Hepatitis B Surface Antigen Seroprevalence among Prevaccine and Vaccine Era Children in Bangladesh

Bangladesh introduced hepatitis B vaccine in a phased manner during 2003-2005 into the routine childhood vaccination schedule. This study was designed to evaluate the impact of the introduction of hepatitis B vaccine in Bangladesh by comparing hepatitis B surface antigen (HBsAg) prevalence among chi...

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Published inThe American journal of tropical medicine and hygiene Vol. 99; no. 3; pp. 764 - 771
Main Authors Paul, Repon C, Rahman, Mahmudur, Wiesen, Eric, Patel, Minal, Banik, Kajal C, Sharif, Ahmad R, Sultana, Sharmin, Rahman, Mizanur, Liyanage, Jayantha, Abeysinghe, Nihal, Kamili, Saleem, Murphy, Trudy, Luby, Stephen P, Mast, Eric E
Format Journal Article
LanguageEnglish
Published United States Institute of Tropical Medicine 01.01.2018
The American Society of Tropical Medicine and Hygiene
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Summary:Bangladesh introduced hepatitis B vaccine in a phased manner during 2003-2005 into the routine childhood vaccination schedule. This study was designed to evaluate the impact of the introduction of hepatitis B vaccine in Bangladesh by comparing hepatitis B surface antigen (HBsAg) prevalence among children born before and after vaccine introduction and to estimate the risk of vertical transmission of chronic hepatitis B virus (HBV) infection from mother to infant. We also evaluated the field sensitivity and specificity of an HBsAg point-of-care test strip. We selected a nationally representative sample of 2,100 prevaccine era and 2,100 vaccine era children. We collected a 5-mL blood sample from each child. One drop of blood was used to perform rapid HBsAg testing. If a child had a positive HBsAg test result with the rapid test, a blood sample was collected from the mother of the HBsAg-positive child and from the mothers of two subsequently enrolled HBsAg-negative children. All samples were tested for serologic markers of HBV infection using standard enzyme-linked immunosorbent assay. One (0.05%) child in the vaccine era group and 27 (1.2%; 95% confidence interval [CI]: 0.8-1.7%) children in the prevaccine era group were HBsAg positive. Mothers of HBsAg-positive children were more likely to be HBsAg positive than mothers of HBsAg-negative children (odds ratios = 4.7; 95% CI: 1.0-21.7%). Sensitivity of the HBsAg rapid test was 91.2% (95% CI: 76.6-98.1%) and specificity was 100% (95% CI: 99.9-100%). The study results suggest that even without a birth dose, the hepatitis B vaccine program in Bangladesh was highly effective in preventing chronic HBV infection among children.
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Financial support: This work was supported by the World Health Organization, Regional Office for South-East Asia, New Delhi, India. J. L. reports grants from GAVI, the Vaccine Alliance, during the conduct of the study.
Authors’ addresses: Repon C. Paul, School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia, and Programme for Emerging Infections, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh, E-mail: repon.paul@unsw.edu.au. Mahmudur Rahman, Ahmad R. Sharif, and Sharmin Sultana, Department of Epidemiology, Institute of Epidemiology Disease Control and Research (IEDCR), Dhaka, Bangladesh, E-mails: mrahman57@hotmail.com, drraihan@gmail.com, and dr.sharmin1579@yahoo.com. Eric Wiesen, Minal Patel, and Eric E. Mast, Global Immunization Division, World Health Organization, Atlanta, GA, E-mails: ejw2@cdc.gov, hgo9@cdc.gov, and eem1@cdc.gov. Kajal C. Banik, Programme for Emerging Infections, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh, E-mail: kajal@icddrb.org. Mizanur Rahman, World Health Organization, SEARO, Dhaka, Bangladesh, E-mail: limon_rnp@yahoo.com. Jayantha Liyanage and Nihal Abeysinghe, World Health Organization, SEARO, New Delhi, India, E-mails: liyanagej@who.int and nihal.ird@gmail.com. Saleem Kamili and Trudy Murphy, Division of Viral Hepatitis, CDC, Atlanta, GA, E-mails: sek6@cdc.gov and nol44m@gmail.com. Stephen P. Luby, Department of Medicine, Stanford University, Stanford, CA, E-mail: sluby@stanford.edu.
ISSN:0002-9637
1476-1645
DOI:10.4269/ajtmh.17-0721