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12.5毫克阿莫曲坦在实现偏头痛相关复合终点方面的疗效:一项针对既往对50毫克舒马曲坦反应不佳患者的双盲、随机、安慰剂对照研究。

Efficacy of almotriptan 12.5 mg in achieving migraine-related composite endpoints: a double-blind, randomized, placebo-controlled study in patients controlled study in patients with previous poor response to sumatriptan 50 mg.

作者信息

Diener Hans-Christoph

机构信息

Department Of Neurology, University of Essen, D-45145 Essen, Germany.

出版信息

Curr Med Res Opin. 2005 Oct;21(10):1603-10. doi: 10.1185/030079905X65448.

Abstract

BACKGROUND

Triptans are not identical and migraine sufferers respond differently to different triptans. Few studies have evaluated the efficacy of switching triptans in migraine patients who have shown poor response to another agent.

OBJECTIVE

To investigate the efficacy and tolerability of almotriptan 12.5 mg in patients who did not achieve 2-h pain relief with sumatriptan 50 mg.

METHODS

This double-blind, placebo-controlled study recruited patients with IHS-defined migraine and at least 2 previous unsatisfactory responses to sumatriptan. Those who did not achieve pain relief (moderate or severe pain decreasing to mild or no pain) 2 h after taking oral sumatriptan 50 mg on an open-label basis for the treatment of their first migraine attack during this trial (Attack 1) were randomized to receive either oral almotriptan 12.5 mg or placebo for the treatment of their next migraine attack (Attack 2).

RESULTS

Of 302 patients receiving sumatriptan 50 mg for the treatment of their first migraine attack, 221 (73%) did not achieve 2-h pain relief and were randomized to almotriptan 12.5 mg or placebo for the treatment of Attack 2. The majority (70%) of randomized patients treating their headache in Attack 2 reported severe pain at baseline characterizing this as a difficult-to-treat population. In the intent-to-treat population (n = 198), significantly more patients in the almotriptan group compared with the placebo group achieved 2-h complete relief (free from pain and migraine-associated symptoms) at 2 h (17.1% vs. 4.4%; p < 0.05) and sustained pain free (20.9% vs. 9.0%; p < 0.05). Adverse events of mild-to-moderate intensity occurred in 7.1% of patients in the almotriptan group compared to 5.1% in the placebo group (not statistically different).

CONCLUSION

Almotriptan is more effective than placebo and similarly well-tolerated for the acute treatment of migraine in patients who responded poorly to oral sumatriptan.

摘要

背景

曲坦类药物并非完全相同,偏头痛患者对不同曲坦类药物的反应也有所不同。很少有研究评估在对另一种药物反应不佳的偏头痛患者中更换曲坦类药物的疗效。

目的

研究12.5毫克阿莫曲坦在未使用50毫克舒马曲坦实现2小时疼痛缓解的患者中的疗效和耐受性。

方法

这项双盲、安慰剂对照研究招募了符合国际头痛协会(IHS)定义的偏头痛患者,且既往至少有2次对舒马曲坦治疗反应不佳。在本次试验(发作1)中,那些在开放标签基础上口服50毫克舒马曲坦治疗首次偏头痛发作后2小时未实现疼痛缓解(中度或重度疼痛减轻至轻度或无疼痛)的患者,被随机分配接受口服12.5毫克阿莫曲坦或安慰剂治疗下一次偏头痛发作(发作2)。

结果

在302例接受50毫克舒马曲坦治疗首次偏头痛发作的患者中,221例(73%)未实现2小时疼痛缓解,并被随机分配接受12.5毫克阿莫曲坦或安慰剂治疗发作2。在发作2中治疗头痛的大多数随机分组患者(70%)在基线时报告有重度疼痛,表明这是一个难以治疗的人群。在意向性治疗人群(n = 198)中,与安慰剂组相比,阿莫曲坦组在2小时时有更多患者实现2小时完全缓解(无疼痛和偏头痛相关症状)(17.1%对4.4%;p < 0.05),且持续无疼痛(20.9%对9.0%;p < 0.05)。阿莫曲坦组7.1%的患者发生轻至中度不良事件,安慰剂组为5.1%(无统计学差异)。

结论

对于口服舒马曲坦反应不佳的偏头痛患者,阿莫曲坦在急性治疗中比安慰剂更有效,且耐受性相似。

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