Effects of intravenous milrinone on left ventricular function in ischemic and idiopathic dilated cardiomyopathy
M-mode echocardiography and Doppler were used to assess the effects of phosphodiesterase inhibition on subendocardial function in dilated cardiomyopathy, and in particular, to study interactions with both systolic and diastolic left ventricular function. Twelve adult patients with dilated cardiomyop...
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Veröffentlicht in: | The American journal of cardiology 1993-01, Vol.71 (2), p.203-209 |
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description | M-mode echocardiography and Doppler were used to assess the effects of phosphodiesterase inhibition on subendocardial function in dilated cardiomyopathy, and in particular, to study interactions with both systolic and diastolic left ventricular function. Twelve adult patients with dilated cardiomyopathy were studied (6 ischemic in origin and 6 idiopathic), 7 of whom were being considered for cardiac transplantation. Cardiac index increased without significant change in heart rate or blood pressure. Longitudinal mitral ring motion, which had been uniformly reduced, increased markedly after intravenous milrinone. Left ventricular cavity size decreased, and shortening fraction, posterior wall thickness, and rates of posterior wall thickening and thinning increased markedly. Left atrial pressure decreased, and isovolumic relaxation time increased. However, the peak velocity and duration of the transmitral E wave increased, with no change in the A wave. Improved longitudinal (subendocardial) function was reflected by improved posterior wall dynamics, and early filling, possibly by augmentation of restoring forces. Thus, severely reduced subendocardial function in dilated cardiomyopathy is potentially reversible, with marked effects on systolic and diastolic function. These previously unrecognized actions of milrinone provide further evidence to justify its snort-term use in supporting the severely depressed myocardium. |
doi_str_mv | 10.1016/0002-9149(93)90739-Y |
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Twelve adult patients with dilated cardiomyopathy were studied (6 ischemic in origin and 6 idiopathic), 7 of whom were being considered for cardiac transplantation. Cardiac index increased without significant change in heart rate or blood pressure. Longitudinal mitral ring motion, which had been uniformly reduced, increased markedly after intravenous milrinone. Left ventricular cavity size decreased, and shortening fraction, posterior wall thickness, and rates of posterior wall thickening and thinning increased markedly. Left atrial pressure decreased, and isovolumic relaxation time increased. However, the peak velocity and duration of the transmitral E wave increased, with no change in the A wave. Improved longitudinal (subendocardial) function was reflected by improved posterior wall dynamics, and early filling, possibly by augmentation of restoring forces. Thus, severely reduced subendocardial function in dilated cardiomyopathy is potentially reversible, with marked effects on systolic and diastolic function. These previously unrecognized actions of milrinone provide further evidence to justify its snort-term use in supporting the severely depressed myocardium.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/0002-9149(93)90739-Y</identifier><identifier>PMID: 8421984</identifier><identifier>CODEN: AJCDAG</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Cardiomyopathy, Dilated - diagnostic imaging ; Cardiomyopathy, Dilated - physiopathology ; Cardiotonic agents ; Cardiotonic Agents - pharmacology ; Cardiovascular disease ; Cardiovascular system ; Drug therapy ; Echocardiography ; Echocardiography, Doppler ; Hemodynamics - drug effects ; Humans ; Male ; Medical research ; Medical sciences ; Middle Aged ; Milrinone ; Myocardial Contraction - drug effects ; Pharmacology. 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Jan 15, 1993</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-88a58d6e7448a36f70356297265baf4f8cd68bb61579e5f5490ac143ec6522353</citedby><cites>FETCH-LOGICAL-c413t-88a58d6e7448a36f70356297265baf4f8cd68bb61579e5f5490ac143ec6522353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/000291499390739Y$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4605233$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8421984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brecker, Stephen J.D.</creatorcontrib><creatorcontrib>Xiao, Han B.</creatorcontrib><creatorcontrib>Mbaissouroum, Mouanodji</creatorcontrib><creatorcontrib>Gibson, Derek G.</creatorcontrib><title>Effects of intravenous milrinone on left ventricular function in ischemic and idiopathic dilated cardiomyopathy</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>M-mode echocardiography and Doppler were used to assess the effects of phosphodiesterase inhibition on subendocardial function in dilated cardiomyopathy, and in particular, to study interactions with both systolic and diastolic left ventricular function. Twelve adult patients with dilated cardiomyopathy were studied (6 ischemic in origin and 6 idiopathic), 7 of whom were being considered for cardiac transplantation. Cardiac index increased without significant change in heart rate or blood pressure. Longitudinal mitral ring motion, which had been uniformly reduced, increased markedly after intravenous milrinone. Left ventricular cavity size decreased, and shortening fraction, posterior wall thickness, and rates of posterior wall thickening and thinning increased markedly. Left atrial pressure decreased, and isovolumic relaxation time increased. However, the peak velocity and duration of the transmitral E wave increased, with no change in the A wave. Improved longitudinal (subendocardial) function was reflected by improved posterior wall dynamics, and early filling, possibly by augmentation of restoring forces. Thus, severely reduced subendocardial function in dilated cardiomyopathy is potentially reversible, with marked effects on systolic and diastolic function. These previously unrecognized actions of milrinone provide further evidence to justify its snort-term use in supporting the severely depressed myocardium.</description><subject>Biological and medical sciences</subject><subject>Cardiomyopathy, Dilated - diagnostic imaging</subject><subject>Cardiomyopathy, Dilated - physiopathology</subject><subject>Cardiotonic agents</subject><subject>Cardiotonic Agents - pharmacology</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular system</subject><subject>Drug therapy</subject><subject>Echocardiography</subject><subject>Echocardiography, Doppler</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Milrinone</subject><subject>Myocardial Contraction - drug effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Pyridones - pharmacology</subject><subject>Ultrasonic imaging</subject><subject>Ventricular Function, Left - drug effects</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU2LFDEQDaKs4-g_UAgioofWpPPRyWVBllUXFvayHvYUMkmFzdKdjEn3wvz7zewMc_AgBELVe1Wv6hVC7yn5RgmV3wkhfacp1180-6rJwHR39wKtqBp0RzVlL9HqRHmN3tT60EJKhTxDZ4r3VCu-QvkyBHBzxTngmOZiHyHlpeIpjiWmnADnhEcIM27AXKJbRltwWJKbY0Nie9XdwxQdtsnj6GPe2vm-hT6OdgaPnS0tOe2e87u36FWwY4V3x3-N_vy8vL343V3f_Lq6-HHdOU7Z3CllhfISBs6VZTIMhAnZ66GXYmMDD8p5qTYbScWgQQTBNbGOcgZOir5ngq3R50Pfbcl_F6izmdqgMI42QdvPDEIILpvWGn38h_iQl5LabKZnTZX2mjUSP5BcybUWCGZb4mTLzlBi9scwe6fN3mmjmXk-hrlrZR-OvZfNBP5UdHS_4Z-OuK3OjqHY5GI90bgkomd79fMDDZphjxGKqS5CcuBjabczPsf_z_EE9QimYQ</recordid><startdate>19930115</startdate><enddate>19930115</enddate><creator>Brecker, Stephen J.D.</creator><creator>Xiao, Han B.</creator><creator>Mbaissouroum, Mouanodji</creator><creator>Gibson, Derek G.</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</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>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19930115</creationdate><title>Effects of intravenous milrinone on left ventricular function in ischemic and idiopathic dilated cardiomyopathy</title><author>Brecker, Stephen J.D. ; Xiao, Han B. ; Mbaissouroum, Mouanodji ; Gibson, Derek G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-88a58d6e7448a36f70356297265baf4f8cd68bb61579e5f5490ac143ec6522353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Biological and medical sciences</topic><topic>Cardiomyopathy, Dilated - diagnostic imaging</topic><topic>Cardiomyopathy, Dilated - physiopathology</topic><topic>Cardiotonic agents</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular system</topic><topic>Drug therapy</topic><topic>Echocardiography</topic><topic>Echocardiography, Doppler</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Milrinone</topic><topic>Myocardial Contraction - drug effects</topic><topic>Pharmacology. Drug treatments</topic><topic>Pyridones - pharmacology</topic><topic>Ultrasonic imaging</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brecker, Stephen J.D.</creatorcontrib><creatorcontrib>Xiao, Han B.</creatorcontrib><creatorcontrib>Mbaissouroum, Mouanodji</creatorcontrib><creatorcontrib>Gibson, Derek G.</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>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brecker, Stephen J.D.</au><au>Xiao, Han B.</au><au>Mbaissouroum, Mouanodji</au><au>Gibson, Derek G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of intravenous milrinone on left ventricular function in ischemic and idiopathic dilated cardiomyopathy</atitle><jtitle>The American journal of cardiology</jtitle><addtitle>Am J Cardiol</addtitle><date>1993-01-15</date><risdate>1993</risdate><volume>71</volume><issue>2</issue><spage>203</spage><epage>209</epage><pages>203-209</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><coden>AJCDAG</coden><abstract>M-mode echocardiography and Doppler were used to assess the effects of phosphodiesterase inhibition on subendocardial function in dilated cardiomyopathy, and in particular, to study interactions with both systolic and diastolic left ventricular function. Twelve adult patients with dilated cardiomyopathy were studied (6 ischemic in origin and 6 idiopathic), 7 of whom were being considered for cardiac transplantation. Cardiac index increased without significant change in heart rate or blood pressure. Longitudinal mitral ring motion, which had been uniformly reduced, increased markedly after intravenous milrinone. Left ventricular cavity size decreased, and shortening fraction, posterior wall thickness, and rates of posterior wall thickening and thinning increased markedly. Left atrial pressure decreased, and isovolumic relaxation time increased. However, the peak velocity and duration of the transmitral E wave increased, with no change in the A wave. Improved longitudinal (subendocardial) function was reflected by improved posterior wall dynamics, and early filling, possibly by augmentation of restoring forces. Thus, severely reduced subendocardial function in dilated cardiomyopathy is potentially reversible, with marked effects on systolic and diastolic function. These previously unrecognized actions of milrinone provide further evidence to justify its snort-term use in supporting the severely depressed myocardium.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8421984</pmid><doi>10.1016/0002-9149(93)90739-Y</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Cardiomyopathy, Dilated - diagnostic imaging Cardiomyopathy, Dilated - physiopathology Cardiotonic agents Cardiotonic Agents - pharmacology Cardiovascular disease Cardiovascular system Drug therapy Echocardiography Echocardiography, Doppler Hemodynamics - drug effects Humans Male Medical research Medical sciences Middle Aged Milrinone Myocardial Contraction - drug effects Pharmacology. Drug treatments Pyridones - pharmacology Ultrasonic imaging Ventricular Function, Left - drug effects |
title | Effects of intravenous milrinone on left ventricular function in ischemic and idiopathic dilated cardiomyopathy |
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