Crossover comparison of efficacy and preference for rizatriptan 10 mg versus ergotamine/caffeine in migraine

被引:39
作者
Christie, S
Göbel, H
Mateos, V
Allen, C
Vrijens, F
Shivaprakash, M
机构
[1] Merck & Co Inc, Dept WS3C 90, Whitehouse Stn, NJ 08889 USA
[2] Ottawa Headache Ctr, Ottawa, ON, Canada
[3] Univ Kiel, Kiel Pain Clin, Kiel, Germany
[4] Ctr Hosp Asturias, Dept Neurol, Oviedo, Spain
[5] Merck Sharp & Dohme Europe, Brussels, Belgium
关键词
rizatriptan; ergotamine; efficacy; preference; migraine;
D O I
10.1159/000067018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rizatriptan is a selective 5-HT1B/1D receptor agonist with rapid oral absorption and early onset of action in the acute treatment of migraine. This randomized double-blind crossover outpatient study assessed the preference for 1 rizatriptan 10 mg tablet to 2 ergotamine 1 mg/caffeine 100 mg tablets in 439 patients treating a single migraine attack with each therapy. Of patients expressing a preference (89.1%), more than twice as many preferred rizatriptan to ergotamine/caffeine (69.9 vs. 30.1%, p ≤ 0.001). Faster relief of headache was the most important reason for preference, cited by 67.3% of patients preferring rizatriptan and 54.2% of patients who preferred ergotamine/caffeine. The co-primary endpoint of being pain free at 2 h was also in favor of rizatriptan. Forty-nine percent of patients were pain free 2 h after rizatriptan, compared with 24.3% treated with ergotamine/caffeine (p ≤ 0.001), rizatriptan being superior within 1 h of treatment. Headache relief at 2 h was 75.9% for rizatriptan and 47.3% for ergotamine/caffeine (p ≤ 0.001), with rizatriptan being superior to ergotamine/caffeine within 30 min of dosing. Almost 36% of patients taking rizatriptan were pain free at 2 h and had no recurrence or need for additional medication within 24 h, compared to 20% of patients on ergotamine/caffeine (p ≤ 0.001). Rizatriptan was also superior to ergotamine/caffeine in the proportions of patients with no nausea, vomiting, phonophobia or photophobia and for patients with normal function 2 h after drug intake (p ≤ 0.001). More patients were (completely, very or somewhat) satisfied 2 h after treatment with rizatriptan (69.8%) than at 2 h after treatment with ergotamine/caffeine (38.6%, p ≤ 0.001). Recurrence rates were 31.4% with rizatriptan and 15.3% with ergotamine/caffeine. Both active treatments were well tolerated. The most common adverse events (incidence ≥ 5% in one group) after rizatriptan and ergotamine/caffeine, respectively, were dizziness (6.7 and 5.3%), nausea (4.2 and 8.5%) and somnolence (5.5 and 2.3%). Copyright © 2003 S. Karger AG, Basel.
引用
收藏
页码:20 / 29
页数:10
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