Nonsteroidal Antiinflammatory Drugs for Axial Spondyloarthritis: A Cochrane Review

被引:30
作者
Kroon, Feline P. B. [1 ]
van der Burg, Lennart R. A. [2 ]
Ramiro, Sofia [1 ,7 ]
Landewe, Robert B. M. [3 ,4 ]
Buchbinder, Rachelle [5 ]
Falzon, Louise [6 ]
van der Heijde, Desiree [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, POB 9600, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Gastroenterol, Leiden, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Clin Immunol & Rheumatol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[4] Atrium Med Ctr, Dept Rheumatol, Heerlen, Netherlands
[5] Monash Univ, Sch Publ Hlth & Prevent Med, Dept Epidemiol & Prevent Med, Monash Dept Clin Epidemiol,Cabrini Hosp, Malvern, Australia
[6] Columbia Univ, Med Ctr, Ctr Behav Cardiovasc Hlth, New York, NY USA
[7] Rijnland Med Ctr, Dept Internal Med, Leiden, Netherlands
基金
英国医学研究理事会;
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ANKYLOSING SPONDYLITIS; AXIAL SPONDYLOARTHRITIS; SYSTEMATIC REVIEW; METAANALYSIS; ASAS/EULAR MANAGEMENT RECOMMENDATIONS; SOCIETY CLASSIFICATION CRITERIA; RANDOMIZED CONTROLLED-TRIAL; SHORT-TERM IMPROVEMENT; ANKYLOSING-SPONDYLITIS; DOUBLE-BLIND; RHEUMATOID-ARTHRITIS; GASTROINTESTINAL TOXICITY; RADIOGRAPHIC PROGRESSION; STRUCTURAL DAMAGE;
D O I
10.3899/jrheum.150721
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To determine the benefits and harms of nonsteroidal antiinflammatory drugs (NSAID) in axial spondyloarthritis (axSpA). Methods. Systematic review using Cochrane Collaboration methodology. Inclusion criteria: randomized controlled trials (RCT) and quasi-RCT (to June 2014), investigating NSAID versus any control for axSpA, and observational studies of longterm effects (= 6 mos) of NSAID on radiographic progression or adverse events. Main outcomes were pain, Bath Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Functional Index, Bath Ankylosing Spondylitis Metrology Index, radiographic progression, number of withdrawals because of adverse events, and number of serious adverse events. Risk of bias was assessed. Results. Thirty-five RCT, 2 quasi-RCT, and 2 cohort studies were included. Twenty-nine RCT and 2 quasi-RCT (n = 4356) were included in pooled analyses [traditional NSAID vs placebo (n = 5), cyclooxygenase-2 (COX-2) vs placebo (n = 3), COX-2 vs traditional NSAID (n = 4), NSAID vs NSAID (n = 24), naproxen vs other NSAID (n = 3), and low-vs high-dose NSAID (n = 5)]. Compared with placebo, both traditional and COX-2 NSAID were consistently more efficacious at 6 weeks and equally safe after 12 weeks. No significant differences in benefits or harms between the 2 NSAID classes and no important differences in benefits or withdrawals because of adverse events between different NSAID were found, especially if studies with high risk of bias were excluded. Single studies suggest NSAID may retard radiographic progression, especially by continuous rather than on-demand NSAID use. Conclusion. High-quality evidence indicates that both traditional and COX-2 NSAID are efficacious for treating axSpA, and harms are not different from placebo in the short term. Various NSAID are equally effective.
引用
收藏
页码:607 / 617
页数:11
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