Safety of medium- to long-term glucocorticoid therapy in rheumatoid arthritis: a meta-analysis

被引:53
作者
Ravindran, Vinod [1 ]
Rachapalli, Satish [1 ]
Choy, Ernest H. [1 ]
机构
[1] Kings Coll London, Sir Alfred Baring Garrod Clin Trials Unit, Acad Dept Rheumatol, Weston Educ Ctr, London SE5 9RJ, England
关键词
Rheumatoid arthritis; Treatment; Glucocorticoid; Meta-analysis; LOW-DOSE PREDNISOLONE; MODIFYING ANTIRHEUMATIC DRUGS; DOUBLE-BLIND; INTRAMUSCULAR METHYLPREDNISOLONE; JOINT DESTRUCTION; CONTROLLED-TRIALS; DISEASE-ACTIVITY; CLINICAL-TRIALS; PLACEBO; SULFASALAZINE;
D O I
10.1093/rheumatology/kep096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methods. MEDLINE, EMBASE and CINAHL databases were searched for RCTs of glucocorticoids in RA. RCTs fulfilling the following criteria were included: double-blinded, placebo-controlled, lasted 1 year or longer, used prednisolone (or equivalent) and in English. Toxicity was assessed by number of the patients withdrawn for adverse events (AEs), and the numbers of serious adverse events (SAEs) and AEs. RCTs were compared by meta-analysis using odd ratios (OR) with 95 CIs. Results. Six RCTs with total of 689 patients met the inclusion criteria. All RCTs lasted 2 years. All studies allowed concomitant use of NSAIDs and DMARDs. Toxicity of glucocorticoid therapy based on number of patients withdrawn was limited (OR 1.09; 95 CI 0.52, 2.25). Using number of AEs per patient-year (OR 1.19; 95 CI 0.91, 1.57) and SAEs (OR 1.06; 95 CI 0.67, 1.67) produced similar results. Efficacy/toxicity ratio was good for glucocorticoid therapy (number needed to harm/number needed to treat 0.25). Conclusion. Medium- to long-term glucocorticoid therapy in RA is associated with limited toxicity compared to placebo.
引用
收藏
页码:807 / 811
页数:5
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