Dopamine therapy does not affect cerebral autoregulation during hypotension in newborn piglets
Hypotensive neonates who have been treated with dopamine have poorer neurodevelopmental outcome than those who have not been treated with dopamine. We speculate that dopamine stimulates adrenoceptors on cerebral arteries causing cerebral vasoconstriction. This vasoconstriction might lead to a rightw...
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description | Hypotensive neonates who have been treated with dopamine have poorer neurodevelopmental outcome than those who have not been treated with dopamine. We speculate that dopamine stimulates adrenoceptors on cerebral arteries causing cerebral vasoconstriction. This vasoconstriction might lead to a rightward shift of the cerebral autoregulatory curve; consequently, infants treated with dopamine would have a higher risk of low cerebral blood flow at a blood pressure that is otherwise considered "safe".
In anaesthetized piglets, perfusion of the brain, monitored with laser-doppler flowmetry, and cerebral venous saturation was measured at different levels of hypotension. Each piglet was studied in two phases: a phase with stepwise decreases in MAP and a phase with stepwise increases in MAP. We randomized the order of the two phases, whether dopamine was given in the first or second phase, and the infusion rate of dopamine (10, 25, or 40 μg/kg/min). In/deflation of a balloon catheter, placed in vena cava, induced different levels of hypotension. At each level of hypotension, fluctuations in MAP were induced by in/deflations of a balloon catheter in descending aorta.
During measurements, PaCO2 and arterial saturation were stable. MAP levels ranged between 14 and 82 mmHg. Cerebral autoregulation (CA) capacity was calculated as the ratio between %-change in cerebrovascular resistance and %-change in MAP induced by the in/deflation of the arterial balloon. A breakpoint in CA capacity was identified at a MAP of 38±18 mmHg without dopamine and at 44±18, 31±14, and 24±14 mmHg with dopamine infusion rates of 10, 25, and 40 μg/kg/min (p = 0.057). Neither the index of steady-state cerebral perfusion nor cerebral venous saturation were affected by dopamine infusion.
Dopamine infusion tended to improve CA capacity at low blood pressures while an index of steady-state cerebral blood flow and cerebral venous saturation were unaffected by dopamine infusion. Thus, dopamine does not appear to impair CA in newborn piglets. |
doi_str_mv | 10.1371/journal.pone.0170738 |
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In anaesthetized piglets, perfusion of the brain, monitored with laser-doppler flowmetry, and cerebral venous saturation was measured at different levels of hypotension. Each piglet was studied in two phases: a phase with stepwise decreases in MAP and a phase with stepwise increases in MAP. We randomized the order of the two phases, whether dopamine was given in the first or second phase, and the infusion rate of dopamine (10, 25, or 40 μg/kg/min). In/deflation of a balloon catheter, placed in vena cava, induced different levels of hypotension. At each level of hypotension, fluctuations in MAP were induced by in/deflations of a balloon catheter in descending aorta.
During measurements, PaCO2 and arterial saturation were stable. MAP levels ranged between 14 and 82 mmHg. Cerebral autoregulation (CA) capacity was calculated as the ratio between %-change in cerebrovascular resistance and %-change in MAP induced by the in/deflation of the arterial balloon. A breakpoint in CA capacity was identified at a MAP of 38±18 mmHg without dopamine and at 44±18, 31±14, and 24±14 mmHg with dopamine infusion rates of 10, 25, and 40 μg/kg/min (p = 0.057). Neither the index of steady-state cerebral perfusion nor cerebral venous saturation were affected by dopamine infusion.
Dopamine infusion tended to improve CA capacity at low blood pressures while an index of steady-state cerebral blood flow and cerebral venous saturation were unaffected by dopamine infusion. Thus, dopamine does not appear to impair CA in newborn piglets.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0170738</identifier><identifier>PMID: 28141842</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animals ; Animals, Newborn ; Aorta ; Arteries ; Balloon catheters ; Biology and Life Sciences ; Blood ; Blood flow ; Blood pressure ; Blood Pressure - drug effects ; Brain ; Brain - drug effects ; Brain - pathology ; Brain - physiopathology ; Care and treatment ; Cerebral blood flow ; Cerebrovascular Circulation - drug effects ; Cerebrovascular system ; Circulatory system ; Dopamine ; Dopamine - pharmacology ; Dopamine - therapeutic use ; Doppler effect ; Dosage and administration ; Drug therapy ; Equilibrium flow ; Homeostasis - drug effects ; Hypotension ; Hypotension - drug therapy ; Hypotension - pathology ; Hypotension - physiopathology ; Infants ; Kinases ; Medical instruments ; Medicine and Health Sciences ; Neonates ; Newborn babies ; Perfusion ; Physical Sciences ; Receptors (physiology) ; Research and Analysis Methods ; Saturation ; Steady state ; Sus scrofa ; Swine ; Variation ; Vasoconstriction</subject><ispartof>PloS one, 2017-01, Vol.12 (1), p.e0170738-e0170738</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Eriksen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Eriksen et al 2017 Eriksen et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c725t-f25a224f37ecd47d47d8f88a928812092a24bb95796cf025b8b338026950c4ac3</citedby><cites>FETCH-LOGICAL-c725t-f25a224f37ecd47d47d8f88a928812092a24bb95796cf025b8b338026950c4ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283654/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283654/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28141842$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Torrens, Christopher</contributor><creatorcontrib>Eriksen, Vibeke Ramsgaard</creatorcontrib><creatorcontrib>Rasmussen, Martin Bo</creatorcontrib><creatorcontrib>Hahn, Gitte Holst</creatorcontrib><creatorcontrib>Greisen, Gorm</creatorcontrib><title>Dopamine therapy does not affect cerebral autoregulation during hypotension in newborn piglets</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Hypotensive neonates who have been treated with dopamine have poorer neurodevelopmental outcome than those who have not been treated with dopamine. We speculate that dopamine stimulates adrenoceptors on cerebral arteries causing cerebral vasoconstriction. This vasoconstriction might lead to a rightward shift of the cerebral autoregulatory curve; consequently, infants treated with dopamine would have a higher risk of low cerebral blood flow at a blood pressure that is otherwise considered "safe".
In anaesthetized piglets, perfusion of the brain, monitored with laser-doppler flowmetry, and cerebral venous saturation was measured at different levels of hypotension. Each piglet was studied in two phases: a phase with stepwise decreases in MAP and a phase with stepwise increases in MAP. We randomized the order of the two phases, whether dopamine was given in the first or second phase, and the infusion rate of dopamine (10, 25, or 40 μg/kg/min). In/deflation of a balloon catheter, placed in vena cava, induced different levels of hypotension. At each level of hypotension, fluctuations in MAP were induced by in/deflations of a balloon catheter in descending aorta.
During measurements, PaCO2 and arterial saturation were stable. MAP levels ranged between 14 and 82 mmHg. Cerebral autoregulation (CA) capacity was calculated as the ratio between %-change in cerebrovascular resistance and %-change in MAP induced by the in/deflation of the arterial balloon. A breakpoint in CA capacity was identified at a MAP of 38±18 mmHg without dopamine and at 44±18, 31±14, and 24±14 mmHg with dopamine infusion rates of 10, 25, and 40 μg/kg/min (p = 0.057). Neither the index of steady-state cerebral perfusion nor cerebral venous saturation were affected by dopamine infusion.
Dopamine infusion tended to improve CA capacity at low blood pressures while an index of steady-state cerebral blood flow and cerebral venous saturation were unaffected by dopamine infusion. Thus, dopamine does not appear to impair CA in newborn piglets.</description><subject>Analysis</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Aorta</subject><subject>Arteries</subject><subject>Balloon catheters</subject><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>Blood flow</subject><subject>Blood pressure</subject><subject>Blood Pressure - drug effects</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Care and treatment</subject><subject>Cerebral blood flow</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Cerebrovascular system</subject><subject>Circulatory system</subject><subject>Dopamine</subject><subject>Dopamine - pharmacology</subject><subject>Dopamine - therapeutic use</subject><subject>Doppler effect</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Equilibrium flow</subject><subject>Homeostasis - drug effects</subject><subject>Hypotension</subject><subject>Hypotension - drug therapy</subject><subject>Hypotension - pathology</subject><subject>Hypotension - physiopathology</subject><subject>Infants</subject><subject>Kinases</subject><subject>Medical instruments</subject><subject>Medicine and Health Sciences</subject><subject>Neonates</subject><subject>Newborn babies</subject><subject>Perfusion</subject><subject>Physical Sciences</subject><subject>Receptors (physiology)</subject><subject>Research and Analysis Methods</subject><subject>Saturation</subject><subject>Steady state</subject><subject>Sus scrofa</subject><subject>Swine</subject><subject>Variation</subject><subject>Vasoconstriction</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</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><sourceid>DOA</sourceid><recordid>eNqNk1trFDEUxwdRbK1-A9EBQfRh11wml3kRSr0tFAreHg1JJjObMptMk4y6395Md1p2pQ8lgYST3_nn5JycongOwRJiBt9d-jE42S8H78wSQAYY5g-KY1hjtKAI4Id7-6PiSYyXABDMKX1cHCEOK8grdFz8-uAHubHOlGltghy2ZeNNLJ1PpWxbo1OpTTAqyL6UY_LBdGMvk_WubMZgXVeut4NPxsXJZF3pzB_lgysH2_UmxafFo1b20Tyb15Pix6eP38--LM4vPq_OTs8XmiGSFi0iEqGqxczopmLT5C3nskacQwRqJFGlVE1YTXULEFFcYcwBojUBupIanxQvd7pD76OYUxMF5BTDmrKKZmK1IxovL8UQ7EaGrfDSimuDD52QIVndGwEZ1pJSpDABFZeN4lARJTVVOlsUy1rv59tGtTGNNi7lBB2IHp44uxad_y0I4piSKgu8mQWCvxpNTGJjozZ9L53x43XcHCOI6_o-KGaAZDijr_5D707ETHUyv9W61ucQ9SQqTisOAa4ZJJla3kHl0ZiN1fnLtTbbDxzeHjhkJpm_qZNjjGL17ev92Yufh-zrPXZtZJ_W0ffj9AfjIVjtQB18jMG0t_WAQEwdc5MNMXWMmDsmu73Yr-Wt002L4H8uABBu</recordid><startdate>20170131</startdate><enddate>20170131</enddate><creator>Eriksen, Vibeke Ramsgaard</creator><creator>Rasmussen, Martin Bo</creator><creator>Hahn, Gitte Holst</creator><creator>Greisen, Gorm</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170131</creationdate><title>Dopamine therapy does not affect cerebral autoregulation during hypotension in newborn piglets</title><author>Eriksen, Vibeke Ramsgaard ; Rasmussen, Martin Bo ; Hahn, Gitte Holst ; Greisen, Gorm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-f25a224f37ecd47d47d8f88a928812092a24bb95796cf025b8b338026950c4ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Aorta</topic><topic>Arteries</topic><topic>Balloon catheters</topic><topic>Biology and Life Sciences</topic><topic>Blood</topic><topic>Blood flow</topic><topic>Blood pressure</topic><topic>Blood Pressure - drug effects</topic><topic>Brain</topic><topic>Brain - drug effects</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Care and treatment</topic><topic>Cerebral blood flow</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Cerebrovascular system</topic><topic>Circulatory system</topic><topic>Dopamine</topic><topic>Dopamine - pharmacology</topic><topic>Dopamine - therapeutic use</topic><topic>Doppler effect</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Equilibrium flow</topic><topic>Homeostasis - drug effects</topic><topic>Hypotension</topic><topic>Hypotension - drug therapy</topic><topic>Hypotension - pathology</topic><topic>Hypotension - physiopathology</topic><topic>Infants</topic><topic>Kinases</topic><topic>Medical instruments</topic><topic>Medicine and Health Sciences</topic><topic>Neonates</topic><topic>Newborn babies</topic><topic>Perfusion</topic><topic>Physical Sciences</topic><topic>Receptors (physiology)</topic><topic>Research and Analysis Methods</topic><topic>Saturation</topic><topic>Steady state</topic><topic>Sus scrofa</topic><topic>Swine</topic><topic>Variation</topic><topic>Vasoconstriction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eriksen, Vibeke Ramsgaard</creatorcontrib><creatorcontrib>Rasmussen, Martin Bo</creatorcontrib><creatorcontrib>Hahn, Gitte Holst</creatorcontrib><creatorcontrib>Greisen, Gorm</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eriksen, Vibeke Ramsgaard</au><au>Rasmussen, Martin Bo</au><au>Hahn, Gitte Holst</au><au>Greisen, Gorm</au><au>Torrens, Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dopamine therapy does not affect cerebral autoregulation during hypotension in newborn piglets</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-01-31</date><risdate>2017</risdate><volume>12</volume><issue>1</issue><spage>e0170738</spage><epage>e0170738</epage><pages>e0170738-e0170738</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hypotensive neonates who have been treated with dopamine have poorer neurodevelopmental outcome than those who have not been treated with dopamine. We speculate that dopamine stimulates adrenoceptors on cerebral arteries causing cerebral vasoconstriction. This vasoconstriction might lead to a rightward shift of the cerebral autoregulatory curve; consequently, infants treated with dopamine would have a higher risk of low cerebral blood flow at a blood pressure that is otherwise considered "safe".
In anaesthetized piglets, perfusion of the brain, monitored with laser-doppler flowmetry, and cerebral venous saturation was measured at different levels of hypotension. Each piglet was studied in two phases: a phase with stepwise decreases in MAP and a phase with stepwise increases in MAP. We randomized the order of the two phases, whether dopamine was given in the first or second phase, and the infusion rate of dopamine (10, 25, or 40 μg/kg/min). In/deflation of a balloon catheter, placed in vena cava, induced different levels of hypotension. At each level of hypotension, fluctuations in MAP were induced by in/deflations of a balloon catheter in descending aorta.
During measurements, PaCO2 and arterial saturation were stable. MAP levels ranged between 14 and 82 mmHg. Cerebral autoregulation (CA) capacity was calculated as the ratio between %-change in cerebrovascular resistance and %-change in MAP induced by the in/deflation of the arterial balloon. A breakpoint in CA capacity was identified at a MAP of 38±18 mmHg without dopamine and at 44±18, 31±14, and 24±14 mmHg with dopamine infusion rates of 10, 25, and 40 μg/kg/min (p = 0.057). Neither the index of steady-state cerebral perfusion nor cerebral venous saturation were affected by dopamine infusion.
Dopamine infusion tended to improve CA capacity at low blood pressures while an index of steady-state cerebral blood flow and cerebral venous saturation were unaffected by dopamine infusion. Thus, dopamine does not appear to impair CA in newborn piglets.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28141842</pmid><doi>10.1371/journal.pone.0170738</doi><tpages>e0170738</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Animals, Newborn Aorta Arteries Balloon catheters Biology and Life Sciences Blood Blood flow Blood pressure Blood Pressure - drug effects Brain Brain - drug effects Brain - pathology Brain - physiopathology Care and treatment Cerebral blood flow Cerebrovascular Circulation - drug effects Cerebrovascular system Circulatory system Dopamine Dopamine - pharmacology Dopamine - therapeutic use Doppler effect Dosage and administration Drug therapy Equilibrium flow Homeostasis - drug effects Hypotension Hypotension - drug therapy Hypotension - pathology Hypotension - physiopathology Infants Kinases Medical instruments Medicine and Health Sciences Neonates Newborn babies Perfusion Physical Sciences Receptors (physiology) Research and Analysis Methods Saturation Steady state Sus scrofa Swine Variation Vasoconstriction |
title | Dopamine therapy does not affect cerebral autoregulation during hypotension in newborn piglets |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T09%3A16%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dopamine%20therapy%20does%20not%20affect%20cerebral%20autoregulation%20during%20hypotension%20in%20newborn%20piglets&rft.jtitle=PloS%20one&rft.au=Eriksen,%20Vibeke%20Ramsgaard&rft.date=2017-01-31&rft.volume=12&rft.issue=1&rft.spage=e0170738&rft.epage=e0170738&rft.pages=e0170738-e0170738&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0170738&rft_dat=%3Cgale_plos_%3EA481039715%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1863196746&rft_id=info:pmid/28141842&rft_galeid=A481039715&rft_doaj_id=oai_doaj_org_article_173ca662b35048adb81b5bac6bc350b7&rfr_iscdi=true |