<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Induruwa I</submitter><funding>National Institute for Health Research (NIHR)</funding><funding>Vivensa Foundation</funding><pagination>145-152</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11569578</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Atrial fibrillation (AF) detected after stroke (AFDAS) may represent a distinct clinical entity to that of known AF (KAF). However, there is limited long-term outcome data available for patients with AFDAS. More information regarding prognosis in AFDAS is required to inform future trial design in these patients.&lt;h4>Patients and methods&lt;/h4>We used data (2015-2019) from a national prospective stroke registry of consecutive patients with acute ischaemic stroke and AF. AFDAS was defined as a new diagnosis of AF after stroke detected on electrocardiograph or cardiac monitoring. The co-primary endpoints were: (1) all-cause mortality; (2) recurrent major adverse cardiovascular events (MACE) at 3 years. Secondary endpoints were: (1) recurrent stroke; (2) functional outcome at discharge; (3) presence of co-existing stroke mechanisms.&lt;h4>Results&lt;/h4>583 patients were included. After a median follow-up of 2.65 years (cumulative 1064 person-years) 309 patients died and 23 had recurrent MACE. Compared with AFDAS, KAF was associated with a higher risk of all-cause mortality (adjusted Hazard Ratio (aHR) 1.56, 95% CI 1.12-2.18), a higher prevalence of co-existing stroke mechanisms (adjusted odds ratio (aOR) 2.28, 95% CI 1.14-4.59), but not poor functional outcome (aOR 1.61, 95% CI 0.98-2.64). A trend towards a higher risk of MACE was observed in patients with KAF, but this was limited by statistical power (aHR 2.90, 95% CI 0.67-12.51). All 14 recurrent strokes occurred in the KAF group (Log-rank &lt;i>p&lt;/i> = 0.03).&lt;h4>Discussion and conclusion&lt;/h4>These data provide further evidence that AFDAS differs to KAF with respect to risk of recurrent stroke, MACE, and all-cause mortality.</pubmed_abstract><journal>European stroke journal</journal><pubmed_title>Recurrent vascular events and mortality outcomes in patients with known atrial fibrillation, compared to atrial fibrillation detected early after stroke.</pubmed_title><pmcid>PMC11569578</pmcid><funding_grant_id>RG85316</funding_grant_id><funding_grant_id>JBGS22/20</funding_grant_id><pubmed_authors>Induruwa I</pubmed_authors><pubmed_authors>Bhakta S</pubmed_authors><pubmed_authors>Hajiev S</pubmed_authors><pubmed_authors>Herlekar R</pubmed_authors><pubmed_authors>McCabe JJ</pubmed_authors><pubmed_authors>Warburton EA</pubmed_authors><pubmed_authors>Khadjooi K</pubmed_authors><pubmed_authors>Sur Roy A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recurrent vascular events and mortality outcomes in patients with known atrial fibrillation, compared to atrial fibrillation detected early after stroke.</name><description>&lt;h4>Introduction&lt;/h4>Atrial fibrillation (AF) detected after stroke (AFDAS) may represent a distinct clinical entity to that of known AF (KAF). However, there is limited long-term outcome data available for patients with AFDAS. More information regarding prognosis in AFDAS is required to inform future trial design in these patients.&lt;h4>Patients and methods&lt;/h4>We used data (2015-2019) from a national prospective stroke registry of consecutive patients with acute ischaemic stroke and AF. AFDAS was defined as a new diagnosis of AF after stroke detected on electrocardiograph or cardiac monitoring. The co-primary endpoints were: (1) all-cause mortality; (2) recurrent major adverse cardiovascular events (MACE) at 3 years. Secondary endpoints were: (1) recurrent stroke; (2) functional outcome at discharge; (3) presence of co-existing stroke mechanisms.&lt;h4>Results&lt;/h4>583 patients were included. After a median follow-up of 2.65 years (cumulative 1064 person-years) 309 patients died and 23 had recurrent MACE. Compared with AFDAS, KAF was associated with a higher risk of all-cause mortality (adjusted Hazard Ratio (aHR) 1.56, 95% CI 1.12-2.18), a higher prevalence of co-existing stroke mechanisms (adjusted odds ratio (aOR) 2.28, 95% CI 1.14-4.59), but not poor functional outcome (aOR 1.61, 95% CI 0.98-2.64). A trend towards a higher risk of MACE was observed in patients with KAF, but this was limited by statistical power (aHR 2.90, 95% CI 0.67-12.51). All 14 recurrent strokes occurred in the KAF group (Log-rank &lt;i>p&lt;/i> = 0.03).&lt;h4>Discussion and conclusion&lt;/h4>These data provide further evidence that AFDAS differs to KAF with respect to risk of recurrent stroke, MACE, and all-cause mortality.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-12T03:20:21.75Z</modification><creation>2025-04-06T01:56:06.638Z</creation></dates><accession>S-EPMC11569578</accession><cross_references><pubmed>39169537</pubmed><doi>10.1177/23969873241272631</doi></cross_references></HashMap>