Hemodilution and intravenous perflubron emulsion as an alternative to blood transfusion: effects on tissue oxygenation during profound hemodilution in anesthetized dogs

BACKGROUND: Intravenously administered perfluorocarbon (PFC) emulsions increase oxygen solubility in plasma. PFC might therefore temporarily replace red cells (RBCs) lost during intraoperative hemorrhage. In patients who have undergone hemodilution, the return of autologous blood may be delayed by t...

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Veröffentlicht in:Transfusion (Philadelphia, Pa.) Pa.), 1998-02, Vol.38 (2), p.145-155
Hauptverfasser: Habler, O.P., Kleen, M.S., Hutter, J.W., Podtschaske, A.H., Tiede, M., Kemming, G.I., Welte, M.V., Corso, C.O., Batra, S., Keipert, P.E., Faithfull, N.S., Messmer, K.F.W.
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container_end_page 155
container_issue 2
container_start_page 145
container_title Transfusion (Philadelphia, Pa.)
container_volume 38
creator Habler, O.P.
Kleen, M.S.
Hutter, J.W.
Podtschaske, A.H.
Tiede, M.
Kemming, G.I.
Welte, M.V.
Corso, C.O.
Batra, S.
Keipert, P.E.
Faithfull, N.S.
Messmer, K.F.W.
description BACKGROUND: Intravenously administered perfluorocarbon (PFC) emulsions increase oxygen solubility in plasma. PFC might therefore temporarily replace red cells (RBCs) lost during intraoperative hemorrhage. In patients who have undergone hemodilution, the return of autologous blood may be delayed by the administration of PFC, and autologous RBCs may be saved for transfusion after surgical bleeding is stopped and PFC is cleared by the reticuloendothelial system. STUDY DESIGN AND METHODS: In 22 anesthetized, hemodiluted dogs (hemoglobin [Hb] 7 g/dL) breathing 100‐percent O2, an intraoperative volume‐compensated blood loss was simulated. The efficacy of three therapeutic regimens in maintaining tissue oxygenation was compared: 1) RBC group (n = 7): maintenance of a Hb > 7 g per dL by transfusion of autologous RBCs; 2) PFC group (n = 7): bolus application of a second‐generation PFC emulsion (60% wt/vol perflubron) and further acute normovolemic hemodilution (ANH) to a Hb of 3 g per dL; and 3) control group (n = 7): further ANH alone to a Hb of 3 g per dL. Systemic and myocardial oxygenation status and tissue oxygenation were assessed. RESULTS: Autologous RBCs transfused to maintain a Hb of 7 g per dL preserved hemodynamics and tissue oxygenation during blood loss. In the PFC and control groups, heart rate and cardiac index increased significantly in response to further ANH. Tissue oxygenation was not different in the PFC and the RBC groups. Direct comparison of the PFC and control groups revealed better tissue oxygenation in the PFC group, as reflected by significantly higher mixed venous, coronary venous, and local tissue pO2 on liver and skeletal muscle. CONCLUSION: Bolus intravenous administration of 60‐ percent (wt/vol) perflubron emulsion and further hemodilution from a Hb of 7 g per dL to one of 3 g per dL were as effective as autologous RBC transfusion in maintaining tissue oxygenation during volume‐compensated blood loss designed to mimic surgical bleeding.
doi_str_mv 10.1046/j.1537-2995.1998.38298193096.x
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PFC might therefore temporarily replace red cells (RBCs) lost during intraoperative hemorrhage. In patients who have undergone hemodilution, the return of autologous blood may be delayed by the administration of PFC, and autologous RBCs may be saved for transfusion after surgical bleeding is stopped and PFC is cleared by the reticuloendothelial system. STUDY DESIGN AND METHODS: In 22 anesthetized, hemodiluted dogs (hemoglobin [Hb] 7 g/dL) breathing 100‐percent O2, an intraoperative volume‐compensated blood loss was simulated. The efficacy of three therapeutic regimens in maintaining tissue oxygenation was compared: 1) RBC group (n = 7): maintenance of a Hb &gt; 7 g per dL by transfusion of autologous RBCs; 2) PFC group (n = 7): bolus application of a second‐generation PFC emulsion (60% wt/vol perflubron) and further acute normovolemic hemodilution (ANH) to a Hb of 3 g per dL; and 3) control group (n = 7): further ANH alone to a Hb of 3 g per dL. Systemic and myocardial oxygenation status and tissue oxygenation were assessed. RESULTS: Autologous RBCs transfused to maintain a Hb of 7 g per dL preserved hemodynamics and tissue oxygenation during blood loss. In the PFC and control groups, heart rate and cardiac index increased significantly in response to further ANH. Tissue oxygenation was not different in the PFC and the RBC groups. Direct comparison of the PFC and control groups revealed better tissue oxygenation in the PFC group, as reflected by significantly higher mixed venous, coronary venous, and local tissue pO2 on liver and skeletal muscle. CONCLUSION: Bolus intravenous administration of 60‐ percent (wt/vol) perflubron emulsion and further hemodilution from a Hb of 7 g per dL to one of 3 g per dL were as effective as autologous RBC transfusion in maintaining tissue oxygenation during volume‐compensated blood loss designed to mimic surgical bleeding.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1046/j.1537-2995.1998.38298193096.x</identifier><identifier>PMID: 9531945</identifier><identifier>CODEN: TRANAT</identifier><language>eng</language><publisher>Edinburgh, UK: Blackwell Science Ltd</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Blood Transfusion ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Dogs ; Fluorocarbons - administration &amp; dosage ; Hemodilution ; Hemodynamics ; Injections, Intravenous ; Medical sciences ; Miscellaneous ; Oxygen - metabolism ; Oxygen Consumption ; Respiration ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Transfusions. Complications. Transfusion reactions. 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PFC might therefore temporarily replace red cells (RBCs) lost during intraoperative hemorrhage. In patients who have undergone hemodilution, the return of autologous blood may be delayed by the administration of PFC, and autologous RBCs may be saved for transfusion after surgical bleeding is stopped and PFC is cleared by the reticuloendothelial system. STUDY DESIGN AND METHODS: In 22 anesthetized, hemodiluted dogs (hemoglobin [Hb] 7 g/dL) breathing 100‐percent O2, an intraoperative volume‐compensated blood loss was simulated. The efficacy of three therapeutic regimens in maintaining tissue oxygenation was compared: 1) RBC group (n = 7): maintenance of a Hb &gt; 7 g per dL by transfusion of autologous RBCs; 2) PFC group (n = 7): bolus application of a second‐generation PFC emulsion (60% wt/vol perflubron) and further acute normovolemic hemodilution (ANH) to a Hb of 3 g per dL; and 3) control group (n = 7): further ANH alone to a Hb of 3 g per dL. Systemic and myocardial oxygenation status and tissue oxygenation were assessed. RESULTS: Autologous RBCs transfused to maintain a Hb of 7 g per dL preserved hemodynamics and tissue oxygenation during blood loss. In the PFC and control groups, heart rate and cardiac index increased significantly in response to further ANH. Tissue oxygenation was not different in the PFC and the RBC groups. Direct comparison of the PFC and control groups revealed better tissue oxygenation in the PFC group, as reflected by significantly higher mixed venous, coronary venous, and local tissue pO2 on liver and skeletal muscle. CONCLUSION: Bolus intravenous administration of 60‐ percent (wt/vol) perflubron emulsion and further hemodilution from a Hb of 7 g per dL to one of 3 g per dL were as effective as autologous RBC transfusion in maintaining tissue oxygenation during volume‐compensated blood loss designed to mimic surgical bleeding.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Transfusion</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Dogs</subject><subject>Fluorocarbons - administration &amp; dosage</subject><subject>Hemodilution</subject><subject>Hemodynamics</subject><subject>Injections, Intravenous</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Oxygen - metabolism</subject><subject>Oxygen Consumption</subject><subject>Respiration</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Transfusions. Complications. Transfusion reactions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Transfusion</topic><topic>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</topic><topic>Dogs</topic><topic>Fluorocarbons - administration &amp; dosage</topic><topic>Hemodilution</topic><topic>Hemodynamics</topic><topic>Injections, Intravenous</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Oxygen - metabolism</topic><topic>Oxygen Consumption</topic><topic>Respiration</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Habler, O.P.</creatorcontrib><creatorcontrib>Kleen, M.S.</creatorcontrib><creatorcontrib>Hutter, J.W.</creatorcontrib><creatorcontrib>Podtschaske, A.H.</creatorcontrib><creatorcontrib>Tiede, M.</creatorcontrib><creatorcontrib>Kemming, G.I.</creatorcontrib><creatorcontrib>Welte, M.V.</creatorcontrib><creatorcontrib>Corso, C.O.</creatorcontrib><creatorcontrib>Batra, S.</creatorcontrib><creatorcontrib>Keipert, P.E.</creatorcontrib><creatorcontrib>Faithfull, N.S.</creatorcontrib><creatorcontrib>Messmer, K.F.W.</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>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Habler, O.P.</au><au>Kleen, M.S.</au><au>Hutter, J.W.</au><au>Podtschaske, A.H.</au><au>Tiede, M.</au><au>Kemming, G.I.</au><au>Welte, M.V.</au><au>Corso, C.O.</au><au>Batra, S.</au><au>Keipert, P.E.</au><au>Faithfull, N.S.</au><au>Messmer, K.F.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemodilution and intravenous perflubron emulsion as an alternative to blood transfusion: effects on tissue oxygenation during profound hemodilution in anesthetized dogs</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>1998-02</date><risdate>1998</risdate><volume>38</volume><issue>2</issue><spage>145</spage><epage>155</epage><pages>145-155</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><coden>TRANAT</coden><abstract>BACKGROUND: Intravenously administered perfluorocarbon (PFC) emulsions increase oxygen solubility in plasma. PFC might therefore temporarily replace red cells (RBCs) lost during intraoperative hemorrhage. In patients who have undergone hemodilution, the return of autologous blood may be delayed by the administration of PFC, and autologous RBCs may be saved for transfusion after surgical bleeding is stopped and PFC is cleared by the reticuloendothelial system. STUDY DESIGN AND METHODS: In 22 anesthetized, hemodiluted dogs (hemoglobin [Hb] 7 g/dL) breathing 100‐percent O2, an intraoperative volume‐compensated blood loss was simulated. The efficacy of three therapeutic regimens in maintaining tissue oxygenation was compared: 1) RBC group (n = 7): maintenance of a Hb &gt; 7 g per dL by transfusion of autologous RBCs; 2) PFC group (n = 7): bolus application of a second‐generation PFC emulsion (60% wt/vol perflubron) and further acute normovolemic hemodilution (ANH) to a Hb of 3 g per dL; and 3) control group (n = 7): further ANH alone to a Hb of 3 g per dL. Systemic and myocardial oxygenation status and tissue oxygenation were assessed. RESULTS: Autologous RBCs transfused to maintain a Hb of 7 g per dL preserved hemodynamics and tissue oxygenation during blood loss. In the PFC and control groups, heart rate and cardiac index increased significantly in response to further ANH. Tissue oxygenation was not different in the PFC and the RBC groups. Direct comparison of the PFC and control groups revealed better tissue oxygenation in the PFC group, as reflected by significantly higher mixed venous, coronary venous, and local tissue pO2 on liver and skeletal muscle. CONCLUSION: Bolus intravenous administration of 60‐ percent (wt/vol) perflubron emulsion and further hemodilution from a Hb of 7 g per dL to one of 3 g per dL were as effective as autologous RBC transfusion in maintaining tissue oxygenation during volume‐compensated blood loss designed to mimic surgical bleeding.</abstract><cop>Edinburgh, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9531945</pmid><doi>10.1046/j.1537-2995.1998.38298193096.x</doi><tpages>11</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Biological and medical sciences
Blood Transfusion
Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis
Dogs
Fluorocarbons - administration & dosage
Hemodilution
Hemodynamics
Injections, Intravenous
Medical sciences
Miscellaneous
Oxygen - metabolism
Oxygen Consumption
Respiration
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
title Hemodilution and intravenous perflubron emulsion as an alternative to blood transfusion: effects on tissue oxygenation during profound hemodilution in anesthetized dogs
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