Fluid resuscitation with deferoxamine hetastarch complex attenuates the lung and systemic response to smoke inhalation

Background. We determined the effect of infusing the iron chelator deferoxamine complexed to hetastarch on the degree of lung dysfunction and systemic abnormalities produced by a severe smoke exposure. Methods. Adult sheep were given a smoke exposure under anesthesia that produced a peak carboxyhemo...

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Veröffentlicht in:Surgery 1996-03, Vol.119 (3), p.340-348
Hauptverfasser: Demling, Robert, LaLonde, Cheryl, Ikegami, Keiichi
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LaLonde, Cheryl
Ikegami, Keiichi
description Background. We determined the effect of infusing the iron chelator deferoxamine complexed to hetastarch on the degree of lung dysfunction and systemic abnormalities produced by a severe smoke exposure. Methods. Adult sheep were given a smoke exposure under anesthesia that produced a peak carboxyhemoglobin between 40% and 45%. Twenty-eight sheep were studied; eight were given smoke alone and resuscitated with sufficient lactated Ringer's solution to maintain baseline hemodynamics. Seven sheep were given a bolus plus 1 ml/kg/hr of a 10% deferoxamine-hetastarch solution for resuscitation; five were given hetastarch alone. The response was compared with eight controls during a period of 24 hours. Results. Smoke alone and smoke with hetastarch resulted in a shunt fraction of greater than 25% and a 50% decrease in compliance, severe airway inflammation, mucosal slough, atelectasis, and some alveolar edema. Increased lipid peroxides measured as malondialdehyde were present in airway fluid. In addition, oxygen consumption increased by 100% early after injury, net 24-hour positive fluid balance was almost 3 L, and a significant increase occurred in liver lipid peroxidation. The group given deferoxamine had a significantly attenuated lung response, with only modest airway damage, lung dysfunction, and minimal systemic changes including a net positive fluid balance of just over 1 L and no liver lipid peroxidation. Conclusions. An iron chelator deferoxamine complexed to hetastarch, given after a severe smoke exposure, significantly attenuates the airway and the systemic inflmmatory (oxidant) injury, indicating free iron release and subsequent increased oxidant activity to be a major etiologic factor.
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We determined the effect of infusing the iron chelator deferoxamine complexed to hetastarch on the degree of lung dysfunction and systemic abnormalities produced by a severe smoke exposure. Methods. Adult sheep were given a smoke exposure under anesthesia that produced a peak carboxyhemoglobin between 40% and 45%. Twenty-eight sheep were studied; eight were given smoke alone and resuscitated with sufficient lactated Ringer's solution to maintain baseline hemodynamics. Seven sheep were given a bolus plus 1 ml/kg/hr of a 10% deferoxamine-hetastarch solution for resuscitation; five were given hetastarch alone. The response was compared with eight controls during a period of 24 hours. Results. Smoke alone and smoke with hetastarch resulted in a shunt fraction of greater than 25% and a 50% decrease in compliance, severe airway inflammation, mucosal slough, atelectasis, and some alveolar edema. Increased lipid peroxides measured as malondialdehyde were present in airway fluid. In addition, oxygen consumption increased by 100% early after injury, net 24-hour positive fluid balance was almost 3 L, and a significant increase occurred in liver lipid peroxidation. The group given deferoxamine had a significantly attenuated lung response, with only modest airway damage, lung dysfunction, and minimal systemic changes including a net positive fluid balance of just over 1 L and no liver lipid peroxidation. Conclusions. An iron chelator deferoxamine complexed to hetastarch, given after a severe smoke exposure, significantly attenuates the airway and the systemic inflmmatory (oxidant) injury, indicating free iron release and subsequent increased oxidant activity to be a major etiologic factor.</description><identifier>ISSN: 0039-6060</identifier><identifier>EISSN: 1532-7361</identifier><identifier>DOI: 10.1016/S0039-6060(96)80121-8</identifier><identifier>PMID: 8619190</identifier><identifier>CODEN: SURGAZ</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Animals ; Biological and medical sciences ; Deferoxamine - pharmacology ; Deferoxamine - therapeutic use ; Female ; Hydroxyethyl Starch Derivatives - pharmacology ; Hydroxyethyl Starch Derivatives - therapeutic use ; Hydroxyl Radical ; Lipid Peroxidation - drug effects ; Lung - pathology ; Lung - physiopathology ; Medical sciences ; Oxygen Consumption - drug effects ; Pharmacology. 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We determined the effect of infusing the iron chelator deferoxamine complexed to hetastarch on the degree of lung dysfunction and systemic abnormalities produced by a severe smoke exposure. Methods. Adult sheep were given a smoke exposure under anesthesia that produced a peak carboxyhemoglobin between 40% and 45%. Twenty-eight sheep were studied; eight were given smoke alone and resuscitated with sufficient lactated Ringer's solution to maintain baseline hemodynamics. Seven sheep were given a bolus plus 1 ml/kg/hr of a 10% deferoxamine-hetastarch solution for resuscitation; five were given hetastarch alone. The response was compared with eight controls during a period of 24 hours. Results. Smoke alone and smoke with hetastarch resulted in a shunt fraction of greater than 25% and a 50% decrease in compliance, severe airway inflammation, mucosal slough, atelectasis, and some alveolar edema. Increased lipid peroxides measured as malondialdehyde were present in airway fluid. In addition, oxygen consumption increased by 100% early after injury, net 24-hour positive fluid balance was almost 3 L, and a significant increase occurred in liver lipid peroxidation. The group given deferoxamine had a significantly attenuated lung response, with only modest airway damage, lung dysfunction, and minimal systemic changes including a net positive fluid balance of just over 1 L and no liver lipid peroxidation. Conclusions. An iron chelator deferoxamine complexed to hetastarch, given after a severe smoke exposure, significantly attenuates the airway and the systemic inflmmatory (oxidant) injury, indicating free iron release and subsequent increased oxidant activity to be a major etiologic factor.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Deferoxamine - pharmacology</subject><subject>Deferoxamine - therapeutic use</subject><subject>Female</subject><subject>Hydroxyethyl Starch Derivatives - pharmacology</subject><subject>Hydroxyethyl Starch Derivatives - therapeutic use</subject><subject>Hydroxyl Radical</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lung - pathology</subject><subject>Lung - physiopathology</subject><subject>Medical sciences</subject><subject>Oxygen Consumption - drug effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Respiratory system</subject><subject>Resuscitation</subject><subject>Sheep</subject><subject>Smoke Inhalation Injury - physiopathology</subject><subject>Smoke Inhalation Injury - therapy</subject><issn>0039-6060</issn><issn>1532-7361</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1TAQRi0EKreFn1DJC4RgEbDj2LFXCFW0IFViAawt154QQ2JfPE5p_z25D90tq1l8Zx46Q8glZ-844-r9N8aEaRRT7I1RbzXjLW_0E7LhUrRNLxR_SjYn5Dk5R_zFGDMd12fkTCtuuGEbcn89LTHQArigj9XVmBP9G-tIAwxQ8oObYwI6QnVYXfEj9XneTvBAXa2QFlcBaR2BTkv6SV0KFB-xwhz9buY2JwRaM8U5_wYa0-im_YoX5NngJoSXx3pBflx_-n71ubn9evPl6uNt44U2tRmGoW0l414YwflgtJBBdNp557VQKnRCMibveq1FDz3XHZjBB962XEKnPRMX5PVh7rbkPwtgtXNED9PkEuQFbb966wXTKygPoC8ZscBgtyXOrjxazuzOt937tjuZ1ii79213fZfHBcvdDOHUdRS85q-OuUPvpqG45COeMMHaTkm5Yh8OGKwy7iMUu34DkocQC_hqQ47_OeQfo1CeRg</recordid><startdate>19960301</startdate><enddate>19960301</enddate><creator>Demling, Robert</creator><creator>LaLonde, Cheryl</creator><creator>Ikegami, Keiichi</creator><general>Mosby, Inc</general><general>Elsevier</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>19960301</creationdate><title>Fluid resuscitation with deferoxamine hetastarch complex attenuates the lung and systemic response to smoke inhalation</title><author>Demling, Robert ; LaLonde, Cheryl ; Ikegami, Keiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-fff22501c39311f9835d348acac8366d435005b78837e7184e9fcd12215e48c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Deferoxamine - pharmacology</topic><topic>Deferoxamine - therapeutic use</topic><topic>Female</topic><topic>Hydroxyethyl Starch Derivatives - pharmacology</topic><topic>Hydroxyethyl Starch Derivatives - therapeutic use</topic><topic>Hydroxyl Radical</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lung - pathology</topic><topic>Lung - physiopathology</topic><topic>Medical sciences</topic><topic>Oxygen Consumption - drug effects</topic><topic>Pharmacology. Drug treatments</topic><topic>Respiratory system</topic><topic>Resuscitation</topic><topic>Sheep</topic><topic>Smoke Inhalation Injury - physiopathology</topic><topic>Smoke Inhalation Injury - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Demling, Robert</creatorcontrib><creatorcontrib>LaLonde, Cheryl</creatorcontrib><creatorcontrib>Ikegami, Keiichi</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>Surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Demling, Robert</au><au>LaLonde, Cheryl</au><au>Ikegami, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluid resuscitation with deferoxamine hetastarch complex attenuates the lung and systemic response to smoke inhalation</atitle><jtitle>Surgery</jtitle><addtitle>Surgery</addtitle><date>1996-03-01</date><risdate>1996</risdate><volume>119</volume><issue>3</issue><spage>340</spage><epage>348</epage><pages>340-348</pages><issn>0039-6060</issn><eissn>1532-7361</eissn><coden>SURGAZ</coden><abstract>Background. We determined the effect of infusing the iron chelator deferoxamine complexed to hetastarch on the degree of lung dysfunction and systemic abnormalities produced by a severe smoke exposure. Methods. Adult sheep were given a smoke exposure under anesthesia that produced a peak carboxyhemoglobin between 40% and 45%. Twenty-eight sheep were studied; eight were given smoke alone and resuscitated with sufficient lactated Ringer's solution to maintain baseline hemodynamics. Seven sheep were given a bolus plus 1 ml/kg/hr of a 10% deferoxamine-hetastarch solution for resuscitation; five were given hetastarch alone. The response was compared with eight controls during a period of 24 hours. Results. Smoke alone and smoke with hetastarch resulted in a shunt fraction of greater than 25% and a 50% decrease in compliance, severe airway inflammation, mucosal slough, atelectasis, and some alveolar edema. Increased lipid peroxides measured as malondialdehyde were present in airway fluid. In addition, oxygen consumption increased by 100% early after injury, net 24-hour positive fluid balance was almost 3 L, and a significant increase occurred in liver lipid peroxidation. The group given deferoxamine had a significantly attenuated lung response, with only modest airway damage, lung dysfunction, and minimal systemic changes including a net positive fluid balance of just over 1 L and no liver lipid peroxidation. Conclusions. An iron chelator deferoxamine complexed to hetastarch, given after a severe smoke exposure, significantly attenuates the airway and the systemic inflmmatory (oxidant) injury, indicating free iron release and subsequent increased oxidant activity to be a major etiologic factor.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>8619190</pmid><doi>10.1016/S0039-6060(96)80121-8</doi><tpages>9</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Deferoxamine - pharmacology
Deferoxamine - therapeutic use
Female
Hydroxyethyl Starch Derivatives - pharmacology
Hydroxyethyl Starch Derivatives - therapeutic use
Hydroxyl Radical
Lipid Peroxidation - drug effects
Lung - pathology
Lung - physiopathology
Medical sciences
Oxygen Consumption - drug effects
Pharmacology. Drug treatments
Respiratory system
Resuscitation
Sheep
Smoke Inhalation Injury - physiopathology
Smoke Inhalation Injury - therapy
title Fluid resuscitation with deferoxamine hetastarch complex attenuates the lung and systemic response to smoke inhalation
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