Author: Anderson, Jana J.; Ho, Frederick K.; Niedzwiedz, Claire L.; Katikireddi, Srinivasa Vittal; Celisâ€Morales, Carlos; Iliodromiti, Stamatina; Welsh, Paul; Pellicori, Pierpaolo; Demou, Evangelia; Hastie, Claire E.; Lyall, Donald M.; Gray, Stuart R.; Forbes, John F.; Gill, Jason M. R.; Mackay, Daniel F.; Berry, Colin; Cleland, John G. F.; Sattar, Naveed; Pell, Jill P.
Title: Remote history of VTE is associated with severe COVIDâ€19 in middle and older age: UK Biobank cohort study Cord-id: 08ynaiuu Document date: 2021_7_20
ID: 08ynaiuu
Snippet: BACKGROUND: Venous thromboembolism (VTE) is a common, lifeâ€threatening complication of COVIDâ€19 infection. COVIDâ€19 riskâ€prediction models include a history of VTE. However, it is unclear whether remote history (>9 years previously) of VTE also confers increased risk of COVIDâ€19. OBJECTIVES: To investigate possible association between VTE and COVIDâ€19 severity, independent of other risk factors. METHODS: Cohort study of UK Biobank participants recruited between 2006 and 2010. Baselin
Document: BACKGROUND: Venous thromboembolism (VTE) is a common, lifeâ€threatening complication of COVIDâ€19 infection. COVIDâ€19 riskâ€prediction models include a history of VTE. However, it is unclear whether remote history (>9 years previously) of VTE also confers increased risk of COVIDâ€19. OBJECTIVES: To investigate possible association between VTE and COVIDâ€19 severity, independent of other risk factors. METHODS: Cohort study of UK Biobank participants recruited between 2006 and 2010. Baseline data, including history of VTE, were linked to COVIDâ€19 test results, COVIDâ€19â€related hospital admissions, and COVIDâ€19 deaths. The risk of COVIDâ€19 hospitalization or death was compared for participants with a remote history VTE versus without. Poisson regression models were run univariately then adjusted stepwise for sociodemographic, lifestyle, and comorbid covariates. RESULTS: After adjustment for sociodemographic and lifestyle confounders and comorbid conditions, remote history of VTE was associated with nonfatal community (RR 1.61, 95% CI 1.02–2.54, p = .039), nonfatal hospitalized (RR 1.52, 95% CI 1.06–2.17, p = .024) and severe (hospitalized or fatal) (RR 1.40, 95% CI 1.04–1.89, p = .025) COVIDâ€19. Associations with remote history of VTE were stronger among men (severe COVIDâ€19: RR 1.68, 95% CI 1.14–2.42, p = .009) than for women (severe COVIDâ€19: RR 1.07, 95% CI 0.66–1.74, p = .786). CONCLUSION: Our findings support inclusion of remote history of VTE in COVIDâ€19 riskâ€prediction scores, and consideration of sexâ€specific risk scores.
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