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氟伐曲坦与佐米曲坦治疗偏头痛急性发作的疗效比较:一项双盲、随机、多中心、意大利研究。

Frovatriptan versus zolmitriptan for the acute treatment of migraine: a double-blind, randomized, multicenter, Italian study.

机构信息

Department of Clinical Neurosciences, National Neurological Institute Carlo Besta, Via Celoria 11, 20133, Milan, Italy.

出版信息

Neurol Sci. 2010 Jun;31 Suppl 1(Suppl 1):S51-4. doi: 10.1007/s10072-010-0273-x.

DOI:10.1007/s10072-010-0273-x
PMID:20464583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2869037/
Abstract

The objective of this study is to assess patients' satisfaction with migraine treatment with frovatriptan (F) or zolmitriptan (Z), by preference questionnaire. 133 subjects with a history of migraine with or without aura (IHS criteria) were randomized to F 2.5 mg or Z 2.5 mg. The study had a multicenter, randomized, double-blind, cross-over design, with each of the two treatment periods lasting no more than 3 months. At the end of the study, patients were asked to assign preference to one of the treatments (primary endpoint). The number of pain-free (PF) and pain-relief (PR) episodes at 2 h, and number of recurrent and sustained pain-free (SPF) episodes within 48 h were the secondary study endpoints. Seventy-seven percent of patients expressed a preference. Average score of preference was 2.9 +/- 1.3 (F) versus 3.0 +/- 1.3 (Z; p = NS). Rate of PF episodes at 2 h was 26% with F and 31% with Z (p = NS). PR episodes at 2 h were 57% for F and 58% for Z (p = NS). Rate of recurrence was 21 (F) and 24% (Z; p = NS). Time to recurrence within 48 h was better for F especially between 4 and 16 h (p < 0.05). SPF episodes were 18 (F) versus 22% (Z; p = NS). Drug-related adverse events were significantly (p < 0.05) less under F (3 vs. 10). In conclusion, our study suggests that F has a similar efficacy of Z, with some advantage as regards tolerability and recurrence.

摘要

本研究旨在通过偏好问卷评估偏头痛患者对曲普坦(F)或佐米曲普坦(Z)治疗的满意度。133 名有偏头痛病史(IHS 标准)的患者伴或不伴先兆,随机分为 F 2.5mg 或 Z 2.5mg。该研究采用多中心、随机、双盲、交叉设计,每个治疗期不超过 3 个月。研究结束时,患者被要求对两种治疗方法中的一种进行偏好选择(主要终点)。次要研究终点为 2 小时内无疼痛(PF)和疼痛缓解(PR)次数,48 小时内复发和持续无疼痛(SPF)次数。77%的患者表达了偏好。偏好平均得分为 2.9 +/- 1.3(F)与 3.0 +/- 1.3(Z;p = NS)。F 组 2 小时 PF 发生率为 26%,Z 组为 31%(p = NS)。F 组 2 小时 PR 发生率为 57%,Z 组为 58%(p = NS)。复发率为 21(F)和 24%(Z;p = NS)。F 在 48 小时内复发的时间更好,尤其是在 4 至 16 小时之间(p < 0.05)。SPF 发生率为 18(F)与 22%(Z;p = NS)。F 组的药物相关不良事件明显(p < 0.05)少于 Z 组(3 比 10)。总之,我们的研究表明,F 与 Z 的疗效相似,在耐受性和复发方面具有一定优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e88c/2869037/5069eac7083b/10072_2010_273_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e88c/2869037/5069eac7083b/10072_2010_273_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e88c/2869037/5069eac7083b/10072_2010_273_Fig1_HTML.jpg

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