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Table 1 Baseline and outcome variables by therapy and indication groups

From: Incident tuberculosis disease in patients receiving biologic therapies in the Western Cape, South Africa from 2007 to 2018

All patients n = 609 n (%)

Therapy groups n = 598a

Indication groups n = 609

TNF-α n = 174 n (%)

Non-TNF-α n = 424

n (%)

pb

IMID n = 348 n (%)

HM n = 261 n (%)

p

AGE IN YEARS at initiation of biologic therapy

 Median (IQR)

41 (22–57)

33 (18–46)

47 (25–59)

< 0.001

28 (13–45)

55 (41–63)

< 0.001

GENDER

 F

311 (51)

73 (42)

232 (55)

0.005

185 (53)

126 (48)

0.223

 M

298 (49)

101 (58)

192 (45)

163 (47)

135 (52)

HIV STATUS at initiation of therapy

 positive

45 (7)

13 (8)

31 (7)

0.946

27 (8)

18 (7)

0.687

 negative

564 (93)

161 (92)

393 (93)

321 (92)

243 (93)

IPT

 yes

211 (35)

119 (78)

83 (20)

< 0.001

206 (59)

5 (2)

< 0.001

 no

398 (65)

55 (22)

341 (80)

142 (41)

256 (98)

SURVIVAL at end of study period

 died

94 (15)

16 (9)

78 (18)

0.005

39 (11)

55 (21)

0.001

 alive

515 (85)

158 (91)

346 (82)

309 (89)

206 (79)

TB INCIDENCE after initiation of biologic therapy

 TB

37 (6)

16 (9)

19 (4)

0.026

29 (8)

8 (3)

0.007

 no TB

572 (94)

158 (91)

405 (96)

319 (92)

253 (97)

  1. apatients receiving both TNF-α and non-TNF-α inhibitors (n = 11) were excluded
  2. bp value compares TNF-α to non-TNF-α only (n = 598) using a Mann-Whitney test for age in years and Chi-Square tests for categorical variables
  3. TNF-α tumour necrosis factor-alpha inhibitors, non-TNF-α non-tumour necrosis factor- alpha inhibitors, IMID immune mediated inflammatory disease, HM haematologic malignancy, IPT isoniazid preventative therapy