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  3. Antiplatelet Use Prior to Anticoagulant Initiation in Patients With Atrial Fibrillation-Related Ischemic Stroke: An ELAN Trial Analysis.
 

Antiplatelet Use Prior to Anticoagulant Initiation in Patients With Atrial Fibrillation-Related Ischemic Stroke: An ELAN Trial Analysis.

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BORIS DOI
10.48620/88482
Publisher DOI
10.5853/jos.2024.04322
PubMed ID
40494580
Description
Background And Purpose
Antiplatelets are often used before direct oral anticoagulant (DOACs) initiation after an acute ischemic stroke related to atrial fibrillation (AF), but the evidence is weak. Here, we explored the risks and benefits of this approach.Methods
A post-hoc analysis of ELAN (Early versus Late Initiation of Direct Oral Anticoagulants in Post-ischemic Stroke Patients with Atrial Fibrillation) trial data (NCT03148457) was conducted to compare the risk of recurrent ischemic stroke, systemic embolism, major bleeding (extracranial or intracranial hemorrhage [ICH]), and vascular death within 30 days (as a composite and as individual outcomes) in participants treated with and without antiplatelets before DOAC initiation after an AF-associated ischemic stroke. We used both logistic and cause-specific Cox proportional hazards regression in inverse probability of treatment weighted models to account for confounding. We calculated the net benefit of antiplatelet use by subtracting the weighted rate of excess bleeding events attributable to antiplatelets from the rate of excess ischemic events possibly prevented by antiplatelets.Results
Among 2,013 participants (median age 77 years, 45.5% female), 1,090 (54.1%) used antiplatelets, and 70 (3.5%) experienced the composite outcome. Antiplatelet use was not associated with the composite outcome (inverse probability of treatment weighted odds ratio [ORweighted] 1.06, 95% confidence interval [CI] 0.66-1.72; inverse probability of treatment weighted hazard ratio [HRweighted] 1.06, 95% CI 0.65-1.72), but showed a lower risk of ischemic stroke recurrence (ORweighted 0.58 [0.30-1.08], HRweighted 0.57 [0.30-1.10]), and a higher risk of major bleeding (ORweighted 1.76 [0.56-6.63], HRweighted 1.88 [0.56-6.39]). Its net benefit was +0.57 (95% CI -1.25 to +2.34) to +0.30 (-1.82 to +2.27) weighted events/100 person-months for ICH weights 1.5 to 3.1.Conclusion
Following an AF-associated ischemic stroke, we found a lower risk of recurrence and no signs of net harm with antiplatelet use before DOAC initiation, despite an increased risk of bleeding.
Date of Publication
2025-05
Publication Type
Article
Keyword(s)
Anticoagulants
•
Antiplatelet bridging
•
Antiplatelets
•
Atrial fibrillation
•
Ischemic stroke
•
Timing
Language(s)
en
Contributor(s)
Polymeris, Alexandros A
Koga, Masatoshi
Strbian, Daniel
Vedamurthy, Adhiyaman
Krishnan, Manju
Branca, Mattia
Department of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
Horvath, Thomas
Clinic of Neurology
Goeldlin, Martinaorcid-logo
Clinic of Neurology
Shim, Gek
Gumbinger, Christoph
Zhang, Liqun
Kristoffersen, Espen Saxhaug
Desfontaines, Philippe
Vanacker, Peter
Alonso, Angelika
Poli, Sven
Nunes, Ana Paiva
Caracciolo, Nicoletta G
Kneihsl, Markus
Kahles, Timo
Giudici, Daria
Räty, Silja
Tiainen, Marjaana
Dawson, Jesse
Fischer, Urs
Clinic of Neurology
Additional Credits
Department of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
Clinic of Neurology
Series
Journal of Stroke
Publisher
Korean Stroke Society
ISSN
2287-6391
Access(Rights)
open.access
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