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非氨酯治疗伦诺克斯-加斯托综合征。

Felbamate in the treatment of Lennox-Gastaut syndrome.

作者信息

Jensen P K

机构信息

Schering-Plough Research Institute, Kenilworth, NJ 07033-0539.

出版信息

Epilepsia. 1994;35 Suppl 5:S54-7. doi: 10.1111/j.1528-1157.1994.tb05969.x.

Abstract

Felbamate (FBM, Felbatol/Taloxa), a new antiepileptic drug (AED), was tested in a placebo-controlled add-on design in 73 patients with therapy refractory Lennox-Gastaut syndrome. Results of the efficacy analysis showed that FBM was statistically significantly more effective (p < 0.05) than placebo for four of five predefined efficacy variables. The total number of seizures, for example, decreased by 26% during treatment with FBM compared with an increase of 5% during placebo (p < 0.001). Retrospective analysis of percentage of patients with specific response rates confirmed results of the predefined efficacy variables. Approximately 50% of patients randomized to FBM obtained at least a 50% reduction in seizure frequency compared with about 15% receiving placebo. In addition, 12-month follow-up data in patients who completed the controlled part of the study confirmed the long-term efficacy of FBM. In general, FBM was well tolerated, with only gastrointestinal symptoms and somnolence seen more often with FBM compared with placebo. FBM is the first compound shown to be effective in a controlled study in patients with Lennox-Gastaut syndrome.

摘要

非氨酯(FBM,商品名Felbatol/Taloxa)是一种新型抗癫痫药物(AED),在一项安慰剂对照的附加治疗设计中,对73例患有难治性Lennox-Gastaut综合征的患者进行了测试。疗效分析结果显示,对于五个预先定义的疗效变量中的四个,非氨酯在统计学上比安慰剂显著更有效(p < 0.05)。例如,在接受非氨酯治疗期间,癫痫发作总数减少了26%,而在接受安慰剂治疗期间增加了5%(p < 0.001)。对具有特定缓解率的患者百分比进行回顾性分析,证实了预先定义的疗效变量的结果。随机接受非氨酯治疗的患者中,约50%的癫痫发作频率至少降低了50%,而接受安慰剂治疗的患者约为15%。此外,完成研究对照部分的患者的12个月随访数据证实了非氨酯的长期疗效。总体而言,非氨酯耐受性良好,与安慰剂相比,仅胃肠道症状和嗜睡在非氨酯治疗时更常见。非氨酯是首个在Lennox-Gastaut综合征患者的对照研究中显示有效的化合物。

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