Abramson Steven B, Greenberg Jeffrey D
New York University Hospital for Joint Diseases, New York, NY, USA.
Nat Clin Pract Rheumatol. 2008 Apr;4(4):182-3. doi: 10.1038/ncprheum0763. Epub 2008 Feb 19.
Scott et al. conducted a systematic review to evaluate the risk of myocardial infarction (MI) associated with cyclo-oxygenase-2 (COX2) inhibitors and traditional NSAIDs. The review found a small increased risk of MI associated with COX2 inhibitors, particularly rofecoxib. Although a fixed-effects model of 14 case-control studies suggested a slightly increased risk of MI with NSAID use, a random-effects model of the same data and analysis of 6 cohort studies found no such link. An increased risk of MI was found in four RCTs of NSAID use in colonic adenoma. In an analysis of 14 RCTs that compared COX2 inhibitors with traditional NSAIDs in patients with arthritis, the odds ratio for MI with COX2 inhibitors was 1.6 (95% CI 1.1-2.4), although most of this risk was accounted for by rofecoxib. COX2 inhibitors were, however, associated with a reduced risk of serious gastrointestinal events. An analysis of previous systematic reviews showed increased risks of MI associated with rofecoxib and celecoxib.
斯科特等人进行了一项系统评价,以评估与环氧化酶-2(COX2)抑制剂和传统非甾体抗炎药相关的心肌梗死(MI)风险。该评价发现,与COX2抑制剂相关的MI风险略有增加,尤其是罗非昔布。尽管14项病例对照研究的固定效应模型表明使用非甾体抗炎药会使MI风险略有增加,但对相同数据的随机效应模型以及6项队列研究的分析未发现此类关联。在四项关于非甾体抗炎药用于结肠腺瘤的随机对照试验中发现MI风险增加。在一项对14项将COX2抑制剂与传统非甾体抗炎药用于关节炎患者的随机对照试验的分析中,COX2抑制剂导致MI的比值比为1.6(95%可信区间1.1 - 2.4),不过这种风险大部分是由罗非昔布导致的。然而,COX2抑制剂与严重胃肠道事件风险降低相关。对既往系统评价的分析显示,罗非昔布和塞来昔布与MI风险增加相关。