Bousser M G, D'Allens H, Richard A
Saint-Antoine Hospital, Paris, France.
J Intern Med. 1993 Aug;234(2):211-6. doi: 10.1111/j.1365-2796.1993.tb00732.x.
To evaluate the efficacy of self-administered subcutaneous sumatriptan in the acute treatment of early-morning migraine attacks.
A double-blind, randomized, placebo-controlled, cross-over study.
Thirteen neurology centres in France.
Patients of either sex, 18-65 years old, with two to six attacks of migraine (according to the International Headache Society (IHS) criteria, with or without aura) per month, of which at least two had to be early-morning migraine attacks. One-hundred-and-one patients were included, 96 being evaluable for the first attack and 81 for the cross-over design.
Two migraine attacks (grade 2/3) were treated with sumatriptan (6 mg) or placebo, with an optional second injection 1-24 h later. Main outcome measures. The primary end-point was headache relief: reduction in headache severity from grade 2/3 (moderate/severe) to grade 1/0 (mild/none) 2 h after treatment.
Sumatriptan was superior to placebo for headache relief (32 [78%] vs. 11 [28%] at the first attack; 29 [73%] vs. 8 [20%] at the second; P < 0.001). Because of a significant carry-over effect for some of the secondary end-points, a parallel-group analysis of the first attack was performed, which confirmed a significantly higher efficacy of sumatriptan for all end-points: pain-free rate (22 [46%] vs. 7 [15%]; P = 0.001) and use of a second injection (26 [53%] vs. 38 [81%]; P = 0.004). Sumatriptan was preferred by 74% of patients vs. 17% for placebo, and 9% expressed no preference (P < 0.0001). After complete relief, headache reappeared in 8/23 (35%) patients with sumatriptan and 3/7 (43%) with placebo. Adverse events were significantly more frequent with sumatriptan but they were minor and transient.
Subcutaneous sumatriptan auto-injection is an effective and well-tolerated acute treatment of early-morning migraine attacks allowing earlier return to normal activity.
评估自行皮下注射舒马曲坦治疗清晨偏头痛发作的急性疗效。
双盲、随机、安慰剂对照、交叉研究。
法国的13个神经科中心。
年龄在18 - 65岁之间的男女患者,每月有2 - 6次偏头痛发作(根据国际头痛协会(IHS)标准,有或无先兆),其中至少2次为清晨偏头痛发作。共纳入101例患者,96例可对首次发作进行评估,81例可用于交叉设计评估。
两次偏头痛发作(2/3级)分别用舒马曲坦(6毫克)或安慰剂治疗,1 - 24小时后可选择再次注射。主要结局指标。主要终点是头痛缓解:治疗2小时后头痛严重程度从2/3级(中度/重度)降至1/0级(轻度/无)。
舒马曲坦在缓解头痛方面优于安慰剂(首次发作时为32例[78%]对11例[28%];第二次发作时为29例[73%]对8例[20%];P < 0.001)。由于某些次要终点存在显著的残留效应,因此对首次发作进行了平行组分析,结果证实舒马曲坦在所有终点上的疗效均显著更高:无痛率(22例[46%]对7例[15%];P = 0.001)和再次注射的使用率(26例[53%]对38例[81%];P = 0.004)。74%的患者更喜欢舒马曲坦,而喜欢安慰剂的患者为17%,9%表示无偏好(P < 0.0001)。完全缓解后,8/23(35%)接受舒马曲坦治疗的患者头痛复发,3/7(43%)接受安慰剂治疗的患者头痛复发。舒马曲坦的不良事件明显更频繁,但均为轻微且短暂的。
皮下注射舒马曲坦自动注射器是治疗清晨偏头痛发作的一种有效且耐受性良好的急性治疗方法,可使患者更早恢复正常活动。