<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schnabel RB</submitter><funding>Bristol Myers Squibb-Pfizer Alliance</funding><funding>German Research Foundation</funding><funding>German Ministry of Education and Research, Berlin, Germany</funding><funding>Union's Horizon 2020 research and innovation programme</funding><funding>Canadian Institutes of HealthResearch</funding><funding>BMBF</funding><funding>German Ministry of Research and Education</funding><funding>Daiichi Sankyo Europe</funding><funding>Accelerating Clinical Trials Network</funding><funding>Population Health Research Institute</funding><funding>ERACoSysMed3</funding><funding>Leducq Foundation</funding><funding>Dutch Heart Foundation</funding><funding>European Union's Horizon Europe research and innovation programme</funding><funding>AFFECT EU</funding><funding>British Heart Foundation</funding><funding>Medtronic</funding><funding>Hamilton Health Sciences</funding><funding>Wolfgang Seefried project funding German Heart Foundation</funding><funding>Heart and Stroke Foundation of Canada</funding><funding>European Union CATCH ME</funding><funding>German Centre for Cardiovascular Research</funding><funding>German Centre for Cardiovascular Research, Berlin, Germany</funding><funding>European Union's Horizon 2020 research and innovation programme</funding><funding>MAESTRIA</funding><funding>Canadian Stroke Prevention Intervention Network</funding><pagination>4902-4916</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11631065</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(46)</volume><pubmed_abstract>&lt;h4>Background and aims&lt;/h4>The optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation.&lt;h4>Methods&lt;/h4>These pre-specified analyses of the NOAH-AFNET 6 (n = 2534 patients) and ARTESiA (n = 4012 patients) trials compared anticoagulation with no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischaemic attack, coronary or peripheral artery disease. Efficacy outcomes were the primary outcomes of both trials, a composite of stroke, systemic arterial embolism (SE), myocardial infarction, pulmonary embolism or cardiovascular death, and stroke or SE. Safety outcomes were major bleeding or major bleeding and deat</pubmed_abstract><journal>European heart journal</journal><pubmed_title>Anticoagulation in device-detected atrial fibrillation with or without vascular disease: a combined analysis of the NOAH-AFNET 6 and ARTESiA trials.</pubmed_title><pmcid>PMC11631065</pmcid><funding_grant_id>847770</funding_grant_id><funding_grant_id>633196</funding_grant_id><funding_grant_id>FKZ 81X2800182</funding_grant_id><funding_grant_id>101095480</funding_grant_id><funding_grant_id>201610PTJ-378238</funding_grant_id><funding_grant_id>Ki 509167694</funding_grant_id><funding_grant_id>BMBF 01ZX1408A</funding_grant_id><funding_grant_id>648131</funding_grant_id><funding_grant_id>01-002-2022-0118</funding_grant_id><funding_grant_id>965286</funding_grant_id><funding_grant_id>031L0239</funding_grant_id><funding_grant_id>AA/18/2/34218</funding_grant_id><pubmed_authors>Schnabel RB</pubmed_authors><pubmed_authors>Zapf A</pubmed_authors><pubmed_authors>Marijon E</pubmed_authors><pubmed_authors>Vardas P</pubmed_authors><pubmed_authors>Healey JS</pubmed_authors><pubmed_authors>Erath JW</pubmed_authors><pubmed_authors>Simantirakis E</pubmed_authors><pubmed_authors>Schotten U</pubmed_authors><pubmed_authors>Kutyifa V</pubmed_authors><pubmed_authors>Camm AJ</pubmed_authors><pubmed_authors>Atar D</pubmed_authors><pubmed_authors>Sehner S</pubmed_authors><pubmed_authors>Rivard L</pubmed_authors><pubmed_authors>Linde C</pubmed_authors><pubmed_authors>Becher N</pubmed_authors><pubmed_authors>Lopes RD</pubmed_authors><pubmed_authors>Benezet-Mazuecos J</pubmed_authors><pubmed_authors>Mabo P</pubmed_authors><pubmed_authors>Chlouverakis G</pubmed_authors><pubmed_authors>Dichtl W</pubmed_authors><pubmed_authors>Toennis T</pubmed_authors><pubmed_authors>Lee SF</pubmed_authors><pubmed_authors>Blomstrom-Lundqvist C</pubmed_authors><pubmed_authors>Lip GYH</pubmed_authors><pubmed_authors>Bertaglia E</pubmed_authors><pubmed_authors>McIntyre WF</pubmed_authors><pubmed_authors>Fierenz A</pubmed_authors><pubmed_authors>Goette A</pubmed_authors><pubmed_authors>Alings M</pubmed_authors><pubmed_authors>Birnie DH</pubmed_authors><pubmed_authors>Benz AP</pubmed_authors><pubmed_authors>Kirchhof P</pubmed_authors><pubmed_authors>Granger CB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anticoagulation in device-detected atrial fibrillation with or without vascular disease: a combined analysis of the NOAH-AFNET 6 and ARTESiA trials.</name><description>&lt;h4>Background and aims&lt;/h4>The optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation.&lt;h4>Methods&lt;/h4>These pre-specified analyses of the NOAH-AFNET 6 (n = 2534 patients) and ARTESiA (n = 4012 patients) trials compared anticoagulation with no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischaemic attack, coronary or peripheral artery disease. Efficacy outcomes were the primary outcomes of both trials, a composite of stroke, systemic arterial embolism (SE), myocardial infarction, pulmonary embolism or cardiovascular death, and stroke or SE. Safety outcomes were major bleeding or major bleeding and deat</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-26T23:12:51.811Z</modification><creation>2025-04-06T17:30:55.59Z</creation></dates><accession>S-EPMC11631065</accession><cross_references><pubmed>39222018</pubmed><doi>10.1093/eurheartj/ehae596</doi></cross_references></HashMap>