Modified ultrafiltration may not improve neurologic outcome following deep hypothermic circulatory arrest

Objective: Modified ultrafiltration (MUF) improves systolic blood pressure and left ventricular performance, as well as lowering transfusion requirements, after cardiopulmonary bypass (CPB). MUF has also been shown to enhance acute cerebral metabolic recovery after deep hypothermic circulatory arres...

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Veröffentlicht in:European journal of cardio-thoracic surgery 2003-08, Vol.24 (2), p.243-248
Hauptverfasser: Myung, Richard J., Kirshbom, Paul M., Petko, Matus, Golden, Jeffrey A., Judkins, Alexander R., Ittenbach, Richard F., Spray, Thomas L., Gaynor, J. William
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container_end_page 248
container_issue 2
container_start_page 243
container_title European journal of cardio-thoracic surgery
container_volume 24
creator Myung, Richard J.
Kirshbom, Paul M.
Petko, Matus
Golden, Jeffrey A.
Judkins, Alexander R.
Ittenbach, Richard F.
Spray, Thomas L.
Gaynor, J. William
description Objective: Modified ultrafiltration (MUF) improves systolic blood pressure and left ventricular performance, as well as lowering transfusion requirements, after cardiopulmonary bypass (CPB). MUF has also been shown to enhance acute cerebral metabolic recovery after deep hypothermic circulatory arrest (DHCA), but whether this improves neurologic outcome is unknown. Methods: Sixteen neonatal piglets underwent CPB and 90 min of DHCA. The hematocrit was maintained between 25 and 30%. Alpha-stat blood gas management was used. After separation from CPB, animals were randomized to 15 min of MUF (n=8) or no intervention (n=8). Neurologic injury was assessed with behavior scores and histologic examination. Standardized behavior scores were obtained on post-operative days 1, 3, and 6 (0=no deficit to 95=brain death). The percentage of injured neurons by hematoxylin and eosin staining and the degree of reactive astrocytosis by glial filbrillary acidic protein (GFAP) immunohistochemistry were assessed to determine histologic scores in the neocortex and hippocampus (0=no injury to 4=diffuse injury). Results: There were no statistically significant differences between groups during CPB. After MUF, the hematocrit was significantly higher (40%±5.7 vs. 28%±3.9, P0.1). There was resolution of deficits by day 6 in all animals. Neuronal injury was present in 81% (13/16) of the animals with no statistically significant differences between groups in incidence or severity. Conclusions: Use of MUF after DHCA does not prevent neuronal injury or improve neurologic outcome in this neonatal swine model.
doi_str_mv 10.1016/S1010-7940(03)00298-7
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William</creator><creatorcontrib>Myung, Richard J. ; Kirshbom, Paul M. ; Petko, Matus ; Golden, Jeffrey A. ; Judkins, Alexander R. ; Ittenbach, Richard F. ; Spray, Thomas L. ; Gaynor, J. William</creatorcontrib><description>Objective: Modified ultrafiltration (MUF) improves systolic blood pressure and left ventricular performance, as well as lowering transfusion requirements, after cardiopulmonary bypass (CPB). MUF has also been shown to enhance acute cerebral metabolic recovery after deep hypothermic circulatory arrest (DHCA), but whether this improves neurologic outcome is unknown. Methods: Sixteen neonatal piglets underwent CPB and 90 min of DHCA. The hematocrit was maintained between 25 and 30%. Alpha-stat blood gas management was used. After separation from CPB, animals were randomized to 15 min of MUF (n=8) or no intervention (n=8). Neurologic injury was assessed with behavior scores and histologic examination. Standardized behavior scores were obtained on post-operative days 1, 3, and 6 (0=no deficit to 95=brain death). The percentage of injured neurons by hematoxylin and eosin staining and the degree of reactive astrocytosis by glial filbrillary acidic protein (GFAP) immunohistochemistry were assessed to determine histologic scores in the neocortex and hippocampus (0=no injury to 4=diffuse injury). Results: There were no statistically significant differences between groups during CPB. After MUF, the hematocrit was significantly higher (40%±5.7 vs. 28%±3.9, P&lt;0.001). There were no significant differences in behavior scores between groups (p&gt;0.1). There was resolution of deficits by day 6 in all animals. Neuronal injury was present in 81% (13/16) of the animals with no statistically significant differences between groups in incidence or severity. Conclusions: Use of MUF after DHCA does not prevent neuronal injury or improve neurologic outcome in this neonatal swine model.</description><identifier>ISSN: 1010-7940</identifier><identifier>EISSN: 1873-734X</identifier><identifier>DOI: 10.1016/S1010-7940(03)00298-7</identifier><identifier>PMID: 12895615</identifier><identifier>CODEN: EJCSE7</identifier><language>eng</language><publisher>Amsterdam: Elsevier Science B.V</publisher><subject>Anesthesia ; Anesthesia depending on type of surgery ; Anesthesia. Intensive care medicine. Transfusions. 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William</creatorcontrib><title>Modified ultrafiltration may not improve neurologic outcome following deep hypothermic circulatory arrest</title><title>European journal of cardio-thoracic surgery</title><addtitle>Eur J Cardiothorac Surg</addtitle><addtitle>Eur J Cardiothorac Surg</addtitle><description>Objective: Modified ultrafiltration (MUF) improves systolic blood pressure and left ventricular performance, as well as lowering transfusion requirements, after cardiopulmonary bypass (CPB). MUF has also been shown to enhance acute cerebral metabolic recovery after deep hypothermic circulatory arrest (DHCA), but whether this improves neurologic outcome is unknown. Methods: Sixteen neonatal piglets underwent CPB and 90 min of DHCA. The hematocrit was maintained between 25 and 30%. Alpha-stat blood gas management was used. After separation from CPB, animals were randomized to 15 min of MUF (n=8) or no intervention (n=8). Neurologic injury was assessed with behavior scores and histologic examination. Standardized behavior scores were obtained on post-operative days 1, 3, and 6 (0=no deficit to 95=brain death). The percentage of injured neurons by hematoxylin and eosin staining and the degree of reactive astrocytosis by glial filbrillary acidic protein (GFAP) immunohistochemistry were assessed to determine histologic scores in the neocortex and hippocampus (0=no injury to 4=diffuse injury). Results: There were no statistically significant differences between groups during CPB. After MUF, the hematocrit was significantly higher (40%±5.7 vs. 28%±3.9, P&lt;0.001). There were no significant differences in behavior scores between groups (p&gt;0.1). There was resolution of deficits by day 6 in all animals. Neuronal injury was present in 81% (13/16) of the animals with no statistically significant differences between groups in incidence or severity. Conclusions: Use of MUF after DHCA does not prevent neuronal injury or improve neurologic outcome in this neonatal swine model.</description><subject>Anesthesia</subject><subject>Anesthesia depending on type of surgery</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Behavior, Animal</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain Chemistry</subject><subject>Brain Ischemia - pathology</subject><subject>Brain Ischemia - prevention &amp; control</subject><subject>Cardiopulmonary Bypass</subject><subject>Deep hypothermic circulatory arrest</subject><subject>Glial Fibrillary Acidic Protein - analysis</subject><subject>Hematocrit</subject><subject>Hemofiltration</subject><subject>Hypothermia, Induced</subject><subject>Medical sciences</subject><subject>Models, Animal</subject><subject>Modified ultrafiltration</subject><subject>Neurologic injury</subject><subject>Neurons - pathology</subject><subject>Random Allocation</subject><subject>Swine</subject><subject>Thoracic and cardiovascular surgery. Cardiopulmonary bypass</subject><subject>Treatment Failure</subject><issn>1010-7940</issn><issn>1873-734X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkEFvFSEUhYmxsbX6EzRsNLoYvQwzMCybRl-btNFYjU03hMdAizLDCIz6_n2ZvqeNiZsLi-_cc89B6BmBNwQIe3tRJlRcNPAK6GuAWnQVf4AOSMdpxWlz-bD8_yD76HFK3wCA0Zo_Qvuk7kTLSHuA3HnonXWmx7PPUVm3zOzCiAe1wWPI2A1TDD8NHs0cgw_XTuMwZx0Gg23wPvxy4zXujZnwzWYK-cbEoSDaRT17lUPcYBWjSfkJ2rPKJ_N09x6iL-_ffT4-qc4-rE6Pj84q3QiWK9630JHW8k4DFRY0ZcqINes5YYISClr0UCIJUzfC9qKm6xLTUkEoIayEP0Qvt3vL2T_mYiwHl7TxXo0mzEly2taCUihguwV1DClFY-UU3aDiRhKQS8fyrmO5FCiByruO5WLwfGcwrwfT36t2pRbgxQ5QSStvoxq1S_dcCw00bFkEWy7M0_-9q3-8q0VSbSUuZfP7r0jF77Is5K08ubySFx9XTft19Ule0VvuJaLD</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Myung, Richard J.</creator><creator>Kirshbom, Paul M.</creator><creator>Petko, Matus</creator><creator>Golden, Jeffrey A.</creator><creator>Judkins, Alexander R.</creator><creator>Ittenbach, Richard F.</creator><creator>Spray, Thomas L.</creator><creator>Gaynor, J. 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William</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-7d50815f78c039f0c36ae9b6d71693130c9d09409e249fd923b101f3913116873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Anesthesia</topic><topic>Anesthesia depending on type of surgery</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Behavior, Animal</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Brain Chemistry</topic><topic>Brain Ischemia - pathology</topic><topic>Brain Ischemia - prevention &amp; control</topic><topic>Cardiopulmonary Bypass</topic><topic>Deep hypothermic circulatory arrest</topic><topic>Glial Fibrillary Acidic Protein - analysis</topic><topic>Hematocrit</topic><topic>Hemofiltration</topic><topic>Hypothermia, Induced</topic><topic>Medical sciences</topic><topic>Models, Animal</topic><topic>Modified ultrafiltration</topic><topic>Neurologic injury</topic><topic>Neurons - pathology</topic><topic>Random Allocation</topic><topic>Swine</topic><topic>Thoracic and cardiovascular surgery. Cardiopulmonary bypass</topic><topic>Treatment Failure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Myung, Richard J.</creatorcontrib><creatorcontrib>Kirshbom, Paul M.</creatorcontrib><creatorcontrib>Petko, Matus</creatorcontrib><creatorcontrib>Golden, Jeffrey A.</creatorcontrib><creatorcontrib>Judkins, Alexander R.</creatorcontrib><creatorcontrib>Ittenbach, Richard F.</creatorcontrib><creatorcontrib>Spray, Thomas L.</creatorcontrib><creatorcontrib>Gaynor, J. William</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cardio-thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Myung, Richard J.</au><au>Kirshbom, Paul M.</au><au>Petko, Matus</au><au>Golden, Jeffrey A.</au><au>Judkins, Alexander R.</au><au>Ittenbach, Richard F.</au><au>Spray, Thomas L.</au><au>Gaynor, J. William</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modified ultrafiltration may not improve neurologic outcome following deep hypothermic circulatory arrest</atitle><jtitle>European journal of cardio-thoracic surgery</jtitle><stitle>Eur J Cardiothorac Surg</stitle><addtitle>Eur J Cardiothorac Surg</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>24</volume><issue>2</issue><spage>243</spage><epage>248</epage><pages>243-248</pages><issn>1010-7940</issn><eissn>1873-734X</eissn><coden>EJCSE7</coden><abstract>Objective: Modified ultrafiltration (MUF) improves systolic blood pressure and left ventricular performance, as well as lowering transfusion requirements, after cardiopulmonary bypass (CPB). MUF has also been shown to enhance acute cerebral metabolic recovery after deep hypothermic circulatory arrest (DHCA), but whether this improves neurologic outcome is unknown. Methods: Sixteen neonatal piglets underwent CPB and 90 min of DHCA. 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Neuronal injury was present in 81% (13/16) of the animals with no statistically significant differences between groups in incidence or severity. Conclusions: Use of MUF after DHCA does not prevent neuronal injury or improve neurologic outcome in this neonatal swine model.</abstract><cop>Amsterdam</cop><pub>Elsevier Science B.V</pub><pmid>12895615</pmid><doi>10.1016/S1010-7940(03)00298-7</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals
subjects Anesthesia
Anesthesia depending on type of surgery
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Animals, Newborn
Behavior, Animal
Biological and medical sciences
Brain - pathology
Brain Chemistry
Brain Ischemia - pathology
Brain Ischemia - prevention & control
Cardiopulmonary Bypass
Deep hypothermic circulatory arrest
Glial Fibrillary Acidic Protein - analysis
Hematocrit
Hemofiltration
Hypothermia, Induced
Medical sciences
Models, Animal
Modified ultrafiltration
Neurologic injury
Neurons - pathology
Random Allocation
Swine
Thoracic and cardiovascular surgery. Cardiopulmonary bypass
Treatment Failure
title Modified ultrafiltration may not improve neurologic outcome following deep hypothermic circulatory arrest
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