Intraventricular hemorrhage after aneurysmal subarachnoid hemorrhage: pilot study of treatment with intraventricular tissue plasminogen activator
Intraventricular (IVen) hemorrhage is considered a predictor of poor outcome after subarachnoid hemorrhage (SAH). This prospective study examines the feasibility and outcome of administration of IVen tissue plasminogen activator (tPA) after aneurysmal SAH. Ten patients with SAH who received IVen tPA...
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Veröffentlicht in: | Neurosurgery 2005-02, Vol.56 (2), p.205-213 |
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description | Intraventricular (IVen) hemorrhage is considered a predictor of poor outcome after subarachnoid hemorrhage (SAH). This prospective study examines the feasibility and outcome of administration of IVen tissue plasminogen activator (tPA) after aneurysmal SAH.
Ten patients with SAH who received IVen tPA after the aneurysm had been secured were compared with 10 age-, sex-, and Glasgow Coma Scale score-matched control patients. The primary end point was third and fourth ventricle clot resolution. IVen blood was quantified by use of the Graeb and Le Roux scales on admission and at an additional time (equal or longer for the control group) after the injection was terminated.
Six men and four women with a mean age of 52 years in each group were evaluated. On average, 3.5 mg tPA was injected 68 +/- 51 hours after admission without ensuing complications. Although the treated group had significantly more IVen blood on admission than control subjects (mean Le Roux scale +/- standard deviation, 11 +/- 3 versus 7.6 +/- 4.2, P = 0.055, and mean Graeb scale +/- standard deviation, 8.5 +/- 2.3 in tPA versus 5.3 +/- 3, P < 0.02), it also had a significant decrease in the amount of IVen blood (mean Le Roux and Graeb scale decrease +/- standard deviation, 6.7 +/- 3.3 and 4.8 +/- 2 in tPA patients versus 0.9 +/- 3.2 and 0.5 +/- 2.6 in control subjects, P = 0.002). The tPA group had a non-statistically significantly shorter length of stay, decreased mortality, and better Glasgow Outcome Scale and modified Rankin Scale scores at discharge. Treated survivors showed a decreased need for shunt placement (2 [22%] of 9 patients versus 5 [83%] of 6 control subjects, P = 0.04).
This pilot study shows that IVen tPA administration is feasible without complications after SAH and may be associated with better outcomes. These results warrant a randomized clinical trial. |
doi_str_mv | 10.1227/01.NEU.0000147973.83688.D8 |
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Ten patients with SAH who received IVen tPA after the aneurysm had been secured were compared with 10 age-, sex-, and Glasgow Coma Scale score-matched control patients. The primary end point was third and fourth ventricle clot resolution. IVen blood was quantified by use of the Graeb and Le Roux scales on admission and at an additional time (equal or longer for the control group) after the injection was terminated.
Six men and four women with a mean age of 52 years in each group were evaluated. On average, 3.5 mg tPA was injected 68 +/- 51 hours after admission without ensuing complications. Although the treated group had significantly more IVen blood on admission than control subjects (mean Le Roux scale +/- standard deviation, 11 +/- 3 versus 7.6 +/- 4.2, P = 0.055, and mean Graeb scale +/- standard deviation, 8.5 +/- 2.3 in tPA versus 5.3 +/- 3, P < 0.02), it also had a significant decrease in the amount of IVen blood (mean Le Roux and Graeb scale decrease +/- standard deviation, 6.7 +/- 3.3 and 4.8 +/- 2 in tPA patients versus 0.9 +/- 3.2 and 0.5 +/- 2.6 in control subjects, P = 0.002). The tPA group had a non-statistically significantly shorter length of stay, decreased mortality, and better Glasgow Outcome Scale and modified Rankin Scale scores at discharge. Treated survivors showed a decreased need for shunt placement (2 [22%] of 9 patients versus 5 [83%] of 6 control subjects, P = 0.04).
This pilot study shows that IVen tPA administration is feasible without complications after SAH and may be associated with better outcomes. These results warrant a randomized clinical trial.</description><identifier>ISSN: 0148-396X</identifier><identifier>EISSN: 1524-4040</identifier><identifier>DOI: 10.1227/01.NEU.0000147973.83688.D8</identifier><identifier>PMID: 15670368</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Case-Control Studies ; Cerebral Hemorrhage - drug therapy ; Cerebral Hemorrhage - etiology ; Cerebral Ventricles - blood supply ; Feasibility Studies ; Female ; Fibrinolytic Agents - administration & dosage ; Humans ; Injections, Intraventricular ; Intracranial Aneurysm - complications ; Male ; Middle Aged ; Pilot Projects ; Prospective Studies ; Subarachnoid Hemorrhage - complications ; Tissue Plasminogen Activator - administration & dosage</subject><ispartof>Neurosurgery, 2005-02, Vol.56 (2), p.205-213</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-44e89bfddd1ede0600cc670623d061519e26f73259d9a9e8953a4b52daca60db3</citedby><cites>FETCH-LOGICAL-c317t-44e89bfddd1ede0600cc670623d061519e26f73259d9a9e8953a4b52daca60db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15670368$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Varelas, Panayiotis N</creatorcontrib><creatorcontrib>Rickert, Kim L</creatorcontrib><creatorcontrib>Cusick, Joseph</creatorcontrib><creatorcontrib>Hacein-Bey, Lotfi</creatorcontrib><creatorcontrib>Sinson, Grant</creatorcontrib><creatorcontrib>Torbey, Michel</creatorcontrib><creatorcontrib>Spanaki, Marianna</creatorcontrib><creatorcontrib>Gennarelli, Thomas A</creatorcontrib><title>Intraventricular hemorrhage after aneurysmal subarachnoid hemorrhage: pilot study of treatment with intraventricular tissue plasminogen activator</title><title>Neurosurgery</title><addtitle>Neurosurgery</addtitle><description>Intraventricular (IVen) hemorrhage is considered a predictor of poor outcome after subarachnoid hemorrhage (SAH). This prospective study examines the feasibility and outcome of administration of IVen tissue plasminogen activator (tPA) after aneurysmal SAH.
Ten patients with SAH who received IVen tPA after the aneurysm had been secured were compared with 10 age-, sex-, and Glasgow Coma Scale score-matched control patients. The primary end point was third and fourth ventricle clot resolution. IVen blood was quantified by use of the Graeb and Le Roux scales on admission and at an additional time (equal or longer for the control group) after the injection was terminated.
Six men and four women with a mean age of 52 years in each group were evaluated. On average, 3.5 mg tPA was injected 68 +/- 51 hours after admission without ensuing complications. Although the treated group had significantly more IVen blood on admission than control subjects (mean Le Roux scale +/- standard deviation, 11 +/- 3 versus 7.6 +/- 4.2, P = 0.055, and mean Graeb scale +/- standard deviation, 8.5 +/- 2.3 in tPA versus 5.3 +/- 3, P < 0.02), it also had a significant decrease in the amount of IVen blood (mean Le Roux and Graeb scale decrease +/- standard deviation, 6.7 +/- 3.3 and 4.8 +/- 2 in tPA patients versus 0.9 +/- 3.2 and 0.5 +/- 2.6 in control subjects, P = 0.002). The tPA group had a non-statistically significantly shorter length of stay, decreased mortality, and better Glasgow Outcome Scale and modified Rankin Scale scores at discharge. Treated survivors showed a decreased need for shunt placement (2 [22%] of 9 patients versus 5 [83%] of 6 control subjects, P = 0.04).
This pilot study shows that IVen tPA administration is feasible without complications after SAH and may be associated with better outcomes. These results warrant a randomized clinical trial.</description><subject>Adult</subject><subject>Aged</subject><subject>Case-Control Studies</subject><subject>Cerebral Hemorrhage - drug therapy</subject><subject>Cerebral Hemorrhage - etiology</subject><subject>Cerebral Ventricles - blood supply</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration & dosage</subject><subject>Humans</subject><subject>Injections, Intraventricular</subject><subject>Intracranial Aneurysm - complications</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>Subarachnoid Hemorrhage - complications</subject><subject>Tissue Plasminogen Activator - administration & dosage</subject><issn>0148-396X</issn><issn>1524-4040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFu1DAQhi0EotvCKyCLA7cEO3YcpzfUFlqpKhcqcbMm9qRrlMSL7RTtY_SNa-hKRZ2D5-Dvn9HoI-QjZzVvmu4z4_XNxW3NSnHZ9Z2otVBa1-f6FdnwtpGVZJK9JpvyrSvRq59H5DilXwVXstNvyRFvVcdKZkMerpYc4R7L6-06QaRbnEOMW7hDCmPGSGHBNe7TDBNN6wAR7HYJ3v0HntKdn0KmKa9uT8NIc0TIcxlK__i8pf7ljuxTWpHuJkizX8IdLhRs9veQQ3xH3owwJXx_6Cfk9uvFj7PL6vr7t6uzL9eVFbzLlZSo-2F0znF0yBRj1pajVCMcU7zlPTZq7ETT9q6HvrCtADm0jQMLirlBnJBPT3N3MfxeMWUz-2Rxmsq9YU1GdUI3kvUFPH0CbQwpRRzNLvoZ4t5wZv4KMYybIsQ8CzH_hJhzXcIfDlvWYUb3HD0YEI-VBI1q</recordid><startdate>200502</startdate><enddate>200502</enddate><creator>Varelas, Panayiotis N</creator><creator>Rickert, Kim L</creator><creator>Cusick, Joseph</creator><creator>Hacein-Bey, Lotfi</creator><creator>Sinson, Grant</creator><creator>Torbey, Michel</creator><creator>Spanaki, Marianna</creator><creator>Gennarelli, Thomas A</creator><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>200502</creationdate><title>Intraventricular hemorrhage after aneurysmal subarachnoid hemorrhage: pilot study of treatment with intraventricular tissue plasminogen activator</title><author>Varelas, Panayiotis N ; Rickert, Kim L ; Cusick, Joseph ; Hacein-Bey, Lotfi ; Sinson, Grant ; Torbey, Michel ; Spanaki, Marianna ; Gennarelli, Thomas A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-44e89bfddd1ede0600cc670623d061519e26f73259d9a9e8953a4b52daca60db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Case-Control Studies</topic><topic>Cerebral Hemorrhage - drug therapy</topic><topic>Cerebral Hemorrhage - etiology</topic><topic>Cerebral Ventricles - blood supply</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration & dosage</topic><topic>Humans</topic><topic>Injections, Intraventricular</topic><topic>Intracranial Aneurysm - complications</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>Subarachnoid Hemorrhage - complications</topic><topic>Tissue Plasminogen Activator - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Varelas, Panayiotis N</creatorcontrib><creatorcontrib>Rickert, Kim L</creatorcontrib><creatorcontrib>Cusick, Joseph</creatorcontrib><creatorcontrib>Hacein-Bey, Lotfi</creatorcontrib><creatorcontrib>Sinson, Grant</creatorcontrib><creatorcontrib>Torbey, Michel</creatorcontrib><creatorcontrib>Spanaki, Marianna</creatorcontrib><creatorcontrib>Gennarelli, Thomas A</creatorcontrib><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>Neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Varelas, Panayiotis N</au><au>Rickert, Kim L</au><au>Cusick, Joseph</au><au>Hacein-Bey, Lotfi</au><au>Sinson, Grant</au><au>Torbey, Michel</au><au>Spanaki, Marianna</au><au>Gennarelli, Thomas A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraventricular hemorrhage after aneurysmal subarachnoid hemorrhage: pilot study of treatment with intraventricular tissue plasminogen activator</atitle><jtitle>Neurosurgery</jtitle><addtitle>Neurosurgery</addtitle><date>2005-02</date><risdate>2005</risdate><volume>56</volume><issue>2</issue><spage>205</spage><epage>213</epage><pages>205-213</pages><issn>0148-396X</issn><eissn>1524-4040</eissn><abstract>Intraventricular (IVen) hemorrhage is considered a predictor of poor outcome after subarachnoid hemorrhage (SAH). This prospective study examines the feasibility and outcome of administration of IVen tissue plasminogen activator (tPA) after aneurysmal SAH.
Ten patients with SAH who received IVen tPA after the aneurysm had been secured were compared with 10 age-, sex-, and Glasgow Coma Scale score-matched control patients. The primary end point was third and fourth ventricle clot resolution. IVen blood was quantified by use of the Graeb and Le Roux scales on admission and at an additional time (equal or longer for the control group) after the injection was terminated.
Six men and four women with a mean age of 52 years in each group were evaluated. On average, 3.5 mg tPA was injected 68 +/- 51 hours after admission without ensuing complications. Although the treated group had significantly more IVen blood on admission than control subjects (mean Le Roux scale +/- standard deviation, 11 +/- 3 versus 7.6 +/- 4.2, P = 0.055, and mean Graeb scale +/- standard deviation, 8.5 +/- 2.3 in tPA versus 5.3 +/- 3, P < 0.02), it also had a significant decrease in the amount of IVen blood (mean Le Roux and Graeb scale decrease +/- standard deviation, 6.7 +/- 3.3 and 4.8 +/- 2 in tPA patients versus 0.9 +/- 3.2 and 0.5 +/- 2.6 in control subjects, P = 0.002). The tPA group had a non-statistically significantly shorter length of stay, decreased mortality, and better Glasgow Outcome Scale and modified Rankin Scale scores at discharge. Treated survivors showed a decreased need for shunt placement (2 [22%] of 9 patients versus 5 [83%] of 6 control subjects, P = 0.04).
This pilot study shows that IVen tPA administration is feasible without complications after SAH and may be associated with better outcomes. These results warrant a randomized clinical trial.</abstract><cop>United States</cop><pmid>15670368</pmid><doi>10.1227/01.NEU.0000147973.83688.D8</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Case-Control Studies Cerebral Hemorrhage - drug therapy Cerebral Hemorrhage - etiology Cerebral Ventricles - blood supply Feasibility Studies Female Fibrinolytic Agents - administration & dosage Humans Injections, Intraventricular Intracranial Aneurysm - complications Male Middle Aged Pilot Projects Prospective Studies Subarachnoid Hemorrhage - complications Tissue Plasminogen Activator - administration & dosage |
title | Intraventricular hemorrhage after aneurysmal subarachnoid hemorrhage: pilot study of treatment with intraventricular tissue plasminogen activator |
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