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Single dose oral meloxicam for acute postoperative pain in adults.

机译:单剂量口服美洛昔康治疗成人急性术后疼痛。

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摘要

BACKGROUND: 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. OBJECTIVES: To assess the efficacy of single dose oral meloxicam in acute postoperative pain, and any associated adverse events. SEARCH STRATEGY: We searched Cochrane CENTRAL (Issue 2, 2009), MEDLINE (June 2009); EMBASE (June 2009); the Oxford Pain Relief Database. SELECTION CRITERIA: Randomised, double-blind, placebo-controlled clinical trials of oral meloxicam for relief of acute postoperative pain in adults. DATA COLLECTION AND ANALYSIS: 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. MAIN RESULTS: 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.
机译:背景:美洛昔康是一种非甾体类抗炎药(NSAID),主要用于治疗与关节炎有关的疼痛。骨关节炎的常规口服剂量为每天15 mg,但老年患者建议降低剂量为7.5 mg。这篇综述旨在通过对已确诊疼痛的患者进行临床研究,评估口服美洛昔康在急性术后疼痛中的疗效和安全性,并使用标准方法在6个小时内对结果进行测量。这种类型的研究已经使用了数十年,以确定药物具有镇痛作用。目的:评估单剂量口服美洛昔康在急性术后疼痛和任何相关不良事件中的疗效。搜索策略:我们搜索了MEDLINE(2009年6月)的Cochrane CENTRAL(2009年第2期); EMBASE(2009年6月);牛津止痛数据库。选择标准:口服美洛昔康缓解成人急性术后疼痛的随机,双盲,安慰剂对照临床试验。数据收集与分析:两位评价作者独立评估了试验质量并提取了数据。我们计划使用经过验证的方程式,使用“疼痛缓解与时间”曲线下的面积,得出美洛昔康在4至6个小时内至少缓解50%疼痛的参与者的比例;使用需要治疗的号码才能受益(NNT);在指定时间内使用抢救镇痛的参与者比例;进行抢救性镇痛的时间;有关不良事件和停药的信息。主要结果:这项研究没有发现研究证实术后疼痛患者口服美洛昔康的研究。作者的结论:在尚无疗效证据的情况下,目前,口服美洛昔康可用于急性术后疼痛,尚无理由将其用于此适应症。由于缺乏在最基本的急性疼痛研究中明确显示镇痛功效的试验,因此应仔细评估在其他适应症中的使用。鉴于此类和类似类别的可用药物数量众多,因此没有紧迫的研究议程。

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