Table 1

Baseline demographics and disease characteristics by washout and direct-switch groups

Washout patients (n  =  449)Direct-switch patients (n  =  597)Overall (n  =  1046)
Age, years56.1 (12.5)53.2 (12.3)54.4 (12.4)
Weight, kg78.9 (21.1)79.1 (20.0)79.0 (20.5)
Gender, female, n (%)359 (80.0)490 (82.1)849 (81.2)
Race, n (%)
    White416 (92.7)551 (92.3)967 (92.4)
    Black27 (6.0)33 (5.5)60 (5.7)
    Other6 (1.3)13 (2.2)19 (1.8)
Duration of disease, years13.0 (10.0)10.6 (9.0)11.6 (9.5)
Previous anti-TNF therapy*, n (%)
    Etanercept226 (50.3)366 (61.3)592 (56.6)
    Infliximab281 (62.6)339 (56.8)620 (59.3)
    Adalimumab193 (43.0)309 (51.8)502 (48.0)
Medications at day 1, n (%)
    Methotrexate307 (68.4)423 (70.9)730 (69.8)
    Azathioprine18 (4.0)25 (4.2)43 (4.1)
    Gold4 (0.9)1 (0.2)5 (0.5)
    Hydroxychloroquine/chloroquine71 (15.8)86 (14.4)157 (15.0)
    Leflunomide66 (14.7)68 (11.4)134 (12.8)
    Sulfasalazine32 (7.1)60 (10.1)92 (8.8)
    Corticosteroids†280 (62.4)331 (55.4)611 (58.4)
Tender joints17.8 (5.9)17.8 (6.1)17.8 (6.0)
Swollen joints13.9 (5.6)13.5 (5.4)13.6 (5.5)
Patient global assessment, VAS 100 mm72.7 (16.7)73.1 (16.4)72.9 (16.5)
HAQ-DI1.7 (0.6)1.7 (0.6)1.7 (0.6)
DAS28 (CRP)‡6.2 (0.7)6.2 (0.7)6.2 (0.7)
CRP (mg/dl)§2.2 (3.0)2.1 (3.0)2.1 (3.0)
Rheumatoid factor positive, n (%)292 (65.0)349 (58.5)641 (61.3)
PPD positive, n (%)9 (2.0)17 (2.8)26 (2.5)
  • Data are presented as mean (SD) unless otherwise indicated. *Patients could have previously received more than one prior anti-tumour necrosis factor (TNF) therapy; two patients, one in the washout and one in the direct-switch group, had received rituxmab more than 12 months before study entry. †Oral and/or injectable. ‡The joint count used was 28. §The upper limit of normal for high sensitivity C-reactive protein (CRP) was 3.00 mg/l. DAS28, disease activity score in 28 joints; HAQ-DI, health assessment questionnaire disability index; PPD, purified protein derivative; VAS, visual analogue scale.