Objective: To investigate the incidence of and factors associated with SARS–CoV-2 testing and infection in immune-mediated inflammatory disease (IMID) patients versus matched non-IMID comparators from the general population. Methods: We conducted a population-based, matched cohort study among adult residents from Ontario, Canada, from January 2020 to December 2020. We created cohorts for the following IMIDs: rheumatoid arthritis (RA), psoriasis, psoriatic arthritis, ankylosing spondylitis, systemic autoimmune rheumatic diseases, multiple sclerosis (MS), iritis, inflammatory bowel disease (IBD), polymyalgia rheumatica, and vasculitis. Each patient was matched with 5 patients without IMIDs based on sociodemographic factors. We estimated the incidence of SARS–CoV-2 testing and infection in IMID patients and non-IMID patients. Multivariable logistic regressions assessed odds of SARS–CoV-2 infection. Results: We studied 493,499 patients with IMIDs and 2,466,946 patients without IMIDs. Patients with IMIDs were more likely to have at least 1 SARS–CoV-2 test versus patients without IMIDs (27.4% versus 22.7%), but the proportion testing positive for SARS–CoV-2 was identical (0.9% in both groups). Overall, IMID patients had 20% higher odds of being tested for SARS–CoV-2 (odds ratio 1.20 [95% confidence interval 1.19–1.21]). The odds of SARS–CoV-2 infection varied across IMID groups but was not significantly elevated for most IMID groups compared with non-IMID comparators. The odds of SARS–CoV-2 infection was lower in IBD and MS and marginally higher in RA and iritis. Conclusion: Patients across all IMIDs were more likely to be tested for SARS–CoV-2 versus those without IMIDs. The risk of SARS–CoV-2 infection varied across disease subgroups.
CITATION STYLE
Eder, L., Croxford, R., Drucker, A. M., Mendel, A., Kuriya, B., Touma, Z., … Widdifield, J. (2023). Understanding COVID-19 Risk in Patients With Immune-Mediated Inflammatory Diseases: A Population-Based Analysis of SARS–CoV-2 Testing. Arthritis Care and Research, 75(2), 317–325. https://doi.org/10.1002/acr.24781
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