A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass
Depression in electroencephalogram (EEG) has been documented clinically and is reproducible in swine at the initiation of cardiopulmonary bypass (CPB) utilizing a crystalloid prime. The physiological cause of this transient alteration in electrical brain activity appears to be associated with the tr...
Gespeichert in:
Veröffentlicht in: | The Journal of extra-corporeal technology 1995-03, Vol.27 (1), p.6-10 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 10 |
---|---|
container_issue | 1 |
container_start_page | 6 |
container_title | The Journal of extra-corporeal technology |
container_volume | 27 |
creator | VOCELKA, C SPIESS, B SOLTOW, L THOMAS, R GOHRA, H AKIMOTO, H ROTHNIE, C KUNZELMAN, K VERRIER, E COCHRAN, R. P |
description | Depression in electroencephalogram (EEG) has been documented clinically and is reproducible in swine at the initiation of cardiopulmonary bypass (CPB) utilizing a crystalloid prime. The physiological cause of this transient alteration in electrical brain activity appears to be associated with the transient drop in arterial pressure. The etiology is unknown but may be attributable to the bolus of the crystalloid prime or micro emboli, either air or fibrin-platelet. Thirteen swine (17-26 kg) were anesthetized and received 4 mg/kg dexamethasone, and following a tracheotomy were ventilated with halothane in 100% O2. Surgical preparation included: sternotomy and preparation for right atrial-aortic CPB. The CPB circuit consisted of a hollow fiber membrane oxygenator, a hard-shell venous reservoir, a roller pump, and PVC tubing. The circuit was randomly primed with either 1200 ml Plasmalyte-A or 10 ml/kg perfluorocarbon emulsion (PFE) and Plasmalyte-A to total 1200 ml. The animals were monitored continuously for systemic hemodynamics and electrocardiogram, and cerebral monitoring included blood flow and bitemporal EEG. Arterial blood gases were measured and PaCO2 was kept between 30-45 mmHg both before and during CPB. Cerebral blood flow (CBF) was measured pre-CPB and at 10 minutes after initiation of CPB. Bitemporal computerized EEG was analyzed every 60 seconds. Total power of each hemisphere, power in frequency bands, and spectral edge were recorded. All animals demonstrated a relative decrease in EEG total power at the onset of CPB. Animals that received PFE demonstrated a more stable arterial blood pressure, an increased CBF, and a lesser decrease and an earlier recovery of the EEG power. |
doi_str_mv | 10.1051/ject/19952716 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77466320</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77466320</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2726-b6bc044bb89422c8e19e87c5129b63a51e5c53bc46fd506c0fdfdbf74b6b6d2b3</originalsourceid><addsrcrecordid>eNpNkTtv2zAUhYkiQe2kHbMGHIJuakhKJKXRCNI2gIEuySzwcdkwoESFlFz4V_Qvh66dotO9w3fOfRyErij5Sgmnty9g5lvadZxJKj6gNetEV7WdIGdoTQhjVaHaFbrI-YUQQUlNP6IVJZQTyeUa_dngCZILS0zRqKTjiGFYQvalmZIfACtr_ex3gP0wpbiDjOdnwBDK3BRhNDA9qxB_JTVgNVpsIIFOKmAdYrTYhfgbq_mvxo_FSM0H6-hwmWZ9nJYwxFGlPdb7SeX8CZ07FTJ8PtVL9PTt_vHuR7X9-f3hbrOtDJNMVFpoQ5pG67ZrGDMt0A5aaThlnRa14hS44bU2jXCWE2GIs85qJ5siFJbp-hJ9OfqWm14XyHM_-GwgBDVCXHIvZSNEzUgBqyNoUsw5gesPbykL95T0hwT6QwL9ewKFvz4ZL3oA-x99fHkBbk6AykYFl9RofP7H1Y2s25bUb3OrkyU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77466320</pqid></control><display><type>article</type><title>A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>VOCELKA, C ; SPIESS, B ; SOLTOW, L ; THOMAS, R ; GOHRA, H ; AKIMOTO, H ; ROTHNIE, C ; KUNZELMAN, K ; VERRIER, E ; COCHRAN, R. P</creator><creatorcontrib>VOCELKA, C ; SPIESS, B ; SOLTOW, L ; THOMAS, R ; GOHRA, H ; AKIMOTO, H ; ROTHNIE, C ; KUNZELMAN, K ; VERRIER, E ; COCHRAN, R. P</creatorcontrib><description>Depression in electroencephalogram (EEG) has been documented clinically and is reproducible in swine at the initiation of cardiopulmonary bypass (CPB) utilizing a crystalloid prime. The physiological cause of this transient alteration in electrical brain activity appears to be associated with the transient drop in arterial pressure. The etiology is unknown but may be attributable to the bolus of the crystalloid prime or micro emboli, either air or fibrin-platelet. Thirteen swine (17-26 kg) were anesthetized and received 4 mg/kg dexamethasone, and following a tracheotomy were ventilated with halothane in 100% O2. Surgical preparation included: sternotomy and preparation for right atrial-aortic CPB. The CPB circuit consisted of a hollow fiber membrane oxygenator, a hard-shell venous reservoir, a roller pump, and PVC tubing. The circuit was randomly primed with either 1200 ml Plasmalyte-A or 10 ml/kg perfluorocarbon emulsion (PFE) and Plasmalyte-A to total 1200 ml. The animals were monitored continuously for systemic hemodynamics and electrocardiogram, and cerebral monitoring included blood flow and bitemporal EEG. Arterial blood gases were measured and PaCO2 was kept between 30-45 mmHg both before and during CPB. Cerebral blood flow (CBF) was measured pre-CPB and at 10 minutes after initiation of CPB. Bitemporal computerized EEG was analyzed every 60 seconds. Total power of each hemisphere, power in frequency bands, and spectral edge were recorded. All animals demonstrated a relative decrease in EEG total power at the onset of CPB. Animals that received PFE demonstrated a more stable arterial blood pressure, an increased CBF, and a lesser decrease and an earlier recovery of the EEG power.</description><identifier>ISSN: 0022-1058</identifier><identifier>EISSN: 2969-8960</identifier><identifier>DOI: 10.1051/ject/19952716</identifier><identifier>PMID: 10150757</identifier><identifier>CODEN: JEXCBD</identifier><language>eng</language><publisher>Reston, VA: American Society of Extra-Corporeal Technology</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Blood Pressure - drug effects ; Cardiopulmonary Bypass ; Cerebrovascular Circulation - drug effects ; Electroencephalography - drug effects ; Electrolytes - administration & dosage ; Electrolytes - therapeutic use ; Emergency and intensive postoperative care (general aspects). Pathophysiology of surgery ; Emulsions ; Fluorocarbons - administration & dosage ; Fluorocarbons - pharmacology ; Health technology assessment ; Intensive care medicine ; Medical sciences ; Microspheres ; Neuroprotective Agents - administration & dosage ; Neuroprotective Agents - pharmacology ; Oxygenators, Membrane ; Plasma Substitutes - administration & dosage ; Plasma Substitutes - therapeutic use ; Solutions ; Swine</subject><ispartof>The Journal of extra-corporeal technology, 1995-03, Vol.27 (1), p.6-10</ispartof><rights>1995 INIST-CNRS</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2726-b6bc044bb89422c8e19e87c5129b63a51e5c53bc46fd506c0fdfdbf74b6b6d2b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,778,782,787,788,23913,23914,25123,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3473880$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10150757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VOCELKA, C</creatorcontrib><creatorcontrib>SPIESS, B</creatorcontrib><creatorcontrib>SOLTOW, L</creatorcontrib><creatorcontrib>THOMAS, R</creatorcontrib><creatorcontrib>GOHRA, H</creatorcontrib><creatorcontrib>AKIMOTO, H</creatorcontrib><creatorcontrib>ROTHNIE, C</creatorcontrib><creatorcontrib>KUNZELMAN, K</creatorcontrib><creatorcontrib>VERRIER, E</creatorcontrib><creatorcontrib>COCHRAN, R. P</creatorcontrib><title>A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass</title><title>The Journal of extra-corporeal technology</title><addtitle>J Extra Corpor Technol</addtitle><description>Depression in electroencephalogram (EEG) has been documented clinically and is reproducible in swine at the initiation of cardiopulmonary bypass (CPB) utilizing a crystalloid prime. The physiological cause of this transient alteration in electrical brain activity appears to be associated with the transient drop in arterial pressure. The etiology is unknown but may be attributable to the bolus of the crystalloid prime or micro emboli, either air or fibrin-platelet. Thirteen swine (17-26 kg) were anesthetized and received 4 mg/kg dexamethasone, and following a tracheotomy were ventilated with halothane in 100% O2. Surgical preparation included: sternotomy and preparation for right atrial-aortic CPB. The CPB circuit consisted of a hollow fiber membrane oxygenator, a hard-shell venous reservoir, a roller pump, and PVC tubing. The circuit was randomly primed with either 1200 ml Plasmalyte-A or 10 ml/kg perfluorocarbon emulsion (PFE) and Plasmalyte-A to total 1200 ml. The animals were monitored continuously for systemic hemodynamics and electrocardiogram, and cerebral monitoring included blood flow and bitemporal EEG. Arterial blood gases were measured and PaCO2 was kept between 30-45 mmHg both before and during CPB. Cerebral blood flow (CBF) was measured pre-CPB and at 10 minutes after initiation of CPB. Bitemporal computerized EEG was analyzed every 60 seconds. Total power of each hemisphere, power in frequency bands, and spectral edge were recorded. All animals demonstrated a relative decrease in EEG total power at the onset of CPB. Animals that received PFE demonstrated a more stable arterial blood pressure, an increased CBF, and a lesser decrease and an earlier recovery of the EEG power.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiopulmonary Bypass</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Electroencephalography - drug effects</subject><subject>Electrolytes - administration & dosage</subject><subject>Electrolytes - therapeutic use</subject><subject>Emergency and intensive postoperative care (general aspects). Pathophysiology of surgery</subject><subject>Emulsions</subject><subject>Fluorocarbons - administration & dosage</subject><subject>Fluorocarbons - pharmacology</subject><subject>Health technology assessment</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Microspheres</subject><subject>Neuroprotective Agents - administration & dosage</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Oxygenators, Membrane</subject><subject>Plasma Substitutes - administration & dosage</subject><subject>Plasma Substitutes - therapeutic use</subject><subject>Solutions</subject><subject>Swine</subject><issn>0022-1058</issn><issn>2969-8960</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkTtv2zAUhYkiQe2kHbMGHIJuakhKJKXRCNI2gIEuySzwcdkwoESFlFz4V_Qvh66dotO9w3fOfRyErij5Sgmnty9g5lvadZxJKj6gNetEV7WdIGdoTQhjVaHaFbrI-YUQQUlNP6IVJZQTyeUa_dngCZILS0zRqKTjiGFYQvalmZIfACtr_ex3gP0wpbiDjOdnwBDK3BRhNDA9qxB_JTVgNVpsIIFOKmAdYrTYhfgbq_mvxo_FSM0H6-hwmWZ9nJYwxFGlPdb7SeX8CZ07FTJ8PtVL9PTt_vHuR7X9-f3hbrOtDJNMVFpoQ5pG67ZrGDMt0A5aaThlnRa14hS44bU2jXCWE2GIs85qJ5siFJbp-hJ9OfqWm14XyHM_-GwgBDVCXHIvZSNEzUgBqyNoUsw5gesPbykL95T0hwT6QwL9ewKFvz4ZL3oA-x99fHkBbk6AykYFl9RofP7H1Y2s25bUb3OrkyU</recordid><startdate>19950301</startdate><enddate>19950301</enddate><creator>VOCELKA, C</creator><creator>SPIESS, B</creator><creator>SOLTOW, L</creator><creator>THOMAS, R</creator><creator>GOHRA, H</creator><creator>AKIMOTO, H</creator><creator>ROTHNIE, C</creator><creator>KUNZELMAN, K</creator><creator>VERRIER, E</creator><creator>COCHRAN, R. P</creator><general>American Society of Extra-Corporeal Technology</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>19950301</creationdate><title>A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass</title><author>VOCELKA, C ; SPIESS, B ; SOLTOW, L ; THOMAS, R ; GOHRA, H ; AKIMOTO, H ; ROTHNIE, C ; KUNZELMAN, K ; VERRIER, E ; COCHRAN, R. P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2726-b6bc044bb89422c8e19e87c5129b63a51e5c53bc46fd506c0fdfdbf74b6b6d2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiopulmonary Bypass</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Electroencephalography - drug effects</topic><topic>Electrolytes - administration & dosage</topic><topic>Electrolytes - therapeutic use</topic><topic>Emergency and intensive postoperative care (general aspects). Pathophysiology of surgery</topic><topic>Emulsions</topic><topic>Fluorocarbons - administration & dosage</topic><topic>Fluorocarbons - pharmacology</topic><topic>Health technology assessment</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Microspheres</topic><topic>Neuroprotective Agents - administration & dosage</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Oxygenators, Membrane</topic><topic>Plasma Substitutes - administration & dosage</topic><topic>Plasma Substitutes - therapeutic use</topic><topic>Solutions</topic><topic>Swine</topic><toplevel>online_resources</toplevel><creatorcontrib>VOCELKA, C</creatorcontrib><creatorcontrib>SPIESS, B</creatorcontrib><creatorcontrib>SOLTOW, L</creatorcontrib><creatorcontrib>THOMAS, R</creatorcontrib><creatorcontrib>GOHRA, H</creatorcontrib><creatorcontrib>AKIMOTO, H</creatorcontrib><creatorcontrib>ROTHNIE, C</creatorcontrib><creatorcontrib>KUNZELMAN, K</creatorcontrib><creatorcontrib>VERRIER, E</creatorcontrib><creatorcontrib>COCHRAN, R. P</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>The Journal of extra-corporeal technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VOCELKA, C</au><au>SPIESS, B</au><au>SOLTOW, L</au><au>THOMAS, R</au><au>GOHRA, H</au><au>AKIMOTO, H</au><au>ROTHNIE, C</au><au>KUNZELMAN, K</au><au>VERRIER, E</au><au>COCHRAN, R. P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass</atitle><jtitle>The Journal of extra-corporeal technology</jtitle><addtitle>J Extra Corpor Technol</addtitle><date>1995-03-01</date><risdate>1995</risdate><volume>27</volume><issue>1</issue><spage>6</spage><epage>10</epage><pages>6-10</pages><issn>0022-1058</issn><eissn>2969-8960</eissn><coden>JEXCBD</coden><abstract>Depression in electroencephalogram (EEG) has been documented clinically and is reproducible in swine at the initiation of cardiopulmonary bypass (CPB) utilizing a crystalloid prime. The physiological cause of this transient alteration in electrical brain activity appears to be associated with the transient drop in arterial pressure. The etiology is unknown but may be attributable to the bolus of the crystalloid prime or micro emboli, either air or fibrin-platelet. Thirteen swine (17-26 kg) were anesthetized and received 4 mg/kg dexamethasone, and following a tracheotomy were ventilated with halothane in 100% O2. Surgical preparation included: sternotomy and preparation for right atrial-aortic CPB. The CPB circuit consisted of a hollow fiber membrane oxygenator, a hard-shell venous reservoir, a roller pump, and PVC tubing. The circuit was randomly primed with either 1200 ml Plasmalyte-A or 10 ml/kg perfluorocarbon emulsion (PFE) and Plasmalyte-A to total 1200 ml. The animals were monitored continuously for systemic hemodynamics and electrocardiogram, and cerebral monitoring included blood flow and bitemporal EEG. Arterial blood gases were measured and PaCO2 was kept between 30-45 mmHg both before and during CPB. Cerebral blood flow (CBF) was measured pre-CPB and at 10 minutes after initiation of CPB. Bitemporal computerized EEG was analyzed every 60 seconds. Total power of each hemisphere, power in frequency bands, and spectral edge were recorded. All animals demonstrated a relative decrease in EEG total power at the onset of CPB. Animals that received PFE demonstrated a more stable arterial blood pressure, an increased CBF, and a lesser decrease and an earlier recovery of the EEG power.</abstract><cop>Reston, VA</cop><pub>American Society of Extra-Corporeal Technology</pub><pmid>10150757</pmid><doi>10.1051/ject/19952716</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1058 |
ispartof | The Journal of extra-corporeal technology, 1995-03, Vol.27 (1), p.6-10 |
issn | 0022-1058 2969-8960 |
language | eng |
recordid | cdi_proquest_miscellaneous_77466320 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Blood Pressure - drug effects Cardiopulmonary Bypass Cerebrovascular Circulation - drug effects Electroencephalography - drug effects Electrolytes - administration & dosage Electrolytes - therapeutic use Emergency and intensive postoperative care (general aspects). Pathophysiology of surgery Emulsions Fluorocarbons - administration & dosage Fluorocarbons - pharmacology Health technology assessment Intensive care medicine Medical sciences Microspheres Neuroprotective Agents - administration & dosage Neuroprotective Agents - pharmacology Oxygenators, Membrane Plasma Substitutes - administration & dosage Plasma Substitutes - therapeutic use Solutions Swine |
title | A perfluorocarbon emulsion prime additive improves the electroencephalogram and cerebral blood flow at the initiation of cardiopulmonary bypass |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T11%3A10%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20perfluorocarbon%20emulsion%20prime%20additive%20improves%20the%20electroencephalogram%20and%20cerebral%20blood%20flow%20at%20the%20initiation%20of%20cardiopulmonary%20bypass&rft.jtitle=The%20Journal%20of%20extra-corporeal%20technology&rft.au=VOCELKA,%20C&rft.date=1995-03-01&rft.volume=27&rft.issue=1&rft.spage=6&rft.epage=10&rft.pages=6-10&rft.issn=0022-1058&rft.eissn=2969-8960&rft.coden=JEXCBD&rft_id=info:doi/10.1051/ject/19952716&rft_dat=%3Cproquest_cross%3E77466320%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77466320&rft_id=info:pmid/10150757&rfr_iscdi=true |