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一项随机、双盲、安慰剂对照研究,旨在评估托吡酯对12至17岁儿童偏头痛预防的疗效和安全性。

Randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of topiramate for migraine prevention in pediatric subjects 12 to 17 years of age.

作者信息

Lewis Donald, Winner Paul, Saper Joel, Ness Seth, Polverejan Elena, Wang Steven, Kurland Caryn L, Nye Jeff, Yuen Eric, Eerdekens Marielle, Ford Lisa

机构信息

Department of Pediatrics, Children's Hospital of the King's Daughters, Eastern Virginia Medical School, 601 Children's Lane, Norfolk, VA 23507-1971, USA.

出版信息

Pediatrics. 2009 Mar;123(3):924-34. doi: 10.1542/peds.2008-0642.

Abstract

OBJECTIVE

Currently, no drugs are Food and Drug Administration-approved for migraine prophylaxis in pediatric patients. The objective of this study was to evaluate the efficacy and safety of topiramate for migraine prevention in adolescents.

METHODS

Adolescents (12-17 years of age) with a >/=6-month history of migraine were assigned randomly to receive 16 weeks of daily treatment with topiramate (50 or 100 mg/day) or placebo. The primary efficacy measure was the percent reduction in monthly migraine attacks, with the use of the 48-hour rule, from the prospective baseline period to the last 12 weeks of the double-blind phase. The 48-hour rule defined a single migraine episode as all recurrences of migraine symptoms within 48 hours after onset. Several secondary efficacy measures were evaluated, including the reduction from baseline in the monthly migraine day rate and the 50% responder rate. Safety and tolerability were also assessed.

RESULTS

A total of 29 (83%) of 35 subjects treated with topiramate at 50 mg/day, 30 (86%) of 35 subjects treated with topiramate at 100 mg/day, and 26 (79.0%) of 33 placebo-treated subjects completed double-blind treatment. Topiramate at 100 mg/day, but not 50 mg/day, resulted in a statistically significant reduction in the monthly migraine attack rate from baseline versus placebo (median: 72.2% vs 44.4%) during the last 12 weeks of double-blind treatment. Topiramate at 100 mg/day, but not 50 mg/day, also resulted in a statistically significant reduction in the monthly migraine day rate from baseline versus placebo. The responder rate favored topiramate at 100 mg/day (83% vs 45% for placebo). Upper respiratory tract infection, paresthesia, and dizziness occurred more commonly in the topiramate groups than in the placebo group.

CONCLUSIONS

The 100 mg/day topiramate group demonstrated efficacy in the prevention of migraine in pediatric subjects. Overall, topiramate treatment was safe and well tolerated.

摘要

目的

目前,尚无药物获美国食品药品监督管理局批准用于小儿偏头痛的预防。本研究的目的是评估托吡酯预防青少年偏头痛的疗效和安全性。

方法

将有≥6个月偏头痛病史的青少年(12 - 17岁)随机分配,接受为期16周的每日托吡酯(50或100毫克/天)或安慰剂治疗。主要疗效指标是根据48小时规则,从前瞻性基线期到双盲期最后12周每月偏头痛发作次数减少的百分比。48小时规则将单次偏头痛发作定义为发作后48小时内偏头痛症状的所有复发。评估了几个次要疗效指标,包括每月偏头痛天数率较基线的降低以及50%缓解率。还评估了安全性和耐受性。

结果

接受50毫克/天托吡酯治疗的35名受试者中有29名(83%)、接受100毫克/天托吡酯治疗的35名受试者中有30名(86%)以及接受安慰剂治疗的33名受试者中有26名(79.0%)完成了双盲治疗。在双盲治疗的最后12周,100毫克/天的托吡酯组(而非50毫克/天的托吡酯组)与安慰剂相比,每月偏头痛发作率从基线有统计学显著降低(中位数:72.2%对44.4%)。100毫克/天的托吡酯组(而非50毫克/天的托吡酯组)与安慰剂相比,每月偏头痛天数率从基线也有统计学显著降低。缓解率有利于100毫克/天的托吡酯组(83%对安慰剂组的45%)。上呼吸道感染、感觉异常和头晕在托吡酯组中比在安慰剂组中更常见。

结论

100毫克/天托吡酯组在预防小儿偏头痛方面显示出疗效。总体而言,托吡酯治疗安全且耐受性良好。

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