Obstetrics Flashcards

1
Q

What are the normal pH ranges at delivery for uterine artery and vein samples during cord gases?

A

Uterine vein (reflects maternal status and placental function): pH 7.2 - 7.44)
Uterine artery (reflects fetal status): pH 7.1 - 7.38

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2
Q

What does the FIGO classification for abnormal uterine bleeding PALM-COEIN stand for?

A

P: Polyps
A: Adenomyosis
L: Leiomyoma (ie fibroids)
M: Malignancy (endometrial, cervical, ovarian)
C: Coagulopathy
O: Ovulatory dysfunction
E: Endometrial
I: Iatrogenic
N: Not yet classified

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3
Q

Is the luteal phase fixed at 14 days, true or false?

A

True. The lifespan of the corpus luteum is 14 days

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4
Q

Which age group has the highest variability in menstrual cycle length on average?

A

<25 year olds have the highest menstrual cycle length variability. Variability declines to be at the lowest in the 35-39 age category. Variability then slightly increases again in the 40-44 category.

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5
Q

Menstrual cycles tend to get shorter with age, true or false?

A

True.

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6
Q

What is the ‘normal’ menstrual blood loss per cycle?

A

25-50ml is considered normal. Menstrual blood loss equal or greater than 80ml is considered abnormal (HOWEVER when defining HMB clinically, impact on physical / emotional / quality of life is the definition. the use of >80ml per cycle should only be used for research work)

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7
Q

A 32-year-old woman presents with symptoms of menorrhagia, dysmenorrhoea and cyclical, localised pelvic pain. The pelvic ultrasound showed no abnormality. What is the next appropriate investigation?

A

Laparoscopy
Allows diagnosis +/- ablation therapy for endometriosis in younger females with cyclical pelvic pain + dysmennhorea + menorrhagia and a normal USS.

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8
Q

What 2 investigations are pre-requisities before performing uterine artery embolisation on fibroids?

A

1) Hysteroscopy
2) MRI pelvis

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9
Q

What is the first-line diagnostic tool for the identification of structural pathology in women with HMB?

A

Transvaginal / transabdominal USS

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10
Q

What is the next appropriate investigation for postmenopausal bleeding with abnormal endometrial thickness on USS?

A

Urgent outpatient hysteroscopy + endometrial biopsy

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11
Q

Which specific test, additional to routine screening, is undertaken on women with HMB in their teenage years or who have had HMB since menarche

A

Testing for coagulation disorders, including von willebrand’s disease

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12
Q

What are contraindications for endometrial ablation?

A

Endometrial ablation is lower risk (but has ~ 20% risk of inadequate resolution leading to eventual hysterectomy) than hysterectomy for those women that suffer with HMB resistant to medical treatment and that do not wish for further children. Contraindications to ablation are;
- Large uterus - either >12 weeks in size or >12 cm in length - not an absolute contraindication but the chance of success lower
- Submucosal fibroid/s >2cm
- Any non-benign endometrial pathology
- Cervical cancer
- Current pelvic infection
- If hysterectomy is required for another condition

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13
Q

What are the 4 features of a menstrual cycle that you should assess and what are the ‘normal’ (5th - 95th centile) values for them?

A

Frequency - should be between every 24-38 days
Variability - there should be max 7-9 days variability between the shortest and longest cycles
Duration - 4-8 days of bleeding per cycle
Volume - subjective, but 25-50ml considered normal, >80 is heavy

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14
Q

What are the different sub-divisions of intermenstrual bleeding (IMB)?

A
  • Cyclic mid-cycle IMB - regular midcycle bleed that can be physiological due to the trough in oestrogen at the time of ovulation
  • Cyclic pre or post menstrual IMB - bleeding that cyclically occurs either in the follicular phase or in the luteal phase
  • Acyclic IMB - IMB that is not cyclical / predictable
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15
Q

Definition of infrequent periods?

A

Periods every >38 days

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16
Q

Definition of frequent periods?

A

Periods every 23 days or less

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17
Q

Definition of irregular periods?

A

10 or more days variation in menstrual cycle lengths

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18
Q

Definition of prolonged menses?

A

> 8 days bleeding per cycle

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19
Q

Acute versus chronic non-gestation AUB?

A

Acute is a one-off episode of abnormal uterine bleeding whereas chronic is an abnormality in frequency, variability, duration or volume that has been present for the majority of the last 6 months or more.

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20
Q

What are polyps?

A

Polyps = localised overgrowth of endometrial stroma and gland tissue. Can be endometrial or endocervical. Can be pedunculated or sessile (flat). Tend to be smaller than fibroids. Don’t tend to be painful. Can cause irregular periods + IMB / spotting.

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21
Q

What are the 3 layers of the uterine wall?

A

Endometrium, myometrium and perimetrium

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22
Q

What is adenomyosis? What are it’s presenting symptoms and what are the classical US findings?

A

Adenomyosis = growth of endometrial tissue within the myometrial layer. Tends to present with dysmennorhoea + menorrhagia and an enlarged, tender uterus.
TVUS shows a globular enlarged uterus, heterogenous echogenicity of the myometrium, loss of clarity of the endo-myometrial junction + linear striations.

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23
Q

What are known risk factors for adenomyosis?

A

Factors that disrupt the endo-myometrial junction (= ^ parity, prev LSCS, prev TOP, uterine curettage) and prolonged oestrogen exposure (advancing age, prev tamoxifen use)
SMOKING MAY BE PROTECTIVE

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24
Q

what are fibroids and how do they typically present?

A

Fibroids are benign smooth muscle tumours of the myometrium. They typically grow larger than polyps, are extremely common (>80% in black women + >70% in white women by age 50), result in prolonged + painful periods and chronic pelvic pain and pressure symptoms.
As women get older there is small but significant risk of malignant transformation of fibroids into leiomyosarcomas = uterine sarcomas arising within a fibroid and presenting with AUB and more rapid fibroid growth. Incidence of uterine sarcoma is essentially non-existent <45 and only ~0.5% in peri and post menopausal women.

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25
Q

What are the major risk factors for endometrial hyperplasia and malignancy?

A

Unopposed exposure to oestrogen + prev Tamoxifen use.
Family history of endometrial, breast or colon cancer
Nulliparity
Late menopause
Obesity
PCOS
Diabetes + hypertension

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26
Q

What features of presentation / investigation in a women with AUB would make you suspect a primary endometrial disorder (AUB-E)?

A

Primary endometrial dysfunction should be considered in women with HMB but regular cycles and a structurally normal uterus and normal clotting. Unknown pathophysiology but may be related to abnormal local haemostasis.

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27
Q

What are the 4 main categories of medications that are commonly implicated in iatrogenic AUB?

A

1) Exogenous sex steroids, especially progesterone-only preparations
2) Drugs that alter hepatic enzyme activity which can affect circulating sex steroid levels (anti-epileptics and anti-TB drugs)
3) Anti-coagulants + anti-platelets
4) Tricyclic antidepressants eg amitriptyline - alter dopamine levels = hyperprolactinaemia = anovulation

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28
Q

What is an isthmocoele?

A

A uterine defect at the site of a previous LSCS incision that can sometimes be a cause of ‘not otherwise classified’ AUB

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29
Q

What are the routine 1st line investigations that should be carried out in primary care for women presenting with HMB?

A

Gynae and general Hx
Exclude pregnancy
FBC to assess for anaemia
Coag screen + VWF if positive response to screening questions or HMB since menarche
Speculum exam with cervical smears + pelvic infection swabs as appropriate
Bimanual examination to assess for pelvic masses / tender / bulky uterus
Request pelvic USS as 1st line if no obvious evidence or strong risk factors for polyps or endometrial malignancy
If polyps / endometrial pathology suspected then outpatient hysteroscopy +/- endometrial biopsy should be 1st line.
USS is more accurate at identifying uterine fibroids than hysteroscopy whereas hysteroscopy is better at identifying polyps and endometrial pathology.

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30
Q

What are the ‘red flag features’ in HMB that warrant referral to one-stop or rapid access gynae clinic?

A

1) Suspected malignancy (persistent intermenstrual / post-coital bleeding / post-menopausal bleeding, cervical lesion or pelvic mass = urgent referral, within 2 weeks)
2) Endometrial biopsy required to exclude endometrial hyperplasia / malignancy (persistent AUB, >45 with treatment failure, irregular bleeding on hormone replacement or tamoxifen)
3) Enlarged uterus (>10weeks clinically or > 10cm on uss)
4) Moderate / Severe anaemia
5) Uterine / ovarian pathology noted on USS
6) Coagulopathy identified
7) Failed medical treatment (after at least 3 months pill or 6 months Mirena)
8) Patient wishes for surgery (ablation / hysterectomy)

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31
Q

Who does NICE define as a high risk patient when presenting with AUB?

A

Those women that either:
- are >45
- have declined or failed medical / conservative treatment
- pathology is suspected based on history / clinical exam

The above should be referred to secondary care.

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32
Q

Appropriate initial Tx of woman with AUB <45 with no history/examination findings consistent with structural pathology?

A

3-6 month trial of medical therapy - ECLIPSE trial showed that outcomes / satisfaction was higher amongst those treated with Mirena coil compared with TXA/NSAIDS/progesterone only pill/COCP

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33
Q

How should symptomatic bacteruria be treated in pregnant women?

A

If symptomatic of UTI, test with dipstick - if evidence of infection send for culture + start on empirical Tx for. 7 days: 1st line = Nitrofurantoin (avoid near term due to risk of neonatal haemolysis). 2nd line = Amoxicillin or Cefalexin
AVOID TRIMETHOPRIM IN PREGNANCY, TERATOGENIC IN 1ST TRIMESTER

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34
Q

How should Asymptomatic bacteruria be treated in pregnant women?

A

All women should be screened for asymptomatic bacteruria at booking - if culture is positive start on 7 days Nitrofurantoin / Amoxicillin / Cefalexin. REPEAT CULTURE AFTER TREATMENT TO ENSURE CLEARED.

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35
Q

Why is asymptomatic bacteruria treated in pregnant women but not the non-pregnant population?

A

Because of the increased risk of progression to pyelonephritis

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36
Q

What is the 1st line treatment for pyelonephritis in pregnancy?

A

A broad spectrum cephalosporin eg cefuroxime.
(also 1st line in the non-pregnant population! )

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37
Q

Combined oral contraceptive pill main mechanism of action?

A

Inhibition of ovulation

38
Q

Progesterone-only pill (excluding desogestrel) main mechanism of action?

A

Thickening cervical mucus

39
Q

Desogestrel pill main mechanism of action?

A

Inhibition of ovulation

40
Q

Main mechanism of action of progesterone-only implant or depot injection?

A

Inhibition of ovulation

41
Q

Mirena coil / IUS main mechanism of action?

A

Prevention of endometrial proliferation

42
Q

Copper coil / IUD main mechanism of action

A

Toxic to sperm (decreases sperm motility and survival) + ovum and inhibits implantation

43
Q

What are the potential risks to the fetus of rubella infection in pregnancy and when is the risk to the fetus at it’s highest?

A

betweRisks: Stillbirth, miscarriage, IUGR, Congenital Rubella Syndrome (congenital deafness, cataracts, cardiac defects [PDA, pulmonary artery stenosis), autism, microencephalopathy)
Risk is highest the earlier in pregnancy Mum is infected. :
< 10 weeks there is a 90% chance of CRS and high chance of multiple defects.
>16 weeks - low chance of deafness / single defects
No case reports of CRS >20 weeks.

44
Q

How should a woman that is non-immune to rubella be managed in pregnancy?

A

There is no longer routine immunity testing for rubella at the booking appointment.
If a woman develops a rash-like illness in pregnancy she should be tested for Rubella IgG (immunity) and IgM (recent exposure / infection) and Parvovirus 19 serology as they present similarly. Any woman with suspected or confirmed rubella should be reported to the local health protection team regardless of vaccination status.
If she is found to be positive for IgM (recent infection)
she should be referred urgently to fetal medicine. There are no treatments to prevent CRS but Human Normal Immunoglobulin can be given to reduce the risk.
If unvaccinated, CANNOT VACCINATE AGAINST RUBELLA IN PREGNANCY but advice to avoid those with rash / might have rubella and to get vaccinated post-natally.

45
Q

When is routine antenatal anti D prophylaxis given to rhesus negative pregnant women?

A

Routine anti-D prophylaxis is given in the 3rd trimester to rhesus neg women. Can either be 2-dose treatment (@ 28 weeks + @ 34 weeks) or 1-dose treatment (between 28-30 weeks). No difference in efficacy, is trust dependent.

46
Q

When is postnatal anti D prophylaxis given to rhesus negative women

A

Umbilical cord sampling is taken at birth. If baby is rhesus positive then anti D is given within 72 hours of delivery.

47
Q

How should HIV positive pregnancies be managed?

A

HIV screening to all pregnant women
In HIV positive women, antepartum, intrapartum + postpartum infant prophylaxis ART is recommended.

If viral load is <50 copies/ml @ 36 weeks then vaginal delivery is recommended. If not then c-section is recommended.
Zidovudine infusion during labour / started 4 hrs before c–section

Zidovudine oral to the infant if viral load <50. If not then they need triple ART.

48
Q

RCOG new guidelines on GBS management in pregnancy

A

UNIVERSAL SCREENING AT BOOKING APPOINTMENT NOT RECOMMENDED. Testing should not be done on maternal request. If GBS UTI then treat at point of diagnosis AND wlll need intrapartum abx. If incidental GCS on vaginal/rectal swab then don’t treat there and then but give intrapartum abx. Any testing should be done at 35-37 wks (3-5 wks before expected delivery date) AND NOT AT THE ONSET OF LABOUR.

If woman prev GBS positive in prev pregnany then explain 50% chance of being positive this pregnancy. Offer them a) testing at 35-37 wks gestation (3-5 wks before anticipated delivery date) with a vaginal + anorectal swab
or b) intrapartum abx prophylaxis.

Intrapartum abx should be offered to all women with a prev BABY with early or late GBS disease regardless of maternal GBS status this pregnancy.

Intrapartum abx for GBS is NOT needed for elective c-sections where the membranes are intact.

ROM at term (37 wks +) in GBS + should start abx stat and offer induction ASAP.
ROM in a GBS negative or unknown woman, offer immediate IOL OR a 24 hr expectant period. After 24 hrs if no natural labour then should induce.

Intrapartum antibiotics are recommended for EVERYONE in pre-term labour (<37 wks) [although not needed for preterm elective c section with intact membranes] or with pyrexia during labour regardless of GBS status. If PROM but >34 wks, can consider induction if known GBS carrier. However if <34wks the risk of prematurity is higher than the risk of GBS.

Membrane sweeps and water births are NOT contraindicated in GBS.

49
Q

Signs/ symptoms of early and late onset GBS disease?

A

Early-onset GBS - 0-6 days
Symptoms: floppy, sleep apnoea/resp distress, reduced feeding / feeding intolerance, blotchy skin, pyrexia, tachy/brady/hypotensive

Late-onset GBS - 7 days - 3 months
Typically presents at septic meningitis -> floppy, bulging fontanelle, turning away from bright light
WHILE INTRAPARTUM ABX REDUCE THE RISK OF EARLY ONSET GBS, THEY DO NOT REDUCE THE RISK OF LATE-ONSET GBS.

50
Q

1st line antibiotic to be given during labour in GBS + women?

A

Benzylpenicillin - loading dose and then every 4 hours during labour. In order to be effective, a dose has to have been given within 4 hours of delivery.

If mild allergy to penicillin, then use a cephalosporin. if severe allergy then use Vancomycin.

51
Q

At what stage in pregnancy would you refer a patient for ECV for breach?

A

Refer if breach at 36 wks.
Done at 36 wks if nulliparous, from 37 weeks if multiparous.
50% chance success.
If converts, unlikely to convert back again.

52
Q

When is folic acid supplementation required until in pregnancy?

A

12 weeks

53
Q

If placenta previa is found on anomaly scan, when is the repeat scan for placenta localisation performed?

A

32 weeks

54
Q

Basic antenatal schedule?

A

<10 wks = booking appointment
10-13 wks = dating scan
18-20 wks = anomaly scan
28 wks = vaccination, 1st anti D given for rhesus neg women
32 weeks = repeat scan if any anomalies on anomaly scan
36 weeks = confirm fetal position, refer for ECV if needed, birth planning

55
Q

What is the standard dose and duration of folic acid in pregnancy?

A

400 micrograms
From pre-conception until 12 wks

56
Q

What are the indications for higher dose folic acid in antenatal care?

A

Obestiy (BMI 30 or more)
Prev neural tube defects or family Hx of neural tube defects
On antiepileptic medication
Diabetic
Sickle cell disease or thalassaemia (take high dose folic acid THROUGHOUT PREGNANCY)

57
Q

Is barrier protection needed if both members of the couple are HIV positive?

A

YES -> to avoid transmission of different viral variants and other STIs

58
Q

Which types of HPV are associated with genital warts + cervical cancer?

A

Genital warts = 6,11
Cervical cancer = 16 + 18

59
Q

What is the presentation of a threatened miscarriage?

A

PV bleeding but cervical os closed and USS in-keeping with normal for dates

60
Q

What is the presentation of an inevitable miscarriage?

A

PV bleeding + membrane rupture or open cervical os

61
Q

What is the presentation of a missed miscarriage?

A

gestational sac with no foetal pole on USS suggesting foetus stopped growing a while ago which has gone underdetected

62
Q

What is the presentation of a complete miscarriage?

A

Empty uterus with no tissue present

63
Q

What is the presentation of an incomplete miscarriage?

A

contents in the uterus and ongoing bleeding

64
Q

What is the typical presentation of intrahepatic cholestasis of pregnancy?

A

2nd half of pregnancy
often family hx
likely to RECUR in later pregnancies
^ risk of preterm labour, stillbirth + fetal distress
the symptoms themself self-resolve after delivery

65
Q

1st line mx for symphysis pubis pain in pregnancy?

A

Advice and reassurance
if intractable -> Obstetric physiotherapy +/ TENS

66
Q

When should you do an extra check of FBC in twin pregnancies to assess for the need for antenatal iron?

A

At 20-24 weeks
(In addition to the 28 week check that is routinely done in non-twin pregnancies)

67
Q

How should DVT in pregnancy be managed?

A

LMWH for the remainder of the pregnancy + 6 wks postpartum AND compression stockings

68
Q

What is the typical presentation of lymphogranulomavenereum?

A

2ndary to chlamydia infection
Stage I - painless genital ulcer
Stage 2 - 10 days to 6 months later - proctocolitis (painful when opening bowels), non-offensive vaginal discharge,+ lymphadenopathy

69
Q

What are contraindications for progesterone-only pill?

A

Active liver disease
Breast cancer <5 years duration

70
Q

What is 1st line treatment for chlamydia infection ?

A

For non-pregnant women + men -> 1st line = PO doxycycline for 1wk (if not tolerated, Azithromycin 1g stat then 500mg OD for 2 days)

For pregnant women -> stat Azithromycin 1g then 500mg for 2 days

Need to treat their CURRENT PARTNERS and advise to abstain until completed antibiotics or until 7 days after Azithromycin.

71
Q

Criteria for referring a patient for pre-eclampsia workup?

A

Rise in BP of 30/20 from booking BP
BP of 160 / 100 or higher
BP of 140/90 WITH proteinuria or symptomatic and IUGR

If borderline raised BP, bring back the next day to repeat

72
Q

Mx of HIV in pregnancy?

A

All HIV positive pregnancies should be notified to the National Study of HIV in Pregnancy and Childhood.

If viral load <50 -> can have planned vaginal delivery
If > 50 = elective c-section at 39 weeks.

Factors that ^ risk of transmission during labour = PROM, preterm delivery, use of fetal scalp electrode, high maternal viral load.

73
Q

typical presentation of uterine leiomyosarcoma?

A

malignant overgrowth of the MYOMETRIUM
-> rapidly growing pelvic mass + lymphadenopathy
Same risk factors as endometrial cancer ie unexposed oestrogen

74
Q

How should a pathological CTG trace be managed?

A

Fetal blood sampling of the presenting part.
If pH < 7.19 = need immediate delivery
-> if fully dilated can do forceps if not then emergency c-section

75
Q

Typical presentation of gonorrhoea conjunctivitis?

A

bilateral purulent conjunctivitis within the first 5 days of life
need prompt Tx as risk of visual loss or corneal ulceration

76
Q

How should you manage the passage of meconium in-utero / meconium-stained liqor?

A

Commence immediate induction if not already in labour
Needs CONTINUOUS fetal monitoring during labour

77
Q

When should an elective c-section for breach be planned?

A

39-40 weeks

78
Q

What defines the UK Perinatal mortality rate?

A

The number of stillbirths and early neonatal (first 7 days of life) deaths per 1,000 births/stillbirths

79
Q

Typical presentation of Conn’s syndrome

A

Conn’s = hyperaldesteronism
= ^ Na and H20 reabsorption (high sodium and high BP)
and increased K+ excretion (hypokalaemia)

Commonly 2ndary to an adrenal adenoma or adrenal hyperplasia

Tx = surgical or spironolactone

80
Q

Typical presentation of Sheehan’s syndrome?

A

Secondary amennorrhoea due to anterior pituitary infarct after a postpartum haemorrhage
may also get hypothyroidism and adrenal insufficiency depending on the size of the infarct

-> get low GNRH + FSH + LH

81
Q

Different methods of TOP and when they are used?

A

All women should be offered a choice between medical or surgical TOP up until 23+6 weeks.
Abortion in the UK is legal until 24 weeks.
After 24 weeks, it is only legal if the mother is at risk or the baby is at risk of having a severe disability.

Up until 9+6 wks, medical abortion can be taken at home. 600mg Mifepristone followed by 400 micrograms PO Misoprostol 48 hrs later.
PRIS TO PRIME

If 10+0 - 23+6 wks then needs to take the misoprostol at the hospital in a clinic or hospital but then can go home for the expulsion.
200mg mifepristone + 800 micrograms of vaginal misoprostol then repeat 400 micrograms misoprostol vaginally/buccally or sublingually every 3 hours until expulsion.

If medical abortion is after 10 weeks then also need anti-D prophylaxis if rhesus negative.

82
Q

Diagnosis and Mx of Premenstrual Syndrome?

A

Recommend keep a 3 month record -> The Daily Record of Severity of Problems (DRSP)

If uncertainty over Dx -> refer to 2ndary care -> they can use GnRh agonists for ovarian suppression for 3 months which can confirm PMS.

Mx:
1st line -> lifestyle

Moderate -> new-generation COCP (Yasmin - drospirenone + ethynylestradiol) continuously (not cyclically)
-> can consider CBT

Severe -> consider 3 month trial of SSRI (if <18 need specialist input first) either continuously or for luteal phase only.

Review after 2 months of Tx, with the woman completing the DRSP throughout.

83
Q

What are contraindications to HRT?

A
  • Active or previous breast-cancer or other oestrogen-dependent cancer
  • Untreated endometrial hyperplasia
  • Undiagnosed abnormal vaginal bleeding
  • Previous or current VTE (unless already on anticoagulation for)
  • Liver disease
  • Thrombophilic disorder
  • Angina or recent MI
84
Q

What are CAUTIONS to HRT?

A
  • Porphyria cutanea tarda
  • Diabetes mellitus
  • At ^ risk of VTE or breast cancer
  • Migraine
  • Prev endometrial hyperplasia
85
Q

HRT risk profiles?

A

Breast cancer ->
Small ^ risk of BC with combined HRT but this is NOT associated with any ^ in mortality from BC.
Oestrogen-only HRT may REDUCE the risk of BC.
Vaginal oestrogen -> no ^ in BC risk

VTE -> higher risk with oral than transdermal. THERE IS NO INCREASED RISK OF VTE WITH TRANSDERMAL

V. small increased risk of ovarian cancer

Endometrial cancer -> Continuous combined HRT reduces the risk. V. small increase in risk with cyclical combined after 5 years of use.

86
Q

For how long after menopause does a women need contraception for?

A

For 2 years after her last period if <50
For 1 year after her last period if >50

87
Q

If a woman’s last period was <12 months ago should she be started on a sequential or continuous regime?

A

If last period < 12 months -> needs to be on a sequential routine
ie continuous oestrogen (ie transdermal or oral) + cyclical progesterone (either for 14 days every month or 14 days every 3 months)

88
Q

Diagnosing menopause?

A

CLINICAL DIAGNOSIS WITH NO NEED FOR A BLOOD TEST IN WOMEN > 45 NOT ON CONTRACEPTION:
* Perimenopause - menopause symptoms + irregular periods in someone > 45
* Menopause -> no period for 12 months (or based on symptoms in someone with a uterus)

WHEN TO USE FSH TO AID DIAGNOSIS:
* > 45 but atypical symptoms
* < 45 with suspected menopause or ovarian insufficiency
* > 50 on progesterone-only contraception (if FSH in premenopausal range then repeat in a year. Need to continue contraception for a year after a menopausal range FSH)

FSH >30 suggests ovarian insufficiency but not sterility. Ideally should do 2x values 4-6 weeks apart for a more robust diagnosis.

89
Q

Does a woman with a uterus need progesterone if they are having vaginal oestrogen?

A

NO
Systemic absorption of vaginal oestrogen is negligible so progesterone doesn’t need to be given, even if they have a uterus

90
Q

Diagnosis of premature ovarian insufficiency?

A

<40 AND Menopausal symptoms / absent or infrequent periods AND raised FSH (>30) on 2x separate ocassions 4-6 wks apart

91
Q

What are contraindications to fetal blood sampling?

A

Maternal infection (HIV, hepatitis, HSV)
Suspected foetal bleeding disorder
<34 weeks gestation

92
Q

Risk and protective factors for hyperemesis?

A

Risk factors = prev eating disorder, primip, molar pregnancy, multiple pregnancy
SMOKING IS PROTECTIVE