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O&G SAQsAntenatal care — medical disorders of pregnancy

O&G SAQs · Antenatal care — medical disorders of pregnancy

Intrahepatic cholestasis of pregnancy — structured SAQ (15 marks)

FRANZCOG-format structured SAQ on moderate ICP (bile acids 78): diagnostic definition, the immediate UDCA bundle with PITCHES caveats, surveillance, and tier-based delivery timing. Per-sub-part marking rubric included.

15 marks20 min2 min readVerification in progress

Target exams

FRANZCOGMRCOGABOG
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Target exams

FRANZCOGMRCOGABOG
Prompt
You are the on-call registrar. A 30-year-old G2P1 at 34 weeks presents with two weeks of nocturnal palm-and-sole pruritus that has worsened despite topical emollients. There is no rash. Her serum bile acids return at 78 micromol/L, ALT 110 IU/L, bilirubin 12 micromol/L, GGT normal. Her CTG is reactive and growth is appropriate. (a) What is the diagnosis and how is it defined? (2 marks) (b) Outline your immediate management plan, with drug names, doses and rationale. (5 marks) (c) Describe your surveillance plan for the remainder of pregnancy. (3 marks) (d) State your plan for delivery timing and the postpartum follow-up. (5 marks)

How this SAQ is marked

Twelve SAQs, 180 marks, two 2-hour papers — roughly 15 marks and 20 minutes each. Marks come from specifics: bile acid thresholds, drug doses, surveillance intervals, and the trial evidence (Ovadia, PITCHES, PITCH) that frames each decision.[1]

Reveal model answer and mark schemeShowHide

(a) Diagnosis and definition (2 marks)

One mark per element. [5][11]

  • Intrahepatic cholestasis of pregnancy (ICP) — a reversible cholestatic disorder of late pregnancy defined by maternal pruritus (palms and soles, worse at night, no primary rash) and elevated serum bile acids.
  • Diagnostic threshold: bile acids above 10 micromol/L using the standard threshold, or above 19 micromol/L using the higher-threshold definition (Mitchell 2021). The normal GGT excludes biliary obstruction as a contributor.

(b) Immediate management (5 marks)

One mark per intervention with drug, dose and rationale. [2][3]

  • Start ursodeoxycholic acid (UDCA) 500 mg twice daily, titrate to a maximum of 2 g per day for symptomatic relief of pruritus. Acknowledge PITCHES showed no perinatal benefit.
  • Topical emollients for skin comfort and chlorpheniramine 4 mg nocte for sleep (it does not affect bile acids).
  • Stratify by bile acid tier — 78 micromol/L places her in the moderate range (40-99); plan delivery 37-38 weeks.
  • Counsel the woman about the bile-acid-stillbirth relationship, the rationale for surveillance and the high recurrence in a future pregnancy.
  • Check coagulation — INR may prolong in moderate-severe disease; supplement vitamin K 10 mg daily if abnormal.
[2]

(c) Surveillance (3 marks)

One mark per element. [1][11]

  • Serial bile acids every 1-2 weeks — track the trajectory; if she reaches 100, escalate the plan.
  • Fetal surveillance — CTG and serial growth scans in moderate-severe disease (the evidence for CTG preventing stillbirth is weak, but surveillance is standard).
  • Exclusion of differential diagnoses — abdominal ultrasound to exclude biliary obstruction; consider viral and autoimmune screens if atypical.

(d) Delivery and postpartum (5 marks)

One mark per element. [1][3][11]

  • Planned delivery at 37-38 weeks for moderate ICP (40-99 micromol/L).
  • Escalate delivery to 35-36 weeks once steroids given if bile acids reach 100 or more.
  • Vaginal induction preferred unless obstetric indication for caesarean.
  • Postpartum follow-up at 6-12 weeks — confirm resolution of pruritus and normalisation of bile acids and LFTs; if persistent, investigate for chronic liver disease.
  • Counsel on contraception — progesterone-only methods safe; oestrogen-containing combined pills generally avoided while LFTs abnormal.
Obstetrics & Gynaecology Pro

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You have read the opening of this SAQ. The complete unit — every section and its primary-source references — is part of the Obstetrics & Gynaecology fellowship library.

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References5ShowHide
  1. [1]Ovadia C, Seed PT, Sklavounos A, et al. Association of adverse perinatal outcomes of intrahepatic cholestasis of pregnancy with biochemical markers: results of aggregate and individual patient data meta-analyses Lancet, 2019.PMID 30773280
  2. [2]Chappell LC, Bell JL, Smith A, et al. Ursodeoxycholic acid versus placebo in women with intrahepatic cholestasis of pregnancy (PITCHES): a randomised controlled trial Lancet, 2019.PMID 31378395
  3. [3]Chappell LC, Gurung V, Seed PT, et al. Ursodeoxycholic acid versus placebo, and early term delivery versus expectant management, in women with intrahepatic cholestasis of pregnancy: semifactorial randomised clinical trial BMJ, 2012.PMID 22695903
  4. [5]Mitchell AL, Ovadia C, Syngelaki A, et al. Re-evaluating diagnostic thresholds for intrahepatic cholestasis of pregnancy: case-control and cohort study BJOG, 2021.PMID 33586324
  5. [11]Westbrook RH, Dusheiko G, Williamson C Pregnancy and liver disease J Hepatol, 2016.PMID 26658682
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