Department of Pediatrics, St George Hospital Medical University Center, University of Balamand, Beirut, Lebanon.
Department of Pediatrics, Hotel Dieu de France Hospital, Beirut, Lebanon.
Seizure. 2020 Jul;79:75-79. doi: 10.1016/j.seizure.2020.04.016. Epub 2020 May 11.
The aim of this study was to evaluate the tolerability and efficacy of lacosamide (LCM) in Lebanese children with focal-onset seizures and to determine if specific variables are predictive of better effectiveness.
This is a retrospective analysis from three medical centers on consecutive children diagnosed with focal onset seizures and initiated on LCM. The seizure frequencies following the introduction of LCM were recorded and compared to the baseline monthly frequency at 3, 6, 12, 18, and 24 months. The primary efficacy variables were the 50% responder and seizure-free rates. The secondary outcome variables included the terminal 6-month seizure remission and percentages of discontinuation due to lack of efficacy or tolerability.
58 patients with a mean age of 10 years experiencing a mean of 36.2 seizures per month during baseline were included. The seizure-free rates were 32.8%, 29.7%, and 12.5% at 6, 12 and 24 months follow up, respectively. Patients concomitantly treated with a sodium channel blocker were less likely to achieve a terminal 6-month seizure remission while the early introduction of LCM resulted in a significantly higher likelihood of attaining such a remission. 74.1% of patients were still maintained on LCM at the last follow-up. The most common adverse events consisted of dizziness, somnolence, nausea, vomiting, and rarely double vision.
LCM is efficacious and overall well tolerated in children with focal-onset seizures and exhibits higher efficacy with early introduction and when added to a non-sodium channel blocker.
本研究旨在评估拉科酰胺(LCM)在黎巴嫩局灶性发作性癫痫患儿中的耐受性和疗效,并确定是否存在特定变量可以预测更好的疗效。
这是一项回顾性分析,来自三个医疗中心,对确诊为局灶性发作性癫痫并开始使用 LCM 的连续儿童进行了分析。记录 LCM 引入后的发作频率,并与基线时的每月频率进行比较,时间为 3、6、12、18 和 24 个月。主要疗效变量为 50%应答者和无发作率。次要结局变量包括终端 6 个月的发作缓解率和因缺乏疗效或耐受性而停药的百分比。
58 名患者的平均年龄为 10 岁,基线时每月平均发作 36.2 次。无发作率分别为 6、12 和 24 个月随访时的 32.8%、29.7%和 12.5%。同时接受钠离子通道阻滞剂治疗的患者达到终端 6 个月发作缓解的可能性较小,而早期引入 LCM 则显著增加了达到缓解的可能性。最后一次随访时,74.1%的患者仍在使用 LCM。最常见的不良反应包括头晕、嗜睡、恶心、呕吐,极少数有复视。
LCM 对儿童局灶性发作性癫痫有效,总体耐受性良好,早期引入和与非钠离子通道阻滞剂联合使用时疗效更高。