多抗药性结核病治疗的良性和安全性:系统性研究

I. G. A. Ari Kusuma Yana, Fauna Herawati
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引用次数: 0

摘要

耐多药结核病是由结核分枝杆菌引起的结核病,结核分枝杆菌对异烟肼和利福平具有耐药性,对其他一线药物有或无耐药性。耐药结核病的发展引起了全世界的关注。2019年,全球有近50万结核病患者,其中78%患有耐多药结核病。近年来,耐多药结核病患者从2018年的186883例增加到2019年的206030例,增加了10%。世卫组织指南建议使用贝达喹啉。与贝达喹啉的有效性和安全性有关的研究仍然很少,因此需要获得合格的信息,使一个国家,特别是印度尼西亚,为使用贝达喹啉治疗做好准备,特别是因为印度尼西亚在全球结核病总数的三分之二中排名第二。目的:评价贝达喹啉联合治疗耐多药结核病的有效性和安全性。方法:文献检索由研究者独立完成,检索数据库为Science Direct、Pubmed和Cochrane,不受研究类型和发表年份的限制。本研究使用的关键词采用布尔运算符组合,即“bedaquiline”与“tuberculosis”和“multi-drug resistant”。结果:7项研究符合纳入标准,给予贝达喹啉干预24周可使平均培养转化时间缩短约60-85天。贝达喹啉的培养转化率百分比(70-85%)高于安慰剂(58%)。最常见的副作用是恶心和高尿酸血症。大多数研究报告贝达喹啉治疗的患者QT间期延长。结论:本系统评价显示贝达喹啉治疗耐多药结核病有效、安全。然而,一些接受贝达喹啉治疗的患者出现了QT间期延长的严重副作用。需要进行进一步的研究,以监测与贝达喹啉治疗耐多药结核病相关的QT间期延长的副作用。
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Efektivitas Dan Keamanan Terapi dengan Rejimen Bedaquiline dalam Terapi Multidrug-Resistant Tuberculosis (TB-MDR): Kajian Sistematis
MDR-TB is a tuberculosis disease caused by Mycobacterium tuberculosis which is resistant to isoniazid and rifampin with or without resistance to other first-line drugs. The development of drug-resistant tuberculosis is causing worldwide concern. Globally in 2019, almost half a million TB sufferers of which 78% had MDR-TB. In recent years, MDR-TB patients increased by 10% from 186,883 patients in 2018 to 206,030 in 2019. Bedaquiline has been recommended by WHO guidelines. Studies related to the effectiveness and safety of Bedaquiline are still few so that there is a need for qualified information to prepare a country, especially Indonesia, for the use of Bedaquiline therapy, especially since Indonesia is ranked second out of two-thirds of the total global TB. Objective: to describe the effectiveness and safety of Bedaquiline in combination therapy for the treatment of MDR-TB. Methods: The literature search was carried out independently by researchers using the online databases of Science Direct, Pubmed, and Cochrane without restrictions on the type of research and year of publication. The keywords used in this study were combined with Boolean operators, namely “bedaquiline” AND “tuberculosis” AND “multi-drug resistant”. Results: Seven studies met the inclusion criteria, the intervention of giving Bedaquiline for 24 weeks can reduce the average time of culture conversion by about 60-85 days. The percentage of culture conversion rate was higher with Bedaquiline (range 70-85%) than placebo (58%). The most common side effects are nausea and hyperuricemia. The majority of studies report a prolongation of the QT interval in patients treated with Bedaquiline. Conclusion: This systematic review showed that Bedaquiline is effective and safe to use in the treatment of MDR-TB. However, serious side effects of QT prolongation occurred in some respondents treated with Bedaquiline. Further studies need to be conducted to monitor the side effects of QT prolongation associated with the administration of Bedaquiline in the treatment of MDR-TB.
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