Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16186
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWilson, Duncan-
dc.contributor.authorCharidimou, Andreas-
dc.contributor.authorAmbler, Gareth-
dc.contributor.authorFox, Zoe V-
dc.contributor.authorGregoire, Simone-
dc.contributor.authorRayson, Phillip-
dc.contributor.authorImaizumi, Toshio-
dc.contributor.authorFluri, Felix-
dc.contributor.authorNaka, Hiromitsu-
dc.contributor.authorHorstmann, Solveig-
dc.contributor.authorVeltkamp, Roland-
dc.contributor.authorRothwell, Peter M-
dc.contributor.authorKwa, Vincent IH-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorLee, Yong-Seok-
dc.contributor.authorKim, Young Dae-
dc.contributor.authorHuang, Yining-
dc.contributor.authorWong, Ka Sing-
dc.contributor.authorJäger, Hans Rolf-
dc.contributor.authorWerring, David J-
dc.date2016-09-02-
dc.date.accessioned2016-09-06T01:55:26Z-
dc.date.available2016-09-06T01:55:26Z-
dc.date.issued2016-09-02-
dc.identifier.citationNeurology 2016; online first: 2 Septemberen_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16186-
dc.description.abstractOBJECTIVE: To determine associations between cerebral microbleed (CMB) burden with recurrent ischemic stroke (IS) and intracerebral hemorrhage (ICH) risk after IS or TIA. METHODS: We identified prospective studies of patients with IS or TIA that investigated CMBs and stroke (ICH and IS) risk during ≥3 months follow-up. Authors provided aggregate summary-level data on stroke outcomes, with CMBs categorized according to burden (single, 2-4, and ≥5 CMBs) and distribution. We calculated absolute event rates and pooled risk ratios (RR) using random-effects meta-analysis. RESULTS: We included 5,068 patients from 15 studies. There were 115/1,284 (9.6%) recurrent IS events in patients with CMBs vs 212/3,781 (5.6%) in patients without CMBs (pooled RR 1.8 for CMBs vs no CMBs; 95% confidence interval [CI] 1.4-2.5). There were 49/1,142 (4.3%) ICH events in those with CMBs vs 17/2,912 (0.58%) in those without CMBs (pooled RR 6.3 for CMBs vs no CMBs; 95% CI 3.5-11.4). Increasing CMB burden increased the risk of IS (pooled RR [95% CI] 1.8 [1.0-3.1], 2.4 [1.3-4.4], and 2.7 [1.5-4.9] for 1 CMB, 2-4 CMBs, and ≥5 CMBs, respectively) and ICH (pooled RR [95% CI] 4.6 [1.9-10.7], 5.6 [2.4-13.3], and 14.1 [6.9-29.0] for 1 CMB, 2-4 CMBs, and ≥5 CMBs, respectively). CONCLUSIONS: CMBs are associated with increased stroke risk after IS or TIA. With increasing CMB burden (compared to no CMBs), the risk of ICH increases more steeply than that of IS. However, IS absolute event rates remain higher than ICH absolute event rates in all CMB burden categories.en_US
dc.titleRecurrent stroke risk and cerebral microbleed burden in ischemic stroke and TIA: A meta-analysisen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleNeurologyen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationStroke Research Centre, UCL, London, UKen_US
dc.identifier.affiliationDepartment of Brain Repair and Rehabilitation, UCL Institute of Neurology, UCL, London, UKen_US
dc.identifier.affiliationThe National Hospital for Neurology and Neurosurgery, UCL, London, UKen_US
dc.identifier.affiliationDepartment of Statistical Science, UCL, London, UKen_US
dc.identifier.affiliationBiomedical Research Centre, UCL, London, UKen_US
dc.identifier.affiliationDepartment of Neurosurgery, Kushiro City General Hospital, Hokkaido, Japanen_US
dc.identifier.affiliationDepartment of Neurology, University Hospital Würzburg, Germanyen_US
dc.identifier.affiliationDepartment of Neurology, Suiseikai Kajikawa Hospital, Hiroshima, Japanen_US
dc.identifier.affiliationDepartment of Neurology, University of Heidelberg, Germanyen_US
dc.identifier.affiliationDepartment of Stroke Medicine, Division of Brain Sciences, Imperial College London, UKen_US
dc.identifier.affiliationNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, UKen_US
dc.identifier.affiliationDepartment of Neurology, Onze Lieve Vrouwe Gasthuis, Amsterdam, the Netherlandsen_US
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationMelbourne Brain Center, University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Neurology, Seoul National University Boramae Medical Center, Seoul, Koreaen_US
dc.identifier.affiliationDepartment of Neurology, Yonsei University College of Medicine, Seoul, Koreaen_US
dc.identifier.affiliationDepartment of Neurology, Peking University First Hospital, Beijing, Chinaen_US
dc.identifier.affiliationDivision of Neurology, Department of Medicine & Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kongen_US
dc.identifier.affiliationLysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, London, UKen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27590288en_US
dc.identifier.doi10.1212/WNL.0000000000003183en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherThijs, Vincent N
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

20
checked on Oct 4, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.