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O&G

Notes, summaries and exam pearls for this rotation. Every note opens as a PDF in a new tab.

Use as a study guide only. These notes are part of a free open-access medical education (FOAMed) project and may contain errors or outdated information. Always verify against current guidelines (e.g. eTG, RACGP, local health district policies) and reputable sources before applying anything to patient care. See the full disclaimer.

From the wards

Clinical pearls & learnings

Tips and tricks collected over the years — a living list that grows with every rotation. Use as a study guide only and check current guidelines before acting on anything.

PV bleeding & gynae pearls

Painful vs non-painful PV bleeding
Painful bleedingNon-painful bleeding
Think first ofEndometriosis > PID, fibroids, adenomyosisCervical ectropion (red, velvety, friable cervix — columnar epithelium extending onto the ectocervix), fibroids, polyps
First investigationTransvaginal ultrasoundCervical co-test (cytology + HPV) to exclude malignancy — never assume ectropion

Ectropion is a benign, common finding — but a friable bleeding cervix looks the same as an early cervical cancer. Examine, swab and co-test before reassuring; postcoital bleeding always warrants a speculum.

Krukenberg tumours

Metastatic (usually bilateral) ovarian tumours with signet-ring cells — most commonly from gastric cancer, then colorectal, breast and appendix. Finding bilateral ovarian masses should prompt a search for a GI primary, not just a gynae work-up.

Contraception & VTE risk

Minimising VTE risk with hormonal therapy

VTE risk by preparation — lowest first

VTE riskPreparationNote
LowestLevonorgestrel IUD, progestogen-only options, local/intrauterine hormonal therapyMinimal VTE risk — the default in anyone with thrombotic risk factors
Low (of combined)Levonorgestrel-containing combined pillsLowest VTE risk of the combined options
HigherCyproterone acetate + ethinylestradiol (Diane-35); other anti-androgenic and third-/fourth-generation progestogensReserve for a clear indication (e.g. significant acne, hirsutism) rather than routine contraception
Emergency contraception
OptionWindowMechanism
Copper IUDUp to 5 days — most effective by far, and works immediatelyCopper is toxic to sperm and ova and induces a sterile endometrial inflammatory reaction — impairs sperm motility and viability so fertilisation does not occur
Levonorgestrel 1.5mgWithin 72 hours (declining efficacy)Synthetic progestogen — delays or inhibits ovulation
Ulipristal acetate (UPA) 30mgWithin 120 hoursSelective progesterone receptor modulator — delays ovulation, effective closer to the LH surge than levonorgestrel

Offer the copper IUD first — most effective and provides ongoing contraception. Note UPA and progestogens can blunt each other's effect: delay hormonal contraception for 5 days after UPA.

Pregnancy complications

Parvovirus B19 in pregnancy
  • Risks to the fetus: severe anaemia and hydrops fetalis (also myocarditis and fetal loss), highest with infection before 20 weeks.
  • Surveillance: weekly ultrasound for ~12 weeks after infection.
  • Measure the middle cerebral artery peak systolic velocity — an elevated MCA-PSV is the non-invasive marker of fetal anaemia and triggers referral for intrauterine transfusion.
Pre-eclampsia

It is a multi-system disease, not just a blood pressure number — hypertension plus evidence of end-organ dysfunction. A spot urine protein:creatinine ratio >30 mg/mmol is significant proteinuria; but proteinuria is not required if there is renal, hepatic, haematological, or neurological involvement, or fetal growth restriction.

Positioning & resuscitation in pregnancy
  • Left lateral tilt (or manual uterine displacement) relieves aortocaval compression by the gravid uterus, improving venous return and uteroplacental blood flow.
  • In maternal cardiac arrest, add amniotic fluid embolism and eclampsia to your reversible-cause list — and plan resuscitative hysterotomy early if there is no ROSC.
  • Maternal deaths are classified as direct (from pregnancy itself) or indirect (pre-existing disease aggravated by pregnancy).
Amniotic fluid embolism

Amniotic fluid entering the maternal circulation triggers an anaphylactoid reaction — massive cytokine release and vasodilation, acute right ventricular failure from pulmonary hypertension with pulmonary oedema, and DIC with catastrophic haemorrhage.

  • A clinical diagnosis of exclusion, usually confirmed retrospectively: sudden hypoxia/respiratory distress, hypotension/cardiovascular collapse, and DIC.
  • Almost always occurs intrapartum or immediately postpartum. Mortality is very high, and neonatal hypoxic-ischaemic encephalopathy is common in survivors.
  • Risk factors: advanced maternal age, multiparity, induction of labour, operative delivery, placental abnormalities. (Artificial rupture of membranes is often cited but the association is weak.)
  • Exclude the far commoner postpartum haemorrhage first — but remember the two coexist, since AFE causes DIC.
  1. Call for help: obstetrics, anaesthetics, ICU, haematology, massive transfusion protocol
  2. High-flow oxygen, secure the airway, aggressive haemodynamic resuscitation
  3. Left lateral tilt / manual uterine displacement to prevent IVC compression
  4. Deliver the fetus urgently — caesarean or instrumental delivery
  5. Correct the coagulopathy: MTP with early cryoprecipitate/fibrinogen, TXA
  6. Refractory: consider ECMO / mechanical circulatory support

Management — a full-team resuscitation

Thrombolysis (e.g. alteplase) is for confirmed massive pulmonary thromboembolism — it is contraindicated in amniotic fluid embolism, where the problem is DIC and bleeding rather than thrombus. Getting this distinction wrong is fatal.

Neonatal outcome markers

Apgar and early neurodevelopment
  • An Apgar <5 at 5 and 10 minutes is a poor prognostic marker and correlates with hypoxic-ischaemic encephalopathy — but it is a description of the newborn's condition, not a measure of asphyxia on its own.
  • The General Movements Assessment at around 3 months corrected age (fidgety movements period) is one of the best early predictors of cerebral palsy — better than neuroimaging or neurological examination alone, and it allows early intervention.