Biton V, Montouris G D, Ritter F, Riviello J J, Reife R, Lim P, Pledger G
Arkansas Epilepsy Program, Little Rock 72205, USA.
Neurology. 1999 Apr 22;52(7):1330-7. doi: 10.1212/wnl.52.7.1330.
Topiramate is effective as adjunctive treatment of partial-onset seizures in adults. The efficacy and safety of topiramate as adjunctive therapy for the treatment of primary generalized tonic-clonic (PGTC) seizures were investigated in a randomized, double-blind, placebo-controlled study.
Eighty patients, 3 to 59 years old, who experienced three or more PGTC seizures during an 8-week baseline phase were randomly assigned to treatment with either topiramate (n = 39) or placebo (n = 41). Topiramate was titrated to target doses of approximately 6 mg/kg/day over 8 weeks and maintained for another 12 weeks.
The median percentage reduction from baseline in PGTC seizure rate was 56.7% for topiramate patients and 9.0% for placebo patients (p = 0.019). The proportion of patients with 50% or higher reduction in PGTC seizure rate was 22/39 (56%) and 8/40 (20%) for the topiramate and placebo groups, respectively (p = 0.001). The median percentage reduction in the rate of all generalized seizures was 42.1% for topiramate patients and 0.9% for placebo patients (p = 0.003). The proportions of patients with 50% or higher reductions in generalized seizure rate were 18/39 (46%) and 7/41 (17%) for the topiramate and placebo groups, respectively (p = 0.003). The most common adverse events were somnolence, fatigue, weight loss, difficulty with memory, and nervousness. Treatment-limiting adverse events occurred in one patient in the topiramate group (anorexia and weight loss) and one in the placebo group (granulocytopenia and thrombocytopenia).
Topiramate is well-tolerated and effective for the adjunctive treatment of PGTC seizures.
托吡酯作为成人部分性发作的辅助治疗药物是有效的。在一项随机、双盲、安慰剂对照研究中,对托吡酯作为辅助疗法治疗原发性全面强直阵挛(PGTC)发作的疗效和安全性进行了研究。
80例年龄在3至59岁之间、在8周基线期经历过3次或更多次PGTC发作的患者被随机分配接受托吡酯治疗(n = 39)或安慰剂治疗(n = 41)。托吡酯在8周内滴定至目标剂量约6mg/kg/天,并维持12周。
托吡酯组患者PGTC发作率较基线降低的中位数百分比为56.7%,安慰剂组为9.0%(p = 0.019)。PGTC发作率降低50%或更高的患者比例,托吡酯组为22/39(56%),安慰剂组为8/40(20%)(p = 0.001)。托吡酯组患者所有全面性发作率降低的中位数百分比为42.1%,安慰剂组为0.9%(p = 0.003)。全面性发作率降低50%或更高的患者比例,托吡酯组为18/39(46%),安慰剂组为7/41(17%)(p = 0.003)。最常见的不良事件为嗜睡、疲劳、体重减轻、记忆困难和紧张。托吡酯组有1例患者出现限制治疗的不良事件(厌食和体重减轻),安慰剂组有1例(粒细胞减少和血小板减少)。
托吡酯耐受性良好,对PGTC发作的辅助治疗有效。