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不同起始剂量瑞替加滨(依佐加滨)治疗部分性发作癫痫患者的安全性和耐受性。

Safety and tolerability of different titration rates of retigabine (ezogabine) in patients with partial-onset seizures.

机构信息

Arkansas Epilepsy Program, 2 Lile Ct, Ste 100, Little Rock, AR 72205, USA.

出版信息

Epilepsy Res. 2013 Nov;107(1-2):138-45. doi: 10.1016/j.eplepsyres.2013.08.021. Epub 2013 Sep 4.

Abstract

Retigabine (RTG; international nonproprietary name)/ezogabine (EZG; US adopted name) is an antiepileptic drug (AED) that prolongs neuronal voltage-gated potassium-channel KCNQ2-5 (Kv 7.2-7.5) opening. This double-blind study evaluated different RTG/EZG dose-titration rates. Patients (N=73) with partial-onset seizures receiving concomitant AEDs were randomized to one of three titration groups, all of which were initiated at RTG/EZG 300mg/day divided into three equal doses. Fast-, medium-, and slow-titration groups received dose increments of 150mg/day every 2, 4, and 7 days, respectively, achieving the target dose of 1200mg/day after 13, 25, and 43 days, respectively. Safety assessments were performed throughout. Discontinuation rates due to treatment-emergent adverse events (TEAEs) were numerically higher in the fast- (10/23) and medium- (7/22) titration groups than in the slow-titration group (3/23) but statistical significance was achieved only for the high-titration group compared with the low-titration group (p=0.024). Stratified analysis, with concomitant AEDs divided into enzyme inducers (carbamazepine, phenytoin, oxcarbazepine) or noninducers, showed that the risk of discontinuation due primarily to TEAEs was significantly higher in the fast- (p=0.010) but not in the medium-titration group (p=0.078) when compared with the slow-titration group. Overall, the slow-titration rate appeared to be best tolerated and was used in further efficacy and safety studies with RTG/EZG.

摘要

瑞替加滨(RTG;国际非专利名称)/依佐加滨(EZG;美国采用的名称)是一种抗癫痫药物(AED),可延长神经元电压门控钾通道 KCNQ2-5(Kv7.2-7.5)的开放。这项双盲研究评估了不同 RTG/EZG 剂量滴定率。接受伴随 AED 治疗的部分发作性癫痫患者(N=73)被随机分为三组滴定组之一,所有组均以 RTG/EZG 300mg/天起始,分为三个相等剂量。快速、中速和慢速滴定组分别以 150mg/天的剂量递增,每 2、4 和 7 天递增一次,分别在 13、25 和 43 天达到 1200mg/天的目标剂量。整个过程中进行安全性评估。由于治疗中出现的不良事件(TEAE)而停药的发生率在快速(10/23)和中速(7/22)滴定组中高于慢速滴定组(3/23),但仅在高剂量组与低剂量组之间达到统计学意义(p=0.024)。分层分析显示,根据伴随 AED 分为酶诱导剂(卡马西平、苯妥英、奥卡西平)或非诱导剂,与慢速滴定组相比,由于主要由 TEAEs 导致停药的风险在快速滴定组中显著更高(p=0.010),但在中速滴定组中无统计学意义(p=0.078)。总的来说,慢速滴定率似乎最耐受,并且在 RTG/EZG 的进一步疗效和安全性研究中使用。

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