GYNECOLOGY Flashcards

1
Q

Menstrual physiology:

A
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2
Q
A
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3
Q

amenorrea dx algo

A
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4
Q
A

BREAST + UTERUS +

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5
Q

BREAST + UTERUS -

Differentiate because pubic and axilary hair are absent

A
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6
Q

breast - uterus +

A

A) Gonadal Dysgenesis (Turner syndrome) 45,X0 (missing x on 23 par)
Short stature ,ovarian insufficiency
Instead of developing ovaries they have streak gonads.
**Fsh levels elevated because of ** no feedback inhibition from estrogen to the pituitary.
Treatment: Estrogen and progesterone replacement.

B)Hypothalamic –Pituitary Failure :Kallman Syndrome: Inability of Hypothalamus to produce Gnrh and also anosmia because the defect is close to olfactory area.
FSH levels are low
Treatment: Estrogen and progesterone replacement for secondary sexual characteristics. *(also known as hypothalamic hypogonadism, familial hypogonadism with anosmia, or hypogonadotropic hypogonadism)

kallman = inherited condition, meaning it ispassed on from parents to their children. Mothers can passon the gene to their daughters and sons, but fathers can usually only pass it onto their daughters. The condition is five times more common in boys (one boy in every 10,000) than in girls.

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7
Q
A
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8
Q

Secondary amenorrhea:

3 main causes:

A
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9
Q

Secondary amenorreah managment ?

A

1.First Step is to rule out Pregnancy through **Beta Hcg **.

Next step:??

2.Thyrotropin TSH:Hypothyroidism can lead to amenorrhea by elevating TRH that in turns elevates prolactin.Treatment:Thyroid replacement
3.Prolactin Level:Elevated prolactin level leads to amenorrhea through Gnrh.
- Medications:Anti psychotics and anti depressants have anti dopamine effect.
- Tumor: Pituitary Tumor and idiopathic.
- Hint:Dopamineand prolactin are inversely related

4 .** Progesterone Challenge** Test: PCT:
Administer a single dose of I/M progesterone or 7 days of oral medroxy-progesterone acetate.(MPA)

-Positive PCT: Withdrawl bleeding is diagnostic of anovulation.
-Negative PCT:reasons may be inadequate Estrogen or outflow tract obstruction.

5. Estrogen-Progesterone Challenge test: EPCT: **
- 21 days of oral estrogen followed by 7 days of MPA> Positive EPCT:
- Withdrawal bleed positive means inadequate estrogen.
- Etiology ?
- FSH?
- ●
Low** FSH = CNS Pathology
- ●High FSH = Ovarian Failure .There can be two causes of Premature Ovarian failure:
- 1. X Chromosome Mosaicism:Premature ovarian failure (POF, OMIM 311360) is defined as the cessation of ovarian function before the age of 40, associated with elevated gonadotropins serum levels **(FSH ≥ 40 UI/l) **and affects at least 1%–3% of women of reproductive age,X chromosome can have multiple kind of defects during ageing in these people like deletions,tranlocations etc…

2.Savage Syndrome:
-1.Ovaries have follicles are present but don’t response to GNRH impulses
-2.Resistant ovary syndrome isone of the disease lead to ovarian failure and secondary amenorrhea. Diagnosis of this disease is based on having a normal 46, XX karyotype, normal secondary sexual characteristics, elevated follicle-stimulating and luteinizing hormone, and normal anti-Müllerian hormone.
————
Negative EPCT:
Absence of withdrawl bleeding
Cause could be outflow tract obstruction
-Asherman Syndrome: Result of extensive Curettage and infection induces Adhesions.
Next Step? Hysterosalpingogram.
Treatment:Hysterscopic adhenolysis followed by estrogen stimulation an inflatable stent is then placed to prevent readhesions**

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9
Q

HEAVY MENSTRUAL BLEEDING

AND

DYSMENO

A
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10
Q

HMB causes:

  • most common sigle cause is DYSFUNCTIONAL UTERINE BLEEDING ( DUB)
  • 2 types :

HMB causes:

A
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11
Q

DUB investigations

A
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12
Q

uterine causes:

HMB causes:

A
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13
Q

systemic causes:

HMB causes:

A
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14
Q

HMB TREATMENT :

A
  1. non hormonal (nsaids or tranexamic acid)
  2. hormonal (levonnogestrel mirena)
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15
Q

emergency menorrhagia

A
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16
Q

Uterine fibroids (leiomyoma):

A

Fibroids are benign tumours of smooth muscle of the myometrium. They are classified according to their location: subserosal, intramural, subendometrial or intra-uterine. They are oestrogen-dependent and shrink with the onset of menopause.

CLINICAL FEATURES:
Lifetime incidence of 60–70% in Caucasian women
Only 1 in 800 develop malignancy
Usually asymptomatic
SYMPTOMS:
Often asymptomatic if small
Menorrhagia
Dysmenorrhoea
Pelvic discomfort ±pain (pressure) including dyspareunia
Bladder dysfunction
Pain with torsion of pedunculatedfibroid
Pain with ‘red degeneration’—only in pregnancy (pain, fever, local tenderness)
Infertility (acts like IUCD if submucosal)
Calcification

MANAGEMENT:
Medical management the same as for DUB :
-Levonorgestrel IUD has now largely taken over as the Preferred option for reduction of bleeding.
-GnRH analogues—especially if >42 years can shrink fibroids (maximum 6 months)—use only immediately pre-operative

●Surgical options:
–myomectomy (remove fibroids only, esp. child-bearing years)
–hysteroscopic resection/endometrial ablation
–hysterectomy
●Other option: uterine embolisation

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17
Q

Premenstrual Syndrome:

A

Premenstrual syndrome (PMS) is defined as a disorder of non-specific somatic, psychological or behavioral symptoms occurring during the late luteal phase of the menstrual cycle.The symptoms of PMS decrease in severity just before and during menstruation. Premenstrual Syndrome:
The most common psychological symptoms are depression and irritability, while headache, bloating and breast tenderness are the most common physical symptoms.

CLASSIFICATION:
It is convenient to classify PMS in terms of severity of symptoms.

Mild:symptoms signal onset of menstruation. No medical advice sought or needed.
Moderate:symptoms annoying but insufficient to interfere with function at home or work. Medical advice sought in about one-third.
Severe:symptoms are such that functions at work or home are disrupted. Medical advice is usually sought. This disruptive form is labelled **PMDD **

Diagnosis:
Thorough history—including diet, exercise habits, psychosocial background, emotional influences and family history
Menstrual calendar—for 3 months, showing timing of the three main symptoms

Physical examination to exclude gynecological, endocrine or other systemic disease; and also include:–breast examination (if breast tenderness)–cervical screening test

Investigations (to exclude other causes):
●–thyroid function tests
●–full blood count
●–electrolytes and creatinine
●–FSH and oestradiol—if perimenopause suspected
●–serum androgens—if oligomenorrhoea present

**MANAGEMENT **
**Explanation, reassurance and insight
**Cognitive-based therapy , which has been shown to have a positive effect in several RCTs,is very Helpful.
●Keeping a diary
●Advise the patient to keep a daily diary of all her symptoms and when they occur over a 2–3 month period. This information should help her to plan around her symptoms: for example, avoid too many social events and demanding business appointments at the time when PMS symptoms are worst.

Dietary advice
1:Advise the patient to eat regularly and sensibly; eat small, frequent meals and aim for ideal weight.Increase amount of low-GI complex carbohydrates, leafy green vegetables and legumes.
Decrease or avoid: refined sugar, salt, alcohol, caffeine (tea, coffee, chocolate), tobacco, red meat and excessive fluid intake during premenstrual phase.
Decrease total protein to 1 g/kg/day; decrease fats.

Exercise
Recommend a program of regular exercise such as swimming, aerobics, jogging or tennis. Such exercise has been proven to decrease depression, anxiety and fluid retention premenstrually
Relaxation
Advise patients to plan activities that they find relaxing and enjoyable at the appropriate time. Consider stress reduction therapy, including meditation, yoga, relaxation techniques and appropriate counselling.Appropriate dress:loosedressing
Medication:

●Pharmaceutical agents that have been used with success in some patients and little or no relief in others include diuretics (e.g. spironolactone), vitamins and minerals (e.g. pyridoxine and evening primrose oil), simple anti-inflammatories (e.g. aspirin, mefenamic acid) and hormonal preparations such as the **OCP. A combination of agents may have to be used.
SUPPLEMENTS:Women often enquire about the use of vitamins, minerals and herbal remedies for PMS. The evidence base for symptom relief so far is as follows:
pyridoxine/vitamin B6 up to 100 mg daily (evidence limited, beware nerve damage to hands/feet with higher doses)
elemental calcium, 1200 mg to 1500 mg daily (two randomisedcontrolled trials have shown significant benefit)elemental magnesium** up to 400 mg daily (minimal evidence)evening primrose oil 500 mg daily (no benefit over placebo)Agnuscastus(Premular®) is an extract of the berries from the chaste tree (several small randomisedcontrolled trials have indicated some benefit over placebo)

ORAL CONTRACEPTION:It is appropriate to use a COC-containing ethinyloestradiol and drospirenone since a meta-analysis of drospirenone, which is a progestogenderivative of spironolactone, concluded that it was effective in reducing the severe symptoms of PMDD.
Moderate to severe PMDD:fluoxetine20 mg (o) or sertraline50 mg (o) daily in morning for 14 days before anticipated onset of menstruation and through to the first full day of menses of each cycle

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18
Q

Atrophic vaginitis:

A

In the absence of oestrogen stimulation, the vaginal and vulval tissues begin to shrink and become thin and dry in old age in post menopausal women. This renders the vagina more susceptible to bacterial attack because of the loss of vaginal acidity. Rarely, a severe attack can occur with a very haemorrhagicvagina and heavy discharge:
●yellowish, non-offensive discharge
●tenderness and dyspareunia
●spotting or bleeding with coitus
●the vagina may be reddened with superficial haemorrhagicareas

TX
Oestrogen cream or pessary(e.g. Ovestin, Vagifem) daily at bedtime for 2–3 weeks, then once or twice weekly
●or
●zinc and castor oil soothing cream
●Note:perform a careful speculum examination.

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19
Q
A
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20
Q

VULVOVAGINAL CANDIDIASIS:
clinic

A
  • Usually in the presence of estrogen.
  • CLINICAL
  • ●Intense vaginal and vulval pruritus
    -●Vulval soreness
    ●Vulval fissures
    Vulvo vaginal erythema(brick red)
    ●Vaginal excoriation and oedema
    White, curd-like discharge
    ●Superficial dyspareunia
    Dysuria
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21
Q

VULVOVAGINAL CANDIDIASIS:
factors predisponing

A

ENDOGENOUS
●Diabetes mellitus●Pregnancy●Immune deficiency, e.g. HIV

EXOGENOUS
●Oral contraceptives (but cessation of the OCP does not usually improve candidiasis)
●MHT or topical oestrogen
●Antibiotics
●Corticosteroid therapy
●Immunosuppressants
●Orogenital/anogenitalintercourse
●IUCD
●Tight-fitting jeans
●Nylon underwear
●Wet bathing suit

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22
Q

vaginal candidiasis
tx ?
chronic vulvovaginal candidiasis tx?

A
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23
Q

resistan infection, candida
tx

A
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24
Q

Trichomonas vaginalis:
clinic
tx

A

Flagellated protozoan Transmitted via sexual intercourse.
In Australia, trichomonasis more common in older women and women from regional and remote areas, especially Aboriginal and Torres Strait Islander
——————-
Profuse, thin discharge (grey to yellow–green in colour) **
Small bubbles may be seen in 20–30%
Vulval itch

Malodorous discharge
●Dyspareunia
●Diffuse erythemaof cervix and vaginal walls
Characteristic punctate appearance on cervix
.
TX
Oral Metronidazole 2 g as a single dose (preferable) or 400 mg bdfor 5 days (if relapse)
●or
●tinidazole 2 g as a single dose
” Sexual PARTNERS must be treated simultaneously “ ●No sexual contact is advised for 7 days after treatment for patient and partner

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25
Q

Bacterial vaginosis:

A

●A white or grey, homogenous discharge
●Malodorous
●No obvious vulvitisor vaginitis
●Liberates an amine-like, fishy odouron admixture of 10% KOH (the amine whiff test)
●Clue cells on wet preparation
●±Dyspareunia and dysuria
●±Pruritus (uncommon)

METRONIDAZOLE OR CLINDAMICINA

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26
Q

Lichen Planus:
clinic
dx
tx

Lichen planus (LP) is a chronic, inflammatory, puriticskin disorder, typically found on the limbs (especially flexor surfaces), mucous membranes (often in the mouth) and genitals –including inside the vagina

A
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27
Q

Lichen sclerosis:lichen sclerosus et atrophicus

A

Complications: if untreated:

●Vulvalatrophy and labial (even clitoral hood) fusion, introitalstenosis
●Lifetime risk of SCC 2–6%

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28
Q

Uterovaginal prolapse: 4 of - uterine prolapse are: -

A

Treatment:Medical:Kegelexercises,Pessaries,Estrogen replacement.

Surgical:anteriorand posterior vaginal wall repair or colporapphy

For uterine prolapse:Sacrohysteropexy

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29
Q

cervix
types:
factor risk

A

-fourth most common cause of cancer
- The most common is squamous cell carcinoma (SCC) 80% of cases. Adenocarcinoma is less common and more difficult to diagnose because it starts higher in the cervix.
- Cervical cancer almost exclusively occurs in women who have been sexually active, due to exposure to human papillomavirus(HPV). Other risk factors include smoking, use of combined oral contraception >5 years, immunosuppressionand exposure to diethylstilboestrol in utero.
- HPV 16 and 18
-

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30
Q

cervix
Who should be screened?

A

Women are invited to commence cervical screening at 25 years (or two years after first sexual intercourse, whichever is later).

●Both HPV-vaccinated and non-vaccinated women should be screened.

●An exit test can be performed at age 70–74 years.

●Women aged 75 years or older may request screening.

●Screening applies only to asymptomatic women. Women with postcoitalor persistent intermenstrual bleeding require a co-test (both HPV test and diagnostic LBC), and referral for an appropriate investigation to exclude malignancy should be considered.10

●For women who experienced first sexual activity at a young age (<14 years) and who had not received the HPV vaccine before sexual debut, a single HPV test between 20 and 24 years of age could be considered on an individual basis

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31
Q

cervix
special groups
hysterectomy
pregnancy
postmeno
inmunodeficient
DES

A
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32
Q

CIN comparison of nomeclature

A
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33
Q

Algorithm for management of low-grade squamous

A
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34
Q

INFERTILITY
female factors
ovulation disorders:
Tubal disease:
uterine and cervical anormalites:

A
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35
Q

INFERTILITY
male factors

A
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36
Q

physical examination nad investigation
man
infertility:

A
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37
Q

physical examination woman infertility:
and investigations first ovulation status:

A
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38
Q

fertility awareness:
chance of fertilization is best during:

A
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39
Q
A

endometriosis

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40
Q

endometriosis
symptoms:

A
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41
Q

dx endometriosis
most acurate test

A

laparoscopy and biopsy

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42
Q

endometriosis
tx

A

ocp
nsaid

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43
Q
A

first line investigation
basal body temperature and cervical mucus dairy
semen analisis
serum progesterona
transvaginal us
rubella inmune status

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44
Q

male infertility investigation
most important endocrine test?

A
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45
Q

female investigation in infertilty

A
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46
Q

infertility tx options

A
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47
Q
A

Poor nutrition and weight ovulation disorders

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48
Q

DX CRITERIA (ROTTERDAM)

LH - TECA- ANDROGENOS + PROGESTERONA
FSH - GRANULOSA - ESTROGENOS

A

EXCLUDE OTHERS:
Hipotiroidismo
hiperprolactinemia
= GnRH DOWN
= fsh y lh down

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49
Q

PCOS SYMPTOMS

A
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50
Q

PCOS
investigations

A

riesgo cancer endometrial

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51
Q

managment PCOS

A
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52
Q
A
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53
Q

Premature Ovarian Failure
Clinical Features:
Investigations
Investigations

A
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54
Q
A
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55
Q

tanner staging

A
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56
Q
A
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57
Q

Klienfelter’s Syndrome –XXY:

A
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58
Q
A
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59
Q
A
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60
Q
A
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61
Q
A

next step would be pelvic examination if she is a virgin (or US trasnvaginal)

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62
Q
A

imperforate hymen

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63
Q
A

hyperprolactinemia

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64
Q
A

STOP METROTEXATE BUT CONTINUE HYDROXICLOROQUINE

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65
Q
A

ULTRASOUND

  • remember the best is hysterosalpingogram
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66
Q

BREAST

A

TRIPLE TEST :

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67
Q

INVESTIGATION X RAY MAMMOGRAPHY

MOST EFFECTIVE TOOL FOR BREAST CANCER
SCREENING 50 YEARS -

A

BREAST ULTRASOUND

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68
Q

Breast imaging for palpable lumps
According to age:

A

<35
35-50
50>

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69
Q

NEEDLE ASPIRATION AND BIOPSY TECHNIQUES

A
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70
Q

Fibrocystic Disease:
clinical features:

A
  • fluctuate with periods!
  • pain tender and swelling
    reassure that is no cancer
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71
Q

FIBROADENOMA

A

REASSURANCE

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72
Q

breast cyst

A
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73
Q

Localized Nodularity:

A

Lactation Cysts

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74
Q

Phyllodes Tumor

A
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75
Q

FAT NECROSIS

Breast

A

Most accurate test : biopsy
reassurance and triple test

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76
Q

Duct Papillomas:

breast

A
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77
Q

mammary duct ectasia:

A
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78
Q

Red Flag Pointers for Breast Lumps

A

*Hard and irregular lump
*Skin dimpling and puckering
*Skin oedema (‘peau d’orange’)
*Nipple discharge
*Nipple distortion
*Nipple eczema
*Postmenopausal women

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79
Q

Diagnosis of Breast Cancer
dx:

A
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80
Q

TX BREAST CANCER

A
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81
Q

Adjuvant Therapy for breast cancer:

A
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82
Q

screening for breast cancer
RISK
1SLIGHTLY
2 MODERATE
3 HIGH

A
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83
Q

Lymphoedema of arm

A
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84
Q

Ductal Carcinoma in Situ
risks:
tx:

A
Paget disease of the nipple:
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85
Q

Paget disease of the nipple:

A
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86
Q

Lumps that require investigations and referral:

A
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87
Q

MASTALGIA

A

CYCLICAL AND NON CYCLICAL

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88
Q

TX MASTALGIA

A
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89
Q

Mastitis carcinomatosa

A
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90
Q

TIETZE SYNDROM

A
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91
Q

breast abcess:

A
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92
Q

Breast Infections
MASTITIS
CLINICAL
candida symptoms?
tx?

A

If systemic symptoms develop:

*Antibiotics:resolution without progression to an abscess will usually be prevented by antibiotics:
*(di/(flu)cloxacillin 500 mg (o) 6 hourly for 10 days or (if hypersensitive to penicillin), cephalexin 500 mg (o) 6 hourly for 10 days)

*If severe cellulitis di/(flu)cloxacillin 2 g (IV) 6 hourly

*Therapeutic ultrasound (2 W/cm 2 for 6 minutes) daily for 2–3 days

*Ibuprofen or paracetamol for pain

.*For** Candida albicans** infection:(fluconazole 200–400 mg (o) daily for 2–4 weeks, second line—nystatin 500 000 U (o) tds

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93
Q
A
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94
Q
A
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95
Q
A
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96
Q
A
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97
Q
A
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98
Q

OSTEOPOROSIS

definition
common sites of fracture:

A

It is also defined by bone mineral density (BMD) as a T score of ≤–2.5.

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99
Q

gold standard of osteoporosis:
t score and z scorea

A
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100
Q

Risk factors for minimal-trauma fracture.
age when to review fracture risk? men and women

A

fall
women
menopause
age

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101
Q

osteoporosis identifyng risk :
average:
high:

A

average risk: clinical assement for risk factors
increase risk: DXA
**high risk: ** DXA (every 2 years)

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102
Q

prevention of osteoporosis:

fracture orevention

A
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103
Q

Calcium and osteoporosis
dosis

vitamin D

A

1300 mg osteoporosis

1300 mg women > 50 years < 1000 mg

1300 mg men > 70 years < 1000 mg

calcium carbonate first line

calcium citrato (if proton pump inhibitor)

*
*
*
remeber to consider the possibility of. a secondary cause

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104
Q

Management of osteoporosis following minimal-trauma fracture:

A
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105
Q

Management of osteoporosis in the absence of fracture:

A
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106
Q

Choice of drug therapy for osteoporosis
summary

A
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107
Q

Bisphosphonates
regimens:

A

inhibiting osteoclasts

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108
Q

Zoledronic acid
adverse effects:

A
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109
Q

Duration of bisphosphonate therapy

A

Bisphosphonates are retained in the skeleton after treatment withdrawal. The beneficial effects on BMD persist for several years after stopping alendronate and zoledronic acid.

●In contrast, BMD decreases within one year of stopping risedronate.

●Long-term bisphosphonate therapy has been linked to an increased risk of skeletal adverse effects such as osteonecrosis of the jaw and atypical fracture of the femur, although the absolute risk remains low. Limiting the duration of bisphosphonate therapy may reduce the incidence of these effects.

Riserdonateis slightly safer option in patients with gastrointestinal irritation

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110
Q

denosumab

A

reducing osteoclast formation and differentiation and increasing osteoclast apoptosis.

Can cause **HYPOCALCEMIA **CHECK
VITAMINA D
CALCIO SERUM
CREATININE CLEAREANCE

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111
Q

Teriparatide

A

Teriparatide is also indicated to be used if the patient has a fracture while on therapy with osteoporosis
-
The maximum lifetime duration of teriparatide is 24 months.
-
DO NOT USE IN:

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112
Q

Romosozumab

A

Romosozumab’suse is limited by strict eligibility criteria for PBS subsidy—●therapy must be started by a specialist, the patient must have a T-score of –3 or less and they must have experienced at least one symptomatic new fracture after at least 12 months of therapy with an antiresorptive drug.

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113
Q

ESTROGEN THERAPY OSTEOPOROSIS

A
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114
Q

how to monitor patients with osteoporosis:

A

BMD

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115
Q

Skeletal adverse effects of drugs used for osteoporosis:

A
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116
Q

Glucocorticoid-induced osteoporosis

A

**The extent of bone loss is related to the dose and the duration of glucocorticoid therapy.

A prednis(ol)one dose of at least 7.5 mg per day, or an equivalent dose of another glucocorticoid is associated with the greatest risk.

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117
Q
A
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118
Q

effectiveness of contraceptive methods.

A
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119
Q

Classification of contraceptive methods

A

Contraceptive methods can be classified by their mechanism of action (hormonal versus non hormonal) or duration of action (long acting versus shorter acting).
** Long-acting reversible contraception(LARCs)**
➢intrauterine contraceptive devices (IUDs)—levonorgestrel-releasing and copper intrauterine IUDs ➢etonogestrelcontraceptive implant

**Shorter-acting hormonal contraception
**➢depot medroxyprogesterone injection
➢combined hormonal contraception—combined oral contraceptives (COCs) and the contraceptive➢vaginal ring
➢progestogen-only contraceptive pills

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120
Q

Hormonal contraception

A
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121
Q

Progestogen-only contraception :
uses:

A

women who are breastfeeding or have a contraindication to taking oestrogen

Progestogen-only contraception is contraindicated in women with active breast cancer within the past 5 years (MEC 4), but has relatively few other contraindications.

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122
Q

Etonogestrel implant (Implanon NXT)

A

3 years
inhibits ovulation
IRREGULAR BLEEDING MOST COMMON EFFECT

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123
Q

Depot medroxyprogesterone acetate:
dosis:
return of fertility?
adverse effect?
age?

A

(amenorrhoea rate 50–70% by 12 months), weight gain (average 2–6%), breast tenderness, mood changes and a delay in return of fertility (mean time 8 months).

Long-term use is associated with **accelerated bone loss. **

For this reason it is not recommended as a first-line contraceptive for women less than 18 and more than 45 years.

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124
Q

Progestogen-only contraceptive pill:

A

The POP (mini-pill) is most commonly prescribed for breastfeeding women for whom an oestrogen contraceptive was previously not recommended. POP is safe from 4 weeks after delivery

evonorgestrel 30 mcg/day

●norethisterone 350 mcg/day

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125
Q

uterine contraceptive devices

absolute contraindications:

A

including young and nulliparous women

All IUDs prevent pregnancy by inhibiting sperm migration and ovum transport and preventing implantation
The levonorgestrel IUD also causes endometrial suppression and cervical mucus thickening and may prevent ovulation.
-
copper IUDs: 99.5% perfect and typical use
-
Absolute contraindications
-active PID,
-undiagnosed abnormal genital tract bleeding
-current or past history of breast cancer for those considering levonorgestrel IUD (MEC 4)

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126
Q

uterine contraceptive devices

Side effects and complications of IUD use:

A

Pregnancy/ectopic pregnancy
- Early removal of the IUD is essential
- IF pregnancy occurs there is an increased risk of abortion and intra-uterine sepsis during the second trimester.
- **risk is low **compared to non users

Pelvic inflammatory disease
- small increased risk of PID in the first 20 days post-insertion

Extrusion, perforation of uterus and translocation
- Factors that increase risk of perforation include breastfeeding, first 6 months postpartum and previous caesarean section.
- translocation of the IUD outside the uterus is proved by X-ray and pelvic ultrasound, referral for removal is mandatory
- woman should attend for a follow-up visit between 3–6 weeks after insertion specifically to exclude infection, perforation or expulsion

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127
Q

Combined hormonal contraception (CHC)

dose:

Combined hormonal contraceptives contain an oestrogen and progestogen, and their main mode of action is inhibition of hypothalamic and pituitary function leading to anovulation

A

COCs in Australia contain ethinyloestradiol(EE), oestradiol valerate (EV), oestradiol (E2) or mestranol and one of a range of progestogens.
-
**EE is the most commonly used oestrogen. The active oestrogen in the newer E2 and EV pills is structurally identical to the E2 produced by the ovaries. **
-
use a dose of 35 mcg EE or less.
-
Formulations containing 50 mcg EE are no longer recommended because there is no known additional benefit from their use and they are associated with an **increased risk of VTE. **

●Women starting on a 20 mcg EE pill are likely to have fewer hormonally related side effects such as headaches or mood swings, but have a higher chance of discontinuation due to breakthrough bleeding.

-
which progesterone ? image

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128
Q

combined oral contraceptive formulations in AUSTRALIA

A
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129
Q

Starting the pill: which COC to use?

A

past menstrual and medical history of the woman should be documented and contraindications excluded:
30 mcg or 35 mcg ethinyloestradiol (EE) with levonorgestrel or norethisterone (e.g. Nordette, Microgynon 30, Monofeme, LevlenED, Brevinor).

*Education and counselling are very important for the woman starting the pill. Suitable patient education should be given.

-
YOUNGS:
Contraception (excluding sterilisation) can be provided without parental consent to adolescents assessed as being able to consent to their own medical treatment.
●Clinicians should be aware of mandatory reporting requirements in their jurisdiction for young people assessed as being at risk of harm (non consensual sexual activity, significant age gap or power differential between the young person and the sexual partner
)

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130
Q

first-line option in adolescence contraception?

A

Long-acting reversible contraception (LARC) (the etonogestrel implant and intrauterine contraceptive devices [IUDs]) is the first-line option in adolescence

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131
Q

Postpartum contraception

A

<6 weeks = progesterona
>6 weeks: estrogenos

-
The etonogestrelimplant can be inserted any time postpartum, including immediately before leaving hospital and during breastfeeding.
-
A levonorgestrel-releasing or copper intrauterine contraceptive device (IUD) can be inserted immediately postpartum (within 48 hours), (>considerar por especialista en otro tiempo)
-
4> semanas es safe DIU , (riks of perforation because of breastfeeding)
-
Depot medroxyprogesterone injection is safe to use immediately postpartum and during breastfeeding. It can be a useful option for those awaiting IUD insertion after delivery.

●Progestogen-only pills (POPs) are commonly prescribed for individuals who are breastfeeding because they do not increase the risk of VTE (unlike combined hormonal contraception). ●The POP can be started immediately after delivery.

  • COP or vaginal ring = 6> semanas
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132
Q

Thromboembolic risk:
Migrane with aura:
migrane without aura:
smokers:
developmental disability:
>35 years:
liver enzyme inducing drugs:

A

All combined hormonal contraceptives (combined oral contraceptives [COCs] or the contraceptive vaginal ring) increase the relative risk of venous thromboembolism (VTE).

-Depot medroxyprogesterone is not associated with a clinically significant risk of VTE. Despite a small increase in VTE risk if started in the first week postpartum, it is considered safe to use immediately postpartum.

●Other progestogen-only contraceptives are not associated with an increased risk of VTE
.
Migrane with aura: Progestogen-only methods of contraception are safe to use for individuals with a current or past history of migraine with aura.

**migrane without aura: **Progestogen-only methods better than COPs
smokers: contraindicated in individuals 35 years or older who smoke 15 or more cigarettes per day;

developmental disability: assessed for their capacity to consent to treatment
>35 years:
*CHC use is safe for healthy non-smoking women until 50 years (MEC 2 for women over 40).
*CHC is not recommended if a woman is over 35 years and has cardiovascular risk factors, including obesity, smoking, diabetes and hypertension (MEC 3/4

liver enzyme inducing drugs:
DMPA and IUDs
antibiotics that interfere (The only exceptions are liver enzyme-inducing rifabutin and rifampicin.)
Other liver enzyme-inducing drugs include many of the older anti-epileptics (e.g. phenytoin, carbamazepine), St John’s wort and protease inhibitors. For women who still request the use of COC, an extended or tricycling regime of a higher dose pill (e.g. containing at least 50 mcg EE) may be effective.

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133
Q

ABSOLUTE AND RELATIVE CONTRAINDICATIONS OF COPS

A
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134
Q

Serious side effects of CHCs

A
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135
Q

MOST COMMON SIDE EFFECTS OF COC

A
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136
Q

Important advice for the patient

A

Important advice for the patient:If a woman vomits within 2 hours of taking an active pill, she should take an additional active pill
A missed pill is defined as one that is taken more than 24 hours late (>48 hours since last pill was taken).
<24 Horas tomar dos

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137
Q

Emergency contraception

A

>70kg or bmi >26 DOUBLE DOSE

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138
Q

vaginal ring

A
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139
Q

delaying a period

A
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140
Q

Lactational amenorrhoea method (LAM)
conditions

A
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141
Q

menopause
premature ovarian failure:
early menopause

A
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142
Q

menopause symptoms and tx

A

The classic vasomotor symptom of menopause is the hot flush. A hot flush lasts 1–2 minutes, begins in the chest and then spreads up over the face and body. There may be associated redness, sweats which can be drenching, panic attacks, palpitations and faintnes.

-
HT is the most effective method for relieving distressing symptoms such as hot flushes, urogenital symptoms, sleeplessness and joint symptoms.
-
strogen + progesterone = has UTERUS (hyperplasia and there is a 5–10 times increased risk of endometrial cancer if only estrogen.)
-
tibolone - no uterus
estrogenos transdermal (less VTE risk)
testosteron - for libido
-
perimenopausal -(12 m) - ** progesterone must be cyclical ** after it trasnfer to continuous
-
Women who are prescribed MHT should be reviewed at least annually
-first line therapy non hormonal lubricant in DRYNESS THEN TOPIC OESTROGEN VAGINAL

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143
Q

PRECONCEPTION CARE
folic acid dosis:
folic acid for women with risk:

A
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144
Q

supplementation preconception care

A
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145
Q

preconception restrictions:

A
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146
Q

pregnancy confirmation:
physical:

A
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147
Q

pregnancy differential:
complications:

A
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148
Q

HORMONAL CHANGES

A
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149
Q

Cardiovascular System Changes

A
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150
Q

Hematologic Changes

A
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151
Q

respiratory system changes
renal changes
inmune changes
gastrointestinal

A

increase estogen -> cholesterol secretion
increase progesterone -> decreased bile acid secretion and muscle relaxation
RISK CHOLELITHIASIS

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152
Q
A
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153
Q

ANTENATAL CARE
TIMING VISITS:

A
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154
Q

routine ANTENATAL SCREENING

A
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155
Q

ROUTINE LAB/DX STUDIES

A

RUBELLA
TSH
<3 CM FUNDUS ERROR REFER!

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156
Q

TIME OF MAJOR PRENATAL TESTS*
important

if the cDNA reveals high risk -> CVS = RISK 1-100 MISCARRIAGE

A
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157
Q

SCREENING TESTS again summary pregnancy

A
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158
Q

dx test pregnancy

A
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159
Q

vaccinations recomended in pregnancy
3

A
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160
Q

glucose challenge in pregnant
when ?

A
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161
Q
A
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162
Q
A
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163
Q
A
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164
Q
A
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165
Q
A
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166
Q
A
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167
Q
A
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168
Q

Vaginal bleeding in early pregnancy:
1-Trimester

A
  1. MISCARRIAGE
  2. ECTOPIC PREGNANCY
  3. MOLAR (rare)

20-40% pregnant women will BLEED 1 TRIMESTER

<6 semanas - hcg se eleva 66% cada 48 horas (sino ectopico)
- hCG > 1500 IU/L PEDIR TRASNV US ***

6-8 SEMANAS
- usar US
- repetir en una semana

> 8 semanas:
- normal US is reassuring

REST IS NOT NECESSARY FOR THREATHNED MISCARRIAGE

ANTI D - ONLY IN COMPLETE MISCARRIAGE

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169
Q

vaginal bleeding 1 trimester investigations:

A
  1. US TV
  2. hCG ( <50% 48 = no viable or ectopic)
  3. maternal blood group and antibody (determine Rhd inmunoglobuline)
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170
Q
A
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171
Q

shoulder tip pain sign
suspect:

A

Of the option, however, shoulder tip pain is the most important sign demanding urgent action. This sign is notcommon but if present in suspected EP, demands urgent surgical action because indicates** free blood in the peritoneum and peritoneal irritation**. The mechanism such pain is produced is thought to be irritation of the diaphragm and the phrenic nerve by the free blood in the peritoneal cavity. Then pain can radiate to the shouldertip especially on the right side

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172
Q
A
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173
Q

risk factors for ectopic pregnancy?

A
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174
Q

ectopic pregnancy most commonly location?

A
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175
Q

vaginal examination in ectopic pregnancy ?

A
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176
Q

->Ectopic Pregnancy

differentials
tx

A
  • METROTEXATE
  • ALL RH (D) NEGATIVES = ANTI D INMUNOGLOBULIN
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177
Q

INEVITABLE, INCOMPLETE, COMPLETE MISCARRIAGE

A
  • inevitable - uterine bleeding, dilatation, contractions.
  • complete
  • incomplete

tx
HOSPITAL
analgesic
heavy bleeding (ergotamine)
vaginal examination and forceps removal
-
residual gestational tissue US
removal surgically by sponge forceps or medically misoprostol

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178
Q

ecotpic pregnancy diagnosis?

A
  • b-hCG
  • <5 not pregnant
    + -> US TV
  • 1000 = fetal heart beat
  • ## no result in US => serial B hcg

SNOWSTORM = MOLAR

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179
Q
A
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180
Q

DEFINITIONS OF MISCARRIAGE

A

as recommended that a fetus be considered potentially viable when the gestation periodhas reached 22 weeks or more, or when the fetus weighs 500 g or more.

ABORTION TERM USED FOR DELIBERATELY TERMINATED

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181
Q
A
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182
Q
A
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183
Q

DEFINITIONS IN MISCARRIAGE

A
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184
Q

THREATNED MISCARRIAGE

A
  • UTERINE BLEEDING (WITH OT WITHOUT PAIN)
  • CERVIX CLOSED
  • US
  • IF subchorionic hematoma preganncy monitered closely
  • NO BED REST
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185
Q

recurrent miscarriage
antiphospholipid syndrome dx and tx:

also cervical incompetence (do cerckage)

A

3 or more sucessive miscarriages
.
lupus anticoagulant
anticardiolipina
anti b2 glicoprotein

tx aspirin and unfractioned heparin

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186
Q

```

~~~

A
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187
Q
A
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188
Q

```

~~~

law on abortion in NSW

A
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189
Q

abortion

A
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190
Q

epilepsy in pregnancy:

A
  • no seizure in 6 months
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191
Q

complications epilepsy on pregnancy

A

Effect of pregnancy on epilepsy
*In most women seizures do not increase during pregnancy
*1-2% incidence of seizures during labour and in 24 hours post delivery

Effect of epilepsy on pregnancy Maternal
*Vaginal bleeding, abruptio placentae, PET, preterm labour Fetal
*Neural tube defects, I UG R, heart and skeletal defects, prematurity.

Newborn
Hemorrhagic disease of newborn***

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192
Q

care and investigations epilepsy pregnancy:

A

Antenatal Care
High risk pregnancy clinic-MDT with neurologist
Continue antiepileptic medication
*Screening for spina bifida: *by nuchal translucency scan for anencephaly, maternal alpha fetoprotein at 16-20 weeks, detailed U/S at 20 weeks which is most predictive for neural tube defects MCQ#########
Monitor anticonvulsant levels once in each trimester
**
Oral Vitamin K **2omg/day during last 1 month of pregnancy.

Intrapartum and Postnatal care
Vaginal delivery at tertiary hospitalI/M 1mg vitamin K to newborn*Breastfeeding is not contraindicated despite the drugs crossing into the breast milk.

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193
Q

DVT pregnancy
when is most risk?
tx?

A

The prevalence of VTE is equally distributed throughout pregnancy, but the day by day risk is greatest in the immediate puerperium. 6 weeks

The major risk factors include caesarean section, obesity, prolonged immobility, preeclampsia, current infection, previous VTE and familial thrombophilia.The preferred treatment of VTE during pregnancy is low molecular weight heparin (LMWH).
Compared withunfractionated heparin, as LMWH does not cross the placenta, there is a reduced risk of bleeding and no thrombocytopenia.

Incidence 1%

Symptoms: Pain, swelling in the leg usually unilateral and **on left leg (80%) **with redness, warmth.

Complication
*pulmonary embolism

Investigation of choiceCompression Doppler US

-If U/S negative =clinical suspicion low, anticoagulation discontinued

  • If clinical suspicion high = repeat doppler U/S, venography or magnetic resonant direct thrombus imaging.
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194
Q

PE in pregnancy
best initial investigation

TX-

A

UNFRACTIONED HEPARINE FOR MASIVE

LMWH FOR PROPHYLAXIS

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195
Q

TX DVT PREGNANCY OVER VIEW:
above the knee
distal DVT

A

LMWH anticoagulant of choice

warfarina contraindicated during pregnancy

Delivery

*Planned delivery preferably *Discontinue therapeutic LMWH 24 hours prior and give prophylactic LMWH until 12 hours prior induction or c-section
*If spontaneous delivery :
- Stop LMWH and send blood for cross match, group and hold.

If high risk of bleeding, unfractionated heparin **is preferred and is has shorter half life and can be completely reversed with **protamine sulphate**
**
Unfractionated heparin also indicated in RENAL FAILURE.

Care during subsequent pregnancy:
*Screen for thrombophilia
*LMWH from 14 weeks to 4 to 6 week post partum
*Compression stocking and avoid immobilization

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196
Q

Gestational diabetes values:

DM vs GDM

A

(oh) * fasting glucose >5.1 mmol
*
(1h)* post 75 gr 1 hour > 10
*
* 2 hour> 8.5

all pregnant women should be screened at 24-28 weeks with 75 gr

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197
Q

unfractioned heparine indicated in pregnancy:

antidote:

A
  • renal failure
  • massive PTE with cardiovascular compromise
  • high risk of bleeding (placenta previa)
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198
Q

risk factors for GDM:

gestational diabetes

A
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199
Q

uncertain values gdm

A

FASTING PLASMA GLUCOSE
<5 mmol/L = normal

5.1-5.9 mmol/L :uncertain. considere lifestyle. OGTT = 16-18 weeks
6.6.0-6.9 mml/L: lifestly advice. OGTT = 16-18 weeks. consider SMBG

RANDOM PLASMA GLUCOSE

9-11mmol/L : signficance unknown. further investigation - fasting or HbA1c.

GLYCATED HAEMOGLOBIN (HbA1c)
- 5,9-6,4 = reasonable predicting a dx of GDM . Lifestyle. consider SMBG

remember - >
OGTT:
1. Fasting(eight hours)
2. 75 g glucose administered orally
3. Blood is collected from a fasting venous sample and two-hour post-glucose challenge venous sample

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200
Q

managment of diabetes
screening and diagnosing type 2 diabetes

A
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201
Q

dx criteria type 2 diabetes adults

asymptomatic

A
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202
Q

GESTATIONAL DIABETES
RECOMENDATIONS

A
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203
Q

GESTATIONAL DIABETES
MANAGEMENT

A
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204
Q

GESTATIONAL DIABETES
follow up:
exams:
-
40% risk of subsequent GDM in pregnancy

A
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205
Q

GESTATIONAL DIABETES COMPLICATIONS
MATERNAL
FETAL

A
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206
Q

GESTATIONAL DAIBETES
DURING PREGNANCY
DURING LABOUR
FOLLOW UP?

A
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207
Q
A
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208
Q
A
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209
Q
A
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210
Q

PROM Premature Rupture of membranes:
risk factors
symptoms
**complications?
**

premature rupture of membranes (PROM) occurs when a patient at ≥ 37 weeks of gestation presents with rupture of membranes (ROM) prior to the start of uterine contractions

PPROM:preterm premature rupture of membranes (PPROM) describes PROM that occurs < 37 weeks of gestation

211
Q

Chorioamnionitis

investigations

A

To prevent chorioamnionitis, it is recommended that all women with PROM more than 18 hours be started on parenteral antibiotic.

212
Q

Management of PPROM:

A

Chorioamnionitis is an absolute contraindication to tocolysis

AB - **Chorioamnionitis is a feared feature of PROM of over 18 hours.

213
Q

memorize this
PPROM

A

Fifty percent of women with PROM women will be in labor in12 hours, 86 % within 24 hours, and 94 % will be established in labor within 48-95 hours. 6% will not establish in labor within 96 hours of PROM.

Chorioamnionitis is a feared feature of PROM of over 18 hours. The most important risk factors for development of chorioamnionitis include: * Increasing numbers of digital vaginal examinations* Longer duration of active labor* Meconium staining of the amniotic fluid

To prevent chorioamnionitis, it is recommended that all women with PROM more than 18 hours be started on parenteral antibiotic.

216
Q

PRETERM LABOUR
criteria

A

The diagnosis of preterm labour must be made carefully

**The criteria or diagnosis are: **

  • The gestational period is less than 36 completed weeks.
  • Uterine contractions, preferably recorded on a tocograph, occur every 5–10 minutes, last or at least 30 seconds and persist or at least 60 minutes.
  • The cervix is >2.5 cm dilated and >75% effaced.

Using these criteria, two-thirds of women presenting with presumed preterm labour will not be in labour. They need reassurance, not drug treatment

217
Q

PRETERM LABOUR
causes :
investigations:

218
Q

PRETERM LABOUR

Fibronectintest

A

Fetal fibronectin (FFN) is an extracellular matrix glycoprotein localized at the maternal-fetal interface of the amniotic membranes, between chorion and decidua, where it is concentrated in this area between decidua and trophoblast. In normal conditions, FFN is found at very low levels in cervicovaginal secretions. Levels greater than or equal to 50 ng/mL at or after 22 weeks have been associated with an increased risk of spontaneous preterm birth. In fact, FFN is one of the best predictors of preterm birth.

Indications
**-Symptomatic women with threatened preterm labour: **
o Between 22+0 and 36+0 weeks gestation and
o Intact membranes and
o Cervical dilatation less than or equal to 3 cm

-OR Asymptomatic women, greater than 22 weeks gestation, with a history of:
o Cervical surgery/trauma or
o PTB in previous pregnancy or
o Late miscarriage in previous pregnancy.

Contraindications of FFN
* Cervical dilatation more than 3 cm
* Ruptured membranes
*Cervical cerclage in situ
* Presence of soaps, gels, lubricants or disinfectants

Relative contraindications*
Visual evidence of moderate or gross bleeding
* Within 24 hours of vaginal intercourse
* A negative fFNresult of less than 10 ng/mL is still valid:
o If a woman reports having intercourse in the previous 24 hours
o In the presence of moderate or gross vaginal bleeding

219
Q

Preterm Labour
Management

220
Q

Preterm Labour
Management
guidelines

224
Q

Abnormal foetal presentations:

225
Q

TRANSVERSE LIE

Abnormal foetal presentations:

226
Q

BREECH PRESENTATIONS

227
Q

breech presentation
management
occipito posterior?
face presentation?

232
Q

shoulder dystocia
read basic

233
Q

shoulder dystocia
management

234
Q

CORD PROLAPSE

237
Q

OBSTRUCTED LABOUR

239
Q

Induction of labour –bishop score

240
Q

Induction of labour –bishop score
GUIDELINES

241
Q

Substance of abuse in pregnancy

medications
teratogenos

A

weeks 1-3 of gestation
●“ all-or-none” effects

●weeks ●3-8 of gestation embryonic period most susceptible time period due to organogenesis

●week 8 of gestation until birth growth and function of organs are affected

242
Q

Substance of abuse in pregnancy

Heavy alcohol

A

Heavy alcohol consumption in pregnancy (>120 g, or 12 standard drinks a day) is associated with:
* 1-IUGR
* 2-Developmental delay and neurological complications in the baby
* 3 -Fetal alcohol syndrome (facial characteristics: low-set ears, elongated midface, small head and upturned nose, skeletal and cardiac malformations). The incidence of FAS is multifactorial and compounded by smoking and other drug abuse, poor diet and social deprivation.

A consumption of seven standard drinks in a week and no more than two in any 1 day spread over at least 2 hours does not appear to have any damaging effects on the fetus or mother. Nevertheless, a pregnant woman should be advised to limit her consumption of alcohol especially during the first trimester, as there is concern about the long-term effects on the neurodevelopment of the child, particularly with numerical problem solving and reading proficiency, which is dose dependent

243
Q

Substance of abuse in pregnancy

Heroin

244
Q

Substance of abuse in pregnancy
cocaine

245
Q

Substance of abuse in pregnancy

Amphetamines

246
Q

Substance of abuse in pregnancy
Cannabis

252
Q

CTG interpretation

A

CTG
variabilidad

253
Q

CTG interpretation
acelerations

254
Q

CTG interpretation

decelerations
types

255
Q

CTG interpretation

Overall impression
reassuring
non reasuring
abnormal:

259
Q

JAUNDICE DURING PREGNANCY
causes 3 :

Systemic disease in pregnancy

A

Jaundice in pregnancy can be caused by
●viral hepatitis,
●intrahepatic cholestasis of pregnancy,
●choledocholithiases,
●HELLP syndrome.

Causes associated with pregnancy Severe hyperemesis gravidarum :

●HELLP
●Acute fatty liver of pregnancy
●Intrahepatic cholestasis of pregnancy

Causes not associatedwithpregnancy
* Viral hepatitis
* Gallstone disease
* Autoimmune hepatitis
* Hemolyticjaundice
* Drug induced

260
Q

JAUNDICE DURING PREGNANCY

ACUTE FATTY LIVER OF PREGNANCY

Systemic disease in pregnancy

261
Q

Cholestasis of pregnancy

Systemic disease in pregnancy

262
Q

HELLP syndrome

Systemic disease in pregnancy

263
Q

THROMBOCYTOPENIA

Systemic disease in pregnancy

266
Q

pulmonary embolism pregnancy daigram

269
Q

Appendicitis

270
Q

POSTPARTUM PSYCHIATRIC PROBLEMS
overview

271
Q

INFECTIOUS DISEASES MEASELS
clinical features:

A

measles complication most common = OTITIS MEDIA

272
Q

INFECTIOUS DISEASES MEASELS
prevention:

A

measles complication most common = OTITIS MEDIA

278
Q
A

NOTE -Interpretation of CMV lgM results in pregnancy requires specialist opinion. Fetal diagnosis is best achieved by a combination of fetal ultrasound, amniocentesis+/-fetal serology; however, the definite diagnosis of fetal infection is by amniocentesis and PCR or the amniotic fluid for CMV. It should be born in mind that positive results do not predict any degree of fetal damage. Since this woman is 16 weeks pregnant, amniocentesis for definite diagnosis is the most appropriate option. Amniocentesis is perfomedin the rather small window of 15-18 (up to 20) weeks. However, repeating the test in 2-4 weeks was the most appropraiteoption if it was an option.

279
Q

round ligament pain
pregnancy

280
Q

food to avoid during pregnancy

281
Q

HEPTATITIS B
SCREENING

A

HEPTATITIS B
ANTENATAL MANAGEMENT

282
Q

HEPTATITIS B
MAGAMENET POTENTIAL EXPOSURE DURING PREGNANCY

A

HEPTATITIS B
NEONATAL MAGAMENET

283
Q

HEPATITIS C
ANTENATAL DIAGNOSIS

A

HEPATITIS C

ANTENATAL MANAGEMENT

284
Q

HEPATITIS C
MANAGEMENT AND FOLLOW UP

285
Q

DIAGNOSIS OF HIV INFECTION IN PREGNANT WOMEN

A

STRATEGTY TO MINIMISE HIV INFECTION IN PREGNANT WOMEN

286
Q

MANAGEMENT OF INFANT RISK HIV

287
Q

ANTI D PROPHYLAXIS

288
Q

ANTI D PROPHYLAXIS
POSTPARTUM

290
Q

HEMOLYTIC DISEASE OF NEW BORN

292
Q
A

blood trasnfusion

294
Q

GESTATIONAL THROPHOBLASTIC DISEASE

A

HYPERMESIS
VAGINAL BLEEDING
UTERUS LARGER THAN EXPECTED

296
Q

HYPERTENSIVE DISEASE

297
Q

MANAGEMENT HYPERTENSION PREGNANCY SUMMARY

298
Q

preeclampsia:

299
Q

preeclampsia

RISK FACTORS:

300
Q

ECLAMPSIA

301
Q

PREECLAMPSIA

ANTIHYPERTENSIVE MEDS
TIME O F BIRTH:

305
Q

hemorrage antepartum > 20 weeks

Inmediate actions just read

306
Q

PLACENTAE PREVIA

DX

SYMPTOMS

INVESTIGATIONS? Important ?

hemorrage antepartum > 20 weeks

307
Q

PLACENTAE PREVIA

TX

risk factors memory ! mcq

308
Q

PLANCETAE ACRETA, INCRETA, PERCRETA

309
Q

VASA PREVIA

310
Q

Abruptio placentae

311
Q

UTERINE RUPTURE

312
Q

BLEEDING>20 WEEKS
ANTEPARTUM BLEEDING SUMMARY

UTERINE RUPTURE
ABRUPTO PLACENTAE
PLACENTAE PREVIA
VASA PREVIA

317
Q
322
Q

Cervical cancer screening

A

2 years after first sexual intercourse or 25–75 years.

HPV test + cell cytology

Negative Result: Every five years.

Unsatisfactory: repeat 6-12 weeks

Positive NON 16-18: Repeat in 12 month. Again positive: Colposcopy.

Positive 16-18: Colposcopy.

Low grade: Repeat in 12 month. Again positive: Colposcopy.

High grade: Colposcopy

323
Q

Breast cancer: Risk factors

A

Risk factors:
- Individuals with age of onset of cancer less than 50 years
- Individuals with ovarian cancer
*Increasing age is a major risk factor.
*Personal history of atypical hyperplasia or lobular carcinoma in situ.
*Strong family history of the disease or mutation in a breast cancer predisposition gene.
*Previous radiotherapy.
*High bone mass or obesity.
-Jewish ancestry
- Breast cancer in a male relative

324
Q

Breast cancer: Screening Low risk

A

Low risk: Family member diagnosed at 50 years or over.

Screening: mammograms
every two years for women aged 50–74 years

325
Q

Breast cancer: Screening Moderate risk

A

Moderate risk:

One 1st degree diagnosed before 50 years
or
Two 1st degree in the same family side at any age
or
Two 2nd degree in the same family side diagnosed before 50 years.

Screening: Annual mammogram for women age 40 years

326
Q

Breast cancer: Screening High risk

A

High risk:

Member of the family in prescence of BRCA 1-2.

or

Two 1st or 2nd degree on the same family side diagnosed with BC or ovarian Ca PLUS:

*Additional relatives with BC or OC.
*BC diagnosed before 40 years.
*Bilateral BC.
*Breast & Ovarian Ca in the same woman.
*BC in a male relative.
*Ashkenazi jewish ancestry.

or

One 1st or 2nd degree with BC < 45 PLUS One 1st or 2nd degree with sarcoma < 45

Screening:

Annual mammogram for women age 40 years

Referral to a cancer clinic for risk assessment, possible genetic testing and management plan.

327
Q

List of all enzyme inducers

A
  • Phenobarbital
  • Primidone
  • Phenytoin
  • Carbamazepine
  • Oxcarbazepine
  • Topiramate
    -ST John’s Wort
328
Q

Non-enzyme inducing anti epileptics

A
  • lamotrigine
  • Levetiracetam
    NOTE: Increase dose in case of OCP as they increase metabolism
329
Q

When does ovulation occur?

A

14th day (midcycle)
- LH surge
- next 24 h (12-36)

330
Q

Ovulation occurring investigation

A

plasma oestradiol peaks
- ovulation to occur in 36-48 hrs

Cervical mucus alteration immediately before ovulation
-more abundant/maximal
- clear and slippery

NOTE: These are less accurate ways to predict ovulation

331
Q

Investigation of choice to predict ovulation has occurred

A

Serum progesterone surge at day 21 (luteal phase)
- level > 20nmol/L

332
Q

Ovulation pain is also known as

A

Mittelschmerz syndrome

333
Q

Ovulation inducing drugs

A

Clomiphene

334
Q

Primary Dysmenorrhoea

A
  • Pain occurs before menses
  • Initial treatments NSAID’s
  • Trial of OCP’s for 2 months upon px request
335
Q

Secondary dysmenorrhoea

A
  • Treat underlying problem

DRAFT

336
Q

Difference between biphasic and triphasic contraceptive pills

A

biphasic: same amount of oestrogen but level of progestin is increased halfway through
triphasic: 3 different doses of oestrogen and progesterone every week for 3 weeks along with sugar pills

337
Q

COCP doses

A
  • low dose: 20mcg of oestrogen.
  • regular dose: 30-35mcg oestrogen.
  • high dose: 50mcg of oestrogen.
338
Q

High dose COCP indications

A
  • Break through bleeding on low dose pills.
  • When low dose pill fails.
  • Concomitant use of enzyme inducing drugs
  • Control of menorrhagia.
339
Q

Approach to PMS

A

1st line: Conservative treatment for 3 menstrual cycles (yoga)
2nd line: COCP, SSRI
3rd: GNRH antagonists due tenderness (danazol) careful because this drug can induce menopause, main complaint of fluid retention spironolactone, main complaint of dysmenorrhoea (mefenamic acid)

BEST method: endometrial ablation, hysterectomy?

DRAFT

340
Q

OCP absolute contraindications

A
  • Pregnancy.
  • < 6 weeks post-partum.
  • Thromboembolic disease.
  • CVA.
  • CAD like known IHD
  • Migraine with aura.
  • Age >35 years and smoking > 15 cigarettes per day.
  • Oestrogen dependent tumours.
  • Active liver disease.
  • Polycythaemia.
  • Undiagnosed vaginal bleeding.
341
Q

OCP relative contraindications

A
  • Age > 35-45
  • BMI > 35
  • Smoker >15 cigarettes per day
  • Breast feeding
  • HT ( >160/ 100)
  • DM
  • Hyperlipidaemia.
  • Depression
  • SLE
  • 4 weeks before and 2weeks after surgery
342
Q

Monthly COCP contents

A

28 pill pack:
* 21 hormonal pills and
*7 sugar pills.

343
Q

COCP administration

A
  • Start on 1st day of menstrual period, continue till 21 days and then 7 sugar pills.
  • Take pill on the same time every day, 1pill /day.
  • On starting sugar pills, the lady gets periods.
  • Protection starts from 1st day of using pills if taken from the 1st day of periods.
  • Or if at any other time of the cycle, alternate methods of contraception should be used
    for 7 days and pregnancy needs to be ruled out.

NOTE: a 24/4 pill pack is also available.

344
Q

COCP advantages

A
  • Decreased menorrhagia, dysmenorrhea and pre-menstrual syndrome. (Periods become
    shorter, lighter and regular).
  • Decreased iron deficiency anaemia.
  • Decreased incidence of functional ovarian cysts, PID, acne, thyroid disorders
345
Q

OCP’s increase the risk of which cancer/s

A

if used more than 5 years:
- cervical
- breast

NOTE: conflicting data, use with caution

346
Q

OCP decreased risk of which cancer/s

A
  • Ovarian cancer 30-50%
  • Colorectal cancer 15-20%
  • Endometrial cancer >30%
347
Q

OCP’s and ovarian cancer

A

OCP’s have no relation to developing ovarian cancer. Some sources have even labelled it as a protective factor

348
Q

COCPs mild side effects

A
  • Break through bleeding
  • Nausea
  • Vomiting
  • Bloating
349
Q

COCPs breakthrough bleeding management

A
  • Usually settles in 3-4 months. If not, check compliance
  • Change from low dose to regular dose
  • Change progesterone to 2nd or 3rd generation if already on regular dose
    OR
  • Another contraceptive or vaginal ring
350
Q

COCPs major side effects

351
Q

Irregular bleeding while on OCP risks

A

– Smoking
– Chronic malabsorption syndrome
– Severe nausea, vomiting and diarrhoea.
– Hepatic enzyme-inducing drugs
(anti-epileptics, anti-tuberculosis and drugs used to treat HIV.)

NOTE: Modafinil is a drug used in patients with a history of narcolepsy can also interfere with contraceptive pills efficacy due to enhanced liver metabolism

352
Q

OCP’s and diarrhoea

A

Severe diarrhoea & vomiting decrease the effectiveness of OCP’s
- take an extra pill add barrier method in addition

353
Q

Missed pills on OCP > 48 h

A

-1st week (1-7) emergency contraception, finish the pack as regular after
- 2nd week (8-14): No need for emergency contraception, finish the pack
- 3rd week (15-21): Next pack of pills should be started without a break (pill-free period omitted)

NOTE: > 7 pills missed, start new fresh pack (exclude pregnancy)

354
Q

Px with hypertension on OCP

A

Change to POP

355
Q

OCP and Otosclerosis

A
  • Systemic hormones from OCP can exacerbate otosclerosis
  • Prescribe IUD instead
356
Q

Px with DVT on OCP

A
  • If px has family history but DOESN’T have DVT herself: POP
  • if px has history of DVT: POP
  • prescribe barrier methods

DRAFT

357
Q

Contraindications to POP

A

Current VTE
Rifampicin (absolute contraindication)
CYP3A4 inducers
malabsorption syndromes
ovarian cysts
previous sex steroid-dependent cancers (breast cancer)
undiagnosed vaginal bleeding
previous ectopic pregnancy
severe active liver disease
successfully treated Breast Cancer > 5 years

358
Q

Absolute contraindication for progesterone implant (Implanon)

A

Breast cancer

359
Q

Contraception of choice in breastfeeding women

A

POP for around 6 months, changing to OCP

360
Q

POP’s in surgery

A

can be given but be on lookout for VTE

361
Q

Progesterone increases the risk of

362
Q

Px on epileptics wanting contraception

A
  • Give IUD (Mirena)
  • IF patient is seizure free for 2 years we can reduce the dose of anti-epileptics and give high dose OCP
  • If patient not seizure free then only high dose OCP

NOTE: anti-epileptics are enzyme inducers and reduce OCP efficacy by 40-50%

363
Q

Postinor-2

A

Progesterone only emergency contraceptive
- 2 tablets at the same time associated with less adverse effects (Virilisation)

DRAFT

364
Q

Best emergency contraception until 5 days

A

1st Ulipristal

2nd Copper IUD

365
Q

IUD best time for insertion

A

During the first 7 days of your menstrual cycle, which starts with the first day of bleeding

366
Q

1st line treatment for Dysfunctional uterine bleeding

A

Mild: NSAID’s & Tranexamic acid
Moderate: COCP or POP
Severe: IV fluids, tranexamic acid, high dose norethisterone

367
Q

HPV vaccination

A

administered in high school

368
Q

Uterine prolapse

A

weakening of the uterosacral ligament

369
Q

risk factors for the development of urinary incontinence

A
  • Obesity (stress)
    – Prenatal urinary incontinence (detrusor)
    – Constipation (stress)
    – Instrumental delivery
    -Third and fourth-degree tears
    -Baby with a birth weight of more than 4.0 kg (detrusor)
370
Q

Post menopause is defined as

A

permanent end of menstruation and fertility, defined as occurring 12 months after the last
menstrual period

371
Q

Most likely cause of post-menopausal bleeding

A

vaginitis due to oestrogen deficiency

372
Q

Age of onset for ovarian cancer

373
Q

HPV can cause what type of cancers

A

– Cancer of cervix.
– Cancer of oro-pharyngeal cavity.
– Squamous cell carcinoma of anus, penis and vagina.
– Cancer of the uterus

374
Q

Cervical cancer risk factors

A

-All women who are or ever have been sexually active.
-Early age at first sexual intercourse.
- after 35
- prolonged use of OCP ( > 5 years)
- immunosuppression
- multiparity (>5)
- persistent HPV infection
-Multiple sexual partners.
-Genital warts virus infection.
-Cigarette smoking

375
Q

genital warts HPV

376
Q

Conservative methods to manage urinary incontinence

A

-Lose weight by 5% or more
-Reduce caffeine intake
-Modify fluid intake-according to hydration status.
-Pelvic floor muscle training
-Treat constipation to avoid straining.
-Treatment of respiratory conditions leading to a chronic cough

377
Q

Investigation of choice for the diagnosis of endometriosis

A

Diagnostic laparoscopy with histopathology

378
Q

What criteria of women that do not need cervical screening?

A

Women who have never engaged in sexual intercourse

379
Q

Mastalgia causes

A
  • cyclical mastalgia (most common)
  • pregnancy
  • caffeine
  • breast cancer
    < 10%
    mastitis carcinomatosa (red and hot breast during lactation)
380
Q

Oral contraceptive pills increase the incidence of which cancer

A

cervical cancer

381
Q

most common type of cervical cancer

A
  • Squamous cell carcinoma 80%
  • adenocarcinoma
382
Q

Stein- Leventhal syndrome is also known as

383
Q

Ovarian cyst: premenopausal cyst less than 5cm and asymptomatic

384
Q

Ovarian cyst: premenopausal cyst 5-7cm and asymptomatic

A

Repeat US in 3-4months and monitor to see if the cyst grows

385
Q

Ovarian cyst: premenopausal cyst >7cm and symptomatic

A

high risk of torsion
Refer to gynaecologist

386
Q

Ovarian cyst: Post menopausal Simple unilateral, unilocular ovarian cysts of <5 cm and low risk of malignancy (normal Ca125)

A

managed conservatively conservatively as the RMI would be zero and 50% of these will resolve spontaneously in 3 months.

387
Q

Ovarian cyst: Post menopausal

A

Cysts of 2–5 cm should be rescanned in 3–4
months.
Women with a moderate-to-high risk RMI should be referred to a referred to a gynaecologist or gynaecological oncologist for consideration of surgical management.

388
Q

Menopause hot flushes due to oestrogen

389
Q

Menopause hot flushes

A

Cyclical oestrogen and progesterone HRT (oestrogen only in hysterectomy)

390
Q

progestogen-only conditions

A

1-Hypertension
2-Superficial thrombophlebitis
3-History of thromboembolism
4-Biliary tract disease
5-Thyroid disease
6-Epilepsy
7-Diabetes without vascular disease

391
Q

Premature menopause

A
  • < 40 years
  • oocytes produce less oestrogen and progesterone, both LH and FSH start to rise
  • Menstrual irregularity and vaginal atrophy
  • increased FSH level is diagnostic
392
Q

Ovarian cancer risk factors

A

– A family history of either ovarian or breast cancer.
– Personal history of breast cancer due to BRACA genes.
– Early menarche.
– Late menopause.
– Nulliparity.
– Increasing age
- obesity

393
Q

sexually active malodorous gray vaginal

A

Gardenerella vaginalis

394
Q

Endometrial cancer risk factor

A

– History of chronic anovulation
– Exposure to unopposed oestrogen
– Polycystic ovary syndrome (PCOS) associated
with chronic anovulation
– Exposure to tamoxifen
– Strong family history of endometrial or colon cancer (Lynch syndrome)
– Nulliparity
– Obesity
– Endometrial thickness more than 8mm in premenopausal woman

395
Q

Lynch syndrome

A

MLH1 + MSH2 mutation
- 40% endometrial cancer
- 10% ovarian cancer

Strong family history of endometrial or colon cancer (<50 years)
- 3 family members
- generational
- (<50 years)

396
Q

Tumour with hair and teeth upon presentation

A

mature cystic teratoma (dermoid tumor)

397
Q

Presentation of PID

A

lower abdominal pain that is gradual in onset and bilateral

Fever, vaginal discharge, dysuria, and occasionally abnormal vaginal bleeding
PID can lead to tubal scarring

diagnostic criteria include
uterine, adnexal, or cervical motion tenderness

398
Q

Risk factors of familial breast-ovarian syndrome

A

1.Two first-degree or second-degree relatives on one side of the family with ovarian or breast cancer.
2.Individuals with age of onset of cancer less than 50 years.
3.Individuals with bilateral or multifocal breast cancer.
4.Individuals with ovarian cancer.
5.Breast cancer in a male relative.
6.Jewish ancestry

399
Q

Breast cancer age cut off

400
Q

Colon cancer age cut off

401
Q

Prostatic cancer age cut off

402
Q

hyperprolactinemia anovulation and should be treated with

A

bromocriptine

403
Q

Minimum time for a couple for infertility before starting treatment

404
Q

gynaecology referral cases

A

– Unexplained pelvic pain.
– Pelvic mass which is tender on bi-manual vaginal examination.
– Primary infertility of greater than a year.
– Patient with suspected diagnosis of endometriosis unresponsive to initial
treatment

405
Q

Painless mass

A
  • rule out malignancy
  • biopsy
406
Q

Indications to use progestogen-only pills

A

1-Age 45 years or more
2-Smokers aged 45 years or more
3-Contraindications to oestrogen
4-Diabetes Mellitus
5-A migraine (combined oral contraceptive pills have absolute contraindication)
6-Well-controlled hypertension
7-Lactation
8-Chloasma (large brown patches on skin)

407
Q

Contraindications to use progestogen-only pills

A
  • pregnancy
  • undiagnosed genital tract bleeding
  • concomitant use of enzyme-inducing drugs
408
Q

Features of dysfunctional uterine bleeding

409
Q

Post menopausal treatment for endometriosis

410
Q

Medical treatment for endometriosis

A
  • OCP
  • continuous progestins
  • danazol
  • GnRH analogues
411
Q

Premenstrual dysmorphic disorder

A

Mimics PMS but displays more severe symptoms that get in the way of the patients ability to function and feeling overwhelmed/ out of control, frequent tearfulness
(abdominal bloating, headaches, reduced libido, reduced concentration and anger management issues)

412
Q

Contraindication to oral administration of oestrogen

A

DVT (liver metabolism is a contraindication)

413
Q

Features of trichomoniasis

A
  • increased frothy, yellowish, fouls smelling vaginal discharge
  • dyspareunia and dysuria.
  • genital area is usually red and sore
414
Q

Treatment of trichomoniasis

A

Metronidazole 2 g

415
Q

severe symptoms of premenstrual dysmorphic
disorder treatment

A

Clomipramine and danazol

416
Q

significant intrauterine adhesions symptoms

A

-Infertility.
-Menstrual irregularities (amenorrhea).
-Cyclic pelvic pain.
-Recurrent pregnancy loss.
The gold standard is diagnostic
hysteroscopy.

417
Q

Pituitary necrosis + hx of postpartum haemorrhage + lactation failure+ signs of early menopause

A

Sheehan’s Syndrome

418
Q

Diagnostic method for Sheehan’s syndrome

419
Q

diagnosis of bacterial vaginosis

A

– Thin, white, fishy, offensive and grey homogeneous discharge.
– Vaginal fluid pH more than 4.5.
Clue cells visualised on a wet preparation of a vaginal swab or Gram-stained smear.
– Fishy odour when adding alkali (potassium hydroxide 10%) to discharge.
- Gardenerella vaginalis
- Relapse rate is more than 50% in 3 months time

420
Q

Treatment of bacterial vaginosis

A

Metronidazole
Clindamycin (if pregnant)

421
Q

premature ovarian failure investigation of choice

A

FSH & LH levels are high and oestradiol levels are low

LOW (<1) LH/FSH ratio

422
Q

Tanner stages

A

I:
- 0–15 years
- None
II:
- Commencement of puberty
-8–15
- Pubic hair first, along with breast budding (pubes flow, boobs grow)
III:
- Increase in hair and pigmentation

423
Q

Menorrhagia features

A
  • menstrual periods lasting over 7 days and/or involving blood loss greater than 80mL
    Ovulatory:
  • Abnormal blood loss at regular intervals
  • uterine issue (leiomyoma, endometriosis, adenomyosis, polyps)

Anovulatory:
- irregular and unpredictable
- Hormonal issue (PCOS, hypothyroidism, hyperprolactinemia, Cushing syndrome)

424
Q

Menorrhagia Investigation

A
  • Exclude pregnancy first
    Ovulatory:
  • Transvaginal US (abdominal if adolescent px)

Anovulatory:
- FBE if anaemia present
- Serum TSH, prolactin, LH (look for signs of hyperthyroidism to consider this)

425
Q

Atrophic vaginitis features

A
  • Atrophic changes 5 years after menopause
  • oestrogen deficiency
  • brown vaginal discharge
  • itching, burning, dryness and irritation
  • dyspareunia
  • can lead to bacterial vaginosis with vaginal discharge
  • increased risk of UTI
  • thinning of bladder and urethral linings leading to chronic dysuria
426
Q

Atrophic vaginitis management

A
  • Topical Oestrogen
427
Q

Atrophic vaginitis contraindication

A
  • Breast cancer (can give SSRI for mood changes)
428
Q

Atrophic vaginitis ddx

A
  • Candidiasis (topical antifungal)
  • Lichen Sclerosis (very potent topical corticosteroids)
429
Q

Postcoital bleeding in post-menopausal woman investigation

A

Co-test of HPV and LBC (Rule out cervical cancer)

430
Q

Most common causes of intrauterine bleeding

A
  • STI (chlamydia cervicitis)
  • cervical ectropion
  • cervical polyp (30-40 years)
431
Q

Primary amenorrhoea

A
  • Turner syndrome (ovarian dysgenesis) (pubes grow normally) 43%
  • Mullerian agenesis 15%
    Imperforated hymen (cyclic abdominal pain, abdominal mass)
432
Q

Most common cause of non-menopausal hot flushes

A
  • Hyperthyroidism
  • Hypertension
433
Q

Primary ovarian insufficiency

A
  • ovarian failure before 40 years of age
  • amenorrhoea = or > 4 months
  • High FSH > 40U/L and LOW oestradiol
  • oestrogen deficiency symptoms
  • increased gonadotropin levels
  • LOW LH/FSH ratio (<1)
434
Q

Primary ovarian insufficiency management

A

Desire to conceive: HRT until menopausal age (51 yo)
Contraception: COCP

  • calcium and Vitamin D supplementation
435
Q

Emergency contraception window

A

5 days post coitus

436
Q

Cervical cancer during pregnancy

A

Same outline as regular screening

BUT if there’s evidence of invasive carcinoma, termination is recommended but dependant on px’s choice

437
Q

CIN grading

A

I: low grade (lower 1/3)
II/III: high grade (entire thickness of the epithelium)

438
Q

Cervical motion tenderness indicates

A

PID or Ectopic pregnancy

439
Q

Pelvic inflammatory disease (PID) dx

A
  • Risk of STD
  • Lower abdominal pain
  • **cervical motion **, uterine, adnexal tenderness
440
Q

Pelvic inflammatory disease (PID) investigation

A
  • Cervical swabs for culture
441
Q

Pelvic inflammatory disease (PID) management

A
  • empirical antibiotics
442
Q

Ovarian teratoma features

A
  • occurs in ages 20-30 years
  • diameter <10cm usually, can exceed 15cm (super rare)
  • made of different cells (hair, teeth, sebum, eyes, bone etc)
  • adnexal location
443
Q

Endometriosis common sites

A
  • ovaries
  • posterior cul-de-sac
  • broad ligament
  • uterosacral ligament
  • rectosigmoid colon
  • bladder
  • distal ureter
444
Q

Green vaginal discharge

A

Chlamydia trachomatous
-trachomonous vaginalis (frothy yellow- green)

445
Q

Drospirenone and ethinylestradiol

A
  • less fluid retention
  • less weight gain
446
Q

Dilation & curettage complications

A

intrauterine adhesions (90%)
- infertility
- amenorrhoea
- cyclic pelvic pain
- recurrent miscarriages

447
Q

intrauterine adhesions investigation

A

transvaginal US (initial)
Hysteroscopy (gold standard)

448
Q

Post menopausal HRT protocol (MHT)

A

Cyclical or sequential therapy
Continuous estrogen + cyclic progestogen
Continuous estrogen for 28 days and then progesterone is added during the last 14 days.
Indication: Peri menopausal women and during 1st year of menopause. Will get cyclical bleeds.

Continuous combined therapy
Continuous estrogen+ continuous progestogen
Indication: after 1 year of menopause. Spotting and breakthrough bleeding is common in the first 3-4 months of therapy.

Estrogen alone therapy
In women who had hysterectomy

449
Q

MHT CONTRAINDICATIONS

A

 Age 60 years or older
 Previous DVT
 Previous MI, Uncontrolled HT
 Stroke, Previous TIA
 Breast cancer
 Endometrial cancer
 Undiagnosed vaginal bleeding
 Significant liver disease
 Porphyria/ SLE

450
Q

MHT increase the Risk of:

A

Not to be given after 60 years due to the risk of
VTE and stroke

 Invasive breast cancer (increased with longer duration of combined MHT and persists up to 10 years after MHT is stopped. Risks greater for continuous combined than with cyclical MHT)
 Stroke (usually above 60 years)
 DVT
 Gallbladder disease
 Coronary heart disease (usually above 60 years)

451
Q

MHT Side Effects

A

 Breakthrough bleed- settles in 8 to 12 weeks
 In cyclical if not settled within 2 to 3 months, increase duration of progestogen
 In continuous combined, increase progestogen dose, change type or route or change to tibolone
 Review in 2 to 3 months. If still present investigate
 Nausea- change to transdermal therapy
 Breast tenderness- reduce oestrogen or progestogen
 Initiating therapy with low dose will minimise these side effects

452
Q

MHT FOLLOW UP

A

 Review in 6 to 8 weeks and then at 6 months
and then every 6 – 12 months with general
health check, breast check
 Mammogram every 2 years
 DEXA where indicated
 Vaginal bleed after 6 months of therapy
needs further investigations
 Most guidelines recommend using MHT for 4
to 5 years

453
Q

Hormonal Alternative to continuous
combined MHT (>1y of menopause)

A
  1. Tibolone

 Synthetic steroid with oestrogenic and progestogenic
activity and weak androgenic activity
Less effective than MHT
 Improves bone mineral density and decreases risk of vertebral and non vertebral fractures
 Does not increase breast density but increases risk of breast cancer recurrence
 Increases risk of stroke after 60 years of age
No increased risk of DVT

  1. Conjugated oestrogens + bazedoxifene

 Less effective than MHT
 Increases hip and spine bone density

454
Q

Non hormonal Alternatives to MHT

A

 SSRI like citalopram, escitalopram, paroxetine
 SNRI- venlafaxine, desvenlafaxine
Both of above alleviates vasomotor symptoms
but to a lesser degree than MHT

 Gabapentin-equally effective as low dose
estrogen for vasomotor symptoms.

 Pregabalin

 Clonidine- mildly effective

455
Q

PCOS features

A
  1. Clinical or biochemical hyperandrogenism
    -hirsutism
    - acne
    - deep voice
    - acanthosis nigricans
  2. Menstrual dysfunction
    - irregularity
    - lack of ovulation
  3. Polycystic ovaries on US
456
Q

PCOS Rotterdam Criteria

457
Q

PCOS hormonal changes

A
  • increased serum free testosterone
  • Serum FSH low/normal
  • LH elevated
  • FSH/LH ratio 2:1/3:1 perhaps
458
Q

PCOS biochemical hyperandrogenism

459
Q

Bartholin abscess features

A
  • base of labia minora
  • Neisseria gonorrhoea/ Chlamydia trachomatis
    asymptomatic <3cm: no treatment/warm compress
    symptomatic:
  • < 3cm Incision & drainage
  • > 3cm word catheter
  • marsupialisation if after 1-2 failed then word catheter
  • gland excision if marsupialisation fails
460
Q

Endometrial cancer/hyperplasia risk factors

A

-unopposed oestrogen therapy 2-10%
- increasing age 50-70 years 1-4%
- obesity 2-4%
- chronic anovulation (PCOS) 3%
- late menopause >55 25
- Nulliparity 2%
- Diabetes 2%

461
Q

Smoking protective factor

A

uterine leiomyomas
ulcerative colitis
Parkinson’s

462
Q

Uterine fibroids/leiomyoma risk factors

463
Q

Features of Turner syndrome

A
  • Short stature
  • Webbed neck
  • Puffy hands and feet
  • Coartaction of the aorta
  • cardiac abnormalities
  • high- arched palate
  • absent secondary sexual characteristics during puberty
  • B/L streak ovaries
  • horse shoe kidney
  • obstructed Uteropelvic junction
464
Q

Bacterial vaginosis management

A

1st line: oral metronidazole 7 days (400mg twice daily)
2nd line: vaginal clindamycin (1g at night)

NOTE: for pregnancy: Clindamycin 300mg orally for 7 days initially
or metronidazole 400mg orally 7 days

465
Q

High grade squamous intraepithelial lesion (HSIL)

A
  1. Colposcopy & cervical cytology in 4-6 months
  2. cervical cytology and human papilloma virus typing at 12 months after treatment annually until tested negative BOTH tests for 2 consecutive occasions
  3. Returned to standard 5 yearly screening
466
Q

Most common cause of chronic pelvic pain in developed countries

A

Endometriosis

467
Q

Most common symptom of endometriosis

A

dysmenorrhoea

468
Q

premenopausal management of ovarian cysts

A
  • Asymptomatic women with simple ovarian cyst <5 cm on ultrasound = no follow-up, cysts will resolve within 3 menstrual cycles
  • Simple cysts of 5–7 cm, a repeat ultrasound should be obtained
  • cysts of >7 cm surgical intervention should be considered.
    If surgery is required, a laparoscopic cystectomy is the operation of choice, as aspiration can cause recurrence.
469
Q

Lactation amenorrhoea

A

1st 6 months after delivery
- baby fully breastfed
- woman remains amenorrhoeic

470
Q

Endometrial cancer types

A
  • simple
  • complex
  • cystic glandular (most common in perimenopausal women)
    -atypical simple
  • atypical complex
471
Q

Endometrial cancer features

A
  • bleeding between periods
  • heavy and/or prolonged periods
  • vaginal discharge
  • abdominal pain
472
Q

Treatment of infertility

A
  • < 35 years but BMI > 25, lifestyle modifications for 1st 6 months
  • > 35 years BMI 30-32 metformin (with or without clomiphene citrate)
  • > 32 BMI combined metformin with clomiphene citrate
  • Metformin & clomiphene citrate unsuccessful, then gonadotropins
  • if PCOS present, laparoscopy with ovarian surgery
  • IVF
473
Q

HRT and mammography

A
  • continue HRT (no need to reduce dose or stop) and commence mammography screening as per guidelines
474
Q

HRT and breast cancer

A
  • after 5 years risk of breast cancer increases
  • No breast cancer risk up to 7 years if HRT oestrogen alone (hysterectomy)
  • review medications annually
  • breast cancer screening per normal as other women
475
Q

HRT & PE/DVT/ stroke

A

increased incidence
- oestrogen only not enough evidence

476
Q

HRT reduced incidence

A
  • Osteoporosis/fractures
  • colon cancer
477
Q

Osteoporosis treatment

A
  • Alendronate, risedronate and zoledronic acid: first-line therapy in **postmenopausal osteoporosis **
    and prevent vertebral, Non-vertebral and hip fractures.
  • bisphosphonates: primary prevention of fractures in px who never had minimal trauma fracture, secondary prevention of fractures
  • Strontium ranelate: primary prevention of osteoporosis in women
  • bisphosphonates and raloxifene: secondary prevention of fractures in women who have had minimal trauma fractures
478
Q

Osteoporosis treatment not going to plan, what to do

A
  • BMD T-score of =<-3
  • > 1 symptomatic new
    fracture after at least 12-months of
    continuous therapy
  • > 2 minimal trauma fractures despite being on sufficient doses of bisphosphonates.

switch to teriparatide for 18 months

479
Q

Stress incontinence management

A

Pelvic floor exercises (Kiegel)

480
Q

Urge incontinence management

A

Bladder training

481
Q

Urinary incontinence with cystocele management

A

Anterior colporrhaphy

482
Q

shoulder tip main mainly refers to

A

ectopic pregnancy

483
Q

unilateral dull pain that can become diffuse smooth adnexal mass with or without peritoneal signs

A

ovarian cyst

484
Q

ascites + pleural effusion + ovarian tumour

A

Meig’s syndrome
- Ovarian fibroma
- spindle shaped cells

485
Q

Presence of Signet cells on histology

A

Krukenberg tumour

486
Q

Turner syndrome is also known as

A
  • Gonadal dysgenesis
  • Ovarian dysgenesis
487
Q

Endometriosis diagnostic time period

A

Due to the variability in this condition, there is a diagnostic delay around 8-10 years

488
Q

Post coital bleeding ddx

A

Rule out malignancy first
1-Cervical erosion
2-Cervical polyp
3-Presence of IUCD
4-Cervical cancer
5-Intra-uterine cancer

489
Q

Ectopic pregnancy high risk factors

A

Previous ectopic pregnancy
Previous tubal surgery
Tubal pathology
Past & current use of IUD
IVF

490
Q

Mirena contraindications

A

– History of breast, cervical or uterine cancer.
– History of liver disease.
- Septic abortion
– Uterine abnormalities, such as fibroids, that interfere with the placement or retention of Mirena.
– Current pelvic infection or have a history of a pelvic inflammatory disease (PID).
– Unexplained vaginal bleeding.
-Being at high risk of a sexually transmitted disease

491
Q

Endometrial ablation contraindications

A

– Pregnancy.
– Suspected genital tract infection.
– The desire to preserve fertility.
– Post-menopausal women.

492
Q

Post-menopausal endometrial thickness

A

Suspect endometrial malignancy - endometrial thickness of 4mm or more with vaginal bleeding mandates endometrial biopsy

493
Q

Ovarian cancer diagnostic approach

A

CA-125 test along with transvaginal ultrasound

494
Q

Features of endometritis

A
  • Lower abdominal pain and uterine tenderness (first 24 to 72 hours)
  • Purulent lochia
  • chills, headache
  • malaise
  • anorexia
495
Q

endometritis management

A
  • augmentin
  • triple test
496
Q

Preoperative staging for endometriosis

A

MRI
- visualising soft tissues as well as all pelvic compartments at one time as opposed to US

497
Q

Asymptomatic bacteriuria treatment indication

A
  • Pregnancy
  • elective urological procedures (TURP)
498
Q

Right lower quadrant (RLQ) pain ddx

A

Gynae
-ectopic pregnancy
- tubo-ovarian abscess
- ruptured corpus luteum ovarian cyst
- ovarian torsion
GI
-appendicitis
-inflammatory bowel disease
- diverticulitis
- hernia

499
Q

Features of threatened abortion

A
  • closed cervical os
  • absent history of passing foetal tissue
500
Q

Features of inevitable abortion

A
  • open cervical os
  • bulging of membranes of the os
501
Q

Features of complete abortion

A
  • closed cervical os
  • passing of foetal tissue
502
Q

Features of septic abortion

A
  • uterine infection during any time
  • vaginal bleeding
    -cramping pain
  • fever
  • purulent cervical discharge
503
Q

Features of missed abortion

A
  • Closed cervical os
  • No spotting or bleeding (no foetal tissue passed)
  • Ultrasound scans diagnosis of a non-viable IUP (empty sac)
504
Q

HPV 6 & 11 indicate

A

benign condyloma (genital warts)

505
Q

features of Sertoli-Leydig tumour

A
  • high androgen production
    (seborrhoea, acne, menstrual irregularity, hirsutism, breast atrophy, alopecia, deepening of the voice, and clitoromegaly)
506
Q

Features of Kruckenberg tumour

A
  • Bilateral solid mass on the ovary
    -Metastasis from other organs (stomach, intestine)
507
Q

evidence of glial tissue and
immature cerebellar and cortical tissue

A

Immature teratoma

508
Q

Testosterone cream uses

A
  • Lichen sclerosis
  • vaginal dryness
  • vulvar atrophy
  • post menopause
509
Q

Prader-Willi syndrome

A

deletion of chromosome 15 (70%) after the newborn period:
- hypotonia
- hypogonadism
- hyperphagia
- hypomentia
- obesity

510
Q

Infertility Treatment for premature ovarian failure/ menopause

511
Q

Premature menopause dx

A

occurs spontaneously before 40 years.
- frequent follicular development
- infrequent ovulation

512
Q

HPV can cause what type of cancers

A

– Cervical cancer.
– Cancer of oro-pharyngeal cavity.
– Squamous cell carcinoma of anus, penis and vagina.
– Cancer of the uterus.

513
Q

common cause of gynaecological cancer deaths

A

Ovarian cancer

514
Q

Most common type of ovarian cancer

A

Epithelial ovarian cancer (90%)

515
Q

Treatment of Lichen- sclerosis

A

Potent topical steroids

516
Q

Lichen- Sclerosis dx

A
  • pre-pubertal and peri-menopausal women
    TRIAD: genital itching, soreness and white wrinkled plaques
    in the genital area
    -Dx: biopsy
517
Q

Specific Indications for cone biopsy

A
  1. Fail to visualize Transformation zone in pt with HSIL on her Cervical smear ref
  2. Suspecting early invasive Cx cancer on cytology, biopsy or colposcopic assessment
  3. Suspecting glandular abnormalities on cytology or biopsy
518
Q

chlamydial urethritis treatment

A

Azithromycin 1 g oral

519
Q

Post menopausal + endometrial thickness 4mm or above + vaginal bleeding

A

Suspect Endometrial cancer and refer to gynaec for endometrial biospy

520
Q

GBS treatment

A

The following women should be treated for GBS during labour:
All women with a history of a GBS-related disease – these women should be given intrapartum antibiotics in all their subsequent pregnancies regardless of the swab culture results
All women with a GBS positive swab or urine culture result in the current pregnancy
Premature rupture of membranes for more than 18 hours, or when the time is unknown
Maternal pre- or intra-partum fever of 38°C
Women with unknown status of GBS colonization

521
Q

most important Endocrine test in assessing male infertility

A

FSH : more than 2time the normal indictaed irreversible testicular failure

522
Q

Aromatase inhibitors cause

A
  • increased osteoporosis
  • cardiac abnormalities
523
Q

Cushing syndrome symptoms in women

A
  • anxiety
  • tremulousness
  • weight gain
  • severe fatigue
  • menstrual irregularities
    -hypertension
  • hyperglycaemia
  • Pinkish stria on buttocks, thighs, breast
  • Skin becomes thin and bruises easily
  • check serum cortisol level
524
Q

Contraceptives used in the treatment of acne

A
  • Cyproterone acetate
  • Desogestrel
  • Drospirenone
  • Gestodene