在接受耐药性结核病治疗的患者中,HIV合并感染增加了结核病后死亡的风险。

Argita D Salindri, Maia Kipiani, Nino Lomtadze, Nestani Tukvadze, Zaza Avaliani, Henry M Blumberg, Katherine E Masyn, Richard B Rothenberg, Russell R Kempker, Matthew J Magee
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引用次数: 0

摘要

背景:我们旨在确定结核病(TB)患者常见的预先存在的合并症(包括人类免疫缺陷病毒(HIV)、糖尿病和丙型肝炎病毒(HCV))与结核病治疗后全因死亡率之间的关系。方法:我们对2009-2017年格鲁吉亚国家接受利福平耐药性和多药/广泛耐药(RR和M/XDR)结核病治疗的患者进行了回顾性队列研究。符合条件的参与者年龄在15岁以上,有新诊断的、实验室确认的耐药结核病,并接受二线治疗。暴露包括HIV血清学状态、糖尿病和HCV状态。主要结果是通过与格鲁吉亚国家死亡登记处交叉验证截至2019年11月的生命状态来确定结核病治疗后的死亡率。我们使用病因特异性风险回归估计了患有和不患有合并症的参与者的结核病后死亡率的危险率比(HR)和95%置信区间(CI)。结果:在纳入我们分析的1032名符合条件的患者中,34名(3.3%)参与者在治疗期间死亡,87名(8.7%)参与者在结核病治疗后死亡。在结核病治疗后死亡的患者中,中位死亡时间为结核病治疗结束后21个月(IQR 7-39)。在校正了潜在的混杂因素后,与未合并感染艾滋病毒的参与者相比,合并感染艾滋病毒参与者在结核病治疗后的死亡率危险率更高(校正后的危险比[aHR]=3.74,95%CI 1.77-7.91)。结论:在我们的队列中,结核病后死亡率最常见于结核病治疗结束后的前三年。额外的结核病后护理和随访,特别是在患有结核病和合并症(尤其是艾滋病毒合并感染)的患者中,可以降低结核病治疗后的死亡率。
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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]) 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.

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