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首页> 外文期刊>Seizure: the journal of the British Epilepsy Association >The efficacy and safety of retigabine and other adjunctive treatments for refractory partial epilepsy: A systematic review and indirect comparison
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The efficacy and safety of retigabine and other adjunctive treatments for refractory partial epilepsy: A systematic review and indirect comparison

机译:瑞格他滨及其他辅助治疗对难治性部分性癫痫的疗效和安全性:系统评价和间接比较

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Introduction: Retigabine (RTG) is now approved in Europe and the US for the adjunctive treatment of partial-onset seizures in adults with epilepsy. To support submissions to EU reimbursement authorities, we explored its efficacy and tolerability relative to selected antiepileptic drugs (AEDs). Methods: A systematic review was conducted to identify placebo-controlled trials of RTG and selected AEDs approved for use in a similar position in the management pathway of partial epilepsy (eslicarbazepine acetate [ESL], lacosamide [LCM], pregabalin [PGB], tiagabine [TGB] and zonisamide [ZNS]). Using conventional and network meta-analyses as appropriate, we report efficacy and tolerability outcomes for each AED versus placebo and the performance of RTG relative to other AEDs. Results: Twenty studies met the inclusion criteria: three each for RTG, ESL, LCM, TGB and ZNS; five for PGB. Comparisons comprised 1-5 studies per AED. In the network meta-analysis, RTG was not found to be different from the other AEDs for responder rate (maintenance period), seizure freedom (maintenance period and double-blind period), withdrawals due to adverse events, and incidences of ataxia, dizziness, fatigue and nausea. Differences between RTG and other AEDs were found for a few comparisons, which did not reveal any trends: RTG was associated with a lower responder rate than PGB during the double-blind period, higher withdrawal rate due to any reason than ESL and a higher incidence of somnolence than TGB. Conclusions: Findings suggest that the risk/benefit for RTG is similar to that for comparator AEDs. However, results should be interpreted in the context of the limitations of the analyses.
机译:简介:瑞替加滨(RTG)现在已在欧洲和美国获得批准,用于癫痫成人的部分发作性癫痫的辅助治疗。为了支持向欧盟报销当局提交的材料,我们探讨了其相对于选定的抗癫痫药(AED)的功效和耐受性。方法:进行了系统的审查,以鉴定安慰剂对照的RTG试验和选定的AED,这些药物被批准用于部分癫痫的治疗途径中的相似位置(醋酸依卡西平[ESL],拉考酰胺[LCM],普瑞巴林[PGB],替加巴滨) [TGB]和zonisamide [ZNS])。使用适当的常规和网络荟萃分析,我们报告了每种AED与安慰剂的疗效和耐受性结果,以及RTG与其他AED的相对性能。结果:二十项研究符合纳入标准:RTG,ESL,LCM,TGB和ZNS各三项; PGB五个。比较每个AED包含1-5个研究。在网络荟萃分析中,未发现RTG与其他AED的反应率(维持期),癫痫发作自由度(维持期和双盲期),因不良事件引起的停药以及共济失调,头晕的发生率不同,疲劳和恶心。进行了一些比较,发现RTG与其他AED之间存在差异,但没有发现任何趋势:RTG与双盲期间的应答率低于PGB,由于任何原因导致的退出率高于ESL以及发生率较高相关比TGB的嗜睡。结论:研究结果表明,RTG的风险/益处与对照AED相似。但是,应在分析的局限性范围内解释结果。

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