Moore R Andrew, Derry Sheena, Moore Maura, 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):CD007548. doi: 10.1002/14651858.CD007548.pub2.
Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) used mainly in treating pain associated with arthritis. The usual oral dose for osteoarthritis is 1000 mg daily, and higher doses are not advised in older patients. There are no known systematic reviews of its analgesic efficacy in acute postoperative pain. This review sought to evaluate the efficacy and safety of oral nabumetone 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 whether drugs have analgesic properties.
To assess the efficacy of single dose oral nabumetone in acute postoperative pain, and any associated adverse events.
We searched The Cochrane Library (Issue 2, 2009), MEDLINE (May 2009); EMBASE via Ovid (May 2009); and the Oxford Pain Relief Database.
Randomised, double-blind, placebo-controlled clinical trials of oral nabumetone for relief of acute postoperative pain in adults.
Two review authors independently assessed trial quality and extracted data. The area under the "pain relief versus time" curve was used to derive the proportion of participants with nabumetone and placebo experiencing at least 50% pain relief over 4 to 6 hours, using validated equations. The number needed to treat to benefit (NNT) was calculated using 95% confidence intervals (CI). The proportion of participants using rescue analgesia over a specified time period, and time to use of rescue analgesia, were sought as additional measures of efficacy. Information on adverse events and withdrawals was also collected.
No studies were identified by the searches that examined oral nabumetone in participants with established postoperative pain.
AUTHORS' CONCLUSIONS: In the absence of evidence of efficacy, at present, for oral nabumetone 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.
萘丁美酮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1000毫克,老年患者不建议使用更高剂量。目前尚无关于其在急性术后疼痛中镇痛效果的系统评价。本综述旨在通过对已确诊疼痛患者的临床研究,并使用标准方法在主要6小时内测量结果,来评估口服萘丁美酮在急性术后疼痛中的疗效和安全性。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。
评估单剂量口服萘丁美酮在急性术后疼痛中的疗效以及任何相关不良事件。
我们检索了《考克兰系统评价数据库》(2009年第2期)、MEDLINE(2009年5月);通过Ovid检索EMBASE(2009年5月);以及牛津疼痛缓解数据库。
口服萘丁美酮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。使用经过验证的公式,通过“疼痛缓解与时间”曲线下面积来得出萘丁美酮组和安慰剂组在4至6小时内疼痛缓解至少50%的参与者比例。使用95%置信区间(CI)计算治疗获益所需人数(NNT)。作为疗效的额外衡量指标,还需找出在特定时间段内使用解救镇痛药的参与者比例以及使用解救镇痛药的时间。同时收集有关不良事件和退出试验的信息。
检索未发现研究口服萘丁美酮对已确诊术后疼痛患者的相关研究。
目前在急性术后疼痛中,由于缺乏口服萘丁美酮疗效的证据,其在该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,其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。