GOSH Flashcards

(293 cards)

1
Q

Laparatomy

A

a surgical incision into the abdominal cavity, for diagnosis or in preparation for major surgery

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2
Q

Laparoscopy

A

a small tube with a camera is put into the stomach area

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3
Q

hysteroscopy

A

a TRANSVAGINAL procedure used to examine the inside of the womb (uterus). It’s carried out using a hysteroscope, which is a narrow telescope with a light and camera at the end.

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4
Q

fibroids/leimyomata definition and RF

A

benign tumours of myometrium

if they have a pendunculated stalk ==> a polyp

RF: afro-carribean and FHx. injectable progestogens and COCP are protective!

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5
Q

fibroids/leimyomata aeitiology

A

Grow in response to oestrogen (and progesterone) therefore shrink after meno pause and variable changes during preg

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6
Q

Sx of fibroids/leimyomata

A

usually site dependent rather than size, and usually asymptomatic

  • menorrhagia
  • dysmenorrhoea
  • IMB
  • They only cause pain if torsion or red degeneration

NB/ if big e/n, may cause bladder retention or frequency

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7
Q

red degeneration

A

Result of an inadequate blood supply - pain and uterine tenderness. Common in preg

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8
Q

fibroids/leimyomata complications

A

torsion, degenerations, malignancy

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9
Q

fibroids/leimyomata ix

A

USS but MRI or laparoscopy may be required to distinguish the fibroid from an ovarian mass

Need to differentiate fibroids and adenomyosis w MRI

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10
Q

fibroids/leimyomata tx

A

small - no tx
large - serially measured by examination or USS (?malig)

MEDICAL Mx = GnRH agonists cause temporary amenorrhoea and fibroid shrinkage but nto for F trying to conceive.
SURGICAL Mx = 
hysteroscopic resection
hysterectomy
Uterine artery embolisation
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11
Q

Adenomyosis definition

A

aka endometriosis interna

= presence of endometrium within the myometrium

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12
Q

Adenomyosis associations

A

40yo
asso/w endometriosis and fibroids (need to differentiate from fibroids!)

Usually asx but can present w painful, regular, heavy menstruation. O/E mildly enlarged and tender uterus. Sx subside after menopause

Ix: MRI

MEDICAL Mx = IUS or COCP w or w/o NSAIDs to control menorrhagia and dysmenorrhoea
SURGICAL Mx = hysterectomy

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13
Q

Endometritis aeitiology

A

often secondary to STI, instrumentation of uterus (eg. surgery, IUD), pregnancy/miscarriage/TOP (RPOC)
infx in postmenopausal –> malignancy

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14
Q

Endometritis sx

A
  • persistent and heavy PV bleed + pain
  • tender uterus
  • open os

Tx = broad sepc abx and ERPC if req

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15
Q

Intrauterine polyps

A

benign tumours in the uterus
40-50yo when oestrogen levels v high or postmenopausal F on tamoxifen for breast carcinoma

cause menorrhagia, IMB, and may prolapse through the cervix

Tx = resection or diathermy can cure bleeding problems

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16
Q

Endometrial carcinoma RF and PC

90% ADENOCARCINOMA

A
RF:
 exogenous oestrogen w/o progesterone
 obesity
 PCOS
 nulliparity and late menopause
ovarian tumours
Tamoxifen is a oestrogen agonist in the uterus!

Hx of COCP and pregnancy is protective

Presents w PCB +/- abnormal smears

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17
Q

Endometrial carcinoma ix and tx

A

USS
endometrial bx w Pipelle or hysteroscopy
MRI and CXR (to exclude rare pulmonary spread) req

NB/ staging is only possible following a hysterectomy

Mx of Endometrial carcinoma:
1. hysterectomy + bilateral salpingooophrectomy (BSO) –> XRT for pt w high risk LN involvement
‘Only XRT’ is for those w high risk of extrauterine and evidence of wide spread disease.

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18
Q

Menorrhagia definition and tx

A

heavy menstrual bleed (subjectively or objectively >80ml)

Tx:
1st line = IUS
2nd line = Tranexamic acid (antifibrinolytics) or mefanamic acid (NSAIDs = PG inihibitors)
3rd line = COCP
4th line = high dose progestogens or GnRH analogues –> amenorrhoea

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19
Q

When to do an endometrial bx (Pipelle or hyseroscopy)

A
>10mm in pre-menopausal, >4mm in post-menopausal
>40yo
menorrhagia w IMB
USS suggests polyp
prior to endometrial ablation/diathermy
before insertion of IUS if irreg cycles
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20
Q

causes of PCB

A

cervical Ca
cervical ectropion
cervical polyps
cervicitis/vaginitis

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21
Q

Ambiguous development and intersex

A

A) increased androgen fx in a genetic F
- Congenital adrenal hyperplasia is recessively inherited. Usually presents at birth w ambiguous genitalia. Tx = mineralcorticoid and cortisol replacement

B) reduced androgen fx in a genetic M

  • appears to be female and dx is when ‘she’ presents w amenorrhoea
  • absent uterus and rudimentary testes
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22
Q

PMS sx and tx

A

cyclical nature
tension, irritability, loss of control, bloatedness
GI upset and breast pain

tx = SSRI

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23
Q

cervical ectropion/erosion

A

= is when the columnar epithelium of the endocervix is visible as a red area around the os

Normal in preg, younger F or if on COCP
PC: PV d/c and PCB
Tx = cryotherapy AFTER smear (and colposcopy) has excluded Ca

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24
Q

Cervicitis

A

usually from STI

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25
Cervical polyps
= benign tumours of endocervical epithelium >40yo asx or cause IMB/PCB
26
Mx of abnormal smear
normal --> repeat every 3 years mild dyskaryosis/borderline changes --> repeat in 6 months. if still present then colposcopy mod dyskaryosis --> colposcopy severe dyskaryosis --> urgent colposcopy cervical glandular --> colopscopy, if abnormality not found then hysteroscopy
27
prevention of cervical Ca
1. HPV vaccination | 2. barrier contraceptive education
28
prevention of invasive cervical Ca
3. LLETZ aka diathermy loop excision (complications incl: post-op haemorrhage and increased risk of pre-term delivery)
29
cervical Ca sx (if any) | MOST ARE SQUAMOUS CELL CARCINOMAS (some are adenocarcinomas)
- PCB - offensive vaginal d/c - IMB (- PMB) pain is NOT an early feature
30
tx of cervical Ca
1. microinvasive ie.stage 1Ai --> cone bx (A cone biopsy is done less often than LLETZ. It: is a minor operation to cut out a cone-shaped piece of tissue containing the abnormal cells. only tends to be used if a large area of tissue needs to be removed.) - -> simple hysterectomy 2. stage 1Aii-1Bi --> laparoscopic lymphadenectomy initially and if positive then straight to chemo-XRT. Radical trachelectomy is for F who wish to preserve fertility. NB/ Wertheine's hysterectomy involves pelvic node clearance 3. other stage 1&2A: if LN -ve --> radical hysterectomy if LN involved --> chemo-XRT 4. stage 2B+ or +ve LN --> chemo-XRT alone Indications for chemo-XRT o LN+ve on MRI or after lymphadenectomy o alternative to radical hysterectomy even when LN -ve o surgical margins unclear o palliative XRT for bone pain or haemorrhage
31
Ovarian cyst accidents
= rupture of ovarian cyst contents into peritoneal cavity - intense pain, esp w demoid cyst and endometrioma. Also caused by haemorrhage into a cyst or the peritoneal cavity (if severe e/n can cause hypovolaemic shock). As does torsion of pedicle
32
Common ovarian masses- pore and post menopausal
PREMENOPAUSAL OVARIAN MASS - benign epithelial tumour, follicular/lutein cysts, dermoid cysts, endometriomas POSTMENOPAUSAL OVARIAN MASSES - benign epithelial tumour, malignancy Endometriotic cyst/endometriomas = blood-filled chocolate cysts if seen in the ovaries, that are characteristic of endometriosis Functional cysts = follicular (persistently enlarged follicles) and lutein cysts (persistently enlarged corpora lutea) are only in pre-menopausal F. COCP protects against functional cysts by inhibiting ovulation. Risk of malig so if >5mm for more than 2 months then CA125 levels measured and laparoscopy considered to remove or drain the large cyst
33
ovarian Ca
SILENT killer Ca presenting at stage 3-4; - abdo distention/palpable mass - pain or abnormal bleeding - Breast and GI sx - commonly secondary ovarian met from breast or GIT Ca RF = FHx, nulliparity, early menarche, late menopause NB/signet ring = Krukenberg tumours
34
ovarian Ca mx
TAH w bilateral salpingo-oophrectomy (BSO) at staging laparotomy Debulking all advanced tumours Follow up w chemo (unless bordlerline or stage 1A) Do not offer routine 'second-look' laparoscopy, but can monitor relapse using CA125 and CT
35
Causes of pruritus vulvae
``` o Candidiasis o vulval warts o pubic lices, scabies o derm eg.eczema, psoriaisis, lichen simplex [long hx of itching and soreness, inflamed labia majora, thickened w hyper/hypopigmentation, Avoid irritants such as soapUse emollients and steroid creams], lichen planus [causes irritation w flat, papular, purplish lesions in anogenital area, also affects hair, nails and mucous mem. Tx = high potency steroid creams], lichen sclerosis [Usually post-menopausal. ?AI co-existing w thyroid disease and vitiligo, soreness and pruritus, pink-white papules which coalesce to form skin resembling old-scribe papers w fissures. Can be ass/w malignancy, Tx = ultra potent topical steroids], contact dermatitis o Ca or premalignant stage ```
36
Bartholin's glands if blocked --> cyst and abscess formation
If infx occurs (Staph and E.Coli) - acutely painful and large tender red swelling near the inner wall (because bartholin glands are behind the labia minora) tx = incision and drainage, marsupialization
37
Congenital cysts
commonly arise in vagina smooth white appearance can be golf ball size and often mistaken for prolapse tx = only excise of sx eg.dyspareunia
38
Vulval Ca causes | MOST ARE SQUAMOUS CELL CARCINOMAS
premalignant disease is VIN = presence of atypical cells in the vulval epithelium. 2x types of VIN a) caused by HPV - responsible for the rare Ca in <45yo. Warty and basaloid lesion b) lichen sclerosis - major cause in >45yo, lesion is keratinizing Although VIN is premalignant, vulval Ca often arises de novo and is ass/w lichen sclerosis, immunosuppression, smoking and Paget's disease of vuvla
39
Vulva Ca sx, ix and tx Primary vaginal Ca mainly in older F (PC = bleeding, d/c, mass, ulcer) Clear cell adenocarcinoma of vagina in late teenage years
PC - pruritus, bleeding, d/c, mass ix - bx 1A --> wide local excision w/o lymphadenectomy others --> wide local excision w separate groin node dissection post op XRT if LN +ve, or pre-op to shrink or for palliation
40
Prolpase RF and sx
RF = childbirth, vaginal birth, oestrogen deficiency, obesity and chronic cough, congenital weakness, pelvic masses dragging/lump sensation - worse at end of day o severe prolapse may interfere w sexual intercourse, bleed, d/c or ulcerate. Cystocele --> urinary freq and incomplete bladder emptying.Rectocele --> difficulty defecating. BACK PAIN IS UNUSUAL
41
Prolapse mx
conservative - weight loss, stop smoking, (Ring usually, shelf if severe) pessaries for those unfit for surgery; they act like artificial pelvic floor, changed yearly uterine prolapse --> vaginal hysterectomy (sacrohysteroplexy if want to maintain fertility) Cystocele --> anterior repair Rectocele --> posterior repair NB/cystoceles and rectoceles are collectively known as vaginal wall prolapses Vault prolapse --> sacrocolpoplexy 'Tape' surgery for genuine stress incontinence
42
Genuine stress incontinence definition
= involuntary loss of urine when bladder pressure exceeds maximum urethral pressure in the absence of detrusor contraction dx only confirmed after ruling out overactive bladder using cystometry
43
SUI RF Hx: ask about faecal incontinence as well! ADL - ask pt to prioritise the sx as tx varies!
``` pregnancy vaginal delivery (esp prolonged or instrumental labour) obesity incr age prolapse commonly co-exists previous hysterectomy ```
44
Mx of SUI
conservative - weight loss, stop smoking, treat chronic cough or constipation 1, PFE +/- vaginal cones for at least 3 months 2. cystometry to exclude OAB 3. 'Tape' surgery 4. Surgery = Open Burch Colposuspension 5. Medical = Duloxetine (serotonin reuptake inhibitor)
45
Genuine stress incontinence vs SUI
GSI = a DISORDER diagnosed only after cystometry, of which stress incontinence is the major sx stress incontinence is a SYMPTOM, can be due to GSI, OAB or overflow incontinence
46
OAB definition
= urgency w or w/o urge incontinence, usually w freq or nocturia in the absence of proven infx. SUI is common. Leakage at night or at orgasm. Faecal urgency. Hx of childhood enuresis. High caffeine/energy drink intake. Whereas... Detrusor overactivity is a urodynamic dx char by involuntary detrusor contractions during the filling phase which may be spontaneous or provoked by coughing
47
OAB mx
1. conservative - if excessive, reduce caffeine/fluid intake Commence bladder training for at least 6 weeks (void by the clock at regular intervals rather than at desire). Stop smoking and reduce weight. 2. medical - antimuscarinic eg. oxygbutynin or tolterodine 3. Botox lasts for 6 months or sacral nerve stimulation
48
Acute urinary retention
pt unable to pass urine for 12hr; it is painful and catheterisation is maintained for 48hr while the cause is treated
49
Painful bladder syndrome | and interstitial cystitis
PBS = pt experiences suprapubic pain related to bladder filling, accompanied by freq and nocturia, in the absence of proven pathology Interstitial cystitis is confined to pt w painful bladder sx who have characteristic cystoscopic and histological features. Tx = TCA, baldder trainig, analgesics.
50
Endometriosis result of retrograde menstruation
= growth of endometrial tissue outside the uterus; oestrogen dependent therefore regresses after the menopause and during pregnancy accumulated altered blood is dark brown --> chocolate cysts aka endometrioma in the ovaries Endometriosis can cause inflammation, progressive fibrosis and adhesions (serious enough to render all pelvic organs to be immobile!)
51
Endometriosis sx
- Chronic pelvic pain - CYCLICAL - dysmenorrhoea (painful periods) before onset of menstruation...may be relieved by period - DEEP dyspareunia - subfertility - dyschezia (the ectopic tissues can be anywhere!) during menses - subfertility (due to the adhesions! if v severe, may req IVF) Rupture of a chocolate cyst (blood filled sac) can cause acute pain O/E: tenderness and thickening behind the uterus or in the adnexa on VE. Uterus may be retroverted and immobile (due to adhesions)
52
Endometriosis ix
can only be diagnosed w visualisation (laparoscopy) +/- bx. Active lesions are red vesicles or punctate marks on the peritonium. TVUS to exclude ovarian endometrioma MRI to exclude adenomyosis
53
Endometriosis ddx
Adenmyosis Chronic PID Chronic pelvic pain IBS
54
Endometriosis mx
asx --> no tx Can just use analgesics. OR Trial of hormonal drug to suppress ovarian activity (based on the evidence that sx regress during pregnancy [prescribe COCP or progestogens eg, ED pill or IUS], post-menopausally [GnRH analogues induces a temporary menopausal state] or androgenic [danazol but rarely used due to severe SE]). NB/COCP is often taken back-to-back w/o a break to reduce the freq of painful w/d bleeds. MEDICAL TX DOES NOT IMPROVE FERTILITY|!!! Surgical - Ablation (using either diathermy, laser, microwave or balloon) can be used at time of laparoscopy ('see and treat') - this improves fertility! Laser ablation +/- adhesiolysis Other radical surgeries are dissection of adhesions and removal of ovarian endometriomata, or even a hysterectomy w BSO (LAST RESORT - usually if severe and older F!)
55
Progestogens
Progesterone is the natural type of progestogen, which is a class of hormones that also includes all of the other synthetic progestogens
56
systemic progestogen SE
fluid retention erratic bleeding PMS weight gain
57
Chronic pelvic pain
= intermittent or constant pain in lower abdo or pelvis of at least 6 months, not occurring exclusively w menstruation or intercourse - migraine - low back pain Exclude endometriosis, adenomyosis, IBS [trial of antispasmodics], psych factors. Prescribe analgesic. F w cyclical pain --> COCP or GnRH for 3-6 months before diagnostic laparoscopy.
58
Candidiasis/thrush
= infx w Candida Albicans (fungus). NON-sexually transmitted RF = pregnancy, DM, abx use - asx or cottage cheese d/c w vulval irritation and itching - superficial dyspaneuria and dysuria might occur - inflamed and red vagina/vulva tx = topical imidazoles eg.Canesten or oral fluconazole
59
Bacterial Vaginosis (BV)/ Gardnerella/anaerobic vaginosis
= overgrowth of mixed vaginal flora incl anaerobes eg.Gardnerella and mycoplasma hominis. NON-sexually transmitted - grey white d/c - fishy odour (from amines released by bacteria) - vulva and vagina NOT red NOR itchy dx by raised pH, fishy grey white d/c, positive 'whiff' test, clue cells on microscopy tx = metronidazole or clindamycin cream
60
chlamydia trachomatis
= a bacterial infx - usually asx but can cause urethritis and vaginal d/c dx = NAAT or PCR, NOT seen on microscopy chlamydia -> PID (tubal damage, subfertility,chronic pelvic pain) -> Reiter's syndrome (urethritis, conjunctivitis, arthritis) tx = doxycycline or azithromycin
61
Neisseria Gonorrhoeae
= a bacterial infx - usually asx but can cause urethritis, vaginal d/c, bartholinitis, cervicitis dx = gram - diplococcus on microscopy + endocervical swabs gonorrhoeae -> bacteraemia -> acute septic arthritis tx = penicillin, ciprofloxacin, or CEFTRIAXONE
62
Genital warts/Condylomata acuminata
= HPV 6&11 viral infx - can range from looking like tiny flat patches on vulval skin to cauliflower (papilliform) swellings tx = podophyllin or imiquimod cream cryotherapy or electrocautery for resistant warts high reccurence rate
63
Genital herpes
= herpes simplex virus type 2 infx (type 1 causes cold sores) - primary infx w MULTIPLE small PAINFUL vesicles and ulcers around the introitus - local lymphadenopathy - dysuria - systemic sx - reactivation w secondary infx is less painful and preceeded by localised tingling tx = aciclovir
64
Syphilis
= Spirochaete infx by treponema pallidum - primary Syphilis is a Solitary painleSS vulval lucer (chancre) - untreated secondary syphilis may develop weeks later w a rash, flu-like sx, warty genital or perioral growths (condylomata lata) - Latent syphilis follows, as does tertiary/neurosyphilis tx = parenteral (usually IM) penicillin
65
Trichomoniasis
= flagellate protozoan infx of trichomonas vaginalis - offensive grey-green d/c - vulval irritation - superficial dyspareunia - cervicitis w a punctate erythematous 'strawberry' appearance tx = metronidazole
66
genital ulcer causes
``` herpes (HSV type 2) syphilis chancroid (haemophilus ducreyi) lymphogranuloma venereum (subtype of chlamydia trachomatis) donovanosis/granuloma inguinale ```
67
HIV RF NB/ CD4 <200 or development of opportunistic infx/Ca eg.cervical is diagnostic of AIDS
``` multiple sexual partners partners and self from high prevalence countries partner w known HIV status failure to use barrier contraception presence of other UTIs CSW or been paid for sex IVDU sexual contact w high risk men eg.MSM ```
68
Acute pelvic infx or PID RF = younger, sexually active nuliliparous F
is an inflammatory and infectious disease, and is a complication of a sexually transmitted disease; ascending infx of the bacteria in the vagina and cervix - usually chlamydia Endometritis usually co-exists, as might bilateral salpingitis - perihepatitis presents w RUQ pain (due to adhesions) - asx (esp chlamydial) - bilateral lower abdo pain - vaginal d/c - signs of lower abdo peritonism w bilateral adnexal tenderness and cervical excitation - fever, raised WCC and raised CRP
69
Acute PID ix
Endocervical swab for chlamydia blood cultures if signs of infx pelvic USS to exclude abscess or ovarian cyst laparoscopy w fimbrial bx and culture is gs
70
Acute PID tx
1. parenteral cephalosporin eg. IM ceftriaxone 2. followed by doxycyclin/oflaxcin + metronidazole 3. + analegesic febrile pt should be admitted for IV therapy. Pelvic absecess may req draining compl of PID -> abscess formation or pyosalpinx - > tubal obstruction and subfertility, chronic pelvic infx, chronic pelvic pain - > ectopic pregnancy
71
causes of vaginal d/c
``` physiological candidiasis BV atrophic vaginitis cervical eversion and ectropion ```
72
chronic PID
results of untreated/inadequately treated acute PID - dense pelvic adhesions and obstructed fallopian tubes, possibly dilated w fluid or pus - chronic pelvic pain - dysmenorrhoea - deep dyspareunia - heavy and irregular menstruation - chronic vaginal d/c - subfertility - OE similar to endometrosis w abdo and adnexal tenderness and a fixed retroverted uterus tx = analgesics, sometimes adhesiolysis and salpingectomy is required
73
subfertility definition
conception has not occured after a year of regular unprotected intercourse
74
PCOS many PCOS pt have fhx of T2DM: peripheral insulin resistance and insulin incr androgen production.
2 out of 3: o PCO = 12+ follicles in an enlarged ovary, on USS NB/PCO is genetic o irregular periods = >35 days apart o hirsutism = clinically w acne or XS body hair, OR biochemically w raised serum testosterone
75
PCOS sx
- subfertility (one of the PCOS criteria is irregular periods) - oligomenorrhoea oe amenorrhoea - hrisutism (acne or XS body hair) - obesity - - m/c
76
PCOS ix
TVUS Anovulation is investigated w FSH (raised in ovarian failure, low in hypothalamic diesase, normal in PCOS) LH (not much use), TSH low luteal phase progesterone if anovulatory prolactin (to exclude prolactinoma) hirsutism is investigated w serum testosterone levels (raised in androgen secreting tumour or congenital adrenal hyperplasia) fasting lipids and glucose to screen for complications
77
PCOS complications
infertility obesity m/c LONG TERM RISKS T2DM Endometrial Ca (if persistent amenorrhoea/anovulation due to unopposed oestrogen action)
78
PCOS symptomatic tx (other than subfertility)
weight reduction balanced diet COCP will regulate menstruation and treat hirsutism, at least 3-4 bleeds/yr antiandrogen acetate or spironolactone for hirsutism metformin reduces insulin levels therefore reducing levels of androgens and hirsutism
79
Causes of anovulation
PCOS Premature ovarian failure (no ovarian folllicles present; bone protection w HRT or COCP req) hypothalmic hypogonadism (reduction in GnRH release which reduces stimulation of pit gland to produce FSH and LH) - common in AN hyperprolactinaemia (in turn reduces GnRH release) thyroid disease
80
Advice for induction of ovulation
normal weight stop smoking folic acid and risk of multiple pregnancies w ovulation induction tx of specific causes
81
PCOS tx (re: ovulation induction)
1. Clomifene (max 6 month use) - for ovulation induction; = anti-oestrogen at the hypothalamus and pit gland therefore incr release of FSH and LH. Need USS monitoring in case of multiple follicle maturation If clomifene resistance... 2. + Metformin (insulin sensitising drug) 3. gonadotrophins 4. Laparosocopic ovarian diathermy 5. IVF
82
hypothalamic hypogonodism tx (re: ovulation induction)
reduce weight | if weight normal, then gonaotrophins
83
hyperprolactinaemia (re: ovulation induction)
bromocriptine or cabergoline
84
Azoospermia
NO sperm present ix = examine for presence of vas deferens, check karyotype eg.Klinefelter's 47XXY, CF, hormone profile tx = surgical sperm retrieval then IVF + ICSI or donor insemination
85
Oligospermia
reduced sperm count tx = intrauterine semination, IVF +/- intracytoplasmic sperm injection (ICSI)
86
Asthenospermia | astheno = w/o strength
poor motility sperm
87
Teratospermia | terato = monster
morphologically defective sperms
88
leucospermia
infection
89
semen analysis
last ejaculation 2-7 days ago if abnormal, repeat after 70 days, examine the scrotum, reduce smoking, drinking, drug use eg.sulfasalazine for RA or anabolic steroids reduce exposure to industrial chemicals wear loose clothing and testicular cooling
90
Causes of fertilization failure
tubal damage - infx eg.PID from chlamydia --> adhesiolysis and salpigostomy (incr rate of ectopic!) - endometriosis --> laparoscopic surgery to remove endometriotic deposits - adhesions from surgery cervical problems sexual problems
91
Detection of tubal damage in subfertility
1. Firstly hysteroscopy needs to be performed first to assess the uterine cavity for abnormalities 2. Laparoscopy and dye test allows visualisation and assessment of fallopian tubes. methylene blue dye is injected through the cervix from the outside and can see if it enters or spills from the tubes to test if they are patent 3. hysterosalpingogram - w/o anaesthetic radio-opaque contrast is injected through the cervix to look for spillage using XR. A variant of this is HyCoSy where TVUS and US opaque liquid is used instead, reserved for F w no RF for tubal disease
92
Indications for assisted conception
``` when all other methods have failed unexplained subfertility male factor subfertility [ICSI] tubal blockage [IVF] Genetic disorders ```
93
Assisted conception methods
``` intrauterine insemination IVF intracytoplasmic sperm injection oocyte or sperm donation surrogacy ``` can offer preimplantation genetic diagnosis to >37yo F
94
Complication of assisted conception
Superovulation leading to multiple pregnancies egg collection can lead to intraperitoneal haemmorhage and pelvic infx incr risk of ectopic preg
95
PCOS tx overview
if infertility --> clomifene, +metformin, ovarian diathermy, , gonadotrophins, IVF if menstrual problems --> COCP if acne/hirsutism --> cosmetic tx, COCP +/- cyproterone acetate, spironolactone, eflornithine facial cream
96
Common progestogenic SE
``` BREAST TENDERNESS mood changes like depression erratic bleeding or amenorrhoea acne weight gain reduced libido ```
97
Common oestrogenic SE
nausea headache BREAST TENDERNESS fluid retentino and weight gain
98
COCP missed pill rule
vomit w/i 2hr --> take another pill and follow MPR severe diarrhoea --> continue pills and follow MPR MPR = one or two missed pills anywhere in the cycle is ok. take the missed pill asap, even if 2 at the same time. then continue the pack as normal. if more than 2 pills missed then use condoms for 7 days.
99
COCP and pre-op
stop 4 weeks before surger due to prothrombotic risks
100
COCP complications
``` VTE CVA - MI and strokes HTN focal migraines jaundice liver, cervical and breast Ca ``` risk is increased by smoking, incr age and obesity
101
absolute CI to COCP
* hx of VTE * inherited thrombophilia * >35yo smoker >15/day * BMI>40 * DM w vascular complications * hx of MI/stroke, IHD, severe HTN * migraine w aura * active breast/endometrial Ca * active/chronic liver problems
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Relative CI to COCP
``` age >40yo chronic inflammatory disease renal impairment, DM BMI 35-40 BF and upto 6 months post partum (because lactation is partly suppressed so the piil in CI in puperium is relative CI upto 6 months post partum) ```
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common minor SE to COCP
nausea, headache, BREAST TENDERNESS | breakthrough bleeding in firth few months but tends to settle shortly
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Benefits to COCP
3 per 1000 women get pregnant regular, less painful and lighter periods improves acne and hirsutism protects again ovarian, endometrial and bowel Ca
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POP (progestogen-only pill)/ED pill/ mini pill An alternative to COCP because no CI ;D
same time every day w/o a break common SE: period changes (erratic or amenorrohoea), weight gain, mood changes eg.depression or PMS, breast tenderness MPR = take next one as soon as possible. if >3hr late, use condoms for 2 days
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complications of intrauterine devices
E and the 6P's expulsion - usually w/i 1st month Perforation - of uterine wall at time of insertion Pain Period changes - heavier or more painful (except w progestogenic devices) PID incr risk Pregnancy more like to be ectopic
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Progestogenic effects on period...
LIGHTER! But may be heavier or more erratic
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Absolute CI to intrauterine devices
Endometrial or cervical Ca undiagnosed PV bleed Active/recent pelvic infx current breast Ca (for progestogenic IUS only)
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Relative CI to intrauterine devices
Previous ectopic preg young/nuliparous immunocompromised incl HIV +ve
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Depot progestogens
IM depo-provera every 3 months S= progestogenic + prolonged amenorrhoea and reversible bone loss
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IUD
prevents implantation can be kept in upto 10 years, but replaced b/t 5-10yr
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cause of PMB
``` endometrial Ca endometrial hyperplasia +/- atypia and polyps cervical Ca atrophic vaginitis cervicitis ovarian Ca Cervical polyps ```
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menopause Premature menopause
permanent cessation of menstruation; 12 consecutive months of amenorrhoea premature if <40yo
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PMB ix
bimanual speculum cervical smear TVUS
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Early menopause effects
Psychological sx eg.depression, mood swings | vasomotor sx eg.hot flushes, night sweats --> sleep disturbance,
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Intermediate menopause effects
skin atrophy hair thinning vaginal atrophy can cause burning, itching or pain during sex urinary sx eg.freq, urgency, nocturia, recurrent infx
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Late menopause effects
CVA eg. MI and strokes (due to oestrogen deficiency) and cardiac disease osteoporosis ie. weak bones that predispose to an incr risk of fracture (osteopenia = weak bones)
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RF for osteoporosis development
``` FHx of # low BMI Early menopause (due to oestrogen deficiency) cigarette smoking ETOH abuse Low Ca intake Corticosteroids disease eg.PA, malabsorption syndromes, hyperthyroidism ```
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ix in menopause
raised FSH = few oocytes left May consider TFT as thyroid disease can cause hot flushes. Catecholamines and 5-hydroxyindolacetic acid to dx chromocytoma and carcinoid syndrome. Low progesterone may be secondary to PCOS, DEXA scan for bone density.
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Menopause tx - oestrogen and oestriol, oestradiol (natural oestrogens) - ethinyl oestradiol (synthetic oestrogen) - progestogens eg.levonorgestrel, norethisterone - tibolone = inert synthetic steroid that is is converted in vivo. For F who want amenorrhoea and treat vasomotor, psychological and libido problems
oestrogen only in F who have no uterus oestrogen PLUS PROGESTERONE (to protect uterus lining from endometrial Ca) in F w uterus PO (tablets), transdermally (patch or gel), SC (implant) NB/ progesterone still need to be given to F who had endometrial ablation as not all had been removed, Progestogen can be given sequentially (regular bleeds) or continuously. (amenorrhoea) Perimenopausal -->cyclic HRT Menopausal --> continuous HRT
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HRT pros and cons
Temporarily treats menopausal sx, protects against osteoporosis, reduces urinary sx, improves hair and skin BUT oestrogenic and progestogenic SE, incr risk of breast Ca and VTE
122
Disorders of early pregnancy
``` Spontaneous m/c Recurrent m/c TOP Ectopic preg Hyperemesis gravidarum Gestational trophoblastic neoplasia ```
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Threatened m/c
bleeding but foetus is alive uterus is size expected from the dates os is closed
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inevitable m/c
heavy bleeding foetus may still be alive os is open ie.m/c is about to occur
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incomplete m/c
os is open bleeding might have happened but gradually stopped now. And while some foetal parts have passed there is still some remaining
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complete m/c
all foetal tissues have passed, no evidence of foetus in uterus uterus is no longer enlarrged bleeding has diminished os is closed
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septic m/c
= contents of uterus are infected causing endometritis offensive vaginal loss, tender uterus, absent fever abdo pain and peritonism if pelvic infx
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missed m/c
= "foetus has not developed in utero, but this is not recognised until bleeding occurs or USS is performed." uterus small than expected closed os
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Mx of spontaneous m/c NB/ if infx becomes systemic, endotoxic shock occasionally ensues w hypoT, renal failure, ARDS and DIC Lon term conception rates do not differ b/t the m/x options
admission to ix resus may be required if XS bleeding RPOC in cervical os cause pain, bleeding and vasovagal shock and are removed via a speculum using forceps IM ergometrine to reduce bleeding (by contracting the uterus, but is only used if foetus is non-viable) swabs if ?infx A) expectant - w/i 2-6 weeks. large intact sac ass/w low success rate B) medical - prostaglandin, sometimes preced by antiprogesterone mifepristone C) surgical - evacuation of RPOC under anaesthetic using vacuum aspiration Go for ERPC if heavy bleeding or infx!
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Counselling after m/c
"not result of anything they did or did not do and it could not have been prevented" "I would like to reassure you that there is a high chance of successful further pregnancies" "Refer you to support groups for emotional support" "m/c is unfortunately v common and further ix are reserved for F who have had 3+ m/c"
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recurrent m/c (3 or more in succession)
serial USS in early preg for reassurance emotional support is vital ANTIPHOSPHOLIPID AB SCREEN (causes thrombosis in the placental circulation)- tx w aspirin and LWMH Karytype both parents for chromosomal defects Pelvic USS and hysterosalpingogram for uterine abnormalities
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Grounds for TOP
A. Continuing preg involves risk to pregnant mother B. to prevent grave permanent physical or MH injury to mother C. pregnancy <24wk and pregnancy would involve risk or injury to pregnant mother D. preg <24wk would involve risk or injury to existing children E. susbstantial risk that if child was born, it would suffer from physical or mental abnormalities
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Methods of TOP o Remember to take bloods for Hb, blood group, rhesus status and haemoglobinopathies o Rhesus -ve F to receive anti-D w/i 72hr of TOP o screen for chlamydia o discuss contraception
[<7wk, but also 7-9/52] mifepristone (antiprogesterone) + misopristol or gemporst (PG analogues) 2 days later [7-13/52] --> Suction curretage [13+/52] --> dilatation and evacuation (D&E), preceded by cervcal preparation [13-24/52] --> medical abortion as in early stage [22+/52] --> feticide (= KCl into umbilical vein/foetal heart to prevent live birth).... usually only if there is foetal abnormality
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complications of TOP
- haemorrhage - infx - uterine perforation - failure
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ectopic preg aetiology
no cause is evident but any factor which damages the tubes can cause fertilised oocytes to be caught eg.PID from Chlamydia, assisted conception or pelvic/tubal surgery
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Ectopic sx
scanty dark PV bleed lower abdo pain (initially colicky as the tube tries to extrude the sac, and then becomes constant) collapse and shoulder tip pain suggests intraperitoneal bleed +ve PT amenorrhoea of 4-10weeks O/E rebound tenderness, cervical motion tenderness, maybe tender adnexa uterus is smaller than expected closed os
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ectopic ix
``` hCG PT serum hcG (should be visible if >1000, if lower but rises by more than 2/3 in 48hr then probably an early intrauterine preg, declining/slow rising/pleateauing = non-viable preg or ectopic. USS (if intrauterine preg is not present, could be <5/40, complete m/c or ectopic ```
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Mx of symptomatic ?ectopic Ectopics must be followed up until hcG <20IU/ml to confirm complete resolution
``` Admit NBM FBC & cross-match IV access PT, USS, serum hcG ```
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Tx of ?ectopic
laparoscopy/laparotomy --> during which you do either a salpingectomy or salpingostomy if criteria met... o unruptured ectopic w no cardiac activity o hcG < 3000 Can treat medically w methotrexate if ectopic is..... - small and unruptured - location of pregnancy is not clear (not visualiesd in uterus or adnexae) - hcG <1000 and decling Can conservatively observe as rupture is unlikely
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Hyperemesis gravidarum mx o usually multiparious F o seldom persists beyond 14wk
exclude multiple and molar pregnancy | IVF w antiemetics and thiamine
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gestational trophoblastic neoplasia 2 forms of hyadatidiform mole: complete (entirely paternal origin = sperm + empty egg) and partial (triploid = 2 sperm + 1 egg). If the proliferation is only in the uterus is it an invasive mole, if metastases then it is a choriocarcinoma
- (heavy) PV bleed - severe vomitting - large uterus - early pre-eclampsia and hyperthyroidism - snowstom appearance (of swollen villi w complete moles) on USS - V.high hCG - persistent or rising
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mx of trophoblastic disease NB/ molar preg only precede 50% malignancies as the rest are preceded by miscarriages
1. trophoblastic tissue is removed by suction curretage (ERPC) 2. Remember to register w supraregional centre for F/U. Pt are scored into low risk [give methotrexate] and high risk [combination chemotherapy] according to prognostic variables. 3. Avoid preg and COCP until hCG levels are normal because may incr the need for chemo.
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Types of hysterectomy
TAH = removal of uterus and cervix through abdo incision Laparoscopic hysterectomy is an alternative to TAH vaginal hysterectomy = removal of uterus and cervix after incising the vagina from below Wertheim's radical hysterectomy = removal of parametrium, upper 1/3 of vagina and pelvic L. Usually Wertheim's is performed for stage 1Aii - stage 2 cervical carcinoma
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complications of hysterectomy
immediate: haemorrhage, bladder or ureter damage post-op: VTW, pain, infx long term: prolapse, stress incontience, pain, psychosexual problems
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Dilatation and curettage (D&C)
cervix is dilated and endometrium is scraped to bx it. D&C is a diagnostic procedure not commonly performed
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ERPC
cervix is dilated and retained non-viable foetus or placental tissue is removed using a suction curette (=scrap). similar procedure used for surgical TOP <12/40
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large loop excision of the transformation zone (LLETZ)
involves using cutting diathermy under LA to remove the transformation zone of the cervix where CIN is present
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cone bx
= removal of transformation zone PLUS much of the endocervix by making a circular cut w a scalpel in the cervix, under epidural or spinal a tx option for stage 1Ai Risk: cervical incompetence
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operation for fibroid
myomectomy - done through the cervix or abdominally Uterine A embolisation - alternative to hysterectomy for F who want to preserve fertility
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Estimation of gestational age
1. from LMP 2. [7-14/40] - measure crown rump length (if >1wk dif b/t LMP and scan, use scan) (3. [14-20] - biparietal diameter or femur length if no early scans or LMP known) measurements to calculate gestational age are of little use beyond 20 weeks
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common causes of polyhydramnios
GDM/DM foetal abnormalities ie.not swallowing or XS urination idiopathic
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obstetric abdo exam
1. general appearance, looking for any swelling of ankles and face, possible anaemia areas assessed. 2. Ask for BP and urinalysis 3. Now ask pt to lie flat, semi prone if big belly uterus is palpable at 12-14/40. At 20wk the fundus is at the umbilicus. At sternum at 36wk. 4. inspect the pregnant uterus for striae, linea nigra and scars, esp in the suprapubic area 5. palpate the fundus using the ulnar border. Measure symphysis-fundal height if >24wk 6. palpate foetal parts (head is ballotable b/t two hands (breech is softer and less easy to define and cannot be balloted), back is firm) and estimate the liquor volume If fingers need to dip in far to feel anything, ?polyhydramnios 7. lie [= relationship b/t foetus and long axis of uterus] THIS POINT CAN SAY IF IT IS A SINGLETON OR NOT 8. presentation - breech VS head 9. station/engagement of head - more than 2/5 palpable means not engaged "my aim is to determine whether majority of the head lies in the abdomen or the pelvis" 10. auscultate over the ant shoulder w pinard's stethoscope, should be ~110-160bpm
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antenatal care schedule
1. booking visit at 9-11wk 2. booking scan at 11-13wk; to confirm gestation and viability, and diagnose multiple pregnancy. ALSO chromosomal screening [nuchal translucency, hCG, PAPPA) 3. anomaly scan at 20wk; to detect structural foetal abnormalities. Doppler of uterine A can be used as screening test for IUGR and PE
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Booking bloods
- FBC - for pre existing anaemia - Ab screen eg.Anti-D - identify risk of intrauterine isoimmunisation - Blood glucose - blood test for syphilis. HIV and hep B counselling and screening - rubella immunity - vaccination offered postnatally if req - urinalysis for glucose, protein and nitrites - MC&S - for asx bacturaemia - screen for infx implicated in preterm labour eg.chlamydia, BV - Hb electrophoresis in F at risk of sickle cell anaemia (Afro-carribean) or thalassaemia (mediterranean)
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pregnancy health promotion
- continue meds and ideally adjusted pre-conception - folic acid supplementation, Vit D if minimal exposure to sunlight - coitus is not CI unless proven placenta praevia - avoid ETOH and smoking - reduce risk of infx by only drinking pasteurised milk, avoid soft and blue cheeses, pate and uncooked or partially cooked food - exercise is advised - traveling - risk of VTE is reduced by adequate hydration and compression stockings - additional antenatal classes
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Common 'minor' conditions of pregnancy
``` o itching o symphysis pubis dysfx o heartburn o backache o constipation o ankle swelling o leg cramps o carpel tunnel syndrome o vaginitis due to candidiasis ```
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physiological changes
weight gain, icr blood vol and RBC, but reduced Hb. WCC incr, incr CO and reduced peripheral resistance. incr tidal vol and no change in RR incr renal blood flow so Cr/urea decr delayed gastric emptying thyroid enlargement
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Klinefelter's syndrome
47XXY normal intellect small testes and infertile
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Turner's syndrome
45XO normal intellect infertile
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Structural abnormalities - neural tube defect. Most common NTDs are ... Reduce risk by... NTD is suggest by...
spina bifida and anencephaly Reduce risk by preconceptual folic acid supplementation for 3 months Raised AFP levels and 20 week anomaly scan
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Structural abnormalities - cardiac abnormalities most common cardiac defect is... RF...
VSD more common in F w congenital cardiac disease, DM and prev children w cardiac disease 20 week anomaly scan
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Polyhydramnios Sx: maternal discomfort, large for dates, taut uterus, foetal parts difficult to palpate aietiology: idiopathic, twins (esp twin-twin syndrome), maternal disorders (eg.renal failure, DM), foetal disorders (eg.upper GI obstructions, inability to swallow, myotonic dystrophy)
= XS amniotic fluid (liquor pool >10cm) complications of polyhydramnios: - preterm - abnormal lie and presentation mx: 1. reduce liquor --> if <34/40 and severe then perform amnioreduction OR use NSAIDs to reduce foetal urine output 2. steroids if <34/40 and can deliver vaginally
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Exomphalos
= partial extrusion of abdo content within the peritoneal sac Remember to offer amnio as commonly linked to chromosomal defects
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Gastrochisis
= free loops of bowel in the amniotic cavity
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Diaphragmatic hernia
= abdo content herniate into chest many neonatal deaths eg. from pulmonary hypoplasia
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foetal hydrops
= XS fluid accumulation in 2 or more areas in the foetus Can be immune (due to anaemia, haemolysis due to rhesus) or non-immune secondary to another cause (chromosomal abnormalities, structural abnormalities, cardiac abnormalities, cardiac failure due to anaemia eg.Parvovirus, twin-twin transfusion syndrome)
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ix of foetal hydrops mx depends on the cause
USS, specialist cardiac scan and assessment of middle cerebral A Maternal blood tested for Kleihauer and parvovirus immunoglobulin M testing FBS if ?anaemia amniocentesis for karyotyping
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pregnancy infx suitable for screening
Syphilis, HIV, hep B Rubella + chlyamydia, BV, beta-haemolytic strep
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TORCH syndrome is a group of 5 infectious diseases that are screened for prenatally
``` Toxoplasmosis (teratogenic) Others eg.syphilis (teratogenic) Rubella (teratogenic) CMV (teratogenic) Herpes ```
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prevention of vertical transmission of group B strep
IV penicillin in labour
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mx (and prevention of vertical transmission) of HIV in pregnancy
``` maternal antiretroviral therapy elective CS avoid BF neonatal antiretroviral therapy for 6 weeks screen for other infx ``` if poor resources then nevirapine during labour and for BF...
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CMV in pregnancy
maternal dx from IgM, IgG (foetal dx from amniocentesis at 20+ wk - not advised because most aren't seriously affected) ``` 10% of neonates are sx at birth: o severe neuro problems eg. DEAFNESS (even asx neonates are at risk of DEAFNESS), visual and mental impairment o IUGR o pneumonia o thrombocytopenia ``` no treatment, screening or vaccination
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Rubella aka German measles in pregnancy Rubella in children causes a mild febrile illness w macular rash
if <16/40, offer TOP High % of foetuses are affected o deafness o cardiac disease o eye problems o mental impairment screening identifies those in need of postnatal immunisation (as it is live therefore cannot be given during pregnancy)
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Toxoplasmosis during pregnancy caused by TOXOPLASMA GONDII following contact w cat faeces, soil, or eating infected meat. more common in mainland Europe screening not routine in UK
maternal dx from IgM foetal dx from amniocentesis at 20+ wk. USS may show hydrocephalus o mental impairment o convulsions o spasticity o visual impairment Mx: proven toxoplasmosis treated w spiramycin asap foetal toxoplasmosis treated w combination therapy
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Syphilis in pregnancy caused by treponema pallidum
o m/c or still birth o severe congenital disease prompt tx w benzylpenicillincan prevent congenital syphilis
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Herpes simplex virus (HSV) during pregnancy
neonatal infx is rare but motality high risk of neonatal herpes if primary infx w/i 6 weeks of delivery or active vesicles at time of labour (therefore CS is indicated) o mother will have typical clinical sx mx: screening is of little benefit 1. refer to GUM 2. CS indicated if primary infx w/i 6 weeks of delivery or active vesicles at time of labour (therefore CS is indicated) 3. daily aciclvir in late preg? NB/ the risk is v low for F w recurrent herpes
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Group B strep during pregnancy
foetus can be infected during labour after ROM RF = preterm, prolonged labour, maternal pyrexia ix: positive 3rd trimester screen mx: know GBS carriers (high maternal carrier rate!) and those at high risk are given high dose IV penicillin throughout labour
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Herpes zoster during pregnancy
severe maternal illness in pregnancy can be teratogenic infx 4 weeks prior to delivery can cause severe neonatal infx mx: immunoglobulins are given to prevent if non-immune oral acyclovir given to treat give neonatal immunoglobulin if delivery was near time of infx
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Hepatitis B during pregnancy
universal screening identifies neonates in need of immunoglobulin the child may become a carrier of hep B
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CHLAMYDIA in pregnancy
o neonatal conjunctivitis o preterm labour chlamydia is treated w azithromycin or erythromycin gonorrhoea is treated w cephalosporin (as commonly resistant to penicillin)
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BV in pregnancy | = overgrowth of normal vaginal lactobacilli by anaerobes eg.Gardnerella vaginalis and mycoplasma hominis
ass/w preterm labour and late m/c screening and if previous preterm or positive BV infx <20/40 --> oral clindmycin
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parvovirus [slapped cheek + arthralgia]
can lead to foetal death if infx < 20/40 o foetal anaemia o hydrops if IgM positive, surveillance for anaemia w middle cerebral A Doppler and US
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HIV in pregnancy
can lead to stillbirth, pE, IUGR and prematurity mx: regular CD4 and viral load tests if low CD4 --> prophylaxis against pneumocystic carinii pneumonia (PCP) screen for other STIs, esp CHLAMYDIA
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Assessment of foetal anaemia
Only severe anaemia is detectable as foetal hydrops or XS foetal fluid ix: doppler US of foetal MCA (used fortnightly in at risk pt) --> if suspicious, do FBS [risk of foetal loss, if done after 28 wk, need to be in a place w facilities for immediate delivery if complications arise] tx = in utero transfusion until 36 weeks, at which delivery should be done
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Potential sensitising events
``` TOP or ERPC after m/c Ectopic PV bleeding <12/40 or heavy PV bleed ECV amniocentesis or chorionic villus sampling Intrauterine death Delivery ```
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RBC isoimmunisation
production of maternal anti-D can be prevented by administration of exogenous anti D which 'mops up' foetal RBC that have crossed the placenta
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Prevention of rhesus disease
Anti-D 500 for all rhesus negative F at 28 and 34 week, and postnatally if baby was rhesus postive Anti D w/i 72hr of any sensitising event Kleihauer test performed postnatally to assess no of foetal cells in the maternal circulation (to detect larger feto-maternal haemorrhages)
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pre-eclampsia is due to blood vessel endothelial damage in ass/w an exaggerated maternal inflammatory response --> vasospasm, incr capillary permeability and clotting dysfx dx = >140/90 PLUS >0.3g OR 30mg proteinuria/24hr
vasospasm --> headache incr vasc resistance --> HTN incr capillary permeability --> proteinuria clotting dysfx reduced placental blood flow --> IUGR reduced cerebral perfusion --> drowsiness, visual disturbance, N&V, eclampsia
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Degree of PE
mild: proteinuria + <170/110 mod: proteinuria + 170+/110 severe: <32weeks or w maternal complication
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RF for PE
``` nulliparity prev hx, FHx older mum chronic HTN DM twin pregnancy AI disease renal disease obesity ```
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assessment of urinary protein
1. bedside urinalysis 1+ proteinuria (nb/trace is usually insignificant!) 2. protein:Cr ratio >30mg/mmol 3. 24hr collection > 0.3g/24hr confirms PE
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Haemolysis signs
dark urine raised lactic dehydrogenase (LDH) anaemia
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Elevated liver enzymes
Epigastric pain liver failure abnormal clotting
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Low platelet
normally self limiting
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Complications of PE
maternal - eclampsia - CVA - coagulation problems (HELLP) and DIC - liver and renal failure foetal - IUGR - preterm - placental abruption - hypoxia
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ix if ?PE
MSU urine protein measurement full set of bloods
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screening
observation of high risk, uterine A doppler nb/ aspirin has limited role
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mx of PE
assess all women w new HTN >140/90 in ANDU A) no proteinuria and <170/110 are managed as OP, BP and urinalysis repeated twice/week. USS fortnightly B) if 1+ proteinuria only, then quantification and subsequent r/v 2 days later ``` C) criteria for admission: o symptomatic o 2+ proteinuria on dipstick or >0.3g/24hr o mod/severe PE o ?foetal compromise ``` AntiHTN if BP reaches 17/110. - Methyldopa is best of maintenance but causes drowsiness - oral nifedipine for initial control w IV labetalol as second line w severe HTN - MgSO4 (incr cerebral perfusion) used for tx of eclampsia Steroids are given if risk of preterm DELIVERY: USUALLY CS, CONTINUOUS CTG MONITORING. 1) mild HTN w/o foetal compromise --> monitored for deterioration. Induction of labour at term 2) Mod or severe HTN --> deliver if >34-36wk. if <34wk, steroids and observe in a specialist unit until labour w daily CTG and assessment and freq blood testing 3) severe PE w complcications or feotal distress --> immediate delivery NB/ergometrine can incr BP therefore use oxytocin for active mx of 3rd stage
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postnatal PE care
bloods esp liver enzymes, platelets and renal fx fluid balance monitoring due to ?pulm oedema nad ?resp failure BP measurement and treated for several weeks w b-blocker. 2nd line is nifedipine and captopril.
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mx of essential HTN
change from ACEi and b-blockers to 1st line = methyldopa, 2nd line = nifedipine
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GDM aietiology
placenta affects glucose tolerance (pregnancy is 'diabetogenic') plus lower threshold for excreting glycosuria so develop GDM
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GDM RF
``` prev hx of GDM or FHx PCOS previous baby >4kg unexplained stillbirth obesity (>100kg) polyhydramnios persistent glycosuria ```
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Complications of GDM
maternal - hypoglycaemia (rarely ketoacidosis) - PE - infx - incr chance of instrumental or operative delivery
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mx of GDM
Anomaly and cardiac US induction/LSCS by 39 WEEKS unless v well controlled 1. lifestyle 2. metformin 3. insulin pt education glucose monitoring and insulin adjustment anomaly and cardiac US and foetal surveillance
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pre-conceptual care of F w DM
assess renal fx, BP and retina optimise glucose control prescr folic acid 5mg/day
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Cardiac diseases in preg
A) mild abnormalities eg.mitral valve prolapse, PDA, VSD, ASD do not cause complications B) PULMONARY HTN EG.EISENMENGER'S SYNDROME is CI in pregnancy and usually terminated due to 40% mortality rate C) aortic stenosis and mitral valve disease should both be corrected before getting pregnant
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criteria for Antiphospholipid syndrome
1 death > 10wk IUGR 3 deaths <10wk VTE LUPUS/Anti-lupin Ab mesure on 2 occasions 3 months apart Common complic incl recurrent m/c, IUGR and PE tx= aspirin + LMWH; serial USS and elective induction of labour by TERM. Then post natal anticoagulation is recommended to prevent VTE
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``` VTE risks (pregnancy is a prothrombotic state due to incr blood clotting factors, reduced fibrinolytic activities, altered blood flow by mechanical obstr and immobility) ``` ?PE --> CT or VQ scan ?DVT --> doppler exam leg and venogram mx of VTE: WARFARIN IS TERATOGENIC! Antenatal VTE prophylaxis w LMWH + aspirin is only for F w very high risk But post partum VTE is the cause of most maternal deaths... 6 week of LMWH post partum if previous or strong FHx of VTE, known prothrombotic tendency, CS performed, or 3+ mod RF o >35yo o high parity o obesity o immobilty or major current illness o gross varicose veins o PE o infx high risk VTE ==> 1 week of LMWH
prothrombotic disorders - activated protein C resistance - prothrombin gene variant - protein S and C deficiency - antithrombin III deficiency pre-existing - Previous VTE - FHx of VTE - thrombophilia - incr age/parity - maternal illness - obesity pregnancy related - CS - prolonged labour - severe haemorrhage - hyperemesis - immobility
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Anaemia in pregnancy
- Sickle cell disease in Afro-Carribbeans. Incr perinatal mortality, thrombosis and sickle crises. Mx = exchange transfusion, folic acid, avoid iron. Can test partner and offer prenatal dx if carrier - thalassaemia in south-east asians (beta in mediterranean). Mx = folic acid, avoid iron. Can test partner and offer prenatal dx if carrier - only treat IDA if <11 - reduced MCV, MCH and ferritin - Folic acid deficiency anaemia is v rare
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dietary advice to avoid anaemia
food rich in iron - meat esp kidney and liver - eggs - green veg food rich in folic acid - lightly cooked or raw green veg - fish
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Preterm prevention
A) cervical incompetence (short or v scarred/not strong enough). cervical stitch is only suture if sig shortened, hx of RF suggestive of cervical weakness and electively at 12-14wk B) infx eg.BV, STI, UTI C)foetal reduction offered at 10-14wk D) tx of polyhydramnios E) progesterone suppositories from early preg
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mx of preterm labour can give birth vaginally (reduced risk of resp distress syndrome) but a lot are in breech so many are CS. otherwise the normal CS reasons applies. VENTOUSE IS CI IN PRETERM. give abx for delivery to preterm due to risk of GBS
steroids give once b/t 24-34 weeks. As steroids take 24hr to act, delivery is often artificially delayed using tocolysis eg.nifedipine or atosiban (oxytocin receptor antagonist) but these should not be used for >24hr Remember to call the paediatrician
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Chorioamniocentesis sx mx: immediate delivery whatever the gestation
``` o contractions or abdo pain o fever o tachycardia o uterine tenderness o coloured or offensive liquor ```
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PPROM complications ix: to look for infx, perform HVS, FBC, CRP foetal well-being assessed w CTG
principle complication is preterm delivery | chorioamnionitis = infx of foetus or placenta ... this could have been the cause!
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PPROM presentation AVOID VE But sometime performed to exclude cord prolapse IF the presentation is not cephalic
o gush of clear fluid, followed by further leaking | o pool of fluid in the posterior fornix
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APH (=bleeding after 24wk) causes
common - unknown - placental abruption - placenta praevia rarer - uterine rupture - vasa praevia
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2 x types placenta praevia: marginal major
marginal placenta praevia = placenta in lower segment, NOT over the os major placenta praevia = placenta completely or partially overlying the os
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RF for placenta praevia NB/ a lot of 'low-lying' placenta at 20weeks but only 1 in 10 become praevia at term. USS repeated at 34wk to exclude praevia
twins high parity older F if uterus is scarred
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complications of placental praevia
C section req (if placenta implants in a prev CS scar it may be so deep as to prevent placental separation = placenta accreta or even penetrate the uterine wall into surrounding structures eg.bladder = placenta percreta) haemorrhage may be severe and prolonged after delivery, worsened by placenta accreta and placenta percreta because the lower segment is less able to contact --> may need hysterectomy
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placenta praevia sx
intermittent PAINLESS bleeds - incr in freq and intensity over weeks breech presentation transverse lie foetal head is high and not engaged
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placenta praevia mx
PV bleed --> admission, USS to confirm --> stay until delivery because of risk of massive haemorrhage asx placenta praevia, admission can be delayed until 37 week THEN elective CS at 39weeks. inflatable balloon or hysterectomy commonly needed for placenta accreta
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RF for placental abruption
- IUGR - PE - AI disease - maternal smoking - cocaine usage - prev hx of placental abruption - multiple preg - high parity - trauma and ECV
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placental abruption sx V. high foetal mortality rate
constant painful bleeding w exacerbation - inconsistent to level of shock tachycardia (+/- hypoT) tender and contracting, hard woody uterus difficult to palpate foetus
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ix in placental abruption
CTG FBC, coag screen, cross-match, U&E early delivery w blood products ready
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mx of placental abruption
admit on the basis of PAIN + UTERINE TENDERNESS (even w/o PV bleed) foetal distress --> urgent LSCS no foetal distress + term --> IOL w amniotomy. If foetal distress ensues then go for LSCS foetal death --> labour induced and blood products given (high chance of coagulopathy)
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ruptured vasa praevia -painless moderate pv bleed at amniotomy/ROM + severe foetal distress CS usually isn't fast enough to save foetus
vasa praevia = vessels running in the membrane in front of os/presenting part (usually when the um cord attaches to the mem rather than the placenta)... when the mem ruptures, vessels may rupture too w massive foetal bleeding
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uterine rupture
usually in F w scarred or congenitally abnormal uterus
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?small for date VS ?IUGR
serial measurements of symphysis-funal height BP and urine check due to ass b/t IUGR and PE serial USS serial umbilical A doppler - oligohydramnios w foetal redistribution --> 'head sparing'
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mx of SFD or IUGR
SFD --> recheck growth fortnightly SFD+abnormal doppler values --> delivery if >36wk, preterms req r/v w um A doppler at least twice a week to weigh out risks and benefits. Admit if absent end-diastolic flow
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1st degree tear
injury to perineal skin only mx: no need to suture unless haemostasis is a problem
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2nd degree tear
injury to perineum involving perineal muscles only w/o involvement of anal sphincter mx: need to be sutured to ensure correct appoistion of perineal muscles and skin, by m/w
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3rd degree tear 3A 3B 3C
injury to perineum involving anal sphincter mx: sutured in theatre w adequate analgesia, by obs reg+ anal sphincter must be repaired to avoid incontinence 3A <50% external anal sphincter torn 3B >50% EAS torn 3C BOTH EXTERNAL AND INTERNAL anal sphincter torn
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4th degree tear
involving anal spincter AND anal epithelium mx: sutured in theatre w adequate analgesia, by obs reg+ and general surgeon if req
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RF of ob anal injury 3rd and 4th degree tears can lead to faecal incontinence if not recognised
``` >4kg bb persistent occipoposterior position nulliparity IOL epidural prolonged 2nd stage >1hr shoulder dystocia midline episiotomy instrumental delivery ```
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Multiple pregnancies... Maternal risks: incr surveillance for anaemia, GDM and pe Most common foetal compl: preterm and IUGR and late m/c
aetiology incl: assisted conception, fhx, incr maternal age, parity present w vomiting more marked in early preg, larger uterus and palpable before 12 week
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Twin-twin transfusion syndrome
the 'donor' is volume depleted --> anaemia, IUGR, oligohydramnios 'recipient' gets fluid overloaded --> polycythaemia, cardiac failure, polyhydramnios
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Selective reduction for triplets+ discussed at 12 weeks (after booking at 11-13?)
incr early m/c rate but reduces chance of preterm (and therefore CP) reduction not advised from twins to singleton
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method of multiple delivery
vaginal if first baby is cephalic | induction/CS at around 37-38 weeks (after which time perinatal mortality is increased)
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mechanism of labour: POWER
once in established labour, uterus contracts for 1 min, every 2-3mins --> pulls the cervix up (effacement) there may be poor uterine contractility in nuliparous F
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PASSAGE and stations
pelvic inlet: transverse diameter of 13cm mid-cavity: AP diameter of 11cm hence the internal rotation pelvic outlet: AP diameter 12.5cm station 0 = head is at level of ischial spine station +2 = 2cm below ischial spine station -2 = 2cm above ischial spine
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PASSENGER and attitude and position NB/ presenting part is either cephalic or breech
attitude = degree of flexion of the head on the neck. maximal flexion is called vertex (feel more of the posterior Y fontanelle) extension is called brow (anterior 3 way fontanelle is more central) hyperextension is called face (face feel features of the face) NB/the sagittal suture runs b/t ant and post fontanelles position = degree of rotation of the head: occipito -transverse/anterior/posterior
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Movements of the head
1. engagement in occipito-transverse (OT) entering the pelvic inlet as the transverse diameter is longest 2. desent and flexion (measured by station) 3. rotation 90o to occipito-anterior position in midcavity as transverse and AP diameters are both 11cm therefore like a square and longest diameter is the diagonal one... 4. then it ends in occipito-anterior position in the outlet as the AP diameter is longest 5. descent and extension to delivery 6. restitution: head externally rotates 90o to enable... 7. delivery of anterior --> posterior shoulders
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effacement
= when cervix is drawn up into the lower segment until flat. Commonly accompanied by a 'show' or mucus plug from the cervix or ROM
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Augmentation -->
1. ARM 2. PG gel into posterior vaginal fornix 3. artifical oxytocin
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dilatation of cervix should be around 1cm/hr
first stage should be completed in 12hr. if first dilatation not achieved w/i 12hr then proceed to LSCS active pushing of 2nd stage should be w/i 1hr
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meconium is not a reliable indicator of foetal well being but req CTG monitoring because...
a) risk of meconium aspiration | b) more like to exp hypoxia
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foetal HR auscultation
first stage - every 15 mins second stage -every 5 mins if abnormalities are detected --> CTG
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FBS
<7.20 --> CS 7.2-7.25 --> recheck in 10-30 mins >7.25 --> reassuring
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Analgesia in labour
non-medical - back rubbing - TENS - immersion in water (NOT water birth!) - Entonox/NO inhalation agents (can cause light headedness, nausea, hyperventilation) - diamorphine IM (may feel drowsy or confused) + anti-emetics - Anaesthetics (spinal, pudendal nerve block (quick pain relief to the perineum, vulva, and vagina), epidural anaesthesia)
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CI to epidural
``` Sepsis Coagulopathy or anticoag therapy (unless just LWMH) Active neurological disease Spinal abnormalities Hypovolaemia ```
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compl of epidural
hypotension spinal tap = inadvernt puncture of the dura mata causing CSF leak PDH
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dx of labour
painful contractions w effacement and dilatation of cervix OR painful contr w show or ROM
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labour progress monitoring
2-4 hourly PV exams
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Retained placenta definition
3rd stage > 30mins mx = oxytocin infusion and 10 units injected into the vein of the cord. leave for 1hr placenta manually removed if it has not happened yet. Cross match blood and give IV abx.
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IOL
prostaglandin gel into posterior vaginal fornix eg. MISOPROSTOL. Can repeat in 6hr providing there is no uterine activity. when cxdil >3cm --> amniotomy oxytocin can also be used after any ROM
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Common indications for IOL
``` post date ?IUGR pPROM pe medical disease eg.HTN, GDM ```
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CI to IOL
acute foetal compromise abnormal lie ie.oblique or transverse pelvic obstruction eg.pelvic mass, pelvic deformity relative CI are prev CS
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compl of IOL
failure --> instrumental/CS hyperstimulation --> foetal distress or uterine rupture amniotomy --> cord prolapse incr risk of PPH
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Absolute CI for CS
Vertical uterine scar | multiple prev CS
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safety of VBAC
safest option is vaginal, least safe is emergency CS and elective CS lies in b/t. So overall maternal safety depends on chance of req emergency CS.
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Mx of labour after CS
in hospital and CTG req due to risk of scar rupture Avoid IOL w PG due to risk of rupture CS is preferred unless amniotomy and cervix is ripe or foetal head is engaged scar rupture usually presents as foetal distress, scar pain, cessation of contractions, PV bleed or maternal collapse --> immediate CS
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pPROM
gush of clear fluid followed by uncontrollable intermittent trickle can ?urinary incontinence
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cord prolapse is usually a complication of...
transverse lie or breech presentation
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mx of pPROM
``` speculum to look for pooling of fluids NO VE check lie and presentation vaginal swab to screen for infx CTG or foetal auscultation for foetal distress ``` After 18-24hr --> prescr abx a) Evidence of meconium or infx warrants immediate induction b) Wait - 80% go into spontaneous laboutr w/i 24hr. Measure maternal temp and pulse, foetal HR, measured every 4hr c) IOL - especially if mother is GBS carrier
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ventouse
``` attaches by suction allowing traction (pulling) and if req, w rotation into OA ```
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Non rotational forceps eg. Simpson's, Neville-Barnes
for traction only therefore only suitable if OA have a cephalic curve for head and a pelvic curve
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Rotational forceps eg.Kielland's
no pelvic curve | allows rotation into OA before traction is applied
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compl of instrumental delivery instrumental delivery is indicated if >1hr of active 2nd stage ie.active pushing or if mother is exhausted or foetal distress during 2nd stage prophylactic use of instrumental delivery is indicated to in F w medical problems who should avoid pushing eg.HTN, cardiac disease
- failure - vaginal laceration - third degree tears - blood loss for the foetus - 'chignon' = swelling of scalp where the suction was applied. Diminishes over hours but mark might still be there for days. - facial bruising or facial nerve damage Scalp laceration, cephalhaematoma and neonatal jaundice are more common w ventouse
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occipito-transverse positions in the mid cavity...
need to be rotated therefore descent is achieved w ventouse. Maybe Keilland's
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occipito-posterior positions in the mid cavity...
180o rotation Kielland's forceps (or alt ventouse)
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Pre-requisites for ventouse or forceps delivery
``` head not palpable abdominally ie. deeply engaged head at/below ischial spines FULLY DILATED cervix ie. in 2nd stage KNOWN position of head Adequate analgesia Bladder emptied ```
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Common reasons for CS
elective - prev CS - breech - placenta praevia emergency - failure to progress - foetal distress
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Urgency of CS
Peri/post-mortem - for foetus and mother during maternal arrest/for foetus after maternal death Elective - planned Urgent - maternal/foetal compromise but not immediately life-threatening Emergency - immediate threat to mother or foetus
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compl of CS
- haemorrhage - uterine/wound sepsis - VTE anaesthetics
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Shoulder dystocia | --> Emergency CS
= when additional manouvres are req after normal downward traction has failed to delivery the shoulders after the head has delivered RF = large bb > 4kg prev shoulder dystocia incr maternal BMI, maternal DM Mx: XS traction is uselss and will cause Erb's palsy 1. senior help 2. McRoberts' manouvre (legs hyperextended onto abdo) 3. apply suprapubic pressure 90% success rate... otherwise 4. episiotomy for internal moanouvres eg.Woodscrew's manouvre 5. grasp the posterior arm and bring the hand down 6. symphisiotomy and Zavenelli manouvre (replacement of head back into abdo and proceed w CS)
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Cord prolapse
occurs after ROM (more than half occur at artificial amniotomy!) = umbilical cords presenting below the presenting part (cephalic or breech) Untreated, the cord will be compressed or go into spasm --> foetal hypoxia ``` RF = preterm breech polyhydramnioss abnormal lie twin preg ``` dx: abnormal foetal HR + cord palpated vaginally or appears at the introitus mx: 1. cord is pushed up by the examining finger to prevent it from getting compressed 2. ?tocolytics eg.terbutaline 3. if the cord is already out of the introitus (ie. into the external environment), do not force it back inside but keep it warm 4. get pt into ALL-FOURS toa void compression 5. CS (instrumental if low head and fully dilated cervix)
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Erbs' palsy
--> 'waiter's tip' position
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amniotic fluid embolism
Usually occurs at ROM (but maybe during labour, at CS or TOP) = when liquor enters the maternal circulation --> sudden SOB, hypoxia, hypoT, seizures and cardiac arrest. Can lead to DIC, pulm oedema and adult RDS RF = particularly strong contractions in the presence of polyhydramnios often mistaken for pe or other causes of collapse Mx = resus and supportive, O2, blood test, order blood and FPP. Then transfer to ICU
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Uterine rupture
uterus tearing, either out of the blue or from opening of old CS scar. If the foetus is expelled, the uterus contracts and bleeds from the ruptured site --> acute foetal hypoxia and massive internal maternal haemorrhage. Can occur while foetus is in utero though RF = prev CS, congenital uterine abnormality, dx: foetal HR abnormality - constant lower abdo pain - vaginal bleeding - cessation of contractions - maternal collapse mx = maternal resus w IVF and blood. May need urgent laparotomy
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Uterine inversion
= when fundus inverts into the uterine cavity (dips into the womb) follows traction fo the placenta dx: haermorrhage, pain and profound shock mx: 1. brief attempt to immediately push the fundus up via the vagina 2. GA then replacement where hydrostatic pressure of several litres of warm saline is ran past a clenched fist at the introitus into the vagina
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advantages of BF NB/ early feeding should be on demand
``` bonding cost saving can't give XS protection against infx in neonates proection agaist Ca (for mother) ```
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postnatal contraception
usually 4-6 weeks after delivery progesterone-only preparations are safe for BF COCP suppresses lactation and CI in BF IUD is safe but screen for infx first. Can be inserted at end of 3rd stage or at 6wk puerperium
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PPH ``` causes: aTony Tissue eg.RPOC, clots Thrombus ie.clotting disorder Trauma eg.perineal tears or high vaginal tear (esp after instr vaginal delivery) ```
>500ml loss of blood <24hr of delivery ``` RF = prev PPH prev CS instrumental or CS APH multiple preg or polyhydramnios grand multiparity uterine malformation or fibroids prolonged and induced labour ```
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mx of PPH
1. resus by lying the pt flat, obtain IV access, cross-match blood 2. remove RPOC manually if there is bleeding or if it is not expelled w/i 60mins of delivery 3. PV to exclude uterine inversion and to bi-manually compress the uterus 4. identify and treat the cause 5. IV ergometrine/oxytocin if no obvious trauma 6. EUA (examination under anaesthetics) is performed where the uterus is explored manually for RPOC and tears looked for which wil be sutured 7. if uterine atony persists, PG is injected into the myometrium 8. persistent haemorrhage may req surgery for Rusch balloon, brace suture, uterine A embolization 9. hysterectomy
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secondary PPH
usually due to endometritis +/- retained placental tissue give abx do evacuation of retained products of contraception (ERPC) if no improvement
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Evacuation of retained products of conception (ERPC)
cervix is dilated and a retained non-viable foetus or placental tissue is removed using a suctino curette. similar to surgical therapeutic abortion before 12/40
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treatment for endometriosis
1. mefanamic acid | 2. hormonal contraception, Mirena, COCP
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Prophylactic aspirin given to high for HTN
prev PE renal disease lupus DM and obesity
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Another word for congenital deformity
BIRTH DEFECT
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If day 21 progesterone is low it is a ...
anovulatory problem!
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dysmenorrhoea
painful periods
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dyschezia
painful defecation
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menorrhagia
heavy periods