Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18119
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dc.contributor.authorThomalla, Götz-
dc.contributor.authorBoutitie, Florent-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorSimonsen, Claus Z-
dc.contributor.authorPedraza, Salvador-
dc.contributor.authorLemmens, Robin-
dc.contributor.authorNighoghossian, Norbert-
dc.contributor.authorRoy, Pascal-
dc.contributor.authorMuir, Keith W-
dc.contributor.authorEbinger, Martin-
dc.contributor.authorFord, Ian-
dc.contributor.authorCheng, Bastian-
dc.contributor.authorGalinovic, Ivana-
dc.contributor.authorCho, Tae-Hee-
dc.contributor.authorPuig, Josep-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorEndres, Matthias-
dc.contributor.authorFiehler, Jens-
dc.contributor.authorGerloff, Christian-
dc.date2017-04-20-
dc.date.accessioned2018-07-22T23:26:58Z-
dc.date.available2018-07-22T23:26:58Z-
dc.date.issued2018-01-
dc.identifier.citationInternational Journal of Stroke 2018; 13(1): 66-73-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18119-
dc.description.abstractBackground Diffusion-weighted imaging (DWI) and fluid-attenuated inversion recovery (FLAIR) mismatch was suggested to identify stroke patients with unknown time of symptom onset likely to be within the time window for thrombolysis. Aims We aimed to study clinical characteristics associated with DWI-FLAIR mismatch in patients with unknown onset stroke. Methods We analyzed baseline MRI and clinical data from patients with acute ischemic stroke proven by DWI from WAKE-UP, an investigator-initiated, randomized, placebo-controlled trial of MRI-based thrombolysis in stroke patients with unknown time of symptom onset. Clinical characteristics were compared between patients with and without DWI-FLAIR mismatch. Results Of 699 patients included, 418 (59.8%) presented with DWI-FLAIR mismatch. A shorter delay between last seen well and symptom recognition (p = 0.0063), a shorter delay between symptom recognition and arrival at hospital (p = 0.0025), and history of atrial fibrillation (p = 0.19) were predictors of DWI-FLAIR mismatch in multivariate analysis. All other characteristics were comparable between groups. Conclusions There are only minor differences in measured clinical characteristics between unknown symptom onset stroke patients with and without DWI-FLAIR mismatch. DWI-FLAIR mismatch as an indicator of stroke onset within 4.5 h shows no relevant association with commonly collected clinical characteristics of stroke patients. Clinical Trial Registration URL: http://www.clinicaltrials.gov . Unique identifier: NCT01525290; URL: https://www.clinicaltrialsregister.eu . Unique identifier: 2011-005906-32.-
dc.language.isoeng-
dc.subjectAcute-
dc.subjectWAKE-UP-
dc.subjectclinical trial-
dc.subjectdiffusion-weighted imaging-
dc.subjectdiffusion-weighted imaging and fluid-attenuated inversion recovery mismatch-
dc.subjectfluid-attenuated inversion recovery imaging-
dc.subjectIschaemic Stroke-
dc.subjectMagnetic Resonance Imaging-
dc.titleClinical characteristics of unknown symptom onset stroke patients with and without diffusion-weighted imaging and fluid-attenuated inversion recovery mismatch.-
dc.typeJournal Article-
dc.identifier.journaltitleInternational Journal of Stroke-
dc.identifier.affiliationKlinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany-
dc.identifier.affiliationHospices Civils de Lyon, Service de Biostatistique, Lyon, France-
dc.identifier.affiliationUniversité Lyon 1, Villeurbanne, France-
dc.identifier.affiliationCNRS, UMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, France-
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin (CSB), Charité-Universitätsmedizin Berlin, Berlin, Germany-
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmark-
dc.identifier.affiliationDepartment of Neurology, Hospices Civils de Lyon, Lyon, France-
dc.identifier.affiliationDepartment of Radiology, Institut de Diagnostic per la Image (IDI), Hospital Dr Josep Trueta, Institut d'Investgació Biomèdica de Girona (IDIBGI), Girona, Spain-
dc.identifier.affiliationKU Leuven-University of Leuven, Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND), Leuven, Belgium-
dc.identifier.affiliationUniversity Hospitals Leuven, Department of Neurology, Leuven, Belgium-
dc.identifier.affiliationVIB, Center for Brain & Disease Research, Laboratory of Neurobiology, Leuven, Belgium-
dc.identifier.affiliationInstitute of Neuroscience & Psychology, University of Glasgow, Glasgow, UK-
dc.identifier.affiliationKlinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Berlin, Germany-
dc.identifier.affiliationRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK-
dc.identifier.affiliationStroke Division, Florey Institute of Neuroscience and Mental Health, Heidelberg, Australia-
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationKlinik und Poliklinik für Neuroradiologische Diagnostik und Intervention, Diagnostikzentrum, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany-
dc.identifier.doi10.1177/1747493017706245-
dc.identifier.orcid0000-0002-6614-8417-
dc.identifier.pubmedid28425349-
dc.type.austinJournal Article-
local.name.researcherThijs, Vincent N
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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