La maladie de Parkinson au Canada (serveur d'exploration)

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Recanalization and clinical outcome of occlusion sites at baseline CT angiography in the Interventional Management of Stroke III trial.

Identifieur interne : 001781 ( Ncbi/Merge ); précédent : 001780; suivant : 001782

Recanalization and clinical outcome of occlusion sites at baseline CT angiography in the Interventional Management of Stroke III trial.

Auteurs : Andrew M. Demchuk ; Mayank Goyal ; Sharon D. Yeatts ; Janice Carrozzella ; Lydia D. Foster ; Emmad Qazi ; Michael D. Hill ; Tudor G. Jovin ; Marc Ribo ; Bernard Yan ; Osama O. Zaidat ; Donald Frei ; Rüdiger Von Kummer ; Kevin M. Cockroft ; Pooja Khatri ; David S. Liebeskind ; Thomas A. Tomsick ; Yuko Y. Palesch ; Joseph P. Broderick

Source :

RBID : pubmed:24895878

English descriptors

Abstract

To use baseline computed tomographic (CT) angiography to analyze imaging and clinical end points in an Interventional Management of Stroke III cohort to identify patients who would benefit from endovascular stroke therapy.

DOI: 10.1148/radiol.14132649
PubMed: 24895878

Links toward previous steps (curation, corpus...)


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pubmed:24895878

Le document en format XML

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<term>Endovascular Procedures</term>
<term>Female</term>
<term>Fibrinolytic Agents (therapeutic use)</term>
<term>Humans</term>
<term>Magnetic Resonance Angiography</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Stroke (diagnostic imaging)</term>
<term>Stroke (mortality)</term>
<term>Stroke (therapy)</term>
<term>Tissue Plasminogen Activator (therapeutic use)</term>
<term>Tomography, X-Ray Computed</term>
<term>Treatment Outcome</term>
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<term>Stroke</term>
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<term>Stroke</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Stroke</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cerebral Angiography</term>
<term>Endovascular Procedures</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Angiography</term>
<term>Male</term>
<term>Middle Aged</term>
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<front>
<div type="abstract" xml:lang="en">To use baseline computed tomographic (CT) angiography to analyze imaging and clinical end points in an Interventional Management of Stroke III cohort to identify patients who would benefit from endovascular stroke therapy.</div>
</front>
</TEI>
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<PMID Version="1">24895878</PMID>
<DateCreated>
<Year>2014</Year>
<Month>09</Month>
<Day>24</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>01</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>11</Month>
<Day>25</Day>
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<ISSN IssnType="Electronic">1527-1315</ISSN>
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<Volume>273</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2014</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Radiology</Title>
<ISOAbbreviation>Radiology</ISOAbbreviation>
</Journal>
<ArticleTitle>Recanalization and clinical outcome of occlusion sites at baseline CT angiography in the Interventional Management of Stroke III trial.</ArticleTitle>
<Pagination>
<MedlinePgn>202-10</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1148/radiol.14132649</ELocationID>
<Abstract>
<AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">To use baseline computed tomographic (CT) angiography to analyze imaging and clinical end points in an Interventional Management of Stroke III cohort to identify patients who would benefit from endovascular stroke therapy.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">The primary clinical end point was 90-day dichotomized modified Rankin Scale (mRS) score. Secondary end points were 90-day mRS score distribution and 24-hour recanalization. Prespecified subgroup was baseline proximal occlusions (internal carotid, M1, or basilar arteries). Exploratory analyses were subsets with any occlusion and specific sites of occlusion (two-sided α = .01).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Of 656 subjects, 306 (47%) underwent baseline CT angiography or magnetic resonance angiography. Of 306, 282 (92%) had arterial occlusions. At baseline CT angiography, proximal occlusions (n = 220) demonstrated no difference in primary outcome (41.3% [62 of 150] endovascular vs 38% [27 of 70] intravenous [IV] tissue-plasminogen activator [tPA]; relative risk, 1.07 [99% confidence interval: 0.67, 1.70]; P = .70); however, 24-hour recanalization rate was higher for endovascular treatment (n = 167; 84.3% [97 of 115] endovascular vs 56% [29 of 52] IV tPA; P < .001). Exploratory subgroup analysis for any occlusion at baseline CT angiography did not demonstrate significant differences between endovascular and IV tPA arms for primary outcome (44.7% [85 of 190] vs 38% [35 of 92], P = .29), although ordinal shift analysis of full mRS distribution demonstrated a trend toward more favorable outcome (P = .011). Carotid T- or L-type occlusion (terminal internal carotid artery [ICA] with M1 middle cerebral artery and/or A1 anterior cerebral artery involvement) or tandem (extracranial or intracranial) ICA and M1 occlusion subgroup also showed a trend favoring endovascular treatment over IV tPA alone for primary outcome (26% [12 of 46] vs 4% [one of 23], P = .047).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Significant differences were identified between treatment arms for 24-hour recanalization in proximal occlusions; carotid T- or L-type and tandem ICA and M1 occlusions showed greater recanalization and a trend toward better outcome with endovascular treatment. Vascular imaging should be mandated in future endovascular trials to identify such occlusions. Online supplemental material is available for this article.</AbstractText>
<CopyrightInformation>© RSNA, 2014.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Demchuk</LastName>
<ForeName>Andrew M</ForeName>
<Initials>AM</Initials>
<AffiliationInfo>
<Affiliation>From the Calgary Stroke Program, Dept of Clinical Neurosciences and Radiology, Hotchkiss Brain Inst, Univ of Calgary, 1403 29 St NW, Room 112, Calgary, AB, Canada T2N 2T9 (A.M.D., M.G., E.Q., M.D.H.); Dept of Public Health Sciences, Medical Univ of South Carolina, Charleston, SC (S.D.Y., L.D.F., Y.Y.P.); Depts of Neurology and Rehabilitation Medicine and Radiology, Univ of Cincinnati Academic Health Ctr, Cincinnati, Ohio (J.C., P.K., T.A.T., J.P.B.); Stroke Inst, Univ of Pittsburgh Medical Ctr, Pittsburgh, Pa (T.G.J.); Neurovascular Unit, Dept of Neurology, Hosp Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Spain (M.R.); Melbourne Brain Ctr, The Royal Melbourne Hosp, Univ of Melbourne, Australia (B.Y.); Dept of Radiology, Medical College of Wisconsin, Milwaukee, Wis (O.O.Z.); Colorado Neurologic Inst, Denver, Colo (D.F.); Dept of Neuroradiology, Dresden Univ Stroke Ctr, Univ Hosp, Dresden, Germany (R.v.K.); Dept of Neurosurgery, Radiology and Public Health Sciences, Penn State M.S. Hershey Medical Ctr, Hershey, Pa (K.C.); and UCLA Stroke Ctr, Los Angeles, Calif (D.S.L.).</Affiliation>
</AffiliationInfo>
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<LastName>Goyal</LastName>
<ForeName>Mayank</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Yeatts</LastName>
<ForeName>Sharon D</ForeName>
<Initials>SD</Initials>
</Author>
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<LastName>Carrozzella</LastName>
<ForeName>Janice</ForeName>
<Initials>J</Initials>
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<LastName>Foster</LastName>
<ForeName>Lydia D</ForeName>
<Initials>LD</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Qazi</LastName>
<ForeName>Emmad</ForeName>
<Initials>E</Initials>
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<LastName>Hill</LastName>
<ForeName>Michael D</ForeName>
<Initials>MD</Initials>
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<LastName>Jovin</LastName>
<ForeName>Tudor G</ForeName>
<Initials>TG</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Ribo</LastName>
<ForeName>Marc</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Yan</LastName>
<ForeName>Bernard</ForeName>
<Initials>B</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Zaidat</LastName>
<ForeName>Osama O</ForeName>
<Initials>OO</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Frei</LastName>
<ForeName>Donald</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y">
<LastName>von Kummer</LastName>
<ForeName>Rüdiger</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Cockroft</LastName>
<ForeName>Kevin M</ForeName>
<Initials>KM</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Khatri</LastName>
<ForeName>Pooja</ForeName>
<Initials>P</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Liebeskind</LastName>
<ForeName>David S</ForeName>
<Initials>DS</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Tomsick</LastName>
<ForeName>Thomas A</ForeName>
<Initials>TA</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Palesch</LastName>
<ForeName>Yuko Y</ForeName>
<Initials>YY</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Broderick</LastName>
<ForeName>Joseph P</ForeName>
<Initials>JP</Initials>
</Author>
<Author ValidYN="Y">
<CollectiveName>IMS III Investigators</CollectiveName>
</Author>
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<Language>eng</Language>
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<Grant>
<GrantID>K24 NS072272</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>U01 NS052220</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>U01 NS054630</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>U01 NS077304</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
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<PublicationType UI="D017428">Clinical Trial, Phase III</PublicationType>
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<PublicationType UI="D016449">Randomized Controlled Trial</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Year>2014</Year>
<Month>06</Month>
<Day>05</Day>
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<MedlineTA>Radiology</MedlineTA>
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<Chemical>
<RegistryNumber>EC 3.4.21.68</RegistryNumber>
<NameOfSubstance UI="D010959">Tissue Plasminogen Activator</NameOfSubstance>
</Chemical>
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<CitationSubset>AIM</CitationSubset>
<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList>
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