| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Circulation, Vol 59, 1098-1104, Copyright © 1979 by American Heart Association
TH LeJemtel, E Keung, EH Sonnenblick, HS Ribner, M Matsumoto, R Davis, W Schwartz, AA Alousi and D Davolos
Chronic congestive heart failure not controlled by conventional therapy was
treated with intravenous amrinone, a new non-glycosidic, non- catecholamine
cardiotonic agent. Eight patients with New York Heart Association
functional class III-IV symptoms were hemodynamically monitored. At peak
effect, cardiac index (CI) increased from 1.84 +/- 0.32 to 2.74 +/- 0.44
l/min/m2 (mean +/- SD) (p less than 0.001) and left ventricular filling
pressure (LVFP) decreased from 25.8 +/- 6.2 to 19.5 +/- 6.8 mm Hg (p less
than 0.05), while heart rate and mean aortic blood pressure did not change
significantly. Mean endocardial circumferential fiber shortening (mean
Vcf), determined by echocardiography, increased from 0.61 +/- 0.27 to 0.89
+/- 0.34 cir/sec (p less than 0.05). The duration of action after bolus
infusion varied from 60--90 minutes. During continuous infusion of
amrinone, sustained increases in CI and reductions in LVFP, similar to
those at the time of peak effect after bolus administration, were
maintained for 180 minutes. These marked cardiotonic effects of amrinone in
patients already taking digitalis for severe heart failure occurred without
side effects of arrhythmias or altered arterial pressures. The fact that
the drug is orally active makes amrinone a v:ry promising inotropic agent
for the treatment of chronic heart failure in man.
ARTICLES
Amrinone: a new non-glycosidic, non-adrenergic cardiotonic agent effective in the treatment of intractable myocardial failure in man
This article has been cited by other articles:
![]() |
M. Azuma, M. Yamane, K. Tachibana, Y. Morimoto, and O. Kemmotsu Effects of epinephrine and phosphodiesterase III inhibitors on bupivacaine-induced myocardial depression in guinea-pig papillary muscle Br. J. Anaesth., January 1, 2003; 90(1): 66 - 71. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Uemura, Y. Fujii, and H. Toyooka Inhaled olprinone improves contractility of fatigued canine diaphragm Br. J. Anaesth., March 1, 2002; 88(3): 408 - 411. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Fujii, T. Hoshi, and H. Toyooka Colforsin Daropate Improves Contractility in Fatigued Canine Diaphragm Anesth. Analg., March 1, 2001; 92(3): 762 - 766. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y Fujii and H Toyooka Different effects of olprinone on contractility in nonfatigued and fatigued diaphragm in dogs Can J Anesth, December 1, 2000; 47(12): 1243 - 1248. [Abstract] |
||||
![]() |
A. K. Pridjian, E. D. Frohlich, C. H. VanMeter, P. M. McFadden, and J. L. Ochsner Pharmacologic Support With High-Energy Phosphate Preservation in the Postischemic Neonatal Heart Ann. Thorac. Surg., June 1, 1995; 59(6): 1435 - 1440. [Abstract] [Full Text] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1979 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |