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The Survival Benefits of Antiretroviral Therapy in South Africa

Background. We sought to quantify the survival benefits attributable to antiretroviral therapy (ART) in South Africa since 2004. Methods. We used the Cost-Effectiveness of Preventing AIDS Complications–International model (CEPAC) to simulate 8 cohorts of human immunodeficiency virus (HIV)–infected p...

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Autores principales: April, Michael D., Wood, Robin, Berkowitz, Bethany K., Paltiel, A. David, Anglaret, Xavier, Losina, Elena, Freedberg, Kenneth A., Walensky, Rochelle P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903379/
https://www.ncbi.nlm.nih.gov/pubmed/24307741
http://dx.doi.org/10.1093/infdis/jit584
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author April, Michael D.
Wood, Robin
Berkowitz, Bethany K.
Paltiel, A. David
Anglaret, Xavier
Losina, Elena
Freedberg, Kenneth A.
Walensky, Rochelle P.
author_facet April, Michael D.
Wood, Robin
Berkowitz, Bethany K.
Paltiel, A. David
Anglaret, Xavier
Losina, Elena
Freedberg, Kenneth A.
Walensky, Rochelle P.
author_sort April, Michael D.
collection PubMed
description Background. We sought to quantify the survival benefits attributable to antiretroviral therapy (ART) in South Africa since 2004. Methods. We used the Cost-Effectiveness of Preventing AIDS Complications–International model (CEPAC) to simulate 8 cohorts of human immunodeficiency virus (HIV)–infected patients initiating ART each year during 2004–2011. Model inputs included cohort-specific mean CD4(+) T-cell count at ART initiation (112–178 cells/µL), 24-week ART suppressive efficacy (78%), second-line ART availability (2.4% of ART recipients), and cohort-specific 36-month retention rate (55%–71%). CEPAC simulated survival twice for each cohort, once with and once without ART. The sum of the products of per capita survival differences and the total numbers of persons initiating ART for each cohort yielded the total survival benefits. Results. Lifetime per capita survival benefits ranged from 9.3 to 10.2 life-years across the 8 cohorts. Total estimated population lifetime survival benefit for all persons starting ART during 2004–2011 was 21.7 million life-years, of which 2.8 million life-years (12.7%) had been realized by December 2012. By 2030, benefits reached 17.9 million life-years under current policies, 21.7 million life-years with universal second-line ART, 23.3 million life-years with increased linkage to care of eligible untreated patients, and 28.0 million life-years with both linkage to care and universal second-line ART. Conclusions. We found dramatic past and potential future survival benefits attributable to ART, justifying international support of ART rollout in South Africa.
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spelling pubmed-39033792014-01-27 The Survival Benefits of Antiretroviral Therapy in South Africa April, Michael D. Wood, Robin Berkowitz, Bethany K. Paltiel, A. David Anglaret, Xavier Losina, Elena Freedberg, Kenneth A. Walensky, Rochelle P. J Infect Dis Major Articles and Brief Reports Background. We sought to quantify the survival benefits attributable to antiretroviral therapy (ART) in South Africa since 2004. Methods. We used the Cost-Effectiveness of Preventing AIDS Complications–International model (CEPAC) to simulate 8 cohorts of human immunodeficiency virus (HIV)–infected patients initiating ART each year during 2004–2011. Model inputs included cohort-specific mean CD4(+) T-cell count at ART initiation (112–178 cells/µL), 24-week ART suppressive efficacy (78%), second-line ART availability (2.4% of ART recipients), and cohort-specific 36-month retention rate (55%–71%). CEPAC simulated survival twice for each cohort, once with and once without ART. The sum of the products of per capita survival differences and the total numbers of persons initiating ART for each cohort yielded the total survival benefits. Results. Lifetime per capita survival benefits ranged from 9.3 to 10.2 life-years across the 8 cohorts. Total estimated population lifetime survival benefit for all persons starting ART during 2004–2011 was 21.7 million life-years, of which 2.8 million life-years (12.7%) had been realized by December 2012. By 2030, benefits reached 17.9 million life-years under current policies, 21.7 million life-years with universal second-line ART, 23.3 million life-years with increased linkage to care of eligible untreated patients, and 28.0 million life-years with both linkage to care and universal second-line ART. Conclusions. We found dramatic past and potential future survival benefits attributable to ART, justifying international support of ART rollout in South Africa. Oxford University Press 2014-02-15 2013-12-03 /pmc/articles/PMC3903379/ /pubmed/24307741 http://dx.doi.org/10.1093/infdis/jit584 Text en © The Author 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Major Articles and Brief Reports
April, Michael D.
Wood, Robin
Berkowitz, Bethany K.
Paltiel, A. David
Anglaret, Xavier
Losina, Elena
Freedberg, Kenneth A.
Walensky, Rochelle P.
The Survival Benefits of Antiretroviral Therapy in South Africa
title The Survival Benefits of Antiretroviral Therapy in South Africa
title_full The Survival Benefits of Antiretroviral Therapy in South Africa
title_fullStr The Survival Benefits of Antiretroviral Therapy in South Africa
title_full_unstemmed The Survival Benefits of Antiretroviral Therapy in South Africa
title_short The Survival Benefits of Antiretroviral Therapy in South Africa
title_sort survival benefits of antiretroviral therapy in south africa
topic Major Articles and Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903379/
https://www.ncbi.nlm.nih.gov/pubmed/24307741
http://dx.doi.org/10.1093/infdis/jit584
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