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舒马曲坦。对其药效学和药代动力学特性以及在偏头痛和丛集性头痛急性治疗中的疗效的综述。

Sumatriptan. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in the acute treatment of migraine and cluster headache.

作者信息

Dechant K L, Clissold S P

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 1992 May;43(5):776-98. doi: 10.2165/00003495-199243050-00010.

Abstract

Sumatriptan is a serotonin1 (5-HT1) receptor agonist, which is effective in the acute treatment of migraine headache. Its antimigraine activity is believed to derive from selective vasoconstriction of cranial blood vessels which are dilated and distended during migraine headache and/or from inhibition of neurogenically mediated inflammation in the dura mater. In placebo-controlled comparative studies, sumatriptan reduced migraine headache from 'moderate or severe' to 'mild or none' within 2 hours in 50 to 73% of patients following oral administration of 100 or 200 mg, and within 1 hour in 70 to 80% of patients following subcutaneous doses of 6 to 8 mg or intranasal doses 20 mg into each nostril. In addition, sumatriptan alleviated the accompanying symptoms of nausea, vomiting, and photophobia/phonophobia more effectively than placebo, and permitted higher percentages of patients to resume normal daily activities. Sumatriptan 100 mg orally was more effective in the acute treatment of migraine than oral combination therapy consisting of ergotamine 2 mg plus caffeine 200 mg or aspirin 900 mg plus metoclopramide 10 mg. Pooled data from nearly 5000 patients treated with either oral or subcutaneous sumatriptan in clinical trials indicate that it is well tolerated. However, migraine recurrence within 24 or 48 hours of initial symptom resolution developed in approximately 40% of patients treated with sumatriptan, irrespective of route of administration. It is likely that migraine recurrence is related to the short half-life of the drug (approximately 2 hours). Future studies should attempt to ascertain whether additional doses of sumatriptan will help prevent migraine recurrence in patients with attacks of long duration and if so, should determine the optimum interval between dosages. In conclusion, sumatriptan is an important addition to the range of drugs currently available for acute treatment of migraine. It provides rapid relief from debilitating symptoms in a high percentage of patients, particularly after subcutaneous administration. At this stage in its development a number of questions remain to be answered - most notably whether repeat doses will help prevent recurrent attacks and which patients are most likely to respond to therapy. Nevertheless, sumatriptan presently offers a combination of efficacy and tolerability that is unique in this particular clinical setting.

摘要

舒马曲坦是一种5-羟色胺1(5-HT1)受体激动剂,对偏头痛急性发作的治疗有效。其抗偏头痛活性被认为源于偏头痛发作时扩张和肿胀的颅血管的选择性血管收缩,和/或源于对硬脑膜中神经源性介导的炎症的抑制。在安慰剂对照的比较研究中,口服100或200mg后,50%至73%的患者在2小时内舒马曲坦使偏头痛从“中度或重度”减轻至“轻度或无”,皮下注射6至8mg或每侧鼻孔鼻内给药20mg后,70%至80%的患者在1小时内症状减轻。此外,舒马曲坦比安慰剂更有效地缓解了伴随的恶心、呕吐和畏光/畏声症状,并使更高比例的患者能够恢复正常的日常活动。口服100mg舒马曲坦在偏头痛急性治疗中比由2mg麦角胺加200mg咖啡因或900mg阿司匹林加10mg甲氧氯普胺组成的口服联合疗法更有效。临床试验中近5000例接受口服或皮下舒马曲坦治疗的患者的汇总数据表明其耐受性良好。然而,无论给药途径如何,在接受舒马曲坦治疗的患者中,约40%在初始症状缓解后的24或48小时内出现偏头痛复发。偏头痛复发可能与药物的短半衰期(约2小时)有关。未来的研究应试图确定额外剂量的舒马曲坦是否有助于预防长时间发作患者的偏头痛复发,如果是这样,应确定最佳给药间隔。总之,舒马曲坦是目前可用于偏头痛急性治疗的药物范围中的重要补充。它能使高比例的患者迅速缓解使人衰弱的症状,尤其是皮下给药后。在其研发的现阶段,仍有一些问题有待解答——最值得注意的是重复给药是否有助于预防复发发作以及哪些患者最可能对治疗有反应。尽管如此,舒马曲坦目前提供了在这一特定临床环境中独特的疗效和耐受性组合。

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