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首页> 外文期刊>Headache >Comparative study of a combination of isometheptene mucate, dichloralphenazone with acetaminophen and sumatriptan succinate in the treatment of migraine.
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Comparative study of a combination of isometheptene mucate, dichloralphenazone with acetaminophen and sumatriptan succinate in the treatment of migraine.

机译:异丁烯酸甲酯,双氯酚a与对乙酰氨基酚和琥珀酸舒马曲坦联合治疗偏头痛的比较研究。

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OBJECTIVE: To compare the safety and efficacy of isometheptene mucate, dichloralphenazone with acetaminophen to sumatriptan succinate for the treatment of mild-to-moderate migraine, with or without aura, when taken at the first sign of an attack. BACKGROUND: The Food and Drug Administration approved sumatriptan succinate and the combination of isometheptene mucate, dichloralphenazone with acetaminophen for the treatment of migraine. As part of the stratified treatment of migraine, those patients whose headaches are mild or moderate may benefit from nontriptan medications. Additionally, early treatment of acute migraine before the headache has become moderate or severe may improve response to treatment. METHODS: This was a multicenter, double-blind, randomized, parallel-group study to assess the safety and efficacy of the combination of isometheptene mucate, dichloralphenazone with acetaminophen and sumatriptan succinate in the early stages of a single migraine attack. Patients diagnosed with migraine, with or without aura, as defined by the International Headache Society diagnostic criteria were enrolled. RESULTS: One hundred thirty-seven patients were enrolled in the study. Data for efficacy were available for 126 patients; safety data were available for 128 patients. No statistically significant difference between the two active agents in the patient's response to treatment was demonstrated. Headache recurrence was not significantly different over the 24-hour evaluation period for those patients responding in the first 4 hours. In those with headache recurrence, it was statistically significantly more severe in those patients treated with sumatriptan succinate. Improvement in functional disability was, in general, better among those treated with isometheptene mucate, dichloralphenazone with acetaminophen. Global analysis of efficacy was similar in the two active groups. Patients treated with sumatriptan succinate were somewhat more likely to have adverse effects than the isometheptene mucate, dichloralphenazone with acetaminophen group. CONCLUSIONS: Both isometheptene mucate, dichloralphenazone with acetaminophen and sumatriptan succinate are safe and effective when used early in the treatment of an acute migraine. Several parameters suggest that isometheptene mucate, dichloralphenazone with acetaminophen may have a slight advantage compared with sumatriptan succinate in the early treatment of mild-to-moderate migraine.
机译:目的:比较在发作的第一个症状时服用异丁烯酸双甲酚,双氯苯甲酰胺和对乙酰氨基酚与琥珀酸舒马曲坦的安全性和有效性,以治疗轻度至中度偏头痛(有或没有先兆)。背景:美国食品药品监督管理局(FDA)批准了舒马曲坦琥珀酸酯和异丁烯酸酯,双氯苯乙酮与对乙酰氨基酚的组合治疗偏头痛。作为偏头痛分层治疗的一部分,那些轻度或中度头痛的患者可能会受益于非曲普坦药物。此外,在头痛变得中度或重度之前对急性偏头痛进行早期治疗可能会改善对治疗的反应。方法:这是一项多中心,双盲,随机,平行分组的研究,旨在评估单偏头痛发作初期异丁烯酸甲酯,双氯酚a与对乙酰氨基酚和琥珀酸舒马曲坦联合使用的安全性和有效性。纳入根据国际头痛学会诊断标准定义的诊断为偏头痛,有无先兆的患者。结果:137例患者被纳入研究。已有126例患者的疗效数据;现有128位患者的安全性数据。在患者对治疗的反应中,两种活性剂之间没有统计学上的显着差异。对于在最初4小时内有反应的那些患者,在24小时评估期内头痛复发没有显着差异。在患有头痛复发的患者中,舒马曲坦琥珀酸盐治疗的患者在统计学上更为严重。通常,在异丁烯酸酯,双氯酚a和对乙酰氨基酚治疗的患者中,功能障碍的改善更好。总体疗效分析在两个活动组中相似。琥珀酸舒马曲坦治疗的患者比异对甲基粘液,对乙酰氨基酚组的二氯苯乙酮更可能产生不良反应。结论:早期用于治疗急性偏头痛时,异丁烯酸甲酯,双氯酚phen和对乙酰氨基酚以及舒马曲坦琥珀酸酯都是安全有效的。有几个参数表明,在舒缓中偏头痛的早期治疗中,与异舒马普坦琥珀酸盐相比,异丁烯酸甲酯,对乙酰氨基酚的双氯酚phen可能具有轻微的优势。

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