...
首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months.
【24h】

Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months.

机译:辅助拉莫三嗪局部癫痫患者年龄在1到24个月。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVE: This randomized, double-blind, placebo-controlled trial was conducted to assess the efficacy and tolerability of adjunctive lamotrigine for the treatment of partial seizures in infants aged 1 to 24 months. METHODS: The study used a responder-enriched design in which all patients received adjunctive lamotrigine during an open-label phase (n = 177; maximum maintenance dose 5.1 mg/kg/day for those on non-enzyme-inducing antiepileptic drugs [AEDs] or valproate and 15.6 mg/kg/day for those on enzyme-inducing AEDs). Patients meeting response criteria were randomly assigned to double-blind treatment for up to 8 weeks with continued lamotrigine (n = 19) or to withdrawal from lamotrigine (placebo; n = 19) while background AEDs were maintained. RESULTS: The proportion of treatment failures (patients who met escape criteria or withdrew before completing the double-blind phase) was lower with lamotrigine (58%) than with placebo (84%). This finding was not significant in the primary analysis (two-sided chi(2) test [primary endpoint]). A post hoc sensitivity analysis of the primary endpoint was also performed (p = 0.045 by one-sided, mid-p corrected Fisher exact test). The median time to meet escape criteria was longer with lamotrigine (42 days) than with placebo (22 days) (p = 0.059). During the last 28 days of the open-label phase, 53% of the patients had a >or=50% reduction in frequency of partial seizures with lamotrigine. Additional reduction in partial seizure frequency was observed during the double-blind phase compared with the last 4 weeks of the open-label phase among those randomly assigned to lamotrigine (32% with a >or=25% reduction) but not those randomly assigned to placebo (5% with a >or=25% reduction). Lamotrigine was well tolerated, with an adverse event profile comparable to that observed in older pediatric patients. CONCLUSION: Lamotrigine was well tolerated, and the data indicate that it may be efficacious in the treatment of partial seizures in infants aged 1 to 24 months.
机译:目的:这个随机、双盲、安慰剂对照试验进行评估辅助的疗效和耐受性拉莫三嗪治疗部分癫痫发作在婴儿1到24个月。研究使用responder-enriched设计中所有患者接受辅助拉莫三嗪在一个开放的阶段(n = 177;维持剂量的5.1毫克/公斤/天non-enzyme-inducing抗癫痫药物(aed)或丙戊酸钠和15.6毫克/公斤/天enzyme-inducing aed)。标准被随机分配到双盲治疗与持续8周拉莫三嗪(n = 19)或退出拉莫三嗪(安慰剂;aed维护。治疗失败的患者(遇到逃跑标准或完成之前就退出了双盲阶段)与拉莫三嗪降低比与安慰剂组(58%)(84%)。不显著的主要分析(双面气(2)测试(主要终点))。事后敏感性分析的主要端点也表现(p = 0.045片面的,mid-p纠正Fisher精确检验)。中位数时间满足逃跑时的标准再与拉莫三嗪(42天)安慰剂(22天)(p = 0.059)。天的非盲阶段,53%的病人有> = 50%减少部分的频率癫痫发作与拉莫三嗪。在部分发作期间观察到的与去年相比双盲阶段4在这些周的开放阶段随机分配到拉莫三嗪(32%的>或减少= 25%)但不是那些随机分配给安慰剂(5% >或= 25%减少)。一个与不良事件概要文件年长的儿科患者中观察到。拉莫三嗪是耐受性良好,数据表明它可能是有效的在婴儿1治疗局部癫痫24个月。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号