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O&G TopicsAntenatal care — perinatal infections

O&G · Antenatal care — perinatal infections

Perinatal infections III: HIV, hepatitis B and hepatitis C in pregnancy

Also known as HIV in pregnancy · Mother-to-child HIV transmission · Hepatitis B in pregnancy · HBsAg positive pregnancy · Hepatitis C in pregnancy · Blood-borne viruses in pregnancy · Perinatal hepatitis

Exam-exhaustive FRANZCOG reference on the three blood-borne viral infections in pregnancy — HIV (vertical transmission falling from about 25% without intervention to under 1% with combined antiretroviral therapy and a suppressed viral load; the ACTG 076 legacy; viral-load-driven mode of delivery; neonatal prophylaxis; setting-dependent infant feeding), hepatitis B (70 to 90% perinatal transmission if HBeAg-positive; birth-dose vaccine plus immunoglobulin preventing about 94%; tenofovir for high viral load to reach under 1%), and hepatitis C (vertical transmission around 7%; no proven antenatal intervention). ASID Perinatal Infections anchored, globally tagged to MRCOG and ABOG.

high14 referencesUpdated 26 July 202613 min readVerification in progress

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FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • A detectable HIV viral load near term means the mode-of-delivery decision is viral-load-driven — a planned caesarean is indicated, not optional
  • HBeAg-positive or a high HBV DNA in pregnancy means perinatal hepatitis B transmission risk is 70 to 90% without intervention — birth-dose immunoglobulin and vaccine are mandatory and third-trimester tenofovir is added
  • A delayed or missed birth-dose hepatitis B vaccine in the infant of an HBsAg-positive mother is a preventable catastrophe — the first dose must be within 12 to 24 hours
  • Hepatitis C has no proven antenatal intervention to reduce vertical transmission — do not treat in pregnancy with an unapproved regimen
  • Infant feeding advice is setting-dependent — high-income formula-only advice applied in a resource-limited setting can be harmful; follow the prevailing WHO guidance
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Your progress

Saved on this device.

Practise this topic8 MCQs with explanations

Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • A detectable HIV viral load near term means the mode-of-delivery decision is viral-load-driven — a planned caesarean is indicated, not optional
  • HBeAg-positive or a high HBV DNA in pregnancy means perinatal hepatitis B transmission risk is 70 to 90% without intervention — birth-dose immunoglobulin and vaccine are mandatory and third-trimester tenofovir is added
  • A delayed or missed birth-dose hepatitis B vaccine in the infant of an HBsAg-positive mother is a preventable catastrophe — the first dose must be within 12 to 24 hours
  • Hepatitis C has no proven antenatal intervention to reduce vertical transmission — do not treat in pregnancy with an unapproved regimen
  • Infant feeding advice is setting-dependent — high-income formula-only advice applied in a resource-limited setting can be harmful; follow the prevailing WHO guidance
One-line fellowship answer

Three blood-borne viruses, three different prevention stories. HIV vertical transmission falls from about 25% without intervention to under 1% with combined antiretroviral therapy and a suppressed viral load, with the mode of delivery driven by the viral load and neonatal zidovudine prophylaxis for the infant. Hepatitis B perinatal transmission is 70 to 90% if the mother is HBeAg-positive, but birth-dose hepatitis B vaccine plus immunoglobulin within 12 to 24 hours prevents about 94% of infections, and adding tenofovir in the third trimester for a high viral load reduces transmission to under 1%. Hepatitis C transmits vertically in about 7% of pregnancies, has no vaccine and no proven antenatal intervention, and is treated postpartum with direct-acting antivirals.[1][2][5][11]

A 26-year-old books at 12 weeks. Her HIV screening is positive, her HBsAg is positive, and she asks whether she can breastfeed. Three answers, each with a different evidence base, and the registrar who holds the combined prevention plan passes the station. This topic is the three answers, organised by virus and by the transmission rate each can be driven down to.[1][5][11]

Overview and definition

These three viruses share a route — blood and bodily fluids — and a destination — the infant — and differ on the prevention lever. HIV is driven to under 1% by antiretroviral suppression. Hepatitis B is driven to under 1% by birth-dose immunoprophylaxis plus antiviral prophylaxis. Hepatitis C, for now, is not driven down at all in pregnancy. The candidate who knows which lever belongs to which virus, and the number each reaches, holds the topic.[1][5][11]

HIV

  • Transmission ~25% without intervention; under 1% with cART and suppressed viral load
  • Predominantly intrapartum transmission
  • Prevention: maternal cART, viral-load-driven mode of delivery, neonatal prophylaxis
  • Infant feeding: setting-dependent
  • Landmark: ACTG 076 (zidovudine 8.3% vs 25.5%)

Hepatitis B

  • Transmission 70 to 90% if HBeAg-positive, 5 to 20% if HBeAg-negative
  • ~90% of infected infants develop chronic infection
  • Prevention: birth-dose vaccine + HBIG within 12 to 24 h; tenofovir for high viral load
  • Reaches under 1% with combined immunoprophylaxis and antiviral prophylaxis
  • Vaccine-preventable; birth-dose coverage is the global gap

Hepatitis C

  • Vertical transmission around 7% overall
  • Higher with HIV co-infection
  • No vaccine, no approved antiviral in pregnancy
  • No proven antenatal intervention
  • Treat the mother postpartum with direct-acting antivirals
[1] [2] [5] [11]
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References14ShowHide
  1. [1]Connor EM, Sperling RS, Gelber R, et al. Reduction of maternal-infant transmission of human immunodeficiency virus type 1 with zidovudine treatment. Pediatric AIDS Clinical Trials Group Protocol 076 Study Group N Engl J Med, 1994.PMID 7935654
  2. [2]Townsend CL, Byrne L, Cortina-Borja M, Thorne C, de Ruiter A, Lyall H, Taylor GP, Peckham CS, Tookey PA Earlier initiation of ART and further decline in mother-to-child HIV transmission rates, 2000-2011 AIDS, 2014.PMID 24566097
  3. [3]Townsend CL, Cortina-Borja M, Peckham CS, de Ruiter A, Lyall H, Tookey PA Low rates of mother-to-child transmission of HIV following effective pregnancy interventions in the United Kingdom and Ireland, 2000-2006 AIDS, 2008.PMID 18453857
  4. [4]Peters H, Byrne L, De Ruiter A, et al. Duration of ruptured membranes and mother-to-child HIV transmission: a prospective population-based surveillance study BJOG, 2016.PMID 26011825
  5. [5]Jeng WJ, Yip TC, Lok AS Hepatitis B: A Review JAMA, 2026.PMID 42081318
  6. [6]Cryer AM, Imperial JC Hepatitis B in Pregnant Women and their Infants Clin Liver Dis, 2019.PMID 31266619
  7. [7]Schillie S, Walker T, Veselsky S, et al. Outcomes of infants born to women infected with hepatitis B Pediatrics, 2015.PMID 25896839
  8. [8]Chilaka VN, Konje JC Viral Hepatitis in pregnancy Eur J Obstet Gynecol Reprod Biol, 2021.PMID 33259998
  9. [9]Li W, Jia L, Zhao X, Wu X, Tang H Efficacy and safety of tenofovir in preventing mother-to-infant transmission of hepatitis B virus: a meta-analysis based on 6 studies from China and 3 studies from other countries BMC Gastroenterol, 2018.PMID 30071845
  10. [10]Lu FT, Ni YH Elimination of Mother-to-Infant Transmission of Hepatitis B Virus: 35 Years of Experience Pediatr Gastroenterol Hepatol Nutr, 2020.PMID 32704492
  11. [11]Ades AE, Gordon F, Scott K, et al. Overall Vertical Transmission of Hepatitis C Virus, Transmission Net of Clearance, and Timing of Transmission Clin Infect Dis, 2023.PMID 35403676
  12. [12]Trickey A, Artenie A, Feld JJ, Vickerman P Estimating the annual number of hepatitis C virus infections through vertical transmission at country, regional, and global levels: a data synthesis study Lancet Gastroenterol Hepatol, 2025.PMID 40714038
  13. [13]Dadabhai S, Chou VB, Pinilla M, et al. Effects of preterm birth, maternal ART and breastfeeding on 24-month infant HIV-free survival in a randomized trial AIDS, 2024.PMID 38427596
  14. [14]Eleje GU, Usman HA, Onubogu CU, et al. Seroprevalence, seroconversion, and mother-to-child transmission of dual and triplex infections of HIV, HBV, and HCV among Nigerian obstetric population: A national multicentre prospective cohort study Antivir Ther, 2025.PMID 40243253

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