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The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study

BACKGROUND: Optimal timing for initiating highly active antiretroviral therapy (HAART) in HIV-TB coinfected patients is challenging for clinicians. We aim to evaluate the impact of different timing of HAART initiation on TB outcome of HIV-infected adults in Taiwan. METHODS: A population-based retros...

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Autores principales: Yang, Chin-Hui, Chen, Kuan-Jung, Tsai, Jih-Jin, Lin, Yu-Hui, Cheng, Shu-Hsing, Wang, Kwei-Feng, Chiou, Hung-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058447/
https://www.ncbi.nlm.nih.gov/pubmed/24897928
http://dx.doi.org/10.1186/1471-2334-14-304
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author Yang, Chin-Hui
Chen, Kuan-Jung
Tsai, Jih-Jin
Lin, Yu-Hui
Cheng, Shu-Hsing
Wang, Kwei-Feng
Chiou, Hung-Yi
author_facet Yang, Chin-Hui
Chen, Kuan-Jung
Tsai, Jih-Jin
Lin, Yu-Hui
Cheng, Shu-Hsing
Wang, Kwei-Feng
Chiou, Hung-Yi
author_sort Yang, Chin-Hui
collection PubMed
description BACKGROUND: Optimal timing for initiating highly active antiretroviral therapy (HAART) in HIV-TB coinfected patients is challenging for clinicians. We aim to evaluate the impact of different timing of HAART initiation on TB outcome of HIV-infected adults in Taiwan. METHODS: A population-based retrospective cohort study was conducted through linking the HIV and TB registries of Taiwan Centers for Disease Control (CDC) during 1997 to 2006. Clinical data of HIV-TB co-infected patients, including the presence of immune reconstitution inflammatory syndrome (IRIS), was collected through medical records review. The outcome of interest was all-cause mortality within 1 year following TB diagnosis. The Cox proportional hazard model was used to explore the probability of death and IRIS after TB diagnosis by adjusting for confounding factors and factors of interest. The probability of survival and TB IRIS were calculated by the Kaplan-Meier method and compared between different HAART initiation timing groups by the log-rank test. RESULTS: There were 229 HIV-TB co-infected patients included for analysis and 60 cases (26.2%) died within one year. Besides decreasing age and increasing CD4 lymphocyte count, having started HAART during TB treatment was significantly associated with better survival (adjusted Hazard Ratio was 0.11, 95% CI 0.06–0.21). As to the timing of HAART initiation, there was only non-significant benefit on survival among cases initiating HAART within 15 days, at 16–30 days and at 31–60 days of TB treatment than initiating after 60 days. Cases with HAART initiated after 30 days had lower risk in developing IRIS than cases with HAART initiated earlier. Cases with IRIS had significantly higher rate of re-hospitalization (49% vs. 4%, p < 0.001) and prolonged hospitalization (28 days vs. 18.5 days, p < 0.01). CONCLUSION: The present study found that starting HAART during TB treatment is associated with better one-year survival, although earlier initiation within 60 days of TB treatment did not show statistical differences in survival than later initiation. Initiation of HAART within 30 days appeared to increase the risk of IRIS. Deferring HAART to 31–60 days of TB treatment might be optimal after considering the risks and benefits.
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spelling pubmed-40584472014-06-17 The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study Yang, Chin-Hui Chen, Kuan-Jung Tsai, Jih-Jin Lin, Yu-Hui Cheng, Shu-Hsing Wang, Kwei-Feng Chiou, Hung-Yi BMC Infect Dis Research Article BACKGROUND: Optimal timing for initiating highly active antiretroviral therapy (HAART) in HIV-TB coinfected patients is challenging for clinicians. We aim to evaluate the impact of different timing of HAART initiation on TB outcome of HIV-infected adults in Taiwan. METHODS: A population-based retrospective cohort study was conducted through linking the HIV and TB registries of Taiwan Centers for Disease Control (CDC) during 1997 to 2006. Clinical data of HIV-TB co-infected patients, including the presence of immune reconstitution inflammatory syndrome (IRIS), was collected through medical records review. The outcome of interest was all-cause mortality within 1 year following TB diagnosis. The Cox proportional hazard model was used to explore the probability of death and IRIS after TB diagnosis by adjusting for confounding factors and factors of interest. The probability of survival and TB IRIS were calculated by the Kaplan-Meier method and compared between different HAART initiation timing groups by the log-rank test. RESULTS: There were 229 HIV-TB co-infected patients included for analysis and 60 cases (26.2%) died within one year. Besides decreasing age and increasing CD4 lymphocyte count, having started HAART during TB treatment was significantly associated with better survival (adjusted Hazard Ratio was 0.11, 95% CI 0.06–0.21). As to the timing of HAART initiation, there was only non-significant benefit on survival among cases initiating HAART within 15 days, at 16–30 days and at 31–60 days of TB treatment than initiating after 60 days. Cases with HAART initiated after 30 days had lower risk in developing IRIS than cases with HAART initiated earlier. Cases with IRIS had significantly higher rate of re-hospitalization (49% vs. 4%, p < 0.001) and prolonged hospitalization (28 days vs. 18.5 days, p < 0.01). CONCLUSION: The present study found that starting HAART during TB treatment is associated with better one-year survival, although earlier initiation within 60 days of TB treatment did not show statistical differences in survival than later initiation. Initiation of HAART within 30 days appeared to increase the risk of IRIS. Deferring HAART to 31–60 days of TB treatment might be optimal after considering the risks and benefits. BioMed Central 2014-06-04 /pmc/articles/PMC4058447/ /pubmed/24897928 http://dx.doi.org/10.1186/1471-2334-14-304 Text en Copyright © 2014 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yang, Chin-Hui
Chen, Kuan-Jung
Tsai, Jih-Jin
Lin, Yu-Hui
Cheng, Shu-Hsing
Wang, Kwei-Feng
Chiou, Hung-Yi
The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title_full The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title_fullStr The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title_full_unstemmed The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title_short The impact of HAART initiation timing on HIV-TB co-infected patients, a retrospective cohort study
title_sort impact of haart initiation timing on hiv-tb co-infected patients, a retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058447/
https://www.ncbi.nlm.nih.gov/pubmed/24897928
http://dx.doi.org/10.1186/1471-2334-14-304
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