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Long-term impact of infant immunization on hepatitis B prevalence: a systematic review and meta-analysis

OBJECTIVE: To conduct a systematic review and meta-analysis of the long-term impact of infant vaccination on the prevalence of hepatitis B virus (HBV) infection at the population level. METHODS: We searched online databases for articles reporting comparisons between population cohorts aged ≥ 15 year...

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Detalles Bibliográficos
Autores principales: Whitford, Kate, Liu, Bette, Micallef, Joanne, Yin, J Kevin, Macartney, Kristine, Van Damme, Pierre, Kaldor, John M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Health Organization 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022616/
https://www.ncbi.nlm.nih.gov/pubmed/29962551
http://dx.doi.org/10.2471/BLT.17.205153
Descripción
Sumario:OBJECTIVE: To conduct a systematic review and meta-analysis of the long-term impact of infant vaccination on the prevalence of hepatitis B virus (HBV) infection at the population level. METHODS: We searched online databases for articles reporting comparisons between population cohorts aged ≥ 15 years who were exposed or unexposed to infant HBV immunization programmes. We categorized programmes as universal or targeted to infants whose mothers were positive for hepatitis B surface antigen (HBsAg). We included studies reporting prevalence of hepatitis B core antibody (HBcAb), HBsAg, or both. We evaluated the quality of the study methods and estimated the relative reduction in the prevalence of infection. FINDINGS: Of 26 studies that met the inclusion criteria, most were from China (20 studies). The prevalence of HBV infection in unvaccinated and universally vaccinated cohorts ranged from 0.6% (116 of 20 305 people) to 16.3% (60/367) and from 0.3% (1/300) to 8.5% (73/857), respectively. Comparing cohorts with universal vaccination to those without vaccination, relative prevalences were 0.24 (95% confidence interval, CI: 0.16–0.35) for HBsAg and 0.23 (95% CI: 0.17–0.32) for HBcAb. For populations with targeted vaccination, relative prevalences were 0.32 (95% CI: 0.24–0.43) and 0.33 (95% CI: 0.23–0.45), respectively. CONCLUSION: The residual burden of infection in cohorts offered vaccination suggests that longer-term evaluations of vaccination coverage, timeliness and other aspects of programme quality are needed. As HBV-vaccinated infant cohorts reach adulthood, ongoing analysis of prevalence in adolescents and young adults will ensure that elimination efforts are on track.