Evidence map›Paper›PMID 41614474›Full record

ArticleEuropean stroke journal2026

Automated DWI-FLAIR mismatch assessment in stroke using DWI only.

Joseph Benzakoun, Lauranne Scheldeman, Anke Wouters, Bastian Cheng, Martin Ebinger, Matthias Endres, Jochen B Fiebach, Jens Fiehler, Ivana Galinovic, Keith W Muir and 17 more

Abstract read
In one paragraph

Article in European stroke journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

27 authors.

Joseph BenzakounIMA-BRAIN, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.ORCID 0000-0002-0733-0104
Lauranne ScheldemanDepartment of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, Leuven, Belgium.ORCID 0000-0002-5263-3550
Anke WoutersDepartment of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, Leuven, Belgium.ORCID 0000-0001-5229-2699
Bastian ChengDepartment of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin EbingerDepartment of Neurology, Medical Park Berlin Humboldtmühle, Berlin, Germany.
Matthias EndresDepartment of Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Jochen B FiebachCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Jens FiehlerDepartment of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-8533-7478
Ivana GalinovicCenter for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-4904-8251
Keith W MuirSchool of Cardiovascular & Metabolic Health, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0001-9535-022X
Norbert NighoghossianHospices Civils de Lyon, Department of Neurology and Stroke Center, Lyon University, Lyon, France.
Salvador PedrazaDepartment of Radiology (CDI) and IDIBAPS, Hospital Clinic, Barcelona, Spain.ORCID 0000-0003-2517-4413
Josep PuigDepartment of Radiology (CDI) and IDIBAPS, Hospital Clinic, Barcelona, Spain.ORCID 0000-0003-2791-6599
Claus Z SimonsenDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0003-1363-0266
Vincent ThijsStroke Division, University of Melbourne, Florey Institute of Neuroscience and Mental Health, Melbourne, VIC, Australia.ORCID 0000-0002-6614-8417
Götz ThomallaDepartment of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Emilien MicardCIC, Innovation Technologique, Université de Lorraine, INSERM 1433, Nancy, France.
Bailiang ChenCIC, Innovation Technologique, Université de Lorraine, INSERM 1433, Nancy, France.ORCID 0000-0003-1038-7846
Bertrand LapergueDepartment of Neurology, Foch Hospital, Versailles Saint-Quentin-en-Yvelines University, Suresnes, France.
Grégoire BoulouisDiagnostic and Interventional Neuroradiology Department, CHRU de Tours, Tours, Centre Val de Loire, France.ORCID 0000-0001-8422-9205
Alice Le BerreIMA-BRAIN, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.
Jean-Claude BaronStroke Team, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.
Guillaume TurcStroke Team, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.ORCID 0000-0001-5059-4095
Wagih Ben HassenIMA-BRAIN, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.
Olivier NaggaraIMA-BRAIN, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.
Catherine OppenheimIMA-BRAIN, INSERM U1266, Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, Paris, France.
Robin LemmensDepartment of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, Leuven, Belgium.

Funding

Agence Nationale de la Recherche ANR-18-RHUS-0001FP7 Health 278276Société Française de Neuroradiologie Research grantSociété Française de Radiologie Research grant
6 · The paper itself

Abstract

introductionIn Acute Ischemic Stroke (AIS), mismatch between Diffusion-Weighted Imaging (DWI) and Fluid-Attenuated Inversion-Recovery (FLAIR) helps identify patients who can benefit from thrombolysis when stroke onset time is unknown (15% of AIS). However, visual assessment has suboptimal observer agreement. Our study aims to develop and validate a Deep-Learning model for predicting DWI-FLAIR mismatch using solely DWI data. PATIENTS AND

methodsThis retrospective study included AIS patients from ETIS registry (derivation cohort, 2018-2024) and WAKE-UP trial (validation cohort, 2012-2017). DWI-FLAIR mismatch was rated visually. We trained a model to predict manually-labeled FLAIR visible areas (FVA) matching the DWI lesion on baseline and early follow-up MRIs, using only DWI as input. FVA-index was defined as the volume of predicted regions. Area under the ROC curve (AUC) and optimal FVA-index cutoff to predict DWI-FLAIR mismatch in the derivation cohort were computed. Validation was performed using baseline MRIs of the validation cohort.

resultsThe derivation cohort included 3605 MRIs in 2922 patients and the validation cohort 844 MRIs in 844 patients. FVA-index demonstrated strong predictive value for DWI-FLAIR mismatch in baseline MRIs from the derivation (n = 2453, AUC = 0.85, 95%CI: 0.84-0.87) and validation cohort (n = 844, AUC = 0.86, 95%CI: 0.84-0.89). With an optimal FVA-index cutoff at 0.5, we obtained a kappa of 0.54 (95%CI: 0.48-0.59), 70% sensitivity (378/537, 95%CI: 66-74%) and 88% specificity (269/307, 95%CI: 83-91%) in the validation cohort. DISCUSSION AND

conclusionThe model accurately predicts DWI-FLAIR mismatch in AIS patients with unknown stroke onset. It could aid readers when visual rating is challenging, or FLAIR unavailable.

Indexed as

Diffusion Magnetic Resonance ImagingIschemic StrokeStrokeAgedAged, 80 and overDeep LearningFemaleHumansMaleMiddle AgedRegistriesRetrospective Studiesartificial intelligencedecision support techniquesdiffusion magnetic resonance imagingIschemic strokemagnetic resonance imaging

Identifiers

PMID41614474
PMCPMC12866262

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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.