Freitag Fred, Diamond Merle, Diamond Seymour, Janssen Imke, Rodgers Anthony, Skobieranda Franck
Diamond Headache Clinic, Chicago, IL, USA.
Headache. 2008 Jun;48(6):921-30. doi: 10.1111/j.1526-4610.2007.01053.x.
To evaluate the efficacy and tolerability of coadministration of rizatriptan and acetaminophen in the acute treatment of migraine.
Rizatriptan is a selective 5-HT1B/1D agonist approved for the acute treatment of migraine. Acetaminophen has been studied for acute migraine treatment. In consideration of the prominent central and peripheral mechanisms in migraine, the use of "multi-mechanism therapy" is gaining momentum in the treatment of acute migraine attacks.
This was a randomized, double-blind, placebo-controlled trial conducted at 10 centers. Eligible patients with migraine according to International Headache Society criteria treated a single migraine attack of moderate or severe intensity within 4 h from pain onset. Patients were randomized into 1 of 4 groups (rizatriptan 10 mg + acetaminophen 1000 mg [RA], rizatriptan alone [R], acetaminophen alone [A], and placebo [P]). There were 3 co-primary hypotheses tested sequentially for 2-h pain relief: (1) RA would be superior to P; (2) if the first was fulfilled, RA would be superior to A; and (3) if the first 2 were fulfilled, RA would be superior to R.
Of 173 patients who treated a migraine, 123 patients (71.5%) achieved pain relief within 2 h. RA (90%) was significantly better than P (46%) and A (70%), but only numerically better than R (77%) for 2-h pain relief. No significant differences were seen between the active treatment groups in adverse events.
Rizatriptan coadministered with acetaminophen achieved 2 of the 3 primary hypotheses, proving superior to both acetaminophen and placebo for 2-h pain relief, but failing to achieve superiority to rizatriptan alone. RA was as well tolerated as each of the individual agents.
评估利扎曲普坦与对乙酰氨基酚联合用药在偏头痛急性治疗中的疗效和耐受性。
利扎曲普坦是一种选择性5-HT1B/1D激动剂,已被批准用于偏头痛的急性治疗。对乙酰氨基酚已被研究用于急性偏头痛治疗。鉴于偏头痛突出的中枢和外周机制,“多机制疗法”在急性偏头痛发作的治疗中越来越受到关注。
这是一项在10个中心进行的随机、双盲、安慰剂对照试验。符合国际头痛协会标准的偏头痛患者在疼痛发作后4小时内治疗单次中度或重度强度的偏头痛发作。患者被随机分为4组之一(利扎曲普坦10毫克 + 对乙酰氨基酚1000毫克 [RA组]、单用利扎曲普坦 [R组]、单用对乙酰氨基酚 [A组] 和安慰剂 [P组])。依次对2小时疼痛缓解情况测试3个共同主要假设:(1)RA组优于P组;(2)如果第一个假设成立,RA组优于A组;(3)如果前两个假设成立,RA组优于R组。
在173例治疗偏头痛的患者中,123例患者(71.5%)在2小时内实现疼痛缓解。RA组(90%)在2小时疼痛缓解方面显著优于P组(46%)和A组(70%),但仅在数值上优于R组(77%)。活性治疗组之间在不良事件方面未见显著差异。
利扎曲普坦与对乙酰氨基酚联合用药实现了3个主要假设中的2个,证明在2小时疼痛缓解方面优于对乙酰氨基酚和安慰剂,但未优于单用利扎曲普坦。RA组的耐受性与各单药相当。