Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25091
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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 N-
dc.contributor.authorThomalla, Götz-
dc.contributor.authorLemmens, Robin-
dc.date2020-04-20-
dc.date.accessioned2020-10-15T03:17:17Z-
dc.date.available2020-10-15T03:17:17Z-
dc.date.issued2020-06-
dc.identifier.citationAnnals of Neurology 2020; 87(6): 931-938en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25091-
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 < 70ml, mismatch volume > 10ml, and mismatch ratio > 1.2. Primary efficacy end point was a modified Rankin Scale score of 0-1 at 90 days, adjusted for age and symptom severity. Of 1,362 magnetic resonance imaging-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% confidence interval [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 patterns 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 to be driven not merely by the presence of a PWI-DWI mismatch, although this analysis was underpowered. ANN NEUROL 2020;87:931-938.en
dc.language.isoeng
dc.titleDifferent Mismatch Concepts for Magnetic Resonance Imaging-Guided Thrombolysis in Unknown Onset Stroke.en
dc.typeJournal Articleen
dc.identifier.journaltitleAnnals of Neurologyen
dc.identifier.affiliationDepartment of Stroke Medicine, Claude Bernard University Lyon 1, CREATIS National Center for Scientific Research Mixed Unit of Research 5220-National Institute of Health and Medical Research U1206, National Institute of Applied Sciences of Lyon, Lyon Civil Hospices, Lyon, Franceen
dc.identifier.affiliationGerman Center for Neurodegenerative Diseases, Berlin, Germanyen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationNeurology Clinic, Medical Park Berlin Humboldtmühle, Berlin, Germanyen
dc.identifier.affiliationCentre national de la recherche scientifique, unité mixte de recherche 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, Franceen
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, KU Leuven-University of Leuven, Leuven, Belgiumen
dc.identifier.affiliationCenter for Brain & Disease Research, Laboratory of Neurobiology, Flanders Institute for Biotechnology, Leuven, Belgium..en
dc.identifier.affiliationHospices Civils de Lyon, Service de Biostatistique, F-69003 Lyon, France; Université Lyon 1, F-69100, Villeurbanne, Franceen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Leuven, Belgiumen
dc.identifier.affiliationGerman Center for Cardiovascular Research, Berlin, Germanyen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationDepartment of Neurosciences, Laboratory for Cognitive Neurology, KU Leuven-University of Leuven, Leuven, Belgium..en
dc.identifier.affiliationGrayNumber Analytics, Lomma, Sweden..en
dc.identifier.affiliationInstitute of Neuroscience & Psychology, University of Glasgow, Glasgow, United Kingdom..en
dc.identifier.affiliationDepartment of Radiology, Institute of Diagnostic Imaging, Dr Josep Trueta Hospital, Girona Institute of Biomedical Research, Marti and Julia de Salt Hospital Park - Building M2, Girona, Spain..en
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark..en
dc.identifier.doi10.1002/ana.25730en
dc.type.contentTexten
dc.identifier.orcid0000-0002-5263-3550en
dc.identifier.orcid0000-0003-1980-2540en
dc.identifier.orcid0000-0001-6520-3720en
dc.identifier.orcid0000-0002-6614-8417en
dc.identifier.pubmedid32227638
local.name.researcherThijs, Vincent N
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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