The effects of dobutamine and dopamine on intrapulmonary shunt and gas exchange in healthy humans
The development of intrapulmonary shunts with increased cardiac output during exercise in healthy humans has been reported in several recent studies, but mechanisms governing their recruitment remain unclear. Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, bot...
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description | The development of intrapulmonary shunts with increased cardiac output during exercise in healthy humans has been reported in several recent studies, but mechanisms governing their recruitment remain unclear. Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, both can increase venous admixture/shunt fraction (Qs/Qt). It is possible that, as with exercise, intrapulmonary shunts are recruited with increased cardiac output during dobutamine and/or dopamine infusion that may contribute to the observed increase in Qs/Qt. The purpose of this study was to examine how dobutamine and dopamine affect intrapulmonary shunt and gas exchange. Nine resting healthy subjects received serial infusions of dobutamine and dopamine at incremental doses under normoxic and hyperoxic (inspired O(2) fraction = 1.0) conditions. At each step, alveolar-to-arterial Po(2) difference (A-aDo(2)) and Qs/Qt were calculated from arterial blood gas samples, intrapulmonary shunt was evaluated using contrast echocardiography, and cardiac output was calculated by Doppler echocardiography. Both dobutamine and dopamine increased cardiac output and Qs/Qt. Intrapulmonary shunt developed in most subjects with both drugs and paralleled the increase in Qs/Qt. A-aDo(2) was unchanged due to a concurrent rise in mixed venous oxygen content. Hyperoxia consistently eliminated intrapulmonary shunt. These findings contribute to our present understanding of the mechanisms governing recruitment of these intrapulmonary shunts as well as their impact on gas exchange. In addition, given the deleterious effect on Qs/Qt and the risk of neurological complications with intrapulmonary shunts, these findings could have important implications for use of dobutamine and dopamine in the clinical setting. |
doi_str_mv | 10.1152/japplphysiol.00404.2012 |
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Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, both can increase venous admixture/shunt fraction (Qs/Qt). It is possible that, as with exercise, intrapulmonary shunts are recruited with increased cardiac output during dobutamine and/or dopamine infusion that may contribute to the observed increase in Qs/Qt. The purpose of this study was to examine how dobutamine and dopamine affect intrapulmonary shunt and gas exchange. Nine resting healthy subjects received serial infusions of dobutamine and dopamine at incremental doses under normoxic and hyperoxic (inspired O(2) fraction = 1.0) conditions. At each step, alveolar-to-arterial Po(2) difference (A-aDo(2)) and Qs/Qt were calculated from arterial blood gas samples, intrapulmonary shunt was evaluated using contrast echocardiography, and cardiac output was calculated by Doppler echocardiography. Both dobutamine and dopamine increased cardiac output and Qs/Qt. Intrapulmonary shunt developed in most subjects with both drugs and paralleled the increase in Qs/Qt. A-aDo(2) was unchanged due to a concurrent rise in mixed venous oxygen content. Hyperoxia consistently eliminated intrapulmonary shunt. These findings contribute to our present understanding of the mechanisms governing recruitment of these intrapulmonary shunts as well as their impact on gas exchange. In addition, given the deleterious effect on Qs/Qt and the risk of neurological complications with intrapulmonary shunts, these findings could have important implications for use of dobutamine and dopamine in the clinical setting.</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.00404.2012</identifier><identifier>PMID: 22700799</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Adult ; Anatomy & physiology ; Arterial Pressure - drug effects ; Cardiac Output - drug effects ; Cardiotonic Agents - administration & dosage ; Dobutamine - administration & dosage ; Dopamine ; Dopamine - administration & dosage ; Dose-Response Relationship, Drug ; Echocardiography, Doppler ; Exercise ; Female ; Forced Expiratory Volume - drug effects ; Hemodynamics - drug effects ; Humans ; Hyperoxia - physiopathology ; Infusions, Intravenous ; Male ; Oxygen Consumption - drug effects ; Pharmaceuticals ; Pulmonary Alveoli - blood supply ; Pulmonary Alveoli - drug effects ; Pulmonary Alveoli - physiopathology ; Pulmonary Artery - diagnostic imaging ; Pulmonary Artery - drug effects ; Pulmonary Artery - physiopathology ; Pulmonary Circulation - drug effects ; Pulmonary Diffusing Capacity - drug effects ; Pulmonary Gas Exchange - drug effects ; Respiration ; Side effects ; Time Factors ; Vital Capacity - drug effects</subject><ispartof>Journal of applied physiology (1985), 2012-08, Vol.113 (4), p.541-548</ispartof><rights>Copyright American Physiological Society Aug 15, 2012</rights><rights>Copyright © 2012 the American Physiological Society 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-3d9152472d66ccd2d6a4f65cad99edef79600682cc76df252a25eeffff741f5a3</citedby><cites>FETCH-LOGICAL-c445t-3d9152472d66ccd2d6a4f65cad99edef79600682cc76df252a25eeffff741f5a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3037,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22700799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bryan, Tracey L</creatorcontrib><creatorcontrib>van Diepen, Sean</creatorcontrib><creatorcontrib>Bhutani, Mohit</creatorcontrib><creatorcontrib>Shanks, Miriam</creatorcontrib><creatorcontrib>Welsh, Robert C</creatorcontrib><creatorcontrib>Stickland, Michael K</creatorcontrib><title>The effects of dobutamine and dopamine on intrapulmonary shunt and gas exchange in healthy humans</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>The development of intrapulmonary shunts with increased cardiac output during exercise in healthy humans has been reported in several recent studies, but mechanisms governing their recruitment remain unclear. Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, both can increase venous admixture/shunt fraction (Qs/Qt). It is possible that, as with exercise, intrapulmonary shunts are recruited with increased cardiac output during dobutamine and/or dopamine infusion that may contribute to the observed increase in Qs/Qt. The purpose of this study was to examine how dobutamine and dopamine affect intrapulmonary shunt and gas exchange. Nine resting healthy subjects received serial infusions of dobutamine and dopamine at incremental doses under normoxic and hyperoxic (inspired O(2) fraction = 1.0) conditions. At each step, alveolar-to-arterial Po(2) difference (A-aDo(2)) and Qs/Qt were calculated from arterial blood gas samples, intrapulmonary shunt was evaluated using contrast echocardiography, and cardiac output was calculated by Doppler echocardiography. Both dobutamine and dopamine increased cardiac output and Qs/Qt. Intrapulmonary shunt developed in most subjects with both drugs and paralleled the increase in Qs/Qt. A-aDo(2) was unchanged due to a concurrent rise in mixed venous oxygen content. Hyperoxia consistently eliminated intrapulmonary shunt. These findings contribute to our present understanding of the mechanisms governing recruitment of these intrapulmonary shunts as well as their impact on gas exchange. In addition, given the deleterious effect on Qs/Qt and the risk of neurological complications with intrapulmonary shunts, these findings could have important implications for use of dobutamine and dopamine in the clinical setting.</description><subject>Adult</subject><subject>Anatomy & physiology</subject><subject>Arterial Pressure - drug effects</subject><subject>Cardiac Output - drug effects</subject><subject>Cardiotonic Agents - administration & dosage</subject><subject>Dobutamine - administration & dosage</subject><subject>Dopamine</subject><subject>Dopamine - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Echocardiography, Doppler</subject><subject>Exercise</subject><subject>Female</subject><subject>Forced Expiratory Volume - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Hyperoxia - physiopathology</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Oxygen Consumption - drug effects</subject><subject>Pharmaceuticals</subject><subject>Pulmonary Alveoli - blood supply</subject><subject>Pulmonary Alveoli - drug effects</subject><subject>Pulmonary Alveoli - physiopathology</subject><subject>Pulmonary Artery - diagnostic imaging</subject><subject>Pulmonary Artery - drug effects</subject><subject>Pulmonary Artery - physiopathology</subject><subject>Pulmonary Circulation - drug effects</subject><subject>Pulmonary Diffusing Capacity - drug effects</subject><subject>Pulmonary Gas Exchange - drug effects</subject><subject>Respiration</subject><subject>Side effects</subject><subject>Time Factors</subject><subject>Vital Capacity - drug effects</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkVtLxDAQhYMoul7-ggZ87jpJ02T7Ioh4A8GX9TnEXLZd2qQ2rbj_3nRXRZ-GYc4588FB6ILAnJCCXq1V1zVdtYl1aOYADNicAqF7aJauNCMcyD6aLUQBmSgW4ggdx7gGIIwV5BAdUSoARFnOkFpWFlvnrB4iDg6b8DYOqq29xcqbtHa7JXhc-6FX3di0wat-g2M1-mErWqmI7aeulF_ZpMKVVc1QbXA1tsrHU3TgVBPt2fc8Qa_3d8vbx-z55eHp9uY50wlqyHJTJnQmqOFca5OGYo4XWpmytMY6UXIAvqBaC24cLaiihU3gzglGXKHyE3S9y-3Gt9YabSfcRnZ93SZcGVQt_198XclV-JA5oww4pIDL74A-vI82DnIdxt4nZkkgFzlbsHxSiZ1K9yHG3rrfDwTk1I38243cdiOnbpLz_C_gr--njPwLityRxw</recordid><startdate>20120815</startdate><enddate>20120815</enddate><creator>Bryan, Tracey L</creator><creator>van Diepen, Sean</creator><creator>Bhutani, Mohit</creator><creator>Shanks, Miriam</creator><creator>Welsh, Robert C</creator><creator>Stickland, Michael K</creator><general>American Physiological 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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20120815</creationdate><title>The effects of dobutamine and dopamine on intrapulmonary shunt and gas exchange in healthy humans</title><author>Bryan, Tracey L ; van Diepen, Sean ; Bhutani, Mohit ; Shanks, Miriam ; Welsh, Robert C ; Stickland, Michael K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-3d9152472d66ccd2d6a4f65cad99edef79600682cc76df252a25eeffff741f5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Anatomy & physiology</topic><topic>Arterial Pressure - drug effects</topic><topic>Cardiac Output - drug effects</topic><topic>Cardiotonic Agents - administration & dosage</topic><topic>Dobutamine - administration & dosage</topic><topic>Dopamine</topic><topic>Dopamine - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Echocardiography, Doppler</topic><topic>Exercise</topic><topic>Female</topic><topic>Forced Expiratory Volume - drug effects</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Hyperoxia - physiopathology</topic><topic>Infusions, Intravenous</topic><topic>Male</topic><topic>Oxygen Consumption - drug effects</topic><topic>Pharmaceuticals</topic><topic>Pulmonary Alveoli - blood supply</topic><topic>Pulmonary Alveoli - drug effects</topic><topic>Pulmonary Alveoli - physiopathology</topic><topic>Pulmonary Artery - diagnostic imaging</topic><topic>Pulmonary Artery - drug effects</topic><topic>Pulmonary Artery - physiopathology</topic><topic>Pulmonary Circulation - drug effects</topic><topic>Pulmonary Diffusing Capacity - drug effects</topic><topic>Pulmonary Gas Exchange - drug effects</topic><topic>Respiration</topic><topic>Side effects</topic><topic>Time Factors</topic><topic>Vital Capacity - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bryan, Tracey L</creatorcontrib><creatorcontrib>van Diepen, Sean</creatorcontrib><creatorcontrib>Bhutani, Mohit</creatorcontrib><creatorcontrib>Shanks, Miriam</creatorcontrib><creatorcontrib>Welsh, Robert C</creatorcontrib><creatorcontrib>Stickland, Michael K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bryan, Tracey L</au><au>van Diepen, Sean</au><au>Bhutani, Mohit</au><au>Shanks, Miriam</au><au>Welsh, Robert C</au><au>Stickland, Michael K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of dobutamine and dopamine on intrapulmonary shunt and gas exchange in healthy humans</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2012-08-15</date><risdate>2012</risdate><volume>113</volume><issue>4</issue><spage>541</spage><epage>548</epage><pages>541-548</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><abstract>The development of intrapulmonary shunts with increased cardiac output during exercise in healthy humans has been reported in several recent studies, but mechanisms governing their recruitment remain unclear. Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, both can increase venous admixture/shunt fraction (Qs/Qt). It is possible that, as with exercise, intrapulmonary shunts are recruited with increased cardiac output during dobutamine and/or dopamine infusion that may contribute to the observed increase in Qs/Qt. The purpose of this study was to examine how dobutamine and dopamine affect intrapulmonary shunt and gas exchange. Nine resting healthy subjects received serial infusions of dobutamine and dopamine at incremental doses under normoxic and hyperoxic (inspired O(2) fraction = 1.0) conditions. At each step, alveolar-to-arterial Po(2) difference (A-aDo(2)) and Qs/Qt were calculated from arterial blood gas samples, intrapulmonary shunt was evaluated using contrast echocardiography, and cardiac output was calculated by Doppler echocardiography. Both dobutamine and dopamine increased cardiac output and Qs/Qt. Intrapulmonary shunt developed in most subjects with both drugs and paralleled the increase in Qs/Qt. A-aDo(2) was unchanged due to a concurrent rise in mixed venous oxygen content. Hyperoxia consistently eliminated intrapulmonary shunt. These findings contribute to our present understanding of the mechanisms governing recruitment of these intrapulmonary shunts as well as their impact on gas exchange. In addition, given the deleterious effect on Qs/Qt and the risk of neurological complications with intrapulmonary shunts, these findings could have important implications for use of dobutamine and dopamine in the clinical setting.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>22700799</pmid><doi>10.1152/japplphysiol.00404.2012</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Anatomy & physiology Arterial Pressure - drug effects Cardiac Output - drug effects Cardiotonic Agents - administration & dosage Dobutamine - administration & dosage Dopamine Dopamine - administration & dosage Dose-Response Relationship, Drug Echocardiography, Doppler Exercise Female Forced Expiratory Volume - drug effects Hemodynamics - drug effects Humans Hyperoxia - physiopathology Infusions, Intravenous Male Oxygen Consumption - drug effects Pharmaceuticals Pulmonary Alveoli - blood supply Pulmonary Alveoli - drug effects Pulmonary Alveoli - physiopathology Pulmonary Artery - diagnostic imaging Pulmonary Artery - drug effects Pulmonary Artery - physiopathology Pulmonary Circulation - drug effects Pulmonary Diffusing Capacity - drug effects Pulmonary Gas Exchange - drug effects Respiration Side effects Time Factors Vital Capacity - drug effects |
title | The effects of dobutamine and dopamine on intrapulmonary shunt and gas exchange in healthy humans |
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