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舒马曲坦鼻喷雾剂治疗偏头痛的多次给药疗效及耐受性

Multiple-attack efficacy and tolerability of sumatriptan nasal spray in the treatment of migraine.

作者信息

Diamond S, Elkind A, Jackson R T, Ryan R, DeBussey S, Asgharnejad M

机构信息

Diamond Headache Clinic, Chicago, Ill 60614, USA.

出版信息

Arch Fam Med. 1998 May-Jun;7(3):234-40. doi: 10.1001/archfami.7.3.234.

Abstract

OBJECTIVE

Sumatriptan hemisulfate nasal spray may provide a useful therapeutic option for patients with migraine who find injectable medications inconvenient or uncomfortable and for patients whose migraine-associated nausea and vomiting preclude the use of oral medication. This study was the first US trial to evaluate the effects of sumatriptan nasal spray administered for multiple migraine attacks.

DESIGN/INTERVENTIONS: Sumatriptan nasal spray (5, 10, or 20 mg) was administered via a 1-shot nasal applicator into either nostril for up to 3 migraine attacks occurring over 6 months in a randomized, double-blind, parallel-group, placebo-controlled study.

SETTING

Fifty-six outpatient clinical centers in the United States.

PATIENTS

A total of 1086 men and women diagnosed with migraine with or without aura per International Headache Society criteria.

MAIN OUTCOME MEASURES

Percentage of patients with headache relief (moderate or severe predose pain reduced to mild or none); percentage of patients with no or mild (vs moderate or severe) clinical disability; percentage of patients with nausea, vomiting, photophobia, or phonophobia; adverse events; clinical laboratory test results.

RESULTS

Across attacks, headache relief in the 20-, 10-, and 5-mg drug and placebo groups was experienced 120 minutes postdose by 60%, 54%, 44%, and 32% of patients, respectively (P<.05 for each sumatriptan nasal spray group vs placebo, for the 10-mg vs 5-mg drug group, and for the 20-mg vs 5-mg drug group). Two thirds of the 20-mg patients treating 3 attacks experienced relief at 2 hours postdose for at least 2 of 3 attacks. Clinical disability scores at 120 minutes in the 20-, 10-, and 5-mg drug and placebo groups reflected no or mild impairment in 70%, 67%, 57%, and 50% of patients, respectively (P<.05 for the 10- or 20-mg drug group vs placebo group, and for the 20-mg vs 5- mg drug group). Similar efficacy rates were observed for nausea, photophobia, and phonophobia. For all parameters, individual-attack efficacy rates did not differ from across-attack rates. The incidence of adverse events was not dose related. The most frequently reported adverse event in the active treatment groups was taste disturbance (bad, bitter, or unpleasant).

CONCLUSIONS

Sumatriptan hemisulfate nasal spray (5, 10, or 20 mg) is effective and well tolerated in the treatment of multiple migraine attacks. The 20-mg dose was associated with the highest efficacy rates across the greatest number of parameters.

摘要

目的

对于那些觉得注射药物不方便或不舒适的偏头痛患者,以及那些偏头痛伴发恶心和呕吐而无法使用口服药物的患者,半硫酸舒马曲坦鼻喷雾剂可能提供一种有效的治疗选择。本研究是美国首个评估半硫酸舒马曲坦鼻喷雾剂用于多次偏头痛发作的疗效的试验。

设计/干预措施:在一项随机、双盲、平行组、安慰剂对照研究中,通过单次鼻腔给药器将半硫酸舒马曲坦鼻喷雾剂(5、10或20毫克)喷入任一鼻孔,用于治疗6个月内发生的多达3次偏头痛发作。

地点

美国56个门诊临床中心。

患者

总共1086名男性和女性,根据国际头痛协会标准被诊断为有或无先兆偏头痛。

主要观察指标

头痛缓解的患者百分比(中度或重度给药前疼痛减轻至轻度或无疼痛);无临床残疾或轻度(与中度或重度相比)临床残疾的患者百分比;有恶心、呕吐、畏光或畏声的患者百分比;不良事件;临床实验室检查结果。

结果

在各次发作中,20毫克、10毫克、5毫克药物组和安慰剂组分别有60%、54%、44%和32%的患者在给药后120分钟头痛缓解(各舒马曲坦鼻喷雾剂组与安慰剂组相比、10毫克药物组与5毫克药物组相比、20毫克药物组与5毫克药物组相比,P<0.05)。接受20毫克剂量治疗3次发作的患者中有三分之二在给药后2小时至少有2次发作得到缓解。20毫克、10毫克、5毫克药物组和安慰剂组在120分钟时的临床残疾评分分别显示70%、67%、57%和50%的患者无或轻度受损(10毫克或20毫克药物组与安慰剂组相比、20毫克药物组与5毫克药物组相比,P<0.05)。在恶心、畏光和畏声方面观察到相似的有效率。对于所有参数,单次发作的有效率与各次发作的有效率无差异。不良事件的发生率与剂量无关。活性治疗组中最常报告的不良事件是味觉障碍(不良、苦味或不愉快)。

结论

半硫酸舒马曲坦鼻喷雾剂(5、10或20毫克)在治疗多次偏头痛发作时有效且耐受性良好。20毫克剂量在最多参数方面的有效率最高。

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