Controversies in rheumatoid arthritis glucocorticoid therapy

被引:14
作者
Ruyssen-Witrand, Adeline [1 ,2 ]
Constantin, Arnaud [1 ,3 ]
机构
[1] Hop Pierre Paul Riquet, Ctr Rhumatol, 1 Pl Dr Baylac, F-31059 Toulouse 09, France
[2] Univ Paul Sabatier Toulouse III, Inserm, UMR 1027, Fac Med, 37 Allees Jules Guesdes, F-31000 Toulouse, France
[3] Univ Paul Sabatier Toulouse III, Inserm, UMR 1043, CPTP,Hop Purpan, 1 Pl Dr Baylac, F-31000 Toulouse, France
关键词
Rheumatoid arthritis; Glucocorticoids; Remission; TREAT-TO-TARGET; CONTROLLED-TRIAL; DOUBLE-BLIND; ADRENAL INSUFFICIENCY; TREATMENT STRATEGY; INDUCTION THERAPY; RANDOMIZED-TRIAL; TIGHT CONTROL; ALL-CAUSE; METHOTREXATE;
D O I
10.1016/j.jbspin.2017.12.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite therapeutic innovations in the past 20 years, glucocorticoids (GC) are still widely used for the symptomatic treatment of rheumatoid arthritis (RA). Studies have demonstrated the clinical and structural efficacy of moderate doses (i.e. 30-60 mg/d) GC in addition to disease modifying anti-rheumatic drug (DMARD) initiation in early RA. A combination of a low dose of GC (i.e. 7.5-10 mg/d) and DMARDs increases remission rates and decreases the risk of medium-term structural progression in early RA. Intra-venous and intramuscular administration of GC associated with DMARD initiation or intra-articular GC injections in symptomatic joints in tight control strategies increase remission rates in early RA. However, due to the risk of adverse events such as infections, cardiovascular events, or increased mortality induced by long-term use of GC, even at low-doses (e.g. 5 mg/d), GC should be prescribed at a minimal dose, for the shortest possible duration, and in association with DMARD initiation in early RA or DMARD change in active established RA. (C) 2017 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:417 / 422
页数:6
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