Incidence of septic arthritis in patients with ankylosing spondylitis and seropositive rheumatoid arthritis following TNF inhibitor therapy

被引:4
作者
Kim, Hyung Woo [1 ]
Han, Minkyung [2 ]
Jung, Inkyung [3 ]
Ahn, Sung Soo [4 ,5 ]
机构
[1] Yonsei Univ, Inst Kidney Dis Res, Coll Med, Dept Internal Med, Seoul, South Korea
[2] Yonsei Univ, Dept Biomed Syst Informat, Biostat Collaborat Unit, Coll Med, Seoul, South Korea
[3] Yonsei Univ, Dept Biomed Syst Informat, Div Biostat, Coll Med, Seoul, South Korea
[4] Yonsei Univ, Yongin Severance Hosp, Dept Internal Med, Div Rheumatol,Coll Med, Seoul, South Korea
[5] Yonsei Univ, Yongin Severance Hosp, Dept Internal Med, Div Rheumatol,Coll Med, Dongbaekjukjeon Daero, Yongin 16995, Gyeonggi Do, South Korea
关键词
septic arthritis; AS; seropositive RA; biologics; TNF; PATHOGENESIS; RISK;
D O I
10.1093/rheumatology/keac721
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Septic arthritis (SA) is a serious complication occurring in the joints, and its risk increases with immunosuppressive therapy. This study investigated whether TNF inhibitors increase the risk of SA in patients with AS and seropositive RA (SPRA). Methods We searched the South Korean Health Insurance Review and Assessment Service database for incident cases of AS and SPRA between 2010 and 2020. SA was defined using the diagnostic code M00 and hospital admission. Cox-proportional hazards analysis was conducted to compare the incidence of SA according to TNF inhibitor (infliximab, etanercept, adalimumab/golimumab) use during follow-up. Results Of the 145 129 patients analysed, 1170 (0.8%) developed SA during the follow-up period. Older age; male sex; SPRA diagnosis; comorbidities of hypertension (HTN), diabetes mellitus (DM) and chronic pulmonary disease (CPD); and infliximab and etanercept use increased the incidence of SA in the overall population. However, in patients with AS, only age and renal disease were predictors of SA, and TNF inhibitors did not increase the incidence of SA. Meanwhile, patients with SPRA treated with TNF inhibitors were prone to SA regardless of TNF inhibitor type, and age, HTN, DM and CPD were associated with SA. The incidence of SA was prominent after the first year of commencing TNF inhibitor therapy, for both AS and SPRA. Conclusion TNF inhibitors increase the incidence of SA, specifically in patients with SPRA, but not AS. Importantly, age, comorbidities and the early time period after starting TNF inhibitors were associated with SA, which should be considered simultaneously when initiating TNF inhibitor therapy.
引用
收藏
页码:2740 / 2747
页数:8
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