Effects of biologics on reducing the risks of total knee replacement and total hip replacement in rheumatoid arthritis

被引:2
作者
Chang, Yu-Sheng [1 ,2 ]
Chen, Jin-Hua [3 ,4 ]
Lin, Tzu-Min [2 ,5 ]
Hsu, Hui-Ching [2 ,6 ]
Chen, Wei-Sheng [7 ,8 ]
Lin, Sheng-Hong [1 ,2 ]
Kuo, Pei-, I [5 ]
Lin, Yi-Chun [3 ]
Chang, Chi-Ching [2 ,5 ]
机构
[1] Taipei Med Univ, Dept Internal Med, Div Allergy Immunol & Rheumatol, Shuang Ho Hosp, New Taipei, Taiwan
[2] Taipei Med Univ, Coll Med, Dept Internal Med, Div Allergy Immunol & Rheumatol,Sch Med, Taipei, Taiwan
[3] Taipei Med Univ, Stat Ctr, Off Data Sci, Taipei, Taiwan
[4] Taipei Med Univ, Coll Management, Grad Inst Data Sci, Taipei, Taiwan
[5] Taipei Med Univ Hosp, Dept Internal Med, Div Rheumatol Immunol & Allergy, Taipei, Taiwan
[6] Taipei Med Univ, Wan Fang Hosp, Dept Internal Med, Div Allergy Immunol & Rheumatol, Taipei, Taiwan
[7] Taipei Vet Gen Hosp, Dept Internal Med, Div Allergy Immunol & Rheumatol, Taipei, Taiwan
[8] Natl Yang Ming Univ, Fac Med, Sch Med, Taipei, Taiwan
关键词
biologics; rheumatoid arthritis; total hip replacement; total knee replacement; methotrexate; DMARDs; bDMARDs; epidemiology; treat-to-target; inflammation; JOINT REPLACEMENT; SURGERY; RATES; TRENDS; CLASSIFICATION; ASSOCIATION; CRITERIA; OUTCOMES;
D O I
10.1093/rheumatology/keab671
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives RA damages the joints and increases the risks of total knee replacement (TKR) and total hip replacement (THR). However, the benefits of biologics in preventing TKR or THR remain unclear. Methods This retrospective nationwide study used the 2000-2013 claims-based National Health Insurance dataset. Biologics are reimbursed for refractory cases. The risks of TKR and THR in the biologic cohort were compared with those of an age- and sex-matched csDMARD cohort. A multivariate Cox regression model was used to investigate the benefits of bDMARDs for TKR and THR. Results TKR was performed in 5979 biologic cases and 11 958 matched controls, of which 249 (4.16%) and 871 (7.28%) cases received TKR, respectively. THR was performed in 6245 biologic cases and 12 490 matched controls, of which 159 (2.55%) and 516 (4.13%) cases had THR, respectively. The biologic cohort had significantly lower incidence rates of TKR (11.73 vs 16.33/1000 person-years, P < 0.001) and THR (7.09 vs 9.16/1000 person-years, P < 0.001). After adjustment for confounding factors, the regular bDMARD subgroup (average dose >0.95 defined daily dose/day) had significantly lower risks of TKR (aHR: 0.55, 95% CI: 0.38, 0.81) and THR (aHR: 0.63, 95% CI: 0.40, 0.98). Those without MTX use, with steroid use, with biologic switch, and overlapping antiphospholipid syndrome had significantly higher risks of TKR and THR. Conclusions Compared with the csDMARD cohort, the risks of TKR and THR in the bDMARD cohort were the same as those in the low-to-moderate dose subgroups and significantly lower in those with regular bDMARD use.
引用
收藏
页码:1849 / 1856
页数:8
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