Rabbie Roy, Derry Sheena, Moore R Andrew, McQuay Henry J
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford, UK, OX1 3QT.
Cochrane Database Syst Rev. 2010 Oct 6(10):CD008039. doi: 10.1002/14651858.CD008039.pub2.
Migraine is a common, disabling condition and a burden for the individual, health services and society. Many sufferers do not seek professional help, relying instead on over-the-counter analgesics. Co-therapy with an antiemetic should help to reduce symptoms commonly associated with migraine headaches.
To determine efficacy and tolerability of ibuprofen, alone or in combination with an antiemetic, compared to placebo and other active interventions in the treatment of acute migraine headaches in adults.
We searched Cochrane CENTRAL, MEDLINE, EMBASE and the Oxford Pain Relief Database for studies through 22 April 2010.
We included randomised, double-blind, placebo- or active-controlled studies using self-administered ibuprofen to treat a migraine headache episode, with at least 10 participants per treatment arm.
Two review authors independently assessed trial quality and extracted data. Numbers of participants achieving each outcome were used to calculate relative risk and number needed to treat (NNT) or harm (NNH) compared to placebo or other active treatment.
Nine studies (4373 participants, 5223 attacks) compared ibuprofen with placebo or other active comparators; none combined ibuprofen with a self-administered antiemetic. All studies treated attacks with single doses of medication. For ibuprofen 400 mg versus placebo, NNTs for 2-hour pain-free (26% versus 12% with placebo), 2-hour headache relief (57% versus 25%) and 24-hour sustained headache relief (45% versus 19%) were 7.2, 3.2 and 4.0, respectively. For ibuprofen 200 mg versus placebo, NNTs for 2-hour pain-free (20% versus 10%) and 2-hour headache relief (52% versus 37%) were 9.7 and 6.3, respectively. The higher dose was significantly better for 2-hour headache relief than the lower dose. Soluble formulations of ibuprofen 400 mg were better than standard tablets for 1-hour, but not 2-hour headache relief.Associated symptoms of nausea, vomiting, photophobia and phonophobia and functional disability were reduced within 2 hours, and fewer participants used rescue medication with ibuprofen compared with placebo. Similar numbers of participants experienced adverse events, which were mostly mild and transient.Ibuprofen 400 mg did not differ from rofecoxib 25 mg for 2-hour headache relief, 24-hour headache relief or use of rescue medication.
AUTHORS' CONCLUSIONS: Ibuprofen is an effective treatment for acute migraine headaches, providing pain relief in about half of sufferers, but complete relief from pain and associated symptoms for only a minority. NNTs for all efficacy outcomes were better with 400 mg than 200 mg in comparisons with placebo, and soluble formulations provided more rapid relief. Adverse events were mostly mild and transient, occurring at the same rate as with placebo.
偏头痛是一种常见的致残性疾病,给个人、医疗服务机构和社会带来负担。许多患者不寻求专业帮助,而是依赖非处方镇痛药。联合使用止吐药应有助于减轻与偏头痛相关的常见症状。
比较布洛芬单独使用或与止吐药联合使用与安慰剂及其他活性干预措施在治疗成人急性偏头痛方面的疗效和耐受性。
我们检索了考克兰中心对照试验注册库、医学期刊数据库、荷兰医学文摘数据库以及牛津止痛数据库,检索截至2010年4月22日的研究。
我们纳入了随机、双盲、安慰剂对照或活性药物对照研究,这些研究使用自行服用的布洛芬治疗偏头痛发作,每个治疗组至少有10名参与者。
两名综述作者独立评估试验质量并提取数据。与安慰剂或其他活性治疗相比,达到各结局的参与者数量用于计算相对危险度以及治疗所需人数(NNT)或伤害所需人数(NNH)。
九项研究(4373名参与者,5223次发作)比较了布洛芬与安慰剂或其他活性对照药;没有研究将布洛芬与自行服用的止吐药联合使用。所有研究均采用单剂量药物治疗发作。对于400毫克布洛芬与安慰剂相比,2小时无痛(26%对安慰剂组的12%)、2小时头痛缓解(57%对25%)和24小时持续头痛缓解(45%对19%)的NNT分别为7.2、3.2和4.0。对于200毫克布洛芬与安慰剂相比,2小时无痛(20%对10%)和2小时头痛缓解(52%对37%)的NNT分别为9.7和6.3。较高剂量在2小时头痛缓解方面明显优于较低剂量。400毫克布洛芬的可溶性制剂在1小时头痛缓解方面优于标准片剂,但在2小时头痛缓解方面并非如此。恶心、呕吐、畏光和畏声等相关症状以及功能障碍在2小时内减轻,与安慰剂相比,使用布洛芬的参与者使用急救药物的较少。经历不良事件的参与者数量相似,不良事件大多为轻度且短暂。40(此处原文有误,应为400)毫克布洛芬在2小时头痛缓解、24小时头痛缓解或使用急救药物方面与25毫克罗非昔布无差异。
布洛芬是治疗急性偏头痛的有效药物,约半数患者疼痛得到缓解,但只有少数患者疼痛及相关症状完全缓解。与安慰剂相比,400毫克布洛芬在所有疗效结局方面的NNT均优于200毫克,可溶性制剂缓解更快。不良事件大多为轻度且短暂,发生率与安慰剂相同。