Effects of CI-914 in congestive heart failure due to coronary artery disease or idiopathic cardiomyopathy
dc.contributor.author | Terris, Susan | en_US |
dc.contributor.author | Bourdillon, Patrick D. V. | en_US |
dc.contributor.author | Cheng, David | en_US |
dc.contributor.author | Latts, Jeffrey | en_US |
dc.contributor.author | Olsen, Steven | en_US |
dc.contributor.author | Nicklas, John M. | en_US |
dc.contributor.author | Pitt, Bertram | en_US |
dc.date.accessioned | 2006-04-07T19:26:27Z | |
dc.date.available | 2006-04-07T19:26:27Z | |
dc.date.issued | 1986-09-15 | en_US |
dc.identifier.citation | Terris, 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.uri | http://www.sciencedirect.com/science/article/B6T10-4C6TPHW-TV/2/4a272fda6469f51744aaeee5f4f0e3d1 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/26044 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3751929&dopt=citation | en_US |
dc.description.abstract | The 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.extent | 549981 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Effects of CI-914 in congestive heart failure due to coronary artery disease or idiopathic cardiomyopathy | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Internal Medicine and Specialties | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.contributor.affiliationum | Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, and Warner-Lambert/Parke Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA | en_US |
dc.identifier.pmid | 3751929 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/26044/1/0000117.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0002-9149(86)90282-1 | en_US |
dc.identifier.source | The American Journal of Cardiology | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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