A mathematical model to estimate global hepatitis B disease burden and vaccination impact.
Abstract
BACKGROUND: Limited data are available regarding global hepatitis B virus (HBV)-related morbidity and mortality and potential reduction in disease burden from hepatitis B vaccination. METHODS: A model was developed to calculate the age-specific risk of acquiring HBV infection, acute hepatitis B (illness and death), and progression to chronic HBV infection. HBV-related deaths among chronically infected persons were determined from HBV-related cirrhosis and hepatocellular carcinoma (HCC) mortality curves, adjusted for background mortality. The effect of hepatitis B vaccination was calculated from vaccine efficacy and vaccination series coverage, with and without administration of the first dose of vaccine within 24 h of birth (i.e. birth dose) to prevent perinatal HBV infection. RESULTS: For the year 2000, the model estimated 620,000 persons died worldwide from HBV-related causes: 580,000 (94%) from chronic infection-related cirrhosis and HCC and 40,000 (6%) from acute hepatitis B. In the surviving birth cohort for the year 2000, the model estimated that without vaccination, 64.8 million would become HBV-infected and 1.4 million would die from HBV-related disease. Infections acquired during the perinatal period, in early childhood (<5 years old), and > or = 5 years of age accounted for 21, 48, and 31% of deaths, respectively. Routine infant hepatitis B vaccination, with 90% coverage and the first dose administered at birth would prevent 84% of global HBV-related deaths. CONCLUSION: Globally, most HBV-related deaths result from the chronic sequelae of infection acquired in the perinatal and early childhood periods. Inclusion of hepatitis B vaccine into national infant immunization programs could prevent >80% of HBV-related deaths.
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Among persons with chronic HBV infection, the risk for premature death from cirrhosis or hepatocellular carcinoma is 15%-25%.
“Among persons with chronic HBV infection, the risk for premature death from cirrhosis or hepatocellular carcinoma is 15%–25% (1313).”
From Sexually Transmitted Infections Treatment Guidelines, 2021 (2021) · cites this paper as [1313]
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Sexually Transmitted Infections Treatment Guidelines, 2021
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- Authors
- Goldstein, S. T., Zhou, F., Hadler, S. C., Bell, B. P., Mast, E. E., & Margolis, H. S.
- Affiliations
- Centers for Disease Control and Prevention (US)
- Corresponding author
- Goldstein, Susan T
- Venue
- International Journal of Epidemiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-10-25
- Volume
- 34
- Issue
- 6
- Pages
- 1329-1339
- ISSN
- 0300-5771 (ISSN-L)
- 1464-3685
- OpenAlex
- W2163274841
- Cited by
- 743
- References
- 60
- Citations by year
- 2026: 11 · 2025: 13 · 2024: 15 · 2023: 13 · 2022: 25 · 2021: 45 · 2020: 21 · 2019: 39 · 2018: 29 · 2017: 53 · 2016: 61 · 2015: 74 · 2014: 54 · 2013: 66 · 2012: 57
- FWCI
- 11.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- International Journal of Epidemiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Hepatitis B Virus Studies
- Health Sciences › Medicine › Hepatology › Hepatitis C virus research
- Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
- Keywords
- hepatitis B virus, hepatitis B vaccination, birth dose vaccine, chronic hepatitis B, hepatocellular carcinoma, liver cirrhosis, acute hepatitis B, infant immunization, vaccine impact, global mortality estimates
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Child, Child, Preschool, Hepatitis B, Carcinoma, Hepatocellular, Humans, Infant, Infant, Newborn, Liver Cirrhosis, Liver Neoplasms, Middle Aged, Models, Biological, Sensitivity and Specificity, Vaccination, Global Health, Treatment Outcome, Hepatitis B Vaccines, Immunization Programs, Risk Assessment, Hepatitis B, Chronic
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