首页> 外文期刊>Journal of pharmacology & toxicology. >A Randomized Open-Label Comparison of Lamotrigine and Valproate in Patients with Juvenile Myoclonic Epilepsy
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A Randomized Open-Label Comparison of Lamotrigine and Valproate in Patients with Juvenile Myoclonic Epilepsy

机译:拉莫三嗪和丙戊酸盐在青少年肌阵挛性癫痫患者中的随机开放标签比较

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摘要

The aim of this study was to evaluate the efficacy and tolerability of lamotrigine and valproate in patients with different types of generalized epilepsy characterized by myoclonic seizures as well as compare the efficacy of those two drugs. A pilot, randomized controlled trial analysis of 46 female patients (age 8-30 years) in alarge university hospital. All patients underwent several interictal EEG including routine awake and sleep EEGs. Lamotrigine was started at the dose of 500 mg day~-1and was progressively increased to a mean dose of 1500-2000 mg day~-4 in a time course of 8 weeks. The target maintenance dose for valproate was 800 mg day~-1 after starting valproate at the dose of 200 mg/12 h. The mean dose was reached within 4 weeks. Out of total 46 patients, 46 (100%) had juvenile myoclonic epilepsy; 43 (93.48%) had tonic-clonic; 5 (11%) had myoclonic absences. In the valproate and lamotrigine groups, there was significant reduction (p<0.001,p<0.001) in myoclonic seizure and tonic-clonic seizure frequencies.
机译:这项研究的目的是评估拉莫三嗪和丙戊酸盐在以肌阵挛性癫痫为特征的不同类型的全身性癫痫患者中的疗效和耐受性,并比较这两种药物的疗效。一家大型大学医院对46名女性患者(年龄8-30岁)进行的一项随机对照试验性试验分析。所有患者均接受了几次发作性脑电图检查,包括常规的清醒和睡眠脑电图检查。拉莫三嗪以500 mg·day-1的剂量开始,并在8周的时间内逐渐增加至1500-2000 mg·day-4的平均剂量。丙戊酸盐以200 mg / 12 h的剂量开始服用后,丙戊酸盐的目标维持剂量为800 mg day〜-1。平均剂量在4周内达到。在总共46例患者中,有46例(100%)患有青少年肌阵挛性癫痫; 43(93.48%)人患有强直性阵挛; 5(11%)人患有肌阵挛性缺失。在丙戊酸盐和拉莫三嗪组中,肌阵挛性发作和强直性阵挛性发作频率显着降低(p <0.001,p <0.001)。

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