Table 1.
Characteristics | Mean (SD) or number (percentage) |
Age, years, mean (SD) | 44.4 (14.1) |
Female, n (%) | 1734 (90.4%) |
Race/Ethnicity, n (%) | |
White | 639 (33.3%) |
Non-white | 1102 (57.3%) |
Missing | 181 (9.4%) |
Region, n (%) | |
Europe | 543 (28.3%) |
USA and Canada | 555 (28.9%) |
Latin America | 643 (33.5%) |
Other | 181 (9.4%) |
Time period, n (%) | |
<15 June 2020 | 733 (38.1%) |
16 June–30 September 2020 | 444 (23.1%) |
1 October 2020–12 April 2021 | 745 (38.8%) |
Comorbidities, n (%) | |
0 | 1098 (57.1%) |
1 | 511 (26.6%) |
≥2 | 313 (16.3%) |
Specific comorbidities, n (%) | |
Chronic renal insufficiency or ESRD | 223 (11.8%) |
Hypertension or cardiovascular disease | 597 (31.1%) |
Disease activity, n (%) | |
Remission | 587 (30.5%) |
Minimal or low | 700 (36.4%) |
Moderate | 229 (11.9%) |
Severe or high | 77 (4.0%) |
Missing | 329 (17.1%) |
Prednisone dose*, n (%) | |
0 mg/day | 846 (44.0%) |
1–5 mg/day | 467 (24.3%) |
6–9 mg/day | 78 (4.1%) |
≥10 mg/day | 280 (14.6%) |
Missing | 251 (13.1%) |
Medication category, n (%) | |
Antimalarials only | 665 (34.6%) |
No SLE therapy | 230 (12.0%) |
Oral synthetic drug monotherapy with methotrexate, leflunomide or sulfasalazine only† | 175 (9.1%) |
Oral synthetic drug monotherapy with (mycophenolate/mycophenolic acid, tacrolimus, cyclophosphamide, ciclosporin or azathioprine)† | 630 (32.8%) |
Biologic/Targeted synthetic monotherapy | 45 (2.3%) |
Biologic/Targeted and immunosuppressive drug combination therapy† | 177 (9.2%) |
*All glucocorticoids were converted to prednisone-equivalent doses.
†These patients could be also on antimalarials.
ESRD, end-stage renal disease; SLE, systemic lupus erythematosus.