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Efficacy and tolerability of naproxen/esomeprazole magnesium tablets compared with non-specific NSAIDs and COX-2 inhibitors: a systematic review and network analyses

机译:萘普生/埃索美拉唑镁片与非特异性NSAIDs和COX-2抑制剂的疗效和耐受性:系统评价和网络分析

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摘要

Non-steroidal anti-inflammatory drugs (NSAIDs), such as non-selective NSAIDs (nsNSAIDs) or selective cyclooxygenase-2 (COX-2) inhibitors, are commonly prescribed for arthritic pain relief in patients with osteoarthritis (OA), rheumatoid arthritis (RA), or ankylosing spondylitis (AS). Treatment guidelines for chronic NSAID therapy include the consideration for gastroprotection for those at risk of gastric ulcers (GUs) associated with the chronic NSAID therapy. The United States Food and Drug Administration has approved naproxen/esomeprazole magnesium tablets for the relief of signs and symptoms of OA, RA, and AS, and to decrease the risk of developing GUs in patients at risk of developing NSAID-associated GUs. The European Medical Association has approved this therapy for the symptomatic treatment of OA, RA, and AS in patients who are at risk of developing NSAID-associated GUs and/or duodenal ulcers, for whom treatment with lower doses of naproxen or other NSAIDs is not considered sufficient. Naproxen/esomeprazole magnesium tablets have been compared with naproxen and celecoxib for these indications in head-to-head trials. This systematic literature review and network meta-analyses of data from randomized controlled trials was performed to compare naproxen/esomeprazole magnesium tablets with a number of additional relevant comparators. For this study, an original review examined MEDLINE®, Embase®, and the Cochrane Controlled Trials Register from database start to April 14, 2009. Using the same methodology, a review update was conducted to December 21, 2009. The systematic review and network analyses showed naproxen/esomeprazole magnesium tablets have an improved upper gastrointestinal tolerability profile (dyspepsia and gastric or gastroduodenal ulcers) over several active comparators (naproxen, ibuprofen, diclofenac, ketoprofen, etoricoxib, and fixed-dose diclofenac sodium plus misoprostol), and are equally effective as all active comparators in treating arthritic symptoms in patients with OA, RA, and AS. Naproxen/esomeprazole magnesium tablets are therefore a valuable option for treating arthritic symptoms in eligible patients with OA, RA, and AS.
机译:非类固醇抗炎药(NSAIDs),例如非选择性NSAIDs(nsNSAIDs)或选择性环氧合酶2(COX-2)抑制剂,通常被处方用于骨关节炎(OA),类风湿性关节炎( RA)或强直性脊柱炎(AS)。慢性NSAID疗法的治疗指南包括考虑对那些与慢性NSAID疗法相关的胃溃疡(GUs)风险患者进行胃保护。美国食品和药物管理局已经批准了萘普生/埃索美拉唑镁片,用于缓解OA,RA和AS的体征和症状,并降低患有NSAID相关GUs风险的患者发展GUs的风险。欧洲医学协会已批准该疗法用于有发展为NSAID相关GUs和/或十二指肠溃疡风险的患者的OA,RA和AS的对症治疗,对于这些患者而言,不宜使用较低剂量的萘普生或其他NSAID进行治疗认为足够。在头对头试验中,已将萘普生/艾美拉唑镁片剂与萘普生和塞来昔布的这些适应症进行了比较。进行了这项系统的文献综述和来自随机对照试验的数据的网络荟萃分析,以比较萘普生/埃索美拉唑镁片与许多其他相关比较物。对于本研究,原始审查从数据库开始到2009年4月14日检查了MEDLINE ®,Embase ®和Cochrane对照试验注册簿。使用相同的方法,进行审查更新至2009年12月21日进行。系统评价和网络分析表明,萘普生/埃索美拉唑镁片在几个活性比较剂(萘普生,布洛芬,双氯芬酸,酮洛芬,依托考昔,以及固定剂量的双氯芬酸钠加米索前列醇),与所有活性比较剂在治疗OA,RA和AS患者的关节炎症状中具有同等效力。因此,萘普生/埃索美拉唑镁片是治疗合格的OA,RA和AS患者的关节炎症状的宝贵选择。

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