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. 2020 Jul 28;83(6):1696–1703. doi: 10.1016/j.jaad.2020.07.089

Table I.

Characteristics of the study population of patients tested for COVID-19

Characteristics Patients with IMID on IS therapy (N = 213)
Age, y, mean ± SD 53 ± 15
Age >65 y, n (%) 50 (23.5)
Female sex, n (%) 155 (72.8)
Race or ethnic group, n (%)
 White 112 (52.6)
 Black 74 (34.7)
 Hispanic 3 (1.4)
 Asian 2 (0.9)
 Middle Eastern 3 (1.4)
 Other/unknown 19 (8.9)
COVID-19 positive, n (%) 77 (36.2)
Hydroxychloroquine use, n (%) 28 (13.1)
IS medication class, n (%)
 Biologics 96 (45.1)
 TNF-α inhibitors 56 (26.3)
 TNF-α inhibitor monotherapy 45 (21.1)
 IL-17 inhibitors 7 (3.3)
 IL-12/23 inhibitors 7 (3.3)
 Biologic monotherapy 73 (34.3)
 DMARDs 138 (64.8)
 Apremilast 10 (4.7)
 Azathioprine 25 (11.7)
 Methotrexate 65 (30.5)
 Methotrexate monotherapy 45 (21.1)
 Mycophenolate 23 (10.8)
 DMARD monotherapy 100 (46.9)
 Multidrug therapy 40 (18.8)
 Systemic corticosteroids 22 (10.3)
Comorbidity class, n (%)
 Cardiac 109 (51.2)
 Pulmonary 75 (35.2)
 Renal 11 (5.2)
 Gastrointestinal 45 (21.1)
 Endocrine 133 (62.4)
 Cancer 11 (5.2)
IMID classification, n (%)
 Rheumatoid arthritis/spondylitis 72 (33.8)
 Psoriasis/psoriatic arthritis 29 (13.6)
 Inflammatory bowel disease 38 (17.8)
 SLE/DM, PM/MCTD/ILD/Scl 33 (15.5)
 Others§ 45 (21.1)

DM, Dermatomyositis; DMARD, disease-modifying antirheumatic drug; IL, interleukin; ILD, interstitial lung disease; IMID, immune-mediated inflammatory disease; IS, immunosuppressive; MCTD, mixed connective tissue disease; PM, polymyositis; Scl, scleroderma and systemic sclerosis; SD, standard deviation; SLE, systemic lupus erythematosus; TNF, tumor necrosis factor.

Concomitant use with IS medication.

Any patient taking a medication from a therapeutic class (Supplemental Table I) was included in the respective group, regardless of additional medications taken. Biologics and DMARDs were further subcategorized as shown. Monotherapy designates a patient using a medication without an additional biologic or DMARD. Therapeutics with fewer than 5 patients treated are not shown.

Patients taking medications from both the biologics and DMARD groups or multiple DMARDs within the IMID cohort were also included in the multidrug therapy group.

§

Others includes patients treated with IS therapy for autoimmune blistering conditions, autoimmune hepatitis, atopic conditions, hidradenitis suppurativa, myasthenia gravis, sarcoidosis, urticaria, and uveitis.