Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16752
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dc.contributor.authorThomalla, Gotz-
dc.contributor.authorBoutitie, Florent-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorSimonsen, Claus Z-
dc.contributor.authorNighoghossian, Norbert-
dc.contributor.authorPedraza, Salvador-
dc.contributor.authorLemmens, Robin-
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-
dc.contributor.authorEndres, Matthias-
dc.contributor.authorFiehler, Jens-
dc.contributor.authorGerloff, Christian-
dc.contributor.authorWAKE-UP Investigators-
dc.date2017-02-17-
dc.date.accessioned2017-08-02T05:23:24Z-
dc.date.available2017-08-02T05:23:24Z-
dc.date.issued2017-03-
dc.identifier.citationStroke 2017; 48(3): 770-773en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16752-
dc.description.abstractBACKGROUND AND PURPOSE: We describe clinical and magnetic resonance imaging (MRI) characteristics of stroke patients with unknown time of symptom onset potentially eligible for thrombolysis from a large prospective cohort. METHODS: We analyzed baseline data from WAKE-UP (Efficacy and Safety of MRI-Based Thrombolysis in Wake-Up Stroke: A Randomized, Doubleblind, Placebo-Controlled Trial), an investigator-initiated, randomized, placebo-controlled trial of MRI-based thrombolysis in stroke patients with unknown time of symptom onset. MRI judgment included assessment of the mismatch between visibility of the acute ischemic lesion on diffusion-weighted imaging and fluid-attenuated inversion recovery. RESULTS: Of 1005 patients included, diffusion-weighted imaging and fluid-attenuated inversion recovery mismatch was present in 479 patients (48.0%). Patients with daytime-unwitnessed stroke (n=138, 13.7%) had a shorter delay between symptom recognition and hospital arrival (1.5 versus 1.8 hours; P=0.002), a higher National Institutes of Stroke Scale score on admission (8 versus 6; P<0.001), and more often aphasia (72.5% versus 34.0%; P<0.001) when compared with stroke patients waking up from nighttime sleep. Frequency of diffusion-weighted imaging and fluid-attenuated inversion recovery mismatch was comparable between both groups (43.7% versus 48.7%; P=0.30). CONCLUSIONS: Almost half of the patients with unknown time of symptom onset stroke otherwise eligible for thrombolysis had MRI findings making them likely to be within a time window for safe and effective thrombolysis. Patients with daytime onset unwitnessed stroke differ from wake-up stroke patients with regards to clinical characteristics but are comparable in terms of MRI characteristics of lesion age. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01525290. URL: https://www.clinicaltrialsregister.eu. Unique identifier: 2011-005906-32.en_US
dc.subjectAphasiaen_US
dc.subjectInformed consenten_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectRisk Factorsen_US
dc.subjectStrokeen_US
dc.titleStroke with unknown time of symptom onset: baseline clinical and magnetic resonance imaging data of the first thousand patients in WAKE-UP (efficacy and safety of MRI-Based thrombolysis in WAKE-UP stroke: a randomized, doubleblind, placebo-controlled trial)en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleStrokeen_US
dc.identifier.affiliationKlinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Universitätsklinikum Hamburg-Eppendorf, Germanyen_US
dc.identifier.affiliationKlinik und Poliklinik für Neuroradiologische Diagnostik und Intervention, Diagnostikzentrum, Universitätsklinikum Hamburg-Eppendorf, Germanyen_US
dc.identifier.affiliationService de Biostatistique, Hospices Civils de Lyon, Franceen_US
dc.identifier.affiliationUniversité Lyon 1, Villeurbanne, Franceen_US
dc.identifier.affiliationCNRS, UMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, Franceen_US
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin (CSB), Charité-Universitätsmedizin Berlin, Germanyen_US
dc.identifier.affiliationKlinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Germanyen_US
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Denmarken_US
dc.identifier.affiliationDepartment of Neurology, Hospices Civils de Lyon, Franceen_US
dc.identifier.affiliationDepartment of Radiology, Institut de Diagnostic per la Image (IDI), Hospital Dr Josep Trueta, Institut d'Investgació Biomèdica de Girona (IDIBGI), Spainen_US
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, KU Leuven-University of Leuven, VIB Center for Brain & Disease Research, and Department of Neurology, University Hospitals Leuven, Belgiumen_US
dc.identifier.affiliationInstitute of Neuroscience and Psychology, University of Glasgow, United Kingdomen_US
dc.identifier.affiliationRobertson Centre for Biostatistics, University of Glasgow, United Kingdomen_US
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australiaen_US
dc.type.studyortrialRandomized Controlled Clinical Trial/Controlled Clinical Trialen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28174327en_US
dc.identifier.doi10.1161/STROKEAHA.116.015233en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6614-8417en_US
dc.type.austinJournal Articleen_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
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