Disease areas:
  • heart and blood vessels
  • infections
Last updated:
Author(s):
Jana J Anderson, Frederick K Ho, Claire L Niedzwiedz, Srinivasa Vittal Katikireddi, Carlos Celis-Morales, Stamatina Iliodromiti, Paul Welsh, Pierpaolo Pellicori, Evangelia Demou, Claire E Hastie, Donald M Lyall, Stuart R Gray, John F Forbes, Jason M R Gill, Daniel F Mackay, Colin Berry, John G F Cleland, Naveed Sattar, Jill P Pell
Publish date:
20 July 2021
Journal:
Journal of Thrombosis and Haemostasis
PubMed ID:
34242477

Abstract

BACKGROUND: Venous thromboembolism (VTE) is a common, life-threatening complication of COVID-19 infection. COVID-19 risk-prediction models include a history of VTE. However, it is unclear whether remote history (>9 years previously) of VTE also confers increased risk of COVID-19.

OBJECTIVES: To investigate possible association between VTE and COVID-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 COVID-19 test results, COVID-19-related hospital admissions, and COVID-19 deaths. The risk of COVID-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) COVID-19. Associations with remote history of VTE were stronger among men (severe COVID-19: RR 1.68, 95% CI 1.14-2.42, p = .009) than for women (severe COVID-19: RR 1.07, 95% CI 0.66-1.74, p = .786).

CONCLUSION: Our findings support inclusion of remote history of VTE in COVID-19 risk-prediction scores, and consideration of sex-specific risk scores.

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