Efficacy of etoricoxib, celecoxib, lumiracoxib, non-selective NSAIDs, and acetaminophen in osteoarthritis: a mixed treatment comparison.

Q4 Medicine Open Rheumatology Journal Pub Date : 2012-01-01 Epub Date: 2012-04-03 DOI:10.2174/1874312901206010006
Wb Stam, Jp Jansen, Sd Taylor
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引用次数: 30

Abstract

Objective: To compare the efficacy of etoricoxib, lumiracoxib, celecoxib, non-selective (ns) NSAIDs and acetaminophen in the treatment of osteoarthritis (OA) METHODS: Randomized placebo controlled trials investigating the effects of acetaminophen 4000mg, diclofenac 150mg, naproxen 1000mg, ibuprofen 2400mg, celecoxib 100-400mg, lumiracoxib 100-400mg, and etoricoxib 30-60mg with treatment duration of at least two weeks were identified with a systematic literature search. The endpoints of interest were pain, physical function and patient global assessment of disease status (PGADS). Pain and physical function reported on different scales (VAS or LIKERT) were translated into effect sizes (ES). An ES 0.2 - 0.5 was defined as a "small" treatment effect, whereas ES of 0.5 - 0.8 and > 0.8 were defined as "moderate" and "large", respectively. A negative effect indicated superior effects of the treatment group compared to the control group. Results of all trials were analyzed simultaneously with a Bayesian mixed treatment comparison.

Results: There is a >95% probability that etoricoxib (30 or 60mg) shows the greatest improvement in pain and physical function of all interventions compared. ESs of etoricoxib 30mg relative to placebo, celecoxib 200mg, ibuprofen 2400mg, and diclofenac 150mg were -0.66 (95% Credible Interval -0.83; -0.49), -0.32 (-0.50; -0.14), -0.25 (-0.53; 0.03), and -0.17 (-0.41; 0.08), respectively. Regarding physical functioning, ESs of etoricoxib 30mg relative to placebo, celecoxib 200mg, ibuprofen 2400mg, and diclofenac 150mg were -0.61 (-0.76; -0.46), -0.27 (-0.43; -0.10), -0.20 (-0.47; 0.07), and -0.09 (- 0.33; 0.14) respectively. The greatest improvements in PGADS were expected with either etoricoxib or diclofenac.

Conclusion: The current study estimated the efficacy of acetaminophen, nsNSAIDs, and COX-2 selective NSAIDs in OA and found that etoricoxib 30 mg is likely to result in the greatest improvements in pain and physical function. Differences in PGADS between interventions were smaller.

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依托昔布、塞来昔布、鲁米昔布、非选择性非甾体抗炎药和对乙酰氨基酚治疗骨关节炎的疗效比较
目的:比较依托昔布、lumiracoxib、塞来昔布、非选择性(ns)非甾体抗炎药和对乙酰氨基酚治疗骨关节炎(OA)的疗效。方法:通过系统的文献检索,确定随机安慰剂对照试验,研究对乙酰氨基酚4000mg、双氯芬酸150mg、萘普生1000mg、布洛芬2400mg、塞来昔布100-400mg、lumiracoxib 100-400mg和依托昔布30-60mg治疗时间至少为2周的疗效。感兴趣的终点是疼痛、身体功能和患者疾病状态总体评估(PGADS)。将不同量表(VAS或LIKERT)报告的疼痛和身体功能转化为效应量(ES)。ES 0.2 - 0.5被定义为“小”治疗效果,而ES 0.5 - 0.8和> 0.8分别被定义为“中等”和“大”。负效应表示治疗组的效果优于对照组。所有试验的结果同时进行贝叶斯混合处理比较分析。结果:与所有干预措施相比,依托昔布(30或60mg)对疼痛和身体功能的改善有>95%的可能性。依托昔布30mg相对于安慰剂、塞来昔布200mg、布洛芬2400mg和双氯芬酸150mg的ESs为-0.66(95%可信区间-0.83;-0.49), -0.32 (-0.50;-0.14), -0.25 (-0.53;0.03), -0.17 (-0.41;分别为0.08)。在生理功能方面,依托昔布30mg相对于安慰剂、塞来昔布200mg、布洛芬2400mg和双氯芬酸150mg的ESs为-0.61 (-0.76;-0.46), -0.27 (-0.43;-0.10), -0.20 (-0.47;0.07), -0.09 (- 0.33;分别为0.14)。依托昔布或双氯芬酸对PGADS的改善最大。结论:本研究评估了对乙酰氨基酚、非甾体抗炎药和COX-2选择性非甾体抗炎药治疗OA的疗效,发现依托瑞昔布30mg可能对疼痛和身体功能的改善最大。干预措施之间的PGADS差异较小。
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来源期刊
Open Rheumatology Journal
Open Rheumatology Journal Medicine-Rheumatology
CiteScore
0.80
自引率
0.00%
发文量
2
期刊介绍: ENTHAM Open publishes a number of peer-reviewed, open access journals. These free-to-view online journals cover all major disciplines of science, medicine, technology and social sciences. BENTHAM Open provides researchers a platform to rapidly publish their research in a good-quality peer-reviewed journal. All peer-reviewed accepted submissions meeting high research and ethical standards are published with free access to all.
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