Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study

Background: Even though clinical data support a relation between ischemic stroke and venous thromboembolism (VTE), the strength and time dependence of the association remain to be settled at the population level. We therefore aimed to investigate the association between ischemic stroke and VTE in a...

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Main Author: Rinde, Ludvig Balteskard
Format: Master Thesis
Language:English
Published: UiT Norges arktiske universitet 2017
Subjects:
Online Access:https://hdl.handle.net/10037/12055
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author Rinde, Ludvig Balteskard
author_facet Rinde, Ludvig Balteskard
author_sort Rinde, Ludvig Balteskard
collection University of Tromsø: Munin Open Research Archive
description Background: Even though clinical data support a relation between ischemic stroke and venous thromboembolism (VTE), the strength and time dependence of the association remain to be settled at the population level. We therefore aimed to investigate the association between ischemic stroke and VTE in a prospective population-based cohort. Methods and Results: Participants (n=30 002) were recruited from 3 surveys of the Tromsø study (conducted in 1994–1995, 2001, and 2007–2008) and followed through 2010. All incident events of ischemic stroke and VTE during follow-up were recorded. Cox-regression models with age as time scale and ischemic stroke as a time-dependent variable were used to calculate hazard ratios (HR) of VTE adjusted for cardiovascular risk factors. During a median follow-up time of 15.7 years, 1360 participants developed ischemic stroke and 722 had a VTE. The risk of VTE was highest the first month (HR 19.7;95% CI, 10.1–38.5) and from 1 to 3 months after the stroke (HR 10.6; 95% CI 5.0–22.5), but declined rapidly thereafter. The risk estimates were approximately the same for deep vein thrombosis (HR 19.1; 95% CI, 7.8–38.5), and pulmonary embolism (HR 20.2; 95% CI, 7.4–55.1). Stroke was associated with higher risk for provoked (HR 22.6; 95% CI, 12.5–40.9) than unprovoked VTE (HR 7.4; 95% CI, 2.7–20.1) the first 3 months. Conclusions: The risk of VTE increased during the first 3 months after an ischemic stroke. The particularly high risk of provoked VTE suggests that additional predisposing factors, such as immobilization, potentiate the VTE risk in patients with ischemic stroke.
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geographic Tromsø
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op_rights Attribution-NonCommercial-ShareAlike 3.0 Unported (CC BY-NC-SA 3.0)
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https://creativecommons.org/licenses/by-nc-sa/3.0
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spelling ftunivtroemsoe:oai:munin.uit.no:10037/12055 2025-04-13T14:27:35+00:00 Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study Rinde, Ludvig Balteskard 2017-10-21 https://hdl.handle.net/10037/12055 eng eng UiT Norges arktiske universitet UiT The Arctic University of Norway https://hdl.handle.net/10037/12055 Attribution-NonCommercial-ShareAlike 3.0 Unported (CC BY-NC-SA 3.0) openAccess Copyright 2017 The Author(s) https://creativecommons.org/licenses/by-nc-sa/3.0 VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Hematology: 775 VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Hematologi: 775 MED-3910 Master thesis Mastergradsoppgave 2017 ftunivtroemsoe 2025-03-14T05:17:55Z Background: Even though clinical data support a relation between ischemic stroke and venous thromboembolism (VTE), the strength and time dependence of the association remain to be settled at the population level. We therefore aimed to investigate the association between ischemic stroke and VTE in a prospective population-based cohort. Methods and Results: Participants (n=30 002) were recruited from 3 surveys of the Tromsø study (conducted in 1994–1995, 2001, and 2007–2008) and followed through 2010. All incident events of ischemic stroke and VTE during follow-up were recorded. Cox-regression models with age as time scale and ischemic stroke as a time-dependent variable were used to calculate hazard ratios (HR) of VTE adjusted for cardiovascular risk factors. During a median follow-up time of 15.7 years, 1360 participants developed ischemic stroke and 722 had a VTE. The risk of VTE was highest the first month (HR 19.7;95% CI, 10.1–38.5) and from 1 to 3 months after the stroke (HR 10.6; 95% CI 5.0–22.5), but declined rapidly thereafter. The risk estimates were approximately the same for deep vein thrombosis (HR 19.1; 95% CI, 7.8–38.5), and pulmonary embolism (HR 20.2; 95% CI, 7.4–55.1). Stroke was associated with higher risk for provoked (HR 22.6; 95% CI, 12.5–40.9) than unprovoked VTE (HR 7.4; 95% CI, 2.7–20.1) the first 3 months. Conclusions: The risk of VTE increased during the first 3 months after an ischemic stroke. The particularly high risk of provoked VTE suggests that additional predisposing factors, such as immobilization, potentiate the VTE risk in patients with ischemic stroke. Master Thesis Tromsø University of Tromsø: Munin Open Research Archive Tromsø
spellingShingle VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Hematology: 775
VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Hematologi: 775
MED-3910
Rinde, Ludvig Balteskard
Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title_full Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title_fullStr Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title_full_unstemmed Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title_short Ischemic stroke and risk of venous thromboembolism in the general population. The Tromsø study
title_sort ischemic stroke and risk of venous thromboembolism in the general population. the tromsø study
topic VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Hematology: 775
VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Hematologi: 775
MED-3910
topic_facet VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Hematology: 775
VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Hematologi: 775
MED-3910
url https://hdl.handle.net/10037/12055