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. 2015 Mar 13;350:h1046. doi: 10.1136/bmj.h1046

Table 1.

 Baseline demographic and clinical characteristics of patients with rheumatoid arthritis randomised to treatment with combinations of disease modifying drugs or tumour necrosis factor inhibitors. Figures are means (SD) unless stated otherwise

Combination disease modifying drugs strategy (n=104) Tumour necrosis factor inhibitor strategy (n=101)
Demographic variables
Age (years) 58 (13) 57 (11)
No (%) of women/men 73/31 (70/30) 79/22 (78/22)
No (%) by ethnic group:
 White 89 (86) 92 (91)
 Black (African, Caribbean, other) 6 (6) 2 (2)
 Other 9 (9) 7 (7)
Median (IQR) duration of disease (years) 4.4 (1.6-9.9) 5.9 (2.2-13.4)
Height (m) 1.64 (0.11) 1.66 (0.09)
Weight (kg) 78 (20) 81 (17)
Median (IQR) BMI 29 (24-33) 29 (25-32)
Clinical variables
Disease activity score for 28 joints 6.2 (0.9) 6.3 (0.8)
Tender joint count 16 (7) 18 (7)
Swollen joint count 11 (6) 11 (7)
ESR (mm in first hour) 33 (26) 30 (23)
Patient global visual analogue score (mm) 68 (20) 68 (21)
Health assessment questionnaire score 1.8 (0.6) 1.9 (0.7)
Larsen score 45 (42) 38 (39)
EQ5D score 0.39 (0.31) 0.35 (0.31)
SF-36 physical component summary score 28 (7) 27 (7)
SF-36 mental component summary score 43 (12) 41 (12)
Previous disease modifying drug treatments (No of patients)
Methotrexate 98 97
Sulfasalazine 68 56
Leflunomide 27 29
Other 48 49
Three previous treatments 33 29
Combination drugs at screening 38 39
Prednisolone at screening (mean daily dose) 16 (4 mg) 8 (4 mg)

BMI=body mass index; IQR=interquartile range; ESR=erythrocyte sedimentation rate.