Effects of Combination Dobutamine and Vasopressin Therapy on Microcirculatory Blood Flow in a Porcine Model of Severe Endotoxic Shock

Background Dobutamine (DB) has been recommended in combination with vasopressor therapy in septic shock, given its reported ability to improve mesenteric and microcirculatory perfusion. Vasopressin (VP) is typically reserved as a second-line agent due to the concern of ischemia. The purpose of our s...

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Veröffentlicht in:The Journal of surgical research 2011-11, Vol.171 (1), p.191-198
Hauptverfasser: Holt, Danielle B., M.D, Delaney, Richard R., M.D, Uyehara, Catherine F.T., Ph.D
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creator Holt, Danielle B., M.D
Delaney, Richard R., M.D
Uyehara, Catherine F.T., Ph.D
description Background Dobutamine (DB) has been recommended in combination with vasopressor therapy in septic shock, given its reported ability to improve mesenteric and microcirculatory perfusion. Vasopressin (VP) is typically reserved as a second-line agent due to the concern of ischemia. The purpose of our study was to determine whether combination DB and VP therapy improved microcirculatory blood flow in severe endotoxic shock. Methods Septic shock was induced in 20 anesthetized piglets with injection of E. coli endotoxin. DB (10μg/kg/min, n = 5) and VP (0.04 units/min, n = 10) were administered alone and in combination ( n = 15). Measurements were compared at baseline, following endotoxin administration, and following treatment. Microcirculatory blood flow was determined via the injection of colored microspheres. Results VP completely reversed endotoxin-mediated hypotension with a mean arterial pressure (MAP) of 85 ± 4.5mm Hg, which was not significantly altered with the addition of DB (77 ± 4.9mm Hg). Endotoxin uniformly depressed cardiac output (CO) from baseline (227 ± 10.7 versus 174 ± 12.4mL/min/kg) despite treatment with VP alone or in combination with DB. The addition of DB did not improve the CO in this severe septic shock model. VP was found to shunt microcirculatory flow from the skin and GI tract to vital organs such as the brain, liver, and kidneys, which was not altered with the addition of DB. Conclusions Results indicate that DB is ineffective in increasing CO or improving mesenteric blood flow when used with physiologic replacement doses of VP. In combination, DB is unable to overcome the blood flow distribution achieved with VP administration alone in severe endotoxic shock.
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Vasopressin (VP) is typically reserved as a second-line agent due to the concern of ischemia. The purpose of our study was to determine whether combination DB and VP therapy improved microcirculatory blood flow in severe endotoxic shock. Methods Septic shock was induced in 20 anesthetized piglets with injection of E. coli endotoxin. DB (10μg/kg/min, n = 5) and VP (0.04 units/min, n = 10) were administered alone and in combination ( n = 15). Measurements were compared at baseline, following endotoxin administration, and following treatment. Microcirculatory blood flow was determined via the injection of colored microspheres. Results VP completely reversed endotoxin-mediated hypotension with a mean arterial pressure (MAP) of 85 ± 4.5mm Hg, which was not significantly altered with the addition of DB (77 ± 4.9mm Hg). Endotoxin uniformly depressed cardiac output (CO) from baseline (227 ± 10.7 versus 174 ± 12.4mL/min/kg) despite treatment with VP alone or in combination with DB. The addition of DB did not improve the CO in this severe septic shock model. VP was found to shunt microcirculatory flow from the skin and GI tract to vital organs such as the brain, liver, and kidneys, which was not altered with the addition of DB. Conclusions Results indicate that DB is ineffective in increasing CO or improving mesenteric blood flow when used with physiologic replacement doses of VP. In combination, DB is unable to overcome the blood flow distribution achieved with VP administration alone in severe endotoxic shock.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2009.11.739</identifier><identifier>PMID: 20338585</identifier><identifier>CODEN: JSGRA2</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acid-Base Equilibrium - drug effects ; Acid-Base Equilibrium - physiology ; Animals ; Biological and medical sciences ; Cardiotonic Agents - pharmacology ; Disease Models, Animal ; dobutamine ; Dobutamine - pharmacology ; Drug Therapy, Combination ; endotoxic shock ; General aspects ; Heart Rate - drug effects ; Heart Rate - physiology ; Medical sciences ; microcirculation ; Microcirculation - drug effects ; Microcirculation - physiology ; Severity of Illness Index ; Shock, Septic - drug therapy ; Shock, Septic - physiopathology ; Stroke Volume - drug effects ; Stroke Volume - physiology ; Surgery ; Sus scrofa ; Vasoconstrictor Agents - pharmacology ; vasopressin ; Vasopressins - pharmacology</subject><ispartof>The Journal of surgical research, 2011-11, Vol.171 (1), p.191-198</ispartof><rights>2010</rights><rights>2015 INIST-CNRS</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-e96c6d6fec1e6febbccc8307628e18ba3d1426e59eff30bf31e6e4031c3f1ccc3</citedby><cites>FETCH-LOGICAL-c437t-e96c6d6fec1e6febbccc8307628e18ba3d1426e59eff30bf31e6e4031c3f1ccc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jss.2009.11.739$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24712004$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20338585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holt, Danielle B., M.D</creatorcontrib><creatorcontrib>Delaney, Richard R., M.D</creatorcontrib><creatorcontrib>Uyehara, Catherine F.T., Ph.D</creatorcontrib><title>Effects of Combination Dobutamine and Vasopressin Therapy on Microcirculatory Blood Flow in a Porcine Model of Severe Endotoxic Shock</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Background Dobutamine (DB) has been recommended in combination with vasopressor therapy in septic shock, given its reported ability to improve mesenteric and microcirculatory perfusion. Vasopressin (VP) is typically reserved as a second-line agent due to the concern of ischemia. The purpose of our study was to determine whether combination DB and VP therapy improved microcirculatory blood flow in severe endotoxic shock. Methods Septic shock was induced in 20 anesthetized piglets with injection of E. coli endotoxin. DB (10μg/kg/min, n = 5) and VP (0.04 units/min, n = 10) were administered alone and in combination ( n = 15). Measurements were compared at baseline, following endotoxin administration, and following treatment. Microcirculatory blood flow was determined via the injection of colored microspheres. Results VP completely reversed endotoxin-mediated hypotension with a mean arterial pressure (MAP) of 85 ± 4.5mm Hg, which was not significantly altered with the addition of DB (77 ± 4.9mm Hg). Endotoxin uniformly depressed cardiac output (CO) from baseline (227 ± 10.7 versus 174 ± 12.4mL/min/kg) despite treatment with VP alone or in combination with DB. The addition of DB did not improve the CO in this severe septic shock model. VP was found to shunt microcirculatory flow from the skin and GI tract to vital organs such as the brain, liver, and kidneys, which was not altered with the addition of DB. Conclusions Results indicate that DB is ineffective in increasing CO or improving mesenteric blood flow when used with physiologic replacement doses of VP. 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Delaney, Richard R., M.D ; Uyehara, Catherine F.T., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-e96c6d6fec1e6febbccc8307628e18ba3d1426e59eff30bf31e6e4031c3f1ccc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acid-Base Equilibrium - drug effects</topic><topic>Acid-Base Equilibrium - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Disease Models, Animal</topic><topic>dobutamine</topic><topic>Dobutamine - pharmacology</topic><topic>Drug Therapy, Combination</topic><topic>endotoxic shock</topic><topic>General aspects</topic><topic>Heart Rate - drug effects</topic><topic>Heart Rate - physiology</topic><topic>Medical sciences</topic><topic>microcirculation</topic><topic>Microcirculation - drug effects</topic><topic>Microcirculation - physiology</topic><topic>Severity of Illness Index</topic><topic>Shock, Septic - drug therapy</topic><topic>Shock, Septic - physiopathology</topic><topic>Stroke Volume - drug effects</topic><topic>Stroke Volume - physiology</topic><topic>Surgery</topic><topic>Sus scrofa</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>vasopressin</topic><topic>Vasopressins - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holt, Danielle B., M.D</creatorcontrib><creatorcontrib>Delaney, Richard R., M.D</creatorcontrib><creatorcontrib>Uyehara, Catherine F.T., Ph.D</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 surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holt, Danielle B., M.D</au><au>Delaney, Richard R., M.D</au><au>Uyehara, Catherine F.T., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Combination Dobutamine and Vasopressin Therapy on Microcirculatory Blood Flow in a Porcine Model of Severe Endotoxic Shock</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>171</volume><issue>1</issue><spage>191</spage><epage>198</epage><pages>191-198</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><coden>JSGRA2</coden><abstract>Background Dobutamine (DB) has been recommended in combination with vasopressor therapy in septic shock, given its reported ability to improve mesenteric and microcirculatory perfusion. Vasopressin (VP) is typically reserved as a second-line agent due to the concern of ischemia. The purpose of our study was to determine whether combination DB and VP therapy improved microcirculatory blood flow in severe endotoxic shock. Methods Septic shock was induced in 20 anesthetized piglets with injection of E. coli endotoxin. DB (10μg/kg/min, n = 5) and VP (0.04 units/min, n = 10) were administered alone and in combination ( n = 15). Measurements were compared at baseline, following endotoxin administration, and following treatment. Microcirculatory blood flow was determined via the injection of colored microspheres. Results VP completely reversed endotoxin-mediated hypotension with a mean arterial pressure (MAP) of 85 ± 4.5mm Hg, which was not significantly altered with the addition of DB (77 ± 4.9mm Hg). Endotoxin uniformly depressed cardiac output (CO) from baseline (227 ± 10.7 versus 174 ± 12.4mL/min/kg) despite treatment with VP alone or in combination with DB. The addition of DB did not improve the CO in this severe septic shock model. VP was found to shunt microcirculatory flow from the skin and GI tract to vital organs such as the brain, liver, and kidneys, which was not altered with the addition of DB. Conclusions Results indicate that DB is ineffective in increasing CO or improving mesenteric blood flow when used with physiologic replacement doses of VP. In combination, DB is unable to overcome the blood flow distribution achieved with VP administration alone in severe endotoxic shock.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20338585</pmid><doi>10.1016/j.jss.2009.11.739</doi><tpages>8</tpages></addata></record>
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subjects Acid-Base Equilibrium - drug effects
Acid-Base Equilibrium - physiology
Animals
Biological and medical sciences
Cardiotonic Agents - pharmacology
Disease Models, Animal
dobutamine
Dobutamine - pharmacology
Drug Therapy, Combination
endotoxic shock
General aspects
Heart Rate - drug effects
Heart Rate - physiology
Medical sciences
microcirculation
Microcirculation - drug effects
Microcirculation - physiology
Severity of Illness Index
Shock, Septic - drug therapy
Shock, Septic - physiopathology
Stroke Volume - drug effects
Stroke Volume - physiology
Surgery
Sus scrofa
Vasoconstrictor Agents - pharmacology
vasopressin
Vasopressins - pharmacology
title Effects of Combination Dobutamine and Vasopressin Therapy on Microcirculatory Blood Flow in a Porcine Model of Severe Endotoxic Shock
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