感染人类免疫缺陷病毒的住院患者的结核病:临床特征、死亡率和基于尿的结核病快速筛查降低非洲住院患者艾滋病相关死亡率的意义

Ankur Gupta-Wright, Katherine Fielding, Douglas Wilson, Joep J van Oosterhout, Daniel Grint, Henry C Mwandumba, Melanie Alufandika-Moyo, Jurgens A Peters, Lingstone Chiume, Stephen D Lawn, Elizabeth L Corbett
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引用次数: 0

摘要

背景:结核病(TB)是全球人类免疫缺陷病毒(HIV)感染者的主要杀手,不理想的诊断和管理导致了高病死率。方法:一项前瞻性队列研究,通过筛查马拉维和南非的hiv阳性住院患者,通过痰和尿诊断发现确诊结核病患者(Xpert MTB/RIF和/或确定TB- lam Ag阳性)(基于快速尿液筛查结核病以降低非洲住院患者艾滋病相关死亡率[STAMP]试验)。前瞻性尿液检测(干预组)或回顾性尿液检测(标准护理组)。我们使用分层聚类分析定义基线临床表型,并使用Cox回归分析确定与早期死亡率(≤56天)的关联。结果:2015年10月至2018年9月期间确诊的322例结核病患者中,78.0%的患者尿检≥1阳性。抗逆转录病毒治疗(ART)覆盖率在非新诊断患者中为80.2%,但中位CD4细胞计数为75细胞/µL, HIV病毒载量高。早期死亡率为30.7%(99/322),尽管结核病得到了近乎普遍的及时治疗。在多因素分析中,年龄较大、男性、入院前接受抗逆转录病毒治疗、营养状况不佳、血红蛋白较低和尿检阳性(TB-LAM和/或Xpert MTB/RIF)与死亡率增加相关。聚类分析(基于基线变量)确定了4个患者亚组,其早期死亡率从9.8%到52.5%不等。尽管南非未经调整的死亡率比马拉维低9.3%,但在调整后的模型中,两国的死亡率相似(风险比,0.9;P = .729)。结论:即使在南非,及时住院诊断hiv相关结核病后的死亡率仍然高得令人无法接受。迫切需要加强管理战略,其预测指标可能指导开发和后续使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tuberculosis in Hospitalized Patients With Human Immunodeficiency Virus: Clinical Characteristics, Mortality, and Implications From the Rapid Urine-based Screening for Tuberculosis to Reduce AIDS Related Mortality in Hospitalized Patients in Africa.

Background: Tuberculosis (TB) is the major killer of people living with human immunodeficiency virus (HIV) globally, with suboptimal diagnostics and management contributing to high case-fatality rates.

Methods: A prospective cohort of patients with confirmed TB (Xpert MTB/RIF and/or Determine TB-LAM Ag positive) identified through screening HIV-positive inpatients with sputum and urine diagnostics in Malawi and South Africa (Rapid urine-based Screening for Tuberculosis to reduce AIDS Related Mortality in hospitalized Patients in Africa [STAMP] trial). Urine was tested prospectively (intervention) or retrospectively (standard of care arm). We defined baseline clinical phenotypes using hierarchical cluster analysis, and also used Cox regression analysis to identify associations with early mortality (≤56 days).

Results: Of 322 patients with TB confirmed between October 2015 and September 2018, 78.0% had ≥1 positive urine test. Antiretroviral therapy (ART) coverage was 80.2% among those not newly diagnosed, but with median CD4 count 75 cells/µL and high HIV viral loads. Early mortality was 30.7% (99/322), despite near-universal prompt TB treatment. Older age, male sex, ART before admission, poor nutritional status, lower hemoglobin, and positive urine tests (TB-LAM and/or Xpert MTB/RIF) were associated with increased mortality in multivariate analyses. Cluster analysis (on baseline variables) defined 4 patient subgroups with early mortality ranging from 9.8% to 52.5%. Although unadjusted mortality was 9.3% lower in South Africa than Malawi, in adjusted models mortality was similar in both countries (hazard ratio, 0.9; P = .729).

Conclusions: Mortality following prompt inpatient diagnosis of HIV-associated TB remained unacceptably high, even in South Africa. Intensified management strategies are urgently needed, for which prognostic indicators could potentially guide both development and subsequent use.

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