Freitag Fred G, Forde Grace, Neto Walter, Wang Daniel Z, Schmitt Jennifer, Wu Shu-Chen, Hulihan Joseph
Diamond Headache Clinic, 467 W Deming Place, Chicago, IL 60614-1881, USA.
J Am Osteopath Assoc. 2007 Jul;107(7):251-8.
A substantial proportion of the patient population with migraine headache should be considered for preventive treatment based on the frequency and disability associated with this disorder. Use of the anticonvulsant topiramate was previously examined in two large, double-blind, randomized, placebo-controlled clinical trials of a subset of patients who have 3 to 12 migraine episodes per month.
To better characterize the efficacy of topiramate for prevention of migraine, with or without aura, by pooling and analyzing data from the two large clinical trials.
The pooled intent-to-treat population included 937 patients receiving topiramate at one of three dosages (50 mg/d, 100 mg/d, 200 mg/d) or placebo. Outcome measures included change in mean monthly migraine frequency and categorical responder rate throughout the 26-week doubleblind phase.
At daily doses of 100 and 200 mg, topiramate was associated with significant reductions in mean monthly migraine frequency throughout the double-blind phase compared with placebo (P<.001). Significantly more patients treated with these topiramate doses exhibited high-percentage reductions in monthly migraine frequency (>/=50% [P<.001], >/=75% [P<.001], 100% [P=.049]) versus placebo. The most common adverse events included anorexia, cognitive deficits, diarrhea, fatigue, nausea, and paresthesia. Topiramate (100 mg/d, 200 mg/d) was associated with significant and sustained reductions in mean monthly migraine frequency beginning as early as 1 week into therapy.
Pooled efficacy data from two large, similarly designed, placebo-controlled migraine-prevention trials demonstrated that a statistically significant proportion of patients using topiramate met or exceeded two main outcome guidelines recommended by the International Headache Society (>/=50% and >/=75% reduction in frequency of monthly attacks). Based on efficacy and tolerability, topiramate at a dosage of 100 mg per day (50 mg twice daily) should be the target dosage for most patients with migraine.
鉴于偏头痛患者群体中相当大一部分人因该疾病的发作频率和功能障碍而应考虑接受预防性治疗。先前在两项大型、双盲、随机、安慰剂对照临床试验中,对每月有3至12次偏头痛发作的部分患者使用了抗惊厥药物托吡酯进行研究。
通过汇总和分析两项大型临床试验的数据,更好地描述托吡酯预防有或无先兆偏头痛的疗效。
汇总的意向性治疗人群包括937例接受三种剂量(50毫克/天、100毫克/天、200毫克/天)之一的托吡酯或安慰剂治疗的患者。疗效指标包括在整个26周双盲期内每月偏头痛平均发作频率的变化以及分类缓解率。
在双盲期,与安慰剂相比,每日剂量为100毫克和200毫克时,托吡酯与每月偏头痛平均发作频率显著降低相关(P<0.001)。与安慰剂相比,接受这些托吡酯剂量治疗的患者中,每月偏头痛发作频率显著降低(≥50%[P<0.001]、≥75%[P<0.001]、100%[P=0.049])的患者明显更多。最常见的不良事件包括厌食、认知缺陷、腹泻、疲劳、恶心和感觉异常。托吡酯(100毫克/天、200毫克/天)从治疗第1周起就与每月偏头痛平均发作频率显著且持续降低相关。
两项大型、设计相似、安慰剂对照的偏头痛预防试验的汇总疗效数据表明,使用托吡酯的患者中有统计学意义的比例达到或超过了国际头痛协会推荐的两项主要疗效指南(每月发作频率降低≥50%和≥75%)。基于疗效和耐受性,对于大多数偏头痛患者,每天100毫克(50毫克,每日两次)的托吡酯剂量应作为目标剂量。