O&G Flashcards

1
Q

Components of a gynae hx

A

Personal details

PC

Specific gynaecological questions

Past obstetric hx

Past medical hx

Systems r/v

DHx: allergies, penicillin and latex

FHx

Personal/Social hx

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2
Q

PC in G

A

SOCRATES

NOTEPAD

Impact on QoL

Previous consultations

Order multiple PCs in order of severity/impact on life

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3
Q

Menstrual questions in G Hx

A

FMP

How often, how many days from the first day of bleeding to the next first day?

How long does it last? (/28)

Is it regular or irregular

Heavy (number of pads, flooding, presence of clots)

Is it or the days leading up to it painful

IMB?

PCB?

Vaginal discharge- characterise

Does she experience premenstrual tension?

When was her LMP?

If post-menopausal, has there been PMB?

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4
Q

Sexual/contraceptive questiosn in G

A

Sexually active?

Painful- penetration (superficial dyspareunia) or deep inside (deep), during and or after (delayed)

What contraceptive does she use and has she used in the past?

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5
Q

Cervical smear questions in G

A

When was her last smear

Ever had an abnormal smear?

What was done?

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6
Q

Cervical screening

A

Every 3 years between 25 and 49

Every 5 years between 50 and 64

Not performed after 64 unless never screened or hx of recent abnormal tests

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7
Q

Urinary/prolapse questions in G

A

Frequency (normal is 4-7pd)

Nocturia

Urgency

Leak urine, including when asleep (nocturnal enuresis), if so how severe is it and with what is it associated (e.g. coughing, lifting/straining, urgency)

Dysuria?

Haematuria

Dragging sensation or feel a mass in or at the vagina?

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8
Q

Past obstetric hx in G

A

Have you ever been pregnant?

If yes ask about previous pregnancies in chronological order

Ask how infant was born, weight and how the infant is now. Name

Any major complications in pregnancy or labour?

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9
Q

PMHx in G

A

Previous gynaecological operations

Ask about DVT, DM, lung and CHD, HTN, jaundice etc as in other medical histories

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10
Q

Systems R/V in G

A

CV, Resp, Neuro.

Specifically ask about urinary and GI symptoms

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11
Q

FHx in G

A

FHx of breast, ovarian carcinoma?

DM?

VTE

CHD

HTN

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12
Q

Personal/social history in G

A

Smoke

ETOH

MarriedStable relationship

Support at home?

Where does she live and what sort of accomodation

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13
Q

Allergies in G

A

Ask specifically about penicllin and latex

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14
Q

Abdo exam in G

A

General examination: seek the systemic effects of gynaecological problems and assess general health.

Appearance and weight. T. BP. Pulse and possible anaemia, jaundice or lymphadenopathy.

Comfortably on back with head on pillow. Exposed from xiphisternum to pubic symphysis.

EMPTY BLADDER

Inspect: scars, body hair distribution, irregularities, striae and hernias

Palpate: tenderness, palpate the abdomen generally looking for masses. Then palpate specifically looking for masses from above the umbilicus down to the pubic symphysis. If masses are present, do they arise from the pelvis (can you get below them)

Percuss: look for shifting dullness

Auscultate: BS

Vaginal Examination

Rectal examination

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15
Q

Vaginal examination in G

A

Privacy, explain, use bathroom. Chaperone- name documented in the notes. Use lubricating jelly.

Inspect: vulva and vaginal orifices

Digital bimanual examination

Cusco’s speculum examination

Sim’s speculum examination

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16
Q

Digital bimanual exmaination

A

Assesses pelvic organs

Left hand on aboomen above the pubic symphysis and pushed down so the organs are palpated

Two fingers inserted into the vagina

Uterus: normally the size and shape of a small pear. Size, consistency, regularity, mobility, anteversion/retroversion and tenderness

Cervix: hard or irregular?

Adnexa: lateral to the uterus on either side. Tenderness and size and consistency of any amss assessed. Separate from the uterus

Pouch of Douglas: uterosacral ligaments should be palpable: even, irregular or tender, mass?

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17
Q

Cusco’s speculum

A

Allows inspection of the cervix and vaginal walls.

NB anteverted uterus.

Look for ulceration, spontaneous bleeding or irregularities.

Cervical smear

Slowly withdraw partly closing speculum to allow inspection of the vaginal walls to the introitus and rotate as retract

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18
Q

Sim’s speculum

A

Allows better inspection of the vaginal walls and te prolapse.

Patient in left lateral position.

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19
Q

Rectal examination

A

Appropriate if posterior wall prolapse, to distingusih between an enterocoele and a rectocoele and in assessing malignant cervical disease

May be necessary if a woman complains of cyclical rectal bleeding- ?rectovaginal endometriosis

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20
Q

What is thelarche and when does it begin?

Adrenarche?

Menarche

What controls secondary sexual characteristics?

A

Beginning of breast development: 9-11 y

Growth of pubic hair (11-12)

13y

Oestrogen

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21
Q

D1-4 mensturation

A

Endometrium is shed as hormonal support is withdrawn, myometrial contraction also occurs

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22
Q

D5-13 proliferative phase

A

GnRH stimulate LH and FSH which induce follicular growth

Follicle produces oestradiol and inhibin which suppress FSH.

As oestradiol level rise and reach their maximum they cause a +ve feedback on the hypothalamus/pit and cause LH surge.

Ovulation occurs 36 hours after the LH surge

Oestradiol also promotes endometrial proliferation

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23
Q

D14-28 Luteal/secretory phase

A

Follicle becomes corpus luteum, produces oestradiol but relatively more progesterone, which peaks d21-28

This induces secretory changes in hte endometrium.

Towards the end of the luteal phase, the corpus luteum starts to fail if the egg hasn’t been fertilised and oestradiol/progesterone levels fall.

This decline in hormonal support causes the endometrium to break down, leading to menstruation and the restart of the cycle

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24
Q

What can be used to delay menstruation and why?

A

Continuous administration of exogenous progesterone as it maintains the secretory endometrium

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25
Normal mensturation cut offs
Menarche \<16y Menopause \>45y Mensturation \<8d Blood loss \<80ml Cycle length 23-25 No IMB
26
Menorrhagia
Heavy menstrual bleeding
27
IMB
Bleeding between periods
28
Irregular periods
Periods outside of the range of 23-35d with a variability of \>7d between the shortest and longest cycle
29
Secondary amenorrhoea
Periods stop for 6m or more.
30
Oligomenorrhoea
Irregular periods, \>35d-6m
31
PMB
Bleeding 1 year after the menopause
32
Dysmenorrhoea
Painful periods
33
Premenstrual syndrome
Psychological and physical symptoms worse during the luteal phase
34
Menorrhagia def
Excessive bleeding in otherwise normal menstrual cycle Excessive menstrual blood loss that interferes with the woman's physical, emotional, social and material QoL +/- other smyptoms \>80mL (corresponds to the maximum amount that a woman on a normal diet can lose without becoming Fe deficient)
35
Aetiology and epidemiology HMB (menorrhagia) Rare causes of HMB
1/3rd women complain of HMB Fibroids= 30% HMB Polyps= 10% HMB Thyroid disease, haemostatic disorders and anticoagulant therapy.
36
What differentiates bleeding in malignancy from HMB?
Bleeding in malignancy tends to be irregular
37
Hx in menorrhagia Ex in menorrhagia
Menstrual calendar. Flooding and passage of large clots. Contraception. Anemia. Pelvic signs often absent. Irregular enlargement of the uterus suggests fibroids. Tenderness without enlargement suggests adenomyosis.
38
Ix in menorrhagia
FBC: to check patient's Hb TFTs/Coagulation: to exclude systemic causes (if there are factors indicating this may be the case) Transvaginal USS of hte pelvis: to exclude local organic causes (endometiral thickness, exclude fibroid, mass and detect larger intrauterine polyps (+/- biopsy or hysterectomy if USS is inconclusive)
39
Indications for USS biopsy in HMB
Endometrial thickness \>10mm ?Polyp Woman \>40 with recent onset menorrhagia Treatment failure/ineffective treatment Before insertion of IUS if cycle not regular Prior to endometiral ablation/diathermy as tissue will not be available for pathology If abnormal uterine bleeding has resulted in acute admission
40
Mx of HMB Rx Sx
Exclude pathology Depends on woman's contraceptive needs. 1st line= intrauterine system- not option for woman who wishes to conceive . 90% reduction in blood loss. 2nd line: antifibrinolytics (tranexamic acid) taken during menstruation only. 50% reduction in blood loss NSAIDs (mefanamic acid) inhibit prostaglandin synthesis reducing blood loss by around 30%. NB also useful for dysmenorrhoea. Combined OCP- lighter mesntruation but less effective if pelvic pathology is present. 3rd line: progestogens, high dose orally or by IM will cuase amenorrhoea but bleeding follows withdrawl. GnRH agonists: produces amenorrhoea. Duration is limited to 6 months unless add-back HRT used. **_Sx_** *Hysterposcopic:* Polyp removal (if caused by local abnormalities) Endometrial ablation technique Transcervical resection of fibroid (TCRF). *More radical:* Myomectomy Hysterectomy: Uterine artery ambolisation
41
Features of IUS
Progestogen impregnated IUD is a coil that reduces menstural flow with fewer Ses. Highly effective alternative to medical and surgical treatment. It is contraceptive and also provides the progestogen component of HRT. Distinguish from Cu IUDs that may increase menstrual loss
42
Sx approaches to HMB Hysteroscopic More radical
Hysterposcopic: Polyp removal (if caused by local abnormalities) Endometrial ablation technique: removal/destruction of endometrium- satisfcation is less than with hysterectomy. Most appropriate in older women with pure menorrhagia. Non sterilising. Transcervical resection of fibroid (TCRF). More radical: Myomectomy: removal of fibroids from the myometrium: open or laparoscopic (\<4fibroids, \<8cm diameter). Used if fibroids causing symptoms but fertility is still required. GnRH agonists can be used to reduce size of fibroids first. Hysterectomy: last resort. Uterine artery ambolisation: treats menorrhagia for women who want to retain their uterus.
43
Rx management of HMB
1st line: IUS 2nd line: antifibrinolytics, NSAIDs, OCP 3rd line: progestogens, GnRH analogues
44
When are anovulatory cycles common
Just after menarche and before the menopause
45
What are some causes of IMB/oligomenorrhoea
Anovulatory Pathological: Non malignant Fibroids, uterine and cervical polyps, adenomyosis, ovarian cysts and chronic pelvic infection. Malignant: Overain, cervical and most particulalry endometrial
46
Ix in IMB/oligomenorrhoea
FBC: to asssess the effect of blood loss Ix to exclude malignancy: Cerbical smear USS of the cavity for women \>35 with irregular/IMB and in younger women if treatment has failed, will also detect uterine fibroid or ovarian mass. Endometrial biopsy
47
Mx of Oligomenorrhoea/IMB Rx
Rx where no anatomical cause is detected 1st line: IUS or OCP. 2nd line: 2nd line Rx for menorrhagia Sx: Cervicaly polyp can be excised.
48
Definition of Amenorrhoea
Absence of menstruation 1o= hasn't started by 16, may be manifestation of delayed puberty in which secondary sexual characteristics are not present by age 14. If 2o sexual characteristics are present, problem of menstrual outflow is more likely. 2o= 6m without menstruation in previosly normal mensturation Oligomenorrhoea: \>35d-6m
49
Classification of causes of amenorrhoea
Physiological Pathological
50
Physiological causes of amenorrheoa
Pregnancy, after the menopause, during lactation, constitutional dleay
51
Pathological amenorrhoea Hypothalamus Pituitary Adrenals Ovary Uterus Outflow Tract Drugs
Hypothalamus: Hypothalamic hypogonadism. Pituitary: hyperprolactinaemia; rarer= other pituitary tumours, Sheehan's syndrome Adrenal/Thyroid; hypo/hyperthyroid. CAH/virilising tumours Ovary: * Acquired: PCOS, premature menopause, rare virilizing tumours* * Congnetial: Turner's (most common), other forms of gonadal dysgenesis* Outflow problems: * Congenital: Primary amenorrhoea with normal secondary sexual characteristics. Imperforate hymen and transverse vaginal septum. Rokitansky's syndrome* * Acquired: Usually secodary. Cervical stenosis, Asherman's syndrome, endometrial resection or ablation* Drugs: e.g. antipsychotics, GnRH analgoues, progestogens
52
Hypothalamic hypogonadism Mx
Common, usually due to psychologica, lowe weight or excessive exercise Tumours are a rare cause and may be excluded by MRI. GnRH and FSH/LH and oestradiol are reduced. Bone density may be reduced if there has been prolonged hypo-oestrogenism. Oestrogen replacement (+progesterone for endometrial protection) i.e. OCP/HRT
53
Hyperprolactinaemia Mx
Usually caused by pituitary hyperplasia or adenomas Rx: bromocriptine, carbegoline or Sx
54
Affect of hypothyroidism on prolactin levels
Hyperprolactinaemia leading to amenorrhoea
55
Turners Syndrome
45 XO Short stature, poor secondary sexual characteritsics, normal intelligence. Most common congenital ovarian cause of amenorrhoea
56
Haematoclpos Haematometra
Accumulation of menstrual flow in the vagina or uterus To outflow tract obstruction by either imperforate hymen or transverser vaginal septum
57
Rokitansky's syndrome
Mullerian agenesis Congential malformation characterised by failures of Mullerian duct development resulting in a missing uterus and variable degrees of vaginal hypoplasia. Mullerian agenesis is the aetiology in 15% of cases of primary amenorrhoea
58
Asherman's syndrome
Consequence of excessive curettage in ERPC performed following miscarriage or delivery. Asherman's syndrome, also known as intrauterine adhesions, is a condition where the cavity of the uterus develops scar tissue (adhesions).
59
Mx of osteoporotic risk in primary amenorrhoea
Treat underlying cause Asses # risk. Correct any VitDD and ensure adequate Ca intake. Consider HRT.OCP if amenorrhoea persists for more than 12m
60
What blood results suggests premature ovarian failure?
Persistently elevated FSH and LH in woman younger than 40y/o
61
What factors are suggestive of Asherman's syndrome
Recent Hx of uterine or cervical Sx or severe pelvic infection (endometritis)
62
Definition of PCB
Vaginal bleeding following intercourse that is not menstrual loss Except for first intercourse, this is always abnormal and cervical carcinoma must be excluded.
63
Aetiology of PCB
When the cervix is not covered in health suqamous epithelium it is more likely to bleed after mild trauma.
64
What are the most common causes of PCB
Cervical ectropions Benign polyps Invasive cervical cancer (cervicitis, vaginitis (atrophic)
65
Mx of PCB
Cervical inspection + smear. Polyp- avulsed and sent to histology. Ectropion can be frozen with cryotherapy. Abnormal smear-\> colposcopy
66
Def dysmenorrhoea
Painful menstruation. Associated with high PG levels in the endometrium and is due to contraction and uterine ischaemia.
67
Causes of dysmenorrhoea
Primary: when no orgnaic cause is found. Secondary: when pain is due to pelvic pathology. Fibroids, adenomyosis, endometriosis, PID, ovariant tumours,
68
What differentiates between primary and secondary dysmenorrhoea?
Primary usually coincides with the start of mensturaiton and is very common, particularly in adolescents. Responds to NSAIDs and ovulation suppresions e.g. OCP. Pelvic pathology more likely if medical treatment fails. Secondary: pain often precedes and is relieved by onset of menstruation. Deep dyspareunia and menorrhoagia or irregular mensturation are common. P USS and laparoscopy useful.
69
Def precocious puberty
When menstruation occurs before the age of 10 and/secondary sexual characteristics are evident before age of 8.
70
Causes of precocious puberty Central Ovarian/adrenal
In 80% no pathological cause is found. Central causes: increased GnRH secretion: meningitis, encephalitis, CNS tumours, hydrocephaly and hypothyroieism may prevent normal prepuberatl inhibition of hypothalamic GnRH release. Rx: Ovarian/adrenal causes: increased oestrogen secretion: hormone producing tumours of the ovary/adrenal glands. Regression occurs after removal. McCune-Allbright syndrome.
71
McCune-Albright syndrome
Bone and ovarian cysts Cafe au lait sports Precocious puberty
72
Mx of precocious puberty
GnRH agonists used to inhibit sex hormone secretion causing regression of secondary sexual health characteristics For increased oestrogen secretion cypropterone acetate (antiandrogenic progestogen) can be used
73
CAH in genetic female Aetiology Features Rx
Recessive inheritance. Defective cortisol production usually as a result of 21-hydroxylase deficiency. ACTH exess causes incresed androgen production. Presents at birth with ambiguous genitalia. GC deficiency may cause Addisonian crisis. May present at puberty with enlarged clitoris and amenorrhoea. Cortisol and MC replacemant.
74
AIS in genetic male
Occurs when male has cell receptor insensitvity to androgen which are peripherally converted to oestrogens. Individual appears to be female. Presentation is with amenorrhoea. Uterus absent, rudimentary testes present which are removed due to possible malginant change.
75
Premenstrual syndrome
Psychological, behavioural and physical symptoms that are experienced on a regular basis during te luteal phase of te mesntrual cycle and often resolve by the end of menstruation.
76
Hx in PMS
Cyclical nature rather than symptoms themselves that enable diagnosis. Tnesion, irritability, aggressoin, depression, loss of control. Bloatedness, GI upset, Breast pain
77
Ex in PMS
Menstrual diaries. Psychological evaluation as depression and neurosis may present at PMS
78
Mx of PMS
SSRIs either continuously or intermittently in the second half of the cycle. OCP. GnRH agonists and add back oestrogens. Supplements: evening primrose oil is good for breast tenderness. Pyridoxine 50mg BD can help but may cause neuropathy in excess Vitex agnus-castus extract.
79
Anatomy of the uterus
Superiorly: fundus Laterally to fundus= cornu which is the communication with the fallopiam tubes Supported at the inferior end by the uterosacral and cardinal ligaments. Anteverted in 80% Wall is made of smooth muscle which is lined by endometrium (glandular epithelium) Serosa= peritoneum posteriorly. Also covers the uterus down to the bladder. Laterally the peritoneum is continuouous with the broad ligaments that run between the uterus and pelvic side wall. These are continuous with the fallopian tubest and round ligaements suepriorly and inferiroly contain the uterine blood supply, ureturs and parametrium
80
Uterine blood supply Lymph drainage?
From uterine arteries Pass over the ureturs laterally to the cervix. Pass inferiroly and superiorly supplying the myometrium and endometrium. Anastamose at the cornu with the ovarian blood supply. Inferiorly anastamose with the blood supply to the upper vagina. Lymph to EI Nodes.
81
Blood supply of the dnometrium
Spiral and basal arterioles. Spiral= important in mensturation and nourishment of growing fetus. After ovulation under the influence of progesterone during the luteal phase the glands swell and blood uspply increases.
82
Fibroids definition
Leiomyomata, bening tumours of the myometrium 25% of wmeon. More common near menopause, Afrocaribbean and in FHx. Less common in parous women and those who have taken OCP or injectable progestogens
83
Fibroid sites
Subsersal Intramural Submucosal may form intracavity polyps
84
Aetiology of fibroids
Oestrogen and progesterone dependant Fbiroids regress after menopause
85
Hx in fibroids
50% asymptomatic and discovered at pelvic/abdo exams. Symptoms relate to site rather than size Menstrual problems (30%): menorrhagia, unchanged timing of menses. IMB may occur if fibroid is submucosal or polypoid. Erratic bleeding Pain: dysmenorrhoea, seldom cause pain unless torsion, red degeneration or sarcomatous chnage occur Pressure effects: large fibroids pressing on bladder can cause frequency/urinary retnetion. Hydronephrosis due to ureteric compressoin. Fertility impairment due to obstruction of the tubal ostia or submucous fibroids preventing implamantation. Intramural fibroids that aren't distorting the cavity can also reduce fertility through an unknown mechanism.
86
Ex in Fibroids
Solid mass palpable on pelvic/abdo examination which arises from pelvis and is continuous with the uterus. Multiple small fibroids cause irregular knobbly enlargement of the uterus.
87
Cx of fibroids
Enlargement: can be very slow. Often stop and calcify after menopause although HRT may stimulate further growth. Enlarge in pregnancy. Pedunculated fibroids may undergo torsion Degenerations: result of inadequate blood supply. Red degeneration (more common in pregnancy): pain + uterine tenderness, haemorrhage and necrosis Hyaline/cystic degeneration the fibroid is soft and partly liquefied. Malignancy: 0.1% are leiomyosarcomata. may be malignant change or de novo transformation of myometrium
88
Fibroids in pregnancy
Premature labour Malpresentations Transverse lie Obstructed labour PPH Red degeneration Pedunculated fibroids may tort in post partum period
89
Ix in Fibroids
Dx: USS bu MRI/Laparoscopy may be required to distinguish from ovarian mass Adenomyosis can exist as a fibroid like mass (MRI ddx) Hysteroscopy/hysterosalpingogram to assess distortion of the uterine cavity- if fertility is an issue. To establish fitness: Hb may be low due to vaginal bleeding, may also be high
90
Why may Hb be high in fibroids
They can secrete EPO
91
Mx of fibroids
Asymptomatic with small/slow-growing: no treatment Large fibroids that are not removed should be serially measured by examination or USS. Menorrhagia associated fibroids: \<3cm without distortion of uterine cavity, determine whether woman wants to conceive and use treatment options for menorrhagia: LNG-IUS. Tranexamic, NSAID or OCPs Norethisterone/Depoprovera (Progestetone) \>3cm: refer: Sx intervention. In interim can try NSAIDs/Tranexamic acid. Compressive symptoms: refer Fertility/obstetric symptoms: refer
92
Sx treatment of fibroid
Hysteroscopic: fibroid polyp or small submucous fibroid can be resected. Pretreatment with GnRH agonist for 1-2m can shrink the fibroid, reduce vasculairy and thin the endometirum making resection easier and safer Myomectomy: open or laparoscopic. NB heavy blood loss and small fibroids may be missed. Myomectomy performed if medical treatment has failed but preservation of reproductive function is required. Preceded by 2-3m of GnRH agonist. Perioperative injection of vasopressin into the myometrium reduces blood loss. Adhesions can form at site of myomectomy which can reduce fertility if affecting the endometrial cavity or fallopian tubes. if the endometrial cavity is opened during myomectomy, C-section is indicated in future pregnancy due to risk of rupture. Radical hysterectomy: Pretreatment with GnRH, common indication. Laparoscopic, vaginal or open. Other treatmnents: UAE Ablation
93
Def adenomyosis
Prsece of endometirum and its underlying stroma in the myometrium. Found in 40% of hysterectomy specimens. Associated with endometriosis and fibroids. Symptoms subside postmenopausally.
94
NB in anedomyosis
Endometrial tissues grows into the myometrium. Occassionally may show varying degrees of atypia or invasion
95
Hx of adenomyosis Ex of adenomyosis
Symptoms may be absent but painful, regular, heavy menstruation is common. Uterus is mildly enlarged and tender
96
Dx of adenomyosis
Not easily diagnosed on USS but can be diagnosed on MRI
97
Mx of adenomyosis
IUS OCP +/- NSAIDs may control the menorrhagia or dysmenorrhoea but hysterectomy often required. Oestrogen dependant.
98
Endometritis
Secondary to STI, as a complication of surgery (C-section and intrauterine procedure) or because of foreign tissue e.g. IUD and RPC. Infection in the postmenopausal uterus is commonly due to malginancy
99
Hx and Ex in enodemtritis
Tender uterus with pelvic and systemic infection
100
Pyometra
Pus accumulates in uterus and is unable to escape
101
Mx of endometritis
Antibiotics ERPC
102
Intrauterine polyps
Small bening tumours that grow in to the uterine cavity. Most are endometrial although some come from submucous fibroid. Often found in patients on tamoxifen for breast Ca. Occassionally contian endometrial hyperplasia or carcinoma. Dx at USS/hysteroscopy
103
104
What is the most common genital tract cancer?
Endometrial carcinoma
105
Epidemiology or endometrial carcinoma
Highest prevalence \>60 15% occur premenopausally. \<1% \<35y/o Usually presents early. Adenocarcinoma of columnar gland cells \>90%. Rest is adenosquamous carcinoma- poorer prognosis
106
What increases the risk of endometrial carcinoa?
high oestrogen: progesterone When oestrogen therapy is used unopposed by progestogens
107
Risk factors for endometrial carcinoma Protective
Exogenous: oestrogens without a progestogen Tamoxifen (acts as an agonist in the postmenopausal uterus) Endogenous: Obesity PCOS as it is associated with prolonged amenorrhoea. Nulliparity Late menopause Ovarian granulosa cell tumours (oestrogen secreting) Misc: DM, HTN. Lynch Type 2 syndrome: familal non-polyposis colonic, ovarian and endometrial carcinoma. OCP and pregnancy
108
Premalignant disease in endoemtrial carcinoma
Cystic hyperplasia-\> Endometrial hyperplasia with atypia May cause menstrual abnormalities or PMB Often coexists (40%) with carcinoma elsewhere in the uterine cavity
109
Hx in endoemtrial carcinoma Ex in endometrial carcinoma
PMB: 10% risk of carcinoma. Likelihood that PMB is due to cancer rather than unknown or benign causes increases with age. Premenopausal patients have irregular or IMB or occasionally recent-onset menorrhagia. Cervical semar may contain abnormal columnar cells. Ex: pelvis often appears normal. Atrophic vaginitis may coexist
110
Spread of endometrial carcinoma
Through the moymetrium to the cervix and upper vagina. May be ovarian involvement. Lymphatic spread to pelvci then para-aortic nodes. Staging is surgical and histological and includes LN involvement
111
Endometrial carcinoma staging
Only possible post hysterectomy 1: lesions confined to uterus A: \<0.5 myometrial invasion. B: \>0.5 myometrial invasion Stage 2: as above but in cervix too Stage 3: Tumour invades through the uterus. A: invades serosa or adnexae B: vaginal/parametrial involvement Ci: pelvic node involvement Cii: para-aortic involvement Stage 4: further spread A: bowel or bladder B: distant mets
112
Dx of endometrial carcinoma
USS/hysteroscopy- biopsy required to make diagnosis MRI performe din all patients or if spread is suspected due to other symptoms. CXR to exclude extrapulmonary sprad FBC, RFT, glucose testing. ECG
113
Treatment of endometrial carcinoma
Sx: 75% present with Stage 1. Hysterectomy and bilatreal salpingooophorectomy (BSO) is performed either open or laparoscopically. Routine lymphadenectomy is not beneficial in early stage disase. RTx: External beam radiography used following hysterectomy for those at high risk of LN involvement but not in those with early stage disease. RFs: deep myometrial spread, poor hisotlogy or grade, cerbical stromal involvement. Vaginal vault therapy. Other: Progestogens seldom used. CTx may have a role in high risk early stage and advanced disease.
114
Px for endometrial carcinoma Poor pxic factors
Recurrency common at the vaginal vault. Older age Advanced stage Deep myometrial invasion in Stage 1 and 2 High tumour grade Adenosquamous hisotlogy
115
Uterine sarcomas 3 categories
Rare Leiomyosarcomas: malignant fibroid Endometrial stromal tumours: most common in perimenopausal woman Mixed mullerian tumours: derived from the embryological elements of the uterus and more common in old age. Usually present with irregular/PMB or rapid painful enlargement of a fiborid Treatment with hysterectomy. RTx/CTx can be used adjuvantly but 5 year survival is 30%
116
Px for Endometrial Ca by stage 1 2 3 4
1: 85 2: 70 3-4: 50 4:25 Overall 75
117
First line treatment for dysmenorrhoea?
NSAIDs as they will inhibit PG synthesis, one of the main cuauses of dysmenorrhoea pains.
118
First line treatment in urinary incontinence Urge Stress
Urge: bladder retrianing Stress: pelvic floor muscle training
119
Causes of urinary incontinence
Overactive bladder/urge incontinence: due to detrusor overactivity Stress incontinence: leaking small amounts when coughing or laughing Mixed incontinence Overflow incontinence: due to bladder outlet obstruction e.g. prostate englargement
120
Ix of urinary incontinence
Bladder diaries (\>3d) Vaginal examination to exclude cystocele Urine dipstick and culture
121
Mx of urge incontinence
Conservative: bladder rtraining (lasts for minimum of 6w, idea is to gradually increase the intervals between voiding) Rx: Bladder stabilising drugs: antimuscarinic is first line. Sx: sacral nerve
122
Mx of stress incontinence
Pelvic floor muscle training (minimum of 3 months) Srugical procedures e.g. retropubic mid-uretthral tape procedures
123
Common causes of vaginal d/c Less common causes
Physiological TV BV Gonorrhoea, Chlamydia (rarely PC), ectropion, foreign body, Cervical Ca
124
Features of Candida d/c
Cottage cheese Vulvitis Pruritis
125
Features of TV d/c
Offesnive, yellow/green, frothy d/c Vulvovaginitis Strawberry cervix
126
Features of BV d/c
Offesnive, thin, white/grey, fishy d/c
127
What differentiates between ectopic and threatened miscarriage Ix
Mild suprapubic pain at 10w USS
128
What is the typical symptom of urogenital prolapse
Bearing down, heaviness, dragging sensation
129
Cervical excitation is seen in?
PID and ectopic pregnancy
130
What is the classical history of ectopic pregnancy?
Amenorrhoea Abdo pain Vaginal bleeding In combination with shoulder tip pain- peritoneal bleed
131
What are the types of miscarriage?
Threatened Missed (delayed) Inevitabel incomplete
132
Features of threatened miscarriage
Painless vaginal bleeding before 24w (typically 6-9w) Bleeding often less than mensturation Cervical os is closed Complicates 25% of pregnancies
133
Features of missed (delayed) miscarriage
A gestational sac which contains a dead fetus before 20w without symptoms of expulsion Mother may have light vaginal bleeding/discharge and symptoms of pregnancy which disappear Typically painless Cervical os is closed When the gestational sac is \>25mm and no embryonic/foetal part can be seen it is sometimes described as a blighted ovum or anembryonic pregnancy
134
Features of inevitable miscarriage
Heavy bleeding with clots and pain Cervical os open
135
Features of incomplete miscarriage
Not all products of conception have been expelled Pain and vaginal bleeding Cervical os open
136
Features of complete miscarriage
Spontaenous abortion with expulsion of the entire foetus through the cervice Pain and uterine contractions stop after the foetus has been expelled Dx: USS shows an empty uterus
137
In a female with PMB what is the diagnosis A 72-year-old nulliparous female presents with post menopausal bleeding. She reports that her last cervical screening was 14 years ago. On examination she is found to be obese and hypertensive. What is the most important diagnosis to rule out? Vaginal squamous cell carcinoma Cervical squamous cell carcinoma Endometrial adenocarcinoma Atrophic vaginitis Leiomyosarcoma
In a female with postmenopausal bleeding (PMB), the diagnosis is endometrial cancer until proven otherwise. Although all the options can result in PMB, the question states the most important one to rule out, which in this case would be endometrial adenocarcinoma due to its strong association with PMB and the importance of an early diagnosis prognostically. In addition, the patient in this question has two risk factors for endometrial adenocarcinoma - hypertension and obesity. Other risk factors include diabetes mellitus, polycystic ovarian syndrome, tamoxifen use, late menopause and high levels of oestrogen.
138
Ix of amenorrhoea
Exclud pregnancy Gonadotrophins: low levels indicate hypothalamic cause whereas high levels suggest an ovarian problem (e.g. premature ovarian failure) Prolactin Androgen levels: raised may be seen in PCOS Oestradiol TFTs
139
What are the key signs and symptoms of endometriosis?
Cyclical abdo pain and deep dyspareunia, may be associated with fertility problems
140
What are the classifications of ovarian cysts?
Physiological: follicular, corpus luteum cyst Benign germ cell tumours: dermoid cyst Benign epithelial tumours: serous cystadenoma, mucinous cystadenoma
141
Featrues of follicular cysts
Commonest type of ovarian cyst Due to non-rupture of the dominant follicle or failure of atresia in a non-dominant follicle Commonly regress after several menstrual cycles
142
Features of corpus luteum cyst
If pregnancy doesn't occur corpus luteum cyst usually breaks down and disappears, if this doesnt occur the corpus luteum may fill with blood or fluid and form a cyst. More likely to present with intraperitoneal bleed than physiological cysts.
143
Features of dermoid cysts
Mature cystic teratomas: lined with epithelial tissue Most comon benign ovarian tumour in woman under 30 years. Bilateral in 10-20% Usually asymptomatic Torsion is more likely than with other ovarian tumours
144
Serous cystadenoma
Most common benign epithelial tumour which bears a resemblance to the most common type of ovarian cancer Bilateral in around 20%
145
Mucinous cystadenoma
Second most common benign epithelial tumour Large and amy become massive If ruptures may cause pseudomyxoma peritonei
146
Pseudomyxoma peritonei
Pseudomyxoma peritonei (PMP) is a clinical condition caused by cancerous cells (mucinous adenocarcinoma) that produce abundant mucin or gelatinous ascites.[1] The tumors cause fibrosis of tissues and impede digestion or organ function, and if left untreated, the tumors and mucin they produce will fill the abdominal cavity. This will result in compression of organs and will destroy the function of colon, small intestine, stomach, or other organs. Prognosis with treatment in many cases optimistic,[2] but the disease is lethal if untreated, with death by cachexia, bowel obstruction, or other types of complications. Disease most commonly caused by appendiceal primary cancer
147
A 22 year-old woman and her male partner present to their GP as they been unsuccessfully trying to conceive for 4 months. Her periods have been regular and there is no obvious cause in her history. What is the most appropriate next step in her management? Refer the patient for a laparoscopy and dye test Address how the couple are having sexual intercourse and reassure the patient Refer the patient for a basal temperature test Refer the patient for a luteal phase progesterone test Refer the patient's partner for semen analysis
A healthy couple can expect to take up to one year to conceive. Investigations are therefore usually performed after one year of regular attempts to conceive. It may however be prudent to address any mechanical reasons that are preventing the couple from conceiving, hence the sexual intercourse history.
148
Epidemiology of infertility
Infertility affects around 1 in 7 couples. Around 84% of couples who have regular sex will conceive within 1 year, and 92% within 2 years
149
What are the main causes of infertility? Basic Ix
Male factor (30%) Unexplained (20%) Ovulation failure (20%) Tubal damage (15%) Other causes (15%) Semen analysis Serum progesterone 7d prior to expected next period
150
\<16nmol/l serum progerstogen
Repeat, if consistently low refer to specialist
151
16-30nmol/l serum progestogen
Repeat
152
\>30mnol/l serum progestogen
Indicates ovulation
153
Key counselling points to couples trying to conceive
Folic acid BMI 20-25 Advise regular sexual intercourse very 2-3d Smoking/drinking advice
154
Mx of abnormal cervical smears (around 5% of smears) Moderate dyskaryosis Severe dyskaryosis Suspected invasive cancer Inadequate
Moderate dyskaryosis: consistent with CINII, refer to colposcopy Severe dyskaryosis: Consistent with CINIII refer to colposcopy Suspected Invasive Ca: refer for urgent colposcopy Inadequate: repeat smear, if 3 inadequate samples-\> colposcopy
155
High risk HPV subtypes
16, 18 & 33
156
What are the causative organisms of PID?
Chlamydia- most common N. Gonorrhoeae Mycoplasma genitalium Mycoplasma hominis
157
What are the features of PID?
Lower abdo pain Fever Deep dsypareunia Dyuria and menstrual irregularities may occur Vaginal or cervical discharge Cervical excitation
158
Ix of PID
Screen for chlamydia and Dx
159
Mx of PID
Rx: oral ofloxacin + metronidazole or IM ceftriaxome and oral doxy and oral metronidazole In mild cases of PID, IUD may be left in, however more recent guidelines suggest that removal of IUD may be assocaiteed with better ST outcomes
160
Cx of PID
Infertility Chronic pelvic pain ectopic pregnancy
161
Def of PID
Inflammation/infection of the female pelvic organs including the uterus, fallopian tubes, ovaries and the surroudning peritoneum. Usually as a result of ascending infection from the endocervix.
162
What is the action if a cervical smear shows borderline or low grade dyskaryosis?
If a cervical smear shows borderline or mild (low grade) dyskaryosis, the laboratory will also test the cytology sample for human papillomavirus (HPV). If HPV is found, the woman will be referred for colposcopy within 8 weeks. If HPV is not found, the woman will be returned to the routine screening programme
163
What are the USS features of adenomyosis
Imaging reveals a "boggy" uterus with subendometrial linear striations
164
What is Amsel's criteria for the Dx of BV?
3/4 of: thin, white homogenous d/c clue cells on microscopy: stippled vaginal epithelial cells Vaginal pH \>4.5 Positive whiff test
165
A 53-year-old woman presents with urgency and frequency. Two weeks ago she consulted with a colleague as she felt 'dry' during intercourse. She has been treated for urinary tract infections on multiple occasions in the past but urine culture is always negative. Her only medication is continuous hormone replacement therapy. A vaginal examination is performed which shows no evidence of vaginal atrophy and no masses are felt. An ultrasound is requested: Both kidneys, spleen and liver are normal size. Outline of the bladder normal. 5 cm complex ovarian cyst noted on left ovary. Right ovary and uterus normal What is the most appropriate next step? Refer for urodynamics Pelvic floor muscle training Trial topical oestrogen Urgent referral to gynaecology Refer for bladder retraining
Any ovarian mass in a post-menopausal woman needs to be investigated.- refer to gynae
166
Initial management for ovarian enlargement What are the possible reports
USS Unilocular- more likely to be physiological or benign Complex- multilocular- more likely to be malignant
167
Mx of ovarian enlargement.
Depends on age and symptoms. Premenopausal: conservative approach esp \<35 as malignancy is less common. If the cyst is small (\<5cm) and reported as simple- likely to be benign. Repeat USS in 8-12 w Postmenopausal: physiological cysts are unlikely any postmenopausal woman with an ovarian cyst regardless of nature or size should be referred to gynaecology for assessment
168
How can the risk of ovarian malignancy be calculated?
Serum Ca125 USS Menopausal findigns
169
Definition of premature ovarian failure
Premature menopausal symptoms Elevated gonadtrophin levels \<40y/o
170
Causes of premature ovarian failure
Idiopathic Chemotherapy Autoimmune Radiation
171
Symptoms of premature ovarian failure
Climacteric symptoms: hot flushes, night sweats Infertility Secondary amenorrhoea Raised FSH, LH
172
What is HRT?
Small dose of oestrogen combined with progestogen (in women with a uterus)
173
Side effects of HRT
Nausea Breast tenderness Fluid retention and weight gain
174
Potential Cx of HRT
Increaed risk of breast Ca (increased by addition of a progestogen) Incresed risk of endometrial reduced by addition of a progestogen. Additional risk eliminated if a progestogen is given continuously. Increased risk of VTE, increased by addition of a progestogen Increased risk of stroke Increased risk of IHD if taken more than 10 years after menopause
175
When does the risk of breast cancer in those taken HRT normalise?
After HRT has been stopped for 5 years
176
What are the features of chlamydia infection?
Asymptomatic in ~70% of women and 50% of men Women: cervicitis (discharge, bleeding), dysuria Men: urethral d/c, dysuria
177
Potential complications of chlamydia infection
Epididymitis PID Endometritis Increased incidence of ectopic pregnancies Infertility Reactive arthritis Perihepatitis (Fitz-Hugh Curtis Syndrome)
178
Dx of Chlamydia
NAAT Urine: first void urine sample, vulvovaginal or cervical swab
179
Mx chalmydia
Doxycycline (7d) or azithromycin (1d) If pregnant than erythromycin or amoxicillin For women and asymptomatic men: all partners from 6 months should be contacted For men: all partners from the 4 weeks prior to symptoms Contacts should be treated presumptively
180
Anatomy of the cervix
2-3cm long made up predominantly of elastic connective tissue. Attached posteriorly to the sacrum by the uterosacral ligaments and laterally to the pelvic wall by the cardinal ligaments. Lateral to the cervix is the parametrium which contains conective tissue, uterine vessels and the ureturs
181
Lining of the endovervix Lining of the ectocervix What is the junction between these two types of cell?
Columnar (glandular) epithelium Continuous with the vagina, covered in squamous epithelium Squamocolumnar junction
182
What is the transformation zone Clinical signficance?
Durign puberty and pregnancy, partial eversion of the cervix occurs. The lower pH of the vagina causes the exposed area of clumnar epithelium to undergo metaplasia to squamous epithelium Cells undergoing metaplasia are vulnerable to agents that induce neoplastic change and cervical carcinoma typically originates from this area.
183
Blood supply of the cervix Lymph drainage
Upper vaginal branches of the uterine artery Obturator and itnernal and external iliac nodes, then to common iliac and para-aortic nodes
184
What is the characteristic spread of cervical carcinoma?
Lymph and locally by direct invasion into the uterus, vagina, bladder and rectum
185
Features of cervical ectropion In which people is it common? Symptoms?
When the columnar epithelium of the endocervix is visible as a red area around the os on the surface of the cervix. Due to eversion and is a normal finding in younger women Those who are pregnant/taking the pill Aysmtpomatic, may cause post-coital bleeding.
186
Mx of cervical ectropion
Cryotherapy following colposcopy to exclude carcinoma. Exposed columnar epithelium is also prone to infection
187
Features of acute cervicitis
Rare Results from STD Ulceration and infection occasionally found in severe degrees of prolapse when the cervix protrudes
188
Features of chronic cervicitis
Chronic inflamamtion/infection, often of an ectropion Causes vaginal discharge and may cause inflammatory smears Cryotherapy +/- antibiotics dependant on culture
189
Features of cervical poylps Age group Smyptoms Mx
Benign tumours of the endocervical epithelium More common in women \>40 May be asymptomatic or cause IMB/PCB Small polyps are aveulsed and examined. Still need to Ix bleedign abnormalities.
190
Features of Nabothian follicles
Occur where squamous epitelium has formed by metaplasia over endocevical cells. The columnar cell secreaions are trappped and form retention cysts whcih appear as white/opaque swellings on the ectocervix. Treatment not required unles symptomatic
191
Nabothian follicle
192
Cervical ectropion
193
What is CIN?
Cervical intraepithelial neoplasia Presence of aytpical cells within the squamous epithlium Dyskaryotic exchibiting larger nuclei with frequent mitosis
194
What is the grading of CIN?
CIN-I: mild dysplasia, atypical cells found in the lower third of the epithelium CIN-II: moderate dysplasia, atypical cells foudn in the lower 2/3rds of the epithelium CIN-III: Severe dysplasia, abnormal cells occupy the full thickness of the epithelium= Carcinoma in situ. Malginancy ensures if these abnromal cells invade through the BM
195
Px CINII/III
1/3rd will develop cervical cancer over the next 10 years.
196
Px of CIN-I
Least malignant potential, can progress but commonly regresses spontaneously.
197
When is the peak incidence of CINIII?
\<45, 25-29 years old
198
Which strains of HPV are most frquently associated with cervical cancer? How many are considered high risk?
Types 16, 18, 31 and 33 13/130 different strains, are considered high risk
199
What strains are included in the UK HPV vaccination programme?
Types 16 and 18 as they are responsible for 75 of cervical cancer cases.
200
What other factors increase risk of CIN?
OCP Smoking Immunocompromised
201
Features of UK cervical screening programme
Every 3 years 25-49 Every 5 years 50-64 \>65: offer if they have not had a cervical screenign test since 50 years old or a recent cervical cytology sample is abnormal
202
What is CGIN? What must then be excluded
Cervical glandular intraepithelial neoplasia Adenocarcinoma of the cervix of endometrium should be excluded using both colposcopy and endocervcal curettage or with cone biopsy. Hysteroscopy can be used.
203
Mx of abnromal smear
Normal: continue with normal screening Borderline/mild dyskaryosis: HPV triage: if negative, back to routine recall. If +ve-\> colposcopy Moderate dyskaryosis: colposcopy Severe dyskaryosis: urgen colposcopy CGIN: colposcopy, if abnormality not found-\> hysteroscopy
204
Mx of CINII/III
LLETZ (large loop excision of transformation zone) aka diatheyrmy loop excision.
205
What are the major common complications of LLETZ?
Postoperative haemorrhage- uncommon Risk of subsequent preterm delivery is increased
206
Discussion of abnormal smear with patient
Assume they have cancer- reassure about early warning cells. CINIII- without treatment she has a 30% chance of developing cancer over 8-15 years.
207
Which type of cervical malignancy has a worse prognosis?
Adenocarcinoma
208
What is occult cervical carcinoma?
When there are no symtposm but the diagnosis is made by biopsy or LLETZ
209
Hx in clinical cervical carcinoma? Ex?
PCB, IMB, PMB, an offensive vaginal discharge. Pain is not an early features but later disease which involves ureturs, bladder, rectum and nerves can cause: uraemia, haematuria, rectal bleeding an pain. Smears have usually been missed. Ulcer or mass may be vissible or palpable on the cervix
210
Spread of cervical cancer
Locally: parametrium and vagina and then to the pelvic side wall. Lymphatic spread to the pelvic nodes is an early feature. Ovarian spread is rare with squamous. Haematological spread is later.
211
Staging of cervical carcinoma NB limited due to lack of inclusion of LNs as prognostic consideration
Stage 1: confined to cervix Stage 2: Invasion into the vagina but not the pelvic side wall Stage 3: invasion of the lower vagina or pelvic wall or causing ureteric obstruction Stage 4: invasion of blddder or rectal mucosa or beyond the true pelvis
212
Ix in cervical carcinoma
Dx: Tumour biopsy Vaginal and rectal ecam to assess teh size of the lesion and local invasion. Examination under anaesthetic is performed Cystoscopy for bladder involvement. MRI detects size, spread and LN involvement. To assess patient's fitness for sx: CXR, FBC and U&Es.
213
Treatment of Stage 1aicervical malignancies
Stage 1ai with cone biopsy.: postoperative haemorrhage and preterm labour are the main complications. Simple hysterectomy preferred in older women.
214
Treatment of Stage 1 and 2 cervical malignancy that isn't stage 1ai
Sx or CTx CTx or RTx if: +ve LNs on MRI or after lymphadenectomy. If LNs -ve as an alternative to hysterectomy Surgical resection margins not clear Palliation for bone bain/haemmorrhage. Sx: Wertheim's hysterectomy if LNs not involved. Ovarias left in young monan with squamous carcinoma. Cx: haemorrhage, ureteric and bladder damage, lymphocyst Radical trachedectomy is less invasive procedure for women who wish to conserve fertility. (LNs negatvie|)
215
Wertheim's hysterectomy
Radical abdominal hysterectomy Involves node clearance, hysterectomy and removal of parametrium and upper 1/3rd of vagina Younger women with squamous carcinom are left with ovaries
216
Radical trachedectomy
Removal of 80% of cervix and upper vagina To preserve fertility
217
Stage 2b and worse or +ve LNs
RTx and CTx with platinum agents
218
Mx Recurrent cervix tumours
CTx/RTx Pelvic exenteration can be considered if the disease is central.
219
Pelvic exenteration
Removal of the vagina, the uterus and cervix, the bladder and or the rectum
220
Px for cervical Ca 1a 1b 2 3-4 LNs involved LN-ve Overall
95 80 60 10-30 +ve 40 -ve 80 Overall 65
221
Poor pxic indicators in cervical malignancy
LN +ve Advanced stage Large priamry Poorly differentiated tumour Early recurrence
222
What is usually the cause of death in cervical carcinoma?
uraemia due to ureteric obstruction
223
Stage 1ai/1aii/b in cervical cancer
ai \<3mm depth, \<7mm across aii \<5mm depth, \<7mm across bi clnically visible lesion, greater than ai \<4cm in greatest dimension bii clinically visible lesin, \<4cm
224
Stage 2ai/aii/b in cervical cancer
ai Involvement of upper 2/3rds of vagina without parametrial invasion \<4cm aii \<4cm b Invasion of parametrium
225
Componenets of an obstetric history
Pesronal details PC/HPC Hx of present pregnancy Past obstetric Hx Other Hx: past gynaecological hx, PMH, ROS, DHx, FHx, Social Hx, Allergies, VTE risk
226
PC in ObHx
Why is she in hospital? Common reasons: HTN, pain, antepartum haemorrhage, unstable lie, possible ROM. If the pregnancy has hitherto been uncomplicated, mention this
227
Hx of present pregnancy
Dates: What was the first day of her LMP What was the length of her menstrual cycle, regular? How many weeks gestation (38w= 36w since conception) EDD: Nagle's rule Complications of pregnancy: bleeding, HTN, DM, anaemia, urinary infections, conern about fetal growth, other problems. Ask about hospital admissions during the pregnancy Tests: what tests have been performed e.g. USS, blood tests, prenatal Dx tests
228
Nagle's rule
Subtrate 3m from the date of the LMP, add 7d anjd one year. NB if a cycle \<28d, the EDD will be later and needs to be adjusted (add the number of days \>28 to the date calculated using Nagle's rule. Same applies if shorter.
229
When is the USS dating performed?
11-13w+6
230
USS measurments to date pregnancy
Measurement of crown-rump length between w9 + 14 Head circumference between 14-20w if no early scan and LMP unknown. NB of little use after 20w.
231
What is a consideration re EDD and women recently stopping OCP
Her cycles can be anovulatory and LMP is less useful
232
Past ObHx
Details of past pregnancies in chronological order. Mode and gestation of delivery, if operative, why? Birth weight and sex of the baby Mother/baby had any Cxs? Parity Gravidity
233
Parity
Number of times a woman has delivered potentially viable babies (\>24w) Suffix denotes number of pregnaniecs that have miscarried or been terminated prior to 24w.
234
Nulliparous
Never delivered a potentially live baby, she may have had miscarriages or abortions
235
Muktiparous
Delivered at least one baby at 24w or more
236
Gravidity
Describes the number of times a woman has been pregnant.
237
PGHx in OBHx
Last cervical smear Treated for an abnormal smear Prior contraception Difficulty conceiving
238
PMHx in ObJx
Surgeries CHD HTN DM Psychiatric disease Epilepsy
239
FHx in OBHx
FHx of twins? DM HTN Pre-eclampsia Auto-immune disease VTE or thrombophilia Any inherited disorders
240
SHx in ObHx
Smoke Drink Drugs Stable relationship? Social support Domestic abuse
241
Palpation of the abdomen and what it tells you at \<24w \>24w \>36w
Dates, twins Well-being by assessing size and liquor To check lie, presentation and engagement
242
Ob Ex
General examination Abodminal Examination Consider examination of fundi, reflexes, T, epigastrium, legs, chest etc.
243
General examination in obstetrics
Appearance, T, oedema, anaemia Height and weight Chest, breasts, CVS examined BP and urinalysis Diastolic BP is recorded at as Korotkoff V: when the sound disappears
244
Abdominal examination in pregnancy When is the uterus palpable? Where is it found?
Semi-prone. Exposed from below the breasts to the symphysis pubis. Later pregnancy can include left lateral tilt to avoid aortocaval compression Uterus normally palpable at 12-14w. 20w: umbilicus
245
What may be the cause if a uterus is larger than expected before 20w?
Incorrect dates, full bladder, multiple pregnancy, uterine fibroids, pelvic mass
246
Ob Ex I P P A
I: size of pregnant uterus, look for striae, linea nigra and scars in the suprapubic area. Fetal movements often visible in later pregnancy Palpation: us the fetus adequately grown, is liquor volume normal? what is the lie? What is the presentation? Ausculation: listening over the anterior shoulder the fetal heart should be heard with a Pinard's stethoscope, should be 110-160bpm
247
Steps in palpation
1. Find the funduse using the fingers and the ulnar border of the left hand. Measure the distance to the pubic symphysis with a tape measure. (after 24w this corresponds to the gestation +/- 2cm. Best for small for dates but only 70% sensitive. Look for tenderness or uterine irritability 2. Use both hands to palpate down the fetus towards the pelvis using dipping movements to palpate the fetal parts and liquor volume. Polyhydramnios: bag will be tense and will need to dip far to feel anything. Head can be balloted, breech is softer and cannot be balloted. Lie: longitudinal, transverse, oblique (head/buttocks palpable in one of the iliac fossae) 3. Turn to face the pelvis and press both hands firmly down to assess the presentation. Engagement of the head occurs when the widest diameter descends into the pelvis and is describe as fifths palpable.
248
Fifths palpable
2/5ths= engaged
249
Pawlik's grip
Grasp the presenting fetal part between the thumb and index finger of the examining hand. Uncomfortable and seldom necessary
250
Findings in Ob Ex
Uterine Size: fundus palpable at 12-14w. Umbilicus at 20w. Xiphoid sternum at 36w. Fundal height increases 1cm/week after 24w Presentation: Breech in 20% at 28w. 3% after 37 Engagement: usual in nulliparoius after 37w. Multiparous often not engaged
251
Presnting Ob Ex
252
Gynae Ex presentaiton
253
Definition of preterm delivery? Whenare risks greatest?
24-37w \<34w
254
What are the complications of preterm delivery for the neonate?
Prematurity accounts for 80% of NICU occupancy 20% of perinatal mortality up to 50% of cerebal palsy Chronic lung disease Blindness Minor disability
255
What are the risks at 24w to neonate of preterm delivery?
1/3rd handicapped 1/3rd will die
256
What are the complications of preterm delivery to the mother?
Infection Endometritis C-section
257
Risk factors for spontaneous preterm labour Complications of pregnancy Maternal medical disease Maternal demographs
Previous Hx Lower socioeconomic class Extremes of materanl age Short inter-pregnancy interval Maternal medical disease: renal failure, diabetes, thyroid disease Pregnancy complications: pre-eclampsia, IUGR, male fetal gender, raised Hb, STIs and vaginal infection (BV), previous cerbical surgery, multiple pregnancy, uterine abnormalities, fibroids, UTIs, polyhydramnios, congenital fetal abnormalities, APH
258
Mechanisms of spontaneous preterm labour Multiple pregnancy
Delivery before 34w occurs in 20% of twins and is the mean delivery of triplets Excess liquor, polyhydramnious has the same effect, probably largely mediated by increased stretch
259
Mechanisms of preterm labour Fetal survival response
More common when fetus is at risk: pre-eclampsia and IUGR or there is infection Placental abruption often followed by labour Iatrogenic preterm delivery aims to improve upon this mechanism
260
Mechanisms of preterm labour relating to the reproductive system
Uterine abnormalities e.g. fibroids or congenital abnormalities Cervical incompetence: some follows previous surgery for CIN or multiple dilatations of the cervix, but in others cause is unknown
261
What are the manifestations of infection in pregnancy?
Chorioamnionitis, offensive liquor, neonatal sepsis and endometritis
262
What infective pathogens are risk factors for preterm delivery? What is often seen in preterm delivery caused by infection?
BV, GBS, Trichomonas, Chlamdyia, (commensals) Coexisting cervical component
263
Hx for predicting preterm labour
Those at increased risk Particulalry those with previous Hx of late miscarriage or preterm labour Most women are not identified as high risk on Hx alone
264
Ix for predicting preterm labour
Cervical length on transvaginal sonography is sensitive and specific Defined as from the external to the internal os
265
Prevention of preterm labour
Cervical cerclage (vaginal or abdominal route) usually preprgancny. Ca be used as prophylaxis, prevention or as a "rescue suture" when an incompetent cervix is dilated or Transvaginal progesterone suppositaries or ?antibiotics or fetal reduction or treatment of polyhydramnios through needle aspiration or NSAIDs (if fetal surveillance is intensive) as they reduce fetal urine output or treatment of medical disease
266
NICE guidlines prophylaxis of preterm
Vaginal progesterone or prophylactic cerclage to women: with Hx of spontaneous preterm birth or midtrimester loss between 16 and 34w and in whome a TVUS has been carried out between 16 and 24w of pregnancy and has revealed a cervical length \<25mm Prophylactic vaginal progesterone to women with no Hx of spontaenous preterm bith or miscarriage in whom a TVUS has been performed and reveals a cervical length of \<25mm Consider cerclage in women who have had a TVUS which reveals a cervical length \<25mm and who have had P-PROM or Hx of cervical trauma
267
When is shortened cervical length picked up on TVUS? What is the measurement?
16-24w 25mm
268
What is a consideration for NSAIDs in the foetus?
Can cause premature closure of the FDA
269
What are the contraindications for rescue cervical cerclage? Indications?
Signs of infection or active vaginal bleeding or uterine contractions 16-27+6w with a dilated cervix and exposed unruptured fetal membranes.
270
Hx in preterm labour
Painful contractions, these will stop spontaneously in half of women With cervical incompetence, painless cervical dilatation may occur and woman may experience a dull suprapubic ache or increased discharge Antepartum haemorrhage and fluid loss are common, the latter suggesting ROM
271
Examination in preterm labour
Fever Lie and presentation may be checked Digital vaginal examination is performed unless the membranes have rupture An effaced or dilating cervix confirm the Dx but the course of preterm labour is unpredictable
272
Ix in preterm labour
Cardiotocography and USS to assess fetal state To assess likelihood of delivery: if cervix is effaced fetal fibronectin is helpful. TVS of cerbical length is alos predictive, \>15mm means unlikely Look for infection: vaginal swabs, CRP, WCC (NB steroids will cause it to rise)
273
Broad Mx of preterm labour
Steroids given 24-34w, in those presenting with contraction these can be restricted to women who are fibronectin +ve or have a short cervix, these reduce perinatal morbidity and mortality by promoting pulmonary maturity. NB glucose control. As they take 24h to take effect delivery is often delayed using tocolysis. Repeated doses not recommended Tocolysis: nifedipine or atosiban (oxytocin-R antag) can be given to allow steroids time to act or to allow transfer to a unit with NICU. Delay rather than stop labour and shouldn't be used for more than 24h. Detect and prevent infection Mg Sulphate: neuroprotective for the neonate if given prior to delivery. NB toxic in OD. Mode of delivery in preterm labour
274
Mode of delivery in preterm labour
Vaginal delviery reduces NRDS. Caesarian undertaken only for obstetric indications. Breech is more common in preterm laour Conduct of delivery: membranes are notruptured in membrane. Labour may be slow allowing steroids more time to act. Forceps rather than ventouse are used. Unless immedaite resuscitation is required the cord should not be clamped for 45s. Antibiotics are recommended in actual as opposed to threatened preterm labour due to increased risk and morbidity of GBS
275
NICE Dx of preterm
\<30w clinically suspected preterm labour: treat \>30w: TVU measurment of cervix, \>15mm unlikely preterm labour. Think of alternative dxs. \<15mm treat for preterm If TVS not available, fetal fibronectin +ve: treat, -ve: unlikely in preterm. Do not use TVS and fetal fibronectin in combination to Dx preterm labour
276
NICE Mx of preterm labour
Nifedipine or oxytocin antagonist (atosiban) Maternal corticosteroids Mg Sulphate
277
Definition of preterm prelabour ROM (P-PROM)
Membranes rupture beofre labour at \<37w All the causes of preterm labour may be indicated It occurse before 1/3rd of preterm deliveries
278
What are the Cxs of P-PROM?
Preterm deelivery and follows within 48h of \>50% of cases Infection of fetus or placenta (chorioamnionitis) or cord (funisitis) is common. May be the cause and thus occur before or it may follow Prolapse of the umbilical cord may occur rarely Absence of liquor \<24w can result in pulmonary hypoplasia and postural deformities
279
Hx and Ex in P-PROM
Gush of clear fluid followed by further leaking Ex: lie and presentation are checked. Dx is with a pool of fluid in the posterior fornix on speculum examination Digital examination to exclude cord prolapse if the presentation is not cephalic
280
What are the clinical features of chorioamnionitis?
Contractions or abdo pain Fever Tachycardia Uterine tenderness Coloured or offesnive liquor
281
Ix in P-PROM
Speculum examination, if pooling not observed consider IGF binding proetin 1 test or placental microglobulin-1 test of vaginal fluid If the results are positive, in conjunction with clinical presentation, offer management in keeping with woman having P-PROM, If negative, unlikely she has P-PROM
282
Mx of P-ROM (NICE)
Balance risk of infection with risk of preterm delivery. Identify infection: CRP, WCC, CTG, do not use in isolation Prophylactic antibiotics: Erythromycin (250mg QDS for \<10d or until labour). If erythromycin is CIed consider oral penicllin. Close maternal and fetal surveillance, if gestation reaches 36w, induce labour
283
Why is co-amoxiclav contraindicated in P-PROM as an antibiotic prophylaxis?
Increases risk of NEC in neonate.
284
What are the normal blood changes in pregnancy an and why?
Normally falls to a minmum in the second trimester by about 30/15 Occurs in both normal and chronically hypertensive women due to a reduction in SVR Rises again by term to normal pre-pregnant levels
285
What is the normal increase in protein excretion in pregnancy?
\<0.3g/24h
286
What is the definition of PIH?
When the blood pressure rises by 140/90 Can be either pre-eclampsia or transient HTN Normally after 20 weeks
287
What is pre-eclampsia
HTN and proteinuria (\>0.3g/24h) Appears in hte second half of pregnacny normally with oedema Occasionally proteinuria is absent in early stage of disease
288
What is pre-existing HTN What are the implications?
BP \>140/90 before pregnancy or before 20w gestation or if the woman is on antiHTNs May be 1o or 2o to other disease May also be pre-exisitng proteinuria because of renal disease
289
What are the implications of pre-existing HTN on pre-eclampsia?
6x risk of "superimposed" preeclampsia
290
What is the course of pre-eclampsia
HTN normally precedes proteinuria which is a relatively late sign Variability in time and severity of presentation. The degree of HTN can be used to help asses it Early onset disease tends to be more severe, after delivery may take up to 24h for "cure"
291
Pre-eclampsia epidemiology
6% of nulliparous. Less common in multiparous unless additional risk factors are present
292
What is the recurrence rate of pre-ecl
15% but can be up to 50% if there has been severe disease before 28w.
293
What are the 2 stages of pre-eclampsia pathogenesis
Stage 1: occurs before 20w. Incomplete invasion of spiral arterioles by trophoblasts leading to decreased uteroplacental blood flow. Stage 2: manifestation of disease. Ischaemic placenta induces widespread endothelial cell damage causing vasoconstriction, increased permeability and clotting dysfunction.
294
What are the principal risk factors for pre-ecl
Nulliparity Previous Hx FHx Old maternal age Disorders characterised by microvascular disease: chronic HTN, chronic renal disease, SCD. DM Pregnancies with large placenta: Twin pregnancies, molar, fetal hydrops Autoimmune disease (esp antiphospholipid) Renal disease Obesity
295
What are the classifications for HTN in pre-ecl And pre-eclampsia itself?
\>140/90= mild \>150/100= modetae \>160/100= severe Mild: proteinruia and mild/modearate HTN Moderate: proteinuria and severe HTN with no maternal complications Severe: proteinuria and HTN \<34w or with maternal complications
296
What are the protein cut offs in pre-ecl? Dipstick PCR 24h
Trace: seldom significant +1: possible significant, quantify +2: likely significant, quantify PCR \>30mg/noml: confirmed significant proteinuria 24h collection: \>0.3g.24h
297
Hx of pre-eclampsia Ex
Usually asymptomatic, headache, drowsiness, visual disturbances, N+V or epigastric pain may occur at late stage HTN usually first sign but occasionally absent Oedema may be massive, not postural or of sudden onset Epigastric tenderness suggestive of impending complications Urine dipstick
298
What are the maternal complications of pre-eclampsia?
Eclampsia: grand mal seizures. Mortality can result from hypoxia and concomitant complications. Rx with Mg SO4 CBA: results from failure of cerebral blood flow autoregulation, antiHTNsives can help Liver and coag problems: HELLP syndrome. DIC, liver failure and rupture may occur. Treatment is supportive and may incude MgSO4 prophylaxis Renal failure: fluid balance monitoring, may require haemodialysis Pulmonary oedmea: Severe pre-eclamptic is particulalry vulnerable to fluid overload. PO treated with O2 and frusemide, assisted ventilation. ARDS may develop.
299
What are the fetal complications of pre-ecl?
Perinatal mortality and morbidity are all increased. Stil birth \<34w: IUGR, spontaneous preterm labour. Preterm devliery often required Term: affects grwoth less but still associated with increased morbidity and mortality At all gestations there is an increased risk of placental abruption
300
Dx of pre-ecl Monitoring of pre-eclampsia
If dipstick positive exclude UTI with cultures and quantiy proteins. Blood tests: Hb often high, uric acid elevated. Rapid fall in platelets suggests impending HELLP. ALTs suggest impending liver test or help. LDH levels rise with liver disease and haemolysis RFT: rapidly rising creatinine suggests severe Cxs and renal failure Fetal: USS, umbilical artery doppler and if abnromal CTG to evaluate fetal well-being
301
HELLP syndrome
Haemolysis Elevated Liver enzymes Low Platelets
302
Screening for pre-ecl
HTN and urinaylsis checks in all pregnant women, esp those at high risk. Most common is uterine artery Doppler at 23w.
303
Preventing pre-eclampsia
High risk women: 75mg of aspirin OD from 12w until birth of baby
304
What factors indicate women should be on aspirin for pre-eclampsia risk?
HTN disease during previous pregnancy, CKD, Autoimmune disease, DM, chronic HTN= High risk first pregnancy, \>40y/o, pregnancy interval of more than 10 years, \>BMI, FHx, multiple pregnancy= moderate risk, \>1 of these=aspirin
305
What are the indications for hospital admission according to NICE in pre-ecl
Mild, moderate or sever HTN= admission Significant proteinuria Following admission, should have regular BP monitoring, repeat quanitifcation of proteinuria not necessary. Montor RFT, FBC, LEs
306
What is first line treatment for pre-ecl HTN? Which severities?
Labetalol Moderate and severe, to keep DBP between 80-100 and systolic to \<150
307
Mx of severe HTN or pre-eclampsia
Anticonvulsants: IV Mg SO. Loading dose of 4g followed by a 24hr infusion Anti-HTNs: labetalol (oral or IV), hydralazine (+/- hydralazine) (IV), nifedipine Corticosteroids for fetalo lung maturation: betamethasone (if \<34w)
308
What are the adverse effects of MgSO4
Severe respiratory depression and hypotension Preceded by loss of patellar reflexes NB renal impairment, stop
309
Timing of delivery for pre-eclampsia
\<34w: after discussion with neonatal and anaesthetists and course of corticosteroids if sever HTN develops refractory to Rx. Maternal or fetal indications. \>34w when BP has been controlled and if corticosteroid course complete 34-36+6: depnding on fetal condition \>37w: within 24-48h of onset
310
Conduct of delivery in pre-ecl
\<34w: Csec \>34w: labour can be induced with PGs, epidural analgesisa helps reduce BP. Use anti-HTNs determine need for haematological and biopchemical tests. Do not rountiely limit second stage of labour. if HTN is severe and refractory to treatment, recommend operative birth
311
Post-natal care in pre-ecl
BP: monitor, ask about symptoms each time BP is measured. Monitor bloods Monitor fluid balance. NB PO and ARDS. If urine output is persistently low, use CVP monitoring. If CVP is high (overload) frusemide. If low, fluid but not albumin. If normal and oliguria persists renal failure is likely, K levels indicate need for dialysis BP maintained at 140/90, postnatal treatment is with beta-blocker, nifedipine and ACEI can be seocodn line
312
Aetiology of pre-pregancy 2o HTN
Obesity, DM, renal disease (PCD, RAS, chronic pyelo) Rarer include phaeo, Cushing's, cadiac, coarctation
313
What should be exluded in all hypertensives?
Fundal changes, renal bruit, radiofermoal delay.
314
Ix in pre-existing chronic HTN in pregnacny
To identify secondary HTN, exlude Pheoe as maternal mortality is very high (24h VMA) Look for coexistant disease through renal USS and RFTs Identify pre pregnancy degree of proteinuria to alloiw compairosn later in the pregnancy
315
Mx of pre-pregnancy HTN
Stop ACEI and ARBs due to teratogenicity. Labetalol. Nifedipine second line. Keep dietary Na low. Kepp BP \<150/100. If HTN is severe and refractory offer birth. Screen for pre-ecl Low dose aspirin.
316
Mx of PIH
Take account of additional RFs If HTN is sever admit until moderate levels. Monitor proteinruia at each visit. Labetalol, second line nifedipine, methyldopa Do not offer birth to \<36w unless HTN is severe.
317
Def: APH
Bleeding from genital tract after 24w gestation.
318
What are the causes of APH? Common: Rarer:
Undetermined origin, placental abruption, placenta praevia Incidental genital tract pathology, uterine rupture, vasa preavia, placenta praevia
319
Def: placent praevia Epidimeology How does it change?
Occurs when the placenta is implanted in the lower segment of the uterus Complicates 0.4% of pregnancies at term. At 20w the placenta is low-lying in many more pregancies but appears to move upwards as the pergnancy continues, only 1 in 10 apparently low-lying placenta will be praevia at term.
320
How can placenta praevia be classified?
Marginal (I-II): placenta in lower segment, not over os Major: placenta completely or partially covering os
321
What increases the risk of placenta praecia?
Twins, age of mothers, uterine scarring
322
What are the cxs in placenta praevia?
Obstructs engagement of the head, may necessitate C-sec and cause transverse lie Haemorrhage can be severe and may continue during and after delivery as the lower segement is less able to contract and constrict the maternal blood supply. If placenta implants in previous c-sec scar it may be so deep as to prevent placental separation or even penetrate through the uterine wall into the surrounding structures such as the bladder (placenta accreta and placenta percreta respectively). May provoke massive haemorrhage at delivery and require hysterectomy.
323
Hx and Ex in placenta praevia
Intermittenet painless bleeds which increase in frequency and intensity over several weeks. (1/3rd won't have experienced bleeding before delivery) Ex: breech presentation and transverse lie. No fetal head engagement. Vaginal examination can provoke massive bleeding and is never performed in a woman who is bleeding vaginally until placenta praevia has been excluded. May be found incidentally on USS
324
Ix of placenta praevia
USS Most diagnosed prior to bleeding, if low lying placenta has been dxed at a 2nd trimester USS this is repeated vaginally at 32w to exclude praevia. A placenta \<2cm from the itnernal os is likely to be praevia at term. If close to a previous c-sec scar, 3-d power USS is best to determine if there is placenta accreta. CTG FBC: clotting studies and cross-match
325
Mx of placenta praevia
Admit all women with bleeding. If placenta praevia is found on USS women often stay in hospital until delviery due to risk of haemorrhage. Blood kept available. IV access maintained Steroids if \<34w. If asymptomatic can delay until 37w. Delivery: C-sec at 39w by most senior person available. Intra-operative and PPH are common. May be emergency if bleeding is severe. Accreta or percreta should have been anticipated although it may occur without invasion through a scar. Uterine incision should be made away from the placenta which can be left in situ or hysterectomy. Treatment of haemorrhage can be with compression of the scar after placental removal through a Rusch balloon. Alternatively, hysterectomy
326
Def: placental abruption
When part or all of the placenta separates before fetal delivery. Occurs in 1% of pregnancies
327
Pathology of fetal abruption
Placenta separating may lead to considerable maternal bleeding. Can lead to further placental separation and acute fetal distress. Blood revealed as APH May also enter the liquor Or the moyemtrium (visible haemorrhage is absent in 20%)
328
Types of palcental abruption
Revealed Concealed: bleed into the myometrium
329
Cxs of placental abruption
Fetal death (30% of proven abruptions) Haemorrhage often necessitates blood transfusion: DIC and renal failure may lead to maternal death
330
What are the risk factors for abruption?
**IUGR** **Pre-ecl** **Pre-existing HTN** **Maternal smoking** **Hx of placental abruption (6% risk)** Autoimmune diesase Cocaine usage Multiple pregnancy High maternal parity Trauma Sudden reduction in uterine volume (ROM in woman with polyhydramnios)
331
Hx and Ex in placental abruption
Painful bleeding, often dark. Degree of vaginal bleeding does not reflect severity of the abruption. If pain occurs alone= concealed Ex: tachycardia suggests profound blood loss. hypotension after massvie loss, uterine tender and often contracting. In severe cases the uterus is woody hard and the fetus difficult to palpate. Fetal heart tones abnormal/absent. If coagulation failure has occured, widespread bleeding is evident
332
Ix of placental abruption
Clinical dx Ixs help to establish severity and plan resuscitation CTG: fetal heartbeat, ferquent uterine activity USS may be used to estimate fetal weight and exclude placenta previa but abruption may not be visible. FBC, coagulation screen, cross-match. Catheterisation with hourly UO, regular FBC, Us&Es, CVP monitoring may be required in severe cases.
333
Features of major placental abruption
Maternal collapse Coagulopathy Fetal distress/demise Woddy hard uterus Poor UO or renal failure Degree of vaginal loss is unhelpful
334
Mx of palcental abruption
Admit if pain and uterine tenderness. IV fluids. Steroids if gestation \<34w. Blood transfusion. Opiate analagesia. Delivery: depends on fetal state and gestation: Fetal distress: emergency C-sec No fetal distress but gestation is \>37w induction of labour with amniotomy. Monitor mother and fetal distress. If fetaus is dead: coagulopathy is also likely. Blood products given and labour induced. If there is no fetal distress, pregnacny is preterms and abruption appears to be minor, steroids and pregnancy -\> high risk . PPH is the majory risk
335
336
What is bleeding of undetermined origin
APH small and painless without placenta praevia, may be difficult to find a cause. USS little help.
337
What is vasa praevia
Occurs when fetal BS runs in the membranes in front of the presenting part. rare but occur when the umbilical cord is attached to the membranes rather than the palcenta. Can be detected on USS. When membranes rupture, the vessel may rupture too. Typical presentation is painless, moderate baginal bleeding at amniotomy or SROM which is accompanied by severe fetal distress.
338
NB for APH?
Cervical carcinoma can present in pregnancy. If a cervical smear is overdue the woman with small recurrent or postcoital haemorrhage should undergo speculum exmaintions.
339
Definition of shoulder dystocia Epidemiology. Consequences?
When additional manoeuvres are required after normal downward traction has failed to deliver the shoulders after the head has delivered 1 in 200 deliveries Characteristically results in Erb's palsy (waiter's tip) from excessive traction on the neck leading to damage to the brachial plexus. Delay and unskilled attempts at delivery can be lethal (can be as short as 5 minutes from head to shoulder delivery)
340
Risk factors for dystocia
Large baby (\>4kg although this only accounts for half of all cases) Previous shoulder dystocia Raised maternal BMI Labour induction Low height Maternal diabetes Instrumental delivery Most cases considered unpreventable due to poor ability to predict and the prevention involves C-section
341
Mx of shoulder dystocia
Rapid and skilled intervention Sequence of actions: Because obstruction is at the pelvic inlet, excessive traction is useless. Senior help. Gentle downward traction Legs are hyperextended onto the abdomen Suprapubic pressure applied This method works in 90% alternative methods if this fails involve internal manoeuvres necessitating episiotomy: If the shoulders are transverese, pressure behind the anterior shoulder will rotate it to the widest diameter, combined with pressure on the anterior part of the posterior shoulder (Wood's screw) can force delivery. If this fails, posterior arm is grasped and by extension at the elbow the hand is brought down. The trunk will either follow or rotation of the body using the arm is performed. Last resorts: symphysiotomy Lateral replacement of the urethra with a metal catheter Zavanelli maneuvre: replacement of the head and C-section, usually irreversible fetal damage has occured by this point.
342
McRobert's maneuvre
Leg hyperextnension used in shoulder dystocia
343
Wood's screw manoeuvre
Pressure on anterior shoulder and pressure on anterior part of posterior shoulder used in shoulder dystocia
344
Zavanelli manoeuvre
Reducing head back into uterus prior to c-sec in shoulder dystocia
345
Definition of cord prolapse
Occurs after ROM Umbilical cord descends below the presenting part. Untreated the cord will be compressed or go into spasm and the baby will rapidly become hypoxic. 1 in 500 deliveries
346
Risk factors for cord prolapse
Preterm labour Breech presentation Polyhydramnios Abnormal lie Twin pregnancy (\>50% occur at artificial amniotomy)
347
Dx of cord prolapse
Fetal heart rate abnormality Vaginal palpation of the cord or its appearance at the introitus
348
Mx of cord prolapse
Presenting part must be prevented from compressing the cord: pushed up by the examining finger or tocolytics e.g. terbutaline are given. If the cord is out of the introitus it should be kept warm and moist but not forced back inside. Patient should go on all fours whilst preparation of delivery is undertaken. C-sec usually used but instrumental vaginal delivery is appropriate when the cervix is fully dilated.
349
Def of amniotic fluid embolism
When liqupr enters the maternal circulation causing anaphylaxis with sudden dyspnoea, hypoxia and hypotension. Often accompanied by seizures and cardiac arrest. Acute heart failure is evident. Extremely rare but serious as often causes death. If patient survives for \>30mins she develops DIC, PO and ARDS.
350
Risk factors for amniotic fluid embolism
Membrane rupture, during labour, C-sec, TOP. Multiple mild predisposing factor: strong contractions in the presence of polyhydramnios. Prevention impossible
351
Mx of amniotic fluid emoblism
NB often confused with other causes of collapse and with eclampsia. ABC resusc. O2 and CVP monitoring. Blooods for clotting, FBC, U&Es, cross match. Blood and FFP will be required. ICU admission.
352
Def: uterine rupture
Can be de novo or an old scar. Fetus is extruded. Uterus contracts and bleeds from rupture site causing acue fetal hypoxia and massive internal maternal haemorrhage. Rupture of a lower trasnverse C-sec scar is usually less severe than others as the lower segment is not very vascular. Occurs in 1/1500 pregnancies. and in 0.7% of women who attempt a vaginal delivery after a single previous lower C-sec. Dx made from fetal HR abnormalities, constant lower abdo pain, vaginal bleeding, contraciton cessation, maternal collapse.
353
Risk factors for uterine rupture
Labours with a scarred uterus Classical C-sec or deep myotomy. Rupture before labour is rare Neglected obstrcuted labour is rare in the West. Congenital uterine abnormalities occasionally cause rupture before labour. Preventive mesaures include avoidance of induction and caution when using oxytocin in women with previous C-sec.
354
Mx of uterine rupture
Maternal resus with IV fluid and bloods Bloods taken fro clotting, Hb, X-match Urgent laparotomy for fetal delivery and repair/removal of uterus. Uterine rupture has a high recurrence rate
355
Def uterine inversion
When the fundus inverts into the uterine cavity. Usually follows traction on the placenta and occurs in 1 in 20000 deliveries Haemorrhage, pain and profound shock. Brief immediate attempt to push the fundus up via the vagina. If not, GA and replacement performed with hydrosstatic pressure of several litres of salin which is run past a clenched fist at the introitus.
356
Causes of epileptiform seizures in pregnant
Maternal epilepsy Exlampsia Hypoxia of any cause
357
Mx of epileptfiorm seizures in obstetrics
Assume pre-eclampsia, Mg sulphate ABC
358
What is LA toxicity
Excessive doses or inadvertent IV doses of LA can cause transient cardiac, respiratoey and neurological consequences
359
What is the optimal initial management of cord prolapse in a fully equipped hospital setting?
When cord prolapse is diagnosed before full dilatation, assistance should be immediately called and preparations made for immediate birth in theatre. T here are insufficient data to evaluate manual replacement of the prolapsed cord above the presenting part to allow continuation of labour. This practice is not recommended . To prevent vasospasm, there should be minimal handling of loops of cord lying outside the vagina. To prevent cord compression, it is recommended that the presenting part be elevated either manually or by filling the urinary bladder. Cord compression can be further reduced by the mother adopting the knee–chest or left lateral (preferably with head down and pillow under the left hip) position. Tocolysis can be considered while preparing for caesarean section if there are persistent fetal heart rate abnormalities after attempts to prevent compression mechanically, particularly when birth is likely to be delayed. Although the measures described above are potentially useful during preparation for birth, they must not result in unnecessary delay.
360
What are the aims of antenatal care? (6)
Detect and manage pre-existing maternal disorders that may affect outcome of pregnancy Prevent or detect and manage maternal complications of pregnancy " fetal compications Detect congenital fetal problems Plan with mother the circumstancs of delivery to ensure maximum safety for the mother and baby Provide education and advice regarding lifestyle and 'minor' conditions of pregnancy
361
Preconceptual care, components
Previous pregnancies: implications Health check: better performed before conception Rubella status Strict preconceptual glucose control in diabetics to reduce the incidence of congenital abnormalities Medication optimisation Folic acid supplementation e.g. 0.4mg/day preconceptually. Advice regarding smoking, ETOH, drugs
362
When is the booking visit What is its purpose
Should be before 10 weeks gestation To secreen for potential cxs that may arise during pregnancy: Risk assessment using Hx and Ex. Decide about type and frequency of antenatal care: need to be constantly re-evaluation as the pregnancy proceeds. Check pregnancy gestation and arrange prenatal screening General health chec,
363
Impact of age on pregnancy risk
\<17y/o \>35y/o are at greater risk of obstetric and mediocal cxs. Chromosomal abnormalities increase with age
364
Impact of past obstetric Hx on pregnancy risk
Many obstetric disorders have a small but significant recurrence rate include: preterm labour, small for dates, IUGR, stillbirth, APH, PPH, some congenital abnromalities, rhesus disease, pre-eclampsia, GDM
365
Impact of gynae Hx on pregnancy risk
Hx of subferitility increases perinatal risk: IVF/augmentatin of fertilisation increases likelihood of multiple pregnancy. Previous uterine surgery (e.g. myomectomy) may be an indication for elective C-section Cervical smear Hx
366
Impact on PMHx on pregnancy risk
HTN, DM, autoimmune disease, Hbopathy, thromboembolic disease, CVD, R disease or other serios diseases are at an increased risk of pregancy problems. Direct questions re: depression are useful
367
Impact of FHx on pregnancy risk
DM in first degree relative increases rsik of GDM HTN, thromboembolic, autoimmune disease and pre-eclampsia are also familial
368
Examination at booking visist
General health and nutritional status BMI Baseline BP Incidental disease may be detected e.g. breast carcinoma Abdo examination: limited before third trimester. Uterus palpable from 12w. Fetal heart can be ausucltated at this point. If no recent smear, usually performed 3 months post-natally.
369
Booking visit investigations and details.
USS: 11-13+6 to date using crown-rump length. Also detects multiple pregnancy and allows screening for nuchal translucency. DS screen: nuchal translucency, beta-hCG and pregnancy-associated plasma protein A (PAPPA) = combined test Bloods: FBC (?anaemia). Serum Abs (anti-D) to identify those at risk of intrauterine isoimmunisation. GGT (in those at risk, normally perforemd later in pregnancy). Syphillis test (VDRL). Rubella immunity checked (vaccination postnatally). HIV and HBV screening. Hb electrophoresis. Screening for infections implicatd in preterm labour (e.g. Chlamydia, BV). Urine MC+S because asymptomatic bacteruria in pregnancy can lead to pyelnephritis in (20%) Urinalysis for glucose, protein and nitrites Folic acid supplementation 0.4mg/d Vit d supplementation 10 microg/d recommended for women \>30BMI, SEA or afrocarribean origin or with low sunlight absoprtion. Fe supplementation should not be routine
370
What is the calorific intake in pregnancy? ETOH? Smoking in pregnancy? Dental? Coitus? Infection avodiance Exercise? Seatbelt?
2500 Avoided or \<1 unit Smoking cessation with nicotine replacement therapy Dental cehck up advised Coitus is not contraindicated unless: placenta praevia, or ROMed. Listeriosis is avoided by drinking pasteurised milk and avoiding soft and blue cheese, pate and undercooked or partially cooked prepared foods. Salmonella avoided by cooking eggs and poultry well. Eservices advised. Above and below the bump.
371
What are the two care options for pregnancy in hte UK?
Communiy: core team of midwives. Women can be referred to hospital Consultant-led care Risk assessment for VTE should be considered
372
When is the anomaly USS?
20w: enables detection of most structural fetal abnormalities.
373
What are the USS screening for risk assesments and whena re they performed?
Doppler of the uterine arteries at 23w can be used as a screening test for IUGR and pre-eclampsia. Not performed routinely but in htose at risk
374
What are the NICE recommended appts schedules for antenatal visits in pregnancy?
Uncomplicated: 10 for nulliparous. 7 for multiparous More frequent visits are appropriate for many "high-risk" pregnancies.
375
What are the components of the examination in antenatal visits?
BP Urine dip-\> urine culture/analysis if abnormality found Abdominal exam: lie, engagement (unimportant until 36w) Fetal heart
376
What is the 16w visit in pregnancy for?
Results of screening tests for chromosomal abnormalities. R/v of booking bloods.
377
18-21w purpose of visit
Anomaly scan Repeat scan arranged at 32w if low-lying placenta
378
Purpose of 25w antenatal vist
Exclusion of early onset pre-eclampsia (only in nulliparous)
379
Purpose of 28w antenatal visit
Fundal height FBC and Abs GTT is perforemd if indicated Anti-D given to rhesus-negative women
380
Purpose of 31w antenatal visit
Fundal height, R/v of bloods from 28w (nulliparous only)
381
Purpose of 36, 38, 40 antenatal visits
Fundal height measured Fetal lie and presentation Referral for external cephalic version if presentation if breech (ECV) Pelvic examination inappropriate unless induction is complicated or there is suspicion of obstruction (and placenta praevia has been excluded)
382
Purpose of 41w antenatal visit
Fundal height measure and fetal lie and presentation checked Membrane sweeping is offered as is induciton of labour by 42w.
383
Itching in pregnancy
Common Scleare checked for jaundice and LFTs and bile acids assessed NB although rare liver issue in pregnancy may bpresent with itching
384
Pelvic girdle pain in pregnancy Mx
Formerly pubic symphysis dysfunction Common and causes varying degrees of discomfort PT, corsets, analgesics and even crutches may be used Care with leg abduction required
385
Heartburn in pregnancy Mx
Affects 70%, most marked in supine position Extra pillows are helpful. Diet modification. Antacids can be used Ranitidine in severe cases (NB pre-eclampsia can present with epigastric pain)
386
Backache in pregnancy Mx
Universal and may cause sciatica Most cases resolve after delivery PT, advice on posture and lifting, a firm mattress and corset may all felp
387
Constipation in pregnancy
Common and exacerbated by oral Fe. High fibre intake. Stool softners can be used.
388
Oedema in pregnancy
Common, worsens towards the end (unreliable sign of pre-eclampsia). Sudden increase warrants assessment and FU of BP and urinalyis. Benign oedema is helped by raising feet. Diuretics should not be given.
389
Leg cramps in pregnancy
Affects 30% of women. Treatments unproven but NaCl, Ca salts or quinine may be tried
390
Cause of carpal tunnel syndrome in pregnancy Mx
Due to fluid retention compressing the median nerve. Seldom severe, usually temporary. Splinting of the wrists may help.
391
Vaginitis in pregnancy
DDue to candida infection Common and difficult to treat Itchy, non-offensive, white-grey discharge. Imidazole vaginal pessaires (e.g. clotrimazole) can be used for symptomatic infection.
392
Tiredness in pregnancy
Common, NB often incorrectly attributed to anaemia.
393
Changse in weight in pregnancy
Gain 10-15kg
394
Changes in UT in pregnancy
Uterus increases weight from 50g-1000g Muscle hypertrophy, increased blood flow and contractility. Cervix softens and may start to efface late in third trimester
395
Changes in blood in pregnancy
50% increase in blood volume Increased red cell mass Decreased Hb Increased WCC
396
Changes in CVs in pregnancy
CO: 40% increase Peripheral resitance: 50% reduction BP: falls in mid-regnancy.
397
Changes in lung in pregnancy
Tidal volume: 40% increase No change in RR
398
Changes to Renal Gut Thyroid in pregnacny
Renal blood flow: 40% increase in GFR so creatinine/urea decreased Reduce motility: delayed gastric emptying and constipation Enlargement of thyroid.
399
First trimester Second Third
w1-12 13-27 28-birth
400
Components of a Bishop score Cut offs
Cervical position Cervical consistency Cervical effacement Cervical dilation Fetal station \<5- indicates labour unlikely to start without induction \>9- indicates htat labour will most likely commence spontaneously.
401
402
What is the epidemiology of breech presenation?
present in 25% at 28w. Only occurs in 3% of babies near term
403
What are the different types of breech presentation?
Frank: hips flexed and knees fully extended Footling: one or both feet come first with the bottom at a higher position (rare but carries a higher perinatal morbidity)
404
What are the risk factors for breech presentation?
Uterine malformations: fibroids Placenta praevia Poly/oligohydramnios Fetal abnromality (e.g. CNS malformation, chromosomal disorders). Prematurity (due to increased incidence earlier in gestation)
405
Mx of breech presentation \<36w 36w If reamins breech
Fetaus may turn spontaneously. ECV: success rate of around 60% (RCOG recommend ECV should be offered from 36w in nulliparous and 37 in parous) Planned C-sec or vaginal
406
What information about C-sec and breech is important
Planned C-sec carries a reduced perinatal mortality and early neonatal morbidity for babies with a breech presentation at term compared with planned vaginal birth There is no evidence that the long term health of babies with a breech presentation delivered at term is influenced by how the baby is born
407
Absolite contraindications of ECV
Indication for C-sec irrespective of fetal presentation (e.g. placenta praevia) Severe oligohydramnios or ROM Nonreassuring fetal monitoring test results Hyperextended fetal head Significant fetal or uterine anomaly PLacental abruption Multiple gestation (can be considered for the second twin after delivery of the first twin)
408
What are the relative contraindications of ECV?
Maternal HTN Maternal obesity fetal growth restriction Oligohydramnios Previous C-sec.
409
What differentiates clinically between cholestasis of pregnancy and acute fatty acid of pregnancy?
holestasis of pregnancy is characterised by severe pruritis, whereas acute fatty liver of pregnancy has predominantly non-specific symptoms (e.g. malaise, fatigue, nausea). With a normal FBC and viral screen a diagnosis of HELLP syndrome or viral hepatitis is unlikely.
410
Features of intrahepatic cholestasis of pregnancy (aka obstetric cholestatis) Mx
Intrahepatic cholestasis of pregnancy: caused by impaired bile flow. Leads to build up of bile salts which can then deposit in the skin as well as the placenta. Can be uncomfortable for mohter but may also cause sudden asphyxial events in fetus leading to anoxia and death. pruritus: typically worse on palms, soles and abodmen bilirubin \< 100 occurs in 2nd and 3rd trimester Increased risk of preterm birth Mx: induction at 37w. Ursodeoxycholic acid Vit K supplementaiton
411
Features of acute fatty liver of pregnacny
Rare complication which may occure in third trimester or immediately following delivery Abdo pain, N+V, headache, jaundice, hypoglycaemia, severe disease may result in pre-eclampsia ALT typically elevated e.g. 500u/l Mx: supportive care, stabilised: delivery is the definitive manageemtn NB Gilbert's and DJS may be exacerbated during pregnancy
412
What is the ovarian blood supply? And the ligamental organisation?
From the ovarian artery which anastamoses with branches of the uterine artery in the broad ligament. Overy lie the uretur in the ovarian fossa. Attached to the broad ligament by the mesovarium, the pelvic side wall by the infundibulopelvic ligament and to the uterus by the ovarian ligament
413
From which layer of the ovary does the most common carcinoma derive?
The outer cortex which is covered by germinal epithelium
414
What are the layers of the ovary?
Outer cortex: germinal epithelium Inner medulla: connective tissue and bvs Cortex contains the follicles and theca cells.
415
Whence is oestrogen secretion? What can occur
Granulosa cells in the growing follicles and also by theca cells Rare tumours of these cells secrete oestrogens.
416
What changes occur to the follicles during ovulation
Multiple enlarge every month under influence of FSH Onle one reaches 20mm and ruptures in response to mid cycle LH surge Collapsed follicle becomes a corpus luteum and continues to produce oestrogen and progesterone to maintain the endometrium. If no implantation occurs the corpus luteum involutes and hormone levels decline. If fertilisation occurs hCG from the trophoblast maintains the corpus luteum's function and hormone production until 7-9w when the placenta takes over. Follicular and lutein cysts result from persistence of these structures in nonpregnant women.
417
What are the symptoms of ovarian masses
Often silent and detected either when they are very large and cause abdominal distension or on USS. Acute presentation is associated with "accidents"
418
What are the different types of ovarian cyst accidents?
Rupture of cyst into the peritoneal cavity. Haemaorrhage into a cyst or peritoenal cavity Torsion of the pedcile
419
What are the features of ovarian cyst rupture
Rupture of the cyst contents into the peritoneal cavity causes intense pain. This is especially the cause with an endometrioma or dermoid cyst.
420
What are the features of haemorrhage of a cyst
Can occur into a cyst or the peritoneal cavity. Often causes pain. Peritoneal cavity haemorrhage can occasionally cause hypovolaemic shock
421
What are the features of torsion of the ovary?
Torsion of the pedicle (which is bulky due to the cyst) causes infarction of the ovary and tube and severe pain. Sx and detorsion required urgently to save the ovary
422
What are the features of PCOS?
Causees oligomenorrhoea, hirsutism and subfertility. Actually small multiple, poorly developed follicles rather than cysts
423
What is the most common gonadal dysgeneses?
Turner's
424
Why are benign cysts classified with primary neoplasms of the ovary?
Because they may undrego malignant change
425
What are the three main groups of primary ovarian neoplasms?
Epithelial tumours Germ cell tumours Sex cord tumours
426
What are the most common ovarian masses premenopausally?
Follicular/lutein cysts Dermoid cysts Endometriomas Benign epithelial tumour
427
What are the most common ovarian masses postmenopausally?
Benign epithelial tumour Malignancy
428
Which group of women are epithelial tumours most commonly found in? What are the features of epithelial tumours that make them unique?
Postmenopausal Histology may demonstrate borderline malignancy where malignant histological features are seen without invasion. Such tumours may become frankly malignant and Sx is advised
429
How does the management of borderline epithelial cysts in younger women differ? What is significant following removal of a cyst?
Close observation following removal of the cysts or affected ovary to retain fertility with close observation. Recurrence as a borderline or invasive tumour can occur up to 20y later
430
What is the most common malignant ovarian neoplasm? What is the benign form
Serous adenocarcinoma (50% of malignant neoplasms of the ovary) derives from the peithelial. Serous cystadenoma
431
What proportion of ovarian malignancies is made up of mucinous adenocarcinoma? What are the features?
10% Mucinous cystadenoma can become very large and are less frequently malignant.
432
What is a rare borderline variant of the mucinous cystadenoma? What happens? What should be excluded?
Pseudomyxoma peritonei Abdominal cavity fills with gelatinous mucin secretions. Appendieal primary should be excluded.
433
What proportion of ovarian malignancies are accounted for by endometroid carcinomas?
25% Similar histologically to endometrial carcinoma. with which it is associated in 20%
434
Which ovarian neoplasm has a particulaarly poor prognosis? What proportion of ovarian malignancies are accounted for by this?
Clear cell carcinoma (epithelial tumours) \<10%
435
What are Brenner Tumours
Rare small and usually benign tumours of the ovarian epithelium
436
What are the relavent proprtions of the incidences of the following ovarian malignancies? From which tissue layer do they arise Serous adenocarcinoma Mucinous adenocarcinoma Endometroid carcinoma Clear cell carcinoma
Epiethlium 50% 10% 25% (associated with endometrial carcinoma in 20% of cases) \<10%
437
Whence do germ cell tumours arise? What are the different kingds of GCT?
From undifferentiated primordial germ cells of the gonad
438
What is a teratoma also known as? What tissue do they arise from? What are the features? What is the malignant form?
Dermoid cyst Undifferentiated primordial germs cells of the gonad. Common benign tumours arising in young premenopasual women. May contain fully differentiated tissue from all cell lines. Commonly bilateral, seldom large, asymptomatic. May rupture. The solid teratoma
439
What is a dysgerminoma? Features?
Female equivalent of the seminoma. Very rare, most common ovarian malignancy in younger women. Senesitive to RTx
440
What is the most common ovarian malignancy in younger women?
Dysgerminoma
441
Whence do sex cord tumours arise? What are the different types?
From the stroma of the gona Granulosa cell tumours Tehcomas Fibromas
442
What is a granulosa cell tumour?
Sex cord tumour. Usually malignant but slow growing Rare and found in postmenopausal women. Stimulation of the endometrium may cause bleeding, endometrial hyperplasia, endometrial malignancy and precocious puberty (rarely in young girls)
443
How does a granulosa cell tumour cause endometrial changes? What are these changes?
Secrete high livels of oestrogen and inhibin which can cause bleeding endometrial hyperplasia malignancy
444
What is the tumour marker for granulosa cell tumours? What is used for?
Serum inhibin used to monitor for recurrence
445
What are the features of thecomas?
Rare usually benign Can secrete oestrogens or androgens
446
What are the features of fibromas?
Rare and benign tumours of the sex cord Can cause Meig's
447
What is Meig's?
Ascites and usually right pleural effusions are found in conjunction with a small ovarian mass. Effusion is benign and cured by removal of the mass
448
What is the proportion of ovarian masses are mets? Where are the common sites?
10% of malignant ovarian masses Breast GIT
449
What are Krukenberg tumours
Mets to ovary from gut which contain "signet-ring" cells. Primary malignancy may be difficult to detect and has very poor px
450
What are the features of endometriotic cysts
Endometriosis can cause altered blood to accumulate in "chocolates cysts" In the ovary these are called endometriomas. Rupture is painful though uncommon "Tumour-like condition"
451
What are functional cysts? Which causes more symptoms?
Follicular and lutein cysts are persistently enlarged follicles and CL respectively. Only found in premenopausal women. Protected against by OCP. Lutein cysts. "Tumour-like condition"
452
What is the Mx of functional cysts
Symptomatic treatment. If asymptomatic, cyst is observed with serial USS. Due to remote possibility of malignancy, if an apparent functional cyst \>5mm persists beyond 2 months measure CA125 and consider laparoscopy to remove or drain the cyst
453
What is the 5 year survival rate of ovarian cancer Why
\<35% Due to its silent nature
454
What is the epidemiology of ovarian malignacny
Rates increase with age \>80% in women \>50 Highest age-specific incidence rates in 80-84 OCP use may be protective
455
456
What are the risk factors for ovarian malignancy?
Relate to number of ovulations: Early menarche Late menopause Nulliparity Familial: BRCA1 or 2 (also associated with breast), HNPCC (Lynch, lifetime incidence of bowel 80%) (if \>2 relatives are affected the lifetime risk is 13%) if BRCA1: 50%.
457
What are the protective factors against ovarian malignancy?
Pregnancy Lactation Use of pill
458
Screening for ovarian cancer
Generally foer ealry malignant rather than premalignant Those with BRCA1 and 2 are offered yearly TVUSS and CA125 or prophylactic SPO
459
What are the clinical features in terms of Hx in ovarian malignancy?
Vague/ absent, 70% present with Stage 3-4 disease Warning signs; Persistent abdominal distension (bloating) Feeling full (early satiety) +/- loss of appetite Pelvic or abdo pain Increased urinary urgency and or frequency Vaginal bleeding Ask about breast/GI symptoms as ovarian mass may be met from these sites. NB for overlap with IBS although this usually presents in younger women. Must exclude ovarian cancer in older women.
460
What are the clinical features in terms of Ex in ovarian malignancy?
Cachexia Large abdo or pelvic mass (very large masses are less likely to be malignant) Ascites Breasts should be examined.
461
What are the features that make an ovarian mass more likely to be malignant?
Rapid growth \>5cm Ascietes Advanced age Bilateral masses Solid or septate nature on USS Increased vasculatiry
462
What is the normal spread of ovarian adenocarcinoma?
Usually spreads directly within the pelvis and abdomen (transcoelomic spread) Lymapthic and histological spread can occur. Staging is surgical and histological.
463
What are the stages of ovarian cancer
Stage 1: macroscopically confined to ovaries. 1a: one ovary affected, capsule intact 1b: both ovaries affected, capsule intact 1c: one/both, capsule not intact, or malignant cells in the abdominal cavity (ascites). Stage 2: disease beyond ovaries, confined to pelvis Stage 3: disease is beyond the pelvis but confined to the abdomen (frequent involvement of the omentum, small bowel and peritoneuM) Stage 4: disease is beyond abdomen e.g. lungs or liver parenchyma
464
How is ovarian malignancy detected intiially What is the cut off What is the next action
CA125 should measured in women \>50 with abdominal symptoms. \>35IU/mL USS of abdomen or pelvis If this dentifies ascites or pelvic or abdo mass, urgent referral to secondary care
465
How is ovarian cancer Dx established What is a consideration in women \<40?
CA125 measured if not already done so Measure AFP and hCG as they are at increased risk of germ cell tumours.
466
How is the Risk of malignancy scored for women with ?ovarian cancer What are the possible scores?
RMI= U x Mx CA125 U scored 1 point for: multilocular cysts, solid areas, metastases, ascites, bilateral lesions. M menopausal status: 1= pre, 3= menopausal. CA125= serum level.
467
What is the cut off of RMI?
\>250-\> referred to MDT CT TAP may be performed, but staging usually established surgically.
468
What is the surgical Mx of ovarian Ca
Assess fitness for surgery Midline laparatomy allows assessment of abdo and pelvis Total hysterectomy with BSO and partial omentectomy perfromed. Stage 1: sample retroperitoneal LNs Stage 2 or greater they are all removed through block dissection. Uterus and unilateral ovary may be preserved in younger women following laparoscopic Sx looking to maintain fertility however they require extensive f/u
469
What is the CTx Mx of ovarian Ca?
Confirmed tissue dx. Very early, no CTx Stage 1c: carboplatin 2-4 carboplatin +/- paclitaxel. NB 2/3rds of women with initial response to CTx relapse within 2 years of completing treatment
470
RTx Mx of Ovarian Ca
Only used for dysgerminomas
471
What are the poor Pxic features of ovarian Ca? What normally causes death?
Advanced stage Poorly differentiated tumours Clear Cell tumorus Slow/poor response to CTx Bowel obstruction or perf
472
Symptom control in palliative care of ovarian Ca Pain? N+V Heavy vaginal bleeding Ascites and bowel obstruction
Analgesic ladder, co-analgesics such as antidepressants steroids and cytotoxics may be used. Antiemetics: anticholinergics, antihistamines, dopamine antagonists or 5HT-3 antags (ondanstrenon) High dose progestogens may be helpful. RTx can be used. Ascites: repeated paracentesis. Obstruction can be managed at home and resolution occurs in 1/3rd spontaneously. If partial: metoclopramide (pro-motility and antiemetic) + stool obstructers with enemas for constipation and a trial of dexmethasone. Complete obstruction: cyclizine and odansetron for N+V with hyoscine for spasm. Surgical palliation indicated with acute, single-sight obstruction, may involve insertion of stents. Terminal distress: good symptom control with anxiolytics and analgesics without oversedation
473
What is the definition of palliative care
Active total care of the patient whose disease is incurable Increase QoL Address symptoms
474
Mx of primary dysmenorrhoea
NSAIDs: mefanamic acid and ibuprofen effective in up to 80% ofr women. Combined OCP= second line
475
What is the difference between 1o and 2o dysmenorhhoea
In primary dysmenorrhoea there is no underlying pelvic pathology. It affects up to 50% of menstruating women and usually appears within 1-2 years of the menarche. Excessive endometrial prostaglandin production is thought to be partially responsible. Features pain typically starts just before or within a few hours of the period starting suprapubic cramping pains which may radiate to the back or down the thigh Secondary dysmenorrhoea typically develops many years after the menarche and is the result of an underlying pathology. In contrast to primary dysmenorrhoea the pain usually starts 3-4 days before the onset of the period. Causes include: endometriosis adenomyosis pelvic inflammatory disease intrauterine devices\* fibroids
476
What are the two methods of emergency contraception available in the UK?
Levonorgestrel (single does of a progesterone) Ulipristal (progesterone R modulator)
477
What are the features of levonorgestrel?
should be taken as soon as possible - efficacy decreases with time must be taken within 72 hrs of unprotected sexual intercourse (UPSI)\* single dose of levonorgestrel 1.5mg (a progesterone) mode of action not fully understood - acts both to stop ovulation and inhibit implantation 84% effective is used within 72 hours of UPSI levonorgestrel is safe and well tolerated. Disturbance of the current menstrual cycle is seen in a significant minority of women. Vomiting occurs in around 1% if vomiting occurs within 2 hours then the dose should be repeated can be used more than once in a menstrual cycle if clinically indicated \*may be offered after this period as long as the client is aware of reduced effectiveness and unlicensed indication
478
What are the features of Ulipristal?
a progesterone receptor modulator currently marketed as EllaOne. The primary mode of action is thought to be inhibition of ovulation 30mg oral dose taken as soon as possible, no later than 120 hours after intercourse concomitant use with levonorgestrel is not recommended may reduce the effectiveness of combined oral contraceptive pills and progesterone only pills caution should be exercised in patients with severe asthma repeated dosing within the same menstrual cycle is not recommended breastfeeding should be delayed for one week after taking ulipristal. There are no such restrictions on the use of levonorgestrel
479
What is an alternative to the emergency contraceptive pill and its features?
Intrauterine device (IUD) ## Footnote must be inserted within 5 days of UPSI, or if a women presents after more than 5 days then an IUD may be fitted up to 5 days after the likely ovulation date may inhibit fertilisation or implantation prophylactic antibiotics may be given if the patient is considered to be at high-risk of sexually transmitted infection is 99% effective regardless of where it is used in the cycle may be left in-situ to provide long-term contraception. If the client wishes for the IUD to be removed it should be at least kept in until the next period
480
What are the high risk groups for pre-eclampsia? What is the action taken?
NICE published guidance in 2010 on the management of hypertension in pregnancy. They also made recommendations on reducing the risk of hypertensive disorders developing in the first place. Women who are at high risk of developing pre-eclampsia should take aspirin 75mg od from 12 weeks until the birth of the baby. High risk groups include: hypertensive disease during previous pregnancies chronic kidney disease autoimmune disorders such as SLE or antiphospholipid syndrome type 1 or 2 diabetes mellitus 75mg Aspirin
481
What are the causes of urinary incontinence?
Causes overactive bladder (OAB)/urge incontinence: due to detrusor over activity stress incontinence: leaking small amounts when coughing or laughing mixed incontinence: both urge and stress overflow incontinence: due to bladder outlet obstruction, e.g. due to prostate enlargement
482
What is the initial investigation of UI?
bladder diaries should be completed for a minimum of 3 days vaginal examination to exclude cystocele urine dipstick and culture
483
What is the Mx of urinary incontinence?
Management depends on whether urge or stress UI is the predominant picture. If urge incontinence is predominant: bladder retraining (lasts for a minimum of 6 weeks, the idea is to gradually increase the intervals between voiding) bladder stabilising drugs: antimuscarinic is first-line surgical management: e.g. sacral nerve stimulation If stress incontinence is predominant: pelvic floor muscle training (for a minimum of 3 months) surgical procedures: e.g. retropubic mid-urethral tape procedures
484
D/c features of Candida
'Cottage cheese' discharge Vulvitis Itch
485
Trichomonas vaginalis
Offensive, yellow/green, frothy discharge Vulvovaginitis Strawberry cervix
486
Bacterial vaginosis
Offensive, thin, white/grey, 'fishy' discharge
487
What are the causes of vaginal discharge?
Common causes physiological Candida Trichomonas vaginalis bacterial vaginosis Less common causes Gonorrhoea Chlamydia can cause a vaginal discharge although this is rarely the presenting symptoms ectropion foreign body cervical cancer
488
What are acute causes of pelvic pain? (usually)
Ectopic pregnancy UTI Appendicitis PID Ovarian torsion Miscarriage
489
Hx in ectopic pregnancy?
A typical history is a female with a history of 6-8 weeks amenorrhoea who presents with lower abdominal pain and later develops vaginal bleeding Shoulder tip pain and cervical excitation may be seen
490
Urinary tract infection
Dysuria and frequency are common but women may experience suprapubic burning secondary to cystitis
491
Appendicitis
Pain initial in the central abdomen before localising to the right iliac fossa Anorexia is common Tachycardia, low-grade pyrexia, tenderness in RIF Rovsing's sign: more pain in RIF than LIF when palpating LIF
492
Pelvic inflammatory disease
Pelvic pain, fever, deep dyspareunia, vaginal discharge, dysuria and menstrual irregularities may occur Cervical excitation may be found on examination
493
Ovarian torsion
Usually sudden onset unilateral lower abdominal pain. Onset may coincide with exercise. Nausea and vomiting are common Unilateral, tender adnexal mass on examination
494
Miscarriage
Vaginal bleeding and crampy lower abdominal pain following a period of amenorrhoea
495
Chronic causes of pelvic pain
Endometriosis IBS Ovarian Cyst Urogenital prolapse
496
Endometriosis
Chronic pelvic pain Dysmenorrhoea - pain often starts days before bleeding Deep dyspareunia Subfertility
497
Irritable bowel syndrome
Extremely common. The most consistent features are abdominal pain, bloating and change in bowel habit Features such as lethargy, nausea, backache and bladder symptoms may also be present
498
Ovarian cyst
Unilateral dull ache which may be intermittent or only occur during intercourse. Torsion or rupture may lead to severe abdominal pain Large cysts may cause abdominal swelling or pressure effects on the bladder
499
Urogenital prolapse
Seen in older women Sensation of pressure, heaviness, 'bearing-down' Urinary symptoms: incontinence, frequency, urgency
500
N+V Mx in early pregnancy
Nausea and vomiting are very common in pregnancy, with 70-85% of pregnant women affected. Most cases are mild and do not require treatment, however anti-emetics may be considered if symptoms are persistent, severe and preventing daily activities. Suitable anti-emetics include cyclizine, metoclopramide, prochlorperazine, promethazine, chlorpromazine, domperidone and ondansetron. There is no evidence to suggest that any one of these drugs works better than another.
501
Mx of epilepsy in early pregnancy
Epilepsy affects 0.5% of pregnant women. It is a significant cause of maternal death, and so antiepileptic treatment is continued during pregnancy. However, antiepileptic drugs increase the risk of congenital abnormalities, particularly neural tube defects. Carbamazepine and lamotrigine are the safest drugs to prescribe, whereas sodium valproate should be avoided. This is because it is associated with a higher rate of congenital abnormalities and lower intelligence in children.
502
Preferred drug used in Mx of hyperthyroidism in early pregnancy?
Proplthiouricil
503
Mx of UTI in eraly pregnancy
Nitrofuratonin is preferred Followed by trimethoprim and then cefalexin. NB Nitrofurantoin should be avoided at term due to risk of neonatal haemolysis Trimethoprim should be avoided during early pregnancy due to its action as a folic acid antagonist
504
505
What are the indications for induction of labour?
Indications prolonged pregnancy, e.g. \> 12 days after estimated date of delivery prelabour premature rupture of the membranes, where labour does not start diabetic mother \> 38 weeks rhesus incompatibility
506
What are the methods for induction of labour?
Method membrane sweep intravaginal prostaglandins breaking of waters oxytocin
507
A 19 year-old woman attends her GP for a repeat prescription of her combined oral contraceptive pill (COCP). Since starting it, she has been suffering from severe left sided headaches with changes in her vision before the headache begins. Clinical examination is normal. What is the most appropriate step in her management? Stop the COCP and start treatment on a progesterone only contraceptive pill. Immediately refer her to the emergency department Refer her to a neurologist Commence a different COCP Stop the COCP and start an oestrogen only contraceptive pill
The woman is having migraines with aura - a condition that can increase using the COCP. Women who have migraine with aura should stop the pill immediately - this is because the oestrogen component of the COCP can increase the risk of the women having an ischaemic stroke. A progesterone-only contraceptive pill is therefore the only alternative contraceptive medication that can be prescribed, as the others have oestrogen.
508
What are the factors reducing HIV vertical transmission?
maternal antiretroviral therapy mode of delivery (caesarean section) neonatal antiretroviral therapy infant feeding (bottle feeding)
509
ART in pregnancy
all pregnant women should be offered antiretroviral therapy regardless of whether they were taking it previously if women are not currently taking antiretroviral therapy the RCOG recommend that it is commenced between 28 and 32 weeks of gestation and should be continued intrapartum. BHIVA recommend that antiretroviral therapy may be started at an earlier gestation depending upon the individual situati
510
Mode of delivery in pregnancy (HIV)
Mode of delivery vaginal delivery is recommended if viral load is less than 50 copies/ml at 36 weeks, otherwise caesarian section is recommended a zidovudine infusion should be started four hours before beginning the caesarean section
511
Neonatal antivrial therapy
zidovudine is usually administered orally to the neonate if maternal viral load is \<50 copies/ml. Otherwise triple ART should be used. Therapy should be continued for 4-6 weeks.
512
A 28-year-old pregnant woman is seen at her booking appointment. Her obstetric history revealed she had pre-eclampsia in her last pregnancy. Which of the following medications should this patient be started on at 12-14 weeks gestation to reduce the risk of intrauterine growth retardation?
The following question tests the understanding of secondary prevention of women with pre-eclampsia. There is A level data showing that low-dose aspirin started at 12-14 weeks' gestation is more effective than placebo at reducing occurrence of pre-eclampsia in women at high risk, reducing perinatal mortality and reducing the risk of babies being born small for gestational age . There is some evidence that low molecular weight heparin might reduce the placental insufficiency seen in pre-eclampsia, but long-term safety studies are not yet available. Labetalol and methyldopa are both common antihypertensive drugs used in the acute management of pre-eclampsia, however are not given prophylactically and do not reduce intrauterine growth retardation. Similarly to LMWH, unfractionated heparin has not been proven to prevent the development uteroplacental insufficiency.
513
NICE guidelines suggest that a woman who has a pre-labour rupture of membranes at term...
can either be offered induction of labour approximately 24 hours later or managed expectantly. Induction is often with vaginal PGE2.
514
What is the most appropriate first line investigation in a woman of reproductive age who has not conceived after 1 year of unprotected vaginal intervourse?
The most appropriate first line investigation in this patient is a day 21 progesterone. This is a non-invasive test and can tell you whether the patient is actually ovulating. Both serum prolactin and thyroid function tests are not recommended unless patient's have a specific reason for being tested i.e. a pituitary tumour or signs of overt thyroid disease.
515
What are the risks to the mother and foetus of VZV in pregnancy?
Risks to the mother 5 times greater risk of pneumonitis Fetal varicella syndrome (FVS) risk of FVS following maternal varicella exposure is around 1% if occurs before 20 weeks gestation studies have shown a very small number of cases occurring between 20-28 weeks gestation and none following 28 weeks features of FVS include skin scarring, eye defects (microphthalmia), limb hypoplasia, microcephaly and learning disabilities Other risks to the fetus shingles in infancy: 1-2% risk if maternal exposure in the second or third trimester severe neonatal varicella: if mother develops rash between 5 days before and 2 days after birth there is a risk of neonatal varicella, which may be fatal to the newborn child in around 20% of cases
516
Mx of VZV exposure in pregnant women?
Management of chickenpox exposure if there is any doubt about the mother previously having chickenpox maternal blood should be urgently checked for varicella antibodies if the pregnant women is not immune to varicella she should be given varicella zoster immunoglobulin (VZIG) as soon as possible. RCOG and Greenbook guidelines suggest VZIG is effective up to 10 days post exposure consensus guidelines suggest oral aciclovir should be given if pregnant women with chickenpox present within 24 hours of onset of the rash
517
Features of ectopic pregnancy
A typical history is a female with a history of 6-8 weeks amenorrhoea who presents with lower abdominal pain and later develops vaginal bleeding lower abdominal pain: typically the first symptom. Pain is usually constant and may be unilateral. Due to tubal spasm vaginal bleeding: usually less than a normal period, may be dark brown in colour history of recent amenorrhoea: typically 6-8 weeks from start of last period; if longer (e.g. 10 wks) this suggest another causes e.g. inevitable abortion peritoneal bleeding can cause shoulder tip pain and pain on defecation / urination Examination findings abdominal tenderness cervical excitation (also known as cervical motion tenderness) adnexal mass: NICE advise NOT to examine for an adnexal mass due to an increased risk of rupturing the pregnancy. A pelvic examination to check for cervical excitation is however recommended
518
Examination in ectopic pregnancy?
adnexal mass: NICE advise NOT to examine for an adnexal mass due to an increased risk of rupturing the pregnancy. A pelvic examination to check for cervical excitation is however recommended
519
What are the risk factors for endometrial carcinoma?
obesity nulliparity early menarche late menopause unopposed oestrogen. The addition of a progestogen to oestrogen reduces this risk (e.g. In HRT). The BNF states that the additional risk is eliminated if a progestogen is given continuously diabetes mellitus tamoxifen polycystic ovarian syndrome
520
A 25-year-old woman presents 5 months after having dilation and curettage for a miscarriage. Since this procedure she has not had a period. A pregnancy test is negative. Hysteroscopy is performed which reveals the diagnosis.
Asherman's syndrome, or intrauterine adhesions, may occur following dilation and curettage. This may prevent the endometrium responding to oestrogen as it normally would.
521
Ix in 2o amenorrhoea
exclude pregnancy with urinary or serum bHCG gonadotrophins: low levels indicate a hypothalamic cause where as raised levels suggest an ovarian problem (e.g. Premature ovarian failure) prolactin androgen levels: raised levels may be seen in PCOS oestradiol thyroid function tests
522
Causes of secondary amenorrhoea (after excluding pregnancy)
hypothalamic amenorrhoea (e.g. Stress, excessive exercise) polycystic ovarian syndrome (PCOS) hyperprolactinaemia premature ovarian failure thyrotoxicosis\* Sheehan's syndrome Asherman's syndrome (intrauterine adhesions)
523
Classification of tears following SVD
first degree: superficial damage with no muscle involvement second degree: injury to the perineal muscle, but not involving the anal sphincter third degree: injury to perineum involving the anal sphincter complex (external anal sphincter, EAS and internal anal sphincter, IAS): 3a: less than 50% of EAS thickness torn 3b: more than 50% of EAS thickness torn 3c: IAS torn fourth degree: injury to perineum involving the anal sphincter complex (EAS and IAS) and rectal mucosa
524
Risk factors for perineal tears
Risk factors for perineal tears primigravida large babies precipitant labour shoulder dystocia forceps delivery
525
Mx of mastitis
Mastitis affects around 1 in 10 breast feeding women. The BNF advises to treat 'if systemically unwell, if nipple fissure present, if symptoms do not improve after 12-24 hours of effective milk removal of if culture indicates infection'. The first-line antibiotic is flucloxacillin for 10-14 days. Breast feeding or expressing should continue during treatment. Referral to hospital for review by the surgical team is only appropriate if a breast abscess is suspected. This patient has no palpable lump therefore an abscess is unlikely.
526
Indications for oral antibiotics in mastitis Rx
Infected nipple fissure not improving after 12-24h following effective milk removal Breast milk culture positive Fluclox for 10-14d Erythromycin or clarithromycin if penallergic
527
Predisposing factors for candidiasis
diabetes mellitus drugs: antibiotics, steroids pregnancy immunosuppression: HIV, iatrogenic
528
Mx of candidiasis
options include local or oral treatment local treatments include clotrimazole pessary (e.g. clotrimazole 500mg PV stat) oral treatments include itraconazole 200mg PO bd for 1 day or fluconazole 150mg PO stat if pregnant then only local treatments (e.g. cream or pessaries) may be used - oral treatments are contraindicated
529
Causes of recurrent vaginal candidiasis
compliance with previous treatment should be checked confirm initial diagnosis i.e. high vaginal swab, exclude differential diagnoses such as lichen sclerosus exclude predisposing factors (see above) consider the use of an induction-maintenance regime, with daily treatment for a week followed by maintenance treatment weekly for 6 months
530
Down Syndrome screening tests in pregnancy.
The combined test is recommended at 10-14 weeks gestation. It involves an ultrasound scan for nuchal translucency and a blood test for levels of Beta-human chorionic gonadotrophin (beta-hCG) and pregnancy associated plasma protein A (PAPP-A). In pregnancies with Down Syndrome, PAPP-A is low and beta-hCG raised. If the window for the combined test was missed, at 14-20 gestation, the quadruple test will be offered. This involves a blood test for levels of alfa-fetoprotein (AFP), unconjugated oestriol, beta-hCG and inhibin A. In pregnancies with Down Syndrome, AFP and unconjugated oestriol are low and beta-hCG and inhibin A are raised.
531
Norethisterone 5 mg tds can be used as
a short-term option to rapidly stop heavy menstrual bleeding.
532
Draw the flow chart for the Mx of a woman presenting with menorrhagia
533
Mx of pregnant women with previous Hx of GBS
Group B streptococcus is a bacteria which is put of the natural gut flora and can colonise the vagina. About 50% of babies born to women who carry Group B streptococcus will become carriers themselves but less than 1% will be ill themselves. The largest risk factor for a baby developing Group B streptococcus growth is the mother having a previous baby who has grown it - the risk is increased by a factor of 10. High risk women should be treated with intrapartum antibiotics, this reduces the risk of the baby developing Group B streptococcus. There is no need for antibiotics prior to labour. Having a vaginal or rectal swab will not change management as intrapartum antibiotics would still be recommended even if they were negative. Women who have known GBS carrier status prior to this pregnancy, but have not had a baby with a GBS pregnancy there is not a requirement for IV antibiotics during labour unless another risk factor is present. Offer intrapartum antibiotic prophylaxis using intravenous benzylpenicillin to prevent early-onset neonatal infection for women who have had: a previous baby with an invasive group B streptococcal infection group B streptococcal colonisation, bacteriuria or infection in the current pregnancy.
534
Intrapartum use of GBS for mother antibiotic choice
Benzylpenicllin Clindamycin if penallergic
535
What is first choice empirical antibiotic for use in baby in ?GBS infection
IV benzylpenicillin and gentamicin
536
Risk factors for GBS infection?
Risk factors for Group B Streptococcus (GBS) infection: prematurity prolonged rupture of the membranes previous sibling GBS infection maternal pyrexia e.g. secondary to chorioamnionitis Women found to have GBS infection in the antenatal period should be treated with intravenous antibiotics during labour. This has been shown to reduce early-onset GBS disease in the neonate
537
Extent of the vulva
Area of skin that stretches from the labie majora laterally to mons pubis anteriorly and the perieneum posteriorly. Overlaps the vestibule, the area between the labia minora and the hymen with surrounds the urethral and vaginal orifices
538
What is the epithelium of the vagina What is found anteriorly? Posteriorly? Lymphatic drainage
Squamous epithelium Bladder and urethra Upper third is the pouch of Douglas, lower posterior wall close to the rectum Most occurs via the femoral via the inguinal LNs and to the EIA nodes of the pelvis
539
What are the most common vulval symptoms
Pruritus Soreness Burning Superficial dyspareunia
540
What are the causes of pruritus vulave?
Infections: Candidiasis (+ vaginal d/c) Vulval warts Pubic lice/scabies Dermatological disease: Any condition esp eczma, psoriasis, lichen simplex, lichen sclerosus, lichen planus, contact dermatitis Neoplasia: Carcinoma Premlaignant disease (vulval intraepithelial neiplasia
541
Features of lichen simplex Ix Mx
AKA chronic vulval dermatitis Chronic inflammatory skin condition Presents with severe intractable pruritus, especially at night Labia majora typically inflamed and thicekend with hyper and hypopigmentation. Symptoms can exacerbated by chemical or contact dermatitis May be exacerbated by chemical or contact dermatitis. Linked to stress/ low Fe stores, Vulval biopsy indicated if biopsy in doubt Irritants such as soap should be avoided Emollionts, moderately potent steroid creams and antihistamines
542
Features of liche planus
Affects skin anywhere on the body but particulalry mucosal surfaces Presents with flat, papular purphlish lesions. Can be erosive and more commonly assoicated with pain than pruritus Treatment is with high-potency steroid creams: potent – such as betamethasone dipropionate very potent – such as clobetasol propionate Topical calcineurin inhibitors may be used as second-line therapy Systemic corticosteroids may be used for short periods in severe ongoing disease
543
Features of lichen sclerosus
Vulval epithelium is thin with loss of collagen. May have autoimmune basis and thyroid disease and vitiligo may coexist. Typically postmenopausal. Causes severe pruritis which may be worse at night. Uncontrollable scratiching may cause trauma. Pink-white papules with coalesce. May cause inflammatory adhesions Vulval carcinoma may develop in 5%. Biopsy important to exclude carcinom. treatment with ultra-potent topical steroids.
544
Vulvodynia
Vulvar dysaesthesiia (AKA) Dx of exclusion. No evidence of vulavl disease Can be provoked or spontaneous and subdivided into to site: local or generalised. Hx of UTI, OCP, psychosexual disorders. Topical agents tend to be unhelpful. Oral durgs e.g. amitriptyline or gabapentin used
545
Spontaneous generalised vulvar dysaesthesia
Burning pain that is more common in older patients
546
Vulvar dysaesthesia of the vestibule
Causes superficial dyspareunia or pain using tampons and is more common in younger women in whom introitus damage must be excluded.
547
Features of candidial infection of the vulva
Irritation and soreness of the vulva and anus rather than discharge. topical or oral antifungal therapy may be necessary
548
What is the pathogeneis of Bartholin's cyst/abscess
Blockage of ducts of the glands behind the labia manora causes cyst formation. Infection may occur with Staphy or E Coli and an abscess forms. Treatment is with incision and drainage and marsupialisation.
549
What is marsupialisation
Where an incision is sutured open to reduce the risk of re-formation
550
What are the features of introital damage
Commonly follows childbirth. Overtightening, incorrect apposition at perineal repair or extensive scar tissue can cause superficial dyspareuina. If the introitus is too tight, vaginal dilators or surgey can be used
551
What is Fenton's repair?
The Fenton’s procedure (also called Fenton's repair) is an operation to remove scar tissue and widen the vaginal opening when a woman experiences persistently painful sexual intercourse. Health problems that may require a Fenton’s procedure include: * Lichen planus of the vulva or vagina * Lichen sclerosus of the vulva * Previous surgery on the genitals that results in painful intercourse * Childbirth tears * Episiotomy complications * Radiotherapy to the genitals
552
What is a common error in the consideration of vaginal cysts
Often mistaken for a prolapse
553
What is vaginal adenosis
When columnar epithelium is found in the normally squamous epithelium of the vaginal. Occurs in women whose mothers received diethylstillboestrol in pregnancy Can turn malignant (clear cell carcinoma of the vagina) although often spontaenously resolves. Women with DES exposure in utero undergo annual screening by colposcopy.
554
What is VIN What are the two types
Presence of atypical cells in the vulval epithelium Usual: nearly all VIN is usual. Associated with HPV, CIN, smoking and chornic immunosuppression, Nay be mutlifocal and varied aappearaence. Associated with warty or basaloid SCC. Differentiated: associated with lichen sclerosis, seen in older women, usually unfocal, linked to keratinisiing SCC of the vulva. Higher risk of progression to cancer thean for VIN.
555
Mx of VIN
Pruritus or pain common: emollients or mild topical steroid may help. Gold standard is local surgical excision for symptomatic relief, to confirm histology and exclude invasive disease. 15% of women undergoing excision have unrecongised invasive disease. Therefore if conservative management is used, adequate biopsies must be taken.
556
VIN=
Vulval Intraepithelial Neoplasia
557
Epidemiology for carcinoma of the vulva
5% of genital tract cancers. Most common \>60y/o
558
What is the pathology of vulval carcinoma
95% are SCC. Melanomas, BCC, adenocarcinomas and others accoutn for the rest.
559
Aetiology of vulval carcinoma
VIN is premalignant. However it often arises de novo Associated with lichen sclerosis, ummonsuppresion, smoking and paget's disease of the vulva
560
What is paget's disease of the vulva
Extramammary Paget’s disease (EMPD), also extramammary Paget disease, is a rare, slow-growing, usually noninvasive intraepithelial (in the skin)adenocarcinoma outside the mammary gland and includes Paget's disease of the vulva and the extremely rare Paget's disease of the penis
561
Hx in vulval carcinoma
Pruritus Bleeding or d/c Mass Malignancy often presents late due to unnoticed lesions or embarrassment
562
Ex in carcinoma of vulva
Ulcer or mass Most commonly on the labia majora or clitoris. Inguinal LNs may be enlarged, hard and nodal
563
Spread of vulval carcinoma
Local and via LN-\> superfiical then deep inguinal nodes-\> femoral-\> EIA. Contralateral spread may occur Staging is surigcal and histological 50% present with Stage 1 disease
564
Staging of vulval carcinoma
Stage 1: a: Tumour confined to vulva/perineum, \<2cm in size with stromal invasion \<1mm. Negative nodes. b: Tumour confined to vulva perineum, \>2cm in size or with stromal invasion \>1mm. negative nodes. Stage 2: tumour of any size with adjacent spread, negative nodes. Stage 3: tumour of any size with positive inguinofemoral nodes. Stage 4: tumours invades upper urethra/vagina/rectum, bladder, bone or distant metastases (IVA vs IVB)
565
Ix of vulval carcinoma
Biopsy Fitenss for surgery: CXR, EXG, FBC, U&E, X match
566
Treatment of vulval carcinoma
Stage 1a: wide local excision For other stages: WLE and groin lymphadenectomy through skin-sparing incisions. If the tumours doesn't extende to within 2cm of midline unilateral excision of LNs has emerged. This has replaced the radical vulvectomy. Cxs: wound break down, infection, lymphoaedma, lymphocyst formation and sexual and body image probelms. RTx may be used for large tumours prior to Sx.
567
Px of vulval carcinoma
Many patients die from other age-related disease Surival at Stage 1: \>90% Stage 3-4: 40%
568
Features of secondary vaginal carcinoma
Common and arises from local infiltration from cervix, endometrium or vulva or from metastatic spread from cervix, endometrium or GI tumours
569
Features of rpiamry carcinoma of the vagina
2% of all genital tract malignancies. Affects oder women and is usually squamous. Presents with bleeding or discharge and a mass or ulcer is evident. Treatment with intravaginal RTx or radical surgery. Survival at 5y: 50%
570
Features of clear cell adenocarcinoma of the vagina
Most common in the late teenage years. Most are a rare Cx of DES prescription to mother during pregnacies to try to prevent miscarriage in 1950-70. Radical surgery and RTx: good survival
571
What is the importance of infection in pregnancy?
Maternal illness may be worse e.g. varicella Maternal complications: HIV infection implicated in pre-eclampsia Preterm labour Vertical transmission can cause miscarriage, can be teratogenic or damage developed organ or can cause serious infection in child. Neurologic damage is more common in present of bacterial infrection Antibiotic usage may be limited by potential adverse effects on foetus.
572
Features of CMV
Herpesvirus transmitted by personal contact. Up to 1% of women develop CMV infection, usually subclinical in pregnancy. Common cause of handicap and deafness
573
Fetal effects of CMV infection
Vertical transmission occurs in 40% 10% of infected neonates are symptomatic at birth with IUGR, pneumonia and thrombicytopenia. Most of these will develop serious neurological sequelae: hearing, visual and mental impairment or die Asympthomatic neonates are at risk of deafness.
574
Dx of CMV infection
USS abnromalities inconsitently present but include intracranial or hepatic calcification. Most diagnoiesd using CMV testing. CMV IgM remains positive a long time after infection, which could predate pregnancy, titres willl rise and IgG avidity will be low with recent infection. If maternal infection confirmed: amniocentesis \>6w post maternal infection will confirm or refute vertical trnsmission
575
Mx of CMV infection in pregnancy
Most infected neonates are not seriously affected. Close surveillance for USS abnormlities and fetal blood sampling at 32w may help determine those at greatest risk for severe sequelae. No prenatal treatment and termination may be offered. Routine screening not advised.
576
Herpes simplex virus features
Responsible for most genital herpes Less than 5% of pregnant women have a history of prior infection but man more have Abs
577
Fetal/neonatal effects of HSV
Not teratogenic. Neonatal infeciton is rare but has a high mortality. Vertical transmission occurs at vaginal delivery, particularly if vesicles are present. More likely to occur in context of recent maternal infection because the fetus will not have maternal Abs (Risk \>40%)
578
Dx of HSV infection
Cliinically and swabs are of little use
579
Mx of HSV infection in pregnancy
Referral to GU clinic C-section for those delivering within 6w of primary attack and those with genital lesions from primary infection at time of infection. Risk is less in recurrent herpes and they can have normal labour. Daily aciclovir in late pregnancy may reduce the frequency of recurrences at term. Exposed neonates are given IV aciclovir.
580
NB if there are CNS features in child at risk of HSV infection
LP shuld be performed Aciclovir IV until infection excluded
581
Features of rubella in pregnancy
Congenital rublleea is very rare in UK due to immunisation
582
Effects of rubella on fetus
Maternal infection causes multiple fetal abnromalities including deafness, cardiac disease, eye problems, rmental retardation. Probability and severity decreases with advancing gestation. At 9w the risk is 90% if after 16w risk is very low.
583
Mx of rubella in pregnancy
If a non-immune woman develoips Rubella before 16w, TOP offered. Screening routine at booking to identify those in need of vaccination after end of pregnancy. Rubella vaccine is live and thus contraindicated in pregnancy.
584
Features of toxoplasmosis in pregnancy
Caused by T. gondii Follows contact with cat faeces, soil or eating infected meat. Infection in pregnancy occurs in 0.2% of women in UK but is more common in europe
585
Fetal/neonatal effects of toxoplasmosis
Fetal infection occurs in \<50% More common as pregnancy progresses. Earlier infection leads to more severe sequelae: mental retardation, convulsions, spasiticities and visual impairment.
586
Dx of toxoplasmosis in pregnacny
USS may show hydrocephalus Maternal infection diagnosed after IgM testing. Flase positives and negatives are common Can be diagnosed or excluded using amniocentesis after 20w.
587
Mx of toxoplasmosis
Health education to reduce risk of toxoplasmosis Spiromycin intiated once maternal infection confirmed. Additional combination therapy may be used following confirmation of vertical transmission although TOP may be requested.
588
Features of VZV
Chickenpox in pregnancy is rare but can cause severe maternal illness
589
Fetal/neonatal affects of VZV
Teratogenicity is a rare consequence of early pregnacny infection (which is immediately treated with oral aciclovir). Maternal infection in the 4w preceding pregnancy may cause severe neonatal infection, this is most common if delivery occurs within 5d or 2d before maternal symptoms
590
Mx of VZV in pregnancy
Ig used to prevent and aciclovir to treat infection. Pregnant women exposed are tested to confirm immunity. Ig recommended if they are non-immune Aciclovir if infection occurs. In late pregnancy neonates delivered in the risk period are given Ig. closely monitored and aciclovir if infection occurs.
591
What are the infections screened for in pregnancy
Asymptomatic bacturia: MSU Chlamydia (\<25y/o) HBV HIV Rubella Syphillis
592
Why should parvovirus B19 be tested for if ?Rubella in pregnancy?
As they are clinically indistinguishable.
593
How to treat pain or fever in pregnancy
Paracetamol Ibuporfen may be considered but should not be used beyoind 27w gestation.
594
Features of parvovirus B19 infection
Infects 0.26% of pregnant women and more during epidemics Slapped cheek is calssic but many have arthralgia or are asymptomatic
595
Fetal/neonatal effects of B19
Virus suppresses fetal erythropoiesis causing anaemia and variable degrees of thrombocytopenia Fetal death occurs in 10% of pregnancies usually before 20w
596
Dx of B19
Where materanl exposure or syymtpoms have occurred maternal IgM testing will prompt fetal surveillance Anaemia is detectable on USS as increased blood flow velocity in the fetal middle cerebral arteral and subsequently as oedema (fetal hydrops) from fetal heart failure. Maternal testing may also follow identification hydrops Hydrops and anaemia spontaneously resolves in 50%
597
Mx of B19
Mothers infected are regulalry sacanned Where hydrops is detected, in utero transfusion is given is this is severe. Evidence of severe disease being associated with neurological damage
598
Features of GBS infection in pregnancy
Caused by carriage of Streptococcus agalactiae which is asymptomatic in about 25% of pregnant women
599
Neonatal effects of GBS
The fetus can be infected during labour after ROM. Most commmon in pre term labour or PROM. Maternal fever Early onset GBS occurs in 1 in 500 neonates. Causes severe illness and has a 6% mortality in term and 18% mortality in preterm. IV benzyl can prevent vertical transmission
600
Risk factors for GBS transmission
Previously affected neonate Positive urinary culture for GBS Preterm labour ROM \>18h Maternal fever in labour Treatment is usual for incidental GBS carriage.
601
Strategy 1 vs Strategy 2 for GBS
Strategy 1= treatment based on RFs Strategy 2: screening with vaginal and rectal swabs at 35-37w Treat with IV benzlypenicillin in labour if swabs positive or RFs present
602
Features of HBV in pregnancy
Persitent HBV infeciton presint in 1% of pregnant women up to 25% in those from Asia and Africa. Degree of infectivity depends on Ab status. HBsAb are immunologically cured and of low infectivity. Those with surface Ag but not Ab and those with E Ag are more infectious
603
Neonatal effects of HBV infection
Vertical transmission occurs at delivery. 90% of infected neonates become chronic carriers compared to 10% of adults
604
Mx of HBV infection
Neonatal immunisation reduces the risk of infection by over 90%. Maternal screening is routine in Offer tenofovir disoproxil to women with HBV DNA greater than 107 IU/ml in the third trimester to reduce the risk of transmission of HBV to the baby UK Advise women that there is no risk of transmitting HBV to their babies through breastfeeding if guidance on hepatitis B immunisation has been followed, and that they may continue antiviral treatment while they are breastfeeding.
605
Maternal effects of HIV in pregnancy
Does not hasten progression to AIDS Increased incidence of pre-eclampsia (may be increased by ARTs) Gestational diabetes may be more commmon
606
Neonatal/fetal effects of HIV
Stillbirth, pre-eclampsia, IUGR and prematurity more problem Congenital abnormalities aren't and ARTs not teratogenic NB Folic acid antagonists may be prescribed to HIV infected women. The most important risk is of vertical transmission, beyond 36w, intrapartum or during breastfeedings. 25% of infected neonates develop AIDS by 1y, 40% will develop AIDS by 5y
607
Mx of HIV in pregnancy
HIV +ve women should be managed in conjunction with their physician and have regular CD4 and viral load tests. Prophylaxis against PCP if low CD4 Drug toxicity monitored with LFT, RFT, Hb and blood glucose. Ix for genital tract infections. HAART including zidovudine which reduces viraemia and maternal disease and should be continued throughout pregnancy and delivery. Neonate treated for the first 6w. Therapy in women not already taking HAARTs is usally started at 28w. C-section Reduces vertical transmission to \<1%
608
Features of GAS
Traditionally responsible for puerperal sepsis. Most common bacterium associated with maternal death in which sepsis is the leading cause (50%). Caused by strep pyogenes, NB sore throat. Infection during as opposed to after pregnancy is usally from children. Chorioamnionitis. abdo pain, diarrhoea and severe sepsis may ensue. Infected fetus usually dies in utero Early recognition, culture and high dose antibiotics and ITU required in severe cases..
609
IFV in pregnancy
Immunisation recommended Oseltamivir and zanamivir Admit esp if respiratory symptoms
610
Syphillis in pregnancy
Active disease in pregnacny usually causes miscarriage, severe congenital disease or stillbirth Benzylpenicillin will prevent but not reverse fetal damage. VDRL used for screening/ PCR
611
Implications of TB in pregnancy
Tuberculin testing is safe BCG is live and contraindicated. Dx in late pregnancy is associated with prematurity and IUGR. Treatment with first line drugs and vitamin B6 is safe in pregnancy Streptomycin is contraindicated
612
Implications of HCV infection in pregnancy
Vertical transmission occurs in 6% and is increased by HIV coinfection and high viral load. Infected neonates are prone to chronic hepatitis. C-sec doesn't reduce vertical transmission. Screening restricted to high risk groups
613
Maternal cxs of malaria infection
Severe anaemia and other problems are more common
614
Fetal cxs of malaria
IUGR and stillbirth are more common Congenital malaria complicates 1% of affected pregnancies Artemisin combination therapy appears safe. Intermittent preventative treatment of 2 dosease at least a month apart can prevent maternal and neonatal infection
615
Where is L monocytogenes found? What does it cause? Dx? Prevention
Gram negative bacillus found in pates, soft cheeses and prepacked meals Causes nonspecific febrile illness. If bacteraemia occurs in pregnancy then a potentially fatal infection of the fetus may occur. Blood cultures Avoidance of high risk food.
616
What are the implications of chlamydia/gonorrhoea infection in the neonate
Associated with preterm labour and neonatal conjunctivitis.
617
Treatment of of chlamydia in pregnancy?
azithromycin or erythromycin. NB tetracycline causes fetal tooth discolouration
618
Treatment of gonorrhoea in pregnancy
Cephalosporins due to high prevalence of penicllin resistance
619
Most common causes of BV Implications in pregnancy Mx
Gardnerella vaginalis and mycoplasma hominis Preter, labour and late miscarriage more common Screning and treatment with oral clindamycin reduces the risk of preterm birth.
620
Anatomy and function of the female lower UT system
Voluntary control of urine release achieved by the bladder and urethra Normal function of the filling phase relies upon adequate bladder capacity and competent urethral sphincter. Normal function of the voiding phase is dependant upon detrusor contractility and coordinated urethral relaxation. Bladder has a smooth muscle wall: detrusor muscle Can store around 500mL or urine although first urge to void is at 200mL. Drained by the urethra which is 4cm long and has a muscular wall and external orifice in the vestibule
621
Nervous control of the bladder
PNS: aids voiding SNS: prevent Afferent fibres respond to bladder wall distension Effeerent PNS bass back to the detrusor muscle and cause contraction. Efferent SNS fibres also pass to the detrusor and are inhibted. This is the micturition reflex and is controlled at the level of the pons. The cerebral cortex modulates this through relaxation or contraction of the pelvic floor and the striated muscle of the urethra
622
What are the factors that influence continence.
Prssure in the urethra being greater than in hte bladder. Bladder pressure is influenced by detrusor pressure and intra-abdominal pressure. Urethral pressure is influenced by the inherent urethral muscle tone and by external pressure (pelvic floor and intra-abdominal pressure). The detrusor muscle is expandable, as bladder fills there is no increase in pressure. Increases in abdominal pressure are transmitted equally to the bladder and upper urethra. Therefore coughing does not normally lead to urinary incontinence.
623
When does micturition occur
When bladder pressure exceeds urethral pressure. Achieved volunterily by simultaenous drop in urethral pressure (partly due to pelvic floor relaxation) and in bladder pressure due to detrusor contraction.
624
What are the two main causes of female incontinence?
Uncontrolled increases in detrusor pressure Increased intra-abdominal pressure transmitted to bladder but not urethra Rarer causes include urine bypassing the sphincter through a fistula Or pressure overwhelming the sphincter due to overfilling of thbladder due to neurogenic causes Or outflow obstruction leading to overflow incontiinece
625
What are the implications of uncontrolled increases in detrusor pressure Most common cause
Increased bladder pressure beyond that of the normal urethra due to OAB or urinary urge incontinence (previously called detrusor instability) i
626
What are the implications and cause of increased intra-abdominal pressure transmission to the bladder but not the urethra?
Incontininece, normally as a consequence of the urethral neck slipping from the abdomen. Bladder pressure therefore exceeds urethral pressure when intra-abdominal pressure is raised. This is most commonly caused by urinary stress incontince
627
What are hte common urinary symptoms?
Incontinence Daytime frequency Nocturia Nocturnal enuresis Urgency Bladder pain Urethral pain Dysuria Haematuria
628
What is urinary incontinence?
The complaint of involuntary urinary leakage wihich can be divided into stress incontinence and urge incontinence.
629
What is daytime frequency? Normal?
Number of times a women voids during waking hours Normall 4-7 Increased daytime frequency defined by patients perception
630
What is nocturia
Having to wake at night one or more times to void \<70y/o \>1 per night= abnormal
631
What is nocturnal enuresis
Urinary incontinence during sleep
632
What is urgency?
Sudden compelling desire to pass urine, which is difficult to deter. Most frequently secondary to detrusor overactivity Inflammatory bladder conditions may also present with this
633
What is bladder pain and where is it typiically felt?
Supra or retropubic. Pain occurs with bladder filling and is relieved by emptying it. Pain is indicative of an intravesical pathology such as interstitial cystitis or malignancy
634
What is dysuria?
Pain felt in the bladder or urethra on passing urine, most frequently associated with UTI
635
What are the features of urine dipstick tests?
Blood, glucose, protein, leucocytes and nitrites Nitrites suggestive of infection, if +ve MCS Glycosuria suggests diabetes Haematuria suggests bladder carcinoma or calculi
636
What is a urine diary
When a patient keeps a record for a week of the time and volume of fluid intake and micturition
637
What is the use of postmicturition ultrasound or catheterisation
Exclude chornic urinary retention
638
What is cystometry
Directly measures via a catheter, the pressure in the bladder while the bladder is filled and provoked with coughing. A pressure transducer also placed in vagina or rectum to measure abdominal pressuor.
639
How can true detrusor pressure by caclulated?
Subtraction of the abdominal pressure from the vescile pressure. Should not normally alter with filling or provocation
640
If urinary leaking occurs with coughing in the absence of detrusor contraciton what is the likely diagnosis?
Urodynamic stress incontinence
641
What is the diagnosis if an involuntary detrusor contraction occurs?
Detrusor overactivity
642
What is the use of ultrasonography in investigation of the urinary tract
Excludes incomplete bladder emptying. Checks for congenital abnromalities or abnormalities of the kidneys
643
What is the use of CT urogram?
With the use of contrast the integrity and route of the uretur is examined
644
What is the methylene dye test?
BLue dye is instilled into the bladder, leakage from places other than the urether i.e. fistulae can be seen
645
What is the definition of urinary stress incontinence? Whendoes it become urodynamic stress incontinence What is the most common cause
Complaint of involuntary leakage of urine on effort or exertion, on sneezing or coughing. Once it has been confirmed by urodynamic studies As a result of urethral sphincter weakness, can only be made with certainty after cystometry.
646
What proportion of female incontinence is caused by stress incontinence?
50% Occurs to verying degress in more than 10% of women
647
What are the causes of stress incontinence?
Pregnancy and vaginal delivery Esp: prolonged labour, forceps delivery Obestity and age. Prolapse commonly exists but is not always related. Previous hysterectomy (when indication was not for prolapse or urianry symptoms) may predispose to USI
648
What is the mechanism of stress incontinence
Increase in intra-abdominal pressure, normally the bladder neck is equally compressed and its pressure rises so the P difference remains unchanged. If the bladder neck has slipped below the pelvic floor because its supports are weak it will not be compressed. If the rest of the urethra are unable to compensate the bladder pressure exceeds urethral pressure and incontinence results.
649
Hx in stress incontinence
Disruption of patients life Stress incontinence predominantes, may also complain of frequency, urgency or urge incontinence. It is important to have the patient prioritise her symptoms as treatment for USI vs OAB differs. Faecal incontinence may coexist (perineal tear during childbirth)
650
Ex in Stress incontinence
Sim's speculum, often but not invariable reveals a cystocoele or urethrocoele. Leakage of urine with coughing may be seen. Abdo palpation to exclude bladder distension.
651
Ix in stress incontinence
Urine dipstick Bladder diaries Can measure post-void residual volume by bladder scan Try conservative management before: Cystometry is required to exclude overactive bladder is considered or if overactive bladder symptoms fail to respond to medical treatment
652
UTIs, MCS and antibiotics
Positive for leucocytes and nitrites with symtpoms; send an MSU for MCS and start empirical antibitotics. Symptomatic and negative test for leucoytes or nitrites send an MSU for MCS and consider empirical antibiotics If asymptomatic with postivie L and N, do not offer antibiotics without the results of MSU If asymptomatic and negative for either L or N do not send for MCS as unlikely UTI
653
Mx of stress urinary incontinence
Conservative: Modification of fluid intake Lose weight if obese Cause of chronic cough can be reduced e.g. smoking. 1st line Pelvic floor muscle training Medical: [Duloxetine (not routinely used as second line treatment unless woman prefers not to have surgery] 2nd line Sxical: Considered when conservative measures have failed and woman's QoL is being signficantly impact. Need to be clear that USI is the cause Mid-urethral sling using tension free tape and trans-obturator baginal tape are first line with cure rates up to 90% If sx fails, artifical urinary sphincter may be considered.
654
What is duloxetine and its adverse effects
SNRI that enhances urethral striated sphincter activity Associated with significant and dose-dependant reduction in frequency of incontinence episodes. Can cause nausea, dyspepsia, dry mouth, dizziness, insomnia or drowsiness
655
What are the Cxs of surgery for USI?
Bladder perforation Postoperative voiding difficulty Bleeding Infection de novo detrusor overactivty and suture or mesh erosion
656
What is TVT?
Tension-free vaginal tape: synthetic polypropylene tape placed in a U-shape under the midurethra ander LA or GA, tension adjusted as woman coughs Cystouerthroscopy is performed to ensure there has been no damage to bladder or urethra
657
What is TOT
Transobturator tape Similar to TVT with different insertion methd (via the transobturator foramen) Reduced risk of bladder perf as retropubic space isn't entered.
658
What is injectable periurethral bulking?
Injection of bulking agents for the treatment of USI. Has a low immediate success rate but low morbidity so may be appropriate in patients where surgery has failed or very elderly patients.
659
What is the difference between USI and stress incontinence?
Stress incontinence is a symptom USI is a disorder diagnosed only following cystometry
660
Def OAB?
Urgency with or without urge incontinence, usually with frequency or nocturia in the absence of proven infection.
661
What is detrusor overactivity?
Urodynamic diagnosis characterised by involuntary detrusor contractions during the filling phase which may be spontaenous or provoked by coughing.
662
What is the epidemiology of OAB
causes 35% of female incontinence
663
Aetiology of OAB
Can follow operations for USI in which case it may be caused by bladder neck obstruction. May occasionally occur in hte context of detrusor overactivity occuring the presence of a neuropathy e.g. MS or SC injury
664
Mechanism of incontinence in OAB
Detrudor contraction normally felt as urgency. If strong enough it causes the bladder pressure to overcome the urethral pressure and the patient leaks= urge incontinence. Can occur spontaneously or with provocation e.g. rise in IAP.
665
Hx in OAB
Urgency and urge incontinence Frequency Nocturia Stress incontinence also common Some patients leak at night or at orgasm Hx of childhood enuresis is common Faecal urgency
666
Ex in OAB
often normal but an incidental cystocoele may be present
667
Ix in OAB
Urine dip Urine diary: frequent passage of small volumes of urine, particularly at night and may show high intake of caffeine containing drinks. After lifetyle changes and trial of Rx, cystometry
668
Mx of OAB
Lifestlye changes: Reduce fluid intake, obesity, avoiding caffeine, drugs that alter bladder function such as diuretic and antipsychotics should be reviewed. Conservative: 1st line Bladder training lasting a minimum of 6 weeks Medical: Muscarinic antagonists 2nd line: Oxybutynin or toiterodine or darifenacin, offer durg with lowest acquisition cost 3rd line: oestrogens, mirabegron for symptomatic control Sxical (only after cystometry): Botulinum toxin injection Percutnaeous nerve stimulation Clam augmentation ileocystoplasty is used only for very severe and resistant symptoms, woman has to be willing to self catheterise Urinary diversion (last ditch)
669
Anticholinergics MOA in OAB Adverse effects
Suppress detrusor overactivity Block muscarinic receptors that mediate detrusor smooth-muscle contraction relaxing the detrusor muscle Dry mouth, dizziness (oxybutynin), constipation, blurred vision, drosiness and dizziness. Have also been known to induce delerium
670
MOA of oestrogens in OAB
Many women develop bladder filling symptoms after menopause Improves symptoms of vaginal atrophy. Can reduce symptoms of urgency, urge incontinence, frequency and notcuria
671
Botulinum A MOA in OAB Cxs
Blocks NMJ transmission causing weakness Injected cystoscopicall into the detrusor muscles with sparing of the trigonium. Lasts 6m on average. Voiding dysfunction and urinary retention
672
Features of neuromodulation and sacral nerve stimulation
Continuous stimulation of hte S3 nerve root via an electrical pulse generator improves the ability to suppress detrusor contractions
673
674
Causes of urgency and frequency
UTI Bladder pathology Pelvic mass Overactive bladder USI
675
What is Mixed incontinence
Combination of USI and OAB Dx made at cytometry Most bothersome symptom treated first
676
Def acute urinary intention Features
Patient unable to pass urine for 12h or more. Catheterisation producing as much or more urine than bladder capacity Painful unless due to epidural anaesthesia or failure of the afferent pathway
677
Causes of acute urinary retention Mx
Childbirth: epidural, vulval or perineal pain Sx Drugs such as anticholinergics Retroverted gravid uterus Pelvic mass Neurological disease Catheterisation for 48h whilst cause is treated
678
Features of chronic retention and urinary overflow
1% of incontinence Bladder overdistension eventually causes overflow Can be due to urethral obstruction or detrusor inactivity Pelvic masses and incontinence sx are the most common causes of urethral obstruction Autonomic neuropathies e.g. DM or previous overdistension of the bladder can cause detrusor inactivity. Presentation may mimic stress incontinence or loss may be continuous Examination reveals a distended non-tender bladder Dx with USS or catheter after micturition
679
Features of painful bladder syndrome and interstitial cystitis
PBS= suprapubic pain due to bladder filling accompanied by other symptoms e.g. frequency in the absence of UTI Dx of interstital cystitis reserved for pateitns with painful bladder who have characteristic cystoscopic and histological features. Treatments include dietary modificatiion, bladder training, TCAs, analgesics and intravesical drug infusion
680
What are the most common fistulae causing incontinence
Vesicovaginal Urethrovaginal Commonly as a result of obstructed labour in the developing world, in West normally due to Sx, RTx or Ca. Ix with CTU or cystoscopy. Sx often required
681
Name that fistula!
1. urethrovaginal 2. vesicovaginal 3. vesicouterine 4. ureterovaginal
682
What are the cut offs for anaemia in pregnancy?
Anaemia in pregnancy is defined using different cut off values than in non-pregnant women and varies according to trimester. British Committee for Standards in Haematology (BCSH) guidance gives the following values: first trimester Hb less than 110 g/l second/third trimester Hb less than 105 g/l postpartum Hb less than 100 g/l
683
What are the management options for anaemia in pregnancy?
Royal College of Obstetricians and Gynaecologists (RCOG) guidelines advise for normocytic or microcytic anaemia a trial of oral iron should be considered as the first step, and further investigations only required if no rise in haemaglobin after 2 weeks. Parenteral iron is only indicated if oral iron is not tolerated, absorbed, patient is not compliant or they are near term and there is insufficient time for oral iron to be effective. Blood transfusion is inappropriate at a slighlty low level of haemoglobin without active bleeding.
684
# Define placental abruption Epidemiology
Placental abruption describes separation of a normally sited placenta from the uterine wall, resulting in maternal haemorrhage into the intervening space 1/200 pregnancies
685
What are the associated factors for placental abruption?
Cause - not known but associated factors: proteinuric hypertension multiparity maternal trauma increasing maternal age
686
What are the clinical features of placental abruption
Clinical features shock out of keeping with visible loss pain constant tender, tense uterus normal lie and presentation fetal heart: absent/distressed coagulation problems beware pre-eclampsia, DIC, anuria Presents with sudden abdominal pain in the third trimester. On examination the mother can be seen to be in extreme pain and cold to touch. Bleeding is present in 80% of cases. Absence of visible bleeding does not rule out this diagnosis. Risk factors include: maternal hypertension (common), cocaine, trauma, uterine overdistension, tobacco and previous placental abruption.
687
What are the causative organisms for PID?
Causative organisms Chlamydia trachomatis - the most common cause Neisseria gonorrhoeae Mycoplasma genitalium Mycoplasma hominis
688
What are the features of PID?
Features lower abdominal pain fever deep dyspareunia dysuria and menstrual irregularities may occur vaginal or cervical discharge cervical excitation
689
Ix of PID
screen for Chlamydia and Gonorrhoea
690
Mx of PID
due to the difficulty in making an accurate diagnosis, and the potential complications of untreated PID, consensus guidelines recommend having a low threshold for treatment oral ofloxacin + oral metronidazole or intramuscular ceftriaxone + oral doxycycline + oral metronidazole RCOG guidelines suggest that in mild cases of PID intrauterine contraceptive devices may be left in. The more recent BASHH guidelines suggest that the evidence is limited but that ' Removal of the IUD should be considered and may be associated with better short term clinical outcomes'
691
Cxs of PID
Complications infertility - the risk may be as high as 10-20% after a single episode chronic pelvic pain ectopic pregnancy
692
Def PID
Pelvic inflammatory disease (PID) is a term used to describe infection and inflammation of the female pelvic organs including the uterus, fallopian tubes, ovaries and the surrounding peritoneum. It is usually the result of ascending infection from the endocervix
693
What are the major causes of bleeding in the 1st trimester?
Spontaneous abortion Ectopic pregnancy Hydatidiform mole
694
Causes of bleeding in 2nd trimester?
Spontaneous abortion Hydatidiform mole Placental abruption
695
Causes of bleeding in 3rd trimester?
Bloody show Placental abruption Placenta praevia Vasa praevia
696
Hydatidiform mole features
Typically bleeding in first or early second trimester associated with exaggerated symptoms of pregnancy e.g. hyperemesis. The uterus may be large for dates and serum hCG is very high
697
Features of placenta praevia
Vaginal bleeding, no pain. Non-tender uterus\* but lie and presentation may be abnormal \*vaginal examination should not be performed in primary care for suspected antepartum haemorrhage - women with placenta praevia may haemorrhage
698
Features of vasa praevia
Rupture of membranes followed immediately by vaginal bleeding. Fetal bradycardia is classically seen
699
What are indications for gynae referral in hyperemesis gravidarum?
Failure of oral antiemetics to control symptoms, ketonuria and weight loss (\>5% of pre pregnancy body weight) are all reasons to refer a woman to gynaecology for urgent assessment and intravenous fluids. It is particularly important to keep a low threshold for referral if the woman has a concurrent condition which may be affected by prolonged nausea and vomiting (for example diabetes).
700
Def: hyperemesis gravidarum
Hyperemesis gravidarum describes excessive vomiting during pregnancy. It occurs in around 1% of pregnancies and is thought to be related to raised beta hCG levels. Hyperemesis gravidarum is most common between 8 and 12 weeks but may persist up to 20 weeks\*. \*and in very rare cases beyond 20 weeks
701
Cxs of hyperemesis gravidarum
Wernicke's encephalopathy Mallory-Weiss tear central pontine myelinolysis acute tubular necrosis fetal: small for gestational age, pre-term birth
702
Mx of hyperemsis gravidarum
antihistamines should be used first-line (BNF suggests promethazine as first-line) ginger and P6 (wrist) acupressure: NICE Clinical Knowledge Summaries suggest these can be tried but there is little evidence of benefit admission may be needed for IV hydration
703
Mx of primary herpes infection within 6w of delivery
Oral aciclovir 400 mg TDS (three times daily) until delivery is recommended in the RCOG guidelines for women who present with a primary herpes infection in their third trimester of pregnancy, especially if the woman is expected to deliver within 6 weeks.
704
When is IV aciclovir indicated in HSV infection during pregnancy?
IV aciclovir for the mother or for the infant is only recommended if there has been a preterm pre-labour rupture of membranes or a spontaneous vaginal delivery in the presence of a primary herpes infection.
705
What are the ToRCH infection?
toxoplasmosis, other, rubella, CMV, herpes
706
HSV 6w before delivery?
It can be difficult to differentiate between a primary infection and a recurrent infection and the guidelines recommend suppressive therapy for both infections after 36 weeks until delivery. Recommended method of delivery in a primary infection is a Caesarean section. For a recurrent infection the risk of transmission is low due to maternal antibodies and a Caesarean section is not recommended.
707
Mx of HSV
Management gingivostomatitis: oral aciclovir, chlorhexidine mouthwash cold sores: topical aciclovir although the evidence base for this is modest genital herpes: oral aciclovir. Some patients with frequent exacerbations may benefit from longer term aciclovir
708
A 22-year-old woman presents with a thin, purulent, and mildly odorous vaginal discharge. She also complains of dysuria, intermenstrual bleeding and dyspareunia. A swab shows a Gram negative diplococcus.
IM ceftriaxone + oral azithromycin The 2011 British Society for Sexual Health and HIV (BASHH) guidelines recommend ceftriaxone 500 mg intramuscularly as a single dose with azithromycin 1 g oral as a single dose. The azithromycin is thought to act synergistically with ceftriaxone and is also useful for eradicating any co-existent Chlamydia infections
709
A 27-year-old woman complains of an offensive 'musty', frothy, green vaginal discharge. On examination you an erythematous cervix with pinpoint areas of exudation.
The correct answer is Oral metronidazole The 'strawberry cervix' is actually quite rare outside of examinations - some studies suggest only 2% of patients with Trichomonas vaginalis have this finding
710
A 30-year-old woman presents with an offensive 'fishy', thin, grey vaginal discharge. Testing the discharge shows the pH to be \> 4.5.
Oral metronidazole
711
Amsell's criteria for BV Dx?
Amsel's criteria for diagnosis of bacterial vaginosis - 3 of the following 4 points should be present: thin, white homogenous discharge clue cells on microscopy: stippled vaginal epithelial cells vaginal pH \> 4.5 positive whiff test (addition of potassium hydroxide results in fishy odour)
712
713
714
Mx of PPH
ABC IV syntocinon (oxytocin) 10 units or IV ergometrine 500 micrograms IM carboprost other options include: B-Lynch suture, ligation of the uterine arteries or internal iliac arteries if severe, uncontrolled haemorrhage then a hysterectomy is sometimes performed as a life-saving procedure
715
Secondary PPH
occurs between 24 hours - 12 weeks\*\* due to retained placental tissue or endometritis
716
Primary PPH
occurs within 24 hours affects around 5-7% of deliveries most common cause of PPH is uterine atony (90% of cases). Other causes include genital trauma and clotting factors
717
Use of PGE2 in pregnancy?
Initiating labour
718
Uses of indomethacin and salbutamol in pregnancy?
Tocolytics
719
Use of mifepristone in pregnancy?
Medical abortion
720
Use of oxytocin/ergometrine in pregnancy?
oxytocin / ergometrine is commonly used to encourage smooth muscle contraction in uterine blood vessels, reducing the risk of postpartum haemorrhage.
721
Variable decelerations
Independent of contractions May indicate cord compression
722
Late deceleration
Deceleration of the heart rate which lags the onset of a contraction and does not returns to normal until after 30 seconds following the end of the contraction Indicates fetal distress e.g. asphyxia or placental insufficiency
723
Early deceleration
Deceleration of the heart rate which commences with the onset of a contraction and returns to normal on completion of the contraction Usually an innocuous feature and indicates head compression
724
Baseline bradycardia CTG
Heart rate \< 100 /min Increased fetal vagal tone, maternal beta-blocker use
725
Baseline tachycardia CTG
Heart rate \> 160 /min Maternal pyrexia, chorioamnionitis, hypoxia, prematurity
726
Loss of baseline variability CTG
\< 5 beats / min Prematurity, hypoxia
727
Classification of PPH? What are the four Ts?
Primary postpartum haemorrhage is defined as the loss of 500ml or more from the genital tract within 24 hours of the birth of a baby. This can be further defined as minor haemorrhage (500-1000ml) or major haemorrhage (\>1000ml), and causes 6 deaths/million deliveries. Causes can be grouped into the 'four T's': tone tissue (retained placenta) trauma thrombin (coagulation abnormalities)
728
Vitamin A in pregnancy? FUnctions of vitamin D?
Vitamin A is teratogenic in high doses, and pregnant women should not exceed a daily intake of \>10,000IU. Women are therefore advised to avoid any supplements containing vitamin A, such as normal multivitamin tablets, in pregnancy (NHS Choices). However, as supplements in the UK are now limited to a maximum vitamin A content of 6,000IU, if they have been taking one it should not be cause for concern. Pregnant women are also advised to avoid eating liver, as it has high levels of vitamin A. Vitamin A is a fat soluble vitamin. Functions converted into retinal, an important visual pigment important in epithelial cell differentiation antioxidant Consequences of vitamin A deficiency night blindness
729
HRT Adverse effects?
Side-effects nausea breast tenderness fluid retention and weight gain Potential complications increased risk of breast cancer: increased by the addition of a progestogen increased risk of endometrial cancer: reduced by the addition of a progestogen but not eliminated completely. The BNF states that the additional risk is eliminated if a progestogen is given continuously increased risk of venous thromboembolism: increased by the addition of a progestogen increased risk of stroke increased risk of ischaemic heart disease if taken more than 10 years after menopause Breast cancer in the Women's Health Initiative (WHI) study there was a relative risk of 1.26 at 5 years of developing breast cancer the increased risk relates to duration of use breast cancer incidence is higher in women using combined preparations compared to oestrogen-only preparations the risk of breast cancer begins to decline when HRT is stopped and by 5 years it reaches the same level as in women who have never taken HRT
730
Parity and gravity
Parity is the number of pregnancies a woman has had which have been carried to a viable age; in the UK this is 24 weeks. The number after '+' is the number of pregnancies which have not been carried to a viable age. It can be thought of the number of fetuses/babies which have come from her, in contrast to gravida which is the number of times the uterus has contained a foetus. For example twins are counted as Gravida 1 Parity 2. Parity also does not increase until the foetus is born but gravida technically increases from conception (though in practice from a woman's first appointments with her doctor).
731
Potential Cxs of Chlamydia infection?
Potential complications epididymitis pelvic inflammatory disease endometritis increased incidence of ectopic pregnancies infertility reactive arthritis perihepatitis (Fitz-Hugh-Curtis syndrome)
732
Fitz-Hugh–Curtis syndrome
Fitz-Hugh–Curtis syndrome is a rare complication of pelvic inflammatory disease(PID) named after the two physicians, Thomas Fitz-Hugh, Jr and Arthur HaleCurtis who first reported this condition in 1934 and 1930 respectively.[1][2][3] It involves liver capsule inflammation[4]leading to the creation of adhesions.
733
Ix of Chlamydia
Investigation traditional cell culture is no longer widely used nuclear acid amplification tests (NAATs) are now rapidly emerging as the investigation of choice urine (first void urine sample), vulvovaginal swab or cervical swab may be tested using the NAAT technique
734
Placenta praevia
Associated factors multiparity multiple pregnancy embryos are more likely to implant on a lower segment scar from previous caesarean section
735
Danazol
is a derivative of ethisterone. It can be used to treat endometriosis and fibrocystic breast disease. It will not prevent implantation and can cause virilisation of female fetuses, so is contraindicated in pregnancy.
736
. If magnesium sulphate is not available, or if it fails to terminate the seizure what can be considered?
A BZD e.g. midazolam
737
Guidlines on usage of Mg Sulphate?
should be given once a decision to deliver has been made in eclampsia an IV bolus of 4g over 5-10 minutes should be given followed by an infusion of 1g / hour urine output, reflexes, respiratory rate and oxygen saturations should be monitored during treatment treatment should continue for 24 hours after last seizure or delivery (around 40% of seizures occur post-partum)
738
The major breastfeeding contraindications tested in exams relate to drugs (see below). Other contraindications of note include:
galactosaemia viral infections - this is controversial with respect to HIV in the developing world. This is because there is such an increased infant mortality and morbidity associated with bottle feeding that some doctors think the benefits outweigh the risk of HIV transmission
739
Women who are considering taking the progestogen only pill (POP) should be counselled in what most common side effect?
Women should be advised about the likelihood and types of bleeding patterns expected with POP use. As a general guide: 20% of women will be amenorrhoeic 40% will bleed regularly 40% will have erratic bleeding. Between 10% and 25% of women using a POP will discontinue this method within 1 year as a result of these bleeding patterns.
740
Advise on starting the POP?
Starting the POP if commenced up to and including day 5 of the cycle it provides immediate protection, otherwise additional contraceptive methods (e.g. Condoms) should be used for the first 2 days if switching from a combined oral contraceptive (COC) gives immediate protection if continued directly from the end of a pill packet (i.e. Day 21) Taking the POP should be taken at same time everyday, without a pill free break (unlike the COC) Missed pills if \< 3 hours\* late: continue as normal if \> 3 hours\*: take missed pill as soon as possible, continue with rest of pack, extra precautions (e.g. Condoms) should be used until pill taking has been re-established for 48 hours
741
Other issues around the POP
Other potential problems diarrhoea and vomiting: continue taking POP but assume pills have been missed - see above antibiotics: have no effect on the POP\*\* liver enzyme inducers may reduce effectiveness e.g. rifampicin discussion on STIs
742
Missed POP
if \< 3 hours\* late: continue as normal if \> 3 hours\*: take missed pill as soon as possible, continue with rest of pack, extra precautions (e.g. Condoms) should be used until pill taking has been re-established for 48 hours
743
Def: puerperal pyrexia Causes? Mx?
Causes: endometritis: most common cause urinary tract infection wound infections (perineal tears + caesarean section) mastitis venous thromboembolism Management if endometritis is suspected the patient should be referred to hospital for intravenous antibiotics (clindamycin and gentamicin until afebrile for greater than 24 hours)
744
A 28 -year-old is found to have an ectopic pregnancy at 10 weeks gestation. She undergoes surgical management of the ectopic with a salpingectomy. She is known to be rhesus negative. What is the recommendation with regard to anti-D?
In surgical management of an ectopic pregnancy then Anti-D immunoglobulin should be administered. Anti-D is not required in circumstances where a medical management of the ectopic has been used, nor for treatment of pregnancy of unknown location.
745
Coombs test:
Direct Coombs: Is a investigation used to look for autoimmune haemolytic anaemia, Indirect: Used antenatally to detect antibodies in the maternal blood that can cross the placenta and result in haemolytic disease of the newborn.
746
Listeriosis in pregnancy
pregnant women are almost 20 times more likely to develop listeriosis compared with the rest of the population due to changes in the immune system fetal/neonatal infection can occur both transplacentally and vertically during child birth complications include miscarriage, premature labour, stillbirth and chorioamnionitis diagnosis can only be made from blood cultures treatment is with amoxicillin
747
Blood cultures and LP for Listeria infection
CSF may reveal a pleocytosis, with 'tumbling motility' on wet mounts
748
Side effects of IUD
IUDs make periods heavier, longer and more painful the IUS is associated with initial frequent uterine bleeding and spotting. Later women typically have intermittent light menses with less dysmenorrhoea and some women become amenorrhoeic uterine perforation: up to 2 per 1000 insertions the proportion of pregnancies that are ectopic is increased but the absolute number of ectopic pregnancies is reduced, compared to a woman not using contraception infection: there is a small increased risk of pelvic inflammatory disease in the first 20 days after insertion but after this period the risk returns to that of a standard population expulsion: risk is around 1 in 20, and is most likely to occur in the first 3 months
749
Contraceptives - time until effective (if not first day period):
instant: IUD 2 days: POP 7 days: COC, injection, implant, IUS
750
What is the gold standard Ix for endometriosis?
Diagnostic laparoscopy
751
Mx of fibroids
medical: symptomatic management e.g. with combined oral contraceptive pill. GnRH agonists may reduce the size of the fibroid but are typically useful for short-term treatment surgery is sometimes needed: myomectomy, hysterscopic endometrial ablation, hysterectomy uterine artery embolization
752
Def: endometriosis Epidemiology
Presence and growth of tissue similar to endometrium outside of the uterus 1-2% of women are diagnosed and peak is between 30 and 45. Although prevalence may be 1-20%, asymptomatic
753
Where is enodmetriosis most commonly found? Pathology
Uterosacral ligaments and on or behind the ovaries Occasionally it affects the umbilicus or abdominal wound scars, vagina, bladder rectum, even lungs Oestrogen dependent, regresses after menopause and during pregnancy. Acucumulated altered blood is dark brown and can form a chocolate cyst (endometrioma) in the ovarias. Can cause inflammation with progressive fibrosis and adhesions, in the most severe form the entire pelvis is frozen due to adhesion
754
Aetiology of endometriosis
Retrograde menstruation More distant foci may be through mechanical, lymphatic or blood-borne spread. Degree of inherited predisposition NB poor symptomatic correlation with extent of disease
755
Hx in endometriosis
May be asymptomatic Causes chronic pelvic pain, usually cyclical Dysmeorrhoea before the onset of mensturation Dyspareunia Subfertility Dyschezia Menstrual probloms Rupture of chocolate cyst: acute pain, may be first symptom Cyclical haematuria, rectal bleeding or bleeding from the umbilicus are uncommon and suggestive of severe disease
756
Ex in endometriosis
VE@ tenderness and or thickening behind the uterus or in the adnexa In severe cases the uterus may be retroverted and immobile A rectovaginal nodule of enodmetriosis may be apparent on digital examination or visible on speculm. With mild endometriosis the pelvis feels normal
757
Ix in endometriosis
Laparoscopy with visualisation and biopsy active lesions are red or punctate marks White scars or brown spots represent less active endometriosis TVU may be useful to dx/exclude endometriomas and may also suggest the presence of adenomyosis although MRI is a better investigation for this. If theere is clinical evidence of deeply infiltrating endometriosis extent of involvement can be examined with MRI, Intravenous pyelogram and barium studies CA125 may be raised but of little diagnostic merit
758
When to suspect endometriosis
Symptoms after severeal years of painless periods Pelvic examinatoin likely to be normal Pelvis USS likely to be normal
759
Mx of endometriosis
Asymptomatic do not require treatment although nb in the low risk of missing ovarian ca Symptomatic relief: Pain: offer NSAID e.g. ibuprofen naproxen or mefenamic acid. Paracetamol if NSAIDs CIed. Rx (NB should be in women who do not wish to conceive): Trial hormonal treatment: COCP (not suitable for older women or smokers) Progestogen preparations: denogestrel or IUS cyclical or continuous. Side effects may be severe. GnRH analgoues: induce temprorary menopausal state so side effects mimic the menopause although add back HRT can minimise these If woman does not want hormonal contraception offer an oral progestogen e.g. medroxyprogesterone Sxical: diathermy ec can be used at laparascopy using see and treat approach. (This may improve conception rates) BSO
760
TVU appearance of ovary described as ground glass
Ovarian endometrioma
761
What is important to note in women undergoing BSO for endometriosis
Will need HRT However if endometriosis remains then there is risk of malignant change in ectopic endometrium Consideration should be given to providing a combined preparation
762
Fertility and endometriosis
Found in 25% of diagnostic laps for subfertility.
763
Def: Chronic Pelvic Pain
Intermittent or constant pain in the lower abdomen or pelvis with \>6m duration not occuring exclusively with mesntruation or intercourse Can present in primay care as migraine, low back pain and affects 15% of adult women
764
NB for CPP
Exclude pathological causes Through TVU, MRI or lap as appropriate
765
Possible causes of CPP
Varies over menstrual cycle: endometriosis, adenomyosis (oestrogen important as condition not typically seen in postmenopausal and suppression of ovarian activity cures 2/3rds). Adhesions: ovarian tissue can become trapped followiing Sx and cause cyclical pain IBS Interstitial cystitis. Psychological factors.
766
Mx of CPP
Depends on cause ?IBS: antispasmodics, analgesia Cyclical pain: therapeutic trial using COCP or GnRH analogue with add back HRT for 3-6m before laparscipy. IUS
767
A pregnant 25-year-old woman attends her booking appointment. Although she is symptom-free, urine dipstick indicates a urinary tract infection. Which of the following antibiotics should be avoided in the first trimester of pregnancy? Trimethoprim Amoxicillin Cefalexin Nitrofurantoin Erythromycin
Whether symptomatic or asymptomatic it is important to treat urinary tract infections in pregnancy to prevent progression to pyelonephritis. As trimethoprim is a folate antagonist it should be avoided in the first trimester - this is the time when the neural tube forms and there is a risk of teratogenicity. The other antibiotics listed are not contraindicated in the first trimester. However, erythromycin is not typically used to treat urinary tract infections, and nitrofurantoin should be avoided close to full term as there is a risk of causing neonatal haemolysis. Sulfonamides and quinolones should also be avoided in pregnancy. (BNF 5.1.13)
768
What are gestational trophoblastic disorders?
Describes a spectrum of disorders originating from the placental trophoblast: complete hydatidiform mole partial hydatidiform mole choriocarcinoma
769
What is a complete hydatidiform mole?
Benign tumour of trophoblastic material. Occurs when an empty egg is fertilized by a single sperm that then duplicates its own DNA, hence the all 46 chromosomes are of paternal origin
770
What are the features of hydatidform moles?
Features bleeding in first or early second trimester exaggerated symptoms of pregnancy e.g. hyperemesis uterus large for dates very high serum levels of human chorionic gonadotropin (hCG) hypertension and hyperthyroidism\* may be seen \*hCG can mimic thyroid-stimulating hormone (TSH)
771
What is the Mx of hydatidiform moles? What is the Px?
Management urgent referral to specialist centre - evacuation of the uterus is performed effective contraception is recommended to avoid pregnancy in the next 12 months Around 2-3% go on to develop choriocarcinoma
772
What are the features of partial hydatidiform moles?
n a partial mole a normal haploid egg may be fertilized by two sperms, or by one sperm with duplication of the paternal chromosomes. Therefore the DNA is both maternal and paternal in origin. Usually triploid - e.g. 69 XXX or 69 XXY. Fetal parts may be seen
773
What are the two stages of the first stage of labour?
First stage is broken into two stages: Latent: Time taken for the cervix to completely efface and dilate to 3cm Active: From 3cm to 10cm
774
What are the time limits of the second stage of labour?
Second stage is from 10cm to delivery of the baby 2 hours is the maximum recommended in multiparous women 3 hours is the maximum recommended in nulliparous women Remember, in the context of an epidural, 1 hour of passive second stage (without pushing) is advised
775
What is the third stage of labour?
Third stage is from delivery of the baby to delivery of the placenta and membranes Third stage is from delivery of the baby to delivery of the placenta and membranes Active: Uses uterotonics, clamping of the cord and controlled cord traction Meds include syntocinon and ergometrine: syntometrine, or oxytocin They are generally given as the anterior shoulder is born Physiological: The cord is only clamped when pulseless in the absence of medications and the placenta delivered through maternal efforts alone Should be converted to active management if placenta not delivered in 1hr
776
What are the active forms of managing 3rd stage of labour
Active: Uses uterotonics, clamping of the cord and controlled cord traction Meds include syntocinon and ergometrine: syntometrine, or oxytocin They are generally given as the anterior shoulder is born
777
What is the definition of labour?
Labour may be defined as the onset of regular and painful contractions associated with cervical dilation and descent of the presenting part Signs of labour include regular and painful uterine contractions a show (shedding of mucous plug) rupture of the membranes (not always) shortening and dilation of the cervix
778
What is nexplanon? What are the contraindications?
Implanon was a non-biodegradable subdermal contraceptive implant which has been replaced by Nexplanon. From a pharmacological perspective Nexplanon is the same as Implanon. The two main differences are: the applicator has been redesigned to try and prevent 'deep' insertions (i.e. subcutaneous/intramuscular) it is radiopaque and therefore easier to locate if impalpable Contraindications UKMEC 3\*: ischaemic heart disease/stroke (for continuation, if initiation then UKMEC 2), unexplained, suspicious vaginal bleeding, past breast cancer, severe liver cirrhosis, liver cancer, positive antiphospholipid antibodies\*\* UKMEC 4\*\*: current breast cancer . \*proven risks generally outweigh the advantages \*\*there is some contradiction in the guidance issued by the FSRH but their most recent document (revised 2010) lists positive antiphospholipid antibodies as UKMEC 3 \*\*\*a condition which represents an unacceptable risk if the contraceptive method is used
779
Def: recurrent miscarriage What are the common causes?
Recurrent miscarriage is defined as 3 or more consecutive spontaneous abortions. It occurs in around 1% of women Causes antiphospholipid syndrome endocrine disorders: poorly controlled diabetes mellitus/thyroid disorders. Polycystic ovarian syndrome uterine abnormality: e.g. uterine septum parental chromosomal abnormalities smoking
780
What is TTTS?
Twin-to-twin transfusion syndrome (TTTS) is a relatively common complication of monochorionic twin pregnancies. The two fetuses share a single placenta, meaning that blood can flow between the twins. In TTTS, one fetus, the 'donor' receives a lesser share of the placenta's blood flow than the other twin, the 'recipient'. This is due to abnormalities in the network of placental blood vessels. The recipient may become fluid-overloaded whilst the donor can become anaemic. One fetus may have oligohydramnios and the other may have polyhydramnios as a result of differences in urine production, causing additional problems. In severe cases, TTTS can be fatal for one or both fetuses. TTTS usually occurs in early or mid-pregnancy, thus ultrasound examinations performed between 16 and 24 weeks focus on detecting this condition. After 24 weeks the main purpose of ultrasound examinations is to detect fetal growth restriction.
781
What is the incidence of multiple pregnancies?
The incidence of multiple pregnancies is as follows twins: 1/105 triplets: 1/10,000 Twins may be dizygotic (non-identical, develop from two separate ova that were fertilized at the same time) or monozygotic (identical, develop from a single ovum which has divided to form two embryos). Around 80% of twins are dizygotic
782
What are the risks of monoamniotic monozygotic twins?
Monoamniotic monozygotic twins are associated with: increased spontaneous miscarriage, perinatal mortality rate increased malformations, IUGR, prematurity twin-to-twin transfusions: recipient is larger with polyhydramnios (do laser ablation of interconnecting vessels)
783
What are the predisposing factors for dizygotic twins?
previous twins family history increasing maternal age multigravida induced ovulation and in-vitro fertilisation race e.g. Afro-Caribbean
784
What are the complications of twin preganancies: Antenatally For the fetus? Labour?
Antenatal complications polyhydramnios pregnancy induced hypertension anaemia antepartum haemorrhage Fetal complications - perinatal mortality (twins \* 5, triplets \* 10) prematurity (mean twins = 37 weeks, triplets = 33) light-for date babies malformation (\*3, especially monozygotic) Labour complications PPH increased (\*2) malpresentation cord prolapse, entanglement
785
Mx of twin pregnancies
Management rest ultrasound for diagnosis + monthly checks additional iron + folate more antenatal care (e.g. weekly \> 30 weeks) precautions at labour (e.g. 2 obstetricians present) 75% of twins deliver by 38 weeks, if longer most twins are induced at 38-40 wks
786
Mx of infertility in PCOS
Infertility weight reduction if appropriate the management of infertility in patients with PCOS should be supervised by a specialist. There is an ongoing debate as to whether metformin, clomifene or a combination should be used to stimulate ovulation a 2007 trial published in the New England Journal of Medicine suggested clomifene was the most effective treatment. There is a potential risk of multiple pregnancies with anti-oestrogen\* therapies such as clomifene. The RCOG published an opinion paper in 2008 and concluded that on current evidence metformin is not a first line treatment of choice in the management of PCOS metformin is also used, either combined with clomifene or alone, particularly in patients who are obese gonadotrophins
787
General Mx in PCOS Mx of hirsutism and acne
General weight reduction if appropriate if a women requires contraception then a combined oral contraceptive (COC) pill may help regulate her cycle and induce a monthly bleed (see below) Hirsutism and acne a COC pill may be used help manage hirsutism. Possible options include a third generation COC which has fewer androgenic effects or co-cyprindiol which has an anti-androgen action. Both of these types of COC may carry an increased risk of venous thromboembolism if doesn't respond to COC then topical eflornithine may be tried spironolactone, flutamide and finasteride may be used under specialist supervision
788
Mx of genital warts
Topical podophyllum or cryotherapy are first choice Imiquimod is ssecond line
789
A 48-year-old female smoker attends the GP for information regarding contraception. Her last menstrual period was 9 months ago and she is convinced that she has 'gone through the menopause'. The most suitable form of contraception is: None, this lady has gone through the menopause and is protected The combined oral contraceptive pill for 12 months (COCP) The intrauterine system (IUS) Hormone replacement therapy (HRT) Barrier methods alone
The menopause is a retrospective diagnosis and is said to occurred 12 months after the last menstrual period. Women who menopause under the age of 50 require contraception for at least 2 years after their last menstrual period. Those over the age of 50 require only 1 year of contraception. In view of this, it would be inappropriate to say this lady does not require any contraception because she is protected. Similarly prescribing the COCP for only 12 months would be equally inappropriate. The fact that she is also a smoker would mean that the risks outweigh the benefits of the COCP as she is over the age of 35. Hormone replacement therapy should not be used solely as a form of contraception and barrier methods are less effective than the other types of contraception listed thus the most appropriate answer is the IUS. This will take the patient through the menopause and can be used for 7 years (off-licence) or 2 years after her last menstrual period.
790
What is the advice to women planning pregnancy and taking antiepileptics?
Take folic acid 5mg per day before pregnancy (Risk of congenital defects in non-epileptic mothers 1-2%, in mothers taking antiepileptic medication rises to 3-4%)
791
Sodium valproate in pregnancy
The November 2013 issue of the Drug Safety Update also carried a warning about new evidence showing a significant risk of neurodevelopmental delay in children following maternal use of sodium valproate. The update concludes that sodium valproate should not be used during pregnancy and in women of childbearing age unless clearly necessary. Women of childbearing age should not start treatment without specialist neurological or psychiatric advice.
792
Mx of hyperemesis gravidarum
Management antihistamines should be used first-line (BNF suggests promethazine as first-line) ginger and P6 (wrist) acupressure: NICE Clinical Knowledge Summaries suggest these can be tried but there is little evidence of benefit admission may be needed for IV hydration
793
What proportion of threatened miscarriages go on to miscarry?
25%
794
What is the most common identifiable cause of postcoital bleeding?
Causes no identifiable pathology is found in around 50% of cases cervical ectropion is the most common identifiable causes, causing around 33% of cases. This is more common in women on the combined oral contraceptive pill cervicitis e.g. secondary to Chlamydia cervical cancer polyps trauma
795
A 21-year-old female presents for review. She is 14 weeks pregnant and has been seen by the midwives for her booking visit. There have been no pregnancy related problems to date. Tests taken revealed the following: Blood group:A Rhesus negative What is the most appropriate management regarding her rhesus status? Give first dose of anti-D at 28 weeks No action required unless antenatal vaginal blood loss Give first dose of anti-D as soon as possible Give anti-D just prior to delivery No action required
Rhesus negative woman - anti-D at 28 + 34 weeks NICE recommend giving rhesus negative woman anti-D at 28 weeks followed by a second dose at 34 weeks
796
Cx of DM during pregnancy Maternal Neonatal
Maternal complications polyhydramnios - 25%, possibly due to fetal polyuria preterm labour - 15%, associated with polyhydramnios Neonatal complications macrosomia (although diabetes may also cause small for gestational age babies) hypoglycaemia (secondary to beta cell hyperplasia) respiratory distress syndrome: surfactant production is delayed polycythaemia: therefore more neonatal jaundice malformation rates increase 3-4 fold e.g. sacral agenesis, CNS and CVS malformations (hypertrophic cardiomyopathy) stillbirth hypomagnesaemia hypocalcaemia shoulder dystocia (may cause Erb's palsy)
797
What is Galactocele?
Galactocele typically occurs in women who have recently stopped breastfeeding and is due to occlusion of a lactiferous duct. A build up of milk creates a cystic lesion in the breast. The lesion can be differentiated from an abscess by the fact that a galactocele is usually painless, with no local or systemic signs of infection.
798
What are the NICE guidlines warranting CTG monitoring?
suspected chorioamnionitis or sepsis, or a temperature of 38°C or above severe hypertension 160/110 mmHg or above oxytocin use the presence of significant meconium fresh vaginal bleeding that develops in labour - this was a new point added to the guidelines in 2014 Fresh vaginal bleeds developing in labour could be a sign of placental rupture (the most common cause of antepartum haemorrhage) or placental praevia (second most common cause of antepartum haemorrhage) and therefore monitoring of the baby is required.
799
You are called to see a 32-year-old woman who has vaginal bleeding one hour post delivery. Formal measurement estimates the blood loss at 1200mls including liquor. Blood pressure is 98/52mmHg and heart rate 110bpm. Bleeding is ongoing. Which of the following options is most appropriate? IV access, group O RhD negative blood, tranexamic acid IV access, crossmatch, tranexamic acid IV access, group and save, commence crystalloid infusion IV access, crossmatch, commence crystalloid infusion IV access, commence crystalloid infusion, consider ballon tamponade
This scenario is classed as a major post partum haemorrhage (PPH) due to an estimated blood loss of greater than 1000 mls. An ABCD approach should be instituted with prompt senior involvement. As this is a major PPH, group and save is inappropriate. Tranexamic acid is an antifibrinolytic which may be used in vaginal bleeding secondary to heavy menstrual bleeding, but has no role in PPH. The causes of PPH can be divided into four T's (uterine Tone, Tissue, Trauma and Thrombin). In uterine atony bimanual uterine compression should be trialed first and a Foley catheter passed to ensure an empty bladder. Uterine balloon tamponade is a suitable first line surgical management, but pharmacological measures should be trialled first. These include a bolus of intravenous syntocinon (repeated if necessary), followed by ergometrine, syntocinon infusion and carboprost in turn. A fluid challenge should be instituted in the first instance while blood products are awaited. The RCOG state that up to 3.5L of warmed crystalloid can be infused at an appropriate rate while waiting for blood products.
800
Combined oral contraceptive pill: missed pill If 1 pill missed? If \>1 pill missed
If 1 pill is missed (at any time in the cycle) take the last pill even if it means taking two pills in one day and then continue taking pills daily, one each day no additional contraceptive protection needed If 2 or more pills missed take the last pill even if it means taking two pills in one day, leave any earlier missed pills and then continue taking pills daily, one each day the women should use condoms or abstain from sex until she has taken pills for 7 days in a row. FSRH:'This advice may be overcautious in the second and third weeks, but the advice is a backup in the event that further pills are missed' if pills are missed in week 1 (Days 1-7): emergency contraception should be considered if she had unprotected sex in the pill-free interval or in week 1 if pills are missed in week 2 (Days 8-14): after seven consecutive days of taking the COC there is no need for emergency contraception\* if pills are missed in week 3 (Days 15-21): she should finish the pills in her current pack and start a new pack the next day; thus omitting the pill free interval
801
How does teh FSRH categorise risk factors for the COCP?
1 - no restrictions on the use of contraceptive method 2 - advantages of contraceptive method generally outweigh the theoretical and proven risks 3 - theoretical and proven risks generally outweigh the advantages of the contraceptive method, can still be given based on expert clinical judgement 4 - condition that poses unacceptable risk if the contraceptive method is used
802
What are hte bsolute contraindications for hte COCP?
Migraine with aura Breastfeeding \<6 weeks post-partum Age 35 or over smoking 15 or more cigarettes/day Systolic 160mmHg or diastolic 95mmHg Vascular disease History of VTE Current VTE (on anticoagulants) Major surgery with prolonged immobilisation Known thrombogenic mutations Current and history of ischaemic heart disease Stroke (including TIA) Complicated valvular and congenital heart disease Current breast cancer Nephropathy/retinopathy/neuropathy Other vascular disease Severe (decompensated) cirrhosis Hepatocellular adenoma Hepatoma Raynaud's disease with lupus anticoagulant Positive antiphospholipid antibodies
803
Which of the following is the most commonly recognised risk of combined hormone replacement therapy (HRT)? Leukaemia Endometrial cancer Gallbladder disease Meigs syndrome Cellulitis
Unopposed oestrogen increases the risk of endometrial cancer and remains elevated for 5 or more years after stopping therapy The risk is not eliminated completely with additional sequential progestogen No increased risk has been found with continuous combined HRT Risk of ovarian cancer is higher the longer HRT is taken. But when the HRT is stopped, the risk goes back down to normal over a few years Venous thromboembolism risk is more than doubled with HRT but absolute risk remains small Risk of breast cancer is increased as it simulated delaying menopause. Every year the menopause is naturally delayed, the risk increases by 2.8% With HRT the risk is increased by 2.3% by year The risk of gallbladder disease is increased in women taking HRT - though this risk may be reduced with transdermal administration
804
Mx of gonorrhoea
Management ## Footnote ciprofloxacin used to be the treatment of choice. However, there is increased resistance to ciprofloxacin and therefore cephalosporins are now used the 2011 British Society for Sexual Health and HIV (BASHH) guidelines recommend ceftriaxone 500 mg intramuscularly as a single dose with azithromycin 1 g oral as a single dose. The azithromycin is thought to act synergistically with ceftriaxone and is also useful for eradicating any co-existent Chlamydia infections if ceftriaxone is refused or contraindicated other options include cefixime 400mg PO (single dose)
805
What is the most common cause of septic arthritis in young adults?
Gonorrhoea
806
What are the potential Cxs of gonorrhoea infection?
Disseminated gonococcal infection (DGI) and gonococcal arthritis may also occur, with gonococcal infection being the most common cause of septic arthritis in young adults. The pathophysiology of DGI is not fully understood but is thought to be due to haematogenous spread from mucosal infection (e.g. Asymptomatic genital infection). Initially there may be a classic triad of symptoms: tenosynovitis, migratory polyarthritis and dermatitis. Later complications include septic arthritis, endocarditis and perihepatitis (Fitz-Hugh-Curtis syndrome)
807
Key features of DGI?
Key features of disseminated gonococcal infection tenosynovitis migratory polyarthritis dermatitis (lesions can be maculopapular or vesicular)
808
Features of chorioamnionitis
Chorioamnionitis (which can affect up to 5% of all pregnancies) is a potentially life-threatening condition to both mother and foetus and is therefore considered a medical emergency. It is usually the result of an ascending bacterial infection of the amniotic fluid / membranes / placenta. The major risk factor in this scenario is the preterm premature rupture of membranes (however, it can still occur when the membranes are still intact) which expose the normally sterile environment of the uterus to potential pathogens. Prompt delivery of the foetus (via cesarean section if necessary) and administration of intravenous antibiotics is widely considered the mainstay of initial treatment for this condition.
809
Normal SFH
The measurement of the symphysis-fundal height in centimetres should closely match the foetal gestational age in weeks within 1 or 2 cm from 20 weeks gestation Anything less= small for dates Anything more= polyhydramnios
810
Injectable contraceptive (medroxyprogesterone acetate)
Inhibits ovulation The Faculty for Sexual and Reproductive Health (FSRH) state Progestogen-only injectable contraception works primarily by inhibiting ovulation.
811
Progestogen-only pill (excluding desogestrel)
The Faculty for Sexual and Reproductive Health (FSRH) state All POPs alter cervical mucus to prevent sperm penetration into the upper reproductive tract. In addition, traditional POPs inhibit ovulation but this can be variable.
812
Intrauterine system (levonorgestrel)
The Faculty for Sexual and Reproductive Health (FSRH) state Most of the contraceptive effect of the LNG-IUS is mediated via its progestogenic effect on the endometrium which prevents implantation.
813
You are called to see a 33-year-old patient complaining of vaginal bleeding 12 hours after a vaginal delivery. On arrival, she is alert, complaining of breathlessness and giddiness. Her blood pressure is 97/73 mmHg. She has no history of a bleeding disorder, and you are told she did not tear. She has a blue cannula in situ with nothing attached, and the midwife has bleeped the registrar on call. What is your immediate course of action? Bleep your FY2 Insert a large bore cannula 500mL crystalloid fluid challenge Vaginal examination Give oxytocin
Post-partum haemorrhage should be managed with an ABC approach. This lady is symptomatic and hypotensive. It would be most appropriate to commence a fluid challenge in the first instance whilst awaiting help from your registrar. A blue cannula (22G) however will only provide a flow rate of 31 mL/minute. Insertion of a large bore cannula is thus the priority in this lady who is actively bleeding. A vaginal examination may also prove useful, as you may find that there are retained products of conception in the cervix causing a vasovagal reaction leading to hypotension. However, your registrar would be able to provide you with assistance to perform that after you have begun fluid resuscitation.
814
Cannula size and colour order
Blue 22G (very small - for difficult hand veins) Pink 20G (small - suitable for the majority of patients that require IV fluids) Green 18G (average sized - suitable for IV fluids and smaller blood transfusions) Grey 16G (large - for use in large blood transfusions and emergency use) Brown 14G (very large and painful - again, for emergency use)
815
A 24-year-old woman presents to the emergency department with intermittent abdominal pain and vaginal bleeding. She thinks her last period was 6 weeks ago but cannot be certain. She has never been pregnant before and has no previous gynaecological history. She is systemically well with a blood pressure of 130/85 mmHg and pulse 79 bpm. A pregnancy test performed in the department is positive and transvaginal ultrasound confirms a pregnancy in the adnexa with a fetal heart beat present. What is the most appropriate management in this case? Reassure and discharge with routine follow-up appointment Mifepristone and misoprostol Admit and observe Surgical management - salpingectomy or salpingotomy Methotrexate
This patient has a confirmed ectopic pregnancy. There is no evidence the pregnancy has ruptured but definitive treatment is still the safest course. Expectant management of ectopics may be an option in those without acute symptoms and declining beta-HCG levels. Close monitoring is essential and intervention is advised if symptoms manifest or beta-HCG levels begin to rise. The presence of a fetal heart beat makes both conservative and medical management unlikely to be successful and also risky in terms of rupture, which would be a medical emergency. Surgical removal of the ectopic is the most appropriate option here. If the contralateral tube is healthy then salpingectomy may be the best option. However, if the contralateral tube is damaged, salpingotomy preserves the functional tube and helps minimise the risk of future infertility.
816
'Traditional' POPs (Micronor, Noriday, Nogeston, Femulen) Missed pills
If less than 3 hours late no action required, continue as normal If more than 3 hours late (i.e. more than 27 hours since the last pill was taken) action needed - see below Action required, if needed: take the missed pill as soon as possible. If more than one pill has been missed just take one pill. Take the next pill at the usual time, which may mean taking two pills in one day continue with rest of pack extra precautions (e.g. condoms) should be used until pill taking has been re-established for 48 hours
817
Cerazette (desogestrel) missed pill
If less than 12 hours late no action required, continue as normal If more than 12 hours late (i.e. more than 36 hours since the last pill was taken) action needed - see below Action required, if needed: take the missed pill as soon as possible. If more than one pill has been missed just take one pill. Take the next pill at the usual time, which may mean taking two pills in one day continue with rest of pack extra precautions (e.g. condoms) should be used until pill taking has been re-established for 48 hours
818
First line Ix for endometrial carcinoma
The first step in the investigation of possible endometrial cancer is to preform a trans-vaginal ultrasound scan to measure the endometrial thickness. Different hospitals have different cut-offs for endometrial thickness and further investigation. If the endometrial lining is thickened then a hysteroscopy will be preformed and an endometrial biopsy taken. Treatment for endometrial cancer is usually laparoscopic hysterectomy with bilateral salpingo-oophorectomy, with or without radiotherapy.
819
Grading of Perineal Tears 1 2 3 4
The RCOG has produced guidelines suggesting the following classification of perineal tears: first degree: superficial damage with no muscle involvement second degree: injury to the perineal muscle, but not involving the anal sphincter third degree: injury to perineum involving the anal sphincter complex (external anal sphincter, EAS and internal anal sphincter, IAS): 3a: less than 50% of EAS thickness torn 3b: more than 50% of EAS thickness torn 3c: IAS torn fourth degree: injury to perineum involving the anal sphincter complex (EAS and IAS) and rectal mucosa
820
When should early referrals for infertility be considered in females?
Previous STI \>35y/o Previous pelvic Sx Abnormal genital examination Amenorrhoea
821
When should early referrals for infertility be considered in males?
Previous Sx on genitali Varicocele Significant systemic illness Abnormal genital examination Previous STI
822
A pregnant woman is found to have tested positive syphilis during her routine booking visit bloods. She is currently 12 weeks pregnant. What is the most appropriate management? Oral doxycycline Recommend termination of pregnancy and administer antibiotic therapy Repeat test in 4 weeks and treat if still positive IM benzathine penicillin G IM human normal immunoglobulin (HNIG)
Management benzylpenicillin alternatives: doxycycline the Jarisch-Herxheimer reaction is sometimes seen following treatment. Fever, rash, tachycardia after first dose of antibiotic. It is thought to be due to the release of endotoxins following bacterial death and typically occurs within a few hours of treatment. The 2008 British Association for Sexual Health and HIV (BASHH) guidelines recommend IM benzathine penicillin G in this scenario. Doxycycline should not be used in pregnancy. Immunoglobulins are used to provide protection against viral illnesses such as rubella.
823
young woman of 28 weeks gestation presents to the emergency department with painless vaginal bleeding, she appears well and is haemodynamically stable. Which investigation is most likely to help confirm the diagnosis? Abdominal ultrasound with colour flow doppler Speculum Digital vaginal examination Kleihauer test Full blood count and urea and electrolytes
RCOG guidelines clearly state that the definitive diagnosis of placenta praevia is through ultrasound scan imaging. There is no screening programme for placenta praevia , however the UK National screening committee supports local practices which during the routine 20 week scan, comment and look for evidence of the placenta covering the cervical os. Transvaginal ultrasound scans be safely performed at 20 weeks, in addition to the abdominal ultrasound scan to help improve the accuracy of localisation and RCOG guidelines state that they should be used to confirm the diagnosis of placenta praevia
824
Which of these is correct in regards to the management of endometrial cancer? Most patients present with stage 1 disease, and are therefore amenable to surgery alone Endometrial biopsy is not required for diagnosis Chemotherapy is used more extensively in treatment than radiotherapy Lymphadenectomy in early stage disease is usually beneficial Progestogens are often used in treatment
1: Correct, 75% of patients present with stage 1 disease, which is generally treated with a hysterectomy and bilateral salpingo-oophorectomy. 2: Endometrial biopsy is required for diagnosis. 3: Radiotherapy is used more often than chemotherapy, particularly in treating high-risk patients post-hysterectomy or in pelvic recurrence. 4. Routine lymphadenectomy is not usually beneficial. 5. Progestogens are now seldom used in treatment.
825
A 30-year-old para 1+0 has presented at term in labour. On vaginal examination, the occiput can be palpated posteriorly (near the sacrum). Which of these is correct regarding your further management of these patients? The fetal head may rotate spontaneously to an OA position Delivery is impossible without rotation Augmentation should be avoided if labour is slow If instrumentation is necessary, a ventouse is associated with the most successful outcomes Mothers will generally experience a later urge to push than if position was OA
1: Correct. 2: Delivery is possible in the OP position, however labour is likely to be longer and more painful. 3: Augmentation should be used if progress is slow. 4: Kielland's forceps are associated with the most successful outcomes, however require particular expertise. 5: Generally, women will experience an earlier urge to push in OP than OA.
826
A 38-year-old patient who is undergoing in vitro fertilisation (IVF) for tubal disease presents 4 days after egg retrieval with abdominal discomfort, nausea and vomiting. She has a past medical history of well-controlled Crohn's disease and is currently taking azathioprine maintenance therapy. On examination her abdomen is visibly distended. The most likely diagnosis is: Ruptured ovarian cyst Intestinal obstruction Hyperemesis gravidarum Ovarian hyperstimulation syndrome Pelvic inflammatory disease (PID)
This question concerns complications that may arise during IVF. The most unlikely answer is hyperemesis gravidarum as the patient is not currently pregnant. Given the patient's reason for IVF (tubal disease) - PID may seem like a reasonable answer however it would be likely that this patient would have already been screened for this disease prior to the commencement of IVF and have been appropriately treated. A ruptured cyst would present with a much more acute picture of pain and systemic signs/symptoms. Obstruction may be on a list of differentials considering the patient's past medical history however in the scenario this patient's Crohn's is well-controlled and the patient would present with central colicky pain and bile-stained vomiting. Thus in this scenario ovarian hyperstimulation syndrome is a much more likely diagnosis. This is associated typically with the use of human chorionic gonadotrophin (HCG) in the maturation of follicles during IVF. It presents with lower abdominal discomfort, nausea, vomiting and abdominal distension. Patients may also develop ascites, hypotension and in serious cases acute respiratory distress syndrome and venous thromboembolism. Patients are treated with fluid replacement and thromboprophylaxis. Note: The actual effect on azathioprine during pregnancy is not fully known - the BNF suggests there are some reports of an association between low birth weight and premature births and exposure to the drug however most physicians would advise women with Crohn's disease that are on maintenance treatment with azathioprine to continue taking this drug as the risk of harm from a flare up of Crohn's disease outweighs the risk of harm of taking this medicine.
827
Features of Ovarian hyperstimulation syndrome
Cx seen in some forms of infertility treatment, presence of high levels of luteinized cysts within the ovaries results in high levels of oestrogens and progesterone and also VEGF which leads to increased membrane permeability and loss of fluid from the intravascular compartment. More likely to be seen following gonadotrophin or hCG treatment, more rare in clomifene therapy
828
Classification of OHSS Mild Moderate Severe Crticial
Mild: Abdo pain, bloating Moderate: Mild+ N+V, USS evidence of ascites Severe: Moderate + clinical evidence of ascites, oliguria, HCt \>45% hypoproteinaemia. Crticial: Severe + thromboembolism, ARDS, anuria, tense ascites
829
What is mefenamic acid?
An NSAID not recommended in pregnancy
830
What is tranexamic acid?
Plasminogen activator inhibtor that acts as an antifibrinolytic to prevent heavy menstrual bleeding. Used when a patient wishes to conceive and there is no dysmenorrhoea
831
A 32 year-old lady has a diagnosis of fibroids and has been trying for a baby for 18 months. She has been under investigation at the sub-fertility clinic and no abnormality has been found except for three small submucosal fibroids, for which she does not have any symptoms. Her partner has had sperm analysis which found no abnormality. Which of the following treatments are most appropriate in this situation? Myomectomy Goserelin acetate (GHRH agonist) Endometrial ablation Uterine artery embolisation Ulipristal acetate
Myomectomy is the only treatment option here that will also retain this lady's fertility. Depending on the operation performed, and whether the uterine cavity was entered, the lady would need counselling in regards to delivery, since often a caesarean section is advised due to risk of uterine rupture. GnRH agonists effectively turn off the ovaries, which causes the fibroids to shrink and therefore are easier to remove surgically. On stopping the medication, the fibroids grow back. As this treatment turns off the ovaries, it inhibits ovulation and therefore means that pregnancy is not possible during this time. As a treatment on its own, it would not be suitable in this case as it causes temporary infertility and fibroid regrowth on cessation. However, if combined with a myomectomy, it would provide a suitable treatment option. Endometrial ablation destroys the endometrial lining, therefore meaning that an embryo would not be able to implant. Uterine artery embolisation is not recommended if trying to conceive as it cuts down the blood supply to the uterus significantly, therefore meaning that the fetus would be unable to implant and grow. Ulipristal acetate is a selective progesterone receptor modulator. It is used pre-operatively for women with fibroids as it has been proven to shrink them, thus making surgery easier. This medication affects fertility, thus is not suitable for women trying to get pregnant, unless (like GnRH agonists) it is used for a short period in combination with surgery.
832
Why should a pregnant woman be resuscitated in the left lateral position?
To prevent compression of the IVC reducing venous return to the hear
833
834
Dx of PE in Pregnanacy
ECG and CXR in all patients If CXR normal, compression duplex doppler. CXR normal-\> V/Q CXR abnormal-\> CTPA NB d-dimer is usually raised in first trimester of pregnancy and is thus not useful.
835
CTPA in pregnancy
CTPA slightly increases the lifetime risk of maternal breast cancer(increased by up to 13.6%, background risk of 1/200 for study population). Pregnancy makes breast tissue particularly sensitive to the effects of radiation
836
V/Q Scanning in pregnancy
V/Q scanning carries a slightly increased risk of childhood cancercompared with CTPA (1/280,000 versus less than 1/1,000,000)
837
What are the Fraser Guidelines? What do they constitute?
Used to determine provision of COCP to children under 16y the young person understands the professional's advice the young person cannot be persuaded to inform their parents the young person is likely to begin, or to continue having, sexual intercourse with or without contraceptive treatment unless the young person receives contraceptive treatment, their physical or mental health, or both, are likely to suffer the young person's best interests require them to receive contraceptive advice or treatment with or without parental consent
838
Fraser vs Gillick competence
Some doctors use the term Fraser competency when referring to contraception and Gillick competency when referring to general issues of consent in children.
839
A 35-year-old woman comes to see you, her GP, because she feels tearful and low since the birth of her son 1 month ago and she isn't sleeping well. She says she thinks the baby hates her and feels they aren't bonding, though she is still breast feeding. She has a good family network, including the baby's father and has never suffered with depression in the past. She does not feel suicidal and has not been abusing any substances, you do not feel the baby is at risk. What is the most appropriate management? Refer to social services Antidepressant therapy Cognitive behavioural therapy (CBT) Mindfulness Prescribe zopiclone
The National Institute for Health and Care Excellence recommends that for women without previous history of severe depression, the first line treatment for moderate to severe depression in pregnancy or the post-natal period should be a high intensity psychological intervention (such as CBT). If this is refused, or symptoms do not improve, then an antidepressant should be used. NICE suggests a selective serotonin re-uptake inhibitor (SSRI) or tricyclic antidepressant (TCA). Mindfulness may be useful for women with persistent subclinical depressive symptoms. You would only need to involve social services if you felt that someone in the household may be at risk. According to the British National Formulary (BNF) zopiclone should be avoided whilst breast feeding as it is present in breast milk
840
False Labor
Occurs in the last 4 weeks of pregnancy Presentation: contractions felt in the lower abdomen. The contractions are irregular and occur every 20 minutes. Progressive cervical changes are absent.
841
Braxton Hicks contractions
Braxton Hicks contractions, also known asprodromal labor or practice contractions, or false labor, are sporadic uterine contractions that sometimes start around six weeks into a pregnancy. However, they are not usually felt until the second trimester orthird trimester of pregnancy. [1]
842
You are the junior doctor on the labour ward, and are called to a 27-year-old's first delivery. She underwent spontaneous preterm rupture of membranes at 34 weeks, and now the umbilical cord is palpable vaginally above the level of the introitus. Which of these is correct regarding your management of this patient? ## Footnote Tocolytics, e.g. terbutaline, should be avoided The presenting part of the fetus may be pushed back into the uterus The patient is advised to lie supine The cord may be pushed back into the uterus Natural labour would be the usual delivery method of choice
This is a case of cord prolapse, which occurs after membrane rupture when the umbilical cord descends below the presenting part of the fetus. It can lead to fetal hypoxia and death due to the cord being compressed or going into spasm. 1: Tocolytics should be used to reduce cord compression and allow Caesarean delivery 2: Correct, to avoid compression 3: The patient is advised to go onto all fours 4: The cord should not be pushed back into the uterus 5: Immediate Caesarean section is the delivery method of choice
843
What are the indications for assessment of a newborn by the neonatal team after any degree of meconium?
RR \>60 Grunting HR \<100 \>160 CRT \>3 T \>38 or 37.5 on 2 occasions 30 minutes apart SaO2 \<95 Central cyanosis
844
845
Def Eisenmenger's? With what is it associated? What are its features? Mx?
Reversal of a left to right shunt in a congenital heart defect due to pulmonary hypertension which has occurred as a result of remodelling of pulmonary microvasculature? VSD, ASD, PDA Original murmur may disappear Cyanosis Clubbing RV failure Haemoptysis, embolism Heart-lung transplant required
846
A woman who is 10 weeks pregnant presents to clinic with a pre-existing heart condition. Which of the following put her at the highest risk of complications? Ventricular septal defect Patent ductus arteriosus Coarctation of the aorta Chronic mitral regurgitation Eisenmenger's syndrome
Eisenmenger's syndrome is the correct answer as it has a maternal mortality ranging from 30% to 50%, with a 50% risk of foetal loss if the mother survives. It occurs when a long standing left to right shunt reverses; not only are mother and baby at risk of hypoxaemia but also of thromboembolic events. Isolated VSDs are well tolerated during pregnancy, provided it is not associated with pulmonary hypertension or eisenmenger's, and so considered a low-risk lesion PDA during pregnancy is not associated with additional maternal risk, provided the shunt is small to moderate and the pulmonary artery pressures are normal. Percutaneous closure is now considered first-line therapy, and it is reasonable to close even asymptomatic small PDAs. Following repair of more significant PDAs, women are at no additional risk for complications during pregnancy. Coarctation is well tolerated during pregnancy, although hypertension, heart failure, angina, and aortic dissection are possible complications. Coarctation can be associated with intracerebral aneurysms, which may rupture during pregnancy. It is therefore considered to be a moderate-risk lesion, even when repaired. In chronic mitral regurgitation, the physiologic reduction in SVR partially compensates for the additional volume overload generated by the regurgitant valve. Should heart failure occur, it can be treated safely with nitrates, hydralazine and dihydropyridine calcium channel-blocking agents. It is considered a low risk lesion, especially after repair.
847
Varencline
a nicotinic receptor partial agonist has been shown in studies to be more effective than bupropion nausea is the most common adverse effect. Other common problems include headache, insomnia, abnormal dreams varenicline should be used with caution in patients with a history of depression or self-harm. There are ongoing studies looking at the risk of suicidal behaviour in patients taking varenicline contraindicated in pregnancy and breast feeding
848
Bupropion
a norepinephrine and dopamine reuptake inhibitor, and nicotinic antagonist should be started 1 to 2 weeks before the patients target date to stop small risk of seizures (1 in 1,000) contraindicated in epilepsy, pregnancy and breast feeding. Having an eating disorder is a relative contraindication
849
Smoking in pregnant women
Pregnant women NICE recommended in 2010 that all pregnant women should be tested for smoking using carbon monoxide detectors, partly because 'some women find it difficult to say that they smoke because the pressure not to smoke during pregnancy is so intense.'. All women who smoke, or have stopped smoking within the last 2 weeks, or those with a CO reading of 7 ppm or above should be referred to NHS Stop Smoking Services. Interventions the first-line interventions in pregnancy should be cognitive behaviour therapy, motivational interviewing or structured self-help and support from NHS Stop Smoking Services the evidence for the use of NRT in pregnancy is mixed but it is often used if the above measures failure. There is no evidence that it affects the child's birthweight. Pregnant women should remove the patches before going to bed as mentioned above, varenicline and bupropion are contraindicated
850
A 36-year-old woman suffers from a major postpartum haemorrhage after delivering twins. The obstetric consultant examines her and suspects uterine atony to be the cause. The protocol for major PPH is initiated. Bimanual uterine compression fails to control the haemorrhage. Which drug is an appropriate next step in the management of uterine atony? Intramuscular carboprost Intravenous oxytocin Rectal misoprostol Intravenous carboprost None - proceed immediately to balloon tamponade
Uterine atony is the most common cause of primary postpartum haemorrhage. It entails failure of the uterus to contract fully following the delivery of the placenta, which hinders the achievement of haemostasis. Uterine atony is associated with overdistension, which may be due to multiple gestation, macrosomia, polyhydramnios or other causes. In addition to the usual steps taken in an episode of PPH (including an ABC approach if the patient is unstable), the following management should be initiated in sequence: bimanual uterine compression to manually stimulate contraction intravenous oxytocin and/or ergometrine intramuscular carboprost intramyometrial carboprost rectal misoprostol surgical intervention such as balloon tamponade
851
Mx of PPH?
ABC Bimanual uterine compression IV oxytocin and or ergometrine IM carboprost Intramyometrial carboprost Rectal misoprostol Balloon Tamponade In sequence
852
What are the expected results in DS screening if trisomy present?
Low alpha fetoprotein (AFP) Low oestriol High human chorionic gonadotrophin beta-subunit (-HCG) Low pregnancy-associated plasma protein A (PAPP-A) Thickened nuchal translucency
853
A 40-year-old woman returns to the GP to discuss her recent blood results. A CA 125 was measured after she reported persistent abdominal bloating and urinary urgency over the past 2 months. Her CA 125 level is reported as 15 IU/ml. Normal CA 125 \<35 IU/ml Which one of the following is the most appropriate next action? ## Footnote Refer to gynaecology clinic Give advice on a bladder retraining programme Assess for other cause of symptoms and advise to return if these become more frequent Refer for ultrasound of abdomen and pelvis Re-test CA 125
If serum CA 125 is 35 IU/ml or greater, arrange an ultrasound scan of the abdomen and pelvis If the ultrasound suggests ovarian cancer, refer the woman urgently. For any woman who has normal serum CA125 (less than 35 IU/ml), or CA125 of 35 IU/ml or greater but a normal ultrasound: clinicians should assess her carefully for other clinical causes of her symptoms and investigate if appropriate. If no other clinical cause is apparent, they should advise her to return to her GP if her symptoms become more frequent and/or persistent. Referral to the gynaecology clinic is not warranted at this time. While bladder retraining is a treatment option for overactive bladder syndrome; it is not the most appropriate approach to dealing with this patient's symptoms. From above we can see that referral for an ultrasound would be necessary if CA 125 was raised to sufficient levels but this is not the case. Re-testing CA 125 would also be of no value at this time. In this case, a thorough assessment for alternative causes of this patient's symptoms is the best form of action at this stage.
854
Epilepsy: contraception For women taking phenytoin,carbamazepine, barbiturates, primidone, topiramate, oxcarbazepine:
UKMEC 3: the COCP and POP UKMEC 2: implant UKMEC 1: Depo-Provera, IUD, IUS
855
Epilepsy: contraception For lamotrigine:
UKMEC 3: the COCP UKMEC 1: POP, implant, Depo-Provera, IUD, IUS
856
Def: preterm labour
24-37w Most important before 34w as neonatal risks are greater.
857
What are the causes of preterm delivery?
Can be as a result of spontaneous labour or can be iatrogenic (obstetric induction due to maternal/fetal risks)
858
Neonatal Cxs of preterm labour
Accounts for 80% of NICE occupancy 20% of perinatal mortality 50% of cerebal palsy Chronic lung ndisease Blindness Minor disability Earlier the gestation the greater the risk to the fetus
859
Px of preterm delivery
24w: 1/3rd of neonates die, 1/3tf handicapped by 32w both of these risks are less than 5%
860
Maternal risk of preterm labour
Infection Endometritis post natally
861
Risk factors for spontaneous preterm labaour
Previous Hx Socioeconomic class Maternal age Short inter-pregnancy interval Maternal medical disease e.g. renal failure, DM, thyroid disease Preganancy complications: pre-eclampsia, IUGR, male fetus Raised Hb STIs BV Previous cervical Sx Multiple pregnancy Uterine abnormalities and fibroids UTI Polyhydramnios Congenital fetal abnromalities APH
862
Three mechanisms fo preterm labour (Castle analogy)
Too many defenders: Multiple pregnancy, excess liquor. Probably largely mediated by increased stretch Defenders jumpm out: Fetal surivavl response: pre-eclampsia, IUGR, infection, placental abruption Poor castle design: Uterine abnormalities Cerbical incompetence Enemy knock down walls: Infection, may be subclinical, BV, GBS, Trichomonmas and Chlamydia Poor dental health
863
Prediction of preterm labour: Hx
Those with risk factors Previous Hx of late miscarriage or prteterm labour Often not identified on history alone
864
Ix in predicitng preterm labour
TVS: cervical length is both sensitive and specific
865
Prevention of preterm labour
Limited to women at high risk, strategies should begin by 12w Cervix: cervical cerclage either vaginally or abdominally. Prepregnancy and laparoscopy. Progesterone supplementation: low risk women with short cervix on USS may benefit Infection: screening and treatment of UTIs and BV Fetal reduction: higher order multiple reduction at 10-14w Polyhydramnios: needle aspiration (amnioreduction) or if fetal surveillance is intesive NSAIDs which reduce fetal urine output and cause premature closure of fetal PDA Treatment of medical disease e.g. thyroid disease
866
3 situtations in which cervical cerclage is used?
Elective., 12-14w Scanned regulalry and used if significant shortening Rescue
867
NB re metronidazoole in preterm labour
Increases risk of preterm labour
868
Clinical features of Preterm labour Hx Ex
Painful contractions (stop spontaneously in 50%) and labour will not continue until term Painless cervical dilatation may occur in cervical incompetence or the woman may experience a dull suprapubic ache APH and fluid loss common Fever Lie and presentation checked with palpation DVE is performed unless membranes have ruptured. Effaced or dilating cervix confirms dx but the course of preterum labour is unpredictable
869
Ix in preterm labour
CTG + USS to assess fetal state Fetal fibronectin can be useful. Negative= unlkely delivery. TVS may be used \>15mm means delivery unlikely To look for infection: vaginal swabs, maternal CRP, WCC NB steroids
870
Def: Red blood cell isoimmunisation
Occurs when the mother mounts an immune response against antigens on fetal RBCs that enter her circulation. Resulting Abs then cross the placenta and cause fetal RBC destruction
871
Pathophysiology of RBC isoimmunisation Blood groups
ABO and rhesus genotype Rhesus system consists of 3 linked gene pairs. Aone allele of each pair is dominant to the other. C, D, E. An individual inherits one allele of each pair from each parent in Mendelian fashion D is most significant. Dd/DD express the D antigent and are D rhesus positive. dd= Rhesus negative and will recognise the D antigen as foreign if they are exposed to it
872
Sensitisation in RBC isoimmunisation
Small amounts of fetal blood and cross te placenta during uncomplicated pregnancies and particularly at sensitising events at delivery. If fetus is D-rhesus positive and mother is D-rhesus negative the mother will create anti-D Abs
873
Haemolysis in RBC isoimmunisation
Immunity is permanent and if the mother's immune system is exposed again to the antigen e.g. a subsequent pregnancy, large amounts of Abs are rapidly created. They can cross the plaecnta and bind to fetal RBCs which are then destroyed in the fetal reticuloendothelial system. This causes haemolytic anaemia and ultimately death. Rhesus haemolytic disease. A similar immune response can be mounted against other RBC antigens
874
What are the other antibodies that can be involved in haemolytic disease of newborn?
Anti-C Anti-Kell (not a rhesus) Esp. after blood transfusion
875
What are some potentially sensitising events for haemolysis in newborn?
TOP or ERPC after miscarriage Ectopic pregnancy Vaginal bleeding \<12w or heavy ECV Invasive uterine procedure e.g. amniocentesis or CVS Intrauterine death Delivery
876
Prevention of Rhesus disease
Produciton of maternal anti-D can be prevented by the administration of exogenous anti-D to the mother This mops up fetal RBCs that have crossed the placenta by binding to their Ags, preventing maternal immune recognition. Anti-D usually given even if both parents are known to be rhesus negative due to possibilty of non-paternity NB Anti-D is pointless if sensitisation has already occurred
877
Antenatal use of Anti-D
Anti-D should be given to all women who are rhesus negative at 28w. Also given to such women within 72h of any sensitising event.
878
Anti-D \<12w
Not required for spontaneous miscarriage before 12+0 unless there is intrumentation of the wob In pregnancies \<12w anti-D indicated in ectopic, molar, TOP and intrauterine bleeding where this is heavy, repeated or associated with abdominal pain.
879
Anti-D \<12w alwasy given:
Ectopic or TOP regardless of method of management NB NICE recommends not offering anti-D if ectopic is medically managed although there is no clear evidence to support this
880
Anti-D in 12w-20
For potentially sensitising events between 12 and 20 weeks of gestation, a dose of 250 IU should be administered within 72 hours of the event. Women who are RhD negative presenting with continual uterine bleeding between 12 and 20 weeks of gestation should be given at least 250 IU anti-D Ig, at a minimum of six-weekly intervals. A maternal blood group and antibody screen should be undertaken to determine or confirm the RhD group and check for the presence of immune anti-D in these cases. If anti-D is identified, further history should be obtained and investigation undertaken to determine if this is immune or passive. If this is not clear then the women should be offered anti-D prophylaxis, as the assumption should be made that it is passive.
881
Anti-D 20-Term
Within 72h of sensitising event FMH is required to detect fetal cells in maternal circulation and to estimate the volume of FMH to calculate additional anti-D dosease.
882
What is FMH and when is it used?
Fetal maternal haemorrhage, used to determine the degree of fetal blood loss into the maternal circulation \>20w to determine anti-D dosing
883
Prevention of rheus disease
Booking and 28w: check for Abs Rhesus negative: give anti-D at 28w, after any bleeding or protentially sensitising event and after delivery if fetaus is positive
884
Manifestations of rhesus disease
Mild: neonatal jaundice only More sufficient haemolysis may cause neonatal anaemia. More severe: in utero anaemia-\> cardiac failure ascites and oedema-\> hydrops. Death will follow.
885
Rhesus disease in subsequent pregancies
Worsesns as maternal Ab production increases
886
Mx of rhesus isoimmunisation
Identifiaction of women at risk Assessing if how severely the fetus is anaemic In utero blood transufion or delivery
887
Identifiication of risk for fetal haemolysis
Unsensitised women screened at 28w. If anti-D levels \<10IU/mL, significant fetal problem unlikely, checked every 2-4w \>10IU/mL further investigation Anti-Kell Abs less predictive of severity and USS used earlier
888
How to assesss severity of fetal anaemia
USS Doppler USS of the peak velocity in systle (PSV) in the fetal MCA has high sensitivity for significant anaemia in \<36w. Used fortnightly in at-risk pregnancies Very severe anaemia (\<5g/dL) is detectable as fetal hydrops or excessive fetal fluid. US-guided blood sampling can be used to confirm suspected fetal anaemia.
889
Treatment of fetal anaemia
Fetal blood sampling is performed with rhesus negative, high Hct, CMV-negative blood ready to be injected down needle if anaemia si confirmed. This proicess will need to be continued until delviery at 36w. All neonates born to rehus-negative women should have the blood group checked, FBC, blood film and bilirubin to detect degrees of isoimmunisation
890
What is the lie of the fetus
Describes the relationship of the fetus to the long axis of the uterus
891
What are the different kinds of fetal lie?
Longitudinal Transverse or Oblique
892
What is the proportion of abnromal lie?
1 in 200 births Before term it is normal
893
What are the causes of abnormal lie?
Circumstances that allow more room to turn: e.g. polyhydramnios, high parity (more lax uterus) are the most common causes resulting in an unstable or constantly changing lie Conditions that prevent turning: Fetal and uterine abnormalities and twin pregnancies Conditions that prevent engagement: Placenta praevia, pelvic tumours or uterine deformities Unstable lie in nulliparous women is rare
894
Cxs of abnormal lie
If the head or breech cannot enter the pelvis, labour cannot deliver the fetus. An arm or the umbilical cord may prolapse when membranes rupture If neglected, obstruction eventually causes uterine rupture
895
What is the difference between oblique and transverse lie?
Head in flank= transverse Head in one iliac foss= oblique
896
Mx of abnormal lie
No management required before 37w unless the woman is in labour Agter 37w woman is admitted incase of ROM, USS performed to exclude particular causes e.g. polyhydramnios and placenta praevia ECV unjustified as fetus turns back. If spontaneous version occurs and persists for 48h the mother is discharged. An abnormal lie will usually stabilise before 41w. At 41w or if the woman is in labour the persistently abnromal lie is delivered by Caesarean.
897
Def: breech presentation
Presentation of the buttocks Occurs in 3% of term pregnancies. More common earlier in pregnancy therefore more common in preterm labour
898
Extended breech
70% has both legs extended at the knee
899
Flexed breech
15% Has both legs flexed at the knee
900
Footling breech
15% One or both feet present below the buttocks
901
Causes of breech presentation
No cause found in most Previous breech has occurred in 8% Prematurity Conditions that prevent movement or head engagement are more common
902
Dx of Breech presentation
Only important from 37w or if patient is in labour Upper abo discomofort common Hard head normally palpable and balottable at the fundus USS confirms Dx and can help detect fetal abnormalitiy, pelvic tumour or placenta praevia and ensures the prequisites for ECV are met
903
Cxs of breech presentation
Perinatal and long-term morbidity and mortality are increaesd Fetal abnromalities are more common but even normal breech babies have higher rate of LT neurological handicap which is independent from the mode of delivery. Labour has potential hazards: increased risk of cord prolapse. Also risk of trapped head.
904
Mx of Breech presentation
ECV from 37w Caesareab section (if ECV has failed or is contraindicated) Vaginal delivery
905
Features of ECV
Attempt to turn the baby to a cephalic presentaiton. Reduces the number of breech presentations at term. Success rate is 50% 3% of successfully turned breeches will turn back. Where ECV fails, only 3% will turn spontaneously before delivery
906
ECV technique
Without anaesthetic Made easier with administration of a tocolytic if uterine tone is high or an initial attempt has failed. Breech disengaged from the pelvis and pushed upwards and to the side. USS guided CTG straight after Anti-D for rhesus negative women.
907
Safety of ECV
Risk very low Placental abruption and uterine rupture have been reported. Risk of emergency C-section
908
Factors affecting success of ECV
Low succes rates seen in nulliparous Caucasions Where the breech is engaged Head not easily palpable Uterine tone high Obese women Liquor volume reduced
909
What are the Absolute contraindications to ECV
C-section required anyway e.g. placenta praevia Twins Membranes ruptured APH within last 7d Abnromal CTG Major uterine abnromalitiy
910
Relative contraindications to ECV
Small for dates with abnormal doppler Proteinuric pre-eclampsia Oligohydramnios Major fetal abnormalities Scarred uterus Unstable lie
911
What is the safest method of delivery for singleton term breech?
C section Reduces mortality by 1% and ST morbidity but does not affect LT outcomes. Maternal morbidity is not increased. NB 1/3rd of attempted vaginal breech deliveries ends with emergency C-sections.
912
Unfavourable factors for vaginal breech birth
Contraindications to vaginal delivery Contracted pelvis Footling breech Large baby \>3800g Growth restricted baby Hyperextended fetal neck in labour Lack of suitably trained clinician Previous C-section
913
Vaginal breech birth Intrapartum care
Pushing not encouraged until the buttocks are visible CTG Epidural common In 30% there is slow cervical dilatation in the frist stage or particularly poor descent in the second. Oxytocin not advised-\> C-section
914
What is a common cause of a difficult breech delivery
Injudicious traction causing extension of the head. Once the buttocks distend the perineum an episiotomy may be made but is not essential.
915
Delivery in Breech
Fetus delivers as far as the umbilicus with maternal effort Legs can flexed out of the vagina whilst the back is kept anterior, Once the scapula is visible the arms are hooked down by sweeping it across the chest If arms cannot be reached as they are extended superiorrly, Lovset's procedure is required. Once the back of the neck is visible, the operator supports the entire weight of the fetus on one palm and forearm, with their finger in its mouth to guide the head over the perineum and maintain flexion. The other hand presses against the occiput. If this fails, forceps.
916
What is Lovset's procedure
Required in breech if arms are extended above the head. Hands placed around the body with the thumbs on the sacrum, rotating the baby 180 degrees clockwise then counter-clockwise with gentle downward traction. Allows the shoulders to enter the pelvis
917
What is the Mauricea-Smellie-Veit manouvre
Used in breech to deliver the head: Operator supports the entire weight of the fetus on one palm and forearm. Finger in mouth to guide head over the perinum and maintain flexion. Other hand presses against the occiput
918
What is the purpose of instrumental delivery
Aim is to prevent fetal and maternal morbidity. Shape of the pelvis will only allow delviery if the head it posterior or occasionally anterior
919
What are Simpson's Forceps, Neville-Barnes forceps? When are they suitable
Non-rotational Only suitable when the baby's head is occipitoanterior
920
What are Kiellan'd forceps?
Rotational forceps allowing a malpositioned head to be rotated by the operator to the OA position before the application of traction.
921
Safety of ventouse and forceps
Failure: both methods can fail Maternal Cxs and need for analgesia are greater with forceps. Either instrument can cause vaginal laceration, blood loss or third-degree tears. Cervical and uterine tears are very rare. Fetal complications: worse with the vventous. Lives a chignong which diminishes over hours. Scalps lacerations, cephalohaematomata are more common with ventous Facial bruising, nerve damage and even skull and neck fractures occur with injudicious use of forceps and prolonged traction by either instrument is dangerous. Chaning instrument: associated with increased fetal trauma and is only appropriate if a ventouse has achieved descent to pelvic outlet but is then replaced by a low cavity forceps delivery.
922
What are the indiciations ofor instrumental vaginal delivery?
Prolonged second stage: most common indication Fetal distress; more common in the second stage Prophylactic use indicated to prevent pushing in some women who have medical problems e.g. cardiac disease or HTN In breech delivery to control the head
923
Prolonged second stage, use of instrument
1h of pushing has failed to deliver the baby If the mother is exhausted it may be performed earlier The length of the passive second stage is less important
924
What are the approaches to prevent instrumental delivery
All labours: continuous support with delivery in the most comfortable maternal position possible. Epidural, analgesia, CTG, and induction predispose to instrumental delivery.
925
Epidural analgesia and isntrumental delviery
Epidural increases the risk of instrumental delivery. If used, maternal pushing should be delayed at least an hour after the diagnosis of second stage unless the head is visible. Oxytocin should be considered if descent of the head is poor (Nulliparous women)
926
What determines the type of delivery and the choice of instrument?
Position and descent of the head. With either instrument, if moderate traction does not produce immediate and progressive descent, C-section is indicated
927
Features of a low cavity delivery
Head below the level of the ischial spines with bony prominences palpable vaginally on the lateral wall of the mid pelvis and is usually OA. Forceps/ventouse are appropriate. Pudendal block with perineal infiltration is usually sufficient.
928
Features of a mid-cavity delivery
Head is not palpable adominally but is at or just below the level of the ischial spines. Epidural or spinal. Trialled in theatre if there is doubt about the potential success. May be OA, OT or OP
929
OA mid-cavity delivery
Forceps or ventouse
930
OT mid-cavity
Usually this is as a result of insufficient descent of the head to make it rotate. Descent achieved with ventouse with rotation resulting Non-rotational forceps are contraindicated. Rotational forceps may be able to achieve rotation in situ followed by descent.
931
OP mid-cavity delivery
Often accompanied by extension of the fetal haed. 1/5th may still be abdominally palpable. Need for instrumental delivery is unsuual in multiparous women and if required this position should be suspected. Requires rotation 180deg, Klielland's most effective.
932
What are the prerequisites for instrumental vaginal delivery
Head must not be palpable abdominally Head must be at or below the level of the ischial spines Cervix must be fully dilated, with the second stage reached. Position of the head must be known Adequate analgesia Bladder should be empty Delivery for a valid reason
933
Ventouse vs forceps
Ventous causes: Higher failure rate More fetal trauma no difference in APGAR Less maternal trauma.
934
What is the usual C-section operation?
Lower segment Caesarean section in which the abdominal wall is opened with a suprapubic transverse incision and the lower segment of the uterus is also incised transversely to deliver the baby
935
When might a "classical" C-section be used?
Extreme prematuirty Multiple fibroids Transverse fetus
936
Indications for emergency C-section
Prolonged first stage Fetal distress
937
Features of prolonged first staeg
Diagnosed when dilatation is not imminenet by 12h or earlier if labour was initially rapid. Occasionally ful dilatation is achieved but not all of the criteria for instrumental delivery are met.
938
What are the 3ps of a prolonged labour
Powers: inefficient uterine action Passenger: malposition or malpresentation Passage: pelvic abnormalities and cephalo-pelvic disproportion
939
When is elective C-section usually performed
39w If earlier, steroids should be considered
940
What are the absolute indications for elective caesarean
Placenta praevia Severe antenatal fetal compromise Uncorrectable abnormal lie Previous vertical C-section Gross pelvic deformity
941
What are the relative indications for elective C section?
Breech Severe IUGR Twin pregnancy DM and other diseases Previous C-sec Older nulliparous patients.
942
What are the most common indications for delivery before 34w
Severe pre-eclampsia and IUGR
943
What are the different types of C section
Emergency: immediate threa to mother or fetus e.g. severe fetal distress Urgent: maternal/fetal compromise that is not immediately life threatening e.g. dystocia Scheduled: needing early delivery but no compromise Elective: at time to suit mother and team Peri/post-mortem: for fetus and mother during maternal arrest or for fetus after maternal death
944
What are the maternal complications of C-section
Greater than with a vaginal delivery. Greater when in labour rather than elective. Haemorrhage and the need for transfusion Uterine or wound infection (20%) Bladder/bowel damage. VTE Prophylactic antibiotics and thromboprophylactic measures. 1/5000 will die after caesarean
945
What are the fetal complications of C section
Increased risk of fetal respiratory morbidity at any gestation and should not be before 39w in uncomplicated pregnancy for this reason. Fetal lacerations rre rare Bonding and breastfeeding affected by emergency procedures. Neonatal morbidity and mortality is increased with elective C-section.
946
What are the risks of C-section to subsequent pregnancy
Become increasingly difficult Increase in stilbirths in subsequent pregnancies Increased incidence of placenta praevia, also increased risk of placenta accreta or percreta (best diagnosed with 3D power Doppler)
947
Mx of placenta praevia
Most senior person with anaesthetic support Cross match blood Facilities for internal iliac or uterine artery embolisation are advised Uterine incision should avoid the placenta, which can be left in situ or hysterectomy performed. In less severe cases compression of the placenta with a Rusch balloon may alleviate or reduce haemorrhage. Ultimately delay in performing hysterectomy can be lethal.
948
What is labour
Process whereby the fetus and placenta are expelled from the uterus, usually between 37 and 422 gestation Dx: painful uterine contractions accompany dilatation and effacement of the cervix
949
What are the stages of labour
Stage 1: initiation to full dilatation 2: Dilatation to fetus delivery 3: Delivery of fetus to delivery of placenta
950
What are the 3 mechanical factors determinining the progress of labour
Powers Passage Passenger
951
What are features of the powers of labour
Once labour is established the uterus contract 45-60s every 2-3 minutes This pulls the cervix up: effacement and causes dilatation, this is aided by the pressure of the head as the uterus pushes the head down into the pelvis. Poor uterine activity is a commmon feature of nulliparous women and in induced labour but is rare in multiparous women
952
What factors constitute tthe passage in labour
Bony pelvis Soft tissues
953
What are hte palnes of the pelvis?
Inlet: transverse diameter is 13cm, wider than the 11cm AP diameter Mid-cavity: is almost round, transverse and AP diameters are similar Outlet: AP (12.5cm) is greater than the transverse (11cm) In the lateral wall of the round mid-pelvis, the ischial spines are palpable vaginally and are used as landmarks to assess the head's descent.
954
What is "station" and how is it measured
Level of the descent of the head Measured in relation to the ischial spines Station 0 means the head is above the level of the spines +2 means it is 2 below -2 means it is 2 above
955
What are the features of the soft tissues in passage
Cerbical dilatation is prerequisite for delivery and is dependant on contractions. Pressure of head and the ability of the cervix to soften allows distension. The soft tissues of the vagina and perineum need to be overcome in the second stage.
956
957
What are the features of passenger
Attitude Position Size
958
What is the gregma
Anterior fontanelle
959
960
What is the vertex of fetal head
The area between the occipit (posterior fontanelle) and the bregma (anterior fontanelle)
961
What is the attitude of the fetal head What is the ideal attitude?
Degree of flexion of the head on the neck Maximum flexion keeping the head bowed- vertex presentation. Presenting diameter is 9.5cm running from the anterior fontanelle to below the occiput at the back. Aextension results in a larger diameter
962
What is a brow presentation
Extension of the fetal head by over 90 degrees, increases the diameter to 13cm.
963
What is a face presentation
Extension by 120 degrees.
964
965
What is the position of the fetal head?
The degree of rotation of the head on the neck. If the sagittal suture is transverse, the fetal head will fit the pelvic inlet best. At the outlet the saggital suture must be vertical for the head to fit. Therefore the head must rotate 90 degrees during labour.
966
What is the normal delivery of the fetal head?
OA: occipitut anterior OP in 5% is more difficult.
967
What does position of the OT position imply?
Non-rotation and that delivery without assistance is impossible.
968
What is moulding of the fetal head?
Compression of the fetal head due to the sutures allowing the bones of the head to come together Pressure of the scalp on the cervix to cause localised swelling or caput.
969
Terms describing the fetal head
Presentation: i.e. cephalic or breech Presenting part: lowest part of the fetus palpable e.g. vertex, brow, face Position: OA, OT, OP Attitude: degree of flexion
970
What are the movements of the fetal head in delivery
Engagement in OT Descent and flexion Rotation 90 deg to OA Descent Extension to deliver Restitution and delivery of shoulder
971
972
What is the show?
A pink/white mucus plug form the cerivx and or rupture of membranes
973
What are the phases of Stage 1 of labour?
Latent phase: cervix dilates slowly for first 3cm Active phase: average dilatation is at a rate of 1cm/h in nulliparous and 2cm/h in multiparous Active first stage should not normally last longer than 12h
974
What are the stages of the second stage of labour
Passive: lasts from full dilation until the head reaches the pelvic floor and the woman experienes the desire to push. Rotatio and flexion are commonly completed, may last a few minutes Active: when the mother is pushing/ Fetus is delviered on average after 40 minutes or 20 minuts (multip vs nullip). If it takes \>1h spontaenous delivery becomes decreasingly likely.
975
Process of delivery of the baby
As the head reaches the perineum it extends to come up and out of the pelvis Perineum stretches and often tears Episiotomy is indicated if progress is slow or in fetal distress The head then restitutes, rotating 90 degress to adopt the transverse position in which it entered the pelvis With the next contraction, the shoulders the deliver, with the anterior shoulder coming under the pubic symphysis first, usually aided by lateral body flexion in a posterior direction. Posterior shoulder delivery is aided by flexion in an anterior direction
976
What are the features of a normal 3rd stage of labour
15 mins \<500mL blood loss Uterine muscle fibres contract to compress the BVs formerly supplying the placenta
977
What is the prevalence of perineal trauma following delivery?
Intact in 1/3rd of nullips and in 1/2 of multips
978
What is the difference between induciton and augmentation
Artificial initiation of labour= induction Augmentation= strengthening the contractions of established labour
979
What determines the likelihood of the success of labour induction
Favourability of the cervix (Bishop's score)
980
What are the methods for induction
Natural Medical: PGs Oxyotcin following amniotomy Surgical: Amniotomy
981
Features of inductions with prostaglandins
PGE2 (2mg) Inserted into posterior vaginal fornix, best method in most nullips and multips (unless te cervix is very favourable) Either starts labour or improves the ripeness of the cervix to allow amniotomy. If one dose doesn't improve cervical ripeness, a second dose may be given \>6h later providing there is no uterine activity. \>2 doses are not helpful
982
Features of induction with amniotomy
Forewaters are ruptured with an amnihook (ARM) Oxytocin infusion is usually started within 2h if labour has not ensued. Oxyotcin alone may be used if ROM has already occurred
983
What is natural induction
Cervical sweeping: passing a finger through the cervix and stripping between the membranes at the lower segment of the uterus. At 40w this reduces the chance of induciton and postdates pregnancy
984
What are some common indications for induction
Prolonged pregnancy Suspected growth restriction PROM Pre-eclampsia Medical disease: HTN and DM
985
What are the fetal indications for induction
High risk situations e.g. prolonged pregnancy Suspected IUGR Compromise APH Poort Ob Hx PROM
986
What are the materno-fetal indications for induction?
Pre-eclampsia Maternal disease e.g. DM
987
What are the maternal indications for induction
Social In utero death
988
What are the absolute contraindications to induction
Acute fetal compromise Abnormal lie Placenta praevia Pelvic obstruction or deformity Usually considered inappropriate after \>1 C-sect
989
What are the relative contraindications for induction
One previous C-sec (increased scar rupture rate) Prematurity
990
What is the Mx of induced labour
Because of both the indication and the use of drugs, the fetus is at increased risk during induction CTG following induction with Pg (1hr) or when they stimulate uterine activity Oxyoticn also warrants CTG monitoring Induction increases the time spent in early labour
991
What are the Cxs of induced labour?
Failure/slow start of labour due to ineffcient uterine activity Risk of instrumental delivery or C-section is higher Uterine overactivity: fetal distress and uterine rupture Umbilical cord prolapse at amniotomy PPH more likely IP and PP infection also more likely Prematurity due to acciden e.g. incorrect gestation Amniotic fluid embolism (if Oxyotcin used and ARM not performed)
992
What are the contraindications for VBAC?
Vaginal delivery after C-section: Vertical uterine scar Multiple previous Caesareans (\>2)
993
What are the factors influencingvaginal delviery after one C-sec
60-80% of women will deliver vaingally, others will require an emergency C-sec Factors associated with increased success: Spontaneous labour Inter-pregnancy interal \<2y Low age and BMI Previous Vaginal delivery Previous C-sec was elective or for fetal distress. Smaller subsequent fetus and engagement of the head
994
What are the maternal risks of VBAC?
Vaginal delivery safest, emergency C sec least safe. Risk of blood transfusion or uterine infection higher Serious maternal morbidity is greater with increasing number of C-secs: placenta accreta
995
What are the fetal risks of VBAC?
Higher mortality as risk of antepartum stillbirth elminiated by 39w elective C sec Uterine rupture
996
What is significant in terms of fetal implications of C-sec
TTN is higher in elective C-secs Fetal morbidity is increased with increasing number of prior caesareans
997
Mx of VBAC
Hospital delivery and CTG monitoring advised Induction avoided Augmentation also increases the risk of scar rupture Epidural safe but labour should not be prolonged Scar rupture presents as fetal distress accompanied by scar pain, contraction cessation, vaginal bleeding and maternal collapse. Immediate laparotomy if rupture suspected
998
What is prelabour term ROM
Rupture of membranes without onset of labour Different from PPROM: prelabour preterm rupture of membranes
999
What is hindwater ruptre
Leaking of liquor but membranes remain in front of the fetal head
1000
What are the risks of PROM
Cord prolapse: rare, usually a Cx of transverse lie or breech Risk of infection, increased by vaginal examination, GBS presence, increased duration of membrane rupture
1001
Mx of Prelabour ROM
Confirmation Lie and presentation checked DVE avodied, may be performed if risk of cord prolapse or fetal distress Vaginal swab Fetal auscultation or CTG Induce or await onset of labour
1002
Induciton of labour in prelabour ROM Waiting for labour in ROM
Does not increase risk of C-sec and associated with a lower chance of maternal infection and of NICE admission, particularly if GBS carrier Only 20% do not enter labour spontaenously Maternal pulse, T and fetal HR measured every 4h. Meconium or infection warrants induction. After 18h: antibiotic prophylaxis vs GBS and induction
1003
What is the cut off for antibiotic prophylaxis in Prelabour ROM?
18h vs GBS and induce labour
1004
Metronidazole In pregnancy Risk Conclusion Alternatives Breastfeeding
Possible increased risk of preterm labour Use with caution Clindamycin Safe to breastfeed
1005
Penicillins In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risks Safe
1006
Erythromycin In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known Safe
1007
Cephalosporins In pregnancy Risk Conclusion Alternatives Breastfeeding
Safe Nil known risks
1008
Augmentin In pregnancy Risk Conclusion Alternatives Breastfeeding
Possible increased neonatal risk if preterm birth- NEC Use with caution Penicllins Safe to breastfeed
1009
Tetracyclines In pregnancy Risk Conclusion Alternatives Breastfeeding
Discolour teeth if 2nd trimester Avoid Erythromycin as alternative Safe to breastfeed
1010
Timethoprim In pregnancy Risk Conclusion Alternatives Breastfeeding
Folic acid antagonist Avoid in pregnancy Cephalosporins as an alternative Safe
1011
Fundamentals of analgesic use in pregnancy
Paracetamol best used, codeine if more severe
1012
NSAIDs In pregnancy Risk Conclusion Alternatives Breastfeeding
Closure of fetal DA. Fetal IUGR Possible cerebral haemorrhage Caution (avoid for analgesia) Monitor fetus with USS Paracetamol Safe to breast feed
1013
Aspirin In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk Use if high risk of pre-eclampsia Alternatives NA Safe to breastfeed
1014
Paracetamol In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk Safe Safe to breastfeed
1015
Opiates In pregnancy Risk Conclusion Alternatives Breastfeeding
Maternal/fetal dependancy Only if severe pain or drug dependancy Methadone if opiate addict Beware accumulation in breast feeding
1016
Warfarin In pregnancy Risk Conclusion Alternatives Breastfeeding
Teratogenic Risk of fetal haemorrhage Only use if artifical heart valves and with specialist advice LMWH Safe to breast feed
1017
LMWH In pregnancy Risk Conclusion Alternatives Breastfeeding
Maternal bleeding in OD Safe for fetus Use if indicated Safe to breast feed
1018
Fundamentals of analgesics in pregnancy
Best use paracetamol, plus codeine if more severe
1019
Fundamentals of anticoagulants in pregnancy
Probably underused Warfarin only used in exceptional circumstances
1020
ACEI In pregnancy Risk Conclusion Alternatives Breastfeeding
Fetal renal failure Teratogenic Avoid in pregnancy Methyldopa as alternative Captopril is safe for breast feeding
1021
Methyldopa In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk Best 1st line Safe to breast feed
1022
Beta blockers In pregnancy Risk Conclusion Alternatives Breastfeeding
Possible IUGR if early Caution, 3rd line Methyldopa as alternative Safe to breast feed
1023
Ca antagonists In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk Best second line e.g. nifedipine Safe to breast feed
1024
Thiazide diuretics In pregnancy Risk Conclusion Alternatives Breastfeeding
Maternal hypovolaemia Avoid in pregnancy Methyldopa as alternative Safe to breast feed
1025
Thyroid hormone in pregnancy In pregnancy Risk Conclusion Alternatives Breastfeeding
Use if indicated Monitor thyroid
1026
Propylthiouracil In pregnancy Risk Conclusion Alternatives Breastfeeding
Fetal hypothyroidism Use minimal dose Monitor thyroid
1027
Carbimazole In pregnancy Risk Conclusion Alternatives Breastfeeding
Fetal hypothyroidism, aplasia cutis Use minimum dose Propylthiouracil as alternative Monitor thyroid
1028
Inslin In pregnancy Risk Conclusion Alternatives Breastfeeding
Maternal hypoglycaemia Use with usual precautions Safe to breast feed
1029
Metformin In pregnancy Risk Conclusion Alternatives Breastfeeding
Probably safe Use with caution Insulin as alternative Safe to breast feed
1030
Ciclosporin In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known effects Continue, monitor leveles Probably safe
1031
Azathioprine In pregnancy Risk Conclusion Alternatives Breastfeeding
Minimal risk Continue if indicated Safe to breastfeed
1032
Prednisolone In pregnancy Risk Conclusion Alternatives Breastfeeding
No fetal effects Maternal GDM, HTN Use minimum dose Safe to breastfeed
1033
TCAs In pregnancy Risk Conclusion Alternatives Breastfeeding
Largely safe Use if high risk of relapse Fluoxetine as an alternative Safe to breast feed
1034
SSRIs In pregnancy Risk Conclusion Alternatives Breastfeeding
Paroxetine teratogenic (3% risk), others probably safe Use if high risk of relapse, fluoxetine preferentially Safe to breast feed
1035
Lithium In pregnancy Risk Conclusion Alternatives Breastfeeding
Teratogenic (10% risk) Use only if high risk of relapse Alternatives difficult Watch for toxicity
1036
Neuroleptics in pregnancy In pregnancy Risk Conclusion Alternatives Breastfeeding
Possibly mildly teratogenic although largely unknown Usually continue due to risk of relapse but avoid clozapine Alternatives difficult Probably safe to breast feed
1037
Sodium valproate In pregnancy Risk Conclusion Alternatives Breastfeeding
Impaired childhood cognition, cognition teratogenic (4-9% risk) Minimise combinations and consider cahgne if \<12w Carbamezapine as an alternative Safe to breast feed
1038
Carbamezapine In pregnancy Risk Conclusion Alternatives Breastfeeding
Teratogenic (3% risk) Usually continue Safe to breast feed
1039
Lamotrigine In pregnancy Risk Conclusion Alternatives Breastfeeding
Teratogenic (1-5% risk) Usually continue Safe to breast feed
1040
Fundamentals of antiepileptics in pregnancy
Best sorted preconception Seizure control imperative Minimise combinations and doses High dose folic acid
1041
Steroids Betamethasone and dexamethsone In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk with single course Use if high risk for preterm labour Betamethasone best NA NA
1042
Beta-agonists In pregnancy Risk Conclusion Alternatives Breastfeeding
Nil known risk at anti-asthmatic doses Use if indicated Safe to breast feed
1043
Ursoedoxycholic acid In pregnancy Risk Conclusion Alternatives Breastfeeding
Safe Use for cholestasis
1044
What is the background risk of congenital malformations?
1-2%
1045
Hb in pregnancy
10.5-14 Higher with supplementation High Hb associated with worse perinatal outcomes, rapid drop in platelets suggestive in PET
1046
WBC in pregnancy
5-11 Levels unchanged in pregnancy but rise in labour
1047
Platelets in pregnancy
100-450 Slight drop towards term
1048
Free T4 in pregnancy Free T3 in pregnancy TSH NB
11-22 Slightly lower in early pregnancy 43-45 Slightly lower in early pregnancy 0-4 Aim for 1.5-2 if replacement therapy NB: undertreated and subclinical hypothyroidism associated with cognitive deficit in childhood
1049
Renal function in pregnancy Urea Creatinine Uric acid Na K Prtoein excr NB
2.8-3.8 Lowered in pregnancy 50-80 Lowered in pregnancy x100, should ve Unchanged K usually slighlty low in pregnancy Slightly raised protein excretion Increased renal excretion in pregnancy, high creatinine/uric acid common with PET
1050
Liver funciton in pregnancy ALP ALT AST ALbumin NB
\<500 Raised \<30 Reduced \<35 Reduced 28-37 Reduced Rapid rise in liver enzymes common with complications of PET
1051
ESR in pregnancy
\>30, elevated, no clinical use in pregnancy
1052
CRP in pregnancy
\<8, unchanged by pregnancy
1053
Glucose in pregnancy NB
\<6: fasting \<8 after food Slight fall in pregnancy Tight glucose control improves outcomes with maternal diabetes.
1054
What is breakthrough bleeding?
Irregular bleeding associated with hormonal contraception
1055
What are the causes of breakthrough bleeding?
Bleeding problems are more common with progestogen-only methods: COCP POCP Contraceptive depot IUS Emergency hormonal contraception
1056
Def: puerperium
6w period following delivery when the body returns to its preprgenant state Maternal morbidity and mortality associated with pregnancy is highest during this period
1057
Changes to the genital tract during the puerperium
Uterus contracts and the BVs that supplied the placenta occlude Uterine size reduces over 6w and shouldn't be palpable abdominally within 10d Contractions or after pains may be felts for 4d. Os closes by 3d Lochia, cervical discahrge may be bloo stained for 4w. Menstruation delayed by lactation but occurs after 6w if woman is not lactating
1058
Changes to the CVS during the puerperium
CO and BV decrease to prepregnant levels within a wekk Loss of oedema can take up to 6w BP normalises within 6w
1059
Changes to the urianry tract during the puerperium
Physiological dilatation of pregnancy reduces over 3m GFR decreases
1060
Changes to the blood during the puerperium
U+Es return to normal Hb and HCt rise thie haemoconcentration WCC falls Platelets and clotting factors rise, predisposing to thrombosis
1061
Generalities of postnatal care
Do not separate mother and baby Early mobilisation Couneselling Check uterine involution, lochia, BP, pulse, T daily Analgesia may be required for perineal pain which can be helped through pelvic floor exercises FBC, Fe if appropriate in conjunction with laxatives Discussion of delivery Psych referral if indicated by history
1062
Physiology of lactation
Dependant on prolactin (ant pit) which stimulats milk secretion. Levels of prolactin in conjunction with the decline in oestrogen and progesterone promote milk secretion Oxytocin from post pit stimulations ejection in respoonse to suckling which also stimulates prolactin release Can produce up to 1000ml Since oxytocin is controlled by hypo, emotional or physical stress may inhibit
1063
What is colostrum
A yellow fluid contianing fat-laden cells, proteins (IgAs) and minerals which is passed for the first 3d before the milk comes in
1064
What is the correct positioning for breast feeding
Baby's lower lip should be planted below the nipple so the entire nipple is drawn into the mouth.
1065
Why is Vit K given postpartum?
To reduce the chances of haemorrhagic disease of the newborn
1066
What are the advantages of breastfeeding?
Protextion against infeciton in neonate Bonding Protection against Ca in mother £
1067
Advice about postnatal contraception
Lactation not adequate alone. Usually started 4-6w post delivery Combined contraceptive suppresses lactation and contraindicated if breastfeeding Progesterone only safe IUD safe: screen for infeciton. Insert at end of third stage or at 6w
1068
Def: primary post partum haemorrhage
Loss of \>500mL blood \<24h after delivery \<1000mL after C-sec Occurs in 10%
1069
What are the causes of PPPH?
Retained placenta Uterine causes Vaginal causes Cervical tears Coagulopathy
1070
Features of retained placenta
Occurs in 2.5% of deliveries. Partial separation can cause blood to accumulate in the uterus, which will rise Collapse may occur in the absence of external loss
1071
Features of uterins causes of PPPH
Account for 80% Uterus fails to contract either due to atony, retained placenta Atony is more common with prolonged labour, grand multparity and overdistension of the uterus and fibroids
1072
Features of vaginal causes of PPPH
Accounts for about 20% Bleed from perineal tear or episiotomy may be obvious but bleed from higher vaginal tear must be considered, especially after instrumental
1073
Features of cervical tears and PPPH
Rare but associated with precipitate labour and instrumental delivery
1074
Coagulopathy causing PPPH
Congenital disorders Anticoagulant therapy DIC
1075
Prevention of PPH
Oxytocin in 3rd stage of labour decrease incidence by 60% As effective as ergometrine
1076
Contraindication of ergometrine in PPH prevention
Causes vomiting and is contraindicated in HTNive women
1077
What are the risk factors for PPH?
Previous hx Previous C sec Coagulation defefct or anticoagulant therapy Instrumental/C-sec Retained placenta APH Polyhydramnios, multiple pregnancy Grand multiparity Uterine malformation or fibroids Prolonged/induced labour
1078
Clinical features of PPH
Blood loss should be minimal after placental delivery Enlarged uterus suggest uterine cause Inspect vaginal walls and cervix for tears May be abdominal blood loss e.g. uterine rupture without pain or overt bleeding
1079
Mx of PPH
ABC: nursed flat, cross matched blood. Restore BV. Page anaesthetist, haematologists, seniors Retained placenta should be removed manually if there is bleeeding if it is not expelled within 60mins of delivery Identify and treat cause: examination Bimanual uterine compression Oxytocin and or ergometrine given to contract the uterus If this fails examination under anaesthetic performed for retained placental fragment and inspect of the vagina If uterine atony persists, PgF2 injected into myometrium Persistent haemorrhage despite medical treatment requires surgery. May be compressed using Rusch balloon if bleeding from placental bed alone B-Lynch (brace suture may be used) Uterine artery embolisation Hysterectomy if these fail
1080
Def: secondary PPH
Excessive blood loss occuring 24h-6w after delivery
1081
Causes of secodarry PPH
Due to endometritis +/- retained placental tissue Rarely incidental gnaecological pathology or gestational trophoblastic disease Uterus enlarged and tender with an open internal cervical os.
1082
Ix in secondary PPH
Vaginal swab Blood count Cross-match USS: although difficult to differentiate between blood clot and retained placental tissue Antibiotics ERPC may be used if bleeding is heavy and acute. Chronic can be managed with antibiotics alone. Histlogical examination of evacuated tissues will exclude gestational trophoblastic disease
1083
What is characteristic of endometritis?
Endometritis due to reatined tissue causes bleeding that slows but does not stop with antibiotics and gets worse again once the course is finished
1084
Def postpartum fever
\>38 in first 14d
1085
What are the common causes of postpartum pyrexia
Infection: genital tract sepsis. Most common after C-sec. Prophylactic antibiotics reduce this DVT often causes low grade pyrexia
1086
What organisms most commonly cause postpartum genital sepsis
GAS Staph E. Coli
1087
What are the features of postpartum genital tract sepsis
Lochia may be offesnive Uterus enlarged and tender Urinary infection, chest infeciton, mastitis, perineal infection and wound infection are alos common.
1088
Ix of postpartum pyrexia
Bloods Urine High vaginal Fetal cultures Broad spectrum antibiotics
1089
What proportion of obstetric deaths from DVT occur post-partum?
50%. Early mobilisation and hydration importatnt for all women
1090
What are third day vlues
Temporary emotional lability, affect 50% of women. Support and reassurance
1091
What should be considered in postnatal depression
Postpartum thyroiditis
1092
Mx of pregnant women with Hx of mental illness
See a psychiatrist before delivery MDT plan for postnatal discharge arranged
1093
Pre-eclampsia postnatally
Takes 25h before illness improves. BP peaks 4-5d post delivery and may need treatment for weeks. Fluid balance, renal funciton and UO should be monitored. BP and hpatic/cardiac failures Continue BP measurements for 5d postnatally
1094
What complications of the urinary tract are common in the puerperium
Retention of urine UTI Incontinence
1095
Features of urine retention in the puerperium
Common after delivery, may not be painful after epidural. May present with frequency, stress incontinence or severe abdominal pain. Infection, overflow incontinence and permanent voiding difficulties may follow. Strict fluid charts and abdominal palpation help to identify. Postmicturition USS can be used to assess the residual volume Treatment is with catheteritsation
1096
Incontinence in the puerperium
Occurs in 20% of women Overflow and infection should be excluded using postmicturition ultrasound or catheterisation and an MSU Symptoms of stress incontinence usually improve with pelvic floor exercises
1097
Complications of perineal trauma in the puerperium
Perineal trauma: repaired Pain: persists more than 8w in 10%. Superficial dyspareunia is common. Diclofenac is effective. Paravaginal haematoma: excrutiating pain te perinum a few hours after delivery., sometimes identified on USS. Drained under anaesthetic
1098
Bowel problems in the puerperium
Constipation and haemorrhoids: laxatives Incontinence of faeces or flatus
1099
Features of faecal/flatus incontinence in the puerperium
Affects 4% of women mostly transiently Can be caused by pudendal nerve or anal sphincter damage. Anal manometry and ultrasound used to assess and managed on basis of symptoms. Formal repatir may be required after which deliveries should be by C-sec
1100
What are the risk factors for incontinence following delivery?
Forceps Large babies Shoulder dstocia Persistent OP position
1101
What are the normal flora and pH of the vagina?
Lactobacillus Acidic pH \<4.5 In prepubertal girls and postmenopausal women, lack of oestrogen results in a thin, atrophic epithelium with a higher pH and reduced resistance to infection
1102
What is thrush and its features
Infection with Candida albicans Most common cause of vaginal infection and found in up to 20% of women, often asymptomatically. Cotttage cheese discahrge Vulval irritaiton and itching. Superficial dyspareunia and dysuria may occur. Vagina and or vulva are inflamed or red
1103
Risk factors for thrush
Pregnancy DM Use of antibiotics
1104
Rx of candida
Topical imidazole (e.g. clotrimazole) or oral fluconazole.
1105
What is BV and its features
When normal latcobacilli ar eovergrown by a mixed flora including anaerobes, Garderella and Mycoplasma hominis Found in 12% of women Grey-white discharge Vagina not red or itchy Fishy odor from amines released by bacterial proteolysis
1106
Dx of BV
Raised vaginal pH Positive whiff test (when 10% KOH added) Presence of clue cells
1107
Vulvitis Cottage-cheese discharge
Candida
1108
Grey-white discharge Fishy odor
BV
1109
Rx in BV
Metronidzaole or clindamycin cream
1110
Signficiance of BV obstetrically
Can cause secondary infection in PID Also an association with preterm labour
1111
What is vaginal infection and discharge in children often due to?
Foreign body. May also be due to atrophic vaginitis due to low oestrogen levels
1112
Toxic shock syndrome in a young woman menstruating
Occurs as a rare complication of a retained, hyperabsorbable tampon Toxin producing Staph aureus.: high fever, hypotension and multisystem failure Abx and ICU
1113
What are the principles in the management of STIs?
Screen for concurrent disease Regular sexual partner should also be screened and treated. Partner notification Maintenance of confidentiality. Education Barrier methods of contraception
1114
What is the most common sexually transmitted bacterial organism in the world?
Chlamydia
1115
Symptoms of chlamydia
May be asymptomatic Urethritis and vaginal discharge
1116
What is the significant Cx of chlamydia infeciton?
Pelvic infection (may be silent) Can cause tubal damage leading to subfertility or chornic pelvic pain. Can also cause Reiter;s yndrome
1117
Rx of chlamydia
Azithromycin or doxycylcine
1118
Dx of chlamydia
NAAT
1119
Reiter's syndrome
Urethritis Conjunctivitis Arthritis (see, pee, climb a tree)
1120
Causative organism in chlamydia
Chlamydia trachomatis
1121
Causative organism in gonorrhoea
Neisseria gonorrhoeae
1122
Symptoms of gonorrhoea
Asymptomatic in women, vaginal discharge, urethritis, bartholinitis and cervicitis can occur. Pelvis commonly infected
1123
Systemic complications of gonorrhoea?
Vacteraemia Acute monoarticular septic arthritis
1124
Rx in gonorrhoea
Azithromycin or ceftriaxone
1125
What are condylomata acuminata?
Genital warts
1126
Treatment of genital warts?
Topical podophyllin or imiquimod cream
1127
Genital herpes causative agent?
HSV Type 2. Although Type 1 implication increasing.
1128
Features of genital herpis
Primary infeciton is the worst with multiple small painful vesicles and ulcers around the introitus. Local lymphadenoapthy, dysuria and systemic symptoms are common. Secondary bacterial infection, aspetic meningitis or urinary retention may also occur.
1129
Rx of genital herpes
Aciclovir (also valaciclovir or famciclovir) used in severe infections
1130
Causative organism in syphillis?
Treponema pallidum
1131
Features of primary syphillis
Solitary, painless, vulval ulcer (chancre)
1132
Features of secondary syphillis
Untreated primary, secondary may develop weeks later: Rash, IFV-like symtpoms and warty genital or perioral growths (condylomata lata) Latent syphillis follows
1133
What are the complications of tertiary syphillis
AR Dementia Tabes dorsalis Gummata in skin and bone.
1134
Treatment of syphillis
IM penicillin
1135
Causative organism in trichomonas infection
Trichomonas vaginalis Flagellate protozoan
1136
Symptoms of TV
Grey-green offesnive discharge Vulval irritaiton Superficial dyspaerunia Cervicitis has a punctuate erythematous ("strawberry") appearance)
1137
Treatment of TV
Metronidazole
1138
Causative orgnaism in chancorid
Haemophils ducreyi
1139
Causative organism in lymphogranuloma venereum
Chlamydia subtypes
1140
Causative organism in donovanosis
Calymmatobacterium granulomatis
1141
What are the infective causes of genital ulcerative disease
Herpes Syphillis Chancroid Lymphogranuloma venereum Donovanosis
1142
AIDS=
Development of opportunisitc infections or malignancy CD4 \<200
1143
Smears in HIV +ve women
Yearly due to increased risk of lesion progression
1144
Features of endometrtiis
Infection confined to the cavity of the uterus which, if left untreated, commonly spreads to the utereus Often the result of either instrumentation of the uterus or as a complication of pregnancy or both.
1145
Common orgnaisms causing endometritis
E Coli BV Staph Clostridia Chlamydia Gonococcus
1146
Presentation of endometritis
Persistent and heavy vaginal bleeding accompanied by pain Uterus is tender and the cervical os is commonly open Fever may be absent byt septicaemia can ensure.
1147
Ix and Mx of endometritis
Vaginal and cervical swabs FBC Pelvis USS (not very reliable) Empirial antibiotics ERPC
1148
Def: PID
Traditionally describes sexuallly transmitted pelvic infection, endometritis usually co-exists
1149
Pelvic infection in pregnancy
Almost never occurs in the presence of a viable pregnancy
1150
What are the risk factors for PID
Sexual factors (80%) Multiple partners No use of barrier protection COCP and Mirena IUS are protective.
1151
What causes the spread of asymptomatic STIs to the pelvis?
Usually spontaneous Can be the result of uterine instrumentation e.g. TOP, ERPC, Lap and dye test, intrauterine devices Or complicatins of childbirth and miscarriage (infection often caused by non-sexually transmitted bacteria) Descending infection from the appendix may also occur
1152
Bacteria implicated in PID
Frequently polymicrobial Chlamydia (60%) (asymptomatic- symptoms commonly due to secondary infection) Gonococcus (acute presentation)
1153
Pathology of PID
Endometritis Bilateral salpingitis Ovary sparing normally Fitz-Hugh- Curtis syndomr
1154
Hx in PID
Many have no smyptoms and present later with subfertility and or menstrual problems Bilateral lower abdominal pain with deep dyspareunia is the hallmark Usually with abnormal vaginal bleeding or discharge
1155
Bilateral lower abdominal pain with deep dyspareunia
PID
1156
Ex in PID
Tachycardia, high fever, signs of lower abdominal peritonism with bilateral adnexal tenderness and cervical excitation Pelvic abscess may be palpable
1157
What is cervical excitation
Pain on movement of the cervix
1158
Ix in PID
Endocervical swabs for Chlamydia and gonococcus Blood cultures WBC CRP Pelvis USS helps to exclude abscess or ovarian cyst
1159
What is the gold standard Ix in PID
Laparoscopy with fimbrial biopsy and culture
1160
Mx of PID
Analgesic Parenteral cephalosporin e.g. IM ceftriaxone + foxy and metronidazole or ofloxacin and metronidazole Admit Dx should be reviewed if no significant improvement in 24h and a laparoscopy performed Pelvis abscess may requrie drainage. NB rupture of a large pelvis abscess may be life-threatening
1161
Cx of PID
Early: formation of abscess or pyosalmpinx Later: tubal obstruction and subfertility. Ectopic pregnancy x6 more common following pelvic infection Chance of tubal damage following one episode of acute PID is 12%
1162
What is chronic PID
Persisting infection and is the result of non/inadequate treatment of PID) Dense pelvic adesions and fallopians may be obstructed and dilated with fluid (hydrosalpinx) or pus (pyosalpinx).
1163
Symptoms of Chronic PID
Chronic pelvic pain or dysmenorrhoea Deep dyspareunia Heavy + irregular menstruation Chronic vaginal discharge Subfertility May have similar examination feature sto endometriosis
1164
Abdominal and adnexal tenderness and a fixed retroverted uterus
PID Endometriosis
1165
Dx of chronic PID
Laparoscopy as culture is often negative.
1166
Rx of chronic PID
Analgesics Abx of evidence of active infection. Adhesiolysis Salpingectomy
1167
Features of PID
Silent (chlamydia) Bilateral pain Caginal discharge Cervical excitation Adnexal tenderness Fever WCC and CRP raised
1168
What are the characteristics of physiological vaginal discahrge
Usually non-offensive Increases around ovulation, during prgnancy and in women taking COCP. Exposure of columnar epithelium in cervical eversion and ectropion may cause discharge one infection has been exluded.
1169
Watery vaginal discharge in post-menopausal women
?Fallopian tube carcinoma
1170
Bloody/offensive vaginal discharge
Suggestive of cervical carcinoma but any genital tract malignancy may be responsible.
1171
1172
Def: early neonatal death
Occurs within 7d of delivery
1173
Def: stillbirth
Fetus delivered after 24w
1174
Def: neonatal death
Death within 28d of delivery
1175
Def: miscarriage
Fetus born with no signs of life \<24w. (if born with signs of life \<24w classified as a neonatal death)
1176
Def: perinatal mortality rate Corrected perinatal mortality rate
Sum of stillbirths and early neonatal deaths per 1000 total births Excludes those that are due to congenital malformations
1177
How are causes of neonatal death classified?
Extended Wigglesworth and supplemented by the Obstetric Aberdeen classification sysytem
1178
What is te most common cause of neonatal mortality?
Preterm delivery
1179
What proportion of stillbirths are accounted for by IUGR?
\>10% stillbirths
1180
APH in neonatal death
Occurs in 10%
1181
What are the principle causes of perinatal mortality
Unexplained antepartum stillbirth IUGR Prematurity Congenital anomalies Intrapartum hypoxia APH
1182
Def: maternal death
Death of a woman during pregnancy or within 42d of its cessation from any cause related to or aggravated by the pregnacny
1183
Def: late maternal death
After 42d post-delivery and \<1y
1184
What is the difference between direct and indirect maternal death
Obstetric complication vs previous or new disease but not the result of pregnancy
1185
What are hte factors affecting maternal death rates
Socioeconomic Obstetric Pre-existing health Level of care Reporting methods
1186
What are the obstetric factors affecting maternal death rates?
Extremes of maternal age High parity Multiple pregnancy Multiple previous C-sec
1187
What are the global causes of maternal mortality?
Haemorrhage Obstructed labour infection Severe pre-ecl and the consequences of illegal abortion
1188
What are the main casuses of direct deaths in the UK in pregnancy
Sepsis: most common cause VTE Haemorrhage Hypertensive disease: mostly as a result of ICH Other causes: disorders of early pregnancy (ectopic), genital tract infeciton, amniotic fluid embolism, anaesthesia, acute fatty liver, genital tract trauma
1189
What are the main causes of indirect deaths in the UK?
Cardiac disease: acquired and congenital disease Psychiatric disease Other: drug?ETOH related death, domestic violence, epilepsy and ICH
1190
Provision of contraception to \<16 y/o
Child has capacity Try to get child to discuss with parent Be convinced that the child's physical or mental health will ne affected without the treatment and it is in the child's best interests to have the treatment without parental knowledge
1191
What is the Bolam principle
A doctor is not guilty of negligence if he or she has acted in accordance with the practice accepted as proper by a responsible body of medical men skilled in that particular art.
1192
What is the risk of stillbirth for women induced at 41-42w?
1 in 300
1193
Observations in labour
T, pulse, BP should be monitored If circumstances predispose to abnormalities e.g. epidural, this should be more frequent
1194
What are the Cxs of epidural Mx
Hypotension managed with fluids and ephidrine
1195
How can aortocaval compression be prevented? What is the implication in labour?
By maintaing left lateral tilt Women should not go through labour flat on their back
1196
Hydration in labour
Dehydration is common IV fluids necessary in epidrual
1197
What is Mendelson's syndrome?
Aspiration of stomach content into the lungs during anaesthesia Most common cause of maternal aneasthetic death. Cyanosis. Tachycardia. Massive pulmonary oedema. Bronchospasm, which occurs often (unlike with amniotic fluid embolism). Hypotension. Hypovolaemia with haemoconcentration (the reactive transudation of fluid into the lungs contributes to this).
1198
What are the implciations of Mendelson's syndrome
Eating is often discouraged during labour Ranitidine may be given to reduce stomach acidity
1199
Def and risks of pyrexia in labour
\>37.5 Associated with increased risk of neonatal illness and is not always as a result of chorioamnionitis More common with epidrual anaesthesia and prolonged labour. Cultures of vagina, urine and blood are taken. Antipyretics often administered Antibiotics warranted if fever reaches 38deg or there are other risk factors for sepsis
1200
Urinary tract in labour
Neglected retention of urine can irreversibly damage the detrusor muscle. Epidural usually removes bladder sensation Catheterisation may be needed but not necessarey for all. Women should be encouraged to micturate during labour
1201
What is used to monitory progression in labour?
The partogram
1202
What consitutes hte partogram
Progression in dilatation of the cervix +/- descent of the head Assessed on VE and plotted against time.
1203
What is the usual minimum rate of dilatation after hte latent phase in labour?
1cm/h
1204
What is the most common cause of slow progress in labour?
Inefficient uterine action. Common in nullips and inductions but rarer in multips
1205
Mx of persistently slow progress?
Augmentation initially with amniotomy Then qith oxytocin
1206
What is hyperactive uterine action?
Occurs with excessively strong or frequent or prolonged contractions. Fetal distress occurs as placental bloo flow is diminished Associated with placental abruption, with too much oxytocin or as a side effect of PG administration to induce labour.
1207
Mx of hyperactive uterine action
If there is no evidence of abruption a tocolytic e.g. sablutaoml can be given IV or subcut C-section usually indicated due to fetal distress
1208
Features of nullip labour
First stage: slow progress usually due to inefficient uterine action. Augmentation can sometimes correct passenger probelsms of attitude or position. ARM may be used If ARM fails to produce further cervical dilatation in 1-2h oxytocin may be used and titrated up. CTG monitoring is advised Nullips are at less risk of uterine rupture
1209
Effects of oxytocin in nullip labour
Will usually increase dilatation within 4h if it is going to be succesfull
1210
C-section in nullips in labour, cut off for C-sec
12-16h
1211
Mx of the second stage in nullip labour
If descent is poor, oxytocin should be started and pushing delayed by 2h If epidural has been used, the urge to push characteristic of second stage may be diminshed
1212
What is the cut off for the active stage of labour?
If lasts longer than 1h, spontaneous delivery becomes less likely because of maternal exhaustion. Fetal hypoxia and maternal trauma are also more common. If the head is distending the perineum, episiotomy can be performed. If not, instruments may be used
1213
Features of the first stage in multip labour
Slow progress is unusual. Uterus likely to be effective. Therefore failure to progress is more likely to be the fetal head: its attitude or position Multip also more prone to rupture. Augmentation with oxytocin may only be performed after careful exclusion of malpresentation.
1214
Features of OP presentaiton in labour
Longer More painful Backache Early desire to push, If progress in labour is normal, no action is needed as OP may spontaenously revert to OP. If labour is slow, augmentation is used. If the position is persistent, delivery will be face to pubis and completed by flexion rather than extension. C-section may be required. If associated with prolonged second stage, instrumental delivery usually achieved with rotation to OA using ventouse or Kielland's
1215
When does OT position become significant
If vaginal delivery has not been achieved after 1h of pushing in the second stage. Usually associated with poor powers so rotation with traction may be required Ventouse
1216
Mx of brow presentation
C section
1217
Features of face presentation
Fetal compromise more common. If the chin is anterior, mento-anterior, delivery may be possible. If the chin is mento-posterior, extension of the head over the perineum is impossible and C-section indicated
1218
Common causes of failure to progress in labour
Powers: inefficient uterine action Passenger: fetal size, OT, OP, disorder of flexion e.g. brow Passage: cephalo-pelvic disproportion, cervix
1219
Def of cephalopelvic disproportion
Retrospective dx made on the inability to deliver a particular fetus despite: presence of adequate uterine activity absence of maposition or presentation. Slightly more likely with very large babies, sort women or where the head remains high in a nullip at term.
1220
Featuers of pelvic vaiants
Found in 50-80% of caucasian women. Arthropod (20%) has a narrower inlet with a transverse diameter less than the AP diameter. Android pelvis is heart shaped. Platypelloid levis: oval shape of the inlet persists with the mid pelvis
1221
What conditions contribute to abnormal pelvic architecture?
RIckets and osteolmalacia Poorly healed pelvic fractures Spinal abnormalities Poliomyelitis Congenital malofrmations
1222
What proportion of cerebal palsies can be attributed solely to intrapartum problems?
10%
1223
What are the causes of intrapartum damage to the fetus?
Fetal hypoxia Infeciton/inflammation in labour Meconium aspiration Trauma Fetal blood loss
1224
Def: fetal distress
Hypoxia that may result in fetal damage or death if not reversed or the fetus delivered urently.
1225
What is the fetal scalp pH indicative of fetal distress
\<7.2 Neurological damage becomes common when it is \<7
1226
What are some causes of acute fetal hypoxia in labour?
Placental abruption Hypertonic uterine states Use of oxytocin Prolapse of the umibilcal cord Maternal hypotension
1227
Intrapartum risk factors for fetal distress? Antepartum?
Long labour Mecnoium Use of epidruals and oxytocin IUGR Pre-ecl
1228
What factors are used to diagnose fetal distress?
Color of liquor FHR CTG Fetal ECG monitoring Fetal blood sampling
1229
What is the significance of undiluted meconium on fetal mortality
4x increase in perinatal mortality. Indication for caution and hence closer surveillance with a CTG as: Fetus may aspirate it Hypoxia is more likely
1230
FHR monitoring
Auscultated every 15 mins during first stage Every 5 mins during the second Using Pinard's or Doppler for 60s after a contraction. Distressed fetus normally exhibits abnormal HR patterns which can be heard. Appropriate monitoring for low risk pregnancies. CTG indicated if abnormalities are detected
1231
pH \<7.2 on fetal scalp m,onitoring
Delivery expedited by fastest route possible
1232
CTG DR C BRAVADO
DR: Define risk: other factors e.g. meconium, fever, IUGR C: Contaction per 10 minutes BR: Baseline rate 110-160bpm Tachys associated with fever, fetal infection, fetal hypoxia. Steep sustained deterioration in rate suggests acute fetal distress V Variability: ST variation in FHR should be \>5bpm except during fetal sleep which normally lasts 45 minutes, reduced variability suggests hypoxia A: Accelerations of fetal heart with movements or contractions D: decelerations. Early are synchronous with contractions and are a normal response to head compression. Variable decelerations vary in timing and classically reflect cord compression which can ultimately cause hypoxia Late: persist after the contraction and are suggestive of fetal hypoxia O: Overall assessment
1233
Def uterine hyperstimulation
Contractions \>5/10 minutes
1234
What is the normal baseline variability in FHR?
\>5bpm except during sleep. Prolonged reduction in variability suggests hypoxia
1235
Early decelerations
Synchronous with contractions as a normal response to head compression
1236
Variable decelerations
Vary in timing and may reflect cord compression which may ultimately cause hypoxia
1237
Late decelerations
Persist after the contraction is completed and are suggested of fetal hypoxia
1238
What are the levels of screening for fetal distress
Level 1: intermittenet auscultation, if abnromal, meconium, long or high risk, proceed to Level 2: continuous CTG. If sustained bradycardia, delvier. Level 3: Fetal blood sampling, if abnormal proceed to Level 4: delivery
1239
What are the disadvantages of CTG
Reduces maternal mobility Increases obstetric intervention No proven reduction in mortality or LT handicap More puerperal sepsis
1240
Mx of fetal distress
Left lateral psotion O2 and IV fluids Stop oxytocin infusion with B2 agonists VE to exclude cord prolapse or rapid progress FBS and delivery expedited if \<7.2 If FHR pattern continues or deteriorates a second sample will be needed
1241
Implications of low-grade maternal fever
Strong risk factor for seizures, fetal death and cerebal palsy even in the absence of evidence of infection. Combination with fetal hypoxia is particulalry dangerous.
1242
Features of meconium aspiration
Aspiration by fetus into lungs where it causes a chemical pneumonitis More common in the presence of fetal hypoxia Where the meconium is thick, amnioinfusion of saline reducs the incidence of meconium aspiration although questions remain around maternal safety and this is rarely performed
1243
Causes of fetal blood loss
Vasa praevia Feto-maternal haemorrhage Placental abruption
1244
What is entonox
NO and O2: Gas and air Can casue light headed ness, nausea and hyperventilation
1245
What opiates are used in labour
Pethidine or meptid are widely used Easy administration Analgesic efect may lead to sedation or confusion. Antiemetics usually needed. Opiates can cause respiratory depression in newborn and reversal with naloxone may be indicated
1246
What are the principle complications of spinal anaesthesia?
Hypotension Total spinal analgesia causing respiratory paralysis (rare)
1247
Use of pudendal nerve block
Low-cavity instrumental vaginal deliveries bilateral injection around the pudendal nerve where it pases by the ischial spine
1248
Location of epidural?
L3 and L4 LA injection into the epidural space. Complete sensory and partial motor blockade from the upper abdomen downwards may occur
1249
When may epidural anaesthesia be advised in labour?
If labour is long HTNive women Abolish a premature urge to push Analgesia for insrumental or C-sect
1250
What are the disadvantages of epidural?
Increased midwifery supervision of BP and HR Woman bed bound Urinary retention Maternal fever is more common Instrumental (but not CS) more common Transient hypotension (minimised by IV fluids) Transient fetal bradycardia although rarely precipitates fetal distress
1251
Contraindications to epidural
Sepsis Coaglopathy or anticoagulant therapy (unless LMWH) Active neurological disease Spinal abnormalities Hypovolaemia
1252
What are the major complications of epidrual
Spinal tap Total spinal analgesia Hypotension LA toxicity Higher instrumental delivery rate Poor mobility Urinary retention Maternal fever
1253
Features of spinal tap
Inadvertent puncture of the dura mater causing CSF leakage Leads to severe headache, characteristically worse when sitting up
1254
How does epidural change the approach to second stage of labour
Normal to wait an hour before pushing in second stage Encouraged to push 3 times for 10 seconds during every contraction
1255
Approach to episiotomy
Perineum infiltrated with LA Cut made with scissors from the fourchette to the mother's right side of the perineum
1256
Delivery of placenta
Gentle contunous traction on cord Suprapubic pressure to prevent uterine inversion
1257
Def: retained placenta
3rd stage longer than 30 minutes Oxytocin infusion started and injected into the vein of the cord and milked up In the absence of bleeding, can be left for 1h
1258
First degree perineal tear
Injury to skin only
1259
Second degree perineal tear
Involving the perianal muscles but not anal sphincter
1260
Third degree tear
Involving anal sphincter complex 3a: \<50% of external anal sphincter 3b: \>50% of external anal shpincter 3c: internal anal sphincter also involved
1261
Fourth degree tear
Involving anal sphincter and epithelium
1262
Mx of first and second degre tears
Sutured under LA Absorbable material used/ Continueous sutures used
1263
Mx of 3rd and 4th degree tears
Occur in 1-3% Sphincter repaired under epidural and spinal anaesthetic Torn ends of the external sphincter are mobilised and sutured usually overlapping Internal sphincter requires seperate suturing if damaged. Antibiotics and laatives given PT assessment 30% have incontinence of flatus or faecas or urgency
1264
What are the risk factors for 3rd/4th degree teasr?
Forceps Large babies Nulliparity And the now obsolete midline episiotomy
1265
What are the principles of fast labour
Early diagnosis of labour 2-hourly VEs Early correction of slow progress with amniotomy and oxytocin C section by 12h if delivery not imminent.
1266
What are the criteria for home birth?
Woman's request Low risk 37-41w Cephalic Clear liquor Normal FHR All maternal obs normal
1267
What are the 3 principle routes for gynaecological operations?
Abdominal route through a lower tranverse incision (Pfannsteil) or vertical midline Vaginal route Laparoscopic
1268
Features of diagnostic hysteroscopy
Rigid or flexible hysteroscope passed through the cervix Cavity distended using CO2 or saline Can be performed without anaesthetic, cervical LA block or under GA Used as an adjunct to endometrial biopsy
1269
What is TCRE?
Transcervical resection of endometrium
1270
What is TCRF
Transcervical resection of fibroid
1271
What are the Cxs or hysteroscopic surgery
Uterine perforation Fluid overload
1272
When is TCRE best used?
With bleeding that is heavy but regular and painless In women approaching menopause Doesn't ensure sterility NB biopsy to be taken before diatherym
1273
What is a Veress needle
Used in laparscopy to insufflate the abdomen with CO2
1274
What is lap and dye?
When dye is passed through the cervix to assess tubal patency
1275
What are the advantages of laparscopic surgery?
Better visualisation of tissues Less tissue handling Less infection Reduced hopsital stay Faster postoperative recovery with less pain
1276
What are hte indications for hysterectomy
Menstural disorders Fibroids Endometriosis Chronic PID Treatment of pelvic malignancy Prolapse PPH
1277
What is the approach to hysterectomy
1: Blood: anastamosis between uterine and ovarain arteries, if hte ovaries are removed the ovarian artery and vein ar ligated instead Round ligament 2: Blood: main uterine artery Cardinal ligament. Bladder dissected off the cervix and upper vagina to prevent injury to it or the ureters 3: Cervicovaginal branches of the uterine artery Uterosacral ligament
1278
What are the different types of hysterectomy?
TAH VH Lap H Wertheim's H
1279
What happens in a subtotal hysterectomy?
Cervix is reatined
1280
What is the indication for VH?
Uterine prolapse
1281
What is LAVH?
Laparoscopically assisted vaginal hysterectomy
1282
What is Wertheim's hysterectomy?
Involves removal of hte parametrium Upper third of the vagina Pelvic LNs Indication is Stage 1a(ii)-2 cervical carcinoma
1283
What is Shcauta's hysterectomy?
Radical hysterectomy performed vaginally
1284
What are hte Cxs of hysterectomy?
Mortality: 1 in 10000 Immediate: haemorrhage, bladder or uteric injury Postoperative: VTE, apin, retention and infetion of urine. Wound and chest infection. Pelvic haematoma. LMWH and prophylactic antibiotics Long term: prolapse, genuine stress incontinence, premature menopause, pain and psychosexual problems
1285
Features of D&C
Dilatation and curettage Cervix dilated with steel rods Hegar dilators of increasing size Endometrium is curetted to biopsy it This is diagnostic procedure inferior to hysteroscopy and is not commonly performed
1286
What is LLETZ
Surgery for CIN Involves using cutting diathermy under LA to remove the transformation zone of the cerix Increases risk of subsequent preterm delivery
1287
What is a cone biopsy
Removal of the transformation zone and the enodcervix by making a circular ct Used to stage early cervical carcinoma and is sufficient for Stage 1ai Increased cervical damage means there is a significant risk of subsequent preterm delivery
1288
What is the approach to repairing a cystocoele
Excision of prolapsed vaginal wall and plication of the bladder base and fascia Vagina then closed
1289
What is the approach to repairing a rectocoele
Levator ani on each side plicated
1290
What is important to ascertain in vaginal prolapse repair?
Whether the patient is sexually active as it may lead to overtightening of the vagina Other complications include urinary retention
1291
What is hysteropexy?
Re-suspension of the prolapsed uterus using a strip of non-absorbable bifurcated mesh to lift the uterus and hold it in place One end is attached to the cervix and the other to the anterior longitudinal ligament over hte sacrum.
1292
What is sacrocolpoplexy?
Used for prolapse of the vaginal vault after hysterectomy Mesh attached from vaginal vault to the sacrum
1293
What is TVT?
Tension free vaginal tape Vertical incision made on the anterior vaginal wall over the midurethral section. Lateral dissection around hte urethra Tape is introduced vaginally with trocards entering the retropubic space. Cystoscopy performed to ensure there is no bladder perforation. If the tape is over tightened, acute urinary retention may occur
1294
What is Burch colposuspension
Involves dissection into the extraperitoneal space over the bladder and anterior vaginal wall. Vaginal wall on either side of the bladder neck is hitched up to the iliopectineal ligaement on either side of the pubic symphysis. Usually performed for failed tape procedures
1295
What are the operations for fibroids?
Myomectomy Uterine artery embolisation (for women who do not want a hysterectomy but do not wish to preserve fertility) Hysterectomy
1296
What are the risks of myomectomy
Adhesions Uterine rupture during labour Perioperative haemorrhage: requiring transfusion and rarely, hysterectomy
1297
How are the risks of thromboembolism minimised in gynae sx?
Stop OCP 4w prior to major abdominal surgery If HRT is not stopped, LMWH must be used All mobilised early and given TEDs LMWH given according to risk assessment
1298
Thromboprophylaxis in gynae surgery Low risk
Minor surgery or major surgey \<30 mins with no risk factors
1299
Thromboprophylaxis in gynae surgery Moderate risk
Consider Teds or subcut LMWH for Sx \>30 mins Obesity Gross varicose veins Current infection Prior immobility Major current illness
1300
Thromboprophylaxis in gynae surgery High risk
Use LMWH for 5d or until mobile for C sx Prolonged Sx History of DVT Thrombophilia \>3 moderate risk factors
1301
What is a foley catheter?
Indwelling transurethral catheter
1302
When is a suprapubic catheter used in gynae sx?
Following surgery for genuine stress incontinence so that the ability to pass urine urethrally can be assessed before catheter removal
1303
What are the principle causes of perinatal mortality?
Unexplained Preterm delivery IUGR Congenital abnormalities Intrapartum including hypoxia Placental abruption
1304
What are the major associations with cerebal palsy? Minor?
Prematurity IUGR Infection Pre-ecl Congenital abnormalities Intrapartum fetal distress Postnatal events Autoimmune disease Multiple pregnanc Placental abruption
1305
Def: SFD
Small for dates Weight of the fetus is less than the tenth centile for its gestation, if at term 2.7kg
1306
Def: IUGR
Describes fetuses that have failed to reach their own "growth potential" In utero growth is slowed May end up SFD
1307
Def: fetal compromsie
Chronic situation when conditions for normal growth and neurological development are not optimum. Most identfiiable causes involve poor nutrient transfer through the placenta: placental dysfunction. Commonly there is IUGR but this may also be absent.
1308
What are the aims of fetal surveillance?
Identify high risk pregnancy Monitor the fetus for growth and well being Intervene at an appropriate time balancing the risk of in utero compromise against those of intervention/prematurity
1309
What factor prepregnancy are suggestive of a high risk pregnancy
Poor past obstetric history or very small baby Maternal disease Assisted conception Extremes of reproductive age Heavy smoking or drug abuse
1310
What factors during pregnancy are suggestive of a high-risk pregnancy?
HTN, proteinuria Vaginal bleeding SFD baby Prolonged pregnancy Multiple pregnancy
1311
What are the Ixs used to identify high-risk pregnancies?
Cervical scan at 23w Uterine artery Doppler Maternal blood tests e.g. PAPP-A
1312
What is PAPP-A?
Placental hormone the maternal level of which is reduced in the first trimester with chromosomal abnormallities Used as a DS screnning Low level also constitutes a high risk for IUGR, placental abruption and consequent stillbirth
1313
What are the features of maternal uterine artery doppler
Uterine circulation develops a low resistancei in pregnancy. Abnormal waverforms at 23w suggest failure of low resistance circulation and identifies 75% of pregnancies at risk of adverse neonatal outcomes in the early third trimester esp: pre-ecl, IUGR, palcental abruption. Most sensitive at 23w
1314
What is the cornerstone of identifying SFD?
Measurement of the symphysis fundal height
1315
What is USS used for in antenatal care?
USS asessment of fetal growth, which are subsequently recorded on centile charts. Rate of growth can be determined by previous scans Pattern of smallness may often help e.g. the fetal abdomen will often stop enlarging before the head which is spared: asymmetrical growth restriction Allows for consitutional non-pathological determinents of fetal grwoth Benefits: serial USS safe and useful. Limitations: one-off USS in later pregnancy are of limited benefit
1316
What is suggestive of placental dysfunction?
Reduced flow in umbilical artery in fetal diastole compared to systole suggests placental dysfunction.
1317
What are the benefits and limitations of doppler umbilical artery waveforms
Umbilical artery waveforms help identify which small fetuses are actually growth restricted and therefore copromosied. Also predates CTG abnormalities and correlates well with severe compromise. Limitations: Doppler is not a useful screening tool in low-risk pregnancies
1318
What is the use of doppler wavforms of the fetal circulation?
So all major fetal vessels can be seen but the most commonly measured are the MCA and the ductus venosus, With fetal compromise, the MCA often develops a low resistance pattern in comparison to the thoracic aorta or the renal vessels- head sparing effect. Velocity of flow also increases with fetal anaemia. Benefits: use is restricted to high-risk preegnancies and specific situtations. Limitations: routine use does not reduce perinatal mortality or morbidity
1319
Incraesed diastolic flow in the MCA on fetal doppler?
Suggests reduced resistance in the fetal MCA. Suggests head sparing Indicative of fetal compromise
1320
What are the features of USS assessment of biophysical profile?
Limb movements Tone Breathing movements Liquor volume Scored 2 each out of 8 CTG also included and the score is out of 10 Low score suggests fetal compromise Benefits: it is useful in high-risk pregnacny where CTG or doppler give equivocal results. Limitations: time consuming and of little use in low risk pregnancy
1321
What is a kick chart?
The mother records the number of individual movements that she experiences every day Benefits: most compromised features have reduced movements in the days or hours before demise, reduction in fetal movements is an indication for more sophisticated testing. Limitations: compromised fetuses stop moving only shortly before death, of limited benefit in reducing perinatal mortality
1322
SFD Other cut off
\<10th centile \<3rd centile i.e. 97th centile
1323
What are the constitutioal determinants of fetal size and health?
Affect growth and birth weight without causing IUGR Low maternal height and weight Asian Female fetal gender All associated with smaller babies
1324
What are the pathological determinants of fetal growth causing IUGR?
Pre-existing maternal disease Maternal pregnancy complications Multiple pregnancy Smoking Drug usage Infection eg. CMV Extreme malnutrition Congenital (chromosomal included) abnormalities Male obesity DM and Male gender All assocaited with increased risk of adverse outcomes
1325
Cx of IUGR
Stillbirth Cerebal palsy Preterm delivery: both iatrogenic and spontaenous Maternal risks
1326
Dx of SFD
Made using ultrasound. Umbilical artery doppler Amniotic fludi volume (often reduced) with fetal redistribution of blood flow apaprent in MCA CMV infection or chromosomal abnormality testing may be indicated CTG: only become abnormal when severe compromise or fetal distress is present
1327
SFD
1328
IUGR
1329
Mx of SFD
Growth recheced at fortnightly fetus Small but consistently growing fetus with normal umbilical artery doppler values does not need internvention
1330
Mx of IUGR at term
Small for dates with abnormal Doppler values is delivered if beyond 36w Induction or c-sect required
1331
Mx of IUGR at preterm
Aim is to prevent in utero demise or neurological damage with ongoing placental dysfunction whil maximising the gestation to avoid cxs of prematurity. IUGR fetus with anbormal doppler values is reviewed twice a week. I fabsent end-diastolic flow is seen the mother is admitted, given steroids if pre-34w and has a daily CTG A severely preterm IUGR is delayed until the CTG or fetal dopplers become abnormal.
1332
Def: SFD
Fetus's weight or estimated weight is below the tenth/fifth/third centile
1333
Def: IUGR
Implies compromise: growth has slowed or is less than expected, taking into account constitutional factors
1334
Def: prolonged pregnancy
\>42w NB risks of perinatal mortality and morbidity start between 41 and 42w.
1335
What is the risk of still birth between 37w and 43 w
0. 35 at 37w 2. 12 at 43w
1336
What are the risks of prolonged pregnancy
Stillbirth Neonatal illness and encephalopathy Meconium passage Dx of fetal distress
1337
Mx of prolonged pregnancy
From 41w: examine patient vaginally and induce, unless cervix very unfavourable or patient prefers to wait If no indcution: sweep cervix and arrange daily CTG If CTG abnormal: delivery by c-sect
1338
What is the probability of twin pregnancy? Triplet?
1 in 80 1 in 1000
1339
What are the types of multiple pregnancy?
DZ MZ
1340
What are the features of DZ twins?
2/3rds of all multiple pregnancies or triplets results from fertilisation of different oocytes by different sperm May be of different sex and are no more genetically similar than siblings from different pregnancies
1341
Features of MZ twins
Result from mitotic division of a single zygote into identical twins. Whether they share the same amnion or placenta depends on the time at which division occured
1342
What are DCDA twins?
Dichorionic diamniotic MZ twins. When division occurs before day 3: leads to twins with separate placentas and amnions
1343
What are MCDA twins?
Monochroionic diamniotic MZ twins Occurs with division between d4 and 8 Leads to twins with a shared placenta but separate amnions
1344
What are MCMA twins?
Monochroionic monoamniotic twins Occurs with later division (9-13d) and is very rare Twins have a shared placenta and single amniotic sac
1345
What are the issues with MC twins
Monochorionic twins have a higher fetal loss rate, particulalry before 24w
1346
What are the most common types of MZ twins?
MCDA (70%) DCDA (30%) MCMA: very rare
1347
What factors contribute to the likelihood of multiple pregnancy?
Assisted conception Genetic factors Increasing maternal age Parity Geenrally affect DZ twins
1348
Dx of multiple pregnancy
Vomiting may be more marked in early pregnancy Uterus is large for dates. May feel multiple fetal poles in later pregnancies
1349
Multiple pregnancy and antepartum complications
Virtually all obstetric risks are exagerrated in multiple pregnancies Maternal: GDM and pre-ecl more common Anaemia: greater increase in blood volume and dilutional effect and also becuase more Fe and folic acid are needed. Fetal: Twins have greater mortality (x6) LT handicap (5x increase) Triplets fare worse with 18x risk of ganidcap Preterm delivery, IUGR, monochorionicity
1350
What are the antepartum risks for all multiples?
Miscarriage: first trimester death. Late miscarriage more common in MC twins Preterm labour: main cause of perinatal mortality. 40% of twins and 80% triplet pregnancies deliver \<36w. IUGR Congenital abnormalities are more common per baby in dichorionic Co-twin death: if one of a pair of DC twins dies, the other usuallly survies although the risk of preterm delivery is increased
1351
Why and what are the Cxs of monochorionicity?
Result largely from the shared blood supply in the single placenta. Twin-twin transfuision syndrome IUGR Co-twin death Monoamniotic twins
1352
What is twin-twin transfusion syndomre
Occurs only in 15% of MCDA twins Results from unequeal blood distribution through vascular anastamoses of the shared placenta. One twin is volume depleted and develpops anaemia, IUGR and oligohydramnios. The other gets fluid overloaded and may develop polycytheamia, cardiac failure and massive polyhydramnios. Both twins are at very high risk of in utero death or severely preterm delivery. Even with optimal treatment, survival of both twins occurs in 50% with one twin in 80%. 10% of survivors have neurological disability
1353
How is TTTS staged?
Quintero system 1-5
1354
What is a particular problem in IUGR of MC twins
Where the umbilical artery waveform of the smaller twin is very erratic (selective IUGR with intermittenet absent or reversed end diastolic flow- sIUGR with iAREDF) which may be the result of superficial artery artery anastomoses. Sudden in utero death occurs in up to 20%
1355
What occurs wth co-twin death?
The drop in BP of the dead twin allows acute transfusion of blood from one to the other which may rapidly lead to hypovolaemia and in 30% death or neurological damage
1356
What are the features of monoamniotic twins
Not only the placenta but the amniotic sac is also shared. The cords are always entangled. In utero demise is sudden.
1357
What are the intrapartum Cxs of multiple pregnacny?
Malpresentation of the first twin occurs in 20% Second twin has an increased risk of death after the first has been delivered because of cord prolapse, hypoxia, tetanic uterine contraction, placental abruption, may present as a breech PPH more common.
1358
Mx of twin pregnancies antepartum
High risk pregnancy Fe and folic acid supplementation prescribed. Selective reduction can be discussed, only indicated in twins when one of them has a congenital abnormalitiy. Transvaginal US of cervical length may identify those at most risk of preterm delivery. Idenfy IUGR
1359
What is the lambda sign?
Sign of dichorionic twins Dividing membrane is thicker as it meets the placenta
1360
What is the T sign?
Thin dividing memrane as it meets the placenta. MZ twins
1361
Mx of TTTS?
Laser photocoagulation of the placental anastomoses in a fetal medicine centre is the preferred treatment.
1362
Intrapartum Mx of multiple pregnancies
Mode: C-sect: reduces risk of death and hypoxia in second twin. vaginal can be discussed when the first fetus is cephalic, regardless of the lie of the second. Method: Induction or C-sec is usualy at 37-38w (DC) or 34-37w(MC) after which time perinatal mortality is increased. CTG monitoring due to increased risk of fetal hypoxia, particularly for the second twin.
1363
Delivery of twins
First as normal Second: Maternal contractions often diminish after the first twin. Usually these return after a few miinutes, oxytocin can be started if not. Lie of the second twin is cehcked and ECV performed if not longitudinal. Once the head or breech enters the pelvis, the membranes are ruptured and pushing again beings. Delivery usually achieved within 20 mins of the first. Excessive delay is associated with increased mortality.
1364
What is breech extraction
Performed under general, epidural or spinal anaesthesia. Involves inserting a hand into the uterus, grasping the feet and guiding them down.
1365
What are the different classifications of congenital abnormalities?
Structural Chromosomal Inherited or as a result of intrauterine infection or durg exposure
1366
What is the prevalence of congenital abnormalities? Major?
Affect 2% of all pregnancies 1% major
1367
What proportion of perinatal deaths are accounted for by congenital abnormalities?
25%
1368
What makes a good screening test?
Cheap High sensitivity and specificity Is safe Must also be an acceptable diagnostic test Condition must be serious enough to warrant testing
1369
What is the difference between a screening and a diagnostic test?
Screening teast is available for all women and gives a measure of the risk of the fetus being affected by a particular disorder A diagnostic test is performed on women with a "high risk" to confirm or refute the possibility e.g. this fetus doesn't have down syndrome
1370
What is sensitivity
Proprotion of subjects with the condition classified by a test as screen positive for a condition
1371
What is NPV
Probability that a subject who is screen negative will not have the condition
1372
What is the specifcity of a test?
Proportion of subjects without the condition who are classified as screen negative
1373
What is the screen positive rate?
The proportion of subjects who are classified as high risk by a tst
1374
What is the PPV?
Probability that a subject who is screen positive will have the condition
1375
When is AFP raised at screening tests?
In neural tube defects. May also indicate a higher risk of third trimester Cxs Seldom used as USS is more accurate
1376
What components constitute the DS screening test?
beta-HCG PAPP-A AFP Oestriol Inhibin A Results can be integrated with other risk factors e.g. amternal age and USS measurements to screen for trisomies 21, 18, 13
1377
Larger nuchal translucency=
Greater risk of DS Also indicates a higher risk of structural (particulalry cardiac) abnormalities in addition, 50% of fetuses with trisomies have structural abnormalities e.g. exomphalos
1378
When is nuchal translucency test performed?
11 and 14w
1379
What is nuchal translucenecy?
Space between skin and soft tissue overlying the cervical spien
1380
What may polyhydramnios indicate? And so?
May be the result of a fetal abnoramlity Warrants a repeat, detailed USS examination
1381
Features of amniocentesis
Diagnostic test involving removal of amniotic fuid using a USS guided fine gauge needle. Safest performed at 15w 1% miscarry
1382
What can be diagnosed using amniocentesis?
Infections e.g. CMV and toxoplasmosis Inherited disorders e.g. sickle-cell anaemia, thalassaemia, CF
1383
Features of CVS
Involves biopsy of the trophoblast by passing a fine gauge needle through the abdominal wall or cervix and into the placenta after 11w. Higher miscarriage rate than amniocentesis Can be performed at 11w.
1384
Down's syndrome=
Trisomy 21 Usually the result of non-dysjunction at meiosissis May arise as a result of a balanced chromosomal translocation in the parents. More common with advancing maternal age.
1385
What is the most common chromosomal abnormality
DS
1386
What are the clinical features of DS?
Mental retardation Characteristic facies: epicanthic folds and flat facial profile Congenital cardiac disease (50%) Abundant neck skin Intestinal stenosis Umbilical hernia hypotonia Predisposition to leukaemia Simian palmar crease Recurrence rate is low unless it is the result of a balanced partental translocation
1387
USS in DS
Thickened nuchal translucenecy Some structural abnormalities Absent or shortened nasal bone TR
1388
Blood test results in DS
Low PAPP-A (1st trimester) Low AFP (1st/2nd trimester) Low oestriol High inhibin High HCG
1389
What is Trisomy 18
Edward's syndrome
1390
What is Trisomy 13
Patau's syndrome
1391
Patau's syndrome | (Trisomy 13)
1392
Clinical features of Patau Syndrome
Polydactyly Microcephaly and mental retardation Clef-lip and palate Cardiac defects Renal defects Umbilical hernia Rocker-bottom feet
1393
Rocker-bottom feet
Patau (Trisomy 13)
1394
Edwards syndrome | (Trisomy 18)
1395
Clinical features of Edwards
Prominent occiput Mental retardation Low set ears Short neck Overlapping fingers Mircognathia Congenital heart defects Renal malformation Limited hip abductio
1396
Kilnfelters
47 XXY Males have normal intellect, small testes, infertile
1397
Turners syndrome
45 XO Affected individuals are female, infertile but with preserved intellect
1398
What is the triple test for DS?
Blood test at 16w using AFP, hCG and oestriol Not hugely accurate, should only be used when screening occurs later than 14w
1399
What is the combined test for DS?
Maternal age PAPP-A Beta-hCG Nuchal translucency as measured by USS at 11-14w
1400
What are neural tube defects?
Result of failure of closure of the neural tube. Neural tissue often exposed allowing degradation. Best known examples are spina bifida (severe disability), anaencephaly (incompatible with life(
1401
How can NTDs be prevented
Preconceputal folica cid supplementation for 3months at 0.4mg/d
1402
Risk of NTDs
1 in 200 Recurrent NTDs occur in 1 in 10 pregnancies but this risk is greatly reduced by high dose folic acid.
1403
What is ventriculomegaly
Often due to NTDs, aqueduct stenosis or agenesis fo the copus callosum Px depends on severity and cause
1404
Akinesia syndromes in utero
Cause abnormal posture and are usualy lethal Polyhydramnios follows impaired swallowing
1405
Frog eye appearance on USS?
Anencephaly
1406
Epidmeiology of congenital cardiac defects
Occur in 1% of pregnancies More common in women with congenital cardiac disease or women who have had previously affected offsrping and when other structural/chromosomal abnormalities are present.
1407
In utero therapy for congenital defects
Medical: Steroids to mature lungs Antiarrythmic drugs NSAIDs for polyhydramnios Surgical: Laser treatment for TTTS Amnioreduction for polyhydramnios Pleuramniotic shunt for hydrops/effusions Vesicoamniotic shunt for urethral valves Bllod/platelet transfusion Tracheal occlusion for diaphragmatic hernia Valvoplasty for critical AS Cord occlusion of monochorionic twins Open: Neural tube defect surgery
1408
What is exomphalos
Partial extrusion of the abdominal contents in the peritoneal sac Fifty percent of affected infants have chromosomal problem and amniocentesis is offered. Isolated, small defects have a good prognosis after postnatal surgery.
1409
Exomphalos
1410
What is gastrochisis
Free loops of bowel in the amniotic cavity and is assoicated with ohter abnormalities. More common when the mother is very young Postnatal surgery is indicated: \>90% survive
1411
Gastroschisis
1412
What are diaphragmatic hernias
Cause the abdominal contents to herniate into the chest leading to pulmonary hypoplasia Associated abnromalities are common. 60% with isolated defects survive. In utero tracheal occlusion can improve prognosis in severe cases
1413
Pleural effusions in utero
May cause pulmonary hypoplasia and hydrops. in utero shunting isuseful
1414
What are CCAMs and pulmonary sequestrations?
Congenital cystic adenomatous malformations and pulmonary sequestrations are visisble as solid or cystic masses of varying sizes. Px usually good
1415
Featuers of oesophageal atresia and traceho-oesophageal fistulae?
Stomach non-visible or small. Polyhydramnios
1416
WWhat is a classic double bubble of the stomach associated with?
Duodenal atreasia,c aused by stomach and dilated upper duodenum. DS very common Polyhydramnios
1417
What does lower gut atresia cause?
Dilated bowel +/- polyhydramnios Meconium ileus due to CF is common
1418
Hydronephrosis in utero
Can be mild to severe Unilateral or bilateral Due to obstructino or reflux More prone to infection and therefore renal damage
1419
What do posterior urethral valves cause?
Obstruct the male urethra, cause oligohydramnios, bladder and renal dilation and damge which can range from lethal to renal failure in adulthood.
1420
What are skeletal dysplasia syndromes?
Affect the limbs, when they are lethal e.g. thanatophoric dysplasia, chest is frequently small
1421
What is the cause of isolated limb abnormalities
Amniotic bands- constriction deformities involving the amnion
1422
What is fetal hydrops?
Occurs when fluid accumulates in two or more areas in the fetus. Has a high mortality and is rarer in late pregnancy due to its high mortality
1423
What are the causes of fetal hydrops
Immune: anaemia and haemolysis (e.g. rhesus) Non-immune: 1. Chromsomal e.g. DS 2. Cardiac abnromalities or arrythmias 3. Structural abnromalities e.g. pleural effusion can cause hydrops 4. Anaemia causing cardiac failure (e.g. parvovirus infection), FMH or fetal alpha thalassaemia major 5. TTTS
1424
Ix of fetal hydrops
USS assessment: MCA Kleihauer and aprvovirus, CMV and toxoplasmosis testing Fetal blood sampling
1425
When can hydrops be cured?
Only possible where anaemia (transfusion) or compression by fluid collection e.g. pleural effusion (vesicoamniotic shunting) have caused hydrops
1426
Def: polyhydramnios
Increased liquor volume. Deepest liquor pool \>10cm
1427
Causes of polyhydramnios
Idiopathic Maternal disorders (established and GDM), renal failure Twins (esp TTTS) Fetal anomaly (particuallry upper GI obstructions or inability to swallow)
1428
Clinical features of polyhydramnios
Maternal discomfort Large for dates Taut uterus Difficult palpation of fetal parts
1429
Cxs of polyhydramnios
Preterm labour Maternal discomfort Abnormal lie Malpresentation
1430
Mx of polyhydramnios
To diagnose fetal anomaly: detailed USS To diagnose DM: maternal blood glucose To reduce liquor: If \<34w and severe, amnioreduction, or use of NSAIDs to reduce fetal urine output Consider steroids if \<34w Delivery: vaginal unless persistent unstable lie or other obstetric indication
1431
What are the consequences of raised fetal blood glucose levels
Induces fetal hyperinsulinaemia leading to fetal fat deposition and excessive growth-\> macrosmia
1432
Why does glucose tolerance decrease in pregnancy?
Altered carbohydrate metabolism and the antaonistic effects of human placental lactogen, progesterone and cortisol. Pregnancy is diabetogenic.
1433
What is significant about renal glucose excretion in pregnancy?
Threshold for glycosuria decreases, therefore glucose in urine may occur at physiological blood concentrations
1434
Pre-existing diabetics in pregnancy
Insulin requirements increase
1435
Def: GDM
Carbohydrate intolerance which is diagnosed in pregnancy and may or may not resolve after pregnancy
1436
NICE definition of GDM
Fasting plasma glucose level of \>5.6 2 hour plasma glucose level of \>7.8 after a 75g glucose load (GTT)
1437
Fetal cxs in DM
T1DM and T2DM are similalrly effected. GDM less so Congenital abnormalities: neural tube and cardiac defects and are related to periconceptual glucose control Preterm labour Reduced fetal lung maturity Raised birthweight: dystocia and birth trauma Fetal compromise Fetal disress Sudden fetal death are more common
1438
How does polyhydramnios arise in GDM?
Fetal pancreatic islet cell hyperplasia leads ot hyperinsulinaemia and fat deposition Leads to incresased UO and polyhydramnios
1439
Maternal cxs of DM in pregnancy
INsulin requirements increase DKA rare Hypoglycaemia may result from attempts to achieve optimum glucose control Infection: UTI, wound or endometrial more common Pre-ecl more common Pre-existing IHD aggravated C-sect or instrumental delivery more likely. Diabetic nephropathy associated with poorer fetal outcomes but doesn't deteriorate in pregnancy **Diabetic retinopathy often deteriorates and may need to be treated in pregnancy**
1440
Preconceptual care of diabetic women wishing to conceive
Baseline RFTs, BP and retina Glucose optimised 5mg folic acid/d BP control with labetalol or methyldopa
1441
How is DM monitored during pregnancy
HbA1c
1442
Who should be screened for GDM?
BMI \>30 Previous macrosmic baby Previous unexplained still birth Previous GDM First degree relative with GDM Family origin with high prevalence of DM
1443
Dx test for GDM
OGTT
1444
Mx of DM in pregnancy
Non-drug treatment: lifestyle changes Medication: Offer metformin if lifestyle changes do not impact on blood glucose levels in 1-2w Insulin as alternative to metformin. If fasting glucose above 7, insulin and metformin. NB advise women to always have fasting acting glucose source available
1445
Fetal monitoring in DM
Normal USS Fetal echocardiography is also indicated.
1446
Mx of pre-ecl risk in DM in pregnancy
75mg daily from 12w
1447
NB in any pregnant woman presenting unwell with hyperglycaemia
DKA
1448
Timing and mode of delivery in GDM
By 39w. Offer C-sect if fetal weight exceeds 4kg Glucose levels maintained by sliding scale of insulin and dextrose infusion during labour
1449
What are the common complications for the neonate immediately after delivery in GDM
Hypoglycaemia due to its accustomisation to hyperglycaemia RDS occurs even after 38w.
1450
Mx of GDM after delivery
Dose of insulin can be changed to prepregnant doses
1451
Indications for GTT in pregnancy
Risk factors Polyhydramnios Persistent glycosuria (2+ on 1 occasion or 1+ on 2 occassions)
1452
Draw Mx of GDM
1453
Folllow up to women with GDM after delivery
OGTT at 3m 50% will be diagnosed as diabetic within the next 10y
1454
Why is an ejection systolic murmur heard in 90% of pregnant women?
40% increase in CO. 40% increase in BV 50% reduction in SVR BP drops, flow rate increases. Increased blood flow produces a flow murmur
1455
How does the ECG change in pregnancy?
Left axis shift Inverted T waves
1456
How are women with cardiac disease assessed prepregnancy
Echo
1457
Mx of labour in women with cardiac disease
Fludi balance monitoring Elective epidural analgesia Elective forceps delivery helps avoid the additional stress of pushing Antibiotics for those at risk of endocarditis
1458
Mx of PDA, VSD and ASD in pregnant women
Do not usually cause complicatiosn
1459
Pulmonary HTN and pregnancy e.g. Eisenmenger's syndrome
High maternal mortality rate (40%) Pregnancy contraindicated and usually terminated
1460
AS in pregnancy
Severe disease causes an inability to increase cardiac output when required and should be corrected before pregnancy. Beta-blockade often used Epidrual analgesia is contraindicated. Thromboprophylaxis required for aortic valves
1461
Mitral valve disease and pregnancy
Should be treated before pregnancy In severe stenosis HF may develop late in pregnancy and beta blockade should be used. Artificial metal valves are particularly prone to thrombosis and warfarin is used after the first 12w despite risk to fetus
1462
What is peripartum cardiomyopathy
Rare cause of HF specific to pregnancy Develops in the last month or the first 6m after pregnancy in the absence of a recognisable cause. Cause of maternal death and leads to permanent LVD in \>50% Treatment is supportive with diruetics and ACEI
1463
Asthma in pregnancy
Doesn't need to be a change in control as medication generally safe Women on LT steroids require an increased dose in labour because the chronically suppressed addrenal cortex is unable to produce adequate steroids for the stress of labour
1464
Supplementation in epileptics during pregnancy
Folic acid 5mg daily 36w: Oral vit K Fetal echocardiography and anomaly scan are important to exclude fetal abnormalities
1465
Cxs of hypothyroidism in pregnancy
High perinatal mortality. Even subclinical hypothyroidism is associated with: miscarriage preterm delivery intellectual impairment in childhood Also associated with an increased risk of pre-eclampsia, particulalry if antithroid antibodies are pregsent. TSH monitored
1466
Cause of neonatal thyrotoxicosis and goritre
Antithyroid Abs in mother suffering from Graves disease that cross the placenta
1467
Implications of poorly controlled hyperthyroidism in pregnancy?
Risk of thyrotoxicosis: acute symptoms and HF usually near or at delivery. Treated with PTU rather than carbimazole
1468
Propylthiouracil
Used to treat hyperthyroidism in pregnancy Can cross the placenta and occasionally causes neonatal hypothyroidism
1469
Features of postpartum thyoridtis
Common and can cause postnatal depression Risk factors: Antithyroid Abs T1DM Transient and usually subclinical hyperthyroidism usually about 3 months postpartum, folled by 4 months of hypothyroidism which is permanent in 20%
1470
Clinical features of acute fatty liver in pregnancy
Acute hepatorenal failure, DIC and hypoglycemia Early symptoms: malaise, vomiting, jaundice and vague epigastric pain. Early dx and prompt delivery essential. Correction of clotting defects and hypoglycaemia Supportive treatment with blood products, fluid blanace and occasionally dialysis
1471
Mx of intrahepatic cholestasis of pregnancy
Vit K 10mg/d to reduce risk of haemorrhage Ursodeoxychlic acid Induction at 38w
1472
Why does intrahepatic cholestasis of pregnancy occur?
Due to increased sensitivity to the cholestatic effects of oestrogen
1473
Dx of antihphospholipid syndrome
1+ clinical criteria: Vascular thrombosis 1+ death of fetus \>10w Pre-ecl or IUGR requiring delivery \<34w 3+ fetal losses \<10w, otherwise unexplained With laboratory criteria: Lupus anticoagulant or high anticardiolipin Abs or anti-b2 glycoprotein Ab (Measured twice \>3m apart)
1474
What are the adverse outcomes of antiphospholipid syndrome?
Due to placental thrombosis: Recurrent miscarriage IUGR Early pre-ecl Fetal loss rate is high
1475
Mx of antiphospholipid syndrome
2% of pregnant women have the Abs Mx with aspirin and LMWH and is restricted to those with the syndrome. Pregnancy is managed as a high risk, with serial USS and elective induction of labour at least by term. Postnatal anticoagulation
1476
Pregnancy in CKD
Inadvisable if creatinine level is \>200mmol as renal function often deteriorates late in the pregnancy
1477
Differentiation between proteinuria in CKD and pre-ecl
CKD present \<20w
1478
Fetal cxs of CK
Pre-ecl IUGR Polyhydramnios Preterm delivery
1479
Mx of CKD in pregnancy
USS for fetal growth RFTs Screen for UTIs Control of HTN Dialysis Vaginal delivery appropriate
1480
UTI in pregnancy
Associated with preterm labour and increased perinatal morbidity and mortality Asymptomatic bacteriuria affects 5% but is more likely (20%) to lead to pyelonephritis in pregnancy
1481
ECG and PE in pregnancy
ECG changes of normal pregnancy can mimic those of a PE
1482
LMWH dosing in pregnancy
More is needed than in nonpregnant women as clearance is more rapid
1483
Risk assessment for VTE High Intermediate Moderate
1484
Maternal and fetal risks of obesity in pregnacny
Maternal: High risk of thromboembolism, pre-ecl, DM C-sec, wound infections, difficult sx, PPH, maternal death Fetal: Higher rate of congenital abnromalities, DM and pre-ecl x2-3 perinatal mortality
1485
Mx of obesity in pregnancy
Preconceptual advise 5mg folic acid High risk if \>35BMI: screen for GDM, and BP surveillance. BMI \>40 require formal anaesthetic risk assessment
1486
BPAD and pregnancy
Well or at low risk of relapse, stop Li Unwell or at high risk, continue Li with blood monitoring due to increased excretion during pregnancy Higher risk of maternal sucidie and postnatal medication is important
1487
Paroxetine in pregnancy
May cause cardiac defects and is not advised
1488
Clozapine and olanzapine in pregnancy
Usually avoided
1489
Risks and management of opiate use in pregnancy
Not teratogenic, use associated with: preterm delivery, IUGR, stillbirth, developmental delay and SIDS Methadone maintenance
1490
Risk and management of cocaine use in pregnancy
Probably teratogenic and can cause childhood intellectual impairment. Associated with IUGR and placental abruption as well as preterm delivery, stillbirth and SIDS COunsellying
1491
Ecstasy and pregnancy
Teratogenic: cardiac defects, gastroschisis Pregnancy cxs similar to that of cocaine Counselling
1492
BZDs and pregnancy
Associated with facial clefts, cause neonatal hypotonia
1493
Fetal alcohol syndomre
Facial abnormalities IUGR Microcephaly Developmental delay \>18 units per day
1494
What are alcohol spectrum disorders
Encompass lesser variants of fetal alcohol syndrome
1495
Risks of smoking in pregnancy
Dose dependent Increased risk of Miscarraige IUGR Preterm birth Placental abruption Stillbirth SIDS
1496
Fe deficiency anaemia in pregnancy
Folic acid deficiency may coexist Symptoms absent until Hb \<9 MCV reduces but may initially be normal Ferritin levels reduced Treatment is with oral Fe, can cause GI upset In severe cases IV Fe is quicker
1497
Foods rich in Fe
Meat, particulalry kidney, and liver, eggs, green vegetables
1498
Foods rich in folic acid
lightly cooked or raw green vegetables. Fish
1499
Adult HbA
2 alpha 2 beta
1500
Fetal HbF
2 alpha 2 gamma
1501
Maternal complications of sickle cell disease
More frequent crises Pre-ecl Thrombosis Infections
1502
Fetal cxs of SCD
Miscarraige IUGR Preterm labour Death
1503
Mx of SCD in pregnancy
Regular exchange blood transfusions Infection screening Hydration Folic acid supplementation Fe avoided because of overload
1504
Def: perimenopause
Time beginning with the first features of the approaching menopause e.g. vasomotor symtpoms and mesntural irregulatiry and ends 12 months after the last menstrual period
1505
Def: surgical menopause
Following BSO
1506
Causes of premature menopause
Premature ovarian failure Infections Autoimmune disease CTx Ovarian dysgensis Metabolic disease
1507
Mx of premature menopause
Oocyte donation for fertility treatment HRT until 50
1508
20% of PMB caused by
Endometrial carcinoma Cervical carcinoma Premalignant endometrial hyperplasia with cytological atypia
1509
Purulent blood stained vaginal discahrge ina post menopausal woman
Investiage to exclude endometrial cancer or (uncommonly) a divertiuclar avscess draining via the uterus or vagina
1510
Causes of PMB
Endometrial carcinoma Endometrial hyperplasia +/- atypia and polyps Cervical carcinoma Atrophic vaginitis Cervicitis Ovarian Ca Cervical polyps
1511
Mx of PMB
Bimanual and pseculum +/- cervical smear TVS to measure endometrial thickness, thickened endometrial cavity or fluid filled cavity: malignancy, hyperplasia or polyps
1512
Early, intermediate and late effects of menopause
Early: psychological symptoms Intermediate: skin atrophy, genital tract atrophy, urinary tract atrophy Late: Cerebrovascular accidents, cardiac disease, bony fractures
1513
What are the vasomotor symptoms of menopause?
Hot flushes and night sweats May begin before periods stop and are usually present for less than 5y
1514
Symptoms of vaginal atrophy
Dyspareunia Cessation of sexual activity Itching Burning Dryness Urinary symptoms: frequency, urgency, notcuria, incontinence, recurrent infection
1515
What are the risk factors for osteoporosis Genetic Constitutional Environmental Drugs Disease
1516
When are FSH levels best measured
Between days 2 and 5 of the cycle to aboid the mid cycle preovulatory increase and the luteal phase suppression
1517
AMH measurement
Produced by small ovarian follicles and give a direct measurement of ovarian reserve, low levels are consistent with ovarian failure. AMH levels are stable throughout the menstrual cycle and so can be measured on any day
1518
Ix in ?premature ovarian failure
FSH (AMH) TFTs Catecholamnies LH, oestradiol and progesterone
1519
Why is the hip better than the spine in terms of estimating bone density?
Spine may have falsely increased values due to osteophytes from OA, kyphosis, scoliosis and aortic calcification
1520
HRT single combined
Oestrogen alone in women who have had a hysterectomy Combined with progestogens in those who ahve not.
1521
Delivery of oestrogens Delivery of progestogens
Oral Transdermal Subcut Orally Transdermally IUS
1522
Why are synthetic oestrogens not used for the HRT?
Because of their greater metabolic impact
1523
What oestrogens are used in HRT
Oestradioll, oestrone, oestriol Synthesised from plants
1524
What progestogens are used in HRT
levonorgestrel Norethisterone
1525
What is tibolone
Synthetic steroid compound that is inert but is converted in vivo to metabolites with oestrogenic, progestogenic, and andorgenic actions. Used in post-menopausal women who desire amenorrhoea and treats vasomotor, psychological and libido problems Conserves bone mass
1526
Oestrogen only HRT
Used in women after hysterectomy May be concenrs about a remnant of endometrium in the cervical stump if it was a subtotal hysterectomy. If this is suspected, presence or absence of bleeding following HRT is a useful test
1527
What is sequential HRT and its effects
10-14d every 4w or 1`4d every 13w Leads to monthly bleeds or 3 monthly bleeds
1528
What is continuous HRT and its effects
Used every day Leads to no bleeds
1529
When is the IUS useful in menopause
During the perimenopausal period if there is menorrhagia
1530
Post-menopause, preferred HRT
Continuous combined regmines because of the lack of induced bleeding and because it may reduce the risk of endometrial cancer Continuous combined therapy induces endometrial atrophy. IU delivery may be used but can be technically difficult in older women
1531
Mx of urogenital symptoms of menopause
Vaginal administration by cream or pessary (oestriol) or oestradiol by table ot ring
1532
Benefits of oestrogens in menopausal symptoms
Oestrogen reduces vasomotor symptoms Oestrogens also reduced vaginal atrophic symptoms May improve sexuality Testosterone can be added
1533
Benefits of HRT for osteoporosis
HRT reduces the risk of #s
1534
Benefits of HRT in CRC
HRT reduces the risk of CRC by 1/3rd
1535
Risks of HRT: breast cancer
Combined but not oestrogen only HRT increases risk Risk fallson stopping combined therapy and normalises after 5y
1536
Risks of HRT: endometrial cancer
Unopposed oestrogen replacement therapy increases endometrial cancer risk
1537
Risks of HRT: VTE
HRT increases risk of VTE x2
1538
Risks of HRT: gall bladder
Oral HRT increases risk of gallbladder disease
1539
Non-oestrogen therapy for vasomotor symptoms of menopause
Progestogens Clonidine: of lmited value SSRIs: are ffective in ST Gabapentin may be effective
1540
Bisphosphonates in menopause
e.g. alendronate, risendronate and ibandronate Used in prevention and treatment of osteoporosis Princple adverse effect is irritation of the upper GI May affect fetal skeleton, so aren't advised in women wishing to conceive
1541
Strontium ranelate
Decreases the risk of osteoporotic vertebral and hip #s
1542
Raloxifene
Selective oestrogen receptor modulator, reduces the incidence of osteoporosis-related vertebral 's
1543
Denosumab
RANKL Ab Used whe bisphosphonates are contraindicated
1544
Def: septic miscarriage
The contents of hte uterus are infected causing endometritis. Vaginal loss is usually offensive, uterus is tender and a fever may be present. If plevic infection occurs there is abdominal pain and peritonsim
1545
What is the cause of \>60% one off sporadic miscarriages?
Isolated non-recurring chromosomal abnormalities.
1546
Ix in ?miscarraige
USS: will show uterine contents. If in doubt, the scan should be repeated 1w later. Bloods: HCG levels (if raised and no intrauterine gestational sac is visible, ectopic) FBC Rhesus group
1547
Mx of miscarriage
Admit: if ectopic, septic or heavy bleeding Resus: contents in cervical os. IM ergometrine will reduce bleeding but is only used if the fetus is non-viable If there is a fever, swabs for culture and IV antibiotics Anti-D is gient to women who are rhesus negative
1548
Mx of threatened miscarriage
90% of women in whom fetal heart activity is detected at 8w will not miscarry
1549
Mx of non-viable intrauterine pregnancy
Expectant Medical: prostaglandins Surgical: ERPC
1550
Cxs of miscarriage
Vaginal bleeding with expectant or medical management can be heavy Risks of expectant/medical management include need for surgical evacuation, risk of infection is not incresed. Infection may become systemic leading to endotoxic shock
1551
Counselling after miscarriage
Miscarriage was not result of anything they did Reassurance as to the high chance of successful pergnancies is important Referral to a support group
1552
Causes of recurrent miscarriage
Antiphospholipid Abs: LMWH and aspirin Chromsoomal defects: parental karyotyping, CVS or amniocentesis. Use of donor oocytes Anatomical: uterine abnormalities (USS or hysterosalpingoram), cervical incompetence (\>16w) Infection Obesity Smoking PCOS Excess caffeiene intake Higher maternal age
1553
Statuatory grounds for abortion in the UK
1554
Surgical methods of abortion
Suction curettaeg (7-13w) Dilatation and evacuation (\>13w) Antibiotic cover required for both
1555
Medical methods of abortion
Antiprogesterone: mifepritsone + prrostaglandin (mifeprostol, gemeprost, PGE1 analogues (36-48h later) is the most effective in \<7w and can be used up to 9w Prostaglandin alone can be used Byeond 22w: KCI injected into the umbilical vein or fetal heart
1556
What are the cxs of TOP
Haemorrhage Infection Uterine perforation Cervical trauma Failure
1557
What is the most common site of ectopic pregnancy?
Fallopian tube (95%)
1558
Sites of ectopics
1559
Hx of ectopic
Lower abdominal pain Scanty dark vaginal bleeding Pain may be initially colicky (as the tube tries to exude the sca) and then become constant Syncopal episodes and shoulder tip pain suggests intraperitoneal blood loss
1560
Ix in ectopic
Pregnancy test USS: TV Quantitative serum hCG is useful if the uterus is empty ifmaternal \>1000IU then if a uterine pregnancy were present it should be visible on TVS. If the level is lower but rises more than 66% in 48h, an earlier but intrauterine pregnancy is normal. Declining or slower rising levles of hCG suggest an ectopic or nonviable intrauterine pregnancy
1561
What is a heterotropic pregnancy
When an intrauterine and an ectopic pregnacny coexist
1562
Mx of symptomatic suspected pregnancy
NBM ABC FBC and cross-match Pregnancy test USS Laparoscopy or medical management if criteria met.
1563
What are the issues with salpingostomy
10% chance a repeat surgery for persisting ectopic is required- detected by failure of serum hCG to fall on follow up. Increased risk of repeat ectopic as damaged tube remains
1564
Medical management of ectopic
If the ectopic is unruptured, with no cardiac activity and an hCG level \<3000 IU Methotrexate as a systemic sinlg edose can be used. Serial hCGs are used to confrm that trophoblastic tissue has gone. SSecond dose may be required.
1565
Conservative management of ectopic
If the ectopic is small and unrupture or if the location of the pregnancy is not clear and hCG le3vles are low and declining. Careful observation may suffice
1566
Cx of ectopic pregnancy
Serial hCG to confirm resolution. 70% will have subsequent successful pregnancy following salpingectomy
1567
Def: hypermesis gravidarum
When N+V is so severe as to cause severe dehydration, weight loss or electrolyte disturbance.
1568
Mild NVP
Nausea and occasional morning vomiting 50% pregnant women No treatment required
1569
Moderate NVP
More persistent vomiting 5% pregnant women Often admitted to hsopital
1570
Severe NVP
Hyperemesis gravidarum
1571
Mx of hyperemsis gravidarum
Exclude predisposing conditions: UTI, multiple or molar pregnancy IV rehydration Antiemetics: promethyazine or cyclizine metoclopramide second line Thiamine Steroids in severe cases
1572
Def: gestatuiational trophoblastic disease
Trohpohblastic tissue which is part of the blastocyst that normally invades the endometrium proliferates in a more aggressive way than is normal: hCG secreted in excess Prolifreation can be localised and noninvasive. May also have characteristics of malignant tissue, invasive in the uterus alone= invasive mole. If metastasises= choreocarcinoma
1573
What is a complete hydatidiform mole
Entirely paternal in origin. When one sperm fertilises an empty oocyte and undergoes mitosis. Result is diploid tissue, usually 46XX
1574
What is a partial hydatidiform mole
Triploid, derived from two sperms entering one oocyte. Variable evidence of a foetus
1575
What is gestational trophoblastic neiplasia
When there is evidence of persistence of gestational trophoblastic disease (hydatidiofrm mole, invasive mole, choriocarcinoma), commonly defined as elevation of hCG.
1576
Hx and Ex in GTD
Heavy vaginal bleeding, hyperemesis Uterus large for dates, pre-eclampsia and hyperthyroidism can occur
1577
Snowstorm appearance of swollen villi
Complete hydatidiform mole
1578
Mx of GTD
Trophoblastic tissue removed by ERPC and diagnosis confirmed histologically Bleeding often heavy Serial hCG levels taken, pesristent or rising levels are suggestive of malignancy. Pregnancy and COCP avoided until hCG levels are normal as they may increase the need for CTx
1579
Cx of GTD
Recurrence of molar pregnancy occurs in 1 in 60, after every subsequent pregnancy, further hCG samples are required to exclude disease recurrence GTN (molar pregnancy only accounts for 50% as malignancy may also follow miscarriages and normal pregnancy, usualy presents as persistent vaginal bleeding)
1580
Mx of GTN
Highly malignant but very sensitive to CTx Patients are risk stratified Low risk: methotrexate and folic acid High risk: Combination CTx
1581
What is the difference between primary and secondary infertility?
Primary: female never conceived Secondary: previously conceived even if the pregnancy ended in miscarraige or TOP
1582
What are the four basic conditions required for pregnancy?
1: Egg must be produced (anovulation) 2. Adequate sperm must be released (Male factor) 3. Sperm must reach the egg (fallopain tube damage, 25%, sexual 5% and cervical 5% problems may also prevent fertilisation) 4. Fetilised egg must implant
1583
What are the most common factors contributing to suberfitility
Ovulatory 30% Male 25% Tubal 25% Coital 5% Cervical \<5% Unxeplained 30% Because more than one cause may be present, the percentage total is \>100%
1584
Why does fertility decline with increasing age?
Mainly due to reduced genetic quality of remaining oocytes rather than ovulatory problems
1585
What is the dominant follicle
The largest follicle with sufficeient gonadotrophin receptors which competes with the other follicles for diminishing stimulating hormones. It is the most likely to survive and continue growth. Development is coregulated by inhibin B which also suppresses FSH
1586
Ix of ovaulation
D21 progesterone (or progesterone 7d before the end of the cycle) 2. USS can monitor follicular growth: not performed 3. Over the counter LH predictor kits that analyse urine 4. Temperature charts
1587
What is PCO?
Characteristic TVS appearnace of \>12 small follciles in an enlarged ovary. Found in 20% of women, the majority of whom have regular ovulatory cycles. Development of other features leads to diagnosis of full syndrome
1588
Clinical dx of PCOS criteria
\>2 of: ``` PCO on USS Irregular periods (\>35d) ``` Hisutism: clinical (acne or hirsutism) and or biochemical (raised testosterone)
1589
Pathophysiology of PCOS
Disordered LH production with peripheral insulin resistance Combination of raised LH and insulin acitng on PCO leads to increased ovarian androgen production.
1590
What are the additional Ix indicated in PCOS?
Bllods: FSH investigated (raised in ovarian failure, low in hypothalamic disease, normal in PCOS), Prolactin (to exclude a prolactinoma) and TSH. Serum testosterone. LH USS Other: DM screening and abnormal lipids or FHx of CVD
1591
Clinical feautres of PCOS
None Subfertility Oligomenorrhoea or amenorrhoea Hisutism and or acne Obesity Miscarriage
1592
Cxs of PCOS
50% develop T2DM 30% develop GDM Endometrial C more common in women with many years of amenorrhoea due to unopposed oestrogen action
1593
Treatment of PCOS symtpoms other than infertility
Advice re diet and exercise which should result in reduction of insulin levels and improvement in all PCOS symptoms Treatment with COCP will regulate mesntruation and treat hirsutism At least three to four bleeds per year, whether spontaenous or induced, are necessary to protect hte endomertium Cyproterone acetate (anti-androgen) or spironolactone are effective treatments for hisutsim but conception must be avoided. Metformin can be used (also promotes ovulation)
1594
Causes of anovulation
Hyptholamus: Hypothalamic hypogonadism: reduction in GnRH causes amenorrhoea. Occurs with anoerxia nervosa. Kallman's syndrome (can be treated with exogenous gonadotrophins- bone protection with OCP or HRT required) Pituitary: Hyperprolacinaemia: suppresses GnRH release (CT indicated if neurological symptoms are present) treated with dopamine antagonist restores ovulation. Sx needed if this fails Pituitary damage: pressure from tumours, Sheehan's Ovarian: Preamture ovarian failure Gonadal dysgenesis Luteinised unruptured follicle syndrome Thyroid: Hyper or hypo Androgen secreting tumours
1595
What is Kallman's snydomre
Occurs when GnRH secreting neurones fail to develop
1596
What is a consideration of exogenous GnRH therapy?
Osteoporosis LT managed by OCP or HRT
1597
What is luteinised unruptured follicle syndrome
Present whena a follicle develops but the egg is never released
1598
Lifestlye changes to induce ovulation
Advice regarding risks Folic acid Restoration of normal weight Treat specific causes Smoking should cease
1599
Treatment of PCOS
Clomifene: first line ovulation induction drug in PCOS. Limited to 6m used. Anti-oestrogen. Only given at start of the cycle from 2-6 Metformin: second line (has a lower live birth rate compared to clomifene) although it doesn't increase the risk of multiple pregnancy Increases the effectiveness of clomifene in clomifene resistant women. Laparoscopic ovarian diathermy: as effective as gonadotrophis and with lower multiple pregnancy rate. Can also check tubal patency during the procedure Gonadotrophins
1600
Considerations of clomifene therapy
Given for 6m and at the start of the cylce from days 2 to 6. Monitored by TVS to assess ovarian response and endometrial thickenss. If no respons than the dose can be increased from 50 to 100 and even 150mg/day If three or more follicles develop then cycle cancellation indicated to reduce the risk of multiple pregnancy. Leads to endometrial thinning
1601
Use of gonadtrophin induction of ovulation
Used when clomifene has failed but also in hypothalamic hypogonadism Mutliple pregnanices are a consideration so a low-dose step up regiment is followed. Once a follicle is of sufficient size, ovulation can be stimulated by injection of hCG or recombinant LH. GnRH pumps can be used to stimulate FSH and LH production form the pituitary in a physiological manner.
1602
What are the side effects of ovulation induction
Mutliple pregnancy: more likely with clomifene or gonadotrophins but not metformin Ovarian hyperstimulation syndrome: gonadtrophins and rarely clomifene overstimulates the follicles which can get very large and painful (more common during IVF) Ovarian and breast carcinomas: generally not a risk
1603
Features of Ovarian hyperstimulation syndrome
Risk factors include gonadotrophin stimulation, age \<35y, previous OHSS, ovaries of PCO morphology Prevention includes using lowest effective gonadotrophin doses, USS monitoring, coasting (withdrawing gonadotrophins for a few days) or cancelling IVF cycle. In severe cases hypovolaemia, electrolyte disturbances, ascites, thromboembolism and pulmonary oedema may develop. OHSS can be fatal Admission may be required: restoration of intravascular volume, electrolyte monitoring, analgesia and thromboprophylaxis
1604
On what is spermatogenesis dependant?
Pituitary LH and FSH LH acts via testosterone production in the Leydig cells of the testis FSH controls sertoli cells which are involved in synthesis and transport of sperm Takes 7d for sperm to develop fully
1605
Features of male semen analysis
Sample produced by mastrubation with last ejaculation having occurred 2-7d previously. Must be analysed within 1-2h of produciton Abnormal analysis must e repeated after 12w. If persistently abnormal, examination and investigations of the male must follow.
1606
Features of normal semen Vollume Sperm Count Progressive motility
\>1.5ml \>15m \>32%
1607
Azoospermia
No sperm present
1608
Oligospermia
\<15m/ml
1609
Severe oligospermia
\<5m/ml
1610
Asthenospermia
Absent or low motility
1611
Causes of abnormal semen analysis
Unknown Smoking/ETOH/drugs/chemicals/inadequate local cooling Genetic Antisperm Abs
1612
Ix and treatment of male factor
Semen: if abnormal repeat and examine scrotum and optimise lifestyle factors If oligospermic then: intrauterine insemination If moderate to severe oligospermia: IVF with intracytoplasmic sperm inection If azoospermic: examine for presence of vas deferens, check karyotype, CF, hormone profile, surgical sperm retreival
1613
Common causes of abnormal/absent sperm release
Idiopathic Drug exposure: sulfasalzine, anabolic steroids Varicocoele Antisperm Abs Other causes: infection, mumps orchitis, testicular abnormalities, obstruction to delivery (e.g. congenital absence of the vas deferens), hypothalamic problems, Kallman's, hyperprolactinaemia, rterograde ejaculation (due to neurological disease secondary to DM or TURP)
1614
Kallman's
hypogonadotrophic hypogonadism
1615
With what is vas deferens agenesis associated?
CF
1616
What do high levels of FSH and LH with low testosterone in males suggest?
Primary testicular failure e.g. due to: cryptorchidism, surgery, RTx or CTx.
1617
Causes of tubal damage
Infection: PID: main cause. If there are peritubal adhesions or clubbed and closed fimbrial ends, laparsocopic adhesiolysis and salpingostomy can be performed. Ectopic rates increased Endometriosis Previous surgery/sterilisation
1618
Causes of cervical problems in failure to fertilise
Antibody production Infection in hte vagina or verxi that prevents adequate mucus Cone biopsy IUI to bypass cervix often used
1619
Tests for detection of tubal damage
Lap and dye Hysterosalpingogram
1620
HSG
Hysterosalpingogram Radio-opaque contrast injected through the cervix. Spillage from the fimbrial end can be seen on XR. Can also be done transvaginally.
1621
How is ovarian reserve measured and what is its significance in IVF
AMH Must be present for IVF to be performed i.e. premature ovarian failure cannot use IVF
1622
What are the stages of IVF
Multiple follicular development Ovulation and egg collection Fertilisation and culture Embryo transfer
1623
What are the cxs of assisted conception
Superovulation Egg collection: intraperitoneal haemorrhage and pelvic infection may complicated the USS-guided aspiration of mature follicles necessary for IVF Pregnancy: increased multiples, rates of ectopics, increased perinatal mortality and morbidity.
1624
What is the Pearl Index?
The risk of pregnancy per 100 women years of using the given contraceptive
1625
What are the considerations for contraceptives in women with IBD?
Malabsorption can reduce th efficacy of oral contraception Alternative methods should be used such as combined patches, progesterone only injectables and implants Depo-provera should not be a first line option as it increases the risk of osteoporosis
1626
Cut off for natural contraception when breat feeding Contraceptive option afterwards?
21d Combined pill reduces breast milk volume and should be avoided 6w postpartum and is relatively contraindicated 6-6m post partum. Progestogen only methods have no effect and can be used in the 6 weeks postpartum
1627
Advice to perimenopausal women re contraception
\<50y/o: continue contraception for at least 2y after the LMP \>50y/o at least 1y,
1628
What are the different types of hormaonal contraception?
Progestogen as a tablet: progestogen only pill (mini pill) Progestogen as a depot: Nexplanon, Depo-Provera or in the levonorgesrel containing IUS 3: Combined hormonal contraception: COC Transdermal patch Vaginal ring
1629
How does the COCP work
Exerting negative feedback on gonadotrophin release inhibiting ovulation. Also thin the endometrium and thicken cervical mucus
1630
What are the dosing regimens for COCP and what does it contain?
3w on, 1w off Most contain synthetic oestrogens: ethinyldoestradiol Bleeding occurs at the end of the pill packet due to withdrawal of hormonal inhibition. Pill packets can be taken back to back to reduce the frequency of the withdrawal bleed
1631
What is oestradiol valarate
Natural oestrogen found in some new types of COC
1632
Feautres of ethinyloestradiol containing COC
Monophasic containing same dose of both hormones every day. Standard dose pill: 30-40 Low dose: 20 Usual choice is 30-35 ug Bleeding determined by type of progestogen rather than oestrogen dose or the phasic regmin
1633
Features of COCP containing oestradiol valerate
Natural oestrogen combined with a synthetic progestogen: dienogest Four phases of oestrogen and progestogen dose over 26 days followed by 2 fill days.
1634
What are the common progestogenic side effects?
Depression PMS-tension like symptoms Bleeding, amenorrhoea Acne Breast discomfort Weight gain Reduced libido
1635
What are the common oestrogenic side effects
Nausea Headaches Increased mucus Fluid retention and weight gain HTN Breast tenderness and fullness Bleeding
1636
What are the other noncontraceptive uses of the COCP
Menstrual cycle control Menorrhagia PMS symptoms Dysmenorrhoea Acne/hirsutism Prevention of recurrent simple ovarian cysts
1637
COC in reduced absorption
If woman suffering from D+V or taking some oral antibiotics. Should follow missed pill instructions for day of the illness If she vomits within 2h of taking the pill she should take another one or follow the rules for missed pill If she is taking broad spectrum antibiotics she should use condoms for the course and for 7d post course If she takes liver inducing drugs, increased dose may be required
1638
What are the instructions for missed standard strength preparations Low strength?
One or two missed pills nayhere in the pack not a problem Only one pill can be missed Forgotten pill should be taken ASAP and pack cntinued as normal but should use condoms for 7d. If there are less than seven pills remaining in the packet, avoid a pill-free break by running straight into the next packet.
1639
Pill and surgery
Normally stopped 4 weeks before. Not discontinued before minor surgery
1640
Counselling women starting pill
Advise of major cxs and benefits Stop smoking Advise to seek medical attention if symptoms suggestive of major cxs Advise re absorption issue Stress the importance of F/U and BP monitoring
1641
What are the major risks of the COCP?
VTE and MI (multiplied by smoking, obestity), more common with 3rd generation pills. Cerebrovascular accident Focal migraine HTN Jaundice Liver, cervical and breast carcinoma
1642
What are the absolute contraindications to COCP?
Hx of VTE Hx of cerebrovascular accidant, IHD, HTN Migraine with aura Active breast/endometrial cancer Inherited thrombopilia Pregnancy Smokers \>35, smoking \>15/d BMI \>40 DM with vascular Cxs Acute/chronic liver disease
1643
What are the relative contraindications to the COCP?
Smokers Chronic inflammatory disease Renal impairment, DM Age \>40 BMI 35-40 Breastfeeding up to 6m postpartum
1644
What should be done if breakthrough bleeding doesn't stop after 3m
Consider changing the pill to one containing a more potent progestogen or using an increased strength for ethinyloestradiol.
1645
What are the advantages of the COCP
Contraceptive Non-contraceptive benefits: Regular, less painful and lighter mesntruation Protection against simple ovarian cysts, benign breast cysts, fibroids and endometriosis. May improve features of PCOS. Reduced risk of PID Reduction in incidence of ovarian, endometrial and bowel carcinoma
1646
What are the features of the combined transdermal patch
Adhesive patch that releases ethinyloestradiol and the progestogen norelgestromin. A new patch is applied weekly for 3 consecutive weeks then replaced. This is followed by a patch free week
1647
What is Evra
Combined transdermal patch
1648
What is Nuvargin
Combined vaginal ring
1649
Features of Nuvaring
Latex free, releases a daily dose of ethinyloestradiol and progestogen. Inserted and worn for 3w Removed to allow for a 7d ringe free break and a withdrawal bleed. New ring is then inserted. Reduced synthetic oestrogen side effects. Shouldn't be remved during intercourse
1650
What are the features of the mini-pill
Contains a low dose (350mg norethisterone) and must be taken every day without a break and at the same time +/-3h MOA: makes cervical mucus hostile to sperm and inhibits ovulation in 50% Progestogenic side effects: vaginal spotting, PMS-like symptoms Functional ovarian cysts can occur. Can be used in those in whom COCP is contraindicated.
1651
Missed POP
Not taken within 3h Another should be taken ASAP and condoms used for 2d
1652
What is Cerazette
A different POP, contains a higher dose and inhibits ovulation in 90% of cycles. More effective and can be taken within a 12h window
1653
What is the benefit of depot progesteogen administration
Bypass portal circulation Similar MOA to minipill Ovulation normally also prevented. Also protect against functional ovarian cysts and ectopic pregnancy.
1654
What are the features of Depo-Provera
Contains medroxyprogesterone acetate Administered by IM very 3m. Often causes irregular bleeding in the first weeks but this is usually followed by amenorrhoea. Bone density decreases over first 2-3y then stabilises and is regiained after stopping. Other methods are preferred in teenagers to allow them to reach peak bone mass. Useful during lactation
1655
What is Noristerat
Alternative depot injection with similar efficacy to Depo-Provera. Lasts 8w Recommended as a ST interim contraceptive.
1656
What are the features of Nexplanon
Single 40mm rod containing progestogen inserted into the upper arm using LA. Lasts 3y Side effects include progestogenic symptoms, irregular bleeding especially in the first year.
1657
What is Levonelle What are its features
Contains a single 1.5mg dose of levonorgestrel Morning after pill. Taken within 24h and no later than 72 Affects sperm function and endometrial reciptivity. 95% success if used within 24h 58% if delayed until 72h Vomiting may occur plus menstrual distrubances
1658
What is ellaOne What are its features
Selective progesterone receptor modulator (like mifepristone) Prevents or delays ovulation Can be used up to 120h after unprotected intervourse. It will reduce the effectiveness of progesterone containing contraceptives and so women should use condoms or avoid unprotected intercourse until the next period.
1659
IUD as an emergency contraceptive
Usually prevents implantation and is the most efficacious method Can be inserted up to 5d after either the episode of intercourse or the expected day of ovulation. Antibiotic prophylaxis usually given at the time of insertion
1660
What is the failure rate of the male condom?
2-15 per 100 woman years
1661
Features of copper containing IUDs
Operate primarily by preventing fertilisaiton with the Cu ions being toxic to sperm Also block implantation Copper either wound around an inert frame which sits within the uterine cavity or threads which are attached to the fundus
1662
What is the Mirena coil and its features
IUD that contain the progestogen levonorgestrel Released locally over 5y Known as the IUS. Contraceptive effects are local through changes to the cervical mucus and uterotubal fluid which impair sperm migration coupled with endometrial changes, impeding implantation. Also reduces menstrual loss and pain. Systemic side effects are low. Irregular ligt bleeding is the main problem
1663
What are the Cx of IUS?
Pain or cervical shock: due to inreased vaginal tone can complicate insertion, devices can be expelled within first month. Perforation of the uterie wall can occur at insertion or afterwards. Expulsion or preforation will cause the threads to disappear but they may also have been cut too short. If the threads are not visible- USS, if it is not present then an XR will reveal whether it is in the abdomen. Heavier or more painful menstruation can occur (with non-progestogen devices) Increased risk of PID if women have symptomatic STIs when the coil is inserted. Increased risk of infection Increased risk of ectopic pregnancy if pregnancy does occur, although the risk of ectopic pregnancy is lower than in a woman using no contraception. If not ectopic, IUD should be removed to reduce the risk of miscarraige
1664
What are the absolute contraindications to the IUD
Endometrial or cervical cancer Undiagnosed vaginal bleeding Active/recent pelvic infection Current breast cancer (for progesteogen IUS) Pregnancy
1665
What are the relative contraindications to the IUD?
Previous ectopic Exessive menstrual loss (unless IUS0 Multiple sexual partners Young/nullip Immunocompromised
1666
What is the counselling that should be given before inserting IUD
Advise of major risks Seek medical help if: IMB Experiences pelvic pain or a vaginal discharge If she feels she might be pregnant Advise to check for strings after each period
1667
What is the most common technique for female sterilisation?
Filshie clips that are applied to the fallopian tubes laparoscopically, occluding the lumen.
1668
What is an alternative to tube clipping for female sterilisation
Transcervical sterilisation: Hysteroscopic placement of microinserts into the proximal part of each tubal lumen Inserts expand, causing fibrosis and occlusion of the lumen, which is confirmed 3m later with a hysterosalpingogram
1669
Reversal of female sterilisation
Not possible with hysteroscopic Not guaranteed with Filshie clips Not available on the NHS
1670
Difference beween endometriosis and adenoymosis?
Endometriosis: presence and grwoth of tissue similar to endometrium outside of the uterus. Adenoymosis: growth of endometrial tissue in myomterium
1671
A 47-year-old woman,comes to the clinic to discuss contraception. She stopped having her periods 12 months ago. She is normotensive with a blood pressure recording of 122/78 mmHg in clinic. She smokes 10 cigarettes per day. She has a past history of breast cancer, successfully treated 4 years ago. You advise: Cerazette (Progesterone-only-pill) No longer requires contraception Copper Intrauterine Device (Cu-IUD) Rigevidon (Combined oral contraceptive pill) Depot injection
This woman has entered the postmenopausal period as she has not had a period for 12 months. Even though she is postmenopausal she still requires contraception because she is under the age of 50. Guidelines advise: 'Women using non-hormonal methods of contraception can be advised to stop contraception after 1 year of amenorrhoea if aged over 50 years, 2 years if the woman is aged under 50 years.' (FSRH) A copper coil is the best option for this woman because of her past history of breast cancer. All other methods, as they are hormonal, are a UKMEC Category 3, and this may be considered an unacceptable risk.
1672
COCP in women \>40
COCP use in the perimenopausal period may help to maintain bone mineral density COCP use may help reduce menopausal symptoms a pill containing 40 years
1673
1675
What are the 3 categories to describe a CTG
Normal Non-reassuring Abnormal
1676
A 30-year-old female presents to her GP seeking contraception. She has three children and states she has completed her family. She is open to long-acting reversible contraception. After receiving advice about all options available, she opts for the copper IUD. Besides pregnancy, which of the following is it important to exclude? Migraines with aura Pelvic inflammatory disease History of ectopic pregnancy History of venous thromboembolism Smoking history
Pelvic inflammatory disease is an absolute contraindication to the insertion of a copper IUD. Women at risk, such as those with multiple sexual partners or symptoms suggestive of pelvic inflammatory disease, should be tested and, if necessary, treated for any infections which could cause pelvic inflammatory disease such as Chlamydia trachomatis and Neisseria gonorrhoeae . Testing for these infections is done using endocervical swabs. Insertion of a copper IUD is in itself a risk for developing pelvic inflammatory disease, however this risk is low in women who are at low risk of sexually transmitted infections.
1677
Potential issues with IUDs
Make periods heavier, longer and more painful IUS associated with inital frequent uterine bleeding and spotting Uterine perforation Increased risk of ectopic pregnancies (in women using contraception, NB lower than in woman not using contraception) Increased risk of PID for 20d after insertion Risk of insertion in 1/20
1678
A 21-year-old female presents to her GP asking for medication to prevent menstruation when she goes away on holiday in 2 weeks' time. She is a non-smoker and has no significant past medical history. What would be the drug of choice for short-term cessation of menstruation in this case? Depot medroxyprogesterone acetate Combined oral contraceptive Cerazette Oral norethisterone GnRH analogue
This patient does not have any menstrual problems and wants short-term cessation of her menses. Norethisterone 5 mg three times a day is licensed for the postponement of periods, and is often prescribed to women who wish not to have a period when going on holiday. It must be started three days prior to the expected onset on menstruation. Menstruation resumes as normal two to three days after stopping the tablets. Note that this is a high dose and should not be used for longer than it is needed i.e. in the short-term. You may wish to read the following article regarding the risk of venous thromboembolism with norethisterone Norethisterone 5 mg TDS can also be used to rapidly stop heavy menstrual bleeding.
1679
A 32-year-old gravid 2, para 2 at 24 weeks gestation attends an antenatal clinic and wishes to discuss delivery options for her pregnancy. On history, you find that her previous pregnancies were delivered by vaginal and elective caesarean section respectively. Which of the following is an absolute contraindication for vaginal delivery following previous cesarean section? Chorioamnionitis Classical caesarean scar Post-term dates Pre-eclampsia Two previous caesarean sections
Planned vaginal birth after caesarean (VBAC) is contraindicated in patients with previous classical caesarean scars, previous episodes of uterine rupture and patients with other contraindications to vaginal birth (e.g. placenta praevia). Women with two or more previous caesarean sections may be offered VBAC. The other options in this question are not absolute contraindications.
1680
Indications for C section
absolute CPD placenta praevia grades 3/4 pre-eclampsia post-maturity IUGR fetal distress in labour/prolapsed cord failure of labour to progress malpresentations: brow placental abruption: only if fetal distress; if dead deliver vaginally vaginal infection e.g. active herpes cervical cancer (disseminates cancer cells)
1681
Cxs of C section
DVT/PE PPH Infeciton: wound, endometritis, UTI Retained placental tissue, ileus, ureteric trauma, transient abdominal distension
1682
Diagnosis of Sheehan's
by inadequate prolactin and gonadotropin stimulation tests in patients with a history of severe PPH.
1683
A 36-year-old nulliparous presents at 37 weeks gestation with the report of a reduction in foetal movements for the past 3 hours associated with abdominal cramping and a small amount of peri vaginal bleeding. Her pregnancy has been otherwise uneventful. It is decided that a cardiotocography (CTG) is needed to further investigate her presentation. Which of the following features of a CTG is a worrying sign and would prompt further investigation? Stable baseline heart rate of 91 bpm with normal variability Single early deceleration Baseline variability of 6 beats / min Multiple early decelerations Single prolonged deceleration for 3 minutes duration
According to NICE guidelines, bradycardia or a single prolonged deceleration that persists for \>3 minutes or more is an abnormal CTG results and indicates the need for urgent investigation.
1684
A 34-year-old gravid 3, para 2 presents in spontaneous labour and has an uncomplicated vaginal delivery. 30 minutes after delivery, the patient reports heavy vaginal bleeding which you estimate to be around 700mL. Which of the following is true regarding postpartum haemorrhage (PPH)? Active management of third stage of labour increases risk of PPH Prophylactic oxytocics in the third stage of labour do not reduce risk of PPH Most cases of PPH have no identifiable risk factors Oxytocin is not as effective as misoprostol in the management of PPH Age is the strongest risk factor for PPH
The correct answer is 3.) most cases of PPH have no identifiable risk factors. In terms of the other options, active management of the third stage of labour has been shown to lower maternal bleeding and reduce the risk of PPH. Similarly, prophylactic oxytocics are routinely used in third stage management as they have been shown to effectively reduce risk of PPH. Oxytocin is 1st line in the management of PPH and has been shown to be more effective than misoprostol. While age is a risk factor for PPH, it is not the strongest risk factor.
1685
A 30-year-old female presents to her GP for advice about contraception. She is provided with information and advice regarding all methods of contraception available and decides to opt for a copper IUD. A pregnancy test done at the surgery is negative. She has a regular 28-day cycle. At what point in her menstrual cycle can the IUD be inserted? Days 1-7 Days 8-14 Days 15-21 Days 22-28 Anytime during cycle
The copper IUD can be fitted at any point during the menstrual cycle. It can also be fitted immediately after first or second-trimester abortion, and from 4 weeks postpartum. Note the importance of advising the patient to refrain from intercourse or use adequate contraception to prevent pregnancy until the IUD is fitted.
1686
A 32-year-old female with long standing hypothyroidism is confirmed as pregnant at 8 weeks gestation. She is taking 75 micrograms of levothyroxine and this dose has remain unchanged over the past 18 months. Blood tests show the following: fT411.7 pmol/L TSH2.77 mU/L What is the most appropriate action in relation to this woman's levothyroxine dose? Increase to 100 micrograms daily Maintain at 75 micrograms per day Reduce to 50 micrograms per day Change to liothyronine Reduce to 25 micrograms per day
Although the thyroid function tests are normal, thyroxine demands increase during pregnancy, and most woman require their dose increased by at least 25-50 micrograms levothyroxine. Therefore, it would be sensible to increase the dose to 100 micrograms in this case.
1687
women with established hypothyroidism who become pregnant should have their dose increased 'by
at least 25-50 micrograms levothyroxine'\* due to the increased demands of pregnancy. The TSH should be monitored carefully, aiming for a low-normal value
1688
Interactions of levothyroxine
iron: absorption of levothyroxine reduced, give at least 2 hours apart
1689
How long does the combined contraceptive patch last?
4w For the first 3w the patch is worn every day and needs to be changed each week During the 4th week if the patch is not worn there will be a withdrawal bleed
1690
For delays in changing the patch, different rules apply depending what week of the patch cycle the woman is in. If the patch change is delayed at the end of week 1 or week 2:
If the delay in changing the patch is less than 48 hours, it should be changed immediately and no further precautions are needed. If the delay is greater than 48 hours, the patch should be changed immediately and a barrier method of contraception used for the next 7 days. If the woman has had sexual intercourse during this extended patch-free interval or if unprotected sexual intercourse has occurred in the last 5 days, then emergency contraception needs to be considered.
1691
For delays in changing the patch, different rules apply depending what week of the patch cycle the woman is in. If the patch removal is delayed at the end of week 3:
The patch should be removed as soon as possible and the new patch applied on the usual cycle start day for the next cycle, even if withdrawal bleeding is occurring. No additional contraception is needed. If patch application is delayed at the end of a patch-free week, additional barrier contraception should be used for 7 days following any delay at the start of a new patch cycle.
1692
A 20-year-old pregnant lady is found to be anaemic 10 weeks gestation. A full blood count is ordered: Hb85 g/L MCV95 fL The lab also reports a high reticulocyte count. A blood film shows target cells and Howell-Jolly bodies. What is the most likely cause of the anaemia? Folate defficiency Anaemia of chronic disease Iron defficiency Thalassaemia Sickle cell disease
The full blood count confirms a normocytic anaemia. Folate and B12 deficiency cause megaloblastic anaemia which is characterised by macrocytosis. Iron deficiency and thalassaemia typically cause microcytosis. Therefore, based on the MCV it can be inferred that sickle cell disease is the most likely answer. In addition, the Howell-Jolly bodies suggest hyposplenism which can occur in Sickle cell disease due to splenic infarctions. The high reticulocyte count suggests increased destruction (e.g. haemolysis) or increased loss (e.g. bleeding) of red cells. Sickle cell disease results in a chronic haemolytic anaemia due to premature destruction of abnormally shaped red cells. This would result in a high reticulocyte count.
1693
Abnormal category for CTG
Within the abnormal category lie the following: Heart rate - \>180 BPM or \<100 BPM Variability - Less than 5 for over 90 minutes Decelerations - Non-reassuring variable decelerations for over 30 minutes since starting conservative measures to improve occuring with over 50% of contractions OR late decelerations present for over 30 minutes not improving with conservative measures occurring with over 50% of contractions OR bradycardia or a single prolonged deceleration lasting 3 minutes or more.
1694
A 15 year old girl presents with amenorrhoea, having never started her periods. Which element of her history would lead you to reassure her that there is no need to investigate yet? She has not developed breasts or axillary/pubic hair Family history of late menarche History of acne and scanty, dark facial hair She is sexually active Cyclical abdominal pain
Primary amenorrhoea can be diagnosed in women above the age of 14 with no secondary sexual characteristics, or above the age of 16 with secondary sexual characteristics. Primary amenorrhoea is commonly constitutional and has a familial distribution; in these cases there is no anatomical or physiological abnormality and patients will generally start menstruating by the age of 18. Lack of breast or body hair development suggests this is true primary amenorrhoea and so warrants investigation. Acne and facial hair may suggest virilisation, e.g. in polycystic ovarian syndrome. In a woman who is sexually active, pregnancy may be a cause of amenorrhoea and should always be excluded. Cyclical abdominal pain associated with amenorrhoea may suggest an anatomical abnormality such as an imperforate hymen.
1695
Requirements for instrumental delivery FORCEPS
Fully dilated cervix generally the second stage of labour must have been reached OA position preferably OP delivery is possible with Keillands forceps and ventouse. The position of the head must be known as incorrect placement of forceps or ventouse could lead to maternal or fetal trauma and failure Ruptured Membranes Cephalic presentation Engaged presenting part i.e. head at or below ischial spines the head must not be palpable abdominally Pain relief Sphincter (bladder) empty this will usually require catheterization
1696
A women of child bearing age comes into your GP surgery. She wishes to try to conceive for a baby in one years time and does not wish to conceive sooner due to barrister exams she has this year. She ideally wants to fall pregnant soon after her exams. Which of the follow methods of contraception is most associated with delayed return to fertility? Intrauterine system Condoms Combined oral contraceptive pill Depo-Provera Progesterone only pill
Condoms work as a barrier contraceptive and do not affect ovulation and hence do not delay fertility. The intrauterine system (IUS) works by thickening cervical mucous and in some women may prevent ovulation, however the majority of women still ovulate. After removal of the IUS the majority of women regain fertility immediately. The combined oral contraceptive pill can delay return to normal menstrual cycle in some women but the majority will be able to conceive within a month of stopping. The progesterone only pill is less likely to delay return to normal cycle as it does not contain oestrogen. Because Depo-Provera lasts up to 12 weeks, it can take several months for the body to return to the normal menstrual cycle and hence delay fertility. For this reason, it is the least appropriate method for this woman who wants to return to ovulatory cycles immediately.
1697
Adverse effects of injectables contraceptives
Irregular bleeding Weight gain May potentially increase risk of osteoporosis: only used in adolescents if no alternative Not quickly reversible and there is a variable return to fertility
1698
A pregnant woman asks for advice about alcohol consumption during pregnancy. Which one of the following is in line with current NICE guidelines? 1 to 2 units once or twice per week throughout pregnancy Avoid first and second trimester. If then chooses to drink 1 to 4 units no more than twice per week 1 to 2 units once per week throughout pregnancy Avoid first trimester. If then chooses to drink 1 to 2 units once or twice per week Avoid alcohol throughout pregnancy
the government now recommend pregnant women should not drink. The wording of the official advice is 'If you are pregnant or planning a pregnancy, the safest approach is not to drink alcohol at all, to keep risks to your baby to a minimum. Drinking in pregnancy can lead to long-term harm to the baby, with the more you drink the greater the risk.'
1699
A hepatitis B serology positive woman gives birth to a healthy baby girl. She is surface antigen positive. What treatment should be given to the baby? Hep B vaccine Hep B vaccine and 0.5 millilitres of HBIG within 12 hours of birth 0.5 millilitres of HBIG within 12 hours of birth only Hep B vaccine and 0.5 millilitres of HBIG within 12 hours of birth with a further hepatitis vaccine at 1-2 months and a further vaccine at 6 months No treatment required
This question tests your knowledge of the Hepatitis B vaccine schedule in baby's born at risk of developing hepatitis B. For babies who are born to mothers who are hepatitis B surface antigen positive, or are known to be high risk of hepatitis B, should receive the first dose of hepatitis B vaccine soon after birth and those born to mother's who are surface antigen positive should also receive 0.5 millilitres of hepatitis B immunoglobulin within 12 hours of birth. The baby should then further receive a second dose of hepatitis B vaccine at 1-2 months and at 6 months.
1700
A 28-year-old woman who is 32 weeks pregnant presents with itch. On examination her abdomen is non tender with the uterus an appropriate size for her gestation. There is no visible rash, although she is mildly jaundiced. Her heart rate is 74/min, blood pressure 129/62mmHg, respiratory rate 20/min, oxygen saturations are 98% in air, temperature 36.8°C. A set of blood results reveal: Hb110 g/lNa+139 mmol/lBilirubin54 µmol/l Platelets243 109/lK+4.1 mmol/lALP353 u/l WBC8.2 109/lUrea4.6 mmol/lALT84 u/l Neuts5.7 109/lCreatinine74 µmol/lγGT207 u/l Lymphs1.8 \* 109/lAlbumin34 g/l What is the most likely cause of her symptoms? Intrahepatic cholestasis of pregnancy HELLP syndrome Pre-eclampsia Acute fatty liver of pregnancy Biliary colic
The answer here is intrahepatic cholestasis of pregnancy. This is a common cause of itch in the third trimester of pregnancy. It will give a cholestatic picture of liver function tests (LFTs) with a high ALP and GGT, with a lesser rise in ALT. Patients may also be jaundiced with right upper quadrant pain and steatorrhoea. Ursodeoxycholic acid is a common treatment. The cholestatic LFTs could indicate biliary colic, however the absence of abdominal pain here makes it very unlikely. Acute fatty liver of pregnancy also occurs in the third term of pregnancy but a hepatic picture would be expected on LFTs, with a rise in ALT/AST greater than that of ALP, a raised white cell count and potential clotting abnormalities. This condition is rare and patients are likely to be unwell with nausea, vomiting, jaundice and possible encephalopathy. In HELLP syndrome you would see a haemolytic anaemia, the mild anaemia seen here does not correlate with this and also low platelets not seen here. This lady is not hypertensive and does not have any other features of pre-eclampsia so this is unlikely. In late pre-eclampsia a hepatic derangement of LFTs might be seen.
1701
28-year-old woman presents the Emergency Department at 35-weeks gestation with lower abdominal pain and vaginal bleeding. She is alert and responsive. Physical examination revealed a heart rate of 115 bpm, blood pressure of 90/60 mmHg and O2 saturation of 99%. On neurological exam, her pupils were dilated and her reflexes were brisk. Hb115 g/l Platelets250 \* 109/l WBC5 \* 109/l PT12 seconds APTT30 seconds Which of the following underlying conditions would most likely explain the findings on physical exam? HELLP syndrome Heroin abuse Cocaine abuse Disseminated intravascular coagulopathy Pre-eclampsia
pre-eclampsia and HELLP syndrome are known causes of placental abruption, which typically presents with hyperreflexia. HELLP syndrome can be ruled out since the full blood count shows no indication of anaemia or low platelets as would be expected in this condition. Dilated pupils + hyperreflexia seen on physical examination point towards cocaine abuse. Heroin abuse would often present with pinpointed pupils and has not been associated with an increased risk of placental abruption. Although pre-eclampsia in pregnancy is associated with an increased risk of placental abruption, the findings on physical exam are more consistent with that of cocaine abuse. Disseminated intravascular coagulopathy is a complication placental abruption, not an underlying cause. Additionally, the normal partial thromboplastin time (PTT) and activated partial thromboplastintime (APTT) decrease the likelihood of underlying DIC.
1702
Risks of smoking in pregnancy
Increased risk of miscarriage Increased risk of pre-term labour Increased risk of stillbirth IUGR Increased risk of sudden unexpected death in infancy
1703
Risks of ETOH in pregnancy
Fetal alcohol syndrome (FAS) learning difficulties characteristic facies: smooth philtrum, thin vermilion, small palpebral fissures IUGR & postnatal restricted growth microcephaly Binge drinking is a major risk factor for FAS
1704
Risks of cocaine in pregnancy?
Maternal risks hypertension in pregnancy including pre-eclampsia placental abruption Fetal risk prematurity neonatal abstinence syndrome
1705
Risks of heroin in pregnancy
Risk of neonatal abstinence syndrome
1706
You are reviewing your patients on the post-natal ward and are discussing a patient who suffered from gestational diabetes during her pregnancy. Post-delivery her blood glucose levels have now returned to normal. The consultant asks you what sort of follow up patients like this have with regards to the gestational diabetes? Fasting BGL before being discharged No follow up Fasting blood glucose level (BGL) 6-13 weeks post-partum 6 monthly Hb1Ac levels 75g 2 hour Oral Glucose Tolerance Test (OGTT)
One of the first things that needs to be insured is that women who have been diagnosed with gestational diabetes should discontinue the blood-glucose lowering therapy immediately after the birth. Before discharge the BGL must be tested to ensure there is no persisting hyperglycaemia Remind women who suffered gestational diabetes during pregnancy of the symptoms of hyperglycaemia Explain the risk of gestational diabetes in future pregnancies Offer lifestyle advice to those whose BGL have returned to normal after delivery Offer a fasting plasma glucose test 6-13 weeks after the birth - this usually takes place at the 6 week post-natal check at the GP
1707
A 24-year-old woman comes to the sexual health clinic. She states she has had 3 episodes of unprotected sex within the last 4 days. She states she uses the combined oral contraceptive pill (COCP) but does not take this regularly and has missed several pills in her current packet. She states that she last had a period 10 days ago. What should she be offered for emergency contraception? Levonorgestrel Cu-IUD Nothing as she is covered by her COCP Mirena coil Ulipristal acetate
This woman requires emergency contraception because she had several episodes of unprotected sexual intercourse (UPSI) and has missed pills in her current packet of COCP. It is not clear if she has real contraceptive cover due to her poor compliance with taking the COCP. The copper-bearing intrauterine device (Cu-IUD) is the best method for this woman as she has presented 4 days after UPSI. It is difficult to assess her expected ovulation date as her periods could be withdrawal bleeds from her intermittent COCP use. The Cu-IUD has a low documented failure rate so women should initially be offered this as a means of emergency contraception. It also serves the dual purpose of long-term reversible contraception which may benefit this woman as she has difficulty taking the COCP. As this woman has poor compliance she should first be offered a pregnancy test before insertion of Cu-IUD. As this woman has presented within 120 hours of UPSI she can be offered ulipristal acetate (ellaOne) but this would be a second choice to a Cu-IUD. Levonorgestrel (Levonelle One) is not indicated for use after 72 hours of UPSI. Mirena coil is not used for emergency contraception.
1708
A woman comes to the GP surgery as she has a long term medical condition but wishes to try to conceive. Which of the following conditions is NOT an indication for high dose folic acid? Obesity Coeliac disease Epilepsy treated with sodium valproate Depression treated with an SSRI Type 1 diabetes
SSRIs are taken safely by many women during pregnancy. The associated effect on the foetus is centred around the instant withdrawal that occurs at birth, and the baby may be initially jittery and hypotonic, rather than with any neural tube malformations.
1709
Prevention of neural tube defects (NTD) during pregnancy:
all women should take 400mcg of folic acid until the 12th week of pregnancy women at higher risk of conceiving a child with a NTD should take 5mg of folic acid until the 12th week of pregnancy women are considered higher risk if any of the following apply: → either partner has a NTD, they have had a previous pregnancy affected by a NTD, or they have a family history of a NTD → the woman is taking antiepileptic drugs or has coeliac disease, diabetes, or thalassaemia trait. → the woman is obese (defined as a body mass index [BMI] of 30 kg/m2 or more).
1710
A 22 year old woman who is 7 weeks pregnant attended the early pregnancy assessment unit with vaginal bleeding. The ultrasound scan confirmed a viable intrauterine pregnancy and she was discharged. A few days later, her endocervical swab results are noted to have isolated Chlamydia trachomatis. She is allergic to azithromycin. What is the most suitable management? Topical clindamycin Oral flucloxacillin Oral doxycycline Oral levofloxacin Oral erythromycin
Chlamydia infection in pregnancy is associated with premature delivery, amnionitis and puerperal infection. If cervical chlamydia infection is present at delivery, there is a high likelihood of neonatal chlamydia. Neonatal chlamydia can include complications such as conjunctivitis and pneumonia. Patients should be referred to a sexual health clinic for a full sexual health screen and for contact tracing. Suitable treatments in pregnancy include erythromycin, amoxicillin or azithromycin. Doxycycline is contraindicated in pregnancy due to the risk of teeth and bone abnormalities in the fetus. Repeat testing sometime after completion of treatment is recommended in pregnancy to ensure therapeutic cure.
1711
A 27 year-old lady is day 1 post emergency caesarean section for failure to progress in the first stage. She has been complaining of pain and heavy vaginal bleeding since delivery and in the morning was noted to have heavy, offensive lochia and a boggy poorly contracted uterus above the umbilicus. What is the most appropriate treatment? Urgent ultrasound scan Speculum examination Examination under anaesthesia IV antibiotics and review after first dose Urgent MRI scan
This is a typical history of retained products, which can happen after caesarean section if care is not taken to make sure that all the placental membranes are removed. The uterus does not contract down well as the products are still in the cavity, and the discharge is offensive suggesting that the products have become infected. This lady needs and urgent examination under anaesthesia to remove the products. The products often pass by themselves without the need for anaesthesia, however after day 1 this is unlikely so intervention is needed. Sometimes a scan would be done before but with a history this clear, it is not necessary. It is also hard to pick up products on scan sometimes as they can be very small. A speculum examination would be helpful to show is the os was still open, however the os remains open in heavy bleeding so this information would not give us a diagnosis. IV antibiotics are probably needed in this case, however the infection will not resolve until the products are removed and therefore surgery is also needed. An MRI is not helpful in this situation as it is not useful for detecting intrauterine pathology, and would probably take a long time to organise which is unhelpful in this acute situation.
1712
A 22-year-old female, gravidity 1 and parity 0 at 10 weeks' gestation is involved in a high speed vehicle collision and her abdomen hits the steering wheel. Maternal vital signs are stable. No uterine contractions are present, and there is no vaginal bleeding. U/S shows an intact placenta. Which is the most appropriate next step? Caesarean delivery Betamethasone Blood type and Rhesus testing Induce labour Discharge home on bed rest
Important points: A pregnant woman with abdominal trauma should have Rhesus testing asap because women who are Rhesus-negative should be given anti-D to prevent Rhesus isoimmunization.
1713
A 17-year-old girl who is nine weeks pregnant has a surgical termination of pregnancy. She feels well a few hours after the procedure. Which of the following risks is most common following a TOP? Infection Haemorrhage Uterine perforation Cervical trauma Failure
Infection can happen in up to 10% of TOP cases. Antibiotics are given to reduce the risk of infection. Signs and symptoms of an infection are unlikely to occur so soon after the procedure. Retained tissue pregnancy occurs in less than 1% of cases. Haemorrhage occurs in less than 1% of cases, but is more likely to occur in pregnancies greater than 20 weeks gestation. Failure occurs in less than 1% of cases. Injury to the cervix occurs in less than 1% of cases.
1714
A 16-year-old girl comes to your GP surgery worried that she has not yet started her periods. She is quite short, has a webbed neck, low set ears and widely space nipples. A heart murmur is heard on auscultation. What type of murmur are you most likely to hear? Systolic, loudest over the pulmonary valve Diastolic, loudest over the pulmonary valve Systolic, loudest over the aortic valve Systolic, loudest over mitral valve Diastolic, loudest over mitral valve
From the clinical picture, you should have a differential diagnosis of Turner's syndrome. Patients with Turner's syndrome are prone to have bicuspid aortic valve, aortic valve stenosis and/or aortic coarctation. For this reason, you would be expecting to hear a systolic murmur which is loudest over the aortic region.
1715
A 24 year old woman presents to your surgery with vaginal discharge. She says it smells quite strongly, but isn't itchy. She has no dysuria or dyspareunia. She has no post-coital bleeding. On examination, there is a watery discharge with an odour. There is no erythema to the labia. Her cervix looks healthy and there is no cervical excitation. What is the most likely diagnosis? ## Footnote Gonorrhoea Bacterial vaginosis Chlamydia Herpes simplex Candidiasis
Clearly you would want more information about sexual history for this lady, and in all likelihood would send triple swabs regardless. However, a diagnosis of Gonorrhoea is unlikely given the healthy looking cervix. You would also expect a more green and purulent discharge for Gonorrhoea rather than a watery discharge. Gonorrhoea is particularly problematic as it can present with a normal examination, however is not often associated with an odour. In a similar line, you would expect to see more problems with the cervix for a diagnosis of Chlamydia and a more mucopurulent discharge. Chlamydia can also cause cervical excitation which this lady does not have. Herpes simplex doesn't tend to cause vaginal discharge, and would instead present as a crop of ulcers or tingling type sensations around the vulva. Patients can have a flu like illness, and may have some lymphadenopathy. For candidiasis, or thrush, you would expect a lot more itching in the history. It would also be more likely to have a thick creamy consistency like cottage cheese. There is a higher probability with thrush that you would get vulval irritation. Bacterial vaginosis is the most likely diagnosis on balance. It gives a characteristic fishy odour, and is often a thin watery discharge that can have a green or white hue. It often doesn't cause irritation or soreness, and can be completely asymptomatic. Diagnosis would be confirmed with a vaginal pH \> 4.5 and clue cells on microscopy.
1716
A 34-year-old woman who is 35 weeks pregnant presents to her general practitioner with painful blisters affecting the vagina and cervix, along with inguinal lymphadenopathy. She has never had these symptoms before. The GP diagnoses primary genital herpes. Which of the following management strategies is most appropriate? Simple analgesia only Oral aciclovir for 5 days Oral aciclovir until delivery and delivery by caesarean section Caesarean section Oral aciclovir until delivery
Guidelines issued by the Royal College of Obstetricians and Gynaecologists state that women who present with first-episode genital herpes during their third trimester should be managed with daily suppressive oral aciclovir 400mg until delivery. Delivery should be by caesarean section due to a high risk of neonatal HSV (herpes simplex virus) transmission. It can be difficult to clinically distinguish between primary and recurrent episodes of genital herpes. If a patient has not noticed the symptoms in the past it is recommended that management is initiated on the assumption that it is the first episode. Type-specific HSV antibody testing can be performed in order to confirm or refute this, but this can take 2-3 weeks to yield results - hence the recommendation to initiate the above management plan which can later be modified if appropriate.
1717
A 29 year-old woman who is taking antidepressant therapy for moderate depression visits her general practitioner (GP) to talk about becoming pregnant. After discussion, the woman and her GP agree that she should continue antidepressant therapy if she falls pregnant in the near future. Which of the following drugs must be avoided in pregnancy due to risk both of fetal malformation and maternal hypertensive crisis? Phenelzine Imipramine Sertraline Fluoxetine Amitriptyline
There are no antidepressants licensed for use during pregnancy, however it is not uncommon for medication to be continued if a patient is already taking it and is likely to struggle without it. Phenelzine is a monoamine-oxidase inhibitor (MAOI). The BNF strongly advises that MAOIs be avoided in pregnancy due to an increased risk of neonatal malformations. Maternal hypertensive crisis has also been reported in association with this class of antidepressant. Fluoxetine and sertraline are selective serotonin reuptake inhibitors. They are associated with a small increased risk of congenital heart disease and can cause neonatal withdrawal symptoms. Imipramine and amitriptyline are tricyclic antidepressants. Imipramine use during pregnancy is associated with a wide range of neonatal symptoms including tachycardia and respiratory depression.
1718
A 25-year-old present 8 weeks after her last menstrual period. She complains of severe nausea, vomiting and vaginal spotting. Pregnancy test was positive and transvaginal ultrasound showed an abnormally enlarged uterus. Which of the following test results would be expected in this patient? High beta hCG, high TSH, high thyroxine High beta hCG, low TSH, high thyroxine High beta hCG, high TSH, low thyroxine Low beta hCG, low TSH, high thyroxine Low beta hCG, high TSH, low thyroxine
The clinical presentation in this question is consistent with that of a molar pregnancy. A basic understanding of physiology is needed to answer this question correctly. Molar pregnancies are characterised by significantly high levels of beta hCG for gestational age, and are therefore used as a tumour marker of gestational trophoblastic disease. The biochemical structure of beta hCG is very similar to that of luteinizing hormone (LH), follicle-stimulating hormone (FSH), and thyroid-stimulating hormone (TSH). That being said, high levels of beta hCG can stimulate the thyroid gland to produce thyroxine (T4), and then triiodothyronine (T3). This can result in signs and symptoms of thyrotoxicosis. High levels of T4 and T3 have a negative feedback effect on the pituitary gland to stop secretion of TSH, causing and overall reduction in TSH levels.
1719
A 19-year-old woman has a positive pregnancy test and is found to have an ectopic pregnancy after an intrauterine pregnancy is excluded. She has no pain or other symptoms at this time. Her serum beta-human chorionic gonadotropin (B-hCG) level is 1397 IU/L. A transvaginal ultrasound reveals a 29mm adnexal mass but no heartbeat. There is no free fluid in the abdomen. She says she would like a follow-up appointment following her treatment. What is the first line treatment? Methotrexate Urgent laparoscopic salpingectomy Monitor B-hCG Misoprostol Mifepristone
The National Institute for Health and Care Excellence (NICE) states that if a woman has a small (\<35mm) unruptured ectopic pregnancy with no visible heartbeat, a serum B-hCG level of \<1500 IU/L, no intrauterine pregnancy and no pain, then first line treatment should be with methotrexate as long as the patient is willing to attend for follow-up. Methotrexate is an antimetabolite chemotherapeutic drug. It interferes with DNA synthesis and disrupts cell multiplication^1 thus preventing the pregnancy from developing. The other treatment option is laparoscopic salpingectomy (or salpingotomy where there is risk of infertility). This should be offered where the ectopic is larger than 35mm, is causing severe pain or if the B-hCG level is \>1500. There is a risk of infertility if a problem arises with the remaining Fallopian tube in the future.
1720
USS of hydatidform mole
On ultrasound, the mole appears as a solid collection of echoes with numerous small anechoic spaces which resembles a bunch of grapes (also known as 'snow-storm' appearance).
1721
A 25-year-old receives a letter from her GP explaining that her first smear showed mild dyskaryosis, and she was Human Papilloma Virus (HPV) positive. She was subsequently referred to the colposcopy clinic where she underwent treatment for cervical intraepithelial neoplasia (CIN) stage 1. Which cell cycle protein does the HPV E6 protein inhibit in the process of cell transformation? ## Footnote pRB c-RAF p53 PTEN c-Ras
The E6 protein binds to p53, preventing it from halting cell division. The E7 protein binds to pRb. The Human Papilloma Virus (HPV) is the causative agent in almost all cervical carcinomas. It is spread easily via sexual transmission, and although most types do not cause cancer, persistence of high-risk oncogenic types, such as 16, 18, 33 and 45 cause cell transformation and neoplasia. The aim of the cervical screening programme is to prevent cervical intraepithelial neoplasia from progressing to cancer. HPV itself is a double-stranded DNA virus, consisting of an icosahedral capsid (encoded by L1 and L2) and proteins E1-E7 (involved in replication and cell transformation). HPV invades keratinocytes of the skin and mucous membranes and uses the host DNA replication machinery to replicate itself. HPV enters the basal compartment and as the surface cells naturally shed, the HPV infected cells migrate upwards and begin to replicate, resulting in a huge increase in viral copy number. Normally, the E2 protein blocks the E6 and E7 proteins, but when HPV DNA integrates into host cell DNA, E2 is inhibited. The E6 protein inhibits the tumour suppressor p53 and the E7 protein inhibits pRb, enabling uncontrolled cell division. HPV evades the immune response as there is no active cytolysis, it is not blood borne, it can disable antigen presenting cells and inhibit interferon synthesis. Most people do eventually mount an immune response to HPV. It is not known why some people are persistently infected with HPV, but it could be related to an inherent problem in immunity, as well as other co-factors, such as smoking and multiparity. The HPV vaccine consists of the L1 nucleocapsid protein (Gardasil uses L1 proteins from 6, 11, 16 and 18), which is non-oncogenic. Intramuscular injection of the vaccine means that stromal dendritic cells encounter the protein, producing a robust antibody response against L1, thus protecting against HPV infection.
1722
UKMEC 1-4
UKMEC1 - No restriction UKMEC2 - Advantages \> Disadvantages UKMEC3 - Disadvantages \> Advantages UKMEC4 - Unacceptable risk
1723
UKMEC 3
- \> 35 years old and smoker of \< 15 cigarettes per day - BMI \> 35 - Migraine with no aura - Family history of deep vein thrombosis or pulmonary embolism in first degree relative \< 45 years old - Controlled hypertension - Immobility e.g. Wheelchair use - Breast feeding and 6 weeks to 6 months postpartum
1724
UKMEC 4
- \>35 years old and smoker of \> 15 cigarettes per day - migraine with aura - Personal history of deep vein thrombosis or pulmonary embolism - Personal history of stroke or ischaemic heart disease - Uncontrolled hypertension - Breast cancer - Recent major surgery with prolonged immobilisation - Breast feeding and \< 6 weeks postpartum
1725
A woman who is 28 weeks pregnant presents with shortness of breath and unilateral leg oedema. You suspect a pulmonary embolism and consult your seniors as to the best test to confirm the diagnosis. Which of the following is the best reason to choose a ventilation/perfusion (V/Q) scan over CT pulmonary angiography (CTPA)? It requires less specialist training to perform It is cheaper There is less radiation to the breast tissue It is less harmful to the foetus It is easier to interpret
Breast tissue in premenopausal women is highly sensitive to radiation; in the long-term, CTPA confers a 14% increased risk against the background for breast cancer in pregnant women who are under 40 years old and should therefore be avoided. In 2012 NHS costing report documented the cost of a V/Q scan as £162 with CTPA as £100; both cost an additional £20 each for reporting. There is often more disagreement between radiologists as to the presence or absence of a PE on V/Q scan and so results are given as high or low probability in the context of a scoring system such as the Wells score. Radiation exposure to the fetus with V/Q scans and CTPA are equivocal
1726
A 20 year-old woman who is 30 weeks pregnant wishes to visit rural Burundi to attend a family funeral. Her general practitioner explains that this is a high risk area for malaria and advises her against visiting whilst pregnant, but the woman is adamant that she will go. Which of the following drugs should be offered as prophylaxis? ## Footnote Atovaquone Piperaquine Doxycycline No antimalarial prophylaxis can be prescribed in pregnancy Mefloquine
Travel to malarial areas should ideally be avoided during pregnancy. However, if travel is unavoidable then the benefits of taking prophylaxis are usually considered to outweigh the risks. Mefloquine is recommended by the Royal College of Obstetricians and Gynaecologists (RCOG) as the drug of choice for prophylaxis in the second and third trimesters. Although chloroquine is considered to be relatively safe, the RCOG states that with very few areas in the world free from chloroquine-resistance, mefloquine is essentially the only drug considered safe for prophylaxis in pregnant travellers. Doxycycline, like other tetracyclines, should be avoided in pregnancy due to effects on skeletal development and discoloration of teeth. Piperaquine has been found to be teratogenic in animal studies. There is insufficient information about the effect of atovaquone in pregnancy.
1727
1728
Which of the following presentations has the greatest mortality and morbidity? Occipitoposterior presentation at delivery Footling presentation at delivery Face presentation at delivery Transverse lie at 30 weeks Breech presentation at 20 weeks
Footling presentations are a rare but the most risky form of breech- there is a 5-20% risk of cord prolapse, which can obstruct foetal blood flow and is an obstetric emergency. 40% of babies are breech at 20 weeks but only 3% at term- there is still plenty of room for the foetus to turn around and resolve to head down. In occipitoposterior presentation the posterior fontanelle is found in the posterior quadrant of the pelvis; greater rotation is required so labour is usually longer. There is a greater rate of intervention- 22% require forceps and 5% require caesarean section. Face presentations normally occur by chance when the head extends rather than flexes as it engages. 99% rotate so the chin lies behind the symphysis and the head can be born by flexion; in 1%the chin rotations to the sacrum and caesarean section is indicated. Transverse lie is where the shoulder is presenting. It occurs in multiparous women due to their uterine muscles being less tight than a nulliparous woman. Extracephalic version may be attempted from 32 weeks and thus is manageable at 30 weeks.
1729
A 28-year-old patient presents with painless vaginal spotting. Her last menstrual period was 9 weeks ago. Transvaginal ultrasound showed an ectopic pregnancy of 3-cm in diameter and beta-hCG of 1000 lU/litre. She was given a single dose of methotrexate and reassessed at day 4. Her beta-hCG levels rose to 1,300 IU/litre. What would be the next best management step? Second dose of methotrexate Second measurement of beta-hCG levels Laparoscopic surgery with salpingectomy Laparoscopic surgery with salpingostomy Emergency laparotomy
This question tests the understanding of the management of ectopic pregnancy. According to the NICE guidelines, systemic methotrexate should be offered to women who have all of the following No significant pain An unruptured ectopic pregnancy with adnexal mass less than 35mm with no visible heart beat A serum hCG less than 1,500 IU/liter No intrauterine pregnancy ( as confirmed by ultrasound) In addition to the criterion mentioned above, it is important to be familiar with the contraindications of using methotrexate. Once given, the patient should have her beta-hCG levels measured twice (at day 4 and day 7). Normally, beta-hCG levels rise on day 4 compared to pre-treatment levels. This is due to the death of trophoblastic cells. A second beta-hCG level should therefore be taken at day 7 and ensure that levels are dropping. Although a second dose of methotrexate is a common approach ,it should only be considered if the beta-hCG levels do not fall \>15% on day 7 compared with day 4. Laparoscopic surgery is preferred in women with ruptured ectopic pregnancy not meeting the criteria for medical treatment. The decision to have a salpingotomy over salpingectomy depends on the condition of the contralateral tube and desire for future fertility. In this scenario, laparoscopic surgery should be considered if medical therapy with methotrexate fails. An emergency laparotomy is not indicated in this patient, as she is stable.
1730
Causes of hyperechogenic bowel?
CF Down's CMV
1731
Causes of increased nuchal translucency
Down's Congenital Abdominal wall defects
1732
A 37-year-old woman in her second pregnancy has delivered a live male infant. She has no past medical history of note. Ten minutes after delivery, she complains of a sudden onset severe occipital headache that is associated with vomiting. On examination there is evidence of photophobia. Shortly after this she losses consciousness and has a Glasgow coma score of 8. What is the most likely diagnosis? Extra-dural haematoma Sheehan's syndrome Sub-dural haematoma Subarachnoid haemorrhage Intracerebral haemorrhage
A subarachnoid haemorrhage (SAH) is a type of stroke which is usually the result of bleeding from a berry aneurysm in the Circle of Willis. Key clinical features include a sudden onset headache which reaches maximum severity in seconds to minutes ('thunderclap headache') and meningitic symptoms (for example photophobia and neck stiffness).
1733
What are the long term Cxs of PCOS?
Subfertility DM Stroke and TIA Coronary artery disease Obstructive sleep apnoea Endometrial Ca
1734
A 27-year-old primiparous woman has had a prolonged first stage of labour and the foetal heart rate on auscultation was 172 beats per minute. Cardiotocography (CTG) is initiated. Over the last 30 minutes the CTG has changed. The latest recording shows a baseline foetal heart rate of 175 beats per minute, a baseline variability of 7 beats per minute, some accelerations are present and there are variable decelerations. What is the next step? Do nothing as the CTG is not worrying Conservative measures and take foetal blood sample Plan immediate delivery Conservative measures (change position, optimise hydration) only Give IV oxytocin to initiate contractions
Cardiotocography (CTG) is used to assess foetal well being by measuring the foetal heart rate and maternal contractions. A normal trace is reassuring but an abnormal trace can require further monitoring or require additional investigations. There are four important features when interpreting a CTG: Baseline foetal heart rate Baseline variability Presence of accelerations Presence/absence of decelerations The CTG described in this case has 2 non-reassuring features - the foetal heart rate is 175 bpm and there are variable decelerations. This makes the CTG abnormal but it does not require urgent intervention as there is no bradycardia or prolonged late decelerations. NICE guidelines suggest that conservative measures should be initiated and a foetal blood sample should be taken in order to determine the next step in management. Planning for delivery will be discussed with the consultant obstetrician after the foetal blood sample is obtained. While oxytocin may help to initiate contractions in order to move into the 2nd stage of labour, this should not be done until foetal well being is confirmed through foetal blood sample.
1735
What are the characteristic levels for normal bladder function?
Should have a voiding detrusor pressure risk of \<70cm Peak flow rate of \>15ml/s High voiding detrusor pressure with low peak flow rate is indicative of bladder outflow obstruction
1736
A 34-year-old woman attends a routine antenatal clinic at 16 weeks gestation. She has no significant past medical history but suffers with occasional frontal headaches. She is noted to have a blood pressure of 148/76mmHg. Urinalysis reveals; pH6.5 Protein+1 Nitrates0 Leuc0 Blood0 What is the most likely diagnosis? Gestational hypertension Pre-eclampsia HELLP Nephrotic syndrome Chronic hypertension
The answer here is chronic hypertension. At 16 weeks gestation, this lady is too early into her pregnancy to have developed any of the pregnancy related causes of hypertension. The small amount of protein in her urine may also indicate relatively long standing hypertension. Intermittent frontal headaches are a common occurrence and are not a sign of pre-eclampsia in this case. Pre-eclampsia and gestational hypertension would only occur after 20 weeks gestation. Pre-eclampsia with significant proteinuria, gestational hypertension without. Nephrotic syndrome would be associated with a larger degree of proteinuria.
1737
A 35-year-old woman comes to see you in clinic with a 12 month history of heavy periods with clots and flooding. She does not experience any pelvic pain. On examination she has a palpable bulky uterus. You book her in for a transvaginal ultrasound scan and decide to start her on some treatment in the interim. What is the most appropriate first line management? Levonorgestrel releasing intrauterine system Oral norethisterone Combined oral contraceptive pill Depot injection Tranexamic acid
This is a question regarding management of menorrhagia. In this scenario, this lady most likely has uterine fibroids and is therefore appropriately being sent for transvaginal ultrasound for further assessment. NICE Clinical Knowledge Summaries dictate that tranexamic acid or NSAIDs are the most suitable 1st line agents to use to manage symptoms while awaiting results of investigations. Since the patient does not have pelvic pain, tranexamic acid is most appropriate. It would not be appropriate to insert a levonorgestrel releasing IUS before delineating the anatomy in someone whom you're suspicious of fibroids.
1738
A 21-year-old woman presents to the emergency department with a 2 day history of nausea and severe constant pain localised since onset to the right iliac fossa. There is no fever nor diarrhoea and no vaginal bleeding. She is on the contraceptive implant that was placed 5 months ago. You suspect ovarian torsion. How would you definitively diagnosis this? Laparotomy Laparoscopy CT abdomen pelvis with contrast CT abdomen pelvis without contrast Transvaginal and transabdominal ultrasound
Ovarian torsion can only be definitively diagnosed invasively. Laparoscopy (keyhole) is the usual method of surgery and allows diagnosis by visual inspection and also allows management with detorsion. Laparotomy (open) is another option for surgery but is usually reserved for patients with suspected or confirmed malignancy to prevent seeding and malignant spread. Laparotomy may also be used for those patients in whom laparoscopy may be difficult, for example due to size, either obesity or small size in infants. Ultrasound is the imaging modality of choice to confirm clinical suspicion of ovarian torsion, but cannot provide a definitive diagnosis. Combining transvaginal with transabdominal methods of ultrasound provides the best images of reproductive organs. Features on ultrasound include visualisation of the twisting of vessels (whirlpool sign), ovarian oedema, and reduced blood flow to and within the ovary when examining with colour Doppler. Diagnostic reliability of non-invasive imaging is also dependent on sonographer/radiologist expertise. CT would show similar findings to ultrasound, but this is more costly and has the added risk of radiation. In a CT with contrast, there would be lack of enhancement of the affected ovary. A CT without contrast is appropriate for imaging renal stones but would not demonstrate ovarian torsion or structural changes within organs very well. N.B. Differential diagnoses for this presentation would be appendicitis and ectopic pregnancy. These can be ruled out from the history. Appendicitis: Abdominal pain was localised since onset to the right iliac fossa rather than starting as diffuse and localising later on. There is no diarrhoea. There is no fever. Ectopic pregnancy: There is no vaginal bleeding. This patient is on the contraceptive implant.
1739
A 25-year-old para 1+0 presents at 36 weeks with painless vaginal bleeding. She reports that she has had intermittent spotting over the last 4 weeks, but they have increased in volume and frequency. Her blood pressure is 125/80mmHg and her heart rate is 85bpm. On examination, her abdomen is soft and non-tender, and the fetal head is not engaged and high. What examination should you perform to confirm your initial working diagnosis? LFTs and urine dipstick Vaginal examination Abdominal ultrasound Vaginal ultrasound Cardiotocography of the fetus
The findings in this case are classical of placenta praevia. 1. These investigations would be used to partly investigate pre-eclampsia 2: Vaginal examinations should always be avoided in a pregnant woman with unexplained vaginal bleeding 3: Correct, this should show a low-lying placenta 4: Vaginal investigations should always be avoided in a pregnant woman with unexplained vaginal bleeding 5: This would elicit any fetal distress, however would not confirm a diagnosis of placenta praevia
1740
A 64 year-old obese lady presents to the rapid access clinic after one episode of post menopausal bleeding. She has an ultrasound scan which shows an endometrial thickness of 4mm. A pipelle biopsy comes back as negative. What is the most appropriate management? Serial ultrasound scans every 6 months Follow up 1 year Discharge Hysteroscopy and endometrial biopsy Repeat pipelle 3 months
The correct answer here is discharge the patient back to her GP, while obviously telling the patient to report back if she has any further episodes of vaginal bleeding. The combination of the endometrium being thin on scan and there being no histological evidence of abnormal tissue is reassuring enough to say at the moment her risk of endometrial cancer is low. Pipelle biopsies are shown to have a very high sensitivity in detecting endometrial cancer (\>99%). Without any further episodes of vaginal bleeding repeating a pipelle in 3 months is not indicated. As the sensitivity of pipelle biopsy is so high, a hysteroscopy and endometrial biopsy is not needed in this case. This is an invasive procedure, which is uncomfortable as an outpatient and therefore often needs a general anaesthetic, which carries further risks. Sometimes a hysteroscopy and endometrial biopsy is needed, for example if the pipelle is not possible in the outpatient setting (e.g. due to patient not tolerating it, a stenosed cervix etc.) or if there is other pathology, for example polyps, which need to be visualised. Ultrasound scanning has not been shown to be a reliable screening test for endometrial cancer, and therefore repeating the ultrasound scans is not helpful. There is no need to follow the patient up in 1 year, as if she does not have any further episodes of bleeding the risk of endometrial cancer remains low. It is however very important to explain to the patient that even though this time she was low risk, she could be in early stages or still go on to develop endometrial cancer, and therefore she should see her GP immediately about any further episodes of vaginal bleeding.
1741
A 76 year old woman presents with post-menopausal bleeding for the past 4 months. She is diagnosed with well-differentiated adeno-carcinoma (stage II) on endometrial biopsy. There is no evidence of metastatic disease. Which is the most appropriate treatment? Transcervical endometrial resection Total abdominal hysterectomy Provera (medroxyprogesterone acetate) Wertheim's radical hysterectomy Total abdominal hysterectomy with bilateral salpingo-oophorectomy
Total abdominal hysterectomy with bilateral salpingo-oophorectomy is the treatment of choice for stage I and II endometrial carcinoma. Provera is a progesterone used as a hormonal treatment for endometrial carcinoma - it acts by slowing the growth of malignant cells in the endometrium. Wertheim's radical hysterectomy includes removal of lymph nodes and is used to treat stage IIB endometrial carcinoma.
1742
A 28-year-old woman with rheumatoid arthritis asks for advice about conception. Which one of the following statements is true? Methotrexate may be continued during pregnancy as long as the woman takes folic acid 5mg daily NSAIDs should be avoided in the first and second trimester Woman with rheumatoid should be encouraged to conceive as soon as possible (ideally within 1 year) after diagnosis to minimise the risk of complications TNF-α blockers are absolutely contraindicated in pregnancy Hydroxychloroquine is considered safe during pregnancy
Hydroxychloroquine is considered safe during pregnancy
1743
Methotrexate in pregnancy
methotrexate is not safe in pregnancy and needs to be stopped at least 3 months before conception
1744
What is significant about anaesthetics in pregnant woman with RA?
patients should be referred to an obstetric anaesthetist due to the risk of atlanto-axial subluxation
1745
NSAIDs in pregnancy
NSAIDs may be used until 32 weeks but after this time should be withdrawn due to the risk of early close of the ductus arteriosus
1746
Sulfasalazine and hydroxychloroquine in pregnancy
Considered safe
1747
Leflunomide in pregnancy
Is not considered safe
1748
A 32-year-old nulliparous female is induced into labour at 39 weeks gestation due to a history of pre-eclampsia and intrauterine growth restriction. Her cervix is favourable and she has undergone artificial rupture of membranes. On inspection of the partogram you note that there has been no uterine activity. What treatment is most suitable? Syntometrine Vaginal prostaglandin (PGE2) No treatment required Syntocinon Caesarian section
Syntocinon is a synthetic oxytocin analogue and is the drug of choice for stimulating labour when the contractions are considered too weak.
1749
A 33-year-old female presents to her GP as she missed her Noriday pill (progestogen only) this morning and is unsure what to do. She normally takes the pill at around 0900 and it is now 1230. What advice should be given? Take missed pill as soon as possible and advise condom use until pill taking re-established for 48 hours Take missed pill as soon as possible and omit pill break at end of pack Perform a pregnancy test Take missed pill as soon as possible and no further action needed Emergency contraception should be offered
Take missed pill as soon as possible and advise condom use until pill taking re-established for 48 hours
1750
A 27-year-old woman presents 1 week following a first trimester miscarriage with continued low abdominal pain and vaginal bleeding. She is tearful and explains she had a previous miscarriage a year ago and wants this process to be over as soon as possible. A trans-vaginal ultrasound is performed and an incomplete miscarriage is suspected. What is the most appropriate management of this patient? Oral misoprostol Admit for observation Intravenous syntocinon infusion Oral mifepristone Vaginal misoprostol
An incomplete miscarriage occurs when some, but not all, of the products of conception are expelled from the uterus. Retained products of conception pose an infection risk to the mother and so should be treated promptly. Bleeding in miscarriage can be serious and physiological signs of shock should not be missed. The National Institute of Health and Care Excellence (NICE) recommends that during an incomplete miscarriage, medical management of miscarriage should be offered where 'expectant management' is unacceptable to the patient. A single dose of misoprostol 600 micrograms as a vaginal pessary is first line medical management of an incomplete miscarriage. If this is not tolerated then oral administration is acceptable. Other management options include manual vacuum aspiration under local anaesthetic and surgical management under general anaesthetic. Medical management as opposed to expectant management is often offered to women who have previously had a traumatic experience of pregnancy, such as a previous miscarriage or still birth.
1751
A 33-year-old woman is reviewed regarding her asthma control. You notice from her records that she has never had a cervical smear and raise this with her. She responds that she is a lesbian and has never had sex with a man. What is the most appropriate advice to give? She does not need to have a smear She may need to have a smear if her partner has previously had heterosexual relationships She should have cervical screening as per normal She does not need to have a smear but does need a one-off HPV test She should be referred to colposcopy clinic for a case-based assessment
HPV, the causative agent of cervical cancer, can be transmitted during lesbian sex. Lesbian and bisexual women should therefore have cervical screening as normal. Unfortunately the uptake amongst lesbian women is around 10 times worse than the general female population, sometimes as a consequence of incorrect advice from healthcare professionals.
1752
What is oxybutynin
Anti-muscarinic used in treatment of detrusor muscle over-activity
1753
A 34-year-old woman from Zimbabwe presents with continuous dribbling incontinence after having her 2nd child. Apart from prolonged labour the woman denies any complications related to her pregnancies. She is normally fit and well. A.Bladder diary for 3 days B.Urodynamic studies C.Bladder drill training for 6 weeks D.Pelvic floor exercises 3 months E.Oxybutynin F.IV urography G.Urinary dye studies H.None of the above
Vesicovaginal fistulae should be suspected in patients with continuous dribbling incontinence after prolonged labour and from a country with poor obstetric services. A dye stains the urine and hence identifies the presence of a fistula.
1754
A 36-year-old with menorrhagia has is investigated and found to have a 1.5 cm uterine fibroid which is not distorting the uterine cavity. She has three children and wants ongoing contraception, but is using only condoms at the moment. What is the most appropriate initial treatment for her menorrhagia? Intrauterine system GnRH agonist Tranexamic acid Refer for consideration of a myomectomy Combined oral contraceptive pill
As the fibroid is less than 3 cm medical treatment can be tried. NICE Clinical Knowledge Summaries recommend an intrauterine system initially, which will also provide contraception.
1755
Treatment options for TTTS
Indomethacin to reduce foetal urine output Laser obliteration of placental vascular communications Selective foetal reduction After birth, the donor may require blood transfusions to treat anaemia. The recipient twin may need exchange transfusions/ heart failure medications.
1756
A 32-year-old woman comes to see her GP asking to be put on the combined oral contraceptive pill as she has recently started a new sexual relationship. She does not want any long acting contraceptives and has tried the progesterone only pill in the past and had side effects. Which one of the following would be an absolute contraindications to prescribed the combined oral contraceptive pill? Migraine without aura 1st degree relative with a history of venous thromboembolism Smoking 10 cigarettes a day HIV positive and using antiretrovirals Systemic Lupus Erythematosus
When prescribing the oral contraceptive pill there are a number of risk factors that must be screened for. These risk factors are split into a four point scale with level 4 being considered an unacceptable health risk. All answer except for Systemic Lupus Erythematosus are considered level 3 where the disadvantages generally outweigh the advantages but prescription can be given if deemed appropriate.
1757
A 30-year-old who is currently 27 weeks pregnant comes to see you about a thin, white discharge. Swabs are taken and clue cells are seen on microscopy. Which treatment do you initiate? Metronidazole 400mg bd for 7 days Single dose of metronidazole 2g Intravaginal clindamycin cream 2% od for 7 days Intravaginal metronidazole gel 0.75% od for 5 days Oral clindamycin 300mg bd for 7 days
Offer treatment to all pregnant women with symptomatic bacterial vaginosis (BV). If a pregnant woman is incidentally found to have BV and has no symptoms, discuss with the woman's obstetrician whether treatment is appropriate. Oral metronidazole is the treatment of choice. High-dose regimens are not recommended during pregnancy. Intravaginal metronidazole gel or clindamycin cream are alternative choices if the woman prefers a topical treatment or is unable to tolerate oral metronidazole. Oral clindamycin is not widely recommended in primary care because of an increased risk of pseudomembranous colitis.
1758
What are the most likely locations of ectopic pregnancy?
These are the various sites of ectopic pregnancy and their prevalence in % : tubal ectopic: 93-97% ampullary ectopic: most common ~70% of tubal ectopics and ~65% of all ectopics isthmal ectopic: ~12% of tubal ectopics and ~11% of all ectopics fimbrial ectopic: ~11% of tubal ectopics and ~10% of all ectopics interstitial ectopic/cornual ectopic: 3-4%; also essentially a type of tubal ectopic ovarian ectopic/ovarian pregnancy; 0.5-1% cervical ectopic/cervical pregnancy; rare \<1% scar ectopic: site of previous Caesarian section scar; rare abdominal ectopic: rare; ~1.4%
1759
A 26-year-old woman presents to her general practitioner requesting contraception. She has a past medical history of severe Crohn's disease. Her periods are regular with a 29 day interval and 5 days of bleeding. Her body mass index is 23kg/m² and she does not smoke. Which of the following methods of contraception would it be most appropriate to prescribe? Qliara (Dienogest with estradiol valerate) Micronor (Norethisterone) Microgynon 30 (Ethinylestradiol with levonorgestrel) Cerazette (Desogestrel) Evra transdermal patch (Ethinylestradiol with norelgestromin)
Oral contraceptives should be used with caution in patients with a history of inflammatory bowel disease affecting the small bowel due to the risk of malabsorption. There is no evidence to suggest that the efficacy of the Evra patch is reduced.
1760
A 27-year-old woman attends colposcopy as she had moderate dyskaryosis on her recent cervical smear. On colposcopy she has aceto-white changes and a punch biopsy followed by cold coagulation. Histology of the biopsy shows CIN II. When should she next be offered cervical screening? 1 month 6 weeks 6 months 12 months Return to normal screening, every 3 years
This woman has been treated for cervical intraepithelial neoplasia (CIN) at her colposcopy appointment. She requires follow-up to determine if the lesion has been adequately treated. Women who have been treated for CIN II should be offered cervical screening at 6 months and 12 months post-treatment. This should then be followed by annual screening for a total of 10 years. If a woman has a positive-test after treatment they should return to colposcopy.
1761
A 30 year old type 2 diabetic presents to the diabetics clinic advising that she wishes to become pregnant. The patient normally has good glycaemic control and is currently being treated with metformin and gliclazide. What advice should you give her about potential changes to her medication during pregnancy? Patient may continue on metformin but gliclazide must be stopped Patient can continue on both medications Patient may continue on gliclazide but metformin must be stopped Both drugs must be stopped and the patient must be switched to insulin Both drugs must be stopped and the patient must be switched to liraglutide
The correct answer is that the patient may be continued on metformin but that the gliclazide must be stopped. In the management of type 2 diabetes in pregnancy 'women with pre-existing diabetes can be treated with metformin, either alone or in combination with insulin'. While it is likely that the patient will be required to switch to insulin it is not an absolute requirement. Both gliclazide and liraglutide are contraindicated in pregnancy.
1762
A 30-year-old woman is 24 weeks pregnant and she receives a letter about her routine cervical smear. She asks her GP if she should make an appointment for her smear. All her smears in the past have been negative. What should the GP advise? Reschedule the smear to occur at least 12 weeks post-delivery Take the smear now This smear can be missed, she will be re-entered for routine screening in 3 years Perform a speculum exam to visualise the cervix for abnormalities Seek advice of an obstetric consultant
NICE guidelines suggest that a woman who has been called for routine screening wait until 12 weeks post-partum for her cervical smear. If a smear has been abnormal in the past and a woman becomes pregnant then specialist advice should be sought. If a previous smear has been abnormal, a cervical smear can be performed mid-trimester as long as there is not a contra-indication, such as a low lying placenta.
1763
A 25-year-old female comes to see her GP with a positive pregnancy test following a missed period. Given her last menstrual period it is estimated that she is 4-5 weeks pregnant. Although the news is unexpected, she is happy to continue with the pregnancy, however she is a known epileptic and is concerned about her medication. Which of the following medications are recommended for epileptics in pregnancy? ## Footnote Sodium valproate Phenytoin Lamotrigine Primidone Phenobarbitone
Anti-epileptics in pregnancy can be a tricky subject. Many are known to cause severe congenital defects (both structural and intellectual) and as such the first line of care is good contraceptive advice and planning with the patient in question. This is however, not always possible and there will always be cases where a patient becomes pregnant whilst on anti-epileptic medication prior to consulting with a doctor. The recent MBRRACE-UK and the NICE clinical guidelines both state that most women with epilepsy and of child bearing age are currently prescribed lamotrigine and during pregnancy this may require a dose increase. Phenytoin, phenobarbitone and sodium valproate are all known to have an adverse effect on cognitive abilities and therefore are usually avoided unless absolutely necessary. Lamotrigine, carbamazepine and levetiracetam are known to have the smallest effects on the developing foetus, however all epileptics who are either pregnant or are planning to become pregnant should be referred to specialist care as soon as possible.
1764
A 35-year-old woman with no significant past medical history presents requesting contraception. She recently got married and says that she is likely to want to start trying for children with her husband in one year. She currently smokes between 15-20 cigarettes per day. Which of the following contraceptives would it be most appropriate to prescribe? ## Footnote Mirena intrauterine device (Levonorgestrel) Cerazette (Desogestrel) Microgynon 30 (Ethinylestradiol with levonorgestrel) Nexplanon implant (Etonogestrel) Depo-provera injection (Medroxyprogesterone acetate)
Microgynon 30 would be contraindicated in this lady as she is over 35 years old and smokes \>15 cigarettes per day. Depo-provera could be used, but can be associated with prolonged amenorrhoea up to 1 year after discontinuation, which would not suit this lady who wants to try for a family in 1 year. The insertion of both Mirena and Implanon and subsequent removal in the space of a year is likely to be more of a burden to this lady than taking an oral contraceptive over the same time period. Cerazette, a progesterone only pill, is not contraindicated and can easily be stopped in 1 year.
1765
Heterotropic pregnancy
describes a very rare situation in which there are simultaneous ectopic and uterine pregnancies. It is usually treated by surgical removal of the ectopic pregnancy.
1766
Mx of VZV in pregnancy
If any doubt about previous chickenpox- urgently check Ab titres If the pregnant womanm is not immune she should be given VZIG which is effective up to 10 days post exposure Should be prescribed oral acyclovir if present within 24h of rash onset
1767
A 26-year-old primigravida presents at 39 weeks with rupture of membranes and bleeding. She describes a flood of cloudy fluid followed by continuous vaginal bleeding. She is very anxious but denies any localised pain or tenderness. Her pregnancy has so far been uncomplicated, but she has not attended her antenatal scans. Cardiotocography shows a resting rate of 105 beats per minute and late decelerations. What is the most likely diagnosis? Placental abruption Bloody show Placenta accreta Vasa praevia Placenta praevia
Vasa praevia describes a complication in which fetal blood vessels cross or run near the internal orifice of the uterus. The vessels can be easily compromised when supporting membranes rupture, leading to frank bleeding. The classic triad of vasa praevia is rupture of membranes followed by painless vaginal bleeding and fetal bradycardia. Unlike placenta praevia, vasa praevia carries no major maternal risk but fetal mortality rates are significant. The two conditions may be difficult to distinguish in acute clinical situations, but for examination purposes a preceding rupture of membranes will usually be emphasised. Although ultrasound scans can detect vasa praevia, many cases are undetectable antenatally.
1768
At her booking visit, a woman mentions to her midwife that she has been previously diagnosed with immune thrombocytopenic purpura (ITP). Which procedure carries the greatest risk of haemorrhage in the newborn? ## Footnote External cephalic version Forceps delivery Prolonged ventouse delivery Fetal blood sampling Caesarean section
Immune thrombocytopenia (ITP) is an autoimmune condition that can occasionally complicate pregnancies, especially if there is placental passage of maternal antiplatelet antibodies. The high pressure exerted by the vacuum during a ventouse delivery can cause bleeding in the neonate. Cephalohaematoma or more severely, subgaleal haemorrhage, can be exacerbated in the context of neonatal thrombocytopenia. Fetal blood sampling and forceps might be used with caution but would not be as high-risk. A Caesarean section would pose a greater risk to the mother, rather than the neonate.
1769
A 26 year old woman with long standing hypertension gives birth to a healthy male child. The patient advises that she wishes to breastfeed the child but is concerned about the medication affecting the baby. Which of the following antihypertensive drugs would NOT be safe for the patient to use while breast feeding? Losartan Enalapril Nifedipine Labetalol Atenolol
The correct answer is Losartan. Losartan is an ARB which are contraindicated in pregnancy unless absolutely essential and not recommended in breast feeding. The other options; Enalapril, Nifedipine, Labetalol and Atenolol are all safer in breast feeding.
1770
A 24-week pregnant woman attends the early pregnancy unit as she has been told that her uterus is small for this date. On ultrasound she is found to have oligohydraminos. Which of the following options is a cause of oligohydraminos? Duodenal atresia Microcephaly Trisomy 21 Bartter's syndrome Renal agenesis
Oligohydraminos is a conditions where there is a deficiency of amniotic fluid during pregnancy. This can often present as smaller symphysiofundal height. Renal agenesis is a cause of oligohydraminos (abnormally low volume of amniotic fluid) as the amniotic fluid is mainly derived from foetal urine
1771
A primiparous 25-year-old woman is in labour. The midwife co-ordinating delivery contacts you as she is concerned that labour is not progressing. She has just examined the cervix and tells you that it is not dilating at a satisfactory rate. What is the minimum acceptable rate of cervical dilatation in the established first stage of labour? 4cm in 4 hours 2cm in 4 hours 2cm per hour 1.5cm per hour 1cm in 4 hours
NICE define delay in the established first stage of labour as: Cervical dilatation of less than 2cm in 4 hours for first labours Cervical dilatation of less than 2cm in 4 hours or a slowing in the progress of labour for second or subsequent labours.
1772
A 36-year-old woman who used to inject heroin has recently been diagnosed HIV positive. She is offered a cervical smear during one of her first visits to the HIV clinic. How should she be followed-up as part of the cervical screening program? Attend colposcopy annually 6 monthly cervical cytology Cervical cytology every three years (normal screening program) Annual cervical cytology Attend colposcopy every three years
Women who are HIV positive are at an increased risk of cervical intra-epithelial neoplasia (CIN) and cervical cancer due to a decreased immune response and decreased clearance of the human papilloma virus. (1) HIV positive women who have low-grade lesions (CIN1) do not clear these lesions and these can progress to high-grade CIN or cervical cancer. Even those women who are effectively treated with antiretrovirals have a high risk of abnormal cytology and an increased risk of false-negative cytology. (1) Women with HIV should be offered cervical cytology at diagnosis.. Cervical cytology should then be offered annually for screening.
1773
A 13 week pregnant woman is diagnosed with bacterial vaginosis (BV) following high vaginal swab results, which were taken due to offensive vaginal discharge. She is otherwise clinically well and has no drug allergies. Which of the following treatments is recommended? No treatment required Amoxicillin Doxycycline Cefalexin Metronidazole
BV is characterised by an overgrowth of mainly anaerobic organisms. It is a common cause of vaginal discharge and is not considered to be a sexually transmitted infection. Approximately 50% of women are asymptomatic. When symptoms are present, BV is characterised by a fishy-smelling vaginal discharge. Symptomatic BV in pregnancy is associated with late miscarriage and preterm delivery. Treatment should be offered to all pregnant woman who are symptomatic. This consists of oral metronidazole 400mg twice daily for 5-7 days (2grams stat dose is not recommended in pregnancy). Treatment is considered on a individual basis for pregnant woman with BV who are asymptomatic. This is because evidence suggests that identification and treatment of asymptomatic pregnant women does not lower the risk of preterm births.
1774
A 22 year old woman attends the family planning clinic enquiring about contraception. She is currently taking carbamazepine for epilepsy and her BMI is 39 kg/m². She has no other past medical history. Which of the following would be the most suitable contraceptive to offer her? ## Footnote Progesterone only pill (POP) Copper intrauterine device Combined oral contraceptive pill (COCP) Progesterone injection (Depo-Provera) Progesterone implant (Nexplanon)
All woman who are taking an enzyme-inducing drug (EID) (carbamazepine is an example of an EID) should be advised to use a reliable contraceptive that is unaffected by EIDs. Examples of contraceptives that are unaffected by EIDs are: Copper intrauterine device Progesterone injection (Depo-provera) Mirena intrauterine system The copper intra-uterine device is usually the preferred option, as it is a non-hormonal method. In the above scenario, the patient is obese with a BMI of 39 kg/m². Therefore, the contraceptive injection (Depo-Provera) would not be the most suitable option. This is because it is associated with weight gain (2-3kg over 1 year). In patients on EIDs who wish to take the COCP (providing there are no contraindications) it is important to inform them that the effectiveness is decreased and there is an increased risk of pregnancy. It is recommended that the dose of oestrogen is increased to 50mcg with no pill-free interval, or reduced to 4 days from 7 days (to reduce the chance of ovulation). In addition, barrier methods would also be advised. This applies when the patient is on an EID and for 4 weeks after stopping. In patients on EIDs who wish to take the POP or progesterone implant, then additional barrier contraception would be required while using EIDs and for 4 weeks after stopping. Note - rifampicin and rifabutin are potent EIDs and require longer periods of using barrier contraception after stopping (8 weeks). If emergency contraception is required, the copper intra-uterine device is again the best option. If levonorgestrel (Levonelle) is used, then double the standard dose is recommended. Ulipristal acetate (ellaOne) is not recommended.
1775
Nancy is a 29 year old lady who has given birth to a baby boy 3 days ago and is keen to discuss future contraception. She was previously on the combined pill but is keen to avoid using anything if she can. She is not breast-feeding. How long after giving birth does she not require any contraception? Up to 28 days She needs contraception immediately after giving birth Up to 21 days Up to 2 months Up to 14 days
Prior to Day 21 postpartum no contraceptive methods are required. In non-breastfeeding women, ovulation may occur as early as Day 28. As sperm can survive for up to 7 days in the female genital tract, contraceptive protection is required from Day 21 onwards if pregnancy is to be avoided.
1776
A 17-year-old female comes to your GP clinic. She has recently travelled to Egypt to see her family, and now has come to visit as she is suffering with per vaginal bleeding and urinary incontinence. She consents to examination with a chaperone present and you identify signs that suggest there have been recent trauma to the genitalia. You suspect this is a case of female genital mutilation. What is the most appropriate course of action? Report this to the police Provide symptomatic treatment only Refer to secondary care for further investigation Contact child protection services Call the family in for a discussion
Female genital mutilation (FGM) is a criminal act. The GMC has now issued guidance that all cases of FGM must be reported to the police in under 18s. The mandatory duty does not apply in over 18s. It also does not apply if a doctor can identify that another doctor has already made a report to the police in connection with the same act of FGM. Providing symptomatic treatment only would be in breach of GMC guidance and would put your registration at risk. Calling in the family for discussion may not be appropriate and may lead to further distress for the patient. You would still need to make a police report. Contacting child protection services may be an additional necessary step, but it is imperative that a police report is made in the first instance. Referring to secondary care for investigation may be useful for treating any symptoms of FGM, but again a police report needs to be made.
1777
Type 1 FGM
Partial or total removal of the clitoris and/or the prepuce (clitoridectomy).
1778
Type 2 FGM
Partial or total removal of the clitoris and the labia minora, with or without excision of the labia majora (excision).
1779
Type 3 FGM
Narrowing of the vaginal orifice with creation of a covering seal by cutting and appositioning the labia minora and/or the labia majora, with or without excision of the clitoris (infibulation).
1780
Type 4 FGM
All other harmful procedures to the female genitalia for non-medical purposes, for example: pricking, piercing, incising, scraping and cauterization.
1781
A 49-year-old lady with a background of hypertension and previous DVT after a flight to Australia comes to see you about hot flushes. They are severely interfering with her sleep and her work as a retail manager. She last had a period 4 months ago and her husband has had a vasectomy. Which of these treatments would you recommend? ## Footnote Cyclical oestrogen with progesterone Oestrogen patches Mirena intrauterine system Clonidine Tibolone
For a woman with a personal or family history of thromboembolic disease, offer lifestyle advice or non-hormonal therapies. For vasomotor symptoms, consider a 2 week trial of Paroxetine/ Fluoxetine/ Citalopram/ Venlafaxine or a 24 week trial of Clonidine. If these measures are inadequate and the woman requires treatment, refer to a specialist in thrombophilia.
1782
Vitamin recommendation in overweight women
Vitamin D
1783
Obese women and 3rd stage of labour
Offer active third stage due to the higher risk of PPH
1784
GDM cut offs in pregnancy
Impaired glucose tolerance 2hour glucose greater than or equal to 7.8 Diabetes random gluocse greater than or equaly to 7 or 2 hour glucose greater than or equal to 7.8
1785
Soft systolic flow murmur audible across the praecordium
Phyisological, due to dilatation across the tricuspid vavle causing mild regurgitant flow.
1786
Warfarin and trimesters
First trimester: highest risk of teratogenicity- fetal warfarin syndrome Still exists in mid and third triemsters
1787
Nasal hypoplasia Vertebral calcinosis Brachydactyly
Fetal warfarin syndrome
1788
CTG vs maternal BP in eclamptic fit
Mother should have BP checked before fetal CTG as it is not possible to deliver the fetus until the mother is stable
1789
22w, unwell with chorioamnionitis mx
Antibiotics Induce labour No steroids
1790
Can cause mid-treimester loss, early meconium and preterm labour Food-borne infection
Listeriosis
1791
Blistering condition, presents with febrile illness and if untreated can lead to maternal and fetal death
Impetigo herpetiformis
1792
A blistering condition that starts at the umbilicus and spreads
Pemphiogid gestationis
1793
A rash of the trunk and upper limbs with abdominal sparing
Prurigo gestationis
1794
Blood sugar reference rangs in pregancny around meals
Pre-meal: \<5.5 1 hour post meal \<7.8