Incidence, determinants and outcomes of pregnancy-associated hepatitis B flares: A regional hospital-based cohort study

Liver Int. 2018 May;38(5):813-820. doi: 10.1111/liv.13594. Epub 2017 Sep 30.

Abstract

Background & aims: There is limited knowledge about hepatitis B virus (HBV) flare among pregnant women. We evaluated the incidence, determinants and outcomes of HBV flare in a multicultural cohort of pregnant HBV-infected women in the United States.

Methods: We performed a retrospective cohort study of pregnant hepatitis B surface antigen-positive women cared for at hospital-based clinics of 4 medical centres in Southeastern Pennsylvania from 2006 to 2015. The main outcome was incident HBV flare (alanine aminotransferase [ALT] ≥2 times upper limit of normal) during pregnancy or within 6 months after delivery. Among patients with flare, we determined development of jaundice (total bilirubin ≥2.5 mg/dL) and hepatic decompensation. Multivariable logistic regression was used to estimate odds ratios (ORs) of HBV flare for risk factors of interest, including timing of flare (during pregnancy versus post-delivery), nulliparity, younger age, HBV e antigen (HBeAg) status, and lack of anti-HBV therapy.

Results: Among 310 pregnant predominantly African HBV-infected women with 388 pregnancies, the incidence of HBV flare was 14% (95% CI, 10-18%) during pregnancy and 16% (95% CI, 11-24%) post-delivery. Jaundice developed in 12% and hepatic decompensation in 2%. Positive HBeAg was associated with HBV flare (OR, 2.55; 95% CI, 1.04-6.20). HBV DNA was measured in 55% of patients, and only 50% were referred for HBV specialty care.

Conclusions: Pregnancy-associated hepatitis B flare occurred in 14% during pregnancy and 16% post-delivery and rarely led to hepatic decompensation. Positive HBeAg was the main risk factor identified. Women did not have adequate HBV monitoring or follow-up during pregnancy.

Keywords: flare; hepatic decompensation; hepatitis B virus; pregnancy.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Alanine Transaminase / blood*
  • Antiviral Agents / therapeutic use
  • DNA, Viral
  • Female
  • Hepatitis B e Antigens / blood*
  • Hepatitis B virus
  • Hepatitis B, Chronic / epidemiology*
  • Humans
  • Incidence
  • Logistic Models
  • Multivariate Analysis
  • Pennsylvania
  • Pregnancy
  • Pregnancy Complications, Infectious / epidemiology*
  • Pregnancy Complications, Infectious / virology
  • Retrospective Studies

Substances

  • Antiviral Agents
  • DNA, Viral
  • Hepatitis B e Antigens
  • Alanine Transaminase