Management of Excessive Itching at 38 Weeks of Gestation
Ursodeoxycholic acid (UDCA) at a dose of 10-15 mg/kg per day is the first-line treatment for pruritus at 38 weeks of gestation, particularly if intrahepatic cholestasis of pregnancy (ICP) is suspected or confirmed. 1
Diagnostic Approach
When a pregnant woman at 38 weeks presents with excessive itching, a systematic approach is needed:
Laboratory testing:
- Serum bile acid levels (most sensitive indicator for ICP)
- Liver function tests (ALT, AST, bilirubin, GGT)
- If bile acids are normal but symptoms persist, repeat testing in 1-2 weeks 2
Physical examination:
- Distribution of pruritus (palms and soles involvement suggests ICP)
- Presence or absence of rash (ICP typically has no primary rash)
- Evidence of excoriations from scratching 2
Treatment Algorithm
First-line treatment:
- UDCA (10-15 mg/kg/day) divided into 2-3 daily doses (typical regimens: 300 mg twice or three times daily, or 500 mg twice daily) 1
- Improvement in pruritus typically occurs within 1-2 weeks
- If pruritus is not relieved, dose can be titrated up to 21-25 mg/kg/day 1
For refractory symptoms:
Alternative or add-on medications:
- S-adenosyl-L-methionine (may have additive effect with UDCA) 1
- Rifampicin (can be combined with UDCA for refractory cases) 1
- Cholestyramine (binds bile acids in gut but has significant side effects) 1
- Caution: Monitor prothrombin time if using cholestyramine as it may exacerbate vitamin K deficiency in cholestasis 1
Symptomatic relief:
Fetal Monitoring and Delivery Planning
At 38 weeks with pruritus, especially if ICP is suspected:
- Begin antenatal fetal surveillance immediately 1
- Consider delivery at 38 weeks of gestation to prevent stillbirth beyond that gestation 1
- Risk stratification based on bile acid levels:
- <40 μmol/L: lower risk
- 40-99 μmol/L: moderate risk (0.3% IUFD risk)
- ≥100 μmol/L: high risk (3.4% IUFD risk) 2
Important Considerations
- Pruritus in ICP can precede the rise in serum bile acid levels by several weeks 1
- Some clinicians make the diagnosis of ICP based on clinical symptoms alone and start UDCA empirically 1
- If UDCA is started empirically before test results are available, elevated bile acid or transaminase levels may never be detected 1
- Persistent abnormalities after delivery should prompt evaluation for other chronic liver diseases 1
Common Pitfalls to Avoid
Misdiagnosis: Not all pruritus in pregnancy is ICP. Consider other pregnancy-specific dermatoses like polymorphic eruption of pregnancy, pemphigoid gestationis, or atopic eruption of pregnancy 3, 4
Inadequate monitoring: Failure to monitor for fetal complications in ICP can lead to adverse outcomes 1
Delayed treatment: Waiting for laboratory confirmation before starting treatment may prolong maternal discomfort 1
Insufficient dosing: Starting with too low a dose of UDCA or not titrating up when needed 1
Overlooking vitamin K deficiency: Cholestasis may lead to vitamin K deficiency and increased bleeding risk, especially if cholestyramine is used 1