Edwards Christopher J, Cooper Cyrus, Fisher David, Field Max, van Staa Tjeerd P, Arden Nigel K
University of Southampton, and Southampton General Hospital, Southampton, UK.
Arthritis Rheum. 2007 Oct 15;57(7):1151-7. doi: 10.1002/art.23003.
To evaluate the effect of disease-modifying antirheumatic drugs (DMARDs) on the likelihood of patients with rheumatoid arthritis (RA) developing septic arthritis (SA).
The United Kingdom General Practice Research Database (GPRD) was used to identify adults with RA, and age-, sex-, and practice-matched control subjects. Subjects were studied between 1987 and 2002. The risk of developing SA (excluding infected joint replacements) for individuals with RA was calculated and the effect of DMARD use determined.
A total of 136,977 subjects (34,250 patients with RA, 102,747 controls) were identified. SA was identified in 345 subjects, of which 321 (236 in patients with RA, 85 in controls) cases occurred during the study period. The incidence rate of SA was 12.9 times higher in subjects with RA than in those without (95% confidence interval [95% CI] 10.1-16.5, P < 0.001). The incident rate ratios (IRRs) for developing SA while receiving DMARDs compared with receiving no DMARDs were different for different medications. Penicillamine (adjusted IRR 2.51, 95% CI 1.29-4.89, P = 0.004), sulfasalazine (adjusted IRR 1.74, 95% CI 1.04-2.91, P = 0.03), and prednisolone (adjusted IRR 2.94, 95% CI 1.93-4.46, P < 0.001) were associated with an increased incidence of SA when compared with not receiving any DMARD. The use of other DMARDs including methotrexate showed no such effect.
Individuals with RA have an increased risk of developing SA. This increased risk can be attributed to both the disease process and the use of DMARDs.
评估改善病情抗风湿药(DMARDs)对类风湿关节炎(RA)患者发生脓毒性关节炎(SA)可能性的影响。
利用英国全科医疗研究数据库(GPRD)确定患有RA的成年人以及年龄、性别和执业地点匹配的对照对象。研究对象为1987年至2002年间的人群。计算RA患者发生SA(不包括感染的关节置换)的风险,并确定使用DMARDs的影响。
共确定了136,977名研究对象(34,250例RA患者,102,747名对照)。在345名研究对象中发现了SA,其中321例(RA患者236例,对照85例)发生在研究期间。RA患者中SA的发病率比无RA者高12.9倍(95%置信区间[95%CI] 10.1 - 16.5,P < 0.001)。接受不同DMARDs治疗与未接受DMARDs治疗相比,发生SA的发病率比(IRRs)因药物不同而有所差异。与未接受任何DMARDs相比,青霉胺(校正IRR 2.51,95%CI 1.29 - 4.89,P = 0.004)、柳氮磺胺吡啶(校正IRR 1.74,95%CI 1.04 - 2.91,P = 0.03)和泼尼松龙(校正IRR 2.94,95%CI 1.93 - 4.46,P < 0.001)与SA发病率增加相关。使用包括甲氨蝶呤在内的其他DMARDs则未显示出此类影响。
RA患者发生SA的风险增加。这种风险增加可归因于疾病进程和DMARDs的使用。