Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32976
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dc.contributor.authorFrey, Benedikt M-
dc.contributor.authorShenas, Farhad-
dc.contributor.authorBoutitie, Florent-
dc.contributor.authorCheng, Bastian-
dc.contributor.authorCho, Tae-Hee-
dc.contributor.authorEbinger, Martin-
dc.contributor.authorEndres, Matthias-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorFiehler, Jens-
dc.contributor.authorGalinovic, Ivana-
dc.contributor.authorBarow, Ewgenia-
dc.contributor.authorKönigsberg, Alina-
dc.contributor.authorSchlemm, Eckhard-
dc.contributor.authorPedraza, Salvador-
dc.contributor.authorLemmens, Robin-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorMuir, Keith W-
dc.contributor.authorNighoghossian, Norbert-
dc.contributor.authorSimonsen, Claus Z-
dc.contributor.authorGerloff, Christian-
dc.contributor.authorThomalla, Götz-
dc.date2023-
dc.date.accessioned2023-06-07T02:37:17Z-
dc.date.available2023-06-07T02:37:17Z-
dc.date.issued2023-07-
dc.identifier.citationStroke 2023-07; 54(7)en_US
dc.identifier.issn1524-4628-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32976-
dc.description.abstractWhite matter hyperintensities of presumed vascular origin (WMH) are the most prominent imaging feature of cerebral small vessel disease (cSVD). Previous studies suggest a link between cSVD burden and intracerebral hemorrhage and worse functional outcome after thrombolysis in acute ischemic stroke. We aimed to determine the impact of WMH burden on efficacy and safety of thrombolysis in the MRI-based randomized controlled WAKE-UP trial of intravenous alteplase in unknown onset stroke. The design of this post hoc study was an observational cohort design of a secondary analysis of a randomized trial. WMH volume was quantified on baseline fluid-attenuated inversion recovery images of patients randomized to either alteplase or placebo in the WAKE-UP trial. Excellent outcome was defined as score of 0-1 on the modified Rankin Scale after 90 days. Hemorrhagic transformation was assessed on follow-up imaging 24-36 hours after randomization. Treatment effect and safety were analyzed by fitting multivariable logistic regression models. Quality of scans was sufficient in 441 of 503 randomized patients to delineate WMH. Median age was 68 years, 151 patients were female, and 222 patients were assigned to receive alteplase. Median WMH volume was 11.4 mL. Independent from treatment, WMH burden was statistically significantly associated with worse functional outcome (odds ratio, 0.72 [95% CI, 0.57-0.92]), but not with higher chances of any hemorrhagic transformation (odds ratio, 0.78 [95% CI, 0.60-1.01]). There was no interaction of WMH burden and treatment group for the likelihood of excellent outcome (P=0.443) or any hemorrhagic transformation (P=0.151). In a subgroup of 166 patients with severe WMH, intravenous thrombolysis was associated with higher odds of excellent outcome (odds ratio, 2.40 [95% CI, 1.19-4.84]) with no significant increase in the rate of hemorrhagic transformation (odds ratio, 1.96 [95% CI, 0.80-4.81]). Although WMH burden is associated with worse functional outcome, there is no association with treatment effect or safety of intravenous thrombolysis in patients with ischemic stroke of unknown onset. URL: https://www. gov; Unique identifier: NCT01525290.en_US
dc.language.isoeng-
dc.subjectalteplaseen_US
dc.subjectcerebral small vessel diseaseen_US
dc.subjectischemic strokeen_US
dc.subjectthrombolytic therapyen_US
dc.titleIntravenous Thrombolysis in Patients With White Matter Hyperintensities in the WAKE-UP Trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleStrokeen_US
dc.identifier.affiliationKlinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, University Medical Center Hamburg-Eppendorf, Germanyen_US
dc.identifier.affiliationUniversité Lyon 1, FranceCNRS, UMR 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, Franceen_US
dc.identifier.affiliationHospices Civils de Lyon, Franceen_US
dc.identifier.affiliationDepartment of Stroke Medicine, Université Claude Bernard Lyon 1, CREATIS CNRS UMR 5220-INSERM U1206, INSA-Lyonen_US
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germanyen_US
dc.identifier.affiliationKlinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Germanyen_US
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germanyen_US
dc.identifier.affiliationDepartment of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Germany (J.F.).en_US
dc.identifier.affiliationCentrum für Schlaganfallforschung Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany (M. Ebinger, M. Endres, J.B.F., I.G.).en_US
dc.identifier.affiliationNeurologie der Rehaklinik Medical Park Humboldtmühle, Berlin, Germanyen_US
dc.identifier.affiliationLeuven - University of Leuven, Department of Neurosciences, Experimental Neurology, Belgiumen_US
dc.identifier.affiliationCenter for Brain & Disease Research, Laboratory of Neurobiology, Campus Gasthuisberg, Belgiumen_US
dc.identifier.affiliationDepartment of Radiology, Institut de Diagnostic per la Image, Hospital Dr Josep Trueta, Institut d'Investigació Biomèdica de Girona (IDIBGI), Parc Hospitalari Martí i Julià de Salt, Girona, Spainen_US
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Belgiumen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen_US
dc.identifier.affiliationInstitute of Neuroscience & Psychology, University of Glasgow, University Avenue, Glasgow, United Kingdomen_US
dc.identifier.affiliationDepartment of Neurology, Aarhus University Hospital, Denmarken_US
dc.identifier.affiliationNeurologyen_US
dc.identifier.doi10.1161/STROKEAHA.122.040247en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-5302-0801en_US
dc.identifier.orcid0009-0003-0903-7897en_US
dc.identifier.orcid0000-0003-2434-1822en_US
dc.identifier.orcid0000-0001-8677-2447en_US
dc.identifier.orcid0000-0002-5073-4665en_US
dc.identifier.orcid0000-0001-6520-3720en_US
dc.identifier.orcid0000-0002-7936-6958en_US
dc.identifier.orcid0000-0003-4904-8251en_US
dc.identifier.orcid0000-0003-2591-1807en_US
dc.identifier.orcid0000-0002-5729-2935en_US
dc.identifier.orcid0000-0003-2517-4413en_US
dc.identifier.orcid0000-0002-4948-5956en_US
dc.identifier.orcid0000-0002-6614-8417en_US
dc.identifier.orcid0000-0001-9535-022Xen_US
dc.identifier.orcid0000-0003-0594-4409en_US
dc.identifier.orcid0000-0003-1363-0266en_US
dc.identifier.orcid0000-0002-6484-8882en_US
dc.identifier.orcid0000-0002-4785-1449en_US
dc.identifier.pubmedid37226772-
local.name.researcherThijs, Vincent N
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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