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贝达喹啉和德拉马尼联合治疗耐多药或耐药患者的治疗结果:来自一个大型全球队列的结果。

Outcome of treatment of MDR-TB or drug-resistant patients treated with bedaquiline and delamanid: Results from a large global cohort.

机构信息

Damien Foundation Nepal, Kathmandu, Nepal.

Moscow Research and Clinical Center for TB Control, Moscow Government's Health Department, Moscow, Russian Federation.

出版信息

Pulmonology. 2021 Sep-Oct;27(5):403-412. doi: 10.1016/j.pulmoe.2021.02.006. Epub 2021 Mar 19.

Abstract

The World Health Organization (WHO) recommends countries introduce new anti-TB drugs in the treatment of multidrug-resistant tuberculosis. The aim of the study is to prospectively evaluate the effectiveness of bedaquiline (and/or delamanid)- containing regimens in a large cohort of consecutive TB patients treated globally. This observational, prospective study is based on data collected and provided by Global Tuberculosis Network (GTN) centres and analysed twice a year. All consecutive patients (including children/adolescents) treated with bedaquiline and/or delamanid were enrolled, and managed according to WHO and national guidelines. Overall, 52 centres from 29 countries/regions in all continents reported 883 patients as of January 31st 2021, 24/29 countries/regions providing data on 100% of their consecutive patients (10-80% in the remaining 5 countries). The drug-resistance pattern of the patients was severe (>30% with extensively drug-resistant -TB; median number of resistant drugs 5 (3-7) in the overall cohort and 6 (4-8) among patients with a final outcome). For the patients with a final outcome (477/883, 54.0%) the median (IQR) number of months of anti-TB treatment was 18 (13-23) (in days 553 (385-678)). The proportion of patients achieving sputum smear and culture conversion ranged from 93.4% and 92.8% respectively (whole cohort) to 89.3% and 88.8% respectively (patients with a final outcome), a median (IQR) time to sputum smear and culture conversion of 58 (30-90) days for the whole cohort and 60 (30-100) for patients with a final outcome and, respectively, of 55 (30-90) and 60 (30-90) days for culture conversion. Of 383 patients treated with bedaquiline but not delamanid, 284 (74.2%) achieved treatment success, while 25 (6.5%) died, 11 (2.9%) failed and 63 (16.5%) were lost to follow-up.

摘要

世界卫生组织(WHO)建议各国在治疗耐多药结核病时引入新的抗结核药物。本研究旨在前瞻性评估贝达喹啉(和/或德拉马尼)为基础的方案在全球范围内连续治疗的大量结核病患者中的疗效。这项观察性前瞻性研究基于全球结核病网络(GTN)中心收集和提供的数据进行分析,每年分析两次。所有接受贝达喹啉和/或德拉马尼治疗的连续患者(包括儿童/青少年)均被纳入,并根据世卫组织和国家指南进行管理。截至 2021 年 1 月 31 日,来自全球 29 个国家/地区的 52 个中心共报告了 883 例患者,29 个国家/地区中的 24 个(其余 5 个国家/地区的比例为 10-80%)提供了其所有连续患者数据的 100%。患者的耐药模式严重(广泛耐药结核病患者>30%;整体队列中耐药药物中位数为 5(3-7),最终结局患者为 6(4-8))。对于有最终结局的患者(883 例中的 477 例,54.0%),抗结核治疗的中位数(IQR)月数为 18(13-23)(以天计为 553(385-678))。痰涂片和培养转阴的患者比例分别为 93.4%和 92.8%(整体队列)和 89.3%和 88.8%(有最终结局的患者),痰涂片和培养转阴的中位数(IQR)时间分别为 58(30-90)天和 60(30-100)天。整体队列和有最终结局的患者的培养转阴时间中位数(IQR)分别为 55(30-90)和 60(30-90)天。在 383 例仅接受贝达喹啉治疗而未接受德拉马尼治疗的患者中,284 例(74.2%)达到治疗成功,25 例(6.5%)死亡,11 例(2.9%)失败,63 例(16.5%)失访。

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