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Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality

OBJECTIVES: Reliable estimates of the joint burden of HIV and tuberculosis epidemics are crucial to planning strategic global and national tuberculosis responses. Prior to the Global Tuberculosis Report 2013, the Global Tuberculosis Programme (GTB) released estimates for tuberculosis–HIV incidence a...

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Autores principales: Pretorius, Carel, Glaziou, Philippe, Dodd, Peter J., White, Richard, Houben, Rein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247264/
https://www.ncbi.nlm.nih.gov/pubmed/25406751
http://dx.doi.org/10.1097/QAD.0000000000000484
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author Pretorius, Carel
Glaziou, Philippe
Dodd, Peter J.
White, Richard
Houben, Rein
author_facet Pretorius, Carel
Glaziou, Philippe
Dodd, Peter J.
White, Richard
Houben, Rein
author_sort Pretorius, Carel
collection PubMed
description OBJECTIVES: Reliable estimates of the joint burden of HIV and tuberculosis epidemics are crucial to planning strategic global and national tuberculosis responses. Prior to the Global Tuberculosis Report 2013, the Global Tuberculosis Programme (GTB) released estimates for tuberculosis–HIV incidence at the global level only. Neither GTB nor United Nations Programme on HIV/AIDS (UNAIDS) published country specific estimates for tuberculosis–HIV mortality. We used a regression approach that combined all available data from GTB and UNAIDS in order to estimate tuberculosis–HIV incidence and mortality at country level. METHODS: A regression method was devised to relate CD4 dynamics (based on national Spectrum files) to an increased relative risk (RR) of tuberculosis disease. The objective function is based on least squares and incorporates all available country-level estimates of tuberculosis–HIV incidence. Global regression parameters, obtained from averaging results over countries with population survey estimates for tuberculosis–HIV burden, were applied to countries with no survey tuberculosis–HIV incidence estimates. RESULTS: The method produced results that are in reasonably close agreement with existing GTB estimates for global tuberculosis–HIV burden. It estimated that tuberculosis–HIV accounts for 12.6% of global tuberculosis incidence, 21.3% of all tuberculosis deaths, and 20% of all HIV deaths as estimated by the Spectrum AIDS Impact Module (AIM). Regional estimates show the highest absolute incidence burden in East and Southeast Asia, and the highest per capita burden in sub-Saharan Africa, where between 12.5% (Central sub-Saharan Africa) and 60.6% (Southern sub-Saharan Africa) of all tuberculosis disease occurs in people living with HIV (PLWH). Tuberculosis mortality follows a similar pattern, except that a disproportionate percentage of global tuberculosis deaths (12.1%) relative to global incidence (8.7%) occurred in Southern sub-Saharan Africa. CONCLUSION: The disaggregation of tuberculosis incidence using a regression method on RR of tuberculosis disease and all available data on HIV burden (from UNAIDS) and tuberculosis–HIV testing (survey, sentinel and routine surveillance data) produces results that closely match GTB estimates for 2011. The tuberculosis–HIV incidence and mortality results were published in the Global Tuberculosis Report 2013. Several limitations of and potential improvements to the process are suggested.
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spelling pubmed-42472642014-12-01 Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality Pretorius, Carel Glaziou, Philippe Dodd, Peter J. White, Richard Houben, Rein AIDS The 2013/14 UNAIDS Estimates Methods: Extending The Scope and Granularity of HIV Estimates OBJECTIVES: Reliable estimates of the joint burden of HIV and tuberculosis epidemics are crucial to planning strategic global and national tuberculosis responses. Prior to the Global Tuberculosis Report 2013, the Global Tuberculosis Programme (GTB) released estimates for tuberculosis–HIV incidence at the global level only. Neither GTB nor United Nations Programme on HIV/AIDS (UNAIDS) published country specific estimates for tuberculosis–HIV mortality. We used a regression approach that combined all available data from GTB and UNAIDS in order to estimate tuberculosis–HIV incidence and mortality at country level. METHODS: A regression method was devised to relate CD4 dynamics (based on national Spectrum files) to an increased relative risk (RR) of tuberculosis disease. The objective function is based on least squares and incorporates all available country-level estimates of tuberculosis–HIV incidence. Global regression parameters, obtained from averaging results over countries with population survey estimates for tuberculosis–HIV burden, were applied to countries with no survey tuberculosis–HIV incidence estimates. RESULTS: The method produced results that are in reasonably close agreement with existing GTB estimates for global tuberculosis–HIV burden. It estimated that tuberculosis–HIV accounts for 12.6% of global tuberculosis incidence, 21.3% of all tuberculosis deaths, and 20% of all HIV deaths as estimated by the Spectrum AIDS Impact Module (AIM). Regional estimates show the highest absolute incidence burden in East and Southeast Asia, and the highest per capita burden in sub-Saharan Africa, where between 12.5% (Central sub-Saharan Africa) and 60.6% (Southern sub-Saharan Africa) of all tuberculosis disease occurs in people living with HIV (PLWH). Tuberculosis mortality follows a similar pattern, except that a disproportionate percentage of global tuberculosis deaths (12.1%) relative to global incidence (8.7%) occurred in Southern sub-Saharan Africa. CONCLUSION: The disaggregation of tuberculosis incidence using a regression method on RR of tuberculosis disease and all available data on HIV burden (from UNAIDS) and tuberculosis–HIV testing (survey, sentinel and routine surveillance data) produces results that closely match GTB estimates for 2011. The tuberculosis–HIV incidence and mortality results were published in the Global Tuberculosis Report 2013. Several limitations of and potential improvements to the process are suggested. Lippincott Williams & Wilkins 2014-11 2014-11-20 /pmc/articles/PMC4247264/ /pubmed/25406751 http://dx.doi.org/10.1097/QAD.0000000000000484 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle The 2013/14 UNAIDS Estimates Methods: Extending The Scope and Granularity of HIV Estimates
Pretorius, Carel
Glaziou, Philippe
Dodd, Peter J.
White, Richard
Houben, Rein
Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title_full Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title_fullStr Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title_full_unstemmed Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title_short Using the TIME model in Spectrum to estimate tuberculosis–HIV incidence and mortality
title_sort using the time model in spectrum to estimate tuberculosis–hiv incidence and mortality
topic The 2013/14 UNAIDS Estimates Methods: Extending The Scope and Granularity of HIV Estimates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247264/
https://www.ncbi.nlm.nih.gov/pubmed/25406751
http://dx.doi.org/10.1097/QAD.0000000000000484
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