Salinas-estabane Ramiro
Social Security System, Monterrey, Nuevo Leon, Mexico.
Adv Ther. 2002 May-Jun;19(3):126-8. doi: 10.1007/BF02850268.
This 6-month open-label study evaluated the efficacy and safety of topiramate monotherapy for partial-onset or primarily generalized seizures in 22 adults with newly diagnosed epilepsy. The initial topiramate dose of 25 mg could be titrated to a maximum effective or maximum tolerated dose of 200 mg/d. Eighteen patients completed the study. The mean topiramate dose was 200 mg/d (range, 75-200 mg/d). Compared with baseline, monthly seizure frequency decreased 89% (median), with 17 patients (94%) achieving complete control. Five patients dropped out of the study. No changes in hematologic, renal, and hepatic function evaluations were noted, and only 1 patient experienced clinical signs significant enough to warrant discontinuation of treatment. In this small study, topiramate in doses ranging from 75 to 200 mg/d was effective and well tolerated as monotherapy in adults with newly diagnosed epilepsy.
这项为期6个月的开放标签研究评估了托吡酯单药治疗对22例新诊断癫痫成人患者部分性发作或原发性全身性发作的疗效和安全性。托吡酯初始剂量为25mg,可滴定至最大有效剂量或最大耐受剂量200mg/d。18例患者完成了研究。托吡酯平均剂量为200mg/d(范围75 - 200mg/d)。与基线相比,每月癫痫发作频率降低了89%(中位数),17例患者(94%)实现了完全控制。5例患者退出研究。血液学、肾脏和肝脏功能评估未见变化,仅有1例患者出现足以停药的明显临床体征。在这项小型研究中,75至200mg/d剂量的托吡酯作为新诊断癫痫成人患者的单药治疗有效且耐受性良好。