Mild Hypothermia Increases Survival from Severe Pressure-Controlled Hemorrhagic Shock in Rats

BACKGROUNDIn previous studies, mild hypothermia (34°C) during uncontrolled hemorrhagic shock (HS) increased survival. Hypothermia also increased mean arterial pressure (MAP), which may have contributed to its beneficial effect. We hypothesized that hypothermia would improve survival in a pressure-co...

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Veröffentlicht in:The Journal of Trauma: Injury, Infection, and Critical Care Infection, and Critical Care, 2001-02, Vol.50 (2), p.253-262
Hauptverfasser: Prueckner, Stephan, Safar, Peter, Kentner, Rainer, Stezoski, Jason, Tisherman, and Samuel A.
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container_issue 2
container_start_page 253
container_title The Journal of Trauma: Injury, Infection, and Critical Care
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creator Prueckner, Stephan
Safar, Peter
Kentner, Rainer
Stezoski, Jason
Tisherman, and Samuel A.
description BACKGROUNDIn previous studies, mild hypothermia (34°C) during uncontrolled hemorrhagic shock (HS) increased survival. Hypothermia also increased mean arterial pressure (MAP), which may have contributed to its beneficial effect. We hypothesized that hypothermia would improve survival in a pressure-controlled HS model and that prolonged hypothermia would further improve survival. METHODSThirty rats were prepared under light nitrous oxide/halothane anesthesia with spontaneous breathing. The rats underwent HS with an initial blood withdrawal of 2 mL/100 g over 10 minutes and pressure-controlled HS at a MAP of 40 mm Hg over 90 minutes (without anticoagulation), followed by return of shed blood and additional lactated Ringer’s solution to achieve normotension. Hemodynamic monitoring and anesthesia were continued to 1 hour, temperature control to 12 hours, and observation without anesthesia to 72 hours. After HS of 15 minutes, 10 rats each were randomized to group 1, with normothermia (38°C) throughout; group 2, with brief mild hypothermia (34°C during HS 15–90 minutes plus 30 minutes after reperfusion); and group 3, with prolonged mild hypothermia (same as group 2, then 35°C [possible without shivering] from 30 minutes after reperfusion to 12 hours). RESULTSMAP during HS and initial resuscitation was the same in all three groups, but was higher in the hypothermia groups 2 and 3, compared with the normothermia group 1, at 45 and 60 minutes after reperfusion. Group 1 required less blood withdrawal to maintain MAP 40 mm Hg during HS and more lactated Ringer’s solution for resuscitation. At end of HS, lactate levels were higher in group 1 than in groups 2 and 3 (p < 0.02). Temperatures were according to protocol. Survival to 72 hours was achieved in group 1 by 3 of 10 rats, in group 2 by 7 of 10 rats (p = 0.18 vs. group 1), and in group 3 by 9 of 10 rats (p = 0.02 vs. group 1, p = 0.58 vs. group 2). Survival time was longer in group 2 (p = 0.09) and group 3 (p = 0.007) compared with group 1. CONCLUSIONBrief hypothermia had physiologic benefit and a trend toward improved survival. Prolonged mild hypothermia significantly increased survival after severe HS even with controlled MAP. Extending the duration of hypothermia beyond the acute phases of shock and resuscitation may be needed to ensure improved outcome after prolonged HS.
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Hypothermia also increased mean arterial pressure (MAP), which may have contributed to its beneficial effect. We hypothesized that hypothermia would improve survival in a pressure-controlled HS model and that prolonged hypothermia would further improve survival. METHODSThirty rats were prepared under light nitrous oxide/halothane anesthesia with spontaneous breathing. The rats underwent HS with an initial blood withdrawal of 2 mL/100 g over 10 minutes and pressure-controlled HS at a MAP of 40 mm Hg over 90 minutes (without anticoagulation), followed by return of shed blood and additional lactated Ringer’s solution to achieve normotension. Hemodynamic monitoring and anesthesia were continued to 1 hour, temperature control to 12 hours, and observation without anesthesia to 72 hours. After HS of 15 minutes, 10 rats each were randomized to group 1, with normothermia (38°C) throughout; group 2, with brief mild hypothermia (34°C during HS 15–90 minutes plus 30 minutes after reperfusion); and group 3, with prolonged mild hypothermia (same as group 2, then 35°C [possible without shivering] from 30 minutes after reperfusion to 12 hours). RESULTSMAP during HS and initial resuscitation was the same in all three groups, but was higher in the hypothermia groups 2 and 3, compared with the normothermia group 1, at 45 and 60 minutes after reperfusion. Group 1 required less blood withdrawal to maintain MAP 40 mm Hg during HS and more lactated Ringer’s solution for resuscitation. At end of HS, lactate levels were higher in group 1 than in groups 2 and 3 (p &lt; 0.02). Temperatures were according to protocol. Survival to 72 hours was achieved in group 1 by 3 of 10 rats, in group 2 by 7 of 10 rats (p = 0.18 vs. group 1), and in group 3 by 9 of 10 rats (p = 0.02 vs. group 1, p = 0.58 vs. group 2). Survival time was longer in group 2 (p = 0.09) and group 3 (p = 0.007) compared with group 1. CONCLUSIONBrief hypothermia had physiologic benefit and a trend toward improved survival. Prolonged mild hypothermia significantly increased survival after severe HS even with controlled MAP. Extending the duration of hypothermia beyond the acute phases of shock and resuscitation may be needed to ensure improved outcome after prolonged HS.</description><identifier>ISSN: 0022-5282</identifier><identifier>EISSN: 1529-8809</identifier><identifier>DOI: 10.1097/00005373-200102000-00010</identifier><identifier>PMID: 11242289</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Blood Pressure ; Disease Models, Animal ; Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care ; Humans ; Hypothermia, Induced ; Intensive care medicine ; Male ; Medical sciences ; Multiple Organ Failure - prevention &amp; control ; Rats ; Rats, Sprague-Dawley ; Resuscitation ; Shock, Hemorrhagic - mortality ; Shock, Hemorrhagic - physiopathology ; Time Factors</subject><ispartof>The Journal of Trauma: Injury, Infection, and Critical Care, 2001-02, Vol.50 (2), p.253-262</ispartof><rights>2001 Lippincott Williams &amp; Wilkins, Inc.</rights><rights>2001 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3840-ce3b978f4b6778b02d39560de2254f46d43ab92ae74d85e7600db6857a11f93e3</citedby><cites>FETCH-LOGICAL-c3840-ce3b978f4b6778b02d39560de2254f46d43ab92ae74d85e7600db6857a11f93e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,776,780,785,786,23909,23910,25118,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=929399$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11242289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Prueckner, Stephan</creatorcontrib><creatorcontrib>Safar, Peter</creatorcontrib><creatorcontrib>Kentner, Rainer</creatorcontrib><creatorcontrib>Stezoski, Jason</creatorcontrib><creatorcontrib>Tisherman, and Samuel A.</creatorcontrib><title>Mild Hypothermia Increases Survival from Severe Pressure-Controlled Hemorrhagic Shock in Rats</title><title>The Journal of Trauma: Injury, Infection, and Critical Care</title><addtitle>J Trauma</addtitle><description>BACKGROUNDIn previous studies, mild hypothermia (34°C) during uncontrolled hemorrhagic shock (HS) increased survival. Hypothermia also increased mean arterial pressure (MAP), which may have contributed to its beneficial effect. We hypothesized that hypothermia would improve survival in a pressure-controlled HS model and that prolonged hypothermia would further improve survival. METHODSThirty rats were prepared under light nitrous oxide/halothane anesthesia with spontaneous breathing. The rats underwent HS with an initial blood withdrawal of 2 mL/100 g over 10 minutes and pressure-controlled HS at a MAP of 40 mm Hg over 90 minutes (without anticoagulation), followed by return of shed blood and additional lactated Ringer’s solution to achieve normotension. Hemodynamic monitoring and anesthesia were continued to 1 hour, temperature control to 12 hours, and observation without anesthesia to 72 hours. After HS of 15 minutes, 10 rats each were randomized to group 1, with normothermia (38°C) throughout; group 2, with brief mild hypothermia (34°C during HS 15–90 minutes plus 30 minutes after reperfusion); and group 3, with prolonged mild hypothermia (same as group 2, then 35°C [possible without shivering] from 30 minutes after reperfusion to 12 hours). RESULTSMAP during HS and initial resuscitation was the same in all three groups, but was higher in the hypothermia groups 2 and 3, compared with the normothermia group 1, at 45 and 60 minutes after reperfusion. Group 1 required less blood withdrawal to maintain MAP 40 mm Hg during HS and more lactated Ringer’s solution for resuscitation. At end of HS, lactate levels were higher in group 1 than in groups 2 and 3 (p &lt; 0.02). Temperatures were according to protocol. Survival to 72 hours was achieved in group 1 by 3 of 10 rats, in group 2 by 7 of 10 rats (p = 0.18 vs. group 1), and in group 3 by 9 of 10 rats (p = 0.02 vs. group 1, p = 0.58 vs. group 2). Survival time was longer in group 2 (p = 0.09) and group 3 (p = 0.007) compared with group 1. CONCLUSIONBrief hypothermia had physiologic benefit and a trend toward improved survival. Prolonged mild hypothermia significantly increased survival after severe HS even with controlled MAP. Extending the duration of hypothermia beyond the acute phases of shock and resuscitation may be needed to ensure improved outcome after prolonged HS.</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</subject><subject>Disease Models, Animal</subject><subject>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</subject><subject>Humans</subject><subject>Hypothermia, Induced</subject><subject>Intensive care medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multiple Organ Failure - prevention &amp; control</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Resuscitation</subject><subject>Shock, Hemorrhagic - mortality</subject><subject>Shock, Hemorrhagic - physiopathology</subject><subject>Time Factors</subject><issn>0022-5282</issn><issn>1529-8809</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFu1DAQhi0EoqvSV0CWkLgFxnYc20e0AlqpCMTCEVmOMyFWnXixk6369mTZpZzwYTyH75-RviGEMnjDwKi3sD4plKg4AIO1QAXH7gnZMMlNpTWYp2QDwHklueYX5KqU0K4Ml8pw_ZxcMMZrzrXZkB-fQuzo9cM-zQPmMTh6M_mMrmChuyUfwsFF2uc00h0eMCP9krGUJWO1TdOcU4y4xnFMOQ_uZ_B0NyR_R8NEv7q5vCDPehcLXp3_S_L9w_tv2-vq9vPHm-2728oLXUPlUbRG6b5uG6V0C7wTRjbQIeey7uumq4VrDXeo6k5LVA1A1zZaKsdYbwSKS_L6NHef068Fy2zHUDzG6CZMS7GqMZKDESuoT6DPqZSMvd3nMLr8YBnYo1371659tGv_2F2jL887lnbE7l_w7HIFXp0BV7yLfXaTD-WRM9wIc6TqE3Wf4oy53MXlHrMd0MV5sP-7rfgNoB6Qrg</recordid><startdate>200102</startdate><enddate>200102</enddate><creator>Prueckner, Stephan</creator><creator>Safar, Peter</creator><creator>Kentner, Rainer</creator><creator>Stezoski, Jason</creator><creator>Tisherman, and Samuel A.</creator><general>Lippincott Williams &amp; Wilkins, 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>200102</creationdate><title>Mild Hypothermia Increases Survival from Severe Pressure-Controlled Hemorrhagic Shock in Rats</title><author>Prueckner, Stephan ; Safar, Peter ; Kentner, Rainer ; Stezoski, Jason ; Tisherman, and Samuel A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3840-ce3b978f4b6778b02d39560de2254f46d43ab92ae74d85e7600db6857a11f93e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</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</topic><topic>Disease Models, Animal</topic><topic>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</topic><topic>Humans</topic><topic>Hypothermia, Induced</topic><topic>Intensive care medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multiple Organ Failure - prevention &amp; control</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Resuscitation</topic><topic>Shock, Hemorrhagic - mortality</topic><topic>Shock, Hemorrhagic - physiopathology</topic><topic>Time Factors</topic><toplevel>online_resources</toplevel><creatorcontrib>Prueckner, Stephan</creatorcontrib><creatorcontrib>Safar, Peter</creatorcontrib><creatorcontrib>Kentner, Rainer</creatorcontrib><creatorcontrib>Stezoski, Jason</creatorcontrib><creatorcontrib>Tisherman, and Samuel A.</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 Trauma: Injury, Infection, and Critical Care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prueckner, Stephan</au><au>Safar, Peter</au><au>Kentner, Rainer</au><au>Stezoski, Jason</au><au>Tisherman, and Samuel A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mild Hypothermia Increases Survival from Severe Pressure-Controlled Hemorrhagic Shock in Rats</atitle><jtitle>The Journal of Trauma: Injury, Infection, and Critical Care</jtitle><addtitle>J Trauma</addtitle><date>2001-02</date><risdate>2001</risdate><volume>50</volume><issue>2</issue><spage>253</spage><epage>262</epage><pages>253-262</pages><issn>0022-5282</issn><eissn>1529-8809</eissn><abstract>BACKGROUNDIn previous studies, mild hypothermia (34°C) during uncontrolled hemorrhagic shock (HS) increased survival. Hypothermia also increased mean arterial pressure (MAP), which may have contributed to its beneficial effect. We hypothesized that hypothermia would improve survival in a pressure-controlled HS model and that prolonged hypothermia would further improve survival. METHODSThirty rats were prepared under light nitrous oxide/halothane anesthesia with spontaneous breathing. The rats underwent HS with an initial blood withdrawal of 2 mL/100 g over 10 minutes and pressure-controlled HS at a MAP of 40 mm Hg over 90 minutes (without anticoagulation), followed by return of shed blood and additional lactated Ringer’s solution to achieve normotension. Hemodynamic monitoring and anesthesia were continued to 1 hour, temperature control to 12 hours, and observation without anesthesia to 72 hours. After HS of 15 minutes, 10 rats each were randomized to group 1, with normothermia (38°C) throughout; group 2, with brief mild hypothermia (34°C during HS 15–90 minutes plus 30 minutes after reperfusion); and group 3, with prolonged mild hypothermia (same as group 2, then 35°C [possible without shivering] from 30 minutes after reperfusion to 12 hours). RESULTSMAP during HS and initial resuscitation was the same in all three groups, but was higher in the hypothermia groups 2 and 3, compared with the normothermia group 1, at 45 and 60 minutes after reperfusion. Group 1 required less blood withdrawal to maintain MAP 40 mm Hg during HS and more lactated Ringer’s solution for resuscitation. At end of HS, lactate levels were higher in group 1 than in groups 2 and 3 (p &lt; 0.02). Temperatures were according to protocol. Survival to 72 hours was achieved in group 1 by 3 of 10 rats, in group 2 by 7 of 10 rats (p = 0.18 vs. group 1), and in group 3 by 9 of 10 rats (p = 0.02 vs. group 1, p = 0.58 vs. group 2). Survival time was longer in group 2 (p = 0.09) and group 3 (p = 0.007) compared with group 1. CONCLUSIONBrief hypothermia had physiologic benefit and a trend toward improved survival. Prolonged mild hypothermia significantly increased survival after severe HS even with controlled MAP. Extending the duration of hypothermia beyond the acute phases of shock and resuscitation may be needed to ensure improved outcome after prolonged HS.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>11242289</pmid><doi>10.1097/00005373-200102000-00010</doi><tpages>10</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Biological and medical sciences
Blood Pressure
Disease Models, Animal
Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care
Humans
Hypothermia, Induced
Intensive care medicine
Male
Medical sciences
Multiple Organ Failure - prevention & control
Rats
Rats, Sprague-Dawley
Resuscitation
Shock, Hemorrhagic - mortality
Shock, Hemorrhagic - physiopathology
Time Factors
title Mild Hypothermia Increases Survival from Severe Pressure-Controlled Hemorrhagic Shock in Rats
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