Université de Montréal, Hôpital Sainte-Justine, Room 5421, 3175 Côte Ste-Catherine, Montréal (Québec) H3T 1C5, Canada.
Can J Neurol Sci. 2012 Nov;39(6):702-11. doi: 10.1017/s0317167100015535.
Lennox-Gastaut syndrome (LGS) is a severe epileptic encephalopathy. Few current treatment options are effective in improving seizure control. This paper reviews the available treatments of LGS and discusses a new option in Canada, rufinamide. It is a wide spectrum anticonvulsant, approved in a number of countries for the treatment of LGS. In a randomized controlled trial in the LGS population, adjunctive rufinamide therapy has been shown to offer significantly greater reduction in total seizure frequency and tonic-atonic seizure frequency in comparison to placebo. Efficacy has been assessed over three years and appears to be sustained. Most adverse events were cognitive (e.g. somnolence) or gastrointestinal in nature and in many cases transient or mild. based on the efficacy and safety data on rufinamide obtained to date, this medication will provide additional benefits to patients with LGS in Canada and is an important consideration for our patients in the adjunctive treatment setting.
朗格汉斯细胞组织细胞增生症(LGS)是一种严重的癫痫性脑病。目前很少有治疗方法能有效改善癫痫发作的控制。本文综述了 LGS 的现有治疗方法,并讨论了加拿大的一种新选择,鲁非酰胺。它是一种广谱抗癫痫药,已在多个国家获得批准,用于治疗 LGS。在 LGS 人群中的一项随机对照试验中,与安慰剂相比,添加鲁非酰胺治疗可显著降低总癫痫发作频率和强直阵挛性癫痫发作频率。疗效已评估三年,且似乎可持续。大多数不良事件为认知(如嗜睡)或胃肠道性质,且在许多情况下为短暂或轻度。基于迄今为止获得的关于鲁非酰胺的疗效和安全性数据,这种药物将为加拿大的 LGS 患者带来额外的益处,并且是辅助治疗环境中我们患者的重要考虑因素。