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. Author manuscript; available in PMC: 2023 Feb 20.
Published in final edited form as: Ann Rheum Dis. 2022 Aug 9;81(12):1742–1749. doi: 10.1136/ard-2022-222954

Table 2.

Rheumatic disease characteristics of patients with SARD with COVID-19 over calendar time

Time period
Overall (n=1449) Early COVID-19 Early treatment Early vaccination Additional vaccination and Delta wave Omicron wave
1 March 2020–30 June 2020 (n=261) 1 July 2020–31 January 2021 (n=492) 1 February 2021–30 June 2021 (n=123) 1 July 2021–16 December 2021 (n=172) 17 December 2021–31 January 2022 (n=401)
Rheumatic disease diagnosis, n ()
 Rheumatoid arthritis 491 (33.9) 90 (34.5) 174 (35.4) 48 (39.0) 45 (26.2) 134 (33.4)
 Psoriatic arthritis and spondyloarthritis 213 (14.7) 31 (11.9) 75 (15.2) 17 (13.8) 32 (18.6) 58 (14.5)
 Systemic lupus erythematosus 190 (13.1) 39 (14.9) 64 (13.0) 16 (13.0) 21 (12.2) 50 (12.5)
 Other inflammatory arthritis* 106 (7.3) 19 (7.3) 38 (7.7) 4 (3.3) 13 (7.6) 32 (8.0)
 PMR and/or GCA 101 (7.0) 23 (8.8) 31 (6.3) 7 (5.7) 14 (8.1) 26 (6.5)
 ANCA-associated vasculitis 68 (4.7) 11 (4.2) 21 (4.3) 7 (5.7) 12 (7.0) 17 (4.2)
 Other vasculitis 33 (2.3) 8 (3.1) 7 (1.4) 4 (3.3) 2 (1.2) 12 (3.0)
 Sjogren’s syndrome 36 (2.5) 2 (0.8) 13 (2.6) 3 (2.4) 5 (2.9) 13 (3.2)
 Systemic sclerosis 35 (2.4) 6 (2.3) 11 (2.2) 5 (4.1) 3 (1.7) 10 (2.5)
 Inflammatory myopathy 33 (2.3) 6 (2.3) 13 (2.6) 1 (0.8) 6 (3.5) 7 (1.8)
 Other connective tissue diseases 37 (2.6) 9 (3.4) 8 (1.6) 3 (2.4) 3 (1.7) 14 (3.5)
 Sarcoidosis 43 (3.0) 9 (3.4) 22 (4.5) 1 (0.8) 4 (2.3) 7 (1.8)
 Multiple rheumatic diagnoses 35 (2.4) 6 (2.3) 9 (1.8) 4 (3.3) 4 (2.3) 12 (3.0)
 Other diagnoses§ 28 (1.9) 2 (0.8) 6 (1.2) 3 (2.4) 8 (4.7) 9 (2.2)
Disease activity, n (%)
 Remission or low activity 1074 (74.1) 181 (69.3) 365 (74.2) 91 (74.0) 131 (76.2) 306 (76.3)
 Moderate or severe activity 259 (17.9) 50 (19.2) 100 (20.3) 23 (18.7) 27 (15.7) 59 (14.7)
 Unknown 116 (8.0) 30 (11.5) 27 (5.5) 9 (7.3) 14 (8.1) 36 (9.0)
Rheumatic disease medications at time of infection, n (%)
 Glucocorticoids 377 (26.0) 80 (30.7) 125 (25.4) 29 (23.6) 42 (24.4) 101 (25.2)
 None 1072 (74.0) 181 (69.3) 367 (74.6) 94 (76.4) 130 (75.6) 300 (74.8)
 Low dose (1–10 mg) 317 (21.9) 70 (26.8) 106 (21.5) 26 (21.1) 36 (20.9) 79 (19.7)
 Moderate/high dose (>10 mg) 53 (3.7) 10 (3.8) 18 (3.7) 3 (2.4) 4 (2.3) 18 (4.5)
 Unknown dose 7 (0.5) 0 (0.0) 1 (0.2) 0 (0.0) 2 (1.2) 4 (1.0)
Conventional synthetic DMARDs and immunosuppressants
 Methotrexate 319 (22.0) 49 (18.8) 108 (22.0) 21 (17.1) 38 (22.1) 103 (25.7)
 Antimalarials 314 (21.7) 58 (22.2) 102 (20.7) 20 (16.3) 36 (20.9) 98 (24.4)
 Sulfasalazine 31 (2.1) 5 (1.9) 8 (1.6) 2 (1.6) 3 (1.7) 13 (3.2)
 Leflunomide 54 (3.7) 12 (4.6) 23 (4.7) 1 (0.8) 5 (2.9) 13 (3.2)
 Mycophenolate mofetil 101 (7.0) 13 (5.0) 27 (5.5) 13 (10.6) 17 (9.9) 31 (7.7)
 Azathioprine 27 (1.9) 9 (3.4) 6 (1.2) 4 (3.3) 2 (1.2) 6 (1.5)
 Calcineurin inhibitor 19 (1.3) 4 (1.5) 5 (1.0) 5 (4.1) 3 (1.7) 2 (0.5)
 Cyclophosphamide 4 (0.3) 3 (1.2) 0 (0) 0 (0) 1 (0.6) 0 (0)
Biologic DMARDs
 TNF inhibitors 292 (20.2) 32 (12.3) 90 (18.3) 26 (21.1) 40 (23.3) 104 (25.9)
 Rituximab 133 (9.2) 17 (6.5) 33 (6.7) 18 (14.6) 25 (14.5) 40 (10.0)
 Belimumab 20 (1.4) 4 (1.5) 1 (0.2) 1 (0.8) 3 (1.7) 11 (2.7)
 Abatacept 31 (2.1) 4 (1.5) 6 (1.2) 3 (2.4) 3 (1.7) 15 (3.7)
 IL-6 inhibitors 45 (3.1) 3 (1.2) 18 (3.7) 3 (2.4) 5 (2.9) 16 (4.0)
 IL-17, IL-12/23, and IL-23 inhibitors 36 (2.5) 8 (3.1) 16 (3.3) 2 (1.6) 3 (1.7) 7 (1.7)
 IL-1 inhibitors 6 (0.4) 0 (0) 0 (0) 0 (0%) 3 (1.7) 3 (0.8)
Targeted synthetic DMARDs
 JAK inhibitors 55 (3.8) 8 (3.1) 21 (4.3) 4 (3.3) 7 (4.1) 15 (3.7)
 Apremilast 5 (0.4) 0 (0) 2 (0.4) 0 (0) 0 (0) 3 (0.8)
IVIG 19 (1.3) 2 (0.8) 7 (1.4) 2 (1.6) 4 (2.3) 4 (1.0)
*

Includes juvenile idiopathic arthritis, other unspecified inflammatory arthritis.

Includes Takayasu’s arteritis, Kawasaki disease, Behcet’s disease, polyarteritis nodosa, other vasculitis.

Includes undifferentiated connective tissue disease, mixed connective tissue disease, antiphospholipid syndrome (without concurrent systemic lupus erythematosus).

§

Includes relapsing polychondritis, IgG4-related disease, sclerosing mediastinitis, periodic fever syndromes, adult-onset Still’s disease.

ANCA, antineutrophil cytoplasmic antibody; DMARD, disease-modifying antirheumatic drug; GCA, giant cell arteritis; IL, interleukin; IVIG, intravenous immune globulin; JAK, Janus kinase; PMR, polymyalgia rheumatica; SARD, systemic autoimmune rheumatic disease; TNF, tumour necrosis factor.