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Article: Global prevalence, cascade of care, and prophylaxis coverage of hepatitis B in 2022: a modelling study

TitleGlobal prevalence, cascade of care, and prophylaxis coverage of hepatitis B in 2022: a modelling study
Authors
Issue Date1-Oct-2023
PublisherElsevier
Citation
The Lancet Gastroenterology & Hepatology, 2023, v. 8, n. 10, p. 879-907 How to Cite?
Abstract

Background

The 2016 World Health Assembly endorsed the elimination of hepatitis B virus (HBV) infection as a public health threat by 2030; existing therapies and prophylaxis measures make such elimination feasible, even in the absence of a virological cure. We aimed to estimate the national, regional, and global prevalence of HBV in the general population and among children aged 5 years and younger, as well as the rates of diagnosis, treatment, prophylaxis, and the future burden globally.

Methods

In this modelling study, we used a Delphi process with data from literature reviews and interviews with country experts to quantify the prevalence, diagnosis, treatment, and prevention measures for HBV infection. The PRoGReSs Model, a dynamic Markov model, was used to estimate the country, regional, and global prevalence of HBV infection in 2022, and the effects of treatment and prevention on disease burden. The future incidence of morbidity and mortality in the absence of additional interventions was also estimated at the global level.

Findings

We developed models for 170 countries which resulted in an estimated global prevalence of HBV infection in 2022 of 3·2% (95% uncertainty interval 2·7–4·0), corresponding to 257·5 million (216·6–316·4) individuals positive for HBsAg. Of these individuals, 36·0 million were diagnosed, and only 6·8 million of the estimated 83·3 million eligible for treatment were on treatment. The prevalence among children aged 5 years or younger was estimated to be 0·7% (0·6–1·0), corresponding to 5·6 million (4·5–7·8) children with HBV infection. Based on the most recent data, 85% of infants received three-dose HBV vaccination before 1 year of age, 46% had received a timely birth dose of vaccine, and 14% received hepatitis B immunoglobulin along with the full vaccination regimen. 3% of mothers with a high HBV viral load received antiviral treatment to reduce mother-to-child transmission.

Interpretation

As 2030 approaches, the elimination targets remain out of reach for many countries under the current frameworks. Although prevention measures have had the most success, there is a need to increase these efforts and to increase diagnosis and treatment to work towards the elimination goals.


Persistent Identifierhttp://hdl.handle.net/10722/340917
ISSN
2023 Impact Factor: 30.9
2023 SCImago Journal Rankings: 8.957
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSeto, Wai Kay Walter-
dc.contributor.authorYuen, Richard Man Fung-
dc.contributor.authorThe Polaris Observatory Collaborators-
dc.date.accessioned2024-03-11T10:48:17Z-
dc.date.available2024-03-11T10:48:17Z-
dc.date.issued2023-10-01-
dc.identifier.citationThe Lancet Gastroenterology & Hepatology, 2023, v. 8, n. 10, p. 879-907-
dc.identifier.issn2468-1253-
dc.identifier.urihttp://hdl.handle.net/10722/340917-
dc.description.abstract<h3>Background</h3><p>The 2016 World Health Assembly endorsed the elimination of hepatitis B virus (HBV) infection as a public health threat by 2030; existing therapies and prophylaxis measures make such elimination feasible, even in the absence of a virological cure. We aimed to estimate the national, regional, and global prevalence of HBV in the general population and among children aged 5 years and younger, as well as the rates of diagnosis, treatment, prophylaxis, and the future burden globally.</p><h3>Methods</h3><p>In this modelling study, we used a Delphi process with data from literature reviews and interviews with country experts to quantify the prevalence, diagnosis, treatment, and prevention measures for HBV infection. The PRoGReSs Model, a dynamic Markov model, was used to estimate the country, regional, and global prevalence of HBV infection in 2022, and the effects of treatment and prevention on disease burden. The future incidence of morbidity and mortality in the absence of additional interventions was also estimated at the global level.</p><h3>Findings</h3><p>We developed models for 170 countries which resulted in an estimated global prevalence of HBV infection in 2022 of 3·2% (95% uncertainty interval 2·7–4·0), corresponding to 257·5 million (216·6–316·4) individuals positive for HBsAg. Of these individuals, 36·0 million were diagnosed, and only 6·8 million of the estimated 83·3 million eligible for treatment were on treatment. The prevalence among children aged 5 years or younger was estimated to be 0·7% (0·6–1·0), corresponding to 5·6 million (4·5–7·8) children with HBV infection. Based on the most recent data, 85% of infants received three-dose HBV vaccination before 1 year of age, 46% had received a timely birth dose of vaccine, and 14% received hepatitis B immunoglobulin along with the full vaccination regimen. 3% of mothers with a high HBV viral load received antiviral treatment to reduce mother-to-child transmission.</p><h3>Interpretation</h3><p>As 2030 approaches, the elimination targets remain out of reach for many countries under the current frameworks. Although prevention measures have had the most success, there is a need to increase these efforts and to increase diagnosis and treatment to work towards the elimination goals.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofThe Lancet Gastroenterology & Hepatology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleGlobal prevalence, cascade of care, and prophylaxis coverage of hepatitis B in 2022: a modelling study-
dc.typeArticle-
dc.identifier.doi10.1016/S2468-1253(23)00197-8-
dc.identifier.scopuseid_2-s2.0-85169786860-
dc.identifier.volume8-
dc.identifier.issue10-
dc.identifier.spage879-
dc.identifier.epage907-
dc.identifier.eissn2468-1253-
dc.identifier.isiWOS:001158110000001-
dc.identifier.issnl2468-1156-

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