Sayfutdinov Zayniddin, Kumar Ajay, Nabirova Dilyara, Gadoev Jamshid, Turaev Laziz, Sultanov Sanjar, Alaverdyan Sevak, Parpieva Nargiza
National Reference Laboratory, Tashkent 100086, Uzbekistan.
International Union Against Tuberculosis and Lung Disease, South-East Asia Office, New Delhi 110016, India.
Int J Environ Res Public Health. 2021 Mar 14;18(6):2965. doi: 10.3390/ijerph18062965.
Tuberculosis patients "resistant to isoniazid and susceptible to rifampicin (Hr-TB)" remain neglected, despite a high burden and poor outcomes. The World Health Organization (WHO) recommends a 6 month regimen consisting of levofloxacin, rifampicin, ethambutol, and pyrazinamide (LRZE) to treat Hr-TB. In contrast, Uzbekistan uses a 9 month regimen (LRZE plus a second-line injectable in the first 3 months). We aimed to assess the treatment outcomes of this novel regimen among Hr-TB patients treated in two regions of Uzbekistan (Fergana and Bukhara) in 2017-2018. We conducted a cohort study involving secondary analysis of routine surveillance data. Of 132 Hr-TB patients, 105 (80%) were successfully treated. Death was the predominant unsuccessful outcome (13, 10%) followed by "treatment failure" (10, 8%) and "lost to follow-up" (4, 2%). High treatment success is an indicator of the potential effectiveness of the novel regimen and adds to the limited global evidence on this issue. However, the sample size was small and there was no comparison group. Since the study was conducted in two regions of Uzbekistan only, the findings have limited generalizability. We recommend future research using an adequate sample size and an appropriate study design (randomized controlled trial or prospective cohort with a control group receiving the WHO-recommended regimen).
尽管耐异烟肼且对利福平敏感的结核病患者(Hr-TB)负担沉重且预后不佳,但他们仍然被忽视。世界卫生组织(WHO)推荐使用一种由左氧氟沙星、利福平、乙胺丁醇和吡嗪酰胺组成的6个月治疗方案(LRZE)来治疗Hr-TB。相比之下,乌兹别克斯坦采用一种9个月的治疗方案(LRZE在前3个月加用一种二线注射剂)。我们旨在评估2017 - 2018年在乌兹别克斯坦两个地区(费尔干纳和布哈拉)接受治疗的Hr-TB患者中这种新方案的治疗效果。我们进行了一项队列研究,对常规监测数据进行二次分析。在132例Hr-TB患者中,105例(80%)成功治愈。死亡是主要的未成功结局(13例,10%),其次是“治疗失败”(10例,8%)和“失访”(4例,2%)。高治疗成功率表明新方案具有潜在有效性,并为该问题的全球有限证据增添了内容。然而,样本量较小且没有对照组。由于该研究仅在乌兹别克斯坦的两个地区进行,研究结果的普遍性有限。我们建议未来的研究采用足够的样本量和合适的研究设计(随机对照试验或前瞻性队列研究,对照组采用WHO推荐的治疗方案)。