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艾滋病毒合并感染会增加开始接受耐多药结核病治疗的患者结核病后死亡风险。

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

作者信息

Salindri Argita D, Kipiani Maia, Lomtadze Nino, Tukvadze Nestani, Avaliani Zaza, Blumberg Henry M, Masyn Katherine E, Rothenberg Richard B, Kempker Russell R, Magee Matthew J

机构信息

Department of Population Health Sciences, Georgia State University School of Public Health, Atlanta, GA, USA; and Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

National Center for Tuberculosis and Lung Diseases, Tbilisi, Georgia; David Tvildiani Medical University, Tbilisi, Georgia; and The University of Georgia, Tbilisi, Georgia.

出版信息

medRxiv. 2024 Mar 26:2023.05.19.23290190. doi: 10.1101/2023.05.19.23290190.

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]) with post-TB mortality. We conducted a retrospective cohort study among persons who initiated treatment for rifampicin-resistant and multi/extensively drug-resistant (RR and 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. Among those who died post-TB treatment, the median time to death was 21 months (interquartile range 7-39) post-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 three years post-TB treatment. Linkage to care for common TB comorbidities post-treatment may reduce post-TB mortality rates.

摘要

关于结核病患者(TB)的常见合并症(包括人类免疫缺陷病毒[HIV]、糖尿病和丙型肝炎病毒[HCV])与结核病后死亡率之间的关系,目前所知甚少。我们对2009年至2017年期间向格鲁吉亚国家结核病监测报告的开始接受耐利福平及耐多药/广泛耐药结核病(RR和M/XDR-TB)治疗的患者进行了一项回顾性队列研究。暴露因素包括HIV血清学状态糖尿病和HCV状态。我们通过与格鲁吉亚死亡登记处交叉验证至2019年11月的生命状态来确定全因结核病后死亡率。我们使用特定病因风险回归估计了有合并症和无合并症参与者结核病后死亡率的调整风险率比(aHR)和95%置信区间(CI)。在1032名符合条件的参与者中,34人(3.3%)在治疗期间死亡,87人(8.7%)在结核病治疗后死亡。在结核病治疗后死亡的患者中,结核病治疗后死亡的中位时间为21个月(四分位间距7-39)。在调整混杂因素后,与无HIV合并感染的参与者相比,合并HIV感染的参与者结核病后死亡率的风险率更高(aHR=3.74,95%CI 1.77-7.91)。在我们的队列中,结核病后死亡率最常发生在结核病治疗后的前三年。治疗后将常见结核病合并症与护理联系起来可能会降低结核病后死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c15/11005638/bd2c1cf6c92d/nihpp-2023.05.19.23290190v2-f0001.jpg

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