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首页> 外文期刊>Clinical therapeutics >Migraine treatment outcomes with rizatriptan in triptan-naive patients: a naturalistic study.
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Migraine treatment outcomes with rizatriptan in triptan-naive patients: a naturalistic study.

机译:利扎曲普坦初治患者的偏头痛治疗结果:一项自然研究。

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摘要

BACKGROUND: The 5-hydroxytryptamine(1B/1D) agonists, or triptans, are the newest class of drugs to become available for the acute treatment of migraine. The class currently includes sumatriptan, zolmitriptan, naratriptan, and rizatriptan. The efficacy of rizatriptan in the acute treatment of migraine has been established against placebo and other oral triptans in controlled comparative trials. OBJECTIVE: The US Migraine Assessment Protocol (USMAP) collected data on the use of rizatriptan in a naturalistic setting reflecting clinical practice. This paper presents results for patients enrolled in the USMAP study who had never taken a triptan before the study. METHODS: At enrollment, 216 patients completed a questionnaire describing their responses to their current nontriptan medications. They were then given specially packaged samples of 4 standard 10-mg rizatriptan tablets and 4 orally disintegrating 10-mg rizatriptan tablets (wafers) and were asked to take a different formulation for each of their next 2 attacks, the sequence to be at their discretion. Within approximately 24 hours after taking rizatriptan, patients were to call a toll-free number to report their responses to rizatriptan using an interactive voice-response system. RESULTS: Within 2 hours after initial dosing of rizatriptan, significantly more patients taking either the rizatriptan tablet or the rizatriptan wafer reported onset of pain relief, had become largely symptom free, and were able to resume usual activities compared with their baseline responses to nontriptans (P < 0.05). In addition, compared with their baseline responses to nontriptans, significantly more patients taking either rizatriptan formulation had mild or no pain 2 hours after dosing (P < 0.05). More than twice as many patients taking the rizatriptan tablets or wafers were either somewhat or very satisfied with the medication compared with their satisfaction with nontriptans (P < 0.05). CONCLUSIONS: In the naturalistic setting of this study, migraineurs who had not previously taken a triptan medication reported more rapid relief of pain, more effective pain relief, and more rapid resumption of normal activities when taking rizatriptan tablets or wafers than when taking a nontriptan medication. Patients dissatisfied with their current nontriptan migraine therapy may benefit from treatment with rizatriptan.
机译:背景:5-羟基色胺(1B / 1D)激动剂或曲普坦是用于偏头痛急性治疗的最新一类药物。该类目前包括舒马曲坦,佐米曲普坦,纳拉曲普坦和利扎曲普坦。在对照比较试验中,已经确定了利扎曲普坦对偏头痛的急性治疗的功效,以对抗安慰剂和其他口服曲普坦。目的:美国偏头痛评估协议(USMAP)收集了利扎曲普坦在自然环境中使用的数据,反映了临床实践。本文介绍了参加USMAP研究的患者的结果,这些患者在研究之前从未服用曲普坦。方法:入组时,有216名患者完成了一份问卷,描述了他们对当前非曲坦类药物的反应。然后,给他们特别包装的4种标准10 mg利扎曲普坦片剂和4种口服崩解性10 mg利扎曲坦片剂(晶圆)的包装样品,并要求他们在接下来的2次发作中分别采取不同的配方,具体顺序由他们自行决定。服用利扎曲普坦后约24小时内,患者将拨打免费电话,以使用交互式语音应答系统报告对利扎曲普坦的反应。结果:首次服用利扎曲普坦后2小时内,服用利扎曲普坦片或利扎曲普坦薄饼的患者报告称疼痛缓解发作明显增加,基本上没有症状,并且与非曲坦类药物的基线反应相比,能够恢复正常活动( P <0.05)。此外,与非曲坦类药物的基线反应相比,服用利扎曲普坦制剂的患者在给药后2小时有轻度疼痛或无疼痛(P <0.05)。与对非曲普坦类药物的满意度相比,服用利扎曲普坦片剂或威化片的患者对药物的某种程度或非常满意的满意度高出两倍以上(P <0.05)。结论:在本研究的自然主义背景下,以前未服用曲普坦药物的偏头痛患者报告说,服用利扎曲坦片剂或威化饼比使用非曲坦药物更能迅速缓解疼痛,更有效地缓解疼痛并能更快地恢复正常活动。对当前非曲普坦偏头痛治疗不满意的患者可从利扎曲普坦治疗中受益。

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