Medical Affairs and Clinical Research, McNeil Consumer Healthcare, Fort Washington, PA 19034, USA.
Headache. 2010 May;50(5):819-33. doi: 10.1111/j.1526-4610.2010.01638.x. Epub 2010 Mar 5.
To evaluate the efficacy and safety of acetaminophen 1000 mg for the treatment of episodic migraine headache.
While acetaminophen is commonly used to treat migraine, there have been limited published clinical trial efficacy results.
DESIGN/METHODS: Ten investigators at 13 private, ambulatory, primary care sites in the United States enrolled and treated 346 outpatient adults 18-72 years of age with migraine headache of moderate to severe intensity into a randomized, placebo-controlled, double-blind clinical trial of 6 hours duration. Each patient was randomly assigned to a single dose of study medication of acetaminophen 1000 mg (n = 177) or placebo (n = 169). The percentage of patients with a reduction in baseline headache pain intensity from severe or moderate to mild or none 2 hours after treatment and the headache pain intensity difference from baseline at 2 hours were the primary efficacy measures. Other measures of pain relief, severity differences from baseline for migraine-associated symptoms of nausea, photophobia, phonophobia, and functional disability, and percentage of patients with migraine-associated symptoms reduced to none were also assessed.
Significantly (P = .001) more patients treated with acetaminophen 1000 mg reported mild to no pain after 2 hours (52.0%) compared with those treated with placebo (32.0%). The mean pain intensity difference from baseline measured at 2 hours was significantly (P < .001) greater for patients treated with acetaminophen 1000 mg (0.82) compared with those treated with placebo (0.46). A significant difference in favor of acetaminophen 1000 mg over placebo was also observed at 1 hour after treatment for the percentage of patients with mild to no pain and for mean pain intensity difference from baseline. Acetaminophen 1000 mg was significantly more effective than placebo for all but 1 (pain reduced to none at 2 hours) clinically important secondary pain relief outcomes. Mean severity changes from baseline in migraine-associated symptoms of nausea, photophobia, phonophobia, and functional disability at 2 and 6 hours were significantly (P < .001) in favor of acetaminophen over placebo; the percentage of patients with no symptoms at 2 and 6 hours statistically significantly favored acetaminophen in 6 of 8 comparisons. Adverse events, overall, and specifically for nausea, were reported more frequently in the placebo group.
Acetaminophen 1000 mg, a nonprescription drug, is an effective and well-tolerated treatment for episodic and moderate migraine headache. In addition, acetaminophen generally provided a beneficial effect on associated symptoms of migraine including nausea, photophobia, phonophobia, and functional disability.
评估对乙酰氨基酚 1000 毫克治疗发作性偏头痛的疗效和安全性。
虽然对乙酰氨基酚常用于治疗偏头痛,但已发表的临床疗效结果有限。
设计/方法:美国 13 个私人、门诊、初级保健地点的 10 名调查员招募并治疗了 346 名年龄在 18-72 岁之间、偏头痛程度为中度至重度的门诊成年人,他们参加了一项为期 6 小时的随机、安慰剂对照、双盲临床试验。每位患者随机接受单次剂量的研究药物对乙酰氨基酚 1000 毫克(n=177)或安慰剂(n=169)。治疗后 2 小时时基线头痛疼痛强度从重度或中度减轻至轻度或无的患者比例以及 2 小时时与基线相比的头痛疼痛强度差异是主要疗效指标。还评估了其他疼痛缓解措施、偏头痛相关症状(恶心、畏光、畏声和功能障碍)的严重程度差异以及偏头痛相关症状减轻至无的患者比例。
接受对乙酰氨基酚 1000 毫克治疗的患者在 2 小时后报告轻度至无疼痛的比例显著(P=0.001)高于接受安慰剂治疗的患者(52.0% vs. 32.0%)。在 2 小时时,与接受安慰剂治疗的患者相比,接受对乙酰氨基酚 1000 毫克治疗的患者的平均疼痛强度从基线的差异显著(P<.001)更大(0.82 对 0.46)。在治疗后 1 小时,接受对乙酰氨基酚 1000 毫克治疗的患者的轻度至无疼痛的比例和与基线相比的平均疼痛强度差异也有显著的优势(P<.001)。在除 1 项(2 小时时疼痛减轻至无)外的所有具有临床意义的次要疼痛缓解结果中,对乙酰氨基酚 1000 毫克的疗效均显著优于安慰剂。在 2 和 6 小时时,与基线相比,偏头痛相关症状(恶心、畏光、畏声和功能障碍)的严重程度变化均值显著(P<.001)有利于对乙酰氨基酚,在 8 项比较中有 6 项在 2 和 6 小时时接受对乙酰氨基酚治疗的患者无症状的比例具有统计学意义。总的来说,在安慰剂组中,不良反应的报告频率更高,特别是恶心。
非处方药物对乙酰氨基酚 1000 毫克是治疗发作性和中度偏头痛头痛的有效且耐受性良好的治疗方法。此外,对乙酰氨基酚通常对偏头痛的相关症状(包括恶心、畏光、畏声和功能障碍)有有益的影响。