Carleton S C, Shesser R F, Pietrzak M P, Chudnofsky C R, Starkman S, Morris D L, Johnson G, Rhee K J, Barton C W, Chelly J E, Rosenberg J, Van Valen M K
Department of Emergency Medicine, University Hospital of Cincinnati, OH 45267-0769, USA.
Ann Emerg Med. 1998 Aug;32(2):129-38. doi: 10.1016/s0196-0644(98)70126-x.
To evaluate intramuscular dihydroergotamine in direct comparison with opioid analgesia in the treatment of acute migraine headache.
This was a prospective, multicenter, double-blind trial performed in the emergency departments of 11 general hospitals in the United States. One hundred seventy-one patients between the ages of 18 and 60 years who presented to the ED with acute migraine headache were enrolled. Patients were randomly assigned to receive either 1 mg dihydroergotamine (DHE) or 1.5 mg/kg meperidine (MEP) by intramuscular injection. The anti-nauseant hydroxyzine (H) was coadministered in both treatment groups.
One hundred fifty-six patients were evaluable. Treatment groups were comparable in sample size, demographics, and baseline measurements of headache pain. Reduction of headache pain as measured on a 100-mm visual analog scale was 41+/-33 mm (53.5% reduction) for the DHE group, and 45+/-30 mm (55.7% reduction) for the MEP group at 60 minutes after treatment (difference=2.2%; 95% confidence interval [CI] -10%, 14.5%; P=.81). Reduction in the severity of nausea and improvement in functional ability were similar between treatment groups. Central nervous system adverse events were less common in the DHE group (DHE 23.5% versus MEP 37.6%, difference-14.1%: 95% CI -28%, 0%). In particular, dizziness was reported less commonly with DHE than MEP (2% versus 15%, difference=-13%: 95% CI -21%, -5%).
In this prospective, double-blind trial of a convenience sample of ED patients randomly assigned to one of two treatment regimens, DHE and MEP were comparable therapies for acute migraine. The use of DHE avoids several problems associated with opioid analgesia, including dizziness.
直接比较肌内注射双氢麦角胺与阿片类镇痛药治疗急性偏头痛的效果。
这是一项在美国11家综合医院急诊科进行的前瞻性、多中心、双盲试验。纳入171例年龄在18至60岁之间因急性偏头痛到急诊科就诊的患者。患者被随机分配接受肌内注射1毫克双氢麦角胺(DHE)或1.5毫克/千克哌替啶(MEP)。两个治疗组均联合使用抗恶心药羟嗪(H)。
156例患者可进行评估。治疗组在样本量、人口统计学特征和头痛疼痛的基线测量方面具有可比性。治疗后60分钟,DHE组在100毫米视觉模拟量表上测得的头痛疼痛减轻程度为41±33毫米(减轻53.5%),MEP组为45±30毫米(减轻55.7%)(差异=2.2%;95%置信区间[CI] -10%,14.5%;P = 0.81)。治疗组之间恶心严重程度的降低和功能能力的改善相似。DHE组中枢神经系统不良事件较少见(DHE组为23.5%,MEP组为37.6%,差异=-14.1%:95% CI -28%,0%)。特别是,与MEP相比,DHE导致头晕的报告较少(2%对15%,差异=-13%:95% CI -21%,-5%)。
在这项对随机分配到两种治疗方案之一的急诊科患者便利样本进行前瞻性双盲试验中,DHE和MEP是治疗急性偏头痛的等效疗法。使用DHE可避免与阿片类镇痛相关的几个问题,包括头晕。