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Severe COVID-19 in patients with immune-mediated rheumatic diseases: A stratified analysis from the SORCOM
Alina Boteanu1, Leticia Leon2,3, Silvia Pérez Esteban4
1Rheumatology Department and IRYCIS, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Insights
Certain therapies like corticosteroids and rituximab increase COVID-19 severity in rheumatic disease patients. Methotrexate and anti-TNF therapy showed no increased risk for severe coronavirus disease 2019.
Area of Science:
- Rheumatology
- Infectious Diseases
- Immunology
Background:
- Patients with immune-mediated rheumatic diseases (IMRD) face risks from infections like COVID-19.
- Understanding risk factors for severe COVID-19 in IMRD is crucial for patient management.
Purpose of the Study:
- To evaluate risk factors for severe coronavirus disease 2019 (COVID-19) in patients with IMRD.
- To stratify risk factors based on systemic autoimmune conditions versus chronic inflammatory arthritis.
Main Methods:
- Observational, cross-sectional multicentre study.
- Included 523 patients with severe acute respiratory syndrome coronavirus-2 infection from 10 Madrid rheumatology departments (Feb 2020-May 2021).
- Logistic regression analyses adjusted for covariates to estimate risk factors for COVID-19 severity (hospital admission or mortality).
Main Results:
- 35.6% of patients required hospital admission; 7.3% died.
- Male gender, older age, diabetes, hypertension, and obesity were associated with severe COVID-19.
- Corticosteroids (>10mg/day), rituximab, sulfasalazine, and mycophenolate use were independently linked to worse outcomes.
Conclusions:
- Confirms harmful effects of corticosteroids, rituximab, mycophenolate, and sulfasalazine in COVID-19 patients with rheumatic diseases.
- Methotrexate and anti-tumour necrosis factor (anti-TNF) therapies were not associated with worse COVID-19 outcomes.
- Severity decreased across pandemic waves; mortality was higher in systemic autoimmune conditions.
Objectives:
The aim of this study is to evaluate risk factors for severe coronavirus disease 2019 (COVID-19) in patients with immune-mediated rheumatic diseases, stratified by systemic autoimmune conditions and chronic inflammatory arthritis.
Methods:
An observational, cross-sectional multicentre study was performed. Patients from 10 rheumatology departments in Madrid who presented with severe acute respiratory syndrome coronavirus-2 infection between February 2020 and May 2021 were included. The main outcome was COVID-19 severity (hospital admission or mortality). Risk factors for severity were estimated, adjusting for covariates (socio-demographic, clinical, and treatments), using logistic regression analyses.
Results:
In total, 523 patients with COVID-19 were included, among whom 192 (35.6%) patients required hospital admission and 38 (7.3%) died. Male gender, older age, and comorbidities such as diabetes mellitus, hypertension, and obesity were associated with severe COVID-19. Corticosteroid doses >10 mg/day, rituximab, sulfasalazine, and mycophenolate use, were independently associated with worse outcomes. COVID-19 severity decreased over the different pandemic waves. Mortality was higher in the systemic autoimmune conditions (univariate analysis, P < .001), although there were no differences in the overall severity in the multivariate analysis.
Conclusions:
This study confirms and provides new insights regarding the harmful effects of corticosteroids, rituximab, and other therapies (mycophenolate and sulfasalazine) in COVID-19. Methotrexate and anti-tumour necrosis factor therapy were not associated with worse outcomes.
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