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Modeling Progress Toward Elimination of Hepatitis B in Australia

BACKGROUND AND AIMS: Chronic hepatitis B (CHB) is a significant global health concern, and the most prevalent blood‐borne virus in Australia. World Health Organization (WHO) member states have committed to global elimination, with targets to diagnose 90% of people living with CHB, treat 80% of those...

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Autores principales: McCulloch, Karen, Romero, Nicole, MacLachlan, Jennifer, Allard, Nicole, Cowie, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187332/
https://www.ncbi.nlm.nih.gov/pubmed/31419332
http://dx.doi.org/10.1002/hep.30899
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author McCulloch, Karen
Romero, Nicole
MacLachlan, Jennifer
Allard, Nicole
Cowie, Benjamin
author_facet McCulloch, Karen
Romero, Nicole
MacLachlan, Jennifer
Allard, Nicole
Cowie, Benjamin
author_sort McCulloch, Karen
collection PubMed
description BACKGROUND AND AIMS: Chronic hepatitis B (CHB) is a significant global health concern, and the most prevalent blood‐borne virus in Australia. World Health Organization (WHO) member states have committed to global elimination, with targets to diagnose 90% of people living with CHB, treat 80% of those eligible, and reduce attributable deaths by 65% by the year 2030. Australia has committed to national targets of 80% diagnosed, 20% on treatment, and a 30% reduction in deaths by 2022. APPROACH AND RESULTS: We constructed and implemented a mathematical model to estimate the burden of CHB incorporating vaccination, phases of infection, cirrhosis progression, and mortality attributed to decompensated cirrhosis and hepatocellular carcinoma and examined the population‐level impact of antiviral therapy. Diversity was integrated according to migration patterns, CHB prevalence by country of birth, Indigenous status, and age. Modelled outcomes were subjected to multivariate uncertainty analysis. Of the estimated 221,420 people living with CHB in Australia in 2017, 68% were diagnosed and 8.7% were receiving treatment (less than one‐third of those estimated to be eligible). Based on current trends, the proportion of people living with CHB who have been diagnosed will reach 71% by 2022 and 81% by 2030, and treatment uptake will rise to 11.2% by 2022 and 12.9% by 2030, resulting in a 5.7% reduction in CHB‐attributable deaths from 2015 to 2030. CHB treatment has prevented approximately 2,300 deaths in Australia between 2000 and 2017. CONCLUSIONS: Australia is not on track to meet local and global targets regarding CHB. Comprehensive and regularly updated modelling approaches accounting for diversity within the population are a useful tool to measure progress and impact of interventions, and quantify further improvements required to meet elimination goals.
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spelling pubmed-71873322020-04-28 Modeling Progress Toward Elimination of Hepatitis B in Australia McCulloch, Karen Romero, Nicole MacLachlan, Jennifer Allard, Nicole Cowie, Benjamin Hepatology Original Articles BACKGROUND AND AIMS: Chronic hepatitis B (CHB) is a significant global health concern, and the most prevalent blood‐borne virus in Australia. World Health Organization (WHO) member states have committed to global elimination, with targets to diagnose 90% of people living with CHB, treat 80% of those eligible, and reduce attributable deaths by 65% by the year 2030. Australia has committed to national targets of 80% diagnosed, 20% on treatment, and a 30% reduction in deaths by 2022. APPROACH AND RESULTS: We constructed and implemented a mathematical model to estimate the burden of CHB incorporating vaccination, phases of infection, cirrhosis progression, and mortality attributed to decompensated cirrhosis and hepatocellular carcinoma and examined the population‐level impact of antiviral therapy. Diversity was integrated according to migration patterns, CHB prevalence by country of birth, Indigenous status, and age. Modelled outcomes were subjected to multivariate uncertainty analysis. Of the estimated 221,420 people living with CHB in Australia in 2017, 68% were diagnosed and 8.7% were receiving treatment (less than one‐third of those estimated to be eligible). Based on current trends, the proportion of people living with CHB who have been diagnosed will reach 71% by 2022 and 81% by 2030, and treatment uptake will rise to 11.2% by 2022 and 12.9% by 2030, resulting in a 5.7% reduction in CHB‐attributable deaths from 2015 to 2030. CHB treatment has prevented approximately 2,300 deaths in Australia between 2000 and 2017. CONCLUSIONS: Australia is not on track to meet local and global targets regarding CHB. Comprehensive and regularly updated modelling approaches accounting for diversity within the population are a useful tool to measure progress and impact of interventions, and quantify further improvements required to meet elimination goals. John Wiley and Sons Inc. 2019-10-14 2020-04 /pmc/articles/PMC7187332/ /pubmed/31419332 http://dx.doi.org/10.1002/hep.30899 Text en © 2019 The Authors. Hepatology published by Wiley Periodicals, Inc., on behalf of American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
McCulloch, Karen
Romero, Nicole
MacLachlan, Jennifer
Allard, Nicole
Cowie, Benjamin
Modeling Progress Toward Elimination of Hepatitis B in Australia
title Modeling Progress Toward Elimination of Hepatitis B in Australia
title_full Modeling Progress Toward Elimination of Hepatitis B in Australia
title_fullStr Modeling Progress Toward Elimination of Hepatitis B in Australia
title_full_unstemmed Modeling Progress Toward Elimination of Hepatitis B in Australia
title_short Modeling Progress Toward Elimination of Hepatitis B in Australia
title_sort modeling progress toward elimination of hepatitis b in australia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187332/
https://www.ncbi.nlm.nih.gov/pubmed/31419332
http://dx.doi.org/10.1002/hep.30899
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