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左乙拉西坦用于治疗伴有肌阵挛发作的特发性全身性癫痫。

Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures.

作者信息

Noachtar S, Andermann E, Meyvisch P, Andermann F, Gough W B, Schiemann-Delgado J

机构信息

Epilepsy Centre, Department of Neurology, University of Munich, Marchioninistr. 15, 81377 Munich, Germany.

出版信息

Neurology. 2008 Feb 19;70(8):607-16. doi: 10.1212/01.wnl.0000297512.18364.40.

Abstract

BACKGROUND

Currently, there are no published randomized controlled trials evaluating the efficacy and safety of adjunctive antiepileptic therapy in idiopathic generalized epilepsy with myoclonic seizures.

METHODS

This randomized, double-blind, placebo-controlled multicenter trial assessed the efficacy and tolerability of adjunctive treatment with levetiracetam 3,000 mg/day in adolescents (>or=12 years) and adults (<or=65 years) with idiopathic generalized epilepsy, who experienced myoclonic seizures on >or=8 days during a prospective 8-week baseline period, despite antiepileptic monotherapy. The 8-week baseline period was followed by 4-week up-titration, 12-week evaluation, and 6-week down-titration/conversion periods.

RESULTS

Of 122 patients randomized, 120 (levetiracetam, n = 60; placebo, n = 60) were evaluable. Diagnoses were either juvenile myoclonic epilepsy (93.4%) or juvenile absence epilepsy (6.6%). A reduction of >or=50% in the number of days/week with myoclonic seizures was seen in 58.3% of patients in the levetiracetam group and in 23.3% of patients in the placebo group (p < 0.001) during the treatment period. Levetiracetam-treated patients were more likely to respond to treatment than patients receiving placebo (OR = 4.77; 95% CI, 2.12 to 10.77; p < 0.001). Levetiracetam-treated patients had higher freedom from myoclonic seizures (25.0% vs 5.0%; p = 0.004) and all seizure types (21.7% vs 1.7%; p < 0.001) during the evaluation period. The only adverse events more frequent with levetiracetam were somnolence and neck pain.

CONCLUSION

These results suggest that levetiracetam is an effective and well-tolerated adjunctive treatment for patients with previously uncontrolled idiopathic generalized epilepsy with myoclonic seizures.

摘要

背景

目前,尚无已发表的随机对照试验评估辅助抗癫痫治疗在伴有肌阵挛发作的特发性全身性癫痫中的疗效和安全性。

方法

这项随机、双盲、安慰剂对照的多中心试验评估了每日3000毫克左乙拉西坦辅助治疗对青少年(≥12岁)和成人(≤65岁)特发性全身性癫痫的疗效和耐受性,这些患者在为期8周的前瞻性基线期内,尽管接受了抗癫痫单药治疗,但仍有≥8天出现肌阵挛发作。8周的基线期之后是4周的剂量递增期、12周的评估期和6周的剂量递减/转换期。

结果

122例随机分组的患者中,120例(左乙拉西坦组60例;安慰剂组60例)可进行评估。诊断为青少年肌阵挛癫痫(93.4%)或青少年失神癫痫(6.6%)。在治疗期间,左乙拉西坦组58.3%的患者每周肌阵挛发作天数减少≥50%,安慰剂组为23.3%(p<0.001)。接受左乙拉西坦治疗的患者比接受安慰剂的患者更有可能对治疗产生反应(比值比=4.77;95%置信区间,2.12至10.77;p<0.001)。在评估期内,接受左乙拉西坦治疗的患者无肌阵挛发作的比例更高(25.0%对5.0%;p=0.004),无所有发作类型的比例也更高(21.7%对1.7%;p<0.001)。左乙拉西坦更常出现的不良事件仅有嗜睡和颈部疼痛。

结论

这些结果表明,左乙拉西坦对先前未得到控制的伴有肌阵挛发作的特发性全身性癫痫患者是一种有效且耐受性良好的辅助治疗药物。

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