Moore R Andrew, Derry Sheena, McQuay Henry J
Pain Research and Nuffield Department of Anaesthetics, University of Oxford, West Wing (Level 6), John Radcliffe Hospital, Oxford, Oxfordshire, UK, OX3 9DU.
Cochrane Database Syst Rev. 2009 Oct 7;2009(4):CD007552. doi: 10.1002/14651858.CD007552.pub2.
Meloxicam is a non-steroidal anti-inflammatory drug (NSAID) used mainly in treating pain associated with arthritis. The usual oral dose for osteoarthritis is 15 mg daily, but lower doses of 7.5 mg are advised in older patients. This review sought to evaluate the efficacy and safety of oral meloxicam in acute postoperative pain, using clinical studies of patients with established pain, and with outcomes measured primarily over 6 hours using standard methods. This type of study has been used for many decades to establish that drugs have analgesic properties.
To assess the efficacy of single dose oral meloxicam in acute postoperative pain, and any associated adverse events.
We searched Cochrane CENTRAL (Issue 2, 2009), MEDLINE (June 2009); EMBASE (June 2009); the Oxford Pain Relief Database.
Randomised, double-blind, placebo-controlled clinical trials of oral meloxicam for relief of acute postoperative pain in adults.
Two review authors independently assessed trial quality and extracted data. We planned to use area under the "pain relief versus time" curve to derive the proportion of participants with meloxicam experiencing least 50% pain relief over 4 to 6 hours, using validated equations; to use number needed to treat to benefit (NNT); the proportion of participants using rescue analgesia over a specified time period; time to use of rescue analgesia; information on adverse events and withdrawals.
No studies were identified by the searches that examined oral meloxicam in patients with established postoperative pain.
AUTHORS' CONCLUSIONS: In the absence of evidence of efficacy, at present, for oral meloxicam in acute postoperative pain, its use in this indication is not justified. Because trials clearly demonstrating analgesic efficacy in the most basic of acute pain studies is lacking, use in other indications should be evaluated carefully. Given the large number of available drugs of this and similar classes, there is no urgent research agenda.
美洛昔康是一种非甾体抗炎药(NSAID),主要用于治疗与关节炎相关的疼痛。骨关节炎的常规口服剂量为每日15毫克,但老年患者建议使用7.5毫克的较低剂量。本综述旨在通过对已确诊疼痛患者的临床研究,并使用标准方法主要在6小时内测量结果,评估口服美洛昔康治疗急性术后疼痛的疗效和安全性。这种类型的研究已经使用了几十年,以确定药物是否具有镇痛特性。
评估单剂量口服美洛昔康治疗急性术后疼痛的疗效以及任何相关不良事件。
我们检索了Cochrane中心对照试验注册库(2009年第2期)、MEDLINE(2009年6月)、EMBASE(2009年6月)以及牛津疼痛缓解数据库。
口服美洛昔康用于缓解成人急性术后疼痛的随机、双盲、安慰剂对照临床试验。
两位综述作者独立评估试验质量并提取数据。我们计划使用“疼痛缓解与时间”曲线下面积,通过验证方程得出服用美洛昔康的参与者在4至6小时内疼痛缓解至少50%的比例;使用需治疗获益人数(NNT);特定时间段内使用解救镇痛药的参与者比例;使用解救镇痛药的时间;不良事件和退出试验的信息。
检索未发现研究口服美洛昔康用于已确诊术后疼痛患者的相关研究。
目前,由于缺乏口服美洛昔康治疗急性术后疼痛疗效的证据,其在此适应症中的使用不合理。由于缺乏在最基本的急性疼痛研究中明确证明镇痛疗效的试验,在其他适应症中的使用应谨慎评估。鉴于此类及类似类别的可用药物众多,目前没有紧迫的研究议程。