The association between systemic glucocorticoid therapy and the risk of infection in patients with rheumatoid arthritis: systematic review and meta-analyses

被引:140
作者
Dixon, William G. [1 ,2 ]
Suissa, Samy [2 ]
Hudson, Marie [2 ]
机构
[1] Univ Manchester, Manchester Acad Hlth Sci Ctr, Arthrit Res UK Epidemiol Unit, Manchester M13 9PT, Lancs, England
[2] McGill Univ, Lady Davis Inst Med Res, Jewish Gen Hosp, Ctr Clin Epidemiol, Montreal, PQ H3T 1E2, Canada
关键词
ANTITUMOR-NECROSIS-FACTOR; LOW-DOSE PREDNISOLONE; MODIFYING ANTIRHEUMATIC DRUGS; METHYLPREDNISOLONE PULSE THERAPY; SERIOUS BACTERIAL-INFECTIONS; RANDOMIZED CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; HERPES-ZOSTER; JOINT ARTHROPLASTY;
D O I
10.1186/ar3453
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Infection is a major cause of morbidity and mortality in patients with rheumatoid arthritis (RA). The objective of this study was to perform a systematic review and meta-analysis of the effect of glucocorticoid (GC) therapy on the risk of infection in patients with RA. Methods: A systematic review was conducted by using MEDLINE, EMBASE, CINAHL, and the Cochrane Central Register of Controlled Trials database to January 2010 to identify studies among populations of patients with RA that reported a comparison of infection incidence between patients treated with GC therapy and patients not exposed to GC therapy. Results: In total, 21 randomised controlled trials (RCTs) and 42 observational studies were included. In the RCTs, GC therapy was not associated with a risk of infection (relative risk (RR), 0.97 (95% CI, 0.69, 1.36)). Small numbers of events in the RCTs meant that a clinically important increased or decreased risk could not be ruled out. The observational studies generated a RR of 1.67 (1.49, 1.87), although significant heterogeneity was present. The increased risk (and heterogeneity) persisted when analyses were stratified by varying definitions of exposure, outcome, and adjustment for confounders. A positive dose-response effect was seen. Conclusions: Whereas observational studies suggested an increased risk of infection with GC therapy, RCTs suggested no increased risk. Inconsistent reporting of safety outcomes in the RCTs, as well as marked heterogeneity, probable residual confounding, and publication bias in the observational studies, limits the opportunity for a definitive conclusion. Clinicians should remain vigilant for infection in patients with RA treated with GC therapy.
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页数:14
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共 100 条
  • [1] [Anonymous], The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses
  • [2] [Anonymous], MCMASTER QUALITY ASS
  • [3] Why has antibiotic prescribing for respiratory illness declined in primary care? A longitudinal study using the General Practice Research Database
    Ashworth, M
    Latinovic, R
    Charlton, J
    Cox, K
    Rowlands, G
    Gulliford, M
    [J]. JOURNAL OF PUBLIC HEALTH, 2004, 26 (03) : 268 - 274
  • [4] Timedependent increase in risk of hospitalisation with infection among Swedish RA patients treated with TNF antagonists (vol 66, pg 1339, 2007)
    Askling, J.
    Fored, C. M.
    Brandt, L.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (11) : 1548 - 1548
  • [5] Time-dependent increase in risk of hospitalisation with infection among Swedish RA patients treated with TNF antagonists
    Askling, Johan
    Fored, C. Michael
    Brandt, Lena
    Baecklund, Eva
    Bertilsson, Lennart
    Feltelius, Nils
    Coster, Lars
    Geborek, Pierre
    Jacobsson, Lennart T.
    Lindblad, Staffan
    Lysholm, Jorgen
    Rantapaa-Dahlqvist, Solbritt
    Saxne, Tore
    van Vollenhoven, Ronald F.
    Klareskog, Lars
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (10) : 1339 - 1344
  • [6] Increased risk of coccidioidomycosis in patients treated with tumor necrosis factor α antagonists
    Bergstrom, L
    Yocum, DE
    Ampel, NM
    Villanueva, I
    Lisse, J
    Gluck, O
    Tesser, J
    Posever, J
    Miller, M
    Araujo, J
    Kageyama, DM
    Berry, M
    Karl, L
    Yung, CM
    [J]. ARTHRITIS AND RHEUMATISM, 2004, 50 (06): : 1959 - 1966
  • [7] Anti-rheumatic drug use and risk of serious infections in rheumatoid arthritis
    Bernatsky, S.
    Hudson, M.
    Suissa, S.
    [J]. RHEUMATOLOGY, 2007, 46 (07) : 1157 - 1160
  • [8] Prevalence of dermatophytosis in patients with rheumatoid arthritis
    Bicer, A
    Tursen, U
    Cimen, OB
    Kaya, TI
    Ozisik, S
    Ikizoglu, G
    Erdogan, C
    [J]. RHEUMATOLOGY INTERNATIONAL, 2003, 23 (01) : 37 - 40
  • [9] Randomised comparison of combined step-down prednisolone, methotrexate and sulphasalazine with sulphasalazine alone in early rheumatoid arthritis
    Boers, M
    Verhoeven, AC
    Markusse, HM
    vandeLaar, MAFJ
    Westhovens, R
    vanDenderen, JC
    vanZeben, D
    Dijkmans, BAC
    Peeters, AJ
    Jacobs, P
    vandenBrink, HR
    Schouten, HJA
    vanderHeijde, DMFM
    Boonen, A
    vanderLinden, S
    [J]. LANCET, 1997, 350 (9074) : 309 - 318
  • [10] Effectiveness of adalimumab for rheumatoid arthritis in patients with a history of TNF-antagonist therapy in clinical practice
    Bombardieri, S.
    Ruiz, A. A.
    Fardellone, P.
    Geusens, P.
    McKenna, F.
    Unnebrink, K.
    Oezer, U.
    Kary, S.
    Kupper, H.
    Burmester, G. R.
    [J]. RHEUMATOLOGY, 2007, 46 (07) : 1191 - 1199