Table 2

Treatments used in patients with AIIRD

AIIRD diagnosis, nImmunosuppressive treatments, n (%)
GCMTXTNFiIL6iAnti-CD20ABAJAKiIL17iMMF
All AIIRD, n=686130 (18.95)176 (25.66)172 (25.07)37 (5.39)87 (12.68)16 (2.33)49 (6.9)48 (7)28 (4.08)
RA, n=26355 (20.91)116 (44.11)47 (17.87)29 (11.03)43 (16.35)15 (5.7)46 (16.9)00
PsA, n=1653 (1.82)36 (21.82)74 (44.85)001
(0.61)
2 (1.2)40 (24.24)0
AxSpA, n=681 (1.47)9 (13.24)48 (70.59)01 (1.47)*008 (11.76)2 (2.94)
SLE, n=10122 (21.78)8 (7.92)007 (6.93)00017 (16.83)
IIM, n=1915 (78.95)2 (10.53)0013 (68.42)0006 (31.58)
LVV, n=2111 (52.38)2 (9.52)1 (4.76)8 (38.1)00000
AAV, n=2612 (46.15)2 (7.69)0018 (69.23)0000
Other vasculitis, n=2311 (47.83)1 (4.35)2 (8.7)05 (21.74)0003 (13.04)
  • *This patient had multiple sclerosis and was treated with ocrelizumab.

  • AAV, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis; ABA, abatacept; AIIRD, autoimmune inflammatory rheumatic diseases; anti-CD20, CD-20 inhibitors; AxSpA, axial spondyloarthritis; GC, glucocorticoids; IIM, idiopathic inflammatory myositis; IL6i, interleukin 6 inhibitors; IL17i, interleukin 17 inhibitors; JAKi, Janus kinase inhibitors; LVV, large vessel vasculitis; MMF, mycophenolate mofetil; MTX, methotrexate; PsA, psoriatic arthritis; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus; TNFi, tumour necrosis factor inhibitors.