{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,15]],"date-time":"2026-07-15T12:02:29Z","timestamp":1784116949155,"version":"3.55.0"},"reference-count":44,"publisher":"American Medical Association (AMA)","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi231081-4\"><jats:title>Importance<\/jats:title><jats:p>Immune-mediated inflammatory diseases (IMIDs) and COVID-19 are independently associated with venous thromboembolisms (VTEs).<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-5\"><jats:title>Objective<\/jats:title><jats:p>To determine if individuals with IMIDs are at higher risk of VTE following COVID-19 infection compared with individuals without IMIDs.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-6\"><jats:title>Design, Setting, and Participants<\/jats:title><jats:p>Population-based matched cohort study using multiple deterministically linked health administrative databases from Ontario, Canada, and including patients testing positive for COVID-19 between January 1, 2020, and December 30, 2021, and followed up until March 31, 2022. Individuals with IMIDs (n\u2009=\u200928\u202f440) who tested positive for COVID-19 were matched with up to 5 individuals without an IMID (n\u2009=\u2009126\u202f437) who tested positive for COVID-19. Matching was based on year of birth, sex, neighborhood income, and rural\/urban residence. Data analysis was performed from August 6, 2022, to August 21, 2023.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-7\"><jats:title>Exposure<\/jats:title><jats:p>Diagnosis of an IMID, identified using algorithms based on diagnostic codes, procedures, and specialist visits.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-8\"><jats:title>Main Outcome and Measure<\/jats:title><jats:p>The main outcome was estimated age- and sex-standardized incidence of VTE. Proportional cause-specific hazard models compared the risk of VTE in people with and without IMIDs. Death was a competing risk. Models adjusted for history of VTE, 2 or more doses of a COVID-19 vaccine 14 or more days prior to COVID-19 diagnosis, and the Charlson Comorbidity Index. Routinely collected health data were used, so the hypothesis tested was formulated after data collection but prior to being granted access to data.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-9\"><jats:title>Results<\/jats:title><jats:p>The study included 28\u202f440 individuals (16\u202f741 [58.9%] female; 11\u202f699 [41.1%] male) with an IMID diagnosed prior to first COVID-19 diagnosis, with a mean (SD) age of 52.1 (18.8) years at COVID-19 diagnosis. These individuals were matched to 126\u202f437 controls without IMIDs. The incidence of VTE within 6 months of COVID-19 diagnosis among 28\u202f440 individuals with an IMID was 2.64 (95% CI, 2.23-3.10) per 100\u202f000 person-days compared with 2.18 (95% CI, 1.99-2.38) per 100\u202f000 person-days among 126\u202f437 matched individuals without IMIDs. The VTE risk was not statistically significantly different among those with vs without IMIDs (adjusted hazard ratio, 1.12; 95% CI, 0.95-1.32).<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi231081-10\"><jats:title>Conclusions and Relevance<\/jats:title><jats:p>In this retrospective population-based cohort study of individuals with IMIDs following COVID-19, individuals with IMIDs did not have a higher risk of VTE compared with individuals without an IMID. These data provide reassurance to clinicians caring for individuals with IMIDs and COVID-19.<\/jats:p><\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2023.37020","type":"journal-article","created":{"date-parts":[[2023,10,9]],"date-time":"2023-10-09T15:01:40Z","timestamp":1696863700000},"page":"e2337020","source":"Crossref","is-referenced-by-count":6,"title":["Venous Thromboembolism After COVID-19 Infection Among People With and Without Immune-Mediated Inflammatory Diseases"],"prefix":"10.1001","volume":"6","author":[{"given":"Rabia","family":"Khan","sequence":"first","affiliation":[{"name":"SickKids Inflammatory Bowel Disease Centre, Division of Gastroenterology, Hepatology and Nutrition, The Hospital for Sick Children, Toronto, Ontario, Canada"},{"name":"Child Health Evaluative Sciences, SickKids Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. 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