Table 1

Baseline characteristics of each treatment cohort (etanercept vs other TNFi) by country: patients with RA

DenmarkFinlandIcelandNorwaySweden
Treatment cohortsEtanerceptoTNFiEtanerceptoTNFiEtanerceptoTNFiEtanerceptoTNFiEtanerceptoTNFi
Episodes, n4968903719233226409773598116813 06717 535
Patients*, n4486667414112330241482456907827411 523
TNFi
 Adalimumab03411016400265020006913
 Certolizumab pegol0148503420<5051902019
 Infliximab0371507890414028706805
 Golimumab04260455092016201798
Female (%)3777 (76)6806 (75)1459 (76)2404 (75)309 (76)573 (74)454 (76)877 (75)10 163 (78)13 418 (77)
Age at TNFi start57 (48–66)57 (47–65)54 (43–62)54 (44–61)52 (41–62)52 (42–61)55 (42–63)55 (44–64)58 (46–66)58 (47–66)
Disease duration (years)
 <1 138 (3)346 (4)69 (4)119 (4)58 (17)97 (15)67 (14)114 (12)703 (5)1044 (6)
 1–51561 (33)2902 (33)487 (26)780 (25)145 (42)267 (40)158 (32)266 (29)3710 (29)4758 (28)
 >53097 (65)5468 (63)1343 (71)2254 (71)146 (42)299 (45)269 (54)537 (59)8472 (66)11 421 (66)
Number previous b/tsDMARDs
 02436 (49)6094 (67)1280 (67)2149 (67)233 (57)476 (62)336 (56)629 (54)7717 (59)10 848 (62)
 11827 (37)1913 (21)539 (28)686 (21)138 (34)169 (22)185 (31)324 (28)3592 (27)4159 (24)
 2498 (10)683 (8)89 (5)292 (9)29 (7)88 (11)59 (10)130 (11)1162 (9)1604 (9)
 3144 (3)241 (3)14 (1)69 (2)6 (1)27 (3)15 (3)61 (5)419 (3)626 (4)
 463 (1)106 (1)1 (0)30 (1)3 (1)13 (2)3 (1)24 (2)177 (1)298 (2)
Clinical measurements
 CRP10.0
(4.0–25.0)
10.0
(4.0–25.0)
10.0
(5.0–26.0)
10.0
(5.0–29.0)
5.0
(3.0–17.0)
7.0
(3.0–17.0)
5.0
(2.0–13.0)
5.0
(2.0–13.0)
9.0
(4.0–24.0)
10.0
(4.0–27.0)
 SJC4 (1–7)4 (2–8)3 (1–7)3 (1–7)5 (2–8)5 (2–10)3 (1–6)3 (1–6)5 (2–9)6 (3–10)
 TJC6 (3–12)7 (3–12)4 (1–7)3 (1–7)6 (2–10)6 (3–11)4 (1–8)4 (1–9)6 (2–10)6 (3–10)
 PGH33 (20–50)35 (20–51)50 (26–69)52 (29–70)70 (50–84)69 (50–82)49 (26–70)50 (28–70)59 (39–75)60 (40–75)
 HAQ†1.3 (0.8–1.8)1.3 (0.8–1.8)1.0 (0.5–1.5)1.0 (0.5–1.5)1.1 (0.8–1.5)1.1 (0.8–1.6)0.6 (0.3–1.0)0.6 (0.3–1.0)1.1 (0.6–1.5)1.1 (0.8–1.6)
 Pain VAS62 (40–77)60 (39–75)50 (27–70)53 (29–72)65 (42–80)67 (45–80)47 (21–70)42 (22–65)60 (38–75)60 (39–75)
 DAS284.7 (3.7–5.6)4.7 (3.7–5.6)4.4 (3.4–5.4)4.3 (3.2–5.3)4.5 (3.6–5.2)4.7 (3.8–5.6)3.9 (3.0–4.8)4.0 (3.0–4.8)4.6 (3.7–5.4)4.7 (3.8–5.5)
 Concomitant methotrexate2978 (60)6339 (70)708 (53)1368 (61)180 (44)350 (45)370 (62)753 (64)8198 (63)12 373 (71)
Comorbidities
 IBD68 (1)200 (2)9 (0)67 (2)1 (0)3 (0)2 (0)22 (2)108 (1)313 (2)
 Diabetes152 (3)212 (2)27 (1)40 (1)4 (1)8 (1)18 (3)28 (2)397 (3)492 (3)
 Thyroidea279 (6)447 (5)47 (2)73 (2)6 (1)4 (1)24 (4)39 (3)622 (5)742 (4)
Smoking
 Current390 (8)600 (7)38 (2)69 (2)47 (11)95 (12)99 (17)184 (16)747 (6)964 (5)
 Former420 (9)603 (7)9 (0)14 (0)102 (25)180 (23)206 (34)352 (30)2537 (19)3039 (17)
 Never754 (15)981 (11)193 (10)270 (8)163 (40)267 (35)180 (30)344 (29)2294 (18)2833 (16)
 Missing3404 (69)6853 (76)1683 (88)2873 (89)97 (24)231 (30)113 (19)288 (25)7489 (57)10 699 (61)
  • Median (quartiles) for continuous variables and number (percentages) for binary variables are displayed. If not otherwise specified, the statistics pertain to treatment episodes. All variables are measured at treatment start.

  • *Patients were allowed starting a treatment with the same molecule several times.

  • †mHAQ in Norway.

  • b/tsDMARD, biologic or targeted synthetic disease-modifying antirheumatic drug; CRP, C reactive protein (mg/L); DAS28, Disease Activity Score based on 28 joint count and CRP; HAQ, Health Assessment Questionnaire; IBD, inflammatory bowel disease; mHAQ, modified Health Assessment Questionnaire; oTNFi, other tumour necrosis factor inhibitors (adalimumab, certolizumab pegol, infliximab, golimumab); PGH, patient’s global health assessment; RA, rheumatoid arthritis; SJC, 28 swollen joint count; TJC, 28 tender joint count; TNFi, tumour necrosis factor inhibitor; VAS, 0–100 Visual Analogue Scale.