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Clinical efficacy and safety of the newer antiepileptic drugs as adjunctive treatment in adults with refractory partial-onset epilepsy: A meta-analysis of randomized placebo-controlled trials

机译:新型抗癫痫药作为辅助治疗成人难治性部分发作性癫痫的临床疗效和安全性:一项随机安慰剂对照试验的荟萃分析

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Objective: To evaluate the clinical efficacy and safety of the newer antiepileptic drugs (AEDs), namely, Eslicarbazepine (ESL), Retigabine/Ezogabine (RTG), Carisbamate (CAR), Lacosamide (LAC), Brivaracetam (BRI) or Perampanel (PER) as adjunctive therapy for adults with partial-onset seizures (POS). Methods: A systematic review of Randomized placebo-controlled Trials (RCTs) of newer AEDs was conducted. Electronic databases and identified bibliographies were searched to retrieve RCTs. The primary outcomes were responder rates and withdrawal rates, adverse effects. Pooled effects of Odds Ratio (OR), Risk Ratio (RR) and Risk Differences (RD) were derived from meta-analysis implemented in Revmen 5.1. Results: In total, 15 RCTs were included. All the studies contained a baseline and treatment phase. The pooled OR of all newer AEDs vs placebo was 2.16 (95%CI: 1.82, 2.57) for responder rates, 1.54 (1.12, 2.10) for withdrawal rates, 1.67 (1.34, 2.08) for adverse effects. The indirect comparisons between individual newer AED and all other newer AEDs suggested the similar results in responder rates (ORs, BRI 1.79 [-1.50, 5.08], RTG 1.41 [0.49, 2.33]). Conclusions: The pooled ORs suggested newer AEDs might be more effective than placebo while with higher incidence of adverse effects. The indirect comparisons suggested BRI, followed by RTG, might be more effective than all other newer AEDs, which could be confirmed by future clinical studies.
机译:目的:评估新型抗癫痫药(AED)的临床疗效和安全性,该药物包括依斯卡西平(ESL),瑞替加滨/依佐加宾(RTG),卡里斯巴马特(CAR),拉可酰胺(LAC),布立西坦(BRI)或Perampanel(PER )作为成人部分发作性癫痫(POS)的辅助治疗。方法:对新型AED的随机安慰剂对照试验(RCT)进行了系统评价。搜索电子数据库和确定的书目以检索RCT。主要结果是缓解率和戒断率,不良反应。风险比(OR),风险比(RR)和风险差异(RD)的汇总效应来自于Revmen 5.1中实施的荟萃分析。结果:总共包括15个RCT。所有研究均包含基线和治疗阶段。所有较新的AED与安慰剂的合并OR分别为:应答者比率为2.16(95%CI:1.82,2.57),停药比率为1.54(1.12,2.10),不良反应为1.67(1.34,2.08)。单个较新的AED与所有其他较新的AED之间的间接比较表明,应答者比率的结果相似(OR,BRI 1.79 [-1.50、5.08],RTG 1.41 [0.49、2.33])。结论:汇总的ORs提示,更新的AED可能比安慰剂更有效,但不良反应的发生率更高。间接比较表明,BRI和RTG可能比所有其他较新的AED更有效,这可以通过未来的临床研究得到证实。

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