Theodore W H, Raubertas R F, Porter R J, Nice F, Devinsky O, Reeves P, Bromfield E, Ito B, Balish M
Clinical Epilepsy Section Medical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892.
Epilepsia. 1991 May-Jun;32(3):392-7. doi: 10.1111/j.1528-1157.1991.tb04668.x.
We performed a randomized, double-blind, three-period cross-over study of felbamate (FBM, 2-phenyl-1,3-propanediol dicarbamate: Carter-Wallace 554) in patients with complex partial seizures. Patients continued carbamazepine (CBZ) throughout the study and were observed in the hospital for the entire trial period. The entry criteria required at least six seizures in a 3-week baseline period (and no more than 1 week with a single seizure) with CBZ alone. Thirty subjects were randomized. Two left the study after randomization, 1 owing to seizure exacerbation, and 1 owing to hyponatremia, which may have been related to CBZ therapy. The daily dosage of 50 mg/kg (maximum 3,000 mg) FBM per day was well tolerated by all 28 patients who completed the study. Only mild adverse experience were observed during the trial. FBM reduced CBZ level (p less than 0.0001; 95% confidence interval -28%, -20%). There was no significant difference in seizure frequency between placebo and FBM periods (one-sided p = 0.172), but when a correction was made for the lower CBZ level noted during FBM periods, the data suggested a strong antiseizure effect of FBM.
我们对患有复杂部分性癫痫的患者进行了一项关于非氨酯(FBM,2-苯基-1,3-丙二醇二氨基甲酸酯:卡特-华莱士554)的随机、双盲、三阶段交叉研究。患者在整个研究过程中持续服用卡马西平(CBZ),并在医院接受了整个试验期的观察。入选标准要求在仅使用CBZ的3周基线期内至少发作6次(且单次发作的时间不超过1周)。30名受试者被随机分组。随机分组后有2人退出研究,1人因癫痫发作加剧,1人因低钠血症,低钠血症可能与CBZ治疗有关。完成研究的所有28名患者对每日50mg/kg(最大3000mg)的FBM剂量耐受性良好。试验期间仅观察到轻度不良事件。FBM降低了CBZ水平(p<0.0001;95%置信区间为-28%,-20%)。安慰剂期和FBM期之间的癫痫发作频率无显著差异(单侧p=0.172),但当对FBM期观察到的较低CBZ水平进行校正后,数据表明FBM具有较强的抗癫痫作用。