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A randomized trial comparing amitriptyline versus topiramate for the prophylaxis of chronic daily headache in pediatric patients

机译:比较阿米替林与托吡酯预防小儿慢性每日头痛的随机试验

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Objective: the goal of this prospective and double-blind study was to compare the efficacy of amitriptyline and topiramate for the prevention of pediatric chronic daily headache (CDH). Research design and methods: fifty-seven children (aged 9-16 yr) diagnosed with CDH were randomly assigned to two groups: group A (n = 29 patients) received amitriptyline 0.5 mg/kg/d and group B (n = 28 patients) received topiramate 25 mg/d increasing up to 100 mg/d according to patient response. Treatment response was monitored for at least 4 months. Results: fifty-five percent of the patients in group A responded to amitriptyline and 61% of patients in group B responded to topiramate as defined by a reduction of more than 50% in monthly headache frequency. There was no significant difference in responder rate or adverse event rate between the two groups (p > 0.05). By the end of the 4-month treatment period, there were no significant differences in the final average severity and monthly frequency of headaches betweenatment groups. Conclusion: these results suggest that the efficacy and tolerability of topiramate is equivalent to that of amitriptyline for reducing the frequency of headache in pediatric CHD patients.
机译:目的:这项前瞻性和双盲研究的目的是比较阿米替林和托吡酯在预防小儿慢性每日头痛(CDH)中的功效。研究设计和方法:将57例诊断为CDH的儿童(9-16岁)随机分为两组:A组(29例)接受阿米替林0.5 mg / kg / d,B组(28例) )接受托吡酯25 mg / d,根据患者反应增加至100 mg / d。监测治疗反应至少4个月。结果:A组中有55%的患者对阿米替林有反应,B组中有61%的患者对托吡酯有反应,定义为每月头痛频率降低50%以上。两组的缓解率或不良事件发生率无显着差异(p> 0.05)。到四个月的治疗期结束时,各治疗组之间的头痛的最终平均严重程度和每月发作频率均无显着差异。结论:这些结果表明托吡酯在降低小儿冠心病患者头痛频率方面的疗效和耐受性与阿米替林相当。

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