Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20149
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dc.contributor.authorCharidimou, Andreas-
dc.contributor.authorTurc, Guillaume-
dc.contributor.authorOppenheim, Catherine-
dc.contributor.authorYan, Shenqiang-
dc.contributor.authorScheitz, Jan F-
dc.contributor.authorErdur, Hebun-
dc.contributor.authorKlinger-Gratz, Pascal P-
dc.contributor.authorEl-Koussy, Marwan-
dc.contributor.authorTakahashi, Wakoh-
dc.contributor.authorMoriya, Yusuke-
dc.contributor.authorWilson, Duncan-
dc.contributor.authorKidwell, Chelsea S-
dc.contributor.authorSaver, Jeffrey L-
dc.contributor.authorSallem, Asma-
dc.contributor.authorMoulin, Solene-
dc.contributor.authorEdjlali-Goujon, Myriam-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorFox, Zoe-
dc.contributor.authorShoamanesh, Ashkan-
dc.contributor.authorAlbers, Gregory W-
dc.contributor.authorMattle, Heinrich P-
dc.contributor.authorBenavente, Oscar R-
dc.contributor.authorJäger, H Rolf-
dc.contributor.authorAmbler, Gareth-
dc.contributor.authorAoki, Junya-
dc.contributor.authorBaron, Jean-Claude-
dc.contributor.authorKimura, Kazumi-
dc.contributor.authorKakuda, Wataru-
dc.contributor.authorTakizawa, Shunya-
dc.contributor.authorJung, Simon-
dc.contributor.authorNolte, Christian H-
dc.contributor.authorLou, Min-
dc.contributor.authorCordonnier, Charlotte-
dc.contributor.authorWerring, David J-
dc.date.accessioned2019-02-04T23:33:59Z-
dc.date.available2019-02-04T23:33:59Z-
dc.date.issued2017-08-
dc.identifier.citationStroke 2017; 48(8): 2084-2090-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20149-
dc.description.abstractBackground and Purpose- We assessed whether the presence, number, and distribution of cerebral microbleeds (CMBs) on pre-intravenous thrombolysis MRI scans of acute ischemic stroke patients are associated with an increased risk of intracerebral hemorrhage (ICH) or poor functional outcome. Methods- We performed an individual patient data meta-analysis, including prospective and retrospective studies of acute ischemic stroke treated with intravenous tissue-type plasminogen activator. Using multilevel mixed-effects logistic regression, we investigated associations of pre-treatment CMB presence, burden (1, 2-4, ≥5, and >10), and presumed pathogenesis (cerebral amyloid angiopathy defined as strictly lobar CMBs and noncerebral amyloid angiopathy) with symptomatic ICH, parenchymal hematoma (within [parenchymal hemorrhage, PH] and remote from the ischemic area [remote parenchymal hemorrhage, PHr]), and poor 3- to 6-month functional outcome (modified Rankin score >2). Results- In 1973 patients from 8 centers, the crude prevalence of CMBs was 526 of 1973 (26.7%). A total of 77 of 1973 (3.9%) patients experienced symptomatic ICH, 210 of 1806 (11.6%) experienced PH, and 56 of 1720 (3.3%) experienced PHr. In adjusted analyses, patients with CMBs (compared with those without CMBs) had increased risk of PH (odds ratio: 1.50; 95% confidence interval: 1.09-2.07; P=0.013) and PHr (odds ratio: 3.04; 95% confidence interval: 1.73-5.35; P<0.001) but not symptomatic ICH. Both cerebral amyloid angiopathy and noncerebral amyloid angiopathy patterns of CMBs were associated with PH and PHr. Increasing CMB burden category was associated with the risk of symptomatic ICH ( P=0.014), PH ( P=0.013), and PHr ( P<0.00001). Five or more and >10 CMBs independently predicted poor 3- to 6-month outcome (odds ratio: 1.85; 95% confidence interval: 1.10-3.12; P=0.020; and odds ratio: 3.99; 95% confidence interval: 1.55-10.22; P=0.004, respectively). Conclusions- Increasing CMB burden is associated with increased risk of ICH (including PHr) and poor 3- to 6-month functional outcome after intravenous thrombolysis for acute ischemic stroke.-
dc.language.isoeng-
dc.subjectcerebral hemorrhage-
dc.subjectcerebral small vessel disease-
dc.subjectMagnetic Resonance Imaging-
dc.subjectprevalence-
dc.subjectStroke-
dc.titleMicrobleeds, Cerebral Hemorrhage, and Functional Outcome After Stroke Thrombolysis.-
dc.typeJournal Article-
dc.identifier.journaltitleStroke-
dc.identifier.affiliationStroke Research Centre, UCL Institute of Neurology, London, United Kingdom-
dc.identifier.affiliationHemorrhagic Stroke Research Group, Massachusetts General Hospital, Boston-
dc.identifier.affiliationDepartment of Neurology, University of Arizona, Tucsonen
dc.identifier.affiliationUCLA Comprehensive Stroke Center, Geffen School of Medicine, Los Angelesen
dc.identifier.affiliationDivision of Neurology, Stroke and Cerebrovascular Health Program, University of British Columbia Hospital, Vancouver, Canada-
dc.identifier.affiliationDepartments of Neurology and Radiology, Hôpital Sainte-Anne, Université Paris Descartes, France-
dc.identifier.affiliationLysholm Department of Neuroradiology, National Hospital, London, United Kingdom-
dc.identifier.affiliationDepartment of Neurological Science, Nippon Medical School Graduate School of Medicine, Tokyo, Japan-
dc.identifier.affiliationDepartment of Rehabilitation Medicine, the Jikei University School of Medicine, Tokyo, Japan-
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Statistical Science, University College London, United Kingdom-
dc.identifier.affiliationDepartment of Medicine (Neurology), McMaster University and Population Health Research Institute, Hamilton, Ontario, Canada-
dc.identifier.affiliationStanford Stroke Center, Palo Alto, CA-
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Neurology, the 2nd Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China-
dc.identifier.affiliationDepartment of Neurology and Center for Stroke Research, Charite Universitätsmedizin, Berlin, Germany-
dc.identifier.affiliationDepartment of Diagnostic and Interventional Neuroradiology, and Neurology, Inselspital, University Hospital Bern, Switzerland-
dc.identifier.affiliationDepartment of Neurology, Tokai University School of Medicine, Japan-
dc.identifier.affiliationUniv. Lille, Inserm, CHU Lille, U1171, Degenerative and Vascular Cognitive Disorders, France-
dc.identifier.doi10.1161/STROKEAHA.116.012992-
dc.identifier.orcid0000-0002-6614-8417-
dc.identifier.pubmedid28720659-
dc.type.austinJournal Article-
dc.type.austinMeta-Analysis-
dc.type.austinResearch Support, Non-U.S. Gov't-
dc.type.austinReview-
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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