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普瑞巴林作为部分性癫痫发作的辅助治疗药物。

Pregabalin as adjunctive therapy for partial seizures.

作者信息

Brodie Martin J

机构信息

Epilepsy Unit, University of Glasgow, Glasgow G11 6NT, Scotland, UK.

出版信息

Epilepsia. 2004;45 Suppl 6:19-27. doi: 10.1111/j.0013-9580.2004.455004.x.

Abstract

The efficacy and safety of pregabalin as adjunctive therapy for patients with partial epilepsy with or without secondary generalization has been studied in three randomized, double-blind, placebo-controlled trials involving 1,052 patients. Patients (> or =12 years of age) participating in the trials were highly refractory to treatment, experiencing at least six seizures and no 4-week seizure-free period during the 8-week baseline phase, even though 73% received at least two antiepileptic drugs and 23% received three. Each fixed-dose study was 12 weeks in duration. In Study 1, patients received pregabalin 50, 150, 300, or 600 mg/day given two times daily with no titration period. Studies 2 and 3 had a 1-week titration to dose levels of 150 and 600 mg/day given three times daily (Study 2), 600 mg/day given two times daily, and 600 mg/day given three times daily (Study 3). Pregabalin, at 150, 300, and 600 mg/day, was significantly superior to placebo in reducing seizure frequency with a clear dose-response relationship. Responder rates, defined as the percentage of patients with > or =50% reduction in seizure frequency from baseline, approached 50% at 600 mg/day. In the effective dose range (150-600 mg/day), seizure freedom in the last 28 days of treatment was 3-17%. There was no difference between two times daily and three times daily dosing regimens. Efficacy was apparent as early as week one. The most commonly reported adverse events were CNS related, and either mild or moderate in intensity and generally self limiting. Few patients (< or =5% in any treatment group) discontinued due to lack of efficacy. These results indicate that pregabalin is highly effective as adjunctive therapy in the treatment of patients with partial seizures with or without secondary generalization.

摘要

三项随机、双盲、安慰剂对照试验对1052例患者进行了研究,以评估普瑞巴林作为辅助治疗药物用于伴有或不伴有继发性全身性发作的部分性癫痫患者的疗效和安全性。参与试验的患者(年龄≥12岁)对治疗具有高度难治性,在8周的基线期内至少经历6次发作且无4周无发作期,尽管73%的患者接受了至少两种抗癫痫药物治疗,23%的患者接受了三种抗癫痫药物治疗。每项固定剂量研究为期12周。在研究1中,患者接受每日50、150、300或600毫克的普瑞巴林治疗,每日给药两次,无滴定期。研究2和3有1周的滴定期,滴定至每日三次给药150和600毫克(研究2)、每日两次给药600毫克以及每日三次给药600毫克(研究3)。每日150、300和600毫克的普瑞巴林在降低癫痫发作频率方面显著优于安慰剂,且具有明确的剂量反应关系。缓解率定义为癫痫发作频率较基线降低≥50%的患者百分比,在每日600毫克时接近50%。在有效剂量范围(每日150 - 600毫克)内,治疗最后28天无癫痫发作的比例为3% - 17%。每日两次和每日三次给药方案之间无差异。疗效早在第1周就很明显。最常报告的不良事件与中枢神经系统相关,强度为轻度或中度,通常为自限性。很少有患者(任何治疗组中≤5%)因缺乏疗效而停药。这些结果表明,普瑞巴林作为辅助治疗药物用于治疗伴有或不伴有继发性全身性发作的部分性癫痫患者具有高度有效性。

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