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类风湿关节炎患者发生脓毒性关节炎的风险和抗 TNF 治疗的效果:来自英国风湿病学会生物制剂注册处的结果。

Risk of septic arthritis in patients with rheumatoid arthritis and the effect of anti-TNF therapy: results from the British Society for Rheumatology Biologics Register.

机构信息

Arthritis Research UK Epidemiology Unit, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.

出版信息

Ann Rheum Dis. 2011 Oct;70(10):1810-4. doi: 10.1136/ard.2011.152769. Epub 2011 Jul 21.

Abstract

OBJECTIVES

To evaluate the risk of septic arthritis (SA) in patients with rheumatoid arthritis (RA) treated with anti-tumour necrosis factor (TNF) therapy.

METHODS

Using data from the British Society for Rheumatology Biologics Register, a prospective observational study, the authors compared the risk of SA between 11 881 anti-TNF-treated and 3673 non-biological disease-modifying antirheumatic drug (nbDMARD)-treated patients.

RESULTS

199 patients had at least one episode of SA (anti-TNF: 179, nbDMARD: 20). Incidence rates were: anti-TNF 4.2/1000 patient years (pyrs) follow-up (95% CI 3.6 to 4.8), nbDMARD 1.8/1000 pyrs (95% CI 1.1 to 2.7). The adjusted HR for SA in the anti-TNF cohort was 2.3 (95% CI 1.2 to 4.4). The risk did not differ significantly between the three agents: adalimumab, etanercept and infliximab. The risk was highest in the early months of therapy. The patterns of reported organisms differed in the anti-TNF cohort. Prior joint replacement surgery was a risk factor for SA in all patients. The rate of postoperative joint infection (within 90 days of surgery) was 0.7%. This risk was not significantly influenced by anti-TNF therapy.

CONCLUSIONS

Anti-TNF therapy use in RA is associated with a doubling in the risk of SA. Physicians and surgeons assessing the RA patient should be aware of this potentially life-threatening complication.

摘要

目的

评估接受肿瘤坏死因子(TNF)拮抗剂治疗的类风湿关节炎(RA)患者发生脓毒性关节炎(SA)的风险。

方法

利用英国风湿病学会生物制剂注册处前瞻性观察性研究的数据,作者比较了 11881 例接受抗 TNF 治疗和 3673 例接受非生物改善病情抗风湿药(nbDMARD)治疗患者的 SA 风险。

结果

199 例患者至少发生过一次 SA(抗 TNF 组 179 例,nbDMARD 组 20 例)。发生率为:抗 TNF 组为 4.2/1000 患者年(pyrs)(95%CI3.64.8),nbDMARD 组为 1.8/1000 pyrs(95%CI1.12.7)。抗 TNF 组发生 SA 的调整 HR 为 2.3(95%CI1.2~4.4)。三种药物之间风险无显著差异:阿达木单抗、依那西普和英夫利昔单抗。风险在治疗早期最高。抗 TNF 组报告的病原体模式不同。关节置换术前是所有患者发生 SA 的危险因素。术后关节感染(术后 90 天内)发生率为 0.7%。该风险未因抗 TNF 治疗而显著改变。

结论

RA 患者接受抗 TNF 治疗与 SA 风险增加两倍相关。评估 RA 患者的内科医生和外科医生应注意这种潜在的威胁生命的并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a9/3168332/de556293e0ba/ard-70-10-1810-fig1.jpg

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