Management of Hepatitis B Surface Antigen Positive Mothers to Prevent Perinatal Transmission
All HBsAg-positive pregnant women should receive comprehensive management including HBV DNA testing, possible antiviral therapy with tenofovir starting at 28-32 weeks gestation if viral load >200,000 IU/mL, and their infants must receive both hepatitis B vaccine and HBIG within 12 hours of birth to prevent perinatal transmission. 1
Screening and Testing Protocol
- All pregnant women must be screened for HBsAg during early prenatal care, regardless of previous vaccination or testing status 1
- Women not tested prenatally should be tested at admission for delivery 1
- For HBsAg-positive pregnant women:
- Test HBV DNA level to guide antiviral therapy decisions 1
- Check liver function tests (ALT/AST, bilirubin, albumin, prothrombin time) at baseline and each trimester 1
- Determine HBeAg status if not already known (helps predict transmission risk) 1
- Repeat HBV DNA quantification at 24-28 weeks of gestation to assess need for antiviral therapy 1
Antiviral Therapy Decision Algorithm
Initiate tenofovir disoproxil fumarate (TDF) if any of the following:
Timing and Duration:
Note: Entecavir is not recommended during pregnancy as it is classified as Pregnancy Category C with insufficient human data on safety 2
Infant Prophylaxis Protocol
For infants born to HBsAg-positive mothers:
For infants born to mothers with unknown HBsAg status:
Post-vaccination testing:
Delivery Considerations
- Cesarean section is NOT recommended solely to prevent HBV transmission 1
- Vaginal delivery is appropriate for HBsAg-positive women, even with high viral loads, if they received antiviral prophylaxis 1
- Ensure maternal HBsAg status is clearly documented in medical records and communicated to the delivery facility 1
Postpartum Care
- Refer HBsAg-positive mothers to appropriate case-management programs 1
- Reassess the need for long-term HBV treatment based on standard criteria 1
- Breastfeeding is safe and should not be discouraged for HBsAg-positive mothers 1
- Exception: Avoid breastfeeding if mothers with detectable HBV DNA have cracked nipples or if the infant has oral ulcers 1
Important Clinical Considerations
- The risk of mother-to-child transmission is negligible (0.04%) when maternal HBV DNA is <200,000 IU/mL 1
- Despite optimal prophylaxis, 1-9% of infants born to HBV-carrying mothers may still develop HBV infection 3
- Research suggests that yeast-recombinant vaccines may have better efficacy than plasma-derived vaccines, especially in preventing late onset infections 4
- Studies comparing different HBIG dosages (100 IU vs 200 IU) found similar efficacy in preventing perinatal transmission when combined with hepatitis B vaccine 5
By following this comprehensive protocol, the risk of perinatal HBV transmission can be significantly reduced, preventing chronic HBV infection in newborns and its associated long-term complications.