Hoernecke R, Doenicke A
Institut für Anästhesiologie, Ludwig-Maximilian-Universität.
Med Klin (Munich). 1993 Nov 15;88(11):642-8.
In a multi-center, double-blind, placebo-controlled crossover study safety and efficacy of oral dihydroergotamine tartrate (DHE) 2 mg, paracetamol 1000 mg, and a fixed combination of these two agents was compared for the relief of migraine attacks. The effect of the four different treatments on severity and duration of migraine headache was assessed pretreatment and at one and two hours post-treatment in the patient diary (10 point numerical rating scale 0 = no pain, 9 = unbearable pain). Nausea, vomiting, photophobia, phonophobia, and adverse events were also recorded in the patient diary.
For 288 patients (81% female, 19% male) of 474 enrolled the results of four consecutive migraine attacks could be evaluated; 186 patients were excluded from the analyses because of missing data or protocol violations. Compared with placebo, headache severity was significantly reduced after all three treatments at one and two hours and all three treatments resulted in statistically significant rapid relief of pain, proving a superior effect of the combination over the mono agents. Duration of headache was significantly shorter when the combination was taken and the number of patients having either no headache or a reduction of pain of more than 50% after one and two hours was bigger in the combination group. Eight adverse events were experienced in patients during placebo treatment, seven in patients during treatment with the fixed combination, five in patients during DHE treatment and two in patients during paracetamol treatment. All adverse events were transitory and none was serious.
The oral combination of 2 mg DHE and 1000 mg paracetamol is safe and effective in the treatment of acute migraine attacks and should be first choice of therapy in patients who do not respond to mild analgesics like paracetamol alone.
在一项多中心、双盲、安慰剂对照的交叉研究中,比较了口服2毫克酒石酸二氢麦角胺(DHE)、1000毫克对乙酰氨基酚以及这两种药物的固定组合对缓解偏头痛发作的安全性和有效性。在患者日记中,于治疗前以及治疗后1小时和2小时评估了四种不同治疗方法对偏头痛严重程度和持续时间的影响(采用10分数字评分量表,0 = 无疼痛,9 = 难以忍受的疼痛)。恶心、呕吐、畏光、畏声及不良事件也记录在患者日记中。
在纳入的474例患者中,288例(81%为女性,19%为男性)连续4次偏头痛发作的结果可进行评估;186例患者因数据缺失或违反方案被排除在分析之外。与安慰剂相比,所有三种治疗在1小时和2小时后头痛严重程度均显著降低,且所有三种治疗均导致疼痛快速缓解具有统计学意义,证明组合药物比单一药物效果更佳。服用组合药物时头痛持续时间显著缩短,且组合药物组在1小时和2小时后无头痛或疼痛减轻超过50%的患者数量更多。安慰剂治疗期间患者出现8例不良事件,固定组合治疗期间患者出现7例,DHE治疗期间患者出现5例,对乙酰氨基酚治疗期间患者出现2例。所有不良事件均为短暂性,无严重不良事件。
2毫克DHE与1000毫克对乙酰氨基酚的口服组合在治疗急性偏头痛发作时安全有效,对于单独使用对乙酰氨基酚等轻度镇痛药无反应的患者应作为首选治疗方法。