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Effects of CI-914 in congestive heart failure due to coronary artery disease or idiopathic cardiomyopathy

dc.contributor.authorTerris, Susanen_US
dc.contributor.authorBourdillon, Patrick D. V.en_US
dc.contributor.authorCheng, Daviden_US
dc.contributor.authorLatts, Jeffreyen_US
dc.contributor.authorOlsen, Stevenen_US
dc.contributor.authorNicklas, John M.en_US
dc.contributor.authorPitt, Bertramen_US
dc.date.accessioned2006-04-07T19:26:27Z
dc.date.available2006-04-07T19:26:27Z
dc.date.issued1986-09-15en_US
dc.identifier.citationTerris, Susan, Bourdillon, Patrick D. V., Cheng, David, Latts, Jeffrey, Olsen, Steven, Nicklas, John, Pitt, Bertram (1986/09/15)."Effects of CI-914 in congestive heart failure due to coronary artery disease or idiopathic cardiomyopathy." The American Journal of Cardiology 58(7): 596-600. <http://hdl.handle.net/2027.42/26044>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4C6TPHW-TV/2/4a272fda6469f51744aaeee5f4f0e3d1en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26044
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3751929&dopt=citationen_US
dc.description.abstractThe hemodynamic effects of CI-914, a phosphodiesterase inhibitor, were studied in 12 patients with left ventricular (LV) dysfunction who were undergoing diagnostic cardiac catheterization. CI-914 was infused intravenously at a rate of 0.8 to 7.0 [mu]g/kg/min for 30 to 60 minutes; hemodynamic values were measured every 10 minutes. No effect was seen in the patient receiving 0.8 [mu]g/kg/min. At infusion rates of 1.2 to 2.4 [mu]g/kg/min, cardiac index increased by 14% (p 2, cardiac index increased by 50% (p 2 (group A). Although systemic vascular resistance decreased in all 8 patients by 26% (p 2; the double product fell from 101 +/- 31 to 91 +/- 23 (NS). In all 12 patients, a linear correlation between peak venous blood concentration and peak effect on cardiac index, systemic vascular resistance and pulmonary artery wedge pressure was observed. The increase in cardiac index associated with a decrease in systemic vascular resistance suggests that part of the favorable hemodynamic effect is attributable to afterload reduction. Nonetheless, the increase in peak +dP/dt in all patients suggests that CI-914 also has a positive inotropic effect. This combination of effects may be of value in the treatment of severe congestive heart failure.en_US
dc.format.extent549981 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleEffects of CI-914 in congestive heart failure due to coronary artery disease or idiopathic cardiomyopathyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USAen_US
dc.identifier.pmid3751929en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26044/1/0000117.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(86)90282-1en_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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