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Table 1 Descriptive characteristics of rheumatoid arthritis patients during first bDMARD or tsDMARD use

From: Incident and recurrent herpes zoster for first-line bDMARD and tsDMARD users in seropositive rheumatoid arthritis patients: a nationwide cohort study

 

Total

TNFα inhibitor

Non-TNFα inhibitor

  

Etanercept

Infliximab

Adalimumab

Golimumab

Tocilizumab

Rituximab

Tofacitinib

Abatacept

Number of participants, N (%)

11,720

2680 (22.9)

1315 (11.2)

3229 (27.6)

1197 (10.2)

1378 (11.8)

67 (0.6)

701 (6.0)

1153 (9.8)

Age, years, median (IQR)

56 (47–64)

55 (45–64)

56 (48–63)

54 (44–62)

55 (46–64)

57 (49–65)

60 (50–67)

56 (47–63)

60 (52–68)

Sex, N (%)

 Men

2152 (18.4)

518 (19.3)

217 (16.5)

581 (18.0)

216 (18.0)

253 (18.4)

11 (16.4)

128 (18.3)

228 (19.8)

 Women

9568 (81.6)

2162 (80.7)

1098 (83.5)

2648 (82.0)

981 (82.0)

1125 (81.6)

56 (83.6)

573 (81.7)

925 (80.2)

No. of csDMARD, N (%)

 ≤1

1790 (15.3)

517 (19.3)

133 (10.1)

450 (13.9)

150 (12.5)

205 (14.9)

26 (38.8)

133 (19.0)

176 (15.3)

 2

5156 (44.0)

1086 (40.5)

590 (44.9)

1378 (42.7)

597 (49.9)

666 (48.3)

21 (31.3)

337 (48.1)

481 (41.7)

 3

3586 (30.6)

798 (29.8)

437 (33.2)

1046 (32.4)

369 (30.8)

372 (27.0)

14 (20.9)

180 (25.7)

370 (32.1)

 ≥4

1188 (10.1)

279 (10.4)

155 (11.8)

355 (11.0)

81 (6.8)

135 (9.8)

6 (9.0)

51 (7.3)

126 (10.9)

Steroids use, mg/day, median (IQR)

4.5 (2.8–6.2)

4.7 (2.9–6.3)

3.9 (2.5–5.9)

4.7 (2.9–6.5)

4.2 (2.5–6.0)

4.1 (2.6–6.0)

4.3 (3.3–6.4)

3.9 (2.5–6.1)

4.8 (3.2–6.4)

Enrollment year, N (%)

 2011

1060 (9.0)

421 (15.7)

161 (12.2)

450 (13.9)

0 (0)

0 (0)

25 (37.3)

0 (0)

3 (0.3)

 2012

1381 (11.8)

547 (20.4)

167 (12.7)

641 (19.9)

0 (0)

0 (0)

17 (25.4)

0 (0)

9 (0.8)

 2013

1294 (11.0)

466 (17.4)

219 (16.7)

488 (15.1)

68 (5.7)

29 (2.1)

9 (13.4)

0 (0)

15 (1.3)

 2014

1822 (15.5)

387 (14.4)

284 (21.6)

386 (12.0)

239 (20.0)

263 (19.1)

2 (3.0)

0 (0)

261 (22.6)

 2015

1393 (11.9)

237 (8.8)

165 (12.5)

268 (8.3)

228 (19.0)

246 (17.9)

3 (4.5)

2 (0.3)

244 (21.2)

 2016

1388 (11.8)

183 (6.8)

122 (9.3)

351 (10.9)

212 (17.7)

274 (19.9)

4 (6.0)

7 (1.0)

235 (20.4)

 2017

1458 (12.4)

181 (6.8)

90 (6.8)

312 (9.7)

232 (19.4)

287 (20.8)

3 (4.5)

171 (24.4)

182 (15.8)

 2018

1765 (15.1)

239 (8.9)

101 (7.7)

304 (9.4)

205 (17.1)

245 (17.8)

4 (6.0)

485 (69.2)

182 (15.8)

 2019

159 (1.4)

19 (0.7)

6 (0.5)

29 (0.9)

13 (1.1)

34 (2.5)

0 (0)

36 (5.1)

22 (1.9)

CCI, N (%)

 1–2

5080 (43.3)

1239 (46.2)

614 (46.7)

1635 (50.6)

481 (40.2)

492 (35.7)

24 (35.8)

244 (34.8)

351 (30.4)

 3–4

4125 (35.2)

902 (33.7)

462 (35.1)

1050 (32.5)

429 (35.8)

540 (39.2)

16 (23.9)

275 (39.2)

451 (39.1)

 ≥5

2515 (21.5)

539 (20.1)

239 (18.2)

544 (16.8)

287 (24.0)

346 (25.1)

27 (40.3)

182 (26.0)

351 (30.4)

FU duration, year, median (IQR)

2.7 (0.8–5.7)

5.4 (1.7–6.7)

4.0 (1.1–6.1)

4.8 (1.1–6.5)

1.4 (0.5–3.1)

1.8 (0.7–3.1)

6.4 (5.3–7.5)

0.6 (0.3–1.0)

1.7 (0.6–3.3)

  1. The number of DMARD types prescribed within 1 year prior to initial biopharmaceutical drug prescription was considered
  2. csDMARDs: methotrexate, sulfasalazine, azathioprine, hydroxychloroquine sulfate, cyclosporine, cyclophosphamide, lefunomide
  3. bDMARD biological disease-modifying anti-rheumatic drugs, tsDMARD targeted synthetic disease-modifying anti-rheumatic drugs, csDMARD conventional synthetic disease-modifying antirheumatic drugs, TNF tumor necrosis factor, N number of people, SD standard deviation, CCI Charlson comorbidity index, FU follow-up, IQR interquartile range