Intraventricular thrombolysis with rt-PA in patients with intraventricular hemorrhage

Dunatov S, Antoncic I, Bralic M, Jurjevic A. Intraventricular thrombolysis with rt‐PA in patients with intraventricular hemorrhage. 
Acta Neurol Scand: 2011: 124: 343–348. 
© 2011 John Wiley & Sons A/S. Objectives –  To evaluate safety, clinical feasibility, and outcome of intraventricular (IVen...

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Veröffentlicht in:Acta neurologica Scandinavica 2011-11, Vol.124 (5), p.343-348
Hauptverfasser: Dunatov, S., Antoncic, I., Bralic, M., Jurjevic, A.
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container_title Acta neurologica Scandinavica
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creator Dunatov, S.
Antoncic, I.
Bralic, M.
Jurjevic, A.
description Dunatov S, Antoncic I, Bralic M, Jurjevic A. Intraventricular thrombolysis with rt‐PA in patients with intraventricular hemorrhage. 
Acta Neurol Scand: 2011: 124: 343–348. 
© 2011 John Wiley & Sons A/S. Objectives –  To evaluate safety, clinical feasibility, and outcome of intraventricular (IVen) administration of recombinant tissue plasminogen activator (rt‐PA) in patients with intraventricular hemorrhage (IVH). Materials and methods –  Forty‐eight patients with IVH who received IVen rt‐PA were compared with 49 age‐, sex‐, Glasgow Coma Scale score‐, and Intracerebral Hemorrhage score‐matched control patients. Patients with IVH of aneurysmal or arteriovenous malformation origin were excluded. External ventricular drainage was inserted as soon as baseline CT was performed and rt‐PA was administered within 12 ± 1 h after the ictal onset. Results –  The outcome after 3 months was evaluated using the modified Rankin Scale (mRS). In addition, Glasgow Outcome Scale (GOS) and mortality were assessed. A good outcome, defined as mRS 0–3, was detected in 27% of patients from the control group vs 58% of patients in the IVen group; P = 0.003. GOS as other outcome scale yielded a significant difference between groups: 20% in the control group, vs 54% in the IVen group; P = 0.001. A statistically significant decrease in mortality was observed in the IVen group: 30% in the control vs 10% in IVen group; P = 0.003. No one patient died because of a complication which could be directly attributed to the IVen thrombolytic therapy. Conclusions –  IVen administration of rt‐PA seems to be safe in cases of IVH. This pilot study shows that it may be associated with better outcomes. Further studies and clinical randomized trials are needed to establish indications and IVen administration protocols.
doi_str_mv 10.1111/j.1600-0404.2010.01481.x
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Acta Neurol Scand: 2011: 124: 343–348. 
© 2011 John Wiley &amp; Sons A/S. Objectives –  To evaluate safety, clinical feasibility, and outcome of intraventricular (IVen) administration of recombinant tissue plasminogen activator (rt‐PA) in patients with intraventricular hemorrhage (IVH). Materials and methods –  Forty‐eight patients with IVH who received IVen rt‐PA were compared with 49 age‐, sex‐, Glasgow Coma Scale score‐, and Intracerebral Hemorrhage score‐matched control patients. Patients with IVH of aneurysmal or arteriovenous malformation origin were excluded. External ventricular drainage was inserted as soon as baseline CT was performed and rt‐PA was administered within 12 ± 1 h after the ictal onset. Results –  The outcome after 3 months was evaluated using the modified Rankin Scale (mRS). In addition, Glasgow Outcome Scale (GOS) and mortality were assessed. A good outcome, defined as mRS 0–3, was detected in 27% of patients from the control group vs 58% of patients in the IVen group; P = 0.003. GOS as other outcome scale yielded a significant difference between groups: 20% in the control group, vs 54% in the IVen group; P = 0.001. A statistically significant decrease in mortality was observed in the IVen group: 30% in the control vs 10% in IVen group; P = 0.003. No one patient died because of a complication which could be directly attributed to the IVen thrombolytic therapy. Conclusions –  IVen administration of rt‐PA seems to be safe in cases of IVH. This pilot study shows that it may be associated with better outcomes. Further studies and clinical randomized trials are needed to establish indications and IVen administration protocols.</description><identifier>ISSN: 0001-6314</identifier><identifier>EISSN: 1600-0404</identifier><identifier>DOI: 10.1111/j.1600-0404.2010.01481.x</identifier><identifier>PMID: 21303348</identifier><identifier>CODEN: ANRSAS</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aneurysm ; Biological and medical sciences ; Case-Control Studies ; Cerebral Hemorrhage - complications ; Cerebral Hemorrhage - drug therapy ; Clinical trials ; Coma ; Drainage ; Female ; Fibrinolytic Agents - administration &amp; dosage ; Fibrinolytic Agents - adverse effects ; Glasgow Outcome Scale ; Hemorrhage ; Humans ; Infusions, Intraventricular ; intracerebral hemorrhage ; intraventricular hemorrhage ; intraventricular thrombolysis ; Male ; Medical sciences ; Middle Aged ; Mortality ; Neurology ; outcome ; Pilot Projects ; Prospective Studies ; recombinant tissue plasminogen activator ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Statistical analysis ; t-Plasminogen activator ; thrombolysis ; Thrombolytic Therapy - adverse effects ; Thrombolytic Therapy - methods ; Tissue Plasminogen Activator - administration &amp; dosage ; Tissue Plasminogen Activator - adverse effects ; Treatment Outcome</subject><ispartof>Acta neurologica Scandinavica, 2011-11, Vol.124 (5), p.343-348</ispartof><rights>2011 John Wiley &amp; Sons A/S</rights><rights>2015 INIST-CNRS</rights><rights>2011 John Wiley &amp; Sons A/S.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4691-2f6796c3d508ceb8049f12a44e1c44feb69542ed78f091ff268c1e9533e761403</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-0404.2010.01481.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0404.2010.01481.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24595402$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21303348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dunatov, S.</creatorcontrib><creatorcontrib>Antoncic, I.</creatorcontrib><creatorcontrib>Bralic, M.</creatorcontrib><creatorcontrib>Jurjevic, A.</creatorcontrib><title>Intraventricular thrombolysis with rt-PA in patients with intraventricular hemorrhage</title><title>Acta neurologica Scandinavica</title><addtitle>Acta Neurol Scand</addtitle><description>Dunatov S, Antoncic I, Bralic M, Jurjevic A. Intraventricular thrombolysis with rt‐PA in patients with intraventricular hemorrhage. 
Acta Neurol Scand: 2011: 124: 343–348. 
© 2011 John Wiley &amp; Sons A/S. Objectives –  To evaluate safety, clinical feasibility, and outcome of intraventricular (IVen) administration of recombinant tissue plasminogen activator (rt‐PA) in patients with intraventricular hemorrhage (IVH). Materials and methods –  Forty‐eight patients with IVH who received IVen rt‐PA were compared with 49 age‐, sex‐, Glasgow Coma Scale score‐, and Intracerebral Hemorrhage score‐matched control patients. Patients with IVH of aneurysmal or arteriovenous malformation origin were excluded. External ventricular drainage was inserted as soon as baseline CT was performed and rt‐PA was administered within 12 ± 1 h after the ictal onset. Results –  The outcome after 3 months was evaluated using the modified Rankin Scale (mRS). In addition, Glasgow Outcome Scale (GOS) and mortality were assessed. A good outcome, defined as mRS 0–3, was detected in 27% of patients from the control group vs 58% of patients in the IVen group; P = 0.003. GOS as other outcome scale yielded a significant difference between groups: 20% in the control group, vs 54% in the IVen group; P = 0.001. A statistically significant decrease in mortality was observed in the IVen group: 30% in the control vs 10% in IVen group; P = 0.003. No one patient died because of a complication which could be directly attributed to the IVen thrombolytic therapy. Conclusions –  IVen administration of rt‐PA seems to be safe in cases of IVH. This pilot study shows that it may be associated with better outcomes. Further studies and clinical randomized trials are needed to establish indications and IVen administration protocols.</description><subject>Aneurysm</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Cerebral Hemorrhage - complications</subject><subject>Cerebral Hemorrhage - drug therapy</subject><subject>Clinical trials</subject><subject>Coma</subject><subject>Drainage</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Fibrinolytic Agents - adverse effects</subject><subject>Glasgow Outcome Scale</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Infusions, Intraventricular</subject><subject>intracerebral hemorrhage</subject><subject>intraventricular hemorrhage</subject><subject>intraventricular thrombolysis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neurology</subject><subject>outcome</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>recombinant tissue plasminogen activator</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Statistical analysis</subject><subject>t-Plasminogen activator</subject><subject>thrombolysis</subject><subject>Thrombolytic Therapy - adverse effects</subject><subject>Thrombolytic Therapy - methods</subject><subject>Tissue Plasminogen Activator - administration &amp; dosage</subject><subject>Tissue Plasminogen Activator - adverse effects</subject><subject>Treatment Outcome</subject><issn>0001-6314</issn><issn>1600-0404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFOGzEQhi3UqqS0r4D2UvW0YWzPeu0DhwgRgkAUodIeLcfxNk53s8HeQPL29ZI0SL10Dp7xzPdb1vyEZBSGNMXZYkgFQA4IOGSQukBR0uHmiAwOg3dkAAA0F5ziMfkY4yLdWIn4gRwzyoFzlAPyeL3sgnl26fR2XZuQdfPQNtO23kYfsxffzbPQ5fejzC-zlel8Ivdt_69y7po2hLn55T6R95Wpo_u8zyfkcXz5_WKS3367ur4Y3eYWhaI5q0SphOWzAqR1UwmoKsoMoqMWsXJToQpkblbKChStKiakpU4VnLtSUAR-Qr7u3l2F9mntYqcbH62ra7N07TpqlZZVMFWI_5JSCclKiT15uifX08bN9Cr4xoSt_ruzBHzZAyZaU1fBLK2PbxwW6dfAEne-41587baHOQXde6gXurdK91bp3kP96qHe6NHdZV8lfb7T-9i5zUFvwm8tSl4W-ufdlebjyfjm5sdEP_A_nmWd9Q</recordid><startdate>201111</startdate><enddate>201111</enddate><creator>Dunatov, S.</creator><creator>Antoncic, I.</creator><creator>Bralic, M.</creator><creator>Jurjevic, A.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>201111</creationdate><title>Intraventricular thrombolysis with rt-PA in patients with intraventricular hemorrhage</title><author>Dunatov, S. ; Antoncic, I. ; Bralic, M. ; Jurjevic, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4691-2f6796c3d508ceb8049f12a44e1c44feb69542ed78f091ff268c1e9533e761403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aneurysm</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Cerebral Hemorrhage - complications</topic><topic>Cerebral Hemorrhage - drug therapy</topic><topic>Clinical trials</topic><topic>Coma</topic><topic>Drainage</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration &amp; dosage</topic><topic>Fibrinolytic Agents - adverse effects</topic><topic>Glasgow Outcome Scale</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Infusions, Intraventricular</topic><topic>intracerebral hemorrhage</topic><topic>intraventricular hemorrhage</topic><topic>intraventricular thrombolysis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neurology</topic><topic>outcome</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>recombinant tissue plasminogen activator</topic><topic>Sarcoidosis. 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Vasculitis</topic><topic>Statistical analysis</topic><topic>t-Plasminogen activator</topic><topic>thrombolysis</topic><topic>Thrombolytic Therapy - adverse effects</topic><topic>Thrombolytic Therapy - methods</topic><topic>Tissue Plasminogen Activator - administration &amp; dosage</topic><topic>Tissue Plasminogen Activator - adverse effects</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dunatov, S.</creatorcontrib><creatorcontrib>Antoncic, I.</creatorcontrib><creatorcontrib>Bralic, M.</creatorcontrib><creatorcontrib>Jurjevic, A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Acta neurologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dunatov, S.</au><au>Antoncic, I.</au><au>Bralic, M.</au><au>Jurjevic, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraventricular thrombolysis with rt-PA in patients with intraventricular hemorrhage</atitle><jtitle>Acta neurologica Scandinavica</jtitle><addtitle>Acta Neurol Scand</addtitle><date>2011-11</date><risdate>2011</risdate><volume>124</volume><issue>5</issue><spage>343</spage><epage>348</epage><pages>343-348</pages><issn>0001-6314</issn><eissn>1600-0404</eissn><coden>ANRSAS</coden><abstract>Dunatov S, Antoncic I, Bralic M, Jurjevic A. Intraventricular thrombolysis with rt‐PA in patients with intraventricular hemorrhage. 
Acta Neurol Scand: 2011: 124: 343–348. 
© 2011 John Wiley &amp; Sons A/S. Objectives –  To evaluate safety, clinical feasibility, and outcome of intraventricular (IVen) administration of recombinant tissue plasminogen activator (rt‐PA) in patients with intraventricular hemorrhage (IVH). Materials and methods –  Forty‐eight patients with IVH who received IVen rt‐PA were compared with 49 age‐, sex‐, Glasgow Coma Scale score‐, and Intracerebral Hemorrhage score‐matched control patients. Patients with IVH of aneurysmal or arteriovenous malformation origin were excluded. External ventricular drainage was inserted as soon as baseline CT was performed and rt‐PA was administered within 12 ± 1 h after the ictal onset. Results –  The outcome after 3 months was evaluated using the modified Rankin Scale (mRS). In addition, Glasgow Outcome Scale (GOS) and mortality were assessed. A good outcome, defined as mRS 0–3, was detected in 27% of patients from the control group vs 58% of patients in the IVen group; P = 0.003. GOS as other outcome scale yielded a significant difference between groups: 20% in the control group, vs 54% in the IVen group; P = 0.001. A statistically significant decrease in mortality was observed in the IVen group: 30% in the control vs 10% in IVen group; P = 0.003. No one patient died because of a complication which could be directly attributed to the IVen thrombolytic therapy. Conclusions –  IVen administration of rt‐PA seems to be safe in cases of IVH. This pilot study shows that it may be associated with better outcomes. Further studies and clinical randomized trials are needed to establish indications and IVen administration protocols.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21303348</pmid><doi>10.1111/j.1600-0404.2010.01481.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Aneurysm
Biological and medical sciences
Case-Control Studies
Cerebral Hemorrhage - complications
Cerebral Hemorrhage - drug therapy
Clinical trials
Coma
Drainage
Female
Fibrinolytic Agents - administration & dosage
Fibrinolytic Agents - adverse effects
Glasgow Outcome Scale
Hemorrhage
Humans
Infusions, Intraventricular
intracerebral hemorrhage
intraventricular hemorrhage
intraventricular thrombolysis
Male
Medical sciences
Middle Aged
Mortality
Neurology
outcome
Pilot Projects
Prospective Studies
recombinant tissue plasminogen activator
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Statistical analysis
t-Plasminogen activator
thrombolysis
Thrombolytic Therapy - adverse effects
Thrombolytic Therapy - methods
Tissue Plasminogen Activator - administration & dosage
Tissue Plasminogen Activator - adverse effects
Treatment Outcome
title Intraventricular thrombolysis with rt-PA in patients with intraventricular hemorrhage
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