Leukoaraiosis, intracerebral hemorrhage, and functional outcome after acute stroke thrombolysis
dc.contributor.author | Kongbunkiat, Kannikar | |
dc.contributor.author | Wilson, Duncan | |
dc.contributor.author | Kasemsap, Narongrit | |
dc.contributor.author | Tiamkao, Somsak | |
dc.contributor.author | Jichi, Fatima | |
dc.contributor.author | Palumbo, Vanessa | |
dc.contributor.author | Hill, Michael D. | |
dc.contributor.author | Buchan, Alastair M. | |
dc.contributor.author | Jung, Simon | |
dc.contributor.author | Mattle, Heinrich P. | |
dc.contributor.author | Henninger, Nils | |
dc.contributor.author | Werring, David J. | |
dc.date | 2022-08-11T08:10:30.000 | |
dc.date.accessioned | 2022-08-23T17:11:11Z | |
dc.date.available | 2022-08-23T17:11:11Z | |
dc.date.issued | 2017-02-14 | |
dc.date.submitted | 2017-03-29 | |
dc.identifier.citation | Neurology. 2017 Feb 14;88(7):638-645. doi: 10.1212/WNL.0000000000003605. Epub Jan 27 2017. <a href="https://doi.org/10.1212/WNL.0000000000003605">Link to article on publisher's site</a> | |
dc.identifier.issn | 0028-3878 (Linking) | |
dc.identifier.doi | 10.1212/WNL.0000000000003605 | |
dc.identifier.pmid | 28130468 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/46218 | |
dc.description | <p>Co-author Nils Henninger is a doctoral student in the Millennium PhD Program (MPP) in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.</p> | |
dc.description.abstract | OBJECTIVE: To perform a systematic review and pooled meta-analysis of published studies to assess whether the presence of leukoaraiosis on neuroimaging before treatment with thrombolysis (IV or intra-arterial) is associated with an increased risk of symptomatic intracerebral hemorrhage (sICH) or poor functional outcome. METHODS: We included studies of patients with acute ischemic stroke, treated with IV or intra-arterial thrombolysis, which assessed functional outcome (3-month modified Rankin Scale [mRS]) or sICH in relation to leukoaraiosis on pretreatment neuroimaging (CT or MRI). We used random-effects models to calculate pooled relative risks (RR) of sICH and poor functional outcome (mRS > /= 2) for any vs no leukoaraiosis (using any rating scale) and for no to mild vs moderate to severe leukoaraiosis (using the Van Swieten or Fazekas Schmidt scale). RESULTS: We identified 15 studies (total n = 6,967). For sICH outcome, the RR was 1.65 (n = 5,551; 95% confidence interval [CI] 1.26-2.16, p = 0.001) with an absolute risk (AR) increase of 2.5% for any leukoaraiosis vs none. The RR was 2.4 (n = 4,192; 95% CI 1.83-3.14, p = 0.001) with an AR increase of 6.2% for moderate to severe vs no to mild leukoaraiosis. For poor functional outcome; the RR was 1.30 (n = 3,401; 95% CI 1.19-1.42, p = 0.001) with an AR increase of 15.4% for any leukoaraiosis vs none. The RR was 1.31 (n = 3,659; 95% CI 1.22-1.42, p = 0.001) with an AR increase of 17.5% for moderate to severe vs no to mild leukoaraiosis. No statistical heterogeneity was noted for any of the analyses. CONCLUSIONS: Leukoaraiosis presence and severity are consistently associated with an increased risk of sICH and poor functional outcome after IV or intra-arterial thrombolysis for acute ischemic stroke. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28130468&dopt=Abstract">Link to Article in PubMed</a> | |
dc.rights | Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Nervous System Diseases | |
dc.subject | Neurology | |
dc.subject | Psychiatry | |
dc.title | Leukoaraiosis, intracerebral hemorrhage, and functional outcome after acute stroke thrombolysis | |
dc.type | Journal Article | |
dc.source.journaltitle | Neurology | |
dc.source.volume | 88 | |
dc.source.issue | 7 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1759&context=psych_pp&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/psych_pp/755 | |
dc.identifier.contextkey | 9942011 | |
refterms.dateFOA | 2022-08-23T17:11:11Z | |
html.description.abstract | <p>OBJECTIVE: To perform a systematic review and pooled meta-analysis of published studies to assess whether the presence of leukoaraiosis on neuroimaging before treatment with thrombolysis (IV or intra-arterial) is associated with an increased risk of symptomatic intracerebral hemorrhage (sICH) or poor functional outcome.</p> <p>METHODS: We included studies of patients with acute ischemic stroke, treated with IV or intra-arterial thrombolysis, which assessed functional outcome (3-month modified Rankin Scale [mRS]) or sICH in relation to leukoaraiosis on pretreatment neuroimaging (CT or MRI). We used random-effects models to calculate pooled relative risks (RR) of sICH and poor functional outcome (mRS > /= 2) for any vs no leukoaraiosis (using any rating scale) and for no to mild vs moderate to severe leukoaraiosis (using the Van Swieten or Fazekas Schmidt scale).</p> <p>RESULTS: We identified 15 studies (total n = 6,967). For sICH outcome, the RR was 1.65 (n = 5,551; 95% confidence interval [CI] 1.26-2.16, p = 0.001) with an absolute risk (AR) increase of 2.5% for any leukoaraiosis vs none. The RR was 2.4 (n = 4,192; 95% CI 1.83-3.14, p = 0.001) with an AR increase of 6.2% for moderate to severe vs no to mild leukoaraiosis. For poor functional outcome; the RR was 1.30 (n = 3,401; 95% CI 1.19-1.42, p = 0.001) with an AR increase of 15.4% for any leukoaraiosis vs none. The RR was 1.31 (n = 3,659; 95% CI 1.22-1.42, p = 0.001) with an AR increase of 17.5% for moderate to severe vs no to mild leukoaraiosis. No statistical heterogeneity was noted for any of the analyses.</p> <p>CONCLUSIONS: Leukoaraiosis presence and severity are consistently associated with an increased risk of sICH and poor functional outcome after IV or intra-arterial thrombolysis for acute ischemic stroke.</p> | |
dc.identifier.submissionpath | psych_pp/755 | |
dc.contributor.department | Morningside Graduate School of Biomedical Sciences | |
dc.contributor.department | Psychiatry | |
dc.contributor.department | Neurology | |
dc.source.pages | 638-645 | |
dc.contributor.student | Nils Henninger | |
dc.description.thesisprogram | Millennium PhD |