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氟伐曲坦与其他曲坦类药物在偏头痛急性治疗中的比较:三项意大利、双盲、随机、交叉、多中心研究的汇总分析。

Frovatriptan versus other triptans in the acute treatment of migraine: pooled analysis of three double-blind, randomized, cross-over, multicenter, Italian studies.

机构信息

Clinica Neurologica, Dipartimento di Scienze Neurologiche, Università di Bologna, Via Ugo Foscolo, 7, 40123 Bologna, Italy.

出版信息

Neurol Sci. 2011 May;32 Suppl 1:S95-8. doi: 10.1007/s10072-011-0551-2.

Abstract

The objective of the study is to systematically review the efficacy and safety of frovatriptan (F) versus rizatriptan (R), zolmitriptan (Z) and almotriptan (A), through a pooled analysis of three individual studies. 414 subjects with a history of migraine with or without aura (IHS criteria) were randomized to F 2.5 mg or R 10 mg (study 1), F 2.5 mg or Z 2.5 mg (study 2), and F 2.5 mg or A 12.5 mg (study 3). The studies had an identical multicenter, randomized, double blind, cross-over design, with each of the two treatment periods lasting not more than 3 months. The number of pain free (PF) and pain relief (PR) episodes at 2 h, and the number of sustained pain free (SPF) and recurrent episodes within the 48 h were the efficacy endpoints. 346 patients were included in the intention-to-treat analysis. Rate of PF episodes at 2 h was 30% with F and 34% with comparators (p = NS). PR episodes at 2 h were 55% for F and 59% for comparators (p = NS). SPF episodes at 48 h were also similar between the two groups (22% F vs. 21% comparators). Rate of recurrence was significantly (p < 0.001) lower under F (27 vs. 40% comparators). Drug-related adverse events were significantly (p < 0.05) less under F, particularly cardiovascular symptoms. Our systematic analysis of individual studies suggests that F has a similar immediate efficacy, but a more sustained effect and a better tolerability than R, Z and A.

摘要

本研究旨在通过对三项独立研究的汇总分析,系统评价曲普坦类药物(如夫罗曲坦 F)与利扎曲坦 R、佐米曲普坦 Z 和阿莫曲坦 A 的疗效和安全性。414 例偏头痛病史(有或无先兆, IHS 标准)患者随机分为 F 2.5mg 或 R 10mg(研究 1)、F 2.5mg 或 Z 2.5mg(研究 2)和 F 2.5mg 或 A 12.5mg(研究 3)组。这些研究采用了相同的多中心、随机、双盲、交叉设计,每个治疗期不超过 3 个月。疗效终点为 2 小时无痛(PF)和缓解(PR)发作次数,以及 48 小时内持续无痛(SPF)和复发发作次数。346 例患者纳入意向治疗分析。2 小时时 PF 发作率 F 组为 30%,对照药组为 34%(p=NS)。2 小时时 PR 发作率 F 组为 55%,对照药组为 59%(p=NS)。两组 48 小时 SPF 发作率也相似(F 组 22%,对照药组 21%)。复发率 F 组显著低于对照药组(p<0.001,27%对 40%)。F 组药物相关不良事件发生率显著低于对照药组(p<0.05),尤其是心血管症状。我们对三项独立研究的系统分析表明,F 的即刻疗效相似,但持续作用更强,耐受性更好。

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