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Delamanid and bedaquiline to treat multidrug-resistant and extensively drug-resistant tuberculosis in children: a systematic review

机译:地拉曼和贝达喹啉治疗儿童多药耐药和广泛耐药结核病:系统评价

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摘要

The new drugs delamanid and bedaquiline are increasingly used to treat multidrug-resistant (MDR-) and extensively drug-resistant tuberculosis (XDR-TB). As evidence is lacking, the World Health Organization recommends their use under specific conditions in adults, delamanid only being recommended in children ≥6 years of age. No systematic review has yet evaluated the efficacy, safety and tolerability of the new drugs in children. A search of peer-reviewed, scientific evidence was performed, to evaluate the efficacy/effectiveness, safety, and tolerability of delamanid or bedaquiline-containing regimens in children with confirmed M/XDR-TB. We used PubMed and Embase to identify any relevant manuscripts in English until 31 December 2016, excluding editorials and reviews. Three out of 96 manuscripts retrieved satisfied the inclusion criteria, while 93 were excluded because dealing exclusively with adults (12: 4 on delamanid and 8 on bedaquiline), being recommendations or guidelines (8 manuscripts), reviews (17 papers) or other studies (56 papers). One of the studies retrieved reported evidence on 19 M/XDR-TB children, 16 of them treated under compassionate use with delamanid (13 achieving consistent bacteriological conversion) and 3 candidates for the drug. Two studies reported details on the first paediatric case treated (and cured) with a delamanid-containing regimen. Eight trials including children were also retrieved (clinicaltrials.gov). Although the methodology used in the study was rigorous, the results are limited by the paucity of the studies available in the literature on the use of new anti-TB drugs in children. In conclusion, more evidence is needed on the use of delamanid and bedaquiline in paediatric patients.
机译:新药地拉曼尼和苯达喹啉被越来越多地用于治疗耐多药(MDR-)和广泛耐药的肺结核(XDR-TB)。由于缺乏证据,世界卫生组织建议在成年人的特定条件下使用它们,仅在≥6岁的儿童中建议使用德拉曼尼德。尚无系统评价评估新药对儿童的疗效,安全性和耐受性。检索经过同行评审的科学证据,以评估在确诊为M / XDR-TB的儿童中使用德拉曼尼德或含苯达喹啉的治疗方案的疗效/有效性,安全性和耐受性。我们使用PubMed和Embase识别了2016年12月31日之前任何相关的英文手稿,但社论和评论除外。检索到的96篇手稿中有3篇符合入选标准,而93篇被排除在外是因为仅与成年人打交道(德拉曼尼德12篇:4篇,苯达喹啉8篇),是推荐或指南(8篇手稿),评论(17篇论文)或其他研究( 56篇论文)。其中一项研究检索了19名M / XDR-TB儿童的报道证据,其中16名儿童经过同情使用德拉曼尼治疗(13名实现了一致的细菌学转化),还有3名候选药物。两项研究报告了使用含德拉曼尼德方案治疗(并治愈)的第一例儿科病例的详细信息。还检索了包括儿童在内的八项试验(clinicaltrials.gov)。尽管该研究中使用的方法学很严格,但结果受到文献中有关在儿童中使用新的抗结核药物的研究不足的限制。总之,在儿童患者中使用地拉曼胺和苯达喹啉需要更多的证据。

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