Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study

Abstract Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naïve patients with atrial fibrillation (AF). Methods and results This historical c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European heart journal 2021
Hauptverfasser: Halvorsen, Sigrun, Johnsen, Søren P, Madsen, Morten, Linder, Marie, Sulo, Gerhard, Ghanima, Waleed, Gislason, Gunnar, Hohnloser, Stefan H, Jenkins, Aaron, Al-Khalili, Faris, Tell, Grethe S, Ehrenstein, Vera
Format: Artikel
Sprache:nor
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title European heart journal
container_volume
creator Halvorsen, Sigrun
Johnsen, Søren P
Madsen, Morten
Linder, Marie
Sulo, Gerhard
Ghanima, Waleed
Gislason, Gunnar
Hohnloser, Stefan H
Jenkins, Aaron
Al-Khalili, Faris
Tell, Grethe S
Ehrenstein, Vera
description Abstract Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naïve patients with atrial fibrillation (AF). Methods and results This historical cohort study included 219 545 AF patients [median age 74 years; 43% women; mean CHA2DS2-VASc (congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, stroke or transient ischaemic attack, vascular disease, age 65–74 years, sex category) score 3.3] initiating apixaban, dabigatran, rivaroxaban, or warfarin in Denmark, Norway, and Sweden (1 January 2013 to 31 December 2016). The primary endpoints were stroke/SE and major bleeding. The median follow-up times were 9.7 (3.9–21.5) months for stroke/SE and 9.6 (3.8–21.3) months for bleeding. Apixaban and warfarin initiators were older and had higher CHA2DS2-VASc scores compared with dabigatran and rivaroxaban initiators. After 1:1 propensity score matching, three cohorts were created: apixaban–warfarin (n = 111 162), dabigatran–warfarin (n = 56 856), and rivaroxaban–warfarin (n = 61 198). Adjusted hazard ratios (HRs) were estimated using a Cox regression. For stroke/SE, adjusted HRs against warfarin were 0.96 [95% confidence interval (CI): 0.87–1.06] for apixaban, 0.89 (95% CI: 0.80–1.00) for dabigatran, and 1.03 (95% CI: 0.92–1.14) for rivaroxaban. For major bleeding, the HRs against warfarin were 0.73 (95% CI: 0.67–0.78) for apixaban, 0.89 (95% CI: 0.82–0.97) for dabigatran, and 1.15 (95% CI: 1.07–1.25) for rivaroxaban. The results in the dabigatran cohort did not hold in all dose-defined subgroups. Conclusion In this large Scandinavian study among AF patients initiating oral anticoagulation, those initiating dabigatran, apixaban, and rivaroxaban had similar rates of stroke/SE to patients initiating warfarin. Rates of major bleeding were lower with apixaban and dabigatran and higher with rivaroxaban, each compared with warfarin.
format Article
fullrecord <record><control><sourceid>cristin</sourceid><recordid>TN_cdi_cristin_nora_10852_91077</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10852_91077</sourcerecordid><originalsourceid>FETCH-cristin_nora_10852_910773</originalsourceid><addsrcrecordid>eNqFjsFKBDEQRIO44Oj6DfYPBJJZJzvjVVYErx68Db2ZZG2JnSXJjOyv-LVG1rtQ0FXUa6gL0eiubeVg7rtL0Sg9dNKY_u1KXOf8oZTqjTaN-N5572yhxbHLGZAnyOhdOUH0wJHlQgU_ieGldgUPkSkXiAnDbyYb8TCH6s6vX5g8pkpXYUlUKU_7RCFgocgPgJBtBYlxIWQ4xuN8ruQes5vAxveYCuQyT6e1WHkM2d3-3Rtx97R7fXyWNtUNxCPXGaNWfdeOg1bb7eZ_4gfQQVlS</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study</title><source>NORA - Norwegian Open Research Archives</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Halvorsen, Sigrun ; Johnsen, Søren P ; Madsen, Morten ; Linder, Marie ; Sulo, Gerhard ; Ghanima, Waleed ; Gislason, Gunnar ; Hohnloser, Stefan H ; Jenkins, Aaron ; Al-Khalili, Faris ; Tell, Grethe S ; Ehrenstein, Vera</creator><creatorcontrib>Halvorsen, Sigrun ; Johnsen, Søren P ; Madsen, Morten ; Linder, Marie ; Sulo, Gerhard ; Ghanima, Waleed ; Gislason, Gunnar ; Hohnloser, Stefan H ; Jenkins, Aaron ; Al-Khalili, Faris ; Tell, Grethe S ; Ehrenstein, Vera</creatorcontrib><description>Abstract Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naïve patients with atrial fibrillation (AF). Methods and results This historical cohort study included 219 545 AF patients [median age 74 years; 43% women; mean CHA2DS2-VASc (congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, stroke or transient ischaemic attack, vascular disease, age 65–74 years, sex category) score 3.3] initiating apixaban, dabigatran, rivaroxaban, or warfarin in Denmark, Norway, and Sweden (1 January 2013 to 31 December 2016). The primary endpoints were stroke/SE and major bleeding. The median follow-up times were 9.7 (3.9–21.5) months for stroke/SE and 9.6 (3.8–21.3) months for bleeding. Apixaban and warfarin initiators were older and had higher CHA2DS2-VASc scores compared with dabigatran and rivaroxaban initiators. After 1:1 propensity score matching, three cohorts were created: apixaban–warfarin (n = 111 162), dabigatran–warfarin (n = 56 856), and rivaroxaban–warfarin (n = 61 198). Adjusted hazard ratios (HRs) were estimated using a Cox regression. For stroke/SE, adjusted HRs against warfarin were 0.96 [95% confidence interval (CI): 0.87–1.06] for apixaban, 0.89 (95% CI: 0.80–1.00) for dabigatran, and 1.03 (95% CI: 0.92–1.14) for rivaroxaban. For major bleeding, the HRs against warfarin were 0.73 (95% CI: 0.67–0.78) for apixaban, 0.89 (95% CI: 0.82–0.97) for dabigatran, and 1.15 (95% CI: 1.07–1.25) for rivaroxaban. The results in the dabigatran cohort did not hold in all dose-defined subgroups. Conclusion In this large Scandinavian study among AF patients initiating oral anticoagulation, those initiating dabigatran, apixaban, and rivaroxaban had similar rates of stroke/SE to patients initiating warfarin. Rates of major bleeding were lower with apixaban and dabigatran and higher with rivaroxaban, each compared with warfarin.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><language>nor</language><ispartof>European heart journal, 2021</ispartof><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4021,26565</link.rule.ids></links><search><creatorcontrib>Halvorsen, Sigrun</creatorcontrib><creatorcontrib>Johnsen, Søren P</creatorcontrib><creatorcontrib>Madsen, Morten</creatorcontrib><creatorcontrib>Linder, Marie</creatorcontrib><creatorcontrib>Sulo, Gerhard</creatorcontrib><creatorcontrib>Ghanima, Waleed</creatorcontrib><creatorcontrib>Gislason, Gunnar</creatorcontrib><creatorcontrib>Hohnloser, Stefan H</creatorcontrib><creatorcontrib>Jenkins, Aaron</creatorcontrib><creatorcontrib>Al-Khalili, Faris</creatorcontrib><creatorcontrib>Tell, Grethe S</creatorcontrib><creatorcontrib>Ehrenstein, Vera</creatorcontrib><title>Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study</title><title>European heart journal</title><description>Abstract Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naïve patients with atrial fibrillation (AF). Methods and results This historical cohort study included 219 545 AF patients [median age 74 years; 43% women; mean CHA2DS2-VASc (congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, stroke or transient ischaemic attack, vascular disease, age 65–74 years, sex category) score 3.3] initiating apixaban, dabigatran, rivaroxaban, or warfarin in Denmark, Norway, and Sweden (1 January 2013 to 31 December 2016). The primary endpoints were stroke/SE and major bleeding. The median follow-up times were 9.7 (3.9–21.5) months for stroke/SE and 9.6 (3.8–21.3) months for bleeding. Apixaban and warfarin initiators were older and had higher CHA2DS2-VASc scores compared with dabigatran and rivaroxaban initiators. After 1:1 propensity score matching, three cohorts were created: apixaban–warfarin (n = 111 162), dabigatran–warfarin (n = 56 856), and rivaroxaban–warfarin (n = 61 198). Adjusted hazard ratios (HRs) were estimated using a Cox regression. For stroke/SE, adjusted HRs against warfarin were 0.96 [95% confidence interval (CI): 0.87–1.06] for apixaban, 0.89 (95% CI: 0.80–1.00) for dabigatran, and 1.03 (95% CI: 0.92–1.14) for rivaroxaban. For major bleeding, the HRs against warfarin were 0.73 (95% CI: 0.67–0.78) for apixaban, 0.89 (95% CI: 0.82–0.97) for dabigatran, and 1.15 (95% CI: 1.07–1.25) for rivaroxaban. The results in the dabigatran cohort did not hold in all dose-defined subgroups. Conclusion In this large Scandinavian study among AF patients initiating oral anticoagulation, those initiating dabigatran, apixaban, and rivaroxaban had similar rates of stroke/SE to patients initiating warfarin. Rates of major bleeding were lower with apixaban and dabigatran and higher with rivaroxaban, each compared with warfarin.</description><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNqFjsFKBDEQRIO44Oj6DfYPBJJZJzvjVVYErx68Db2ZZG2JnSXJjOyv-LVG1rtQ0FXUa6gL0eiubeVg7rtL0Sg9dNKY_u1KXOf8oZTqjTaN-N5572yhxbHLGZAnyOhdOUH0wJHlQgU_ieGldgUPkSkXiAnDbyYb8TCH6s6vX5g8pkpXYUlUKU_7RCFgocgPgJBtBYlxIWQ4xuN8ruQes5vAxveYCuQyT6e1WHkM2d3-3Rtx97R7fXyWNtUNxCPXGaNWfdeOg1bb7eZ_4gfQQVlS</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Halvorsen, Sigrun</creator><creator>Johnsen, Søren P</creator><creator>Madsen, Morten</creator><creator>Linder, Marie</creator><creator>Sulo, Gerhard</creator><creator>Ghanima, Waleed</creator><creator>Gislason, Gunnar</creator><creator>Hohnloser, Stefan H</creator><creator>Jenkins, Aaron</creator><creator>Al-Khalili, Faris</creator><creator>Tell, Grethe S</creator><creator>Ehrenstein, Vera</creator><scope>3HK</scope></search><sort><creationdate>2021</creationdate><title>Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study</title><author>Halvorsen, Sigrun ; Johnsen, Søren P ; Madsen, Morten ; Linder, Marie ; Sulo, Gerhard ; Ghanima, Waleed ; Gislason, Gunnar ; Hohnloser, Stefan H ; Jenkins, Aaron ; Al-Khalili, Faris ; Tell, Grethe S ; Ehrenstein, Vera</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-cristin_nora_10852_910773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>nor</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halvorsen, Sigrun</creatorcontrib><creatorcontrib>Johnsen, Søren P</creatorcontrib><creatorcontrib>Madsen, Morten</creatorcontrib><creatorcontrib>Linder, Marie</creatorcontrib><creatorcontrib>Sulo, Gerhard</creatorcontrib><creatorcontrib>Ghanima, Waleed</creatorcontrib><creatorcontrib>Gislason, Gunnar</creatorcontrib><creatorcontrib>Hohnloser, Stefan H</creatorcontrib><creatorcontrib>Jenkins, Aaron</creatorcontrib><creatorcontrib>Al-Khalili, Faris</creatorcontrib><creatorcontrib>Tell, Grethe S</creatorcontrib><creatorcontrib>Ehrenstein, Vera</creatorcontrib><collection>NORA - Norwegian Open Research Archives</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halvorsen, Sigrun</au><au>Johnsen, Søren P</au><au>Madsen, Morten</au><au>Linder, Marie</au><au>Sulo, Gerhard</au><au>Ghanima, Waleed</au><au>Gislason, Gunnar</au><au>Hohnloser, Stefan H</au><au>Jenkins, Aaron</au><au>Al-Khalili, Faris</au><au>Tell, Grethe S</au><au>Ehrenstein, Vera</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study</atitle><jtitle>European heart journal</jtitle><date>2021</date><risdate>2021</risdate><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>Abstract Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naïve patients with atrial fibrillation (AF). Methods and results This historical cohort study included 219 545 AF patients [median age 74 years; 43% women; mean CHA2DS2-VASc (congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, stroke or transient ischaemic attack, vascular disease, age 65–74 years, sex category) score 3.3] initiating apixaban, dabigatran, rivaroxaban, or warfarin in Denmark, Norway, and Sweden (1 January 2013 to 31 December 2016). The primary endpoints were stroke/SE and major bleeding. The median follow-up times were 9.7 (3.9–21.5) months for stroke/SE and 9.6 (3.8–21.3) months for bleeding. Apixaban and warfarin initiators were older and had higher CHA2DS2-VASc scores compared with dabigatran and rivaroxaban initiators. After 1:1 propensity score matching, three cohorts were created: apixaban–warfarin (n = 111 162), dabigatran–warfarin (n = 56 856), and rivaroxaban–warfarin (n = 61 198). Adjusted hazard ratios (HRs) were estimated using a Cox regression. For stroke/SE, adjusted HRs against warfarin were 0.96 [95% confidence interval (CI): 0.87–1.06] for apixaban, 0.89 (95% CI: 0.80–1.00) for dabigatran, and 1.03 (95% CI: 0.92–1.14) for rivaroxaban. For major bleeding, the HRs against warfarin were 0.73 (95% CI: 0.67–0.78) for apixaban, 0.89 (95% CI: 0.82–0.97) for dabigatran, and 1.15 (95% CI: 1.07–1.25) for rivaroxaban. The results in the dabigatran cohort did not hold in all dose-defined subgroups. Conclusion In this large Scandinavian study among AF patients initiating oral anticoagulation, those initiating dabigatran, apixaban, and rivaroxaban had similar rates of stroke/SE to patients initiating warfarin. Rates of major bleeding were lower with apixaban and dabigatran and higher with rivaroxaban, each compared with warfarin.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0195-668X
ispartof European heart journal, 2021
issn 0195-668X
1522-9645
language nor
recordid cdi_cristin_nora_10852_91077
source NORA - Norwegian Open Research Archives; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
title Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a scandinavian population-based cohort study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T00%3A27%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-cristin&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effectiveness%20and%20safety%20of%20non-vitamin%20K%20antagonist%20oral%20anticoagulants%20and%20warfarin%20in%20atrial%20fibrillation:%20a%20scandinavian%20population-based%20cohort%20study&rft.jtitle=European%20heart%20journal&rft.au=Halvorsen,%20Sigrun&rft.date=2021&rft.issn=0195-668X&rft.eissn=1522-9645&rft_id=info:doi/&rft_dat=%3Ccristin%3E10852_91077%3C/cristin%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true