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[Preprint]. 2022 Jun 20:2022.06.19.22276599. [Version 1] doi: 10.1101/2022.06.19.22276599

Table 2:

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

Time period
Early COVID-19 Early treatment Early vaccination Additional vaccination and Delta wave Omicron wave
Overall (n = 1449) March 1 2020 - June 30 2020 (n = 261) July 1 2020 - Jan 31 2021 (n = 492) Feb 1 2021 - June 30 2021 (n = 123) July 1 2021 - Dec 16 2021 (n = 172) Dec 17 2021 - Jan 31 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 – 10mg) 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%)

SARD, systemic autoimmune rheumatic disease; COVID-19, coronavirus disease 2019; PMR, polymyalgia rheumatica; GCA, giant cell arteritis; ANCA, antineutrophil cytoplasmic antibody; TNF, tumor necrosis factor; IL, interleukin; JAK, Janus kinase; IVIG, intravenous immune globulin

*

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 SLE)

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