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. 2018 May;11(3):148–158.

Table 1.

Patient and Disease Characteristics at Time of TNF Inhibitor Initiation in Patients Who Continued Their Initial Treatment for ≥6 Months

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)
a

CDAI score 10–22.

b

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.