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Hepatitis B immunization for indigenous adults, Australia

OBJECTIVE: To quantify the disparity in incidence of hepatitis B between indigenous and non-indigenous people in Australia, and to estimate the potential impact of a hepatitis B immunization programme targeting non-immune indigenous adults. METHODS: Using national data on persons with newly acquired...

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Autores principales: Wattiaux, Andre Louis, Yin, J Kevin, Beard, Frank, Wesselingh, Steve, Cowie, Benjamin, Ward, James, Macartney, Kristine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Health Organization 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096351/
https://www.ncbi.nlm.nih.gov/pubmed/27821885
http://dx.doi.org/10.2471/BLT.16.169524
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author Wattiaux, Andre Louis
Yin, J Kevin
Beard, Frank
Wesselingh, Steve
Cowie, Benjamin
Ward, James
Macartney, Kristine
author_facet Wattiaux, Andre Louis
Yin, J Kevin
Beard, Frank
Wesselingh, Steve
Cowie, Benjamin
Ward, James
Macartney, Kristine
author_sort Wattiaux, Andre Louis
collection PubMed
description OBJECTIVE: To quantify the disparity in incidence of hepatitis B between indigenous and non-indigenous people in Australia, and to estimate the potential impact of a hepatitis B immunization programme targeting non-immune indigenous adults. METHODS: Using national data on persons with newly acquired hepatitis B disease notified between 2005 and 2012, we estimated incident infection rates and rate ratios comparing indigenous and non-indigenous people, with adjustments for underreporting. The potential impact of a hepatitis B immunization programme targeting non-immune indigenous adults was projected using a Markov chain Monte Carlo simulation model. FINDINGS: Of the 54 522 persons with hepatitis B disease notified between 1 January 2005 and 31 December 2012, 1953  infections were newly acquired. Acute hepatitis B infection notification rates were significantly higher for indigenous than non-indigenous Australians. The rates per 100 000 population for all ages were 3.6 (156/4 368 511) and 1.1 (1797/168 449 302) for indigenous and non-indigenous people respectively. The rate ratio of age-standardized notifications was 4.0 (95% confidence interval: 3.7–4.3). If 50% of non-immune indigenous adults (20% of all indigenous adults) were vaccinated over a 10-year programme a projected 527–549 new cases of acute hepatitis B would be prevented. CONCLUSION: There continues to be significant health inequity between indigenous and non-indigenous Australians in relation to vaccine-preventable hepatitis B disease. An immunization programme targeting indigenous Australian adults could have considerable impact in terms of cases of acute hepatitis B prevented, with a relatively low number needed to vaccinate to prevent each case.
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spelling pubmed-50963512016-11-07 Hepatitis B immunization for indigenous adults, Australia Wattiaux, Andre Louis Yin, J Kevin Beard, Frank Wesselingh, Steve Cowie, Benjamin Ward, James Macartney, Kristine Bull World Health Organ Research OBJECTIVE: To quantify the disparity in incidence of hepatitis B between indigenous and non-indigenous people in Australia, and to estimate the potential impact of a hepatitis B immunization programme targeting non-immune indigenous adults. METHODS: Using national data on persons with newly acquired hepatitis B disease notified between 2005 and 2012, we estimated incident infection rates and rate ratios comparing indigenous and non-indigenous people, with adjustments for underreporting. The potential impact of a hepatitis B immunization programme targeting non-immune indigenous adults was projected using a Markov chain Monte Carlo simulation model. FINDINGS: Of the 54 522 persons with hepatitis B disease notified between 1 January 2005 and 31 December 2012, 1953  infections were newly acquired. Acute hepatitis B infection notification rates were significantly higher for indigenous than non-indigenous Australians. The rates per 100 000 population for all ages were 3.6 (156/4 368 511) and 1.1 (1797/168 449 302) for indigenous and non-indigenous people respectively. The rate ratio of age-standardized notifications was 4.0 (95% confidence interval: 3.7–4.3). If 50% of non-immune indigenous adults (20% of all indigenous adults) were vaccinated over a 10-year programme a projected 527–549 new cases of acute hepatitis B would be prevented. CONCLUSION: There continues to be significant health inequity between indigenous and non-indigenous Australians in relation to vaccine-preventable hepatitis B disease. An immunization programme targeting indigenous Australian adults could have considerable impact in terms of cases of acute hepatitis B prevented, with a relatively low number needed to vaccinate to prevent each case. World Health Organization 2016-11-01 2016-09-16 /pmc/articles/PMC5096351/ /pubmed/27821885 http://dx.doi.org/10.2471/BLT.16.169524 Text en (c) 2016 The authors; licensee World Health Organization. This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.
spellingShingle Research
Wattiaux, Andre Louis
Yin, J Kevin
Beard, Frank
Wesselingh, Steve
Cowie, Benjamin
Ward, James
Macartney, Kristine
Hepatitis B immunization for indigenous adults, Australia
title Hepatitis B immunization for indigenous adults, Australia
title_full Hepatitis B immunization for indigenous adults, Australia
title_fullStr Hepatitis B immunization for indigenous adults, Australia
title_full_unstemmed Hepatitis B immunization for indigenous adults, Australia
title_short Hepatitis B immunization for indigenous adults, Australia
title_sort hepatitis b immunization for indigenous adults, australia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096351/
https://www.ncbi.nlm.nih.gov/pubmed/27821885
http://dx.doi.org/10.2471/BLT.16.169524
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