What are the management and treatment guidelines for hepatitis B in pregnancy?

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Last updated: November 18, 2025View editorial policy

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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

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Breastfeeding Safety for Mothers with Hepatitis B

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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