Acute haemodynamic and metabolic effects of dopexamine, a new dopaminergic receptor agonist, in patients with chronic heart failure
Dopexamine, a new compound with postjunctional dopamine receptor activating and beta adrenoceptor agonist properties, was given to 10 patients with chronic heart failure at diagnostic cardiac catheterisation to investigate its acute haemodynamic and metabolic effects. The drug was administered by in...
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Veröffentlicht in: | British Heart Journal 1985-09, Vol.54 (3), p.313-320 |
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description | Dopexamine, a new compound with postjunctional dopamine receptor activating and beta adrenoceptor agonist properties, was given to 10 patients with chronic heart failure at diagnostic cardiac catheterisation to investigate its acute haemodynamic and metabolic effects. The drug was administered by intravenous infusion in three incremental doses and produced significant dose related increases in cardiac index, stroke volume index, and heart rate and falls in systemic vascular resistance and left ventricular end diastolic pressure; aortic and pulmonary artery pressures were unchanged. Isovolumic phase (max dP/dt and KVmax) and ejection phase (peak aortic blood velocity, maximum acceleration of blood, and maximum rate of change of power with time during ejection) indices of myocardial contractility were all increased by dopexamine but these changes were hard to interpret in the presence of an increase in heart rate. Myocardial efficiency and ejection fraction were both increased and left ventricular end diastolic and end systolic volumes fell. These largely beneficial changes were achieved without a statistically significant increase in myocardial oxygen consumption or disturbance of myocardial metabolic function. Dopexamine was well tolerated but tremor was reported by two patients at the intermediate dose and mild chest pain by two patients at the high dose. |
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The drug was administered by intravenous infusion in three incremental doses and produced significant dose related increases in cardiac index, stroke volume index, and heart rate and falls in systemic vascular resistance and left ventricular end diastolic pressure; aortic and pulmonary artery pressures were unchanged. Isovolumic phase (max dP/dt and KVmax) and ejection phase (peak aortic blood velocity, maximum acceleration of blood, and maximum rate of change of power with time during ejection) indices of myocardial contractility were all increased by dopexamine but these changes were hard to interpret in the presence of an increase in heart rate. Myocardial efficiency and ejection fraction were both increased and left ventricular end diastolic and end systolic volumes fell. These largely beneficial changes were achieved without a statistically significant increase in myocardial oxygen consumption or disturbance of myocardial metabolic function. Dopexamine was well tolerated but tremor was reported by two patients at the intermediate dose and mild chest pain by two patients at the high dose.</description><identifier>ISSN: 0007-0769</identifier><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>EISSN: 2053-5864</identifier><identifier>DOI: 10.1136/hrt.54.3.313</identifier><identifier>PMID: 4041300</identifier><identifier>CODEN: BHJUAV</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Blood Flow Velocity - drug effects ; Cardiotonic agents ; Cardiovascular system ; Chemical Phenomena ; Chemistry ; Dopamine - administration & dosage ; Dopamine - analogs & derivatives ; Dopamine - metabolism ; Dopamine - therapeutic use ; Dose-Response Relationship, Drug ; Female ; Heart Failure - drug therapy ; Heart Rate - drug effects ; Hemodynamics - drug effects ; Humans ; Male ; Medical sciences ; Middle Aged ; Myocardial Contraction - drug effects ; Pharmacology. Drug treatments ; Stroke Volume - drug effects ; Vascular Resistance - drug effects</subject><ispartof>British Heart Journal, 1985-09, Vol.54 (3), p.313-320</ispartof><rights>1986 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Sep 1985</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b4203-c4bbf0f9f883199e677c3e14847a751a0937f3037fe96a1724b863c1dff3c7563</citedby><cites>FETCH-LOGICAL-b4203-c4bbf0f9f883199e677c3e14847a751a0937f3037fe96a1724b863c1dff3c7563</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/PMC481901/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC481901/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,729,782,786,887,27933,27934,53800,53802</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8609124$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4041300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dawson, J R</creatorcontrib><creatorcontrib>Thompson, D S</creatorcontrib><creatorcontrib>Signy, M</creatorcontrib><creatorcontrib>Juul, S M</creatorcontrib><creatorcontrib>Turnbull, P</creatorcontrib><creatorcontrib>Jenkins, B S</creatorcontrib><creatorcontrib>Webb-Peploe, M M</creatorcontrib><title>Acute haemodynamic and metabolic effects of dopexamine, a new dopaminergic receptor agonist, in patients with chronic heart failure</title><title>British Heart Journal</title><addtitle>Br Heart J</addtitle><description>Dopexamine, a new compound with postjunctional dopamine receptor activating and beta adrenoceptor agonist properties, was given to 10 patients with chronic heart failure at diagnostic cardiac catheterisation to investigate its acute haemodynamic and metabolic effects. The drug was administered by intravenous infusion in three incremental doses and produced significant dose related increases in cardiac index, stroke volume index, and heart rate and falls in systemic vascular resistance and left ventricular end diastolic pressure; aortic and pulmonary artery pressures were unchanged. Isovolumic phase (max dP/dt and KVmax) and ejection phase (peak aortic blood velocity, maximum acceleration of blood, and maximum rate of change of power with time during ejection) indices of myocardial contractility were all increased by dopexamine but these changes were hard to interpret in the presence of an increase in heart rate. Myocardial efficiency and ejection fraction were both increased and left ventricular end diastolic and end systolic volumes fell. These largely beneficial changes were achieved without a statistically significant increase in myocardial oxygen consumption or disturbance of myocardial metabolic function. Dopexamine was well tolerated but tremor was reported by two patients at the intermediate dose and mild chest pain by two patients at the high dose.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Flow Velocity - drug effects</subject><subject>Cardiotonic agents</subject><subject>Cardiovascular system</subject><subject>Chemical Phenomena</subject><subject>Chemistry</subject><subject>Dopamine - administration & dosage</subject><subject>Dopamine - analogs & derivatives</subject><subject>Dopamine - metabolism</subject><subject>Dopamine - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Rate - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocardial Contraction - drug effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Stroke Volume - drug effects</subject><subject>Vascular Resistance - drug effects</subject><issn>0007-0769</issn><issn>1355-6037</issn><issn>1468-201X</issn><issn>2053-5864</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</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>eNp9kb2PEzEQxVcIdBwHHS2SJRA02WDHjr1bXHGETykCCkDoGmvWGWcddu1g73J3Nf84DokioKCxNX6_N3rWK4qHjE4Z4_J5G4fpXEz5lDN-qzhlQlbljLKvt4tTSqkqqZL13eJeSps8irqSJ8WJoIJxSk-LnxdmHJC0gH1Y3XjonSHgV6THAZrQ5QmtRTMkEixZhS1eZ8TjhADxeLV7-T3HdSYjGtwOIRJYB-_SMCHOky0MDn32X7mhJaaNWTKkRYgDseC6MeL94o6FLuGDw31WfH796tPibbn88Obd4mJZNmJGeWlE01hqa1tVnNU1SqUMRyYqoUDNGdCaK8tpPrCWwNRMNJXkhq2s5UbNJT8rzvd7t2PT48rkWBE6vY2uh3ijAzj9t-Jdq9fhhxYVqynL_qcHfwzfR0yD7l0y2HXgMYxJK8llXYkqg4__ATdhjD7_TTOlKKNM0F2cyZ4yMaQU0R6TMKp3zercrJ4LzXVuNuOP_kx_hA9VZv3JQYdkoLMRvHHpiFWS1mwmMlbusVwQXh9liN-0VFzN9fsvC30pXyzF5UuhP2b-2Z5v-s3_A_4CpnfJjg</recordid><startdate>19850901</startdate><enddate>19850901</enddate><creator>Dawson, J R</creator><creator>Thompson, D S</creator><creator>Signy, M</creator><creator>Juul, S M</creator><creator>Turnbull, P</creator><creator>Jenkins, B S</creator><creator>Webb-Peploe, M M</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19850901</creationdate><title>Acute haemodynamic and metabolic effects of dopexamine, a new dopaminergic receptor agonist, in patients with chronic heart failure</title><author>Dawson, J R ; Thompson, D S ; Signy, M ; Juul, S M ; Turnbull, P ; Jenkins, B S ; Webb-Peploe, M M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b4203-c4bbf0f9f883199e677c3e14847a751a0937f3037fe96a1724b863c1dff3c7563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Flow Velocity - drug effects</topic><topic>Cardiotonic agents</topic><topic>Cardiovascular system</topic><topic>Chemical Phenomena</topic><topic>Chemistry</topic><topic>Dopamine - administration & dosage</topic><topic>Dopamine - analogs & derivatives</topic><topic>Dopamine - metabolism</topic><topic>Dopamine - therapeutic use</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Rate - drug effects</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocardial Contraction - drug effects</topic><topic>Pharmacology. Drug treatments</topic><topic>Stroke Volume - drug effects</topic><topic>Vascular Resistance - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dawson, J R</creatorcontrib><creatorcontrib>Thompson, D S</creatorcontrib><creatorcontrib>Signy, M</creatorcontrib><creatorcontrib>Juul, S M</creatorcontrib><creatorcontrib>Turnbull, P</creatorcontrib><creatorcontrib>Jenkins, B S</creatorcontrib><creatorcontrib>Webb-Peploe, M M</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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>ProQuest Central</collection><collection>BMJ Journals</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British Heart Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dawson, J R</au><au>Thompson, D S</au><au>Signy, M</au><au>Juul, S M</au><au>Turnbull, P</au><au>Jenkins, B S</au><au>Webb-Peploe, M M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute haemodynamic and metabolic effects of dopexamine, a new dopaminergic receptor agonist, in patients with chronic heart failure</atitle><jtitle>British Heart Journal</jtitle><addtitle>Br Heart J</addtitle><date>1985-09-01</date><risdate>1985</risdate><volume>54</volume><issue>3</issue><spage>313</spage><epage>320</epage><pages>313-320</pages><issn>0007-0769</issn><issn>1355-6037</issn><eissn>1468-201X</eissn><eissn>2053-5864</eissn><coden>BHJUAV</coden><abstract>Dopexamine, a new compound with postjunctional dopamine receptor activating and beta adrenoceptor agonist properties, was given to 10 patients with chronic heart failure at diagnostic cardiac catheterisation to investigate its acute haemodynamic and metabolic effects. The drug was administered by intravenous infusion in three incremental doses and produced significant dose related increases in cardiac index, stroke volume index, and heart rate and falls in systemic vascular resistance and left ventricular end diastolic pressure; aortic and pulmonary artery pressures were unchanged. Isovolumic phase (max dP/dt and KVmax) and ejection phase (peak aortic blood velocity, maximum acceleration of blood, and maximum rate of change of power with time during ejection) indices of myocardial contractility were all increased by dopexamine but these changes were hard to interpret in the presence of an increase in heart rate. Myocardial efficiency and ejection fraction were both increased and left ventricular end diastolic and end systolic volumes fell. These largely beneficial changes were achieved without a statistically significant increase in myocardial oxygen consumption or disturbance of myocardial metabolic function. Dopexamine was well tolerated but tremor was reported by two patients at the intermediate dose and mild chest pain by two patients at the high dose.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>4041300</pmid><doi>10.1136/hrt.54.3.313</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biological and medical sciences Blood Flow Velocity - drug effects Cardiotonic agents Cardiovascular system Chemical Phenomena Chemistry Dopamine - administration & dosage Dopamine - analogs & derivatives Dopamine - metabolism Dopamine - therapeutic use Dose-Response Relationship, Drug Female Heart Failure - drug therapy Heart Rate - drug effects Hemodynamics - drug effects Humans Male Medical sciences Middle Aged Myocardial Contraction - drug effects Pharmacology. Drug treatments Stroke Volume - drug effects Vascular Resistance - drug effects |
title | Acute haemodynamic and metabolic effects of dopexamine, a new dopaminergic receptor agonist, in patients with chronic heart failure |
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