Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25972
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dc.contributor.authorGrosch, Anne Sophie-
dc.contributor.authorKufner, Anna-
dc.contributor.authorBoutitie, Florent-
dc.contributor.authorCheng, Bastian-
dc.contributor.authorEbinger, Martin-
dc.contributor.authorEndres, Matthias-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorFiehler, Jens-
dc.contributor.authorKönigsberg, Alina-
dc.contributor.authorLemmens, Robin-
dc.contributor.authorMuir, Keith W-
dc.contributor.authorNighoghossian, Norbert-
dc.contributor.authorPedraza, Salvador-
dc.contributor.authorSiemonsen, Claus Z-
dc.contributor.authorThijs, Vincent-
dc.contributor.authorWouters, Anke-
dc.contributor.authorGerloff, Christian-
dc.contributor.authorThomalla, Götz-
dc.contributor.authorGalinovic, Ivana-
dc.date2020-
dc.date.accessioned2021-03-03T21:49:57Z-
dc.date.available2021-03-03T21:49:57Z-
dc.date.issued2021-02-04-
dc.identifier.citationFrontiers in Neurology 2020; 11: 623881en
dc.identifier.issn1664-2295
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25972-
dc.description.abstractBackground and Aims: Fluid-attenuated inversion recovery (FLAIR) hyperintense vessels (FHVs) on MRI are a radiological marker of vessel occlusion and indirect sign of collateral circulation. However, the clinical relevance is uncertain. We explored whether the extent of FHVs is associated with outcome and how FHVs modify treatment effect of thrombolysis in a subgroup of patients with confirmed unilateral vessel occlusion from the randomized controlled WAKE-UP trial. Methods: One hundred sixty-five patients were analyzed. Two blinded raters independently assessed the presence and extent of FHVs (defined as the number of slices with visible FHV multiplied by FLAIR slice thickness). Patients were then separated into two groups to distinguish between few and extensive FHVs (dichotomization at the median <30 or ≥30). Results: Here, 85% of all patients (n = 140) and 95% of middle cerebral artery (MCA) occlusion patients (n = 127) showed FHVs at baseline. Between MCA occlusion patients with few and extensive FHVs, no differences were identified in relative lesion growth (p = 0.971) and short-term [follow-up National Institutes of Health Stroke Scale (NIHSS) score; p = 0.342] or long-term functional recovery [modified Rankin Scale (mRS) <2 at 90 days poststroke; p = 0.607]. In linear regression analysis, baseline extent of FHV (defined as a continuous variable) was highly associated with volume of hypoperfused tissue (β = 2.161; 95% CI 0.96-3.36; p = 0.001). In multivariable regression analysis adjusted for treatment group, stroke severity, lesion volume, occlusion site, and recanalization, FHV did not modify functional recovery. However, in patients with few FHVs, the odds for good functional outcome (mRS) were increased in recombinant tissue plasminogen activator (rtPA) patients compared to those who received placebo [odds ratio (OR) = 5.3; 95% CI 1.2-24.0], whereas no apparent benefit was observed in patients with extensive FHVs (OR = 1.1; 95% CI 0.3-3.8), p-value for interaction was 0.11. Conclusion: While the extent of FHVs on baseline did not alter the evolution of stroke in terms of lesion progression or functional recovery, it may modify treatment effect and should therefore be considered relevant additional information in those patients who are eligible for intravenous thrombolysis. Clinical Trial Registration: Main trial (WAKE-UP): ClinicalTrials.gov, NCT01525290; and EudraCT, 2011-005906-32. Registered February 2, 2012.en
dc.language.isoeng
dc.subjectFLAIR hyperintensitiesen
dc.subjectMRIen
dc.subjecthyperintense vesselen
dc.subjectischemic Strokeen
dc.subjectprognosisen
dc.subjectthrombolysisen
dc.subjectwake-up Strokeen
dc.titleExtent of FLAIR Hyperintense Vessels May Modify Treatment Effect of Thrombolysis: A Post hoc Analysis of the WAKE-UP Trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleFrontiers in Neurologyen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationExcellence Cluster NeuroCure, Charite-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, Medical Park Berlin Humboldtmühle, Berlin, Germanyen
dc.identifier.affiliationHospices Civils de Lyon, Service de Biostatistique, Lyon, Franceen
dc.identifier.affiliationUniversité Lyon 1, Villeurbanne, Franceen
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.affiliationKlinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationBerlin Institute of Health (BIH), Berlin, Germanyen
dc.identifier.affiliationStroke Theme, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Heidelberg, VIC, Australiaen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationBerlin Institute of Health (BIH), Berlin, Germanyen
dc.identifier.affiliationGerman Centre for Cardiovascular Research (DZHK), Berlin, Germanyen
dc.identifier.affiliationGerman Center for Neurodegenerative Diseases (DZNE), Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Leuven, Belgiumen
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, Katholieke Universiteit Leuven-University of Leuven, Leuven, Belgiumen
dc.identifier.affiliationLaboratory of Neurobiology, Center for Brain & Disease Research, Flanders Institute for Biotechnology, Leuven, Belgiumen
dc.identifier.affiliationDepartment of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.affiliationDepartment of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationDepartment of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationInstitute of Neuroscience & Psychology, University of Glasgow, Glasgow, United Kingdomen
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.affiliationDepartment of Radiology, Girona Institute of Biomedical Research, Institute of Diagnostic Imaging, Dr. Josep Trueta Hospital, Girona, Spainen
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Aarhus, Denmarken
dc.identifier.affiliationDepartment of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationCenter for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germanyen
dc.identifier.doi10.3389/fneur.2020.623881en
dc.type.contentTexten
dc.identifier.pubmedid33613422
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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