Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22923
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dc.contributor.authorScheldeman, Lauranne-
dc.contributor.authorWouters, Anke-
dc.contributor.authorBoutitie, Florent-
dc.contributor.authorDupont, Patrick-
dc.contributor.authorChristensen, Soren-
dc.contributor.authorCheng, Bastian-
dc.contributor.authorEbinger, Martin-
dc.contributor.authorEndres, Matthias-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorGerloff, Christian-
dc.contributor.authorMuir, Keith W-
dc.contributor.authorNighoghossian, Norbert-
dc.contributor.authorPedraza, Salvador-
dc.contributor.authorSimonsen, Claus Z-
dc.contributor.authorThijs, Vincent-
dc.contributor.authorThomalla, Götz-
dc.contributor.authorLemmens, Robin-
dc.date2020-03-30-
dc.date.accessioned2020-04-14T04:00:53Z-
dc.date.available2020-04-14T04:00:53Z-
dc.date.issued2020-03-30-
dc.identifier.citationAnnals of neurology 2020; online first: 30 March-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22923-
dc.description.abstractTo explore the prevalence of the perfusion-weighted imaging (PWI) - diffusion-weighted imaging (DWI) mismatch and response to intravenous thrombolysis in the WAKE-UP trial. We performed a prespecified post-hoc analysis of ischemic stroke patients screened for DWI - fluid-attenuated inversion recovery (FLAIR) mismatch in WAKE-UP who underwent PWI. We defined PWI-DWI mismatch as ischemic core volume < 70 ml, mismatch volume > 10 ml and mismatch ratio > 1.2. Primary efficacy endpoint was a modified Rankin Scale score of 0-1 at 90 days, adjusted for age and symptom severity. Of 1,362 magnetic resonance imaging (MRI) screened patients, 431 underwent PWI. Of these, 57 (13%) had a double mismatch, 151 (35%) only a DWI-FLAIR mismatch and 54 (13%) only a PWI-DWI mismatch. DWI-FLAIR mismatch was more prevalent than PWI-DWI mismatch (48%; 95% CI 43%-53% vs 26%; 95% CI 22%-30%, p < 0.0001). Screening for either one of the mismatch profiles resulted in a yield of 61% (95% CI 56%-65%). Prevalence of PWI-DWI mismatch was similar in patients with (27%) or without (24%) DWI-FLAIR mismatch (p = 0.52). In an exploratory analysis in the small subgroup of 208 randomized patients with PWI, PWI-DWI mismatch status did not modify the treatment response (p for interaction = 0.73). Evaluating both the DWI-FLAIR and PWI-DWI mismatch pattern in patients with unknown time of stroke onset will result in the highest yield of thrombolysis treatment. The treatment benefit of alteplase in patients with a DWI-FLAIR mismatch seems not merely driven by the presence of a PWI-DWI mismatch, although this analysis was underpowered. This article is protected by copyright. All rights reserved.-
dc.language.isoeng-
dc.titleDifferent mismatch concepts for MRI-guided thrombolysis in unknown onset stroke.-
dc.typeJournal Article-
dc.identifier.journaltitleAnnals of neurology-
dc.identifier.affiliationDepartment of Stroke Medicine, Université Claude Bernard Lyon 1, CREATIS CNRS UMR 5220-INSERM U1206, INSA- Lyon, Hospices Civils de Lyon, Lyon, Franceen
dc.identifier.affiliationKlinik für Neurologie, Medical Park Berlin Humboldtmühle, Berlin, Germanyen
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin (CSB), Charité - Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationCNRS, UMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, Franceen
dc.identifier.affiliationKlinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Leuven, Belgiumen
dc.identifier.affiliationInstitute of Neuroscience & Psychology, University of Glasgow, Glasgow, UKen
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, Leuven, Belgiumen
dc.identifier.affiliationCenter for Brain & Disease Research, Laboratory of Neurobiology, VIB, Leuven, Belgium..en
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin (CSB), Charité - Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationKlinik und Hochschulambulanz für Neurologie, Charité- Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationGerman Center for Cardiovascular Research (DZHK), partner site Berlinen
dc.identifier.affiliationGerman Center for Neurodegenerative Diseases (DZNE), partner site Berlin..en
dc.identifier.affiliationHospices Civils de Lyon, Service de Biostatistique, F-69003 Lyon, France, Université Lyon 1, F-69100, Villeurbanne, Franceen
dc.identifier.affiliationStroke Theme, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurosciences, Laboratory for Cognitive Neurology, KU Leuven - University of Leuven, Leuven, Belgium..-
dc.identifier.affiliationGrayNumber Analytics, Lomma, Sweden..-
dc.identifier.affiliationDepartment of Radiology, Institut de Diagnostic per la Image (IDI), Hospital Dr Josep Trueta, Institut d'Investigació Biomedica de Girona (IDIBGI), Parc Hospitalari Marti i Julia de Salt - Edifici M2, Girona, Spain..-
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark..-
dc.identifier.doi10.1002/ana.25730-
dc.identifier.orcid0000-0002-5263-3550-
dc.identifier.orcid0000-0001-6520-3720-
dc.identifier.orcid0000-0002-6614-8417-
dc.identifier.pubmedid32227638-
dc.type.austinJournal Article-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
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