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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >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
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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

机译:评估托吡酯预防12至17岁小儿偏头痛的功效和安全性的随机,双盲,安慰剂对照研究

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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.
机译:目的。当前,尚无食品和药物管理局批准用于预防小儿偏头痛的药物。这项研究的目的是评估托吡酯预防青少年偏头痛的有效性和安全性。偏头痛病史≥6个月的青少年(12-17岁)被随机分配接受托吡酯(50或100 mg /天)或安慰剂每日治疗16周。主要疗效指标是使用48小时规则从预期基线期到双盲阶段的最后12周,每月偏头痛发作的百分比降低。 48小时规则将单个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。评估了几种次要疗效指标,包括每月偏头痛日率和50%应答率与基线相比降低。还评估了安全性和耐受性。接受50毫克/天托吡酯治疗的35位受试者中的29位(83%),接受100毫克/天托吡酯治疗的35位受试者中的30位(86%)和接受安慰剂治疗的33位受试者中的26位(79.0%)已完成双盲治疗。在双盲治疗的最后12周中,托吡酯100毫克/天,但不是50毫克/天,导致偏头痛的每月偏头痛发作率较安慰剂组有统计学意义的降低(中位数:72.2%vs 44.4%)。托吡酯100毫克/天,但不是50毫克/天,与安慰剂相比,每月偏头痛日率也有统计学上的显着降低。 100 mg /天的应答率偏爱托吡酯(83%vs安慰剂为45%)。托吡酯组比安慰剂组更常见上呼吸道感染,感觉异常和头晕。每天100 mg的托吡酯组证明在预防小儿科患者偏头痛方面有效。总体而言,托吡酯治疗安全且耐受性良好。

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