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Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand

BACKGROUND: The case fatality rate in patients with tuberculosis (TB) associated with human immunodeficiency virus (HIV) has been particularly high in Chiang Rai, Northern Thailand. It was almost 50% before the introduction of antiretroviral therapy in the last decade, and was still at 28% in 2008,...

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Autores principales: Kantipong, Pacharee, Murakami, Kuniko, Moolphate, Saiyud, Aung, Myo Nyein, Yamada, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469094/
https://www.ncbi.nlm.nih.gov/pubmed/23071410
http://dx.doi.org/10.2147/HIV.S33535
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author Kantipong, Pacharee
Murakami, Kuniko
Moolphate, Saiyud
Aung, Myo Nyein
Yamada, Norio
author_facet Kantipong, Pacharee
Murakami, Kuniko
Moolphate, Saiyud
Aung, Myo Nyein
Yamada, Norio
author_sort Kantipong, Pacharee
collection PubMed
description BACKGROUND: The case fatality rate in patients with tuberculosis (TB) associated with human immunodeficiency virus (HIV) has been particularly high in Chiang Rai, Northern Thailand. It was almost 50% before the introduction of antiretroviral therapy in the last decade, and was still at 28% in 2008, despite expanding access to antiretroviral therapy. Reviewing the causes of death may lead to further understanding of the timeline and natural history of TB-HIV coinfection, and in so doing help to devise an effective prevention strategy in Chiang Rai. In this study, we aimed to investigate the distribution of confirmed causes of death in patients coinfected with TB and HIV in Chiang Rai, describe the causes of such deaths along the timeline of TB treatment, and identify predictors of each cause of death. METHODS: In this retrospective study, we reviewed the causes of death for 331 patients who died of TB-HIV coinfection at Chiang Rai Prachanukroh Hospital from 2005 to 2008. Causes of death were confirmed by reviewing medical records, vital registration, and the TB register in the province, as well as obtaining reconfirmation by two experienced HIV physicians. RESULTS: The confirmed causes of death were TB (39%), acquired immune deficiency syndrome (AIDS)-related opportunistic infections other than TB (AOI) (29%), and other systemic diseases which were neither TB nor AIDS-related opportunistic infections (nonTB-nonAOI) (16%). The definitive cause could not be confirmed in the remaining 16% of deaths. After starting the TB treatment, deaths caused by TB occurred earlier compared with deaths caused by AOI, which occurred steadily throughout the course of TB treatment, whilst deaths caused by non-TB-nonAOI increased gradually in later months. Further analysis by multivariate multinomial regression analysis showed that deaths in the first month (adjusted odds ratio [aOR] 4.64, 95% confidence interval [CI] 2.49–8.63), CD4 count ≥ 200 cells/mm(3) (aOR 5.33, CI 1.05–26.10), non-category 1 TB treatment regimens (aOR 5.23, CI 1.04–9.77), and TB meningitis (aOR 3.27, CI 1.37–7.82) were significant predictors of confirmed TB deaths. Moreover, age over 45 years (aOR 3, CI 1.32–6.84) and admission as an inpatient were predictors of death caused by neither TB nor AIDS-related opportunistic infections (aOR 3.08, CI 1.39–6.80). Additional analysis showed that non-Thai patients (aOR 0.35, CI 0.12–0.99), those with an unknown CD4 count at TB diagnosis (aOR 0.16, CI 0.08–0.33), and those without an HIV diagnosis before TB treatment (aOR 0.32, CI 0.18–0.59) were less able to access antiretroviral therapy. CONCLUSION: The timeline and predictors of causes of death may assist in devising an intervention strategy for further reduction of the TB-HIV case fatality rate.
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spelling pubmed-34690942012-10-15 Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand Kantipong, Pacharee Murakami, Kuniko Moolphate, Saiyud Aung, Myo Nyein Yamada, Norio HIV AIDS (Auckl) Original Research BACKGROUND: The case fatality rate in patients with tuberculosis (TB) associated with human immunodeficiency virus (HIV) has been particularly high in Chiang Rai, Northern Thailand. It was almost 50% before the introduction of antiretroviral therapy in the last decade, and was still at 28% in 2008, despite expanding access to antiretroviral therapy. Reviewing the causes of death may lead to further understanding of the timeline and natural history of TB-HIV coinfection, and in so doing help to devise an effective prevention strategy in Chiang Rai. In this study, we aimed to investigate the distribution of confirmed causes of death in patients coinfected with TB and HIV in Chiang Rai, describe the causes of such deaths along the timeline of TB treatment, and identify predictors of each cause of death. METHODS: In this retrospective study, we reviewed the causes of death for 331 patients who died of TB-HIV coinfection at Chiang Rai Prachanukroh Hospital from 2005 to 2008. Causes of death were confirmed by reviewing medical records, vital registration, and the TB register in the province, as well as obtaining reconfirmation by two experienced HIV physicians. RESULTS: The confirmed causes of death were TB (39%), acquired immune deficiency syndrome (AIDS)-related opportunistic infections other than TB (AOI) (29%), and other systemic diseases which were neither TB nor AIDS-related opportunistic infections (nonTB-nonAOI) (16%). The definitive cause could not be confirmed in the remaining 16% of deaths. After starting the TB treatment, deaths caused by TB occurred earlier compared with deaths caused by AOI, which occurred steadily throughout the course of TB treatment, whilst deaths caused by non-TB-nonAOI increased gradually in later months. Further analysis by multivariate multinomial regression analysis showed that deaths in the first month (adjusted odds ratio [aOR] 4.64, 95% confidence interval [CI] 2.49–8.63), CD4 count ≥ 200 cells/mm(3) (aOR 5.33, CI 1.05–26.10), non-category 1 TB treatment regimens (aOR 5.23, CI 1.04–9.77), and TB meningitis (aOR 3.27, CI 1.37–7.82) were significant predictors of confirmed TB deaths. Moreover, age over 45 years (aOR 3, CI 1.32–6.84) and admission as an inpatient were predictors of death caused by neither TB nor AIDS-related opportunistic infections (aOR 3.08, CI 1.39–6.80). Additional analysis showed that non-Thai patients (aOR 0.35, CI 0.12–0.99), those with an unknown CD4 count at TB diagnosis (aOR 0.16, CI 0.08–0.33), and those without an HIV diagnosis before TB treatment (aOR 0.32, CI 0.18–0.59) were less able to access antiretroviral therapy. CONCLUSION: The timeline and predictors of causes of death may assist in devising an intervention strategy for further reduction of the TB-HIV case fatality rate. Dove Medical Press 2012-10-04 /pmc/articles/PMC3469094/ /pubmed/23071410 http://dx.doi.org/10.2147/HIV.S33535 Text en © 2012 Kantipong et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Kantipong, Pacharee
Murakami, Kuniko
Moolphate, Saiyud
Aung, Myo Nyein
Yamada, Norio
Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title_full Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title_fullStr Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title_full_unstemmed Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title_short Causes of mortality among tuberculosis and HIV co-infected patients in Chiang Rai, Northern Thailand
title_sort causes of mortality among tuberculosis and hiv co-infected patients in chiang rai, northern thailand
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469094/
https://www.ncbi.nlm.nih.gov/pubmed/23071410
http://dx.doi.org/10.2147/HIV.S33535
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