Hepatitis B vaccination impact and the unmet need for antiviral treatment in Blantyre, Malawi

  • Alexander J Stockdale
  • James E Meiring
  • Isaac T Shawa
  • Deus Thindwa
  • Niza M Silungwe
  • Maurice Mbewe
  • Rabson Kachala
  • Benno Kreuels
  • Pratiksha Patel
  • Priyanka Patel
  • Marc Y R Henrion
  • Naor Bar-Zeev
  • Todd D Swarthout
  • Robert S Heyderman
  • Stephen B Gordon
  • Anna Maria Geretti
  • Melita A Gordon

Beteiligte Einrichtungen

Abstract

BACKGROUND: Hepatitis B is the leading cause of cirrhosis and liver cancer in sub-Saharan Africa. To reduce mortality, antiviral treatment programs are needed. We estimated prevalence, vaccine impact, and need for antiviral treatment in Blantyre, Malawi.

METHODS: We conducted a household study in 2016-2018. We selected individuals from a census using random sampling and estimated age-sex-standardized hepatitis B surface antigen (HBsAg) seroprevalence. Impact of infant hepatitis B vaccination was estimated by binomial log-linear regression comparing individuals born before and after vaccine implementation. In HBsAg-positive adults, eligibility for antiviral therapy was assessed.

RESULTS: Of 97386 censused individuals, 6073 (median age 18 years; 56.7% female) were sampled. HBsAg seroprevalence was 5.1% (95% confidence interval [CI], 4.3%-6.1%) among adults and 0.3% (95% CI, .1%-.6%) among children born after vaccine introduction. Estimated vaccine impact was 95.8% (95% CI, 70.3%-99.4%). Of HBsAg-positive adults, 26% were HIV-positive. Among HIV-negative individuals, 3%, 6%, and 9% were eligible for hepatitis B treatment by WHO, European, and American hepatology association criteria, respectively.

CONCLUSIONS: Infant HBV vaccination has been highly effective in reducing HBsAg prevalence in urban Malawi. Up to 9% of HBsAg-positive HIV-negative adults are eligible, but have an unmet need, for antiviral therapy.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0022-1899
DOIs
StatusVeröffentlicht - 13.09.2022

Anmerkungen des Dekanats

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

PubMed 34752631