New Appearance of Extraischemic Microbleeds on T2-Weighted Magnetic Resonance Imaging 24 Hours After Tissue-type Plasminogen Activator Administration

It is unknown whether new-extraischemic microbleeds (new-EMBs) develop rapidly after tissue-type plasminogen activator (tPA) infusion. We hypothesized that new-EMBs may develop rapidly after tPA infusion using T2*-weighted MRI (T2*) and investigated the frequency and clinical factors associated with...

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Veröffentlicht in:Stroke (1970) 2013-10, Vol.44 (10), p.2776-2781
Hauptverfasser: Kimura, Kazumi, Aoki, Junya, Shibazaki, Kensaku, Saji, Naoki, Uemura, Junichi, Sakamoto, Yuki
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container_end_page 2781
container_issue 10
container_start_page 2776
container_title Stroke (1970)
container_volume 44
creator Kimura, Kazumi
Aoki, Junya
Shibazaki, Kensaku
Saji, Naoki
Uemura, Junichi
Sakamoto, Yuki
description It is unknown whether new-extraischemic microbleeds (new-EMBs) develop rapidly after tissue-type plasminogen activator (tPA) infusion. We hypothesized that new-EMBs may develop rapidly after tPA infusion using T2*-weighted MRI (T2*) and investigated the frequency and clinical factors associated with new-EMBs. Patients with acute stroke within 3 hours of onset who were treated with tissue-type plasminogen activator (tPA) were studied prospectively. T2* was performed before and 24 hours after tPA therapy. Independent clinical factors associated with new-EMBs development were examined using multivariate logistic regression analysis. A total of 224 patients (121 men; mean age, 76.2±10.6 years) were enrolled in the present study. MBs before tPA infusion were observed in 72 (32.1%) patients. Within 24 hours after tPA infusion, 6 (2.7%) patients had symptomatic intracranial hemorrhage (extraischemic [n=4], and hemorrhagic transformation [n=2]). Follow-up T2* revealed asymptomatic new-EMBs in 11 (4.9%) patients and hemorrhagic transformation in the infarcted area in 65 (29.0%). The total and mean number of new-EMBs were 23 and 1.6±1.3, respectively. Patients with new-EMBs more frequently had symptomatic extraischemic hemorrhage than those without new-EMBs (27.3% [3/11] versus 0.5% [1/213]; P=0.0003). However, the frequency of hemorrhagic transformation was not different between patients with and without new-EMBs (27.3% versus 29.1%; P=0.9999). Multivariate logistic regression demonstrated that the presence of MBs before tPA infusion was the only independent factor associated with new-EMBs (odds ratio, 10.6; 95% confidence interval, 20.68-54.279; P=0.0046). New-EMBs occurred rapidly after tPA infusion in 4.9% of patients. The presence of MBs before tPA therapy was associated with new-EMBs. Patients with new-EMBs are likely to have symptomatic extraischemic hemorrhage.
doi_str_mv 10.1161/STROKEAHA.113.001778
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We hypothesized that new-EMBs may develop rapidly after tPA infusion using T2*-weighted MRI (T2*) and investigated the frequency and clinical factors associated with new-EMBs. Patients with acute stroke within 3 hours of onset who were treated with tissue-type plasminogen activator (tPA) were studied prospectively. T2* was performed before and 24 hours after tPA therapy. Independent clinical factors associated with new-EMBs development were examined using multivariate logistic regression analysis. A total of 224 patients (121 men; mean age, 76.2±10.6 years) were enrolled in the present study. MBs before tPA infusion were observed in 72 (32.1%) patients. Within 24 hours after tPA infusion, 6 (2.7%) patients had symptomatic intracranial hemorrhage (extraischemic [n=4], and hemorrhagic transformation [n=2]). Follow-up T2* revealed asymptomatic new-EMBs in 11 (4.9%) patients and hemorrhagic transformation in the infarcted area in 65 (29.0%). The total and mean number of new-EMBs were 23 and 1.6±1.3, respectively. Patients with new-EMBs more frequently had symptomatic extraischemic hemorrhage than those without new-EMBs (27.3% [3/11] versus 0.5% [1/213]; P=0.0003). However, the frequency of hemorrhagic transformation was not different between patients with and without new-EMBs (27.3% versus 29.1%; P=0.9999). Multivariate logistic regression demonstrated that the presence of MBs before tPA infusion was the only independent factor associated with new-EMBs (odds ratio, 10.6; 95% confidence interval, 20.68-54.279; P=0.0046). New-EMBs occurred rapidly after tPA infusion in 4.9% of patients. The presence of MBs before tPA therapy was associated with new-EMBs. 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The total and mean number of new-EMBs were 23 and 1.6±1.3, respectively. Patients with new-EMBs more frequently had symptomatic extraischemic hemorrhage than those without new-EMBs (27.3% [3/11] versus 0.5% [1/213]; P=0.0003). However, the frequency of hemorrhagic transformation was not different between patients with and without new-EMBs (27.3% versus 29.1%; P=0.9999). Multivariate logistic regression demonstrated that the presence of MBs before tPA infusion was the only independent factor associated with new-EMBs (odds ratio, 10.6; 95% confidence interval, 20.68-54.279; P=0.0046). New-EMBs occurred rapidly after tPA infusion in 4.9% of patients. The presence of MBs before tPA therapy was associated with new-EMBs. Patients with new-EMBs are likely to have symptomatic extraischemic hemorrhage.</description><subject>Acute Disease</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Cerebral Hemorrhage - chemically induced</subject><subject>Cerebral Hemorrhage - diagnostic imaging</subject><subject>Diffusion Magnetic Resonance Imaging</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Pharmacology. Drug treatments</subject><subject>Radiography</subject><subject>Stroke - diagnostic imaging</subject><subject>Stroke - drug therapy</subject><subject>Time Factors</subject><subject>Tissue Plasminogen Activator - administration &amp; dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0039-2499</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc1u1DAUhSMEotPCGyDkDRKbFP8lsZdRNTAVLUVlEMvIca5nDEmc2g7TPgjvi4cZ2oV1dK3v-Mj3ZNkbgs8JKcmHb-vbm8_LelWnkZ1jTKpKPMsWpKA85yUVz7MFxkzmlEt5kp2G8BNjTJkoXmYnSUQlWLHI_nyBHaqnCZRXowbkDFreR69s0FsYrEbXVnvX9gBdQG5Ea5r_ALvZRujQtdqMEBNzC8GN_-yXg9rYcYMoRys3-4BqE8GjtQ1hhjw-TIC-9ioMdnQbGFGto_2tovOo7tKdDSk5Wje-yl4Y1Qd4fdSz7PvH5fpilV_dfLq8qK9yzSUXOa80GFUWqlOUYMWFlJzR1kjgBe86U4hOUq5bwQyQJBoz07ISt0QbqbFkZ9n7w7uTd3czhNgM6ePQ92oEN4eGcFYWJcOUJ5Qf0LSOEDyYZvJ2UP6hIbjZF9I8FpJG1hwKSba3x4S5HaB7NP1vIAHvjoAKWvVmX4MNT1xVVVji8il_5_q00vCrn3fgmy2oPm5TGsZVWeGcYsLIfsrTIYL9BcAgpj8</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>Kimura, Kazumi</creator><creator>Aoki, Junya</creator><creator>Shibazaki, Kensaku</creator><creator>Saji, Naoki</creator><creator>Uemura, Junichi</creator><creator>Sakamoto, Yuki</creator><general>American Heart Association, Inc</general><general>Lippincott Williams &amp; Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131001</creationdate><title>New Appearance of Extraischemic Microbleeds on T2-Weighted Magnetic Resonance Imaging 24 Hours After Tissue-type Plasminogen Activator Administration</title><author>Kimura, Kazumi ; Aoki, Junya ; Shibazaki, Kensaku ; Saji, Naoki ; Uemura, Junichi ; Sakamoto, Yuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4948-47cefa65ada210a4899432bf9e454ddf58d924cb83fe1cb8c03fb360b1cf9c093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acute Disease</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Cerebral Hemorrhage - chemically induced</topic><topic>Cerebral Hemorrhage - diagnostic imaging</topic><topic>Diffusion Magnetic Resonance Imaging</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration &amp; dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Pharmacology. Drug treatments</topic><topic>Radiography</topic><topic>Stroke - diagnostic imaging</topic><topic>Stroke - drug therapy</topic><topic>Time Factors</topic><topic>Tissue Plasminogen Activator - administration &amp; dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Kazumi</creatorcontrib><creatorcontrib>Aoki, Junya</creatorcontrib><creatorcontrib>Shibazaki, Kensaku</creatorcontrib><creatorcontrib>Saji, Naoki</creatorcontrib><creatorcontrib>Uemura, Junichi</creatorcontrib><creatorcontrib>Sakamoto, Yuki</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Kazumi</au><au>Aoki, Junya</au><au>Shibazaki, Kensaku</au><au>Saji, Naoki</au><au>Uemura, Junichi</au><au>Sakamoto, Yuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Appearance of Extraischemic Microbleeds on T2-Weighted Magnetic Resonance Imaging 24 Hours After Tissue-type Plasminogen Activator Administration</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2013-10-01</date><risdate>2013</risdate><volume>44</volume><issue>10</issue><spage>2776</spage><epage>2781</epage><pages>2776-2781</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>It is unknown whether new-extraischemic microbleeds (new-EMBs) develop rapidly after tissue-type plasminogen activator (tPA) infusion. We hypothesized that new-EMBs may develop rapidly after tPA infusion using T2*-weighted MRI (T2*) and investigated the frequency and clinical factors associated with new-EMBs. Patients with acute stroke within 3 hours of onset who were treated with tissue-type plasminogen activator (tPA) were studied prospectively. T2* was performed before and 24 hours after tPA therapy. Independent clinical factors associated with new-EMBs development were examined using multivariate logistic regression analysis. A total of 224 patients (121 men; mean age, 76.2±10.6 years) were enrolled in the present study. MBs before tPA infusion were observed in 72 (32.1%) patients. Within 24 hours after tPA infusion, 6 (2.7%) patients had symptomatic intracranial hemorrhage (extraischemic [n=4], and hemorrhagic transformation [n=2]). Follow-up T2* revealed asymptomatic new-EMBs in 11 (4.9%) patients and hemorrhagic transformation in the infarcted area in 65 (29.0%). The total and mean number of new-EMBs were 23 and 1.6±1.3, respectively. Patients with new-EMBs more frequently had symptomatic extraischemic hemorrhage than those without new-EMBs (27.3% [3/11] versus 0.5% [1/213]; P=0.0003). However, the frequency of hemorrhagic transformation was not different between patients with and without new-EMBs (27.3% versus 29.1%; P=0.9999). Multivariate logistic regression demonstrated that the presence of MBs before tPA infusion was the only independent factor associated with new-EMBs (odds ratio, 10.6; 95% confidence interval, 20.68-54.279; P=0.0046). New-EMBs occurred rapidly after tPA infusion in 4.9% of patients. The presence of MBs before tPA therapy was associated with new-EMBs. Patients with new-EMBs are likely to have symptomatic extraischemic hemorrhage.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>23887835</pmid><doi>10.1161/STROKEAHA.113.001778</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Journals@Ovid Ovid Autoload; MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Acute Disease
Aged
Aged, 80 and over
Biological and medical sciences
Blood. Blood coagulation. Reticuloendothelial system
Cerebral Hemorrhage - chemically induced
Cerebral Hemorrhage - diagnostic imaging
Diffusion Magnetic Resonance Imaging
Female
Fibrinolytic Agents - administration & dosage
Fibrinolytic Agents - adverse effects
Humans
Male
Medical sciences
Middle Aged
Neurology
Pharmacology. Drug treatments
Radiography
Stroke - diagnostic imaging
Stroke - drug therapy
Time Factors
Tissue Plasminogen Activator - administration & dosage
Tissue Plasminogen Activator - adverse effects
Vascular diseases and vascular malformations of the nervous system
title New Appearance of Extraischemic Microbleeds on T2-Weighted Magnetic Resonance Imaging 24 Hours After Tissue-type Plasminogen Activator Administration
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