HIV co-infection increases the risk of post-tuberculosis mortality among persons who initiated treatment for drug-resistant tuberculosis

Little is known regarding the relationship between common comorbidities in persons with tuberculosis (TB) (including human immunodeficiency virus [HIV], diabetes, and hepatitis C virus [HCV]) and post-TB mortality. We conducted a retrospective cohort study among persons who initiated treatment for rifampicin-resistant or multi/extensively drug-resistant (RR or M/XDR) TB reported to the country of Georgia's TB surveillance during 2009-2017. Exposures included HIV serologic status, diabetes, and HCV status. Our outcome was all-cause post-TB mortality determined by cross-validating vital status with Georgia's death registry through November 2019. We estimated adjusted hazard rate ratios (aHR) and 95% confidence intervals (CI) of post-TB mortality among participants with and without comorbidities using cause-specific hazard regressions. Among 1032 eligible participants, 34 (3.3%) died during treatment and 87 (8.7%) died post-TB treatment. The median time to post-TB death was 21 months (interquartile range 7-39) after TB treatment. After adjusting for confounders, the hazard rates of post-TB mortality were higher among participants with HIV co-infection (aHR = 3.74, 95%CI 1.77-7.91) compared to those without HIV co-infection. In our cohort, post-TB mortality occurred most commonly in the first 3 years post-TB treatment. Linkage to care for common TB comorbidities post-treatment may reduce post-TB mortality rates.

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Publication Details

Journal
Scientific Reports
Published
2024-10-11
DOI
https://doi.org/10.1038/s41598-024-68605-2
Citations
10
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
3.89

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article

HIV co-infection increases the risk of post-tuberculosis mortality among persons who initiated treatment for drug-resistant tuberculosis

Matthew James Magee, Zaza Avaliani, Katherine E. Masyn, Nestani Tukvadze et al.
10 citations
Scientific Reports
Tuberculosis Research and Epidemiology
3.89
article

HIV co-infection increases the risk of post-tuberculosis mortality among persons who initiated treatment for drug-resistant tuberculosis

Matthew James Magee, Zaza Avaliani, Katherine E. Masyn, Nestani Tukvadze, Nino Lomtadze, Russell Ryan Kempker, Argita D. Salindri, Henry M. Blumberg, Maia Kipiani, Richard B. Rothenberg
article en
10 citations

Abstract

Little is known regarding the relationship between common comorbidities in persons with tuberculosis (TB) (including human immunodeficiency virus [HIV], diabetes, and hepatitis C virus [HCV]) and post-TB mortality. We conducted a retrospective cohort study among persons who initiated treatment for rifampicin-resistant or multi/extensively drug-resistant (RR or M/XDR) TB reported to the country of Georgia's TB surveillance during 2009-2017. Exposures included HIV serologic status, diabetes, and HCV status. Our outcome was all-cause post-TB mortality determined by cross-validating vital status with Georgia's death registry through November 2019. We estimated adjusted hazard rate ratios (aHR) and 95% confidence intervals (CI) of post-TB mortality among participants with and without comorbidities using cause-specific hazard regressions. Among 1032 eligible participants, 34 (3.3%) died during treatment and 87 (8.7%) died post-TB treatment. The median time to post-TB death was 21 months (interquartile range 7-39) after TB treatment. After adjusting for confounders, the hazard rates of post-TB mortality were higher among participants with HIV co-infection (aHR = 3.74, 95%CI 1.77-7.91) compared to those without HIV co-infection. In our cohort, post-TB mortality occurred most commonly in the first 3 years post-TB treatment. Linkage to care for common TB comorbidities post-treatment may reduce post-TB mortality rates.

Scientific ReportsVol. 14(1)
Emory University (US), Swiss Tropical and Public Health Institute (CH), Georgia State University (US), National Center for Tuberculosis and Lung Disease (GE), University of Georgia (GE), Stanford Medicine (US), David Tvildiani Medical University (GE), Georgia Department of Public Health (US), Stanford University (US)
Vanderbilt University, Emory University, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Fogarty International Center
Good health and well-being
Openalex Percentile: Top 6%
Tuberculosis Research and Epidemiology
3.89
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