What is the screening and management process for cholestasis of pregnancy (intrahepatic cholestasis of pregnancy, ICP) in pregnant women?

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Screening and Management of Cholestasis of Pregnancy

Initial Screening Approach

Any pregnant woman presenting with new-onset pruritus in the second or third trimester should be immediately tested with serum total bile acids and liver transaminases (ALT/AST), using random (non-fasting) samples for convenience. 1, 2

Key Clinical Features to Assess

  • Pruritus characteristics: Generalized itching predominantly affecting palms and soles, worse at night, without a primary rash (only excoriations from scratching) 1, 2
  • Timing: Typically occurs in late second or third trimester 1, 2
  • Physical examination: Absence of rash, vesicles, bullae, or plaques; dark urine and jaundice are uncommon and suggest alternative diagnoses 1
  • Risk factors: Prior ICP (up to 90% recurrence risk), family history, pre-existing liver disease (hepatitis C, cirrhosis, gallstones) 1, 2

Essential Laboratory Testing

Order immediately when ICP is suspected: 1, 2

  • Total serum bile acids (enzymatic assay preferred; results in 4 hours to 4 days vs. 4-14 days for mass spectrometry) 1, 2
  • Liver transaminases (ALT and AST) 1, 2

Diagnostic threshold: Total bile acids >10 μmol/L combined with pruritus confirms ICP 1, 2

Additional testing to exclude alternative diagnoses: 2

  • Complete blood count with platelets (exclude HELLP syndrome)
  • Coagulation studies and glucose (exclude acute fatty liver of pregnancy)
  • Hepatobiliary ultrasound (exclude gallstones/biliary obstruction)
  • Thyroid function tests and renal function (if indicated)

Management Algorithm Based on Bile Acid Levels

Treatment Initiation

Start ursodeoxycholic acid (UDCA) 10-15 mg/kg/day in divided doses immediately upon diagnosis, titrating up to maximum 21 mg/kg/day if needed. 1, 2 UDCA improves maternal pruritus, reduces bile acid levels, and decreases adverse outcomes including preterm birth and stillbirth. 2

Fetal Surveillance

Begin antenatal fetal testing at the gestational age when delivery would be performed in response to abnormal results, or immediately if diagnosed later in gestation. 1, 2 Increase frequency with higher bile acid levels, especially ≥100 μmol/L. 2 Place all ICP patients on continuous fetal monitoring during labor. 2

Delivery Timing (Strictly Based on Peak Bile Acid Levels)

Bile acids ≥100 μmol/L: Deliver at 36 0/7 weeks of gestation 1, 2, 3

Bile acids <100 μmol/L: Deliver between 36 0/7 and 39 0/7 weeks of gestation 1, 2

Bile acids <40 μmol/L: Consider delivery at term (39 weeks) 2

Administer antenatal corticosteroids for fetal lung maturity if delivering before 37 0/7 weeks. 1

Critical Management Pitfalls to Avoid

Never deliver before 37 weeks based on clinical suspicion alone without laboratory confirmation of elevated bile acids. 1, 2, 3 This leads to unnecessary preterm deliveries with associated neonatal morbidity. 3

Never assume normal initial labs permanently rule out ICP. 3 Pruritus can precede bile acid elevation by several weeks. 1, 2

Repeat Testing Strategy

If initial bile acids are normal but pruritus persists without alternative explanation, repeat bile acid and transaminase measurements every 1-2 weeks until symptoms resolve or diagnosis is confirmed. 2, 3 Bile acid levels can increase rapidly during pregnancy, particularly near term. 1, 3

Serial weekly testing is not routinely recommended once diagnosis is established, but repeat testing may guide delivery timing in severe cases. 1

Postpartum Follow-Up

Repeat biochemical testing at 4-6 weeks postpartum if symptoms or abnormal laboratory values persist. 1, 2, 3 ICP typically resolves completely after delivery; persistence suggests underlying chronic liver condition (chronic hepatitis, liver fibrosis/cirrhosis, hepatitis C, cholangitis). 1

Refer to hepatology if results remain abnormal at 4-6 weeks postpartum. 1, 2, 3 Some experts advocate routine hepatitis C testing in all ICP patients given the increased risk and availability of effective treatment. 1

Counseling Points

  • Recurrence risk: Up to 90% in subsequent pregnancies 1, 2
  • Long-term maternal risk: Increased risk of hepatobiliary diseases, particularly within the first year after diagnosis (hepatitis C: HR 4.16, liver fibrosis/cirrhosis: HR 5.11) 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Differential Diagnosis of Intrahepatic Cholestasis of Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Bile Acid Level Testing in Intrahepatic Cholestasis of Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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