Management of Hepatitis B in Pregnancy
All pregnant women with HBV DNA levels >200,000 IU/mL should receive tenofovir disoproxil fumarate starting at 24-32 weeks of gestation and continuing through 12 weeks postpartum to prevent mother-to-child transmission. 1
Screening and Initial Assessment
- Screen all pregnant women for HBsAg in the first trimester, as this is critical for recognizing and reducing mother-to-child transmission risk 1, 2
- Perform triple-panel testing (HBsAg, anti-HBs antibody, and total anti-HBc) at the initial prenatal visit if not previously documented 2
- For women with unknown HBsAg status at delivery, test immediately upon presentation to the birthing facility 2
- Measure HBV DNA and ALT levels at 26-28 weeks of gestation in all HBsAg-positive women to determine need for antiviral prophylaxis 1
Antiviral Therapy Indications and Timing
For Prevention of Vertical Transmission:
- Initiate tenofovir disoproxil fumarate (300 mg daily) at 24-32 weeks of gestation in pregnant women with HBV DNA >200,000 IU/mL (>5.3 log₁₀ IU/mL) 1, 2
- Continue therapy through 12 weeks postpartum 1
- The 2023 EASL guidelines provide the most recent evidence with 100% consensus on this threshold and timing 1
For Maternal Liver Disease:
- Continue tenofovir throughout pregnancy in women with chronic HBV infection and advanced fibrosis or cirrhosis 1
- Women already on entecavir should be switched to tenofovir before or during pregnancy 1
- Monitor HBV DNA and ALT every 12 weeks during pregnancy and at 4-6 weeks postpartum 1
Important caveat: Some guidelines suggest HBeAg-positive status alone as an indication for therapy, but the most recent 2023 EASL guidelines prioritize the viral load threshold of >200,000 IU/mL regardless of HBeAg status 1.
Drug Selection
- Tenofovir disoproxil fumarate is the first-line agent (pregnancy category B, now considered safe with extensive data) 1, 2
- Tenofovir alafenamide (25 mg daily) is an acceptable alternative 2
- Older guidelines mentioned telbivudine and lamivudine, but these are no longer preferred due to resistance concerns with lamivudine and superior safety data for tenofovir 1
Delivery Management
- Vaginal delivery is recommended; cesarean section should not be performed solely to reduce HBV transmission 1, 3, 2
- The exception: Some Asian guidelines suggest cesarean may be considered in HBeAg-positive Asian women with very high viral loads (>6.14 log₁₀ IU/mL) who did not receive antiviral therapy, though this is not universally endorsed 1
- Standard obstetric indications should guide mode of delivery 1, 2
Invasive Prenatal Testing
- Non-invasive prenatal testing is strongly preferred over amniocentesis in HBeAg-positive women or those with HBV DNA >5.3 log₁₀ IU/mL 1
- If amniocentesis is necessary, counsel patients that transmission risk increases with viral loads >7 log₁₀ IU/mL 1, 3
- Chorionic villus sampling should be avoided 1
Neonatal Management
- Administer both hepatitis B vaccine and HBIG within 12 hours of birth to all infants born to HBsAg-positive mothers, regardless of whether maternal antiviral therapy was given 1, 3, 2
- Complete the 3-dose vaccine series at 1 and 6 months 1, 3
- Test infant for HBsAg and anti-HBs at 9-12 months of age to confirm protection 4
Breastfeeding
- Breastfeeding is safe and should be encouraged in HBsAg-positive mothers, including those on tenofovir therapy 1, 5, 3, 2
- The 2023 EASL guidelines state with 100% consensus that breastfeeding should not be discouraged unless mothers have cracked nipples with detectable HBV DNA or the infant has oral ulcers 1
- This contradicts older 2015 US guidelines that recommended against breastfeeding during antiviral therapy—the more recent evidence supports breastfeeding safety 1, 5
Postpartum Monitoring
- Monitor for hepatitis flares after delivery and after stopping antiviral therapy 1, 4
- Check ALT every 1-3 months for 6 months postpartum in women who discontinue therapy 4
- Women who stop therapy postpartum require close monitoring for viral reactivation 1
Interventions NOT Recommended
- Do not administer hepatitis B immunoglobulin to pregnant women (antepartum maternal HBIG is ineffective at reducing transmission regardless of viral load) 1
- Do not delay breastfeeding initiation until after infant immunization 5
- Do not perform cesarean delivery solely for HBV transmission prevention 1, 3, 2
Common Pitfalls
- Failing to check viral load in the third trimester leads to missed opportunities for prophylaxis in high-risk women 1
- Using lamivudine for long-term therapy increases resistance risk; tenofovir is superior 1
- Continuing entecavir during pregnancy when tenofovir is the safer, evidence-based choice 1
- Discouraging breastfeeding based on outdated guidance contradicts current evidence showing safety with proper infant immunoprophylaxis 1, 5