Oxygen Administration Improves Survival but Worsens Cardiopulmonary Functions in Chlorine-exposed Rats
Chlorine is a highly reactive gas that can cause significant injury when inhaled. Unfortunately, its use as a chemical weapon has increased in recent years. Massive chlorine inhalation can cause death within 4 hours of exposure. Survivors usually require hospitalization after massive exposure. No co...
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description | Chlorine is a highly reactive gas that can cause significant injury when inhaled. Unfortunately, its use as a chemical weapon has increased in recent years. Massive chlorine inhalation can cause death within 4 hours of exposure. Survivors usually require hospitalization after massive exposure. No countermeasures are available for massive chlorine exposure and supportive-care measures lack controlled trials. In this work, adult rats were exposed to chlorine gas (LD
) in a whole-body exposure chamber, and given oxygen (0.8 Fi
) or air (0.21 Fi
) for 6 hours after baseline measurements were obtained. Oxygen saturation, vital signs, respiratory distress and neuromuscular scores, arterial blood gases, and hemodynamic measurements were obtained hourly. Massive chlorine inhalation caused severe acute respiratory failure, hypoxemia, decreased cardiac output, neuromuscular abnormalities (ataxia and hypotonia), and seizures resulting in early death. Oxygen improved survival to 6 hours (87% versus 42%) and prevented observed seizure-related deaths. However, oxygen administration worsened the severity of acute respiratory failure in chlorine-exposed rats compared with controls, with increased respiratory acidosis (pH 6.91 ± 0.04 versus 7.06 ± 0.01 at 2 h) and increased hypercapnia (180.0 ± 19.8 versus 103.2 ± 3.9 mm Hg at 2 h). In addition, oxygen did not improve neuromuscular abnormalities, cardiac output, or respiratory distress associated with chlorine exposure. Massive chlorine inhalation causes severe acute respiratory failure and multiorgan damage. Oxygen administration can improve short-term survival but appears to worsen respiratory failure, with no improvement in cardiac output or neuromuscular dysfunction. Oxygen should be used with caution after massive chlorine inhalation, and the need for early assisted ventilation should be assessed in victims. |
doi_str_mv | 10.1165/rcmb.2016-0223OC |
format | Article |
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) in a whole-body exposure chamber, and given oxygen (0.8 Fi
) or air (0.21 Fi
) for 6 hours after baseline measurements were obtained. Oxygen saturation, vital signs, respiratory distress and neuromuscular scores, arterial blood gases, and hemodynamic measurements were obtained hourly. Massive chlorine inhalation caused severe acute respiratory failure, hypoxemia, decreased cardiac output, neuromuscular abnormalities (ataxia and hypotonia), and seizures resulting in early death. Oxygen improved survival to 6 hours (87% versus 42%) and prevented observed seizure-related deaths. However, oxygen administration worsened the severity of acute respiratory failure in chlorine-exposed rats compared with controls, with increased respiratory acidosis (pH 6.91 ± 0.04 versus 7.06 ± 0.01 at 2 h) and increased hypercapnia (180.0 ± 19.8 versus 103.2 ± 3.9 mm Hg at 2 h). In addition, oxygen did not improve neuromuscular abnormalities, cardiac output, or respiratory distress associated with chlorine exposure. Massive chlorine inhalation causes severe acute respiratory failure and multiorgan damage. Oxygen administration can improve short-term survival but appears to worsen respiratory failure, with no improvement in cardiac output or neuromuscular dysfunction. Oxygen should be used with caution after massive chlorine inhalation, and the need for early assisted ventilation should be assessed in victims.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/rcmb.2016-0223OC</identifier><identifier>PMID: 28846437</identifier><language>eng</language><publisher>United States: American Thoracic Society</publisher><subject>Acidosis ; Acute Disease ; Airway management ; Animals ; Ataxia ; Cardiac Output - drug effects ; Chemical Warfare Agents - toxicity ; Chlorine ; Chlorine - toxicity ; Edema ; Fatalities ; Gases ; Heart attacks ; Heart diseases ; Hypercapnia ; Hypercapnia - chemically induced ; Hypercapnia - drug therapy ; Hypercapnia - physiopathology ; Hypoxemia ; Inhalation ; Laboratories ; Male ; Mechanical ventilation ; Mortality ; Original Research ; Oxygen ; Oxygen - pharmacology ; Oxygen therapy ; pH effects ; Railroad accidents & safety ; Rats ; Rats, Sprague-Dawley ; Respiratory Insufficiency - chemically induced ; Respiratory Insufficiency - drug therapy ; Respiratory Insufficiency - physiopathology ; Respiratory therapy ; Rodents ; Seizures ; Signal transduction ; Sulfur ; Survival ; Ventilators ; World War I</subject><ispartof>American journal of respiratory cell and molecular biology, 2018-01, Vol.58 (1), p.107-116</ispartof><rights>Copyright American Thoracic Society Jan 2018</rights><rights>Copyright © 2018 by the American Thoracic Society 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-10a9c759ffbf20a3c1d05a4b389f05b4bb4e29abb401566df42be28e4c2083583</citedby><cites>FETCH-LOGICAL-c424t-10a9c759ffbf20a3c1d05a4b389f05b4bb4e29abb401566df42be28e4c2083583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28846437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okponyia, Obiefuna C</creatorcontrib><creatorcontrib>McGraw, Matthew D</creatorcontrib><creatorcontrib>Dysart, Marilyn M</creatorcontrib><creatorcontrib>Garlick, Rhonda B</creatorcontrib><creatorcontrib>Rioux, Jacqueline S</creatorcontrib><creatorcontrib>Murphy, Angela L</creatorcontrib><creatorcontrib>Roe, Gates B</creatorcontrib><creatorcontrib>White, Carl W</creatorcontrib><creatorcontrib>Veress, Livia A</creatorcontrib><title>Oxygen Administration Improves Survival but Worsens Cardiopulmonary Functions in Chlorine-exposed Rats</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>Chlorine is a highly reactive gas that can cause significant injury when inhaled. Unfortunately, its use as a chemical weapon has increased in recent years. Massive chlorine inhalation can cause death within 4 hours of exposure. Survivors usually require hospitalization after massive exposure. No countermeasures are available for massive chlorine exposure and supportive-care measures lack controlled trials. In this work, adult rats were exposed to chlorine gas (LD
) in a whole-body exposure chamber, and given oxygen (0.8 Fi
) or air (0.21 Fi
) for 6 hours after baseline measurements were obtained. Oxygen saturation, vital signs, respiratory distress and neuromuscular scores, arterial blood gases, and hemodynamic measurements were obtained hourly. Massive chlorine inhalation caused severe acute respiratory failure, hypoxemia, decreased cardiac output, neuromuscular abnormalities (ataxia and hypotonia), and seizures resulting in early death. Oxygen improved survival to 6 hours (87% versus 42%) and prevented observed seizure-related deaths. However, oxygen administration worsened the severity of acute respiratory failure in chlorine-exposed rats compared with controls, with increased respiratory acidosis (pH 6.91 ± 0.04 versus 7.06 ± 0.01 at 2 h) and increased hypercapnia (180.0 ± 19.8 versus 103.2 ± 3.9 mm Hg at 2 h). In addition, oxygen did not improve neuromuscular abnormalities, cardiac output, or respiratory distress associated with chlorine exposure. Massive chlorine inhalation causes severe acute respiratory failure and multiorgan damage. Oxygen administration can improve short-term survival but appears to worsen respiratory failure, with no improvement in cardiac output or neuromuscular dysfunction. Oxygen should be used with caution after massive chlorine inhalation, and the need for early assisted ventilation should be assessed in victims.</description><subject>Acidosis</subject><subject>Acute Disease</subject><subject>Airway management</subject><subject>Animals</subject><subject>Ataxia</subject><subject>Cardiac Output - drug effects</subject><subject>Chemical Warfare Agents - toxicity</subject><subject>Chlorine</subject><subject>Chlorine - toxicity</subject><subject>Edema</subject><subject>Fatalities</subject><subject>Gases</subject><subject>Heart attacks</subject><subject>Heart diseases</subject><subject>Hypercapnia</subject><subject>Hypercapnia - chemically induced</subject><subject>Hypercapnia - drug therapy</subject><subject>Hypercapnia - physiopathology</subject><subject>Hypoxemia</subject><subject>Inhalation</subject><subject>Laboratories</subject><subject>Male</subject><subject>Mechanical ventilation</subject><subject>Mortality</subject><subject>Original Research</subject><subject>Oxygen</subject><subject>Oxygen - pharmacology</subject><subject>Oxygen therapy</subject><subject>pH effects</subject><subject>Railroad accidents & safety</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Respiratory Insufficiency - chemically induced</subject><subject>Respiratory Insufficiency - drug therapy</subject><subject>Respiratory Insufficiency - physiopathology</subject><subject>Respiratory therapy</subject><subject>Rodents</subject><subject>Seizures</subject><subject>Signal transduction</subject><subject>Sulfur</subject><subject>Survival</subject><subject>Ventilators</subject><subject>World War I</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc1LHTEUxYO0qLXuXZVAN92MzedMshFk0CoID1qly5BkMhqZScZk5qH_fTM8lbare-H-zuEeDgAnGJ1iXPPvyY7mlCBcV4gQumn3wCHmlFdMCvmh7IixCnMmD8CnnB8RwkRgvA8OiBCsZrQ5BP3m-eXeBXjejT74PCc9-xjg9TiluHUZ_lrS1m_1AM0yw98xZRcybHXqfJyWYYxBpxd4uQS7yjL0AbYPQ0w-uMo9TzG7Dv7Uc_4MPvZ6yO74dR6Bu8uL2_aqutn8uG7PbyrLCJsrjLS0DZd9b3qCNLW4Q1wzQ4XsETfMGOaI1GUgzOu66xkxjgjHLEGCckGPwNnOd1rM6DrrQkk0qCn5sTyqovbq30vwD-o-bhWXDFO0Gnx7NUjxaXF5VqPP1g2DDi4uWWFJaY24aFhBv_6HPsYlhRKvUKKhjWwoKRTaUTbFnJPr35_BSK0lqrVEtZaodiUWyZe_Q7wL3lqjfwA4spug</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Okponyia, Obiefuna C</creator><creator>McGraw, Matthew D</creator><creator>Dysart, Marilyn M</creator><creator>Garlick, Rhonda B</creator><creator>Rioux, Jacqueline S</creator><creator>Murphy, Angela L</creator><creator>Roe, Gates B</creator><creator>White, Carl W</creator><creator>Veress, Livia A</creator><general>American Thoracic Society</general><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>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201801</creationdate><title>Oxygen Administration Improves Survival but Worsens Cardiopulmonary Functions in Chlorine-exposed Rats</title><author>Okponyia, Obiefuna C ; McGraw, Matthew D ; Dysart, Marilyn M ; Garlick, Rhonda B ; Rioux, Jacqueline S ; Murphy, Angela L ; Roe, Gates B ; White, Carl W ; Veress, Livia A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-10a9c759ffbf20a3c1d05a4b389f05b4bb4e29abb401566df42be28e4c2083583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acidosis</topic><topic>Acute Disease</topic><topic>Airway management</topic><topic>Animals</topic><topic>Ataxia</topic><topic>Cardiac Output - drug effects</topic><topic>Chemical Warfare Agents - toxicity</topic><topic>Chlorine</topic><topic>Chlorine - toxicity</topic><topic>Edema</topic><topic>Fatalities</topic><topic>Gases</topic><topic>Heart attacks</topic><topic>Heart diseases</topic><topic>Hypercapnia</topic><topic>Hypercapnia - chemically induced</topic><topic>Hypercapnia - drug therapy</topic><topic>Hypercapnia - physiopathology</topic><topic>Hypoxemia</topic><topic>Inhalation</topic><topic>Laboratories</topic><topic>Male</topic><topic>Mechanical ventilation</topic><topic>Mortality</topic><topic>Original Research</topic><topic>Oxygen</topic><topic>Oxygen - pharmacology</topic><topic>Oxygen therapy</topic><topic>pH effects</topic><topic>Railroad accidents & safety</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Respiratory Insufficiency - chemically induced</topic><topic>Respiratory Insufficiency - drug therapy</topic><topic>Respiratory Insufficiency - physiopathology</topic><topic>Respiratory therapy</topic><topic>Rodents</topic><topic>Seizures</topic><topic>Signal transduction</topic><topic>Sulfur</topic><topic>Survival</topic><topic>Ventilators</topic><topic>World War I</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okponyia, Obiefuna C</creatorcontrib><creatorcontrib>McGraw, Matthew D</creatorcontrib><creatorcontrib>Dysart, Marilyn M</creatorcontrib><creatorcontrib>Garlick, Rhonda B</creatorcontrib><creatorcontrib>Rioux, Jacqueline S</creatorcontrib><creatorcontrib>Murphy, Angela L</creatorcontrib><creatorcontrib>Roe, Gates B</creatorcontrib><creatorcontrib>White, Carl W</creatorcontrib><creatorcontrib>Veress, Livia A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of respiratory cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okponyia, Obiefuna C</au><au>McGraw, Matthew D</au><au>Dysart, Marilyn M</au><au>Garlick, Rhonda B</au><au>Rioux, Jacqueline S</au><au>Murphy, Angela L</au><au>Roe, Gates B</au><au>White, Carl W</au><au>Veress, Livia A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxygen Administration Improves Survival but Worsens Cardiopulmonary Functions in Chlorine-exposed Rats</atitle><jtitle>American journal of respiratory cell and molecular biology</jtitle><addtitle>Am J Respir Cell Mol Biol</addtitle><date>2018-01</date><risdate>2018</risdate><volume>58</volume><issue>1</issue><spage>107</spage><epage>116</epage><pages>107-116</pages><issn>1044-1549</issn><eissn>1535-4989</eissn><abstract>Chlorine is a highly reactive gas that can cause significant injury when inhaled. Unfortunately, its use as a chemical weapon has increased in recent years. Massive chlorine inhalation can cause death within 4 hours of exposure. Survivors usually require hospitalization after massive exposure. No countermeasures are available for massive chlorine exposure and supportive-care measures lack controlled trials. In this work, adult rats were exposed to chlorine gas (LD
) in a whole-body exposure chamber, and given oxygen (0.8 Fi
) or air (0.21 Fi
) for 6 hours after baseline measurements were obtained. Oxygen saturation, vital signs, respiratory distress and neuromuscular scores, arterial blood gases, and hemodynamic measurements were obtained hourly. Massive chlorine inhalation caused severe acute respiratory failure, hypoxemia, decreased cardiac output, neuromuscular abnormalities (ataxia and hypotonia), and seizures resulting in early death. Oxygen improved survival to 6 hours (87% versus 42%) and prevented observed seizure-related deaths. However, oxygen administration worsened the severity of acute respiratory failure in chlorine-exposed rats compared with controls, with increased respiratory acidosis (pH 6.91 ± 0.04 versus 7.06 ± 0.01 at 2 h) and increased hypercapnia (180.0 ± 19.8 versus 103.2 ± 3.9 mm Hg at 2 h). In addition, oxygen did not improve neuromuscular abnormalities, cardiac output, or respiratory distress associated with chlorine exposure. Massive chlorine inhalation causes severe acute respiratory failure and multiorgan damage. Oxygen administration can improve short-term survival but appears to worsen respiratory failure, with no improvement in cardiac output or neuromuscular dysfunction. Oxygen should be used with caution after massive chlorine inhalation, and the need for early assisted ventilation should be assessed in victims.</abstract><cop>United States</cop><pub>American Thoracic Society</pub><pmid>28846437</pmid><doi>10.1165/rcmb.2016-0223OC</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acidosis Acute Disease Airway management Animals Ataxia Cardiac Output - drug effects Chemical Warfare Agents - toxicity Chlorine Chlorine - toxicity Edema Fatalities Gases Heart attacks Heart diseases Hypercapnia Hypercapnia - chemically induced Hypercapnia - drug therapy Hypercapnia - physiopathology Hypoxemia Inhalation Laboratories Male Mechanical ventilation Mortality Original Research Oxygen Oxygen - pharmacology Oxygen therapy pH effects Railroad accidents & safety Rats Rats, Sprague-Dawley Respiratory Insufficiency - chemically induced Respiratory Insufficiency - drug therapy Respiratory Insufficiency - physiopathology Respiratory therapy Rodents Seizures Signal transduction Sulfur Survival Ventilators World War I |
title | Oxygen Administration Improves Survival but Worsens Cardiopulmonary Functions in Chlorine-exposed Rats |
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