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Improving survival with tuberculosis & HIV treatment integration: A mini-review

Tuberculosis (TB) is a leading cause of morbidity and mortality among HIV-infected patients while HIV remains a key risk factor for the development of active TB infection. Treatment integration is a key in reducing mortality in patients with HIV-TB co-infection. However, this opportunity to improve...

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Autores principales: Naidoo, Kogieleum, Rampersad, Sanisha, Karim, Salim Abdool
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829777/
https://www.ncbi.nlm.nih.gov/pubmed/31670268
http://dx.doi.org/10.4103/ijmr.IJMR_660_19
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author Naidoo, Kogieleum
Rampersad, Sanisha
Karim, Salim Abdool
author_facet Naidoo, Kogieleum
Rampersad, Sanisha
Karim, Salim Abdool
author_sort Naidoo, Kogieleum
collection PubMed
description Tuberculosis (TB) is a leading cause of morbidity and mortality among HIV-infected patients while HIV remains a key risk factor for the development of active TB infection. Treatment integration is a key in reducing mortality in patients with HIV-TB co-infection. However, this opportunity to improve outcomes of both infections is often missed or poorly implemented. Challenges in TB-HIV treatment integration range from complexities involving clinical management of co-infected patients to obstacles in health service-organization and prioritization. This is evident in high prevalence settings such as in sub-Saharan Africa where TB-HIV co-infection rates reach up to 80 per cent. This review discusses published literature on clinical trials and cohort studies of strategies for TB-HIV treatment integration aimed at reducing co-infection mortality. Studies published since 2009, when several treatment guidelines recommended treatment integration, were included. A total of 43 articles were identified, of which a total of 23 observational studies and nine clinical trials were informative on TB-HIV treatment integration. The data show that the survival benefit of AIDS therapy in patients infected with TB can be maximized among patients with advanced immunosuppression by starting antiretroviral therapy (ART) soon after TB treatment initiation, i.e. in patients with CD4+ cell counts <50 cells/μl. However, patients with greater CD4+ cell counts should defer initiation of ART to no less than eight weeks after initiation of TB treatment to reduce the occurrence and extent of immune reconstitution disease and subsequent hospitalization. Addressing operational challenges in integrating TB-HIV care can significantly improve patient outcomes, generate substantial public health impact by decreasing morbidity and death in settings with a high burden of HIV and TB.
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spelling pubmed-68297772019-11-14 Improving survival with tuberculosis & HIV treatment integration: A mini-review Naidoo, Kogieleum Rampersad, Sanisha Karim, Salim Abdool Indian J Med Res Review Article Tuberculosis (TB) is a leading cause of morbidity and mortality among HIV-infected patients while HIV remains a key risk factor for the development of active TB infection. Treatment integration is a key in reducing mortality in patients with HIV-TB co-infection. However, this opportunity to improve outcomes of both infections is often missed or poorly implemented. Challenges in TB-HIV treatment integration range from complexities involving clinical management of co-infected patients to obstacles in health service-organization and prioritization. This is evident in high prevalence settings such as in sub-Saharan Africa where TB-HIV co-infection rates reach up to 80 per cent. This review discusses published literature on clinical trials and cohort studies of strategies for TB-HIV treatment integration aimed at reducing co-infection mortality. Studies published since 2009, when several treatment guidelines recommended treatment integration, were included. A total of 43 articles were identified, of which a total of 23 observational studies and nine clinical trials were informative on TB-HIV treatment integration. The data show that the survival benefit of AIDS therapy in patients infected with TB can be maximized among patients with advanced immunosuppression by starting antiretroviral therapy (ART) soon after TB treatment initiation, i.e. in patients with CD4+ cell counts <50 cells/μl. However, patients with greater CD4+ cell counts should defer initiation of ART to no less than eight weeks after initiation of TB treatment to reduce the occurrence and extent of immune reconstitution disease and subsequent hospitalization. Addressing operational challenges in integrating TB-HIV care can significantly improve patient outcomes, generate substantial public health impact by decreasing morbidity and death in settings with a high burden of HIV and TB. Wolters Kluwer - Medknow 2019-08 /pmc/articles/PMC6829777/ /pubmed/31670268 http://dx.doi.org/10.4103/ijmr.IJMR_660_19 Text en Copyright: © 2019 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Naidoo, Kogieleum
Rampersad, Sanisha
Karim, Salim Abdool
Improving survival with tuberculosis & HIV treatment integration: A mini-review
title Improving survival with tuberculosis & HIV treatment integration: A mini-review
title_full Improving survival with tuberculosis & HIV treatment integration: A mini-review
title_fullStr Improving survival with tuberculosis & HIV treatment integration: A mini-review
title_full_unstemmed Improving survival with tuberculosis & HIV treatment integration: A mini-review
title_short Improving survival with tuberculosis & HIV treatment integration: A mini-review
title_sort improving survival with tuberculosis & hiv treatment integration: a mini-review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829777/
https://www.ncbi.nlm.nih.gov/pubmed/31670268
http://dx.doi.org/10.4103/ijmr.IJMR_660_19
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