Table 1.
Characteristic | Patients using initial TNF inhibitor for ≥6 months (N = 1732) |
---|---|
Female, N (%) | 1294 (74.7) |
White, N (%) | 1502 (86.7) |
Age, median (IQR) | 56 (16.0) |
BMI, median (IQR) | 28.2 (8.6) |
Duration of RA, median, yrs (IQR) | 3 (8) |
CDAI score, median (IQR) | 23.8 (16) |
Moderate disease activity,a N (%) | 777 (44.9) |
High disease activity,b N (%) | 955 (55.1) |
Tender joints, median (IQR) | 8 (8) |
Swollen joints, median (IQR) | 7 (8) |
mHAQ-DI, median (IQR) | .5 (.8) |
Patient pain, median rating (IQR) | 50 (45) |
Patient global assessment, median rating (IQR) | 50 (44) |
Patient-reported fatigue, median rating (IQR) | 50 (55) |
Morning stiffness, median, hrs (IQR) | 1 (1.8) |
Prednisone use, N (%) | 612 (35.3) |
Previous csDMARDs (including current), median, N (IQR) | 1 (1) |
TNF inhibitor monotherapy, N (%) | 230 (13.3) |
TNF inhibitor combination therapy, N (%) | 1502 (86.7) |
Methotrexate alone | 984 (56.8) |
Other csDMARD | 235 (13.6) |
Methotrexate plus other csDMARD | 283 (16.3) |
Initial TNF inhibitor, N (%) | |
Adalimumab | 558 (32.2) |
Etanercept | 541 (31.2) |
Infliximab | 506 (29.2) |
Certolizumab pegol | 87 (5.0) |
Golimumab | 40 (2.3) |
CDAI score 10–22.
CDAI score >22.
BMI indicates body mass index; CDAI, Clinical Disease Activity Index; csDMARD, conventional synthetic disease-modifying antirheumatic drug; IQR, interquartile range; mHAQ-DI, modified Health Assessment Questionnaire-Disability Index; RA, rheumatoid arthritis; TNF, tumor necrosis factor.