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Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study
The benefit of oral anticoagulant (OAC) therapy in atrial fibrillation (AF) and intermediate stroke risk is debated. In a nationwide Norwegian cohort with a non-sex CHA2DS2-VASc risk score of one, this study aimed to investigate (i) stroke and bleeding risk in AF patients with and without OAC treatm...
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Published in: | European heart journal 2024-01, Vol.45 (1), p.57-66 |
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creator | Anjum, Mariam Ariansen, Inger Hjellvik, Vidar Selmer, Randi Kjerpeseth, Lars J Skovlund, Eva Myrstad, Marius Ellekjær, Hanne Christophersen, Ingrid E Tveit, Arnljot Berge, Trygve |
description | The benefit of oral anticoagulant (OAC) therapy in atrial fibrillation (AF) and intermediate stroke risk is debated. In a nationwide Norwegian cohort with a non-sex CHA2DS2-VASc risk score of one, this study aimed to investigate (i) stroke and bleeding risk in AF patients with and without OAC treatment, and (ii) the risk of stroke in non-anticoagulated individuals with and without AF.
A total of 1 118 762 individuals including 34 460 AF patients were followed during 2011-18 until ischaemic stroke, intracranial haemorrhage, increased CHA2DS2-VASc score, or study end. One-year incidence rates (IRs) were calculated as events per 100 person-years (%/py). Cox regression models provided adjusted hazard ratios (aHRs [95% confidence intervals]).
Among AF patients, the ischaemic stroke IR was 0.51%/py in OAC users and 1.05%/py in non-users (aHR 0.47 [0.37-0.59]). Intracranial haemorrhage IR was 0.28%/py in OAC users and 0.19%/py in non-users (aHR 1.23 [0.88-1.72]). Oral anticoagulant use was associated with an increased risk of major bleeding (aHR 1.37 [1.16-1.63]) but lower risk of the combined outcome of ischaemic stroke, major bleeding, and mortality (aHR 0.57 [0.51-0.63]). Non-anticoagulated individuals with AF had higher risk of ischaemic stroke compared to non-AF individuals with the same risk profile (aHR 2.47 [2.17-2.81]).
In AF patients at intermediate risk of stroke, OAC use was associated with overall favourable clinical outcomes. Non-anticoagulated AF patients had higher risk of ischaemic stroke compared to the general population without AF with the same risk profile. |
doi_str_mv | 10.1093/eurheartj/ehad659 |
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A total of 1 118 762 individuals including 34 460 AF patients were followed during 2011-18 until ischaemic stroke, intracranial haemorrhage, increased CHA2DS2-VASc score, or study end. One-year incidence rates (IRs) were calculated as events per 100 person-years (%/py). Cox regression models provided adjusted hazard ratios (aHRs [95% confidence intervals]).
Among AF patients, the ischaemic stroke IR was 0.51%/py in OAC users and 1.05%/py in non-users (aHR 0.47 [0.37-0.59]). Intracranial haemorrhage IR was 0.28%/py in OAC users and 0.19%/py in non-users (aHR 1.23 [0.88-1.72]). Oral anticoagulant use was associated with an increased risk of major bleeding (aHR 1.37 [1.16-1.63]) but lower risk of the combined outcome of ischaemic stroke, major bleeding, and mortality (aHR 0.57 [0.51-0.63]). Non-anticoagulated individuals with AF had higher risk of ischaemic stroke compared to non-AF individuals with the same risk profile (aHR 2.47 [2.17-2.81]).
In AF patients at intermediate risk of stroke, OAC use was associated with overall favourable clinical outcomes. Non-anticoagulated AF patients had higher risk of ischaemic stroke compared to the general population without AF with the same risk profile.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/ehad659</identifier><identifier>PMID: 37995254</identifier><language>eng</language><publisher>England</publisher><subject>Anticoagulants ; Atrial Fibrillation - complications ; Atrial Fibrillation - drug therapy ; Atrial Fibrillation - epidemiology ; Brain Ischemia - epidemiology ; Brain Ischemia - etiology ; Brain Ischemia - prevention & control ; Hemorrhage - chemically induced ; Hemorrhage - complications ; Hemorrhage - epidemiology ; Humans ; Intracranial Hemorrhages - chemically induced ; Intracranial Hemorrhages - epidemiology ; Ischemic Stroke - chemically induced ; Ischemic Stroke - complications ; Ischemic Stroke - drug therapy ; Risk Assessment ; Risk Factors ; Stroke - epidemiology ; Stroke - etiology ; Stroke - prevention & control</subject><ispartof>European heart journal, 2024-01, Vol.45 (1), p.57-66</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-1dfce66bf32d61f70ad1bb8652755da248176eeaf1ba4e84afcb7366930a97483</citedby><cites>FETCH-LOGICAL-c301t-1dfce66bf32d61f70ad1bb8652755da248176eeaf1ba4e84afcb7366930a97483</cites><orcidid>0000-0001-9480-3848 ; 0000-0002-7681-8621 ; 0000-0001-8529-4826 ; 0000-0002-7223-5138</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37995254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anjum, Mariam</creatorcontrib><creatorcontrib>Ariansen, Inger</creatorcontrib><creatorcontrib>Hjellvik, Vidar</creatorcontrib><creatorcontrib>Selmer, Randi</creatorcontrib><creatorcontrib>Kjerpeseth, Lars J</creatorcontrib><creatorcontrib>Skovlund, Eva</creatorcontrib><creatorcontrib>Myrstad, Marius</creatorcontrib><creatorcontrib>Ellekjær, Hanne</creatorcontrib><creatorcontrib>Christophersen, Ingrid E</creatorcontrib><creatorcontrib>Tveit, Arnljot</creatorcontrib><creatorcontrib>Berge, Trygve</creatorcontrib><title>Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>The benefit of oral anticoagulant (OAC) therapy in atrial fibrillation (AF) and intermediate stroke risk is debated. In a nationwide Norwegian cohort with a non-sex CHA2DS2-VASc risk score of one, this study aimed to investigate (i) stroke and bleeding risk in AF patients with and without OAC treatment, and (ii) the risk of stroke in non-anticoagulated individuals with and without AF.
A total of 1 118 762 individuals including 34 460 AF patients were followed during 2011-18 until ischaemic stroke, intracranial haemorrhage, increased CHA2DS2-VASc score, or study end. One-year incidence rates (IRs) were calculated as events per 100 person-years (%/py). Cox regression models provided adjusted hazard ratios (aHRs [95% confidence intervals]).
Among AF patients, the ischaemic stroke IR was 0.51%/py in OAC users and 1.05%/py in non-users (aHR 0.47 [0.37-0.59]). Intracranial haemorrhage IR was 0.28%/py in OAC users and 0.19%/py in non-users (aHR 1.23 [0.88-1.72]). Oral anticoagulant use was associated with an increased risk of major bleeding (aHR 1.37 [1.16-1.63]) but lower risk of the combined outcome of ischaemic stroke, major bleeding, and mortality (aHR 0.57 [0.51-0.63]). Non-anticoagulated individuals with AF had higher risk of ischaemic stroke compared to non-AF individuals with the same risk profile (aHR 2.47 [2.17-2.81]).
In AF patients at intermediate risk of stroke, OAC use was associated with overall favourable clinical outcomes. Non-anticoagulated AF patients had higher risk of ischaemic stroke compared to the general population without AF with the same risk profile.</description><subject>Anticoagulants</subject><subject>Atrial Fibrillation - complications</subject><subject>Atrial Fibrillation - drug therapy</subject><subject>Atrial Fibrillation - epidemiology</subject><subject>Brain Ischemia - epidemiology</subject><subject>Brain Ischemia - etiology</subject><subject>Brain Ischemia - prevention & control</subject><subject>Hemorrhage - chemically induced</subject><subject>Hemorrhage - complications</subject><subject>Hemorrhage - epidemiology</subject><subject>Humans</subject><subject>Intracranial Hemorrhages - chemically induced</subject><subject>Intracranial Hemorrhages - epidemiology</subject><subject>Ischemic Stroke - chemically induced</subject><subject>Ischemic Stroke - complications</subject><subject>Ischemic Stroke - drug therapy</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Stroke - epidemiology</subject><subject>Stroke - etiology</subject><subject>Stroke - prevention & control</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOwzAURC0EouXxAWyQl2wCfsROzK4qjyJVRaKA2EVOfN0a0hhsR4i_p6ilq9mcGWkOQmeUXFKi-BX0YQk6pPcrWGojhdpDQyoYy5TMxT4aEqpEJmX5NkBHMb4TQkpJ5SEa8EIpwUQ-RN08Bf8BWHcG1y2Acd0CBxc_sOuwTsHpFltXB9e2Ojnf4W-Xlng8GbGbOcteR_Pxho6ND4C9xb6Da5yWgGc-fMPC6Q6P7maPTzim3vycoAOr2win2zxGL3e3z-NJNn28fxiPplnDCU0ZNbYBKWvLmZHUFkQbWtelFKwQwmiWl7SQANrSWudQ5to2dcGlVJxoVeQlP0YXm93P4L96iKlaudjA-kQHvo8VKxUvc0IKvkbpBm2CjzGArT6DW-nwU1FS_WmudpqrreZ153w739crMLvGv1f-C512fF0</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Anjum, Mariam</creator><creator>Ariansen, Inger</creator><creator>Hjellvik, Vidar</creator><creator>Selmer, Randi</creator><creator>Kjerpeseth, Lars J</creator><creator>Skovlund, Eva</creator><creator>Myrstad, Marius</creator><creator>Ellekjær, Hanne</creator><creator>Christophersen, Ingrid E</creator><creator>Tveit, Arnljot</creator><creator>Berge, Trygve</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9480-3848</orcidid><orcidid>https://orcid.org/0000-0002-7681-8621</orcidid><orcidid>https://orcid.org/0000-0001-8529-4826</orcidid><orcidid>https://orcid.org/0000-0002-7223-5138</orcidid></search><sort><creationdate>20240101</creationdate><title>Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study</title><author>Anjum, Mariam ; Ariansen, Inger ; Hjellvik, Vidar ; Selmer, Randi ; Kjerpeseth, Lars J ; Skovlund, Eva ; Myrstad, Marius ; Ellekjær, Hanne ; Christophersen, Ingrid E ; Tveit, Arnljot ; Berge, Trygve</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-1dfce66bf32d61f70ad1bb8652755da248176eeaf1ba4e84afcb7366930a97483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anticoagulants</topic><topic>Atrial Fibrillation - complications</topic><topic>Atrial Fibrillation - drug therapy</topic><topic>Atrial Fibrillation - epidemiology</topic><topic>Brain Ischemia - epidemiology</topic><topic>Brain Ischemia - etiology</topic><topic>Brain Ischemia - prevention & control</topic><topic>Hemorrhage - chemically induced</topic><topic>Hemorrhage - complications</topic><topic>Hemorrhage - epidemiology</topic><topic>Humans</topic><topic>Intracranial Hemorrhages - chemically induced</topic><topic>Intracranial Hemorrhages - epidemiology</topic><topic>Ischemic Stroke - chemically induced</topic><topic>Ischemic Stroke - complications</topic><topic>Ischemic Stroke - drug therapy</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Stroke - epidemiology</topic><topic>Stroke - etiology</topic><topic>Stroke - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anjum, Mariam</creatorcontrib><creatorcontrib>Ariansen, Inger</creatorcontrib><creatorcontrib>Hjellvik, Vidar</creatorcontrib><creatorcontrib>Selmer, Randi</creatorcontrib><creatorcontrib>Kjerpeseth, Lars J</creatorcontrib><creatorcontrib>Skovlund, Eva</creatorcontrib><creatorcontrib>Myrstad, Marius</creatorcontrib><creatorcontrib>Ellekjær, Hanne</creatorcontrib><creatorcontrib>Christophersen, Ingrid E</creatorcontrib><creatorcontrib>Tveit, Arnljot</creatorcontrib><creatorcontrib>Berge, Trygve</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anjum, Mariam</au><au>Ariansen, Inger</au><au>Hjellvik, Vidar</au><au>Selmer, Randi</au><au>Kjerpeseth, Lars J</au><au>Skovlund, Eva</au><au>Myrstad, Marius</au><au>Ellekjær, Hanne</au><au>Christophersen, Ingrid E</au><au>Tveit, Arnljot</au><au>Berge, Trygve</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>45</volume><issue>1</issue><spage>57</spage><epage>66</epage><pages>57-66</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>The benefit of oral anticoagulant (OAC) therapy in atrial fibrillation (AF) and intermediate stroke risk is debated. In a nationwide Norwegian cohort with a non-sex CHA2DS2-VASc risk score of one, this study aimed to investigate (i) stroke and bleeding risk in AF patients with and without OAC treatment, and (ii) the risk of stroke in non-anticoagulated individuals with and without AF.
A total of 1 118 762 individuals including 34 460 AF patients were followed during 2011-18 until ischaemic stroke, intracranial haemorrhage, increased CHA2DS2-VASc score, or study end. One-year incidence rates (IRs) were calculated as events per 100 person-years (%/py). Cox regression models provided adjusted hazard ratios (aHRs [95% confidence intervals]).
Among AF patients, the ischaemic stroke IR was 0.51%/py in OAC users and 1.05%/py in non-users (aHR 0.47 [0.37-0.59]). Intracranial haemorrhage IR was 0.28%/py in OAC users and 0.19%/py in non-users (aHR 1.23 [0.88-1.72]). Oral anticoagulant use was associated with an increased risk of major bleeding (aHR 1.37 [1.16-1.63]) but lower risk of the combined outcome of ischaemic stroke, major bleeding, and mortality (aHR 0.57 [0.51-0.63]). Non-anticoagulated individuals with AF had higher risk of ischaemic stroke compared to non-AF individuals with the same risk profile (aHR 2.47 [2.17-2.81]).
In AF patients at intermediate risk of stroke, OAC use was associated with overall favourable clinical outcomes. Non-anticoagulated AF patients had higher risk of ischaemic stroke compared to the general population without AF with the same risk profile.</abstract><cop>England</cop><pmid>37995254</pmid><doi>10.1093/eurheartj/ehad659</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9480-3848</orcidid><orcidid>https://orcid.org/0000-0002-7681-8621</orcidid><orcidid>https://orcid.org/0000-0001-8529-4826</orcidid><orcidid>https://orcid.org/0000-0002-7223-5138</orcidid></addata></record> |
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subjects | Anticoagulants Atrial Fibrillation - complications Atrial Fibrillation - drug therapy Atrial Fibrillation - epidemiology Brain Ischemia - epidemiology Brain Ischemia - etiology Brain Ischemia - prevention & control Hemorrhage - chemically induced Hemorrhage - complications Hemorrhage - epidemiology Humans Intracranial Hemorrhages - chemically induced Intracranial Hemorrhages - epidemiology Ischemic Stroke - chemically induced Ischemic Stroke - complications Ischemic Stroke - drug therapy Risk Assessment Risk Factors Stroke - epidemiology Stroke - etiology Stroke - prevention & control |
title | Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study |
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