Rapid hypothermic aortic flush can achieve survival without brain damage after 30 minutes cardiac arrest in dogs
Neither exsanguination to pulselessness nor cardiac arrest of 30 min duration can be reversed with complete neurologic recovery using conventional resuscitation methods. Techniques that might buy time for transport, surgical hemostasis, and initiation of cardiopulmonary bypass or other resuscitation...
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creator | BEHRINGER, Wilhelm PRUECKNER, Stephan KENTNER, Rainer TISHERMAN, Samuel A RADOVSKY, Ann CLARK, Robert STEZOSKI, S. William HENCHIR, Jeremy KLEIN, Edwin SAFAR, Peter |
description | Neither exsanguination to pulselessness nor cardiac arrest of 30 min duration can be reversed with complete neurologic recovery using conventional resuscitation methods. Techniques that might buy time for transport, surgical hemostasis, and initiation of cardiopulmonary bypass or other resuscitation methods would be valuable. We hypothesized that an aortic flush with high-volume cold normal saline solution at the start of exsanguination cardiac arrest could rapidly preserve cerebral viability during 30 min of complete global ischemia and achieve good outcome.
Sixteen dogs weighing 20-25 kg were exsanguinated to pulselessness over 5 min, and circulatory arrest was maintained for another 30 min. They were then resuscitated using closed-chest cardiopulmonary bypass and had assisted circulation for 2 h, mild hypothermia (34 degrees C) for 12 h, controlled ventilation for 20 h, and intensive care to outcome evaluation at 72 h. Two minutes after the onset of circulatory arrest, the dogs received a flush of normal saline solution at 4 degrees C into the aorta (cephalad) via a balloon catheter. Group I (n = 6) received a flush of 25 ml/kg saline with the balloon in the thoracic aorta; group II (n = 7) received a flush of 100 ml/kg saline with the balloon in the abdominal aorta.
The aortic flush decreased mean tympanic membrane temperature (Tty) in group I from 37.6 +/- 0.1 to 33.3 +/- 1.6 degrees C and in group II from 37.5 +/- 0.1 to 28.3 +/- 2.4 degrees C (P = 0.001). In group 1, four dogs achieved overall performance category (OPC) 4 (coma), and 2 dogs achieved OPC 5 (brain death). In group II, 4 dogs achieved OPC 1 (normal), and 3 dogs achieved OPC 2 (moderate disability). Median (interquartile range [IQR]) neurologic deficit scores (NDS 0-10% = normal; NDS 100% = brain death) were 69% (56-99%) in group I versus 4% (0-15%) in group II (P = 0.003). Median total brain histologic damage scores (HDS 0 = no damage; > 100 = extensive damage; 1,064 = maximal damage) were 144 (74-168) in group I versus 18 (3-36) in group II (P = 0.004); in three dogs from group II, the brain was histologically normal (HDS 0-5).
A single high-volume flush of cold saline (4 degrees C) into the abdominal aorta given 2 min after the onset of cardiac arrest rapidly induces moderate-to-deep cerebral hypothermia and can result in survival without functional or histologic brain damage, even after 30 min of no blood flow. |
doi_str_mv | 10.1097/00000542-200012000-00022 |
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Sixteen dogs weighing 20-25 kg were exsanguinated to pulselessness over 5 min, and circulatory arrest was maintained for another 30 min. They were then resuscitated using closed-chest cardiopulmonary bypass and had assisted circulation for 2 h, mild hypothermia (34 degrees C) for 12 h, controlled ventilation for 20 h, and intensive care to outcome evaluation at 72 h. Two minutes after the onset of circulatory arrest, the dogs received a flush of normal saline solution at 4 degrees C into the aorta (cephalad) via a balloon catheter. Group I (n = 6) received a flush of 25 ml/kg saline with the balloon in the thoracic aorta; group II (n = 7) received a flush of 100 ml/kg saline with the balloon in the abdominal aorta.
The aortic flush decreased mean tympanic membrane temperature (Tty) in group I from 37.6 +/- 0.1 to 33.3 +/- 1.6 degrees C and in group II from 37.5 +/- 0.1 to 28.3 +/- 2.4 degrees C (P = 0.001). In group 1, four dogs achieved overall performance category (OPC) 4 (coma), and 2 dogs achieved OPC 5 (brain death). In group II, 4 dogs achieved OPC 1 (normal), and 3 dogs achieved OPC 2 (moderate disability). Median (interquartile range [IQR]) neurologic deficit scores (NDS 0-10% = normal; NDS 100% = brain death) were 69% (56-99%) in group I versus 4% (0-15%) in group II (P = 0.003). Median total brain histologic damage scores (HDS 0 = no damage; > 100 = extensive damage; 1,064 = maximal damage) were 144 (74-168) in group I versus 18 (3-36) in group II (P = 0.004); in three dogs from group II, the brain was histologically normal (HDS 0-5).
A single high-volume flush of cold saline (4 degrees C) into the abdominal aorta given 2 min after the onset of cardiac arrest rapidly induces moderate-to-deep cerebral hypothermia and can result in survival without functional or histologic brain damage, even after 30 min of no blood flow.</description><identifier>ISSN: 0003-3022</identifier><identifier>EISSN: 1528-1175</identifier><identifier>DOI: 10.1097/00000542-200012000-00022</identifier><identifier>PMID: 11149445</identifier><identifier>CODEN: ANESAV</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Aorta, Abdominal ; Biological and medical sciences ; Body Temperature ; Brain Death ; Brain Ischemia - prevention & control ; Dogs ; Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care ; Heart Arrest, Induced - methods ; Heart Arrest, Induced - mortality ; Hypothermia, Induced - methods ; Hypothermia, Induced - mortality ; Infusions, Intra-Arterial - methods ; Intensive care medicine ; Male ; Medical sciences ; Neurologic Examination ; Sodium Chloride - administration & dosage ; Time Factors ; Treatment Outcome</subject><ispartof>Anesthesiology (Philadelphia), 2000-12, Vol.93 (6), p.1491-1499</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-1c50db5295023fc1e4b18f8c0af32dc44128a4120208d7fe70f8d78e35b2a783</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=827628$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11149445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BEHRINGER, Wilhelm</creatorcontrib><creatorcontrib>PRUECKNER, Stephan</creatorcontrib><creatorcontrib>KENTNER, Rainer</creatorcontrib><creatorcontrib>TISHERMAN, Samuel A</creatorcontrib><creatorcontrib>RADOVSKY, Ann</creatorcontrib><creatorcontrib>CLARK, Robert</creatorcontrib><creatorcontrib>STEZOSKI, S. William</creatorcontrib><creatorcontrib>HENCHIR, Jeremy</creatorcontrib><creatorcontrib>KLEIN, Edwin</creatorcontrib><creatorcontrib>SAFAR, Peter</creatorcontrib><title>Rapid hypothermic aortic flush can achieve survival without brain damage after 30 minutes cardiac arrest in dogs</title><title>Anesthesiology (Philadelphia)</title><addtitle>Anesthesiology</addtitle><description>Neither exsanguination to pulselessness nor cardiac arrest of 30 min duration can be reversed with complete neurologic recovery using conventional resuscitation methods. Techniques that might buy time for transport, surgical hemostasis, and initiation of cardiopulmonary bypass or other resuscitation methods would be valuable. We hypothesized that an aortic flush with high-volume cold normal saline solution at the start of exsanguination cardiac arrest could rapidly preserve cerebral viability during 30 min of complete global ischemia and achieve good outcome.
Sixteen dogs weighing 20-25 kg were exsanguinated to pulselessness over 5 min, and circulatory arrest was maintained for another 30 min. They were then resuscitated using closed-chest cardiopulmonary bypass and had assisted circulation for 2 h, mild hypothermia (34 degrees C) for 12 h, controlled ventilation for 20 h, and intensive care to outcome evaluation at 72 h. Two minutes after the onset of circulatory arrest, the dogs received a flush of normal saline solution at 4 degrees C into the aorta (cephalad) via a balloon catheter. Group I (n = 6) received a flush of 25 ml/kg saline with the balloon in the thoracic aorta; group II (n = 7) received a flush of 100 ml/kg saline with the balloon in the abdominal aorta.
The aortic flush decreased mean tympanic membrane temperature (Tty) in group I from 37.6 +/- 0.1 to 33.3 +/- 1.6 degrees C and in group II from 37.5 +/- 0.1 to 28.3 +/- 2.4 degrees C (P = 0.001). In group 1, four dogs achieved overall performance category (OPC) 4 (coma), and 2 dogs achieved OPC 5 (brain death). In group II, 4 dogs achieved OPC 1 (normal), and 3 dogs achieved OPC 2 (moderate disability). Median (interquartile range [IQR]) neurologic deficit scores (NDS 0-10% = normal; NDS 100% = brain death) were 69% (56-99%) in group I versus 4% (0-15%) in group II (P = 0.003). Median total brain histologic damage scores (HDS 0 = no damage; > 100 = extensive damage; 1,064 = maximal damage) were 144 (74-168) in group I versus 18 (3-36) in group II (P = 0.004); in three dogs from group II, the brain was histologically normal (HDS 0-5).
A single high-volume flush of cold saline (4 degrees C) into the abdominal aorta given 2 min after the onset of cardiac arrest rapidly induces moderate-to-deep cerebral hypothermia and can result in survival without functional or histologic brain damage, even after 30 min of no blood flow.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Aorta, Abdominal</subject><subject>Biological and medical sciences</subject><subject>Body Temperature</subject><subject>Brain Death</subject><subject>Brain Ischemia - prevention & control</subject><subject>Dogs</subject><subject>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</subject><subject>Heart Arrest, Induced - methods</subject><subject>Heart Arrest, Induced - mortality</subject><subject>Hypothermia, Induced - methods</subject><subject>Hypothermia, Induced - mortality</subject><subject>Infusions, Intra-Arterial - methods</subject><subject>Intensive care medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurologic Examination</subject><subject>Sodium Chloride - administration & dosage</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0003-3022</issn><issn>1528-1175</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkFtLAzEQhYMotlb_ggQE31Zz2bjpoxRvUBCk72E2m3QjezPZrfTfm7VrDWQOM3xnBg5CmJI7SpbZPRmfSFnCotKxJPEzdoLmVDCZUJqJUzSPM57wOJ-hixA-Y5sJLs_RjFKaLtNUzFH3AZ0rcLnv2r40vnYaQ-v7KLYaQok1NBh06czO4DD4ndtBhb9dX7ZDj3MPrsEF1LA1GGxvPOYE164ZehOi1RcO4j7vTejxSLbbcInOLFTBXE26QJvnp83qNVm_v7ytHteJ5nLZJ1QLUuSCLQVh3Gpq0pxKKzUBy1mh05QyCbEQRmSRWZMRG1UaLnIGmeQLdHtY2_n2a4j3Ve2CNlUFjWmHoDImGGViBOUB1L4NwRurOu9q8HtFiRrDVn9hq2PY6jfsaL2ebgx5bYp_45RuBG4mAIKGynpotAtHTrLsgUn-A3Flhvs</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>BEHRINGER, Wilhelm</creator><creator>PRUECKNER, Stephan</creator><creator>KENTNER, Rainer</creator><creator>TISHERMAN, Samuel A</creator><creator>RADOVSKY, Ann</creator><creator>CLARK, Robert</creator><creator>STEZOSKI, S. William</creator><creator>HENCHIR, Jeremy</creator><creator>KLEIN, Edwin</creator><creator>SAFAR, Peter</creator><general>Lippincott</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>20001201</creationdate><title>Rapid hypothermic aortic flush can achieve survival without brain damage after 30 minutes cardiac arrest in dogs</title><author>BEHRINGER, Wilhelm ; PRUECKNER, Stephan ; KENTNER, Rainer ; TISHERMAN, Samuel A ; RADOVSKY, Ann ; CLARK, Robert ; STEZOSKI, S. William ; HENCHIR, Jeremy ; KLEIN, Edwin ; SAFAR, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-1c50db5295023fc1e4b18f8c0af32dc44128a4120208d7fe70f8d78e35b2a783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Aorta, Abdominal</topic><topic>Biological and medical sciences</topic><topic>Body Temperature</topic><topic>Brain Death</topic><topic>Brain Ischemia - prevention & control</topic><topic>Dogs</topic><topic>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</topic><topic>Heart Arrest, Induced - methods</topic><topic>Heart Arrest, Induced - mortality</topic><topic>Hypothermia, Induced - methods</topic><topic>Hypothermia, Induced - mortality</topic><topic>Infusions, Intra-Arterial - methods</topic><topic>Intensive care medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurologic Examination</topic><topic>Sodium Chloride - administration & dosage</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BEHRINGER, Wilhelm</creatorcontrib><creatorcontrib>PRUECKNER, Stephan</creatorcontrib><creatorcontrib>KENTNER, Rainer</creatorcontrib><creatorcontrib>TISHERMAN, Samuel A</creatorcontrib><creatorcontrib>RADOVSKY, Ann</creatorcontrib><creatorcontrib>CLARK, Robert</creatorcontrib><creatorcontrib>STEZOSKI, S. William</creatorcontrib><creatorcontrib>HENCHIR, Jeremy</creatorcontrib><creatorcontrib>KLEIN, Edwin</creatorcontrib><creatorcontrib>SAFAR, Peter</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>Anesthesiology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BEHRINGER, Wilhelm</au><au>PRUECKNER, Stephan</au><au>KENTNER, Rainer</au><au>TISHERMAN, Samuel A</au><au>RADOVSKY, Ann</au><au>CLARK, Robert</au><au>STEZOSKI, S. William</au><au>HENCHIR, Jeremy</au><au>KLEIN, Edwin</au><au>SAFAR, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid hypothermic aortic flush can achieve survival without brain damage after 30 minutes cardiac arrest in dogs</atitle><jtitle>Anesthesiology (Philadelphia)</jtitle><addtitle>Anesthesiology</addtitle><date>2000-12-01</date><risdate>2000</risdate><volume>93</volume><issue>6</issue><spage>1491</spage><epage>1499</epage><pages>1491-1499</pages><issn>0003-3022</issn><eissn>1528-1175</eissn><coden>ANESAV</coden><abstract>Neither exsanguination to pulselessness nor cardiac arrest of 30 min duration can be reversed with complete neurologic recovery using conventional resuscitation methods. Techniques that might buy time for transport, surgical hemostasis, and initiation of cardiopulmonary bypass or other resuscitation methods would be valuable. We hypothesized that an aortic flush with high-volume cold normal saline solution at the start of exsanguination cardiac arrest could rapidly preserve cerebral viability during 30 min of complete global ischemia and achieve good outcome.
Sixteen dogs weighing 20-25 kg were exsanguinated to pulselessness over 5 min, and circulatory arrest was maintained for another 30 min. They were then resuscitated using closed-chest cardiopulmonary bypass and had assisted circulation for 2 h, mild hypothermia (34 degrees C) for 12 h, controlled ventilation for 20 h, and intensive care to outcome evaluation at 72 h. Two minutes after the onset of circulatory arrest, the dogs received a flush of normal saline solution at 4 degrees C into the aorta (cephalad) via a balloon catheter. Group I (n = 6) received a flush of 25 ml/kg saline with the balloon in the thoracic aorta; group II (n = 7) received a flush of 100 ml/kg saline with the balloon in the abdominal aorta.
The aortic flush decreased mean tympanic membrane temperature (Tty) in group I from 37.6 +/- 0.1 to 33.3 +/- 1.6 degrees C and in group II from 37.5 +/- 0.1 to 28.3 +/- 2.4 degrees C (P = 0.001). In group 1, four dogs achieved overall performance category (OPC) 4 (coma), and 2 dogs achieved OPC 5 (brain death). In group II, 4 dogs achieved OPC 1 (normal), and 3 dogs achieved OPC 2 (moderate disability). Median (interquartile range [IQR]) neurologic deficit scores (NDS 0-10% = normal; NDS 100% = brain death) were 69% (56-99%) in group I versus 4% (0-15%) in group II (P = 0.003). Median total brain histologic damage scores (HDS 0 = no damage; > 100 = extensive damage; 1,064 = maximal damage) were 144 (74-168) in group I versus 18 (3-36) in group II (P = 0.004); in three dogs from group II, the brain was histologically normal (HDS 0-5).
A single high-volume flush of cold saline (4 degrees C) into the abdominal aorta given 2 min after the onset of cardiac arrest rapidly induces moderate-to-deep cerebral hypothermia and can result in survival without functional or histologic brain damage, even after 30 min of no blood flow.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>11149445</pmid><doi>10.1097/00000542-200012000-00022</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Aorta, Abdominal Biological and medical sciences Body Temperature Brain Death Brain Ischemia - prevention & control Dogs Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care Heart Arrest, Induced - methods Heart Arrest, Induced - mortality Hypothermia, Induced - methods Hypothermia, Induced - mortality Infusions, Intra-Arterial - methods Intensive care medicine Male Medical sciences Neurologic Examination Sodium Chloride - administration & dosage Time Factors Treatment Outcome |
title | Rapid hypothermic aortic flush can achieve survival without brain damage after 30 minutes cardiac arrest in dogs |
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