Evidence map›Paper›PMID 42783370›Full record

Observational studyJAMA network open2026

Antithrombotic Therapy and Bleeding Risk Among Young Adults After Ischemic Stroke.

Anne Rasing, Esmée Verburgt, Merel S Ekker, Mijntje M I Schellekens, Maikel H M Immens, Jamie I Verhoeven, Esther M Boot, Mayte E van Alebeek, Paul J A M Brouwers, Renate M Arntz and 21 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Anne RasingDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Esmée VerburgtDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Merel S EkkerDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Mijntje M I SchellekensDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Maikel H M ImmensDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Jamie I VerhoevenDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Esther M BootDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Mayte E van AlebeekDepartment of Neurology, Gelre Hospital, Apeldoorn, the Netherlands.
Paul J A M BrouwersDepartment of Neurology, Medisch Spectrum Twente, Enschede, the Netherlands.
Renate M ArntzDepartment of Neurology, Medisch Spectrum Twente, Enschede, the Netherlands.
Gert W van DijkDepartment of Neurology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands.
Inge W M van UdenDepartment of Neurology, Catharina Hospital, Eindhoven, the Netherlands.
Rob A R GonsDepartment of Neurology, Catharina Hospital, Eindhoven, the Netherlands.
Tom den HeijerDepartment of Neurology, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands.
Julia H van TuijlDepartment of Neurology, Elisabeth-TweeSteden Hospital, Tilburg, the Netherlands.
Karlijn F de LaatDepartment of Neurology, Haga Hospital, The Hague, the Netherlands.
Anouk G W van NordenDepartment of Neurology, Amphia Hospital, Breda, the Netherlands.
Sarah E VermeerDepartment of Neurology, Rijnstate Hospital, Arnhem, the Netherlands.
Marian S G van ZagtenDepartment of Neurology, Jeroen Bosch Hospital, 's-Hertogenbosch, the Netherlands.
Robert J van OostenbruggeDepartment of Neurology, Maastricht University Medical Centre, Cardiovascular Research Institute Maastricht (CARIM), Maastricht, the Netherlands.
Marieke J H WermerDepartment of Neurology, Leiden University Medical Centre, Leiden, the Netherlands.
Paul J NederkoornDepartment of Neurology, Amsterdam University Medical Centre, Amsterdam, the Netherlands.
Henk KerkhoffDepartment of Neurology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
Fergus A RooyerDepartment of Neurology, Zuyderland Hospital, Sittard-Geleen, the Netherlands.
Frank G van RooijDepartment of Neurology, Frisius Medical Centre, Leeuwarden, the Netherlands.
Ido R van den WijngaardDepartment of Neurology, Haaglanden Medical Centre, The Hague, the Netherlands.
Tim J F Ten CateDepartment of Cardiology, Radboud University Medical Centre, Nijmegen, the Netherlands.
Anil M TuladharDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Edo RichardDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Frank-Erik de LeeuwDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.
Nina A HilkensDepartment of Neurology, Radboud University Medical Centre, Radboud Institute for Medical Research and Innovation, Donders Centre for Medical Neurosciences, Nijmegen, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Antithrombotic therapy is routinely prescribed to young adults after ischemic stroke to prevent recurrent vascular events. However, the long-term balance between potential benefits and bleeding risks of continued antithrombotic therapy in this population remains uncertain. Objective: To determine the short-term and long-term risk of bleeding associated with antithrombotic therapy in young stroke survivors. Design, Setting, and Participants: This cohort study used data from the Observational Dutch Young Symptomatic Stroke Study (ODYSSEY), a prospective, multicenter cohort study conducted in 17 hospitals in the Netherlands. Data were collected between 2013 and 2021. Follow-up data were obtained through standardized questionnaires with subsequent verification based on medical records, with data collection continuing until March 2024. Data were analyzed from October to December 2025. Participants included patients aged 18 to 49 years with a first-ever neuroimaging-proven ischemic stroke who survived the first 30 days after the index event. Exposure: Antithrombotic therapy. Main Outcomes and Measures: The primary outcome was the occurrence of a bleeding event requiring medical evaluation. Bleeding complications were stratified by severity according to the Bleeding Academic Research Consortium criteria. Potential factors associated with bleeding risk included sex, age, stroke severity, stroke cause, vascular risk factors, and antithrombotic therapy during follow-up. As a secondary analysis, bleeding risk was compared with the recurrence risk. The estimated bleeding probability during follow-up was calculated using Kaplan-Meier survival analysis with 95% CIs. Results: In total, 1226 patients were included (median [IQR] age, 44 [38-48] years; 637 male [52.0%]), with a median (IQR) follow-up of 4.2 (2.2-5.9) years. During follow-up, 129 patients experienced at least 1 bleeding event, corresponding to a 5-year cumulative risk of 10.7%. The annual bleeding rate was 2.5 events per 100 person-years. Among patients receiving antiplatelet therapy, the cumulative risk of bleeding at 6 years exceeded that of recurrent vascular events (85 bleeding events [14.7%] vs 105 vascular events [12.9%]). Among patients treated with oral anticoagulants, the cumulative risk of bleeding exceeded the risk of recurrent vascular events at 5 years (22 bleeding events [24.0%] vs 19 vascular events [23.6%]). Conclusion and Relevance: In this cohort study, young stroke survivors receiving antithrombotic therapy were at substantial long-term risk of bleeding. Although bleeding and recurrent ischemic events may differ in their clinical consequences, these findings highlight that bleeding risk should be carefully considered throughout long-term antithrombotic therapy.

Indexed as

Fibrinolytic AgentsHemorrhageIschemic StrokeAdolescentAdultBrain IschemiaFemaleHumansMaleMiddle AgedNetherlandsProspective StudiesRisk FactorsYoung AdultFibrinolytic Agents

Identifiers

PMID42783370
PMCPMC13613175

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.