|
|
||||||||
The Journal of Thoracic and Cardiovascular Surgery, Vol 102, 246-258, Copyright © 1991 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
HR Lee, RE Hershberger, JD Port, R Rasmussen, DG Renlund, JB O'Connell, EM Gilbert, PC Mealey, K Volkman and R Menlove
During a 3-year period we administered enoximone, a phosphodiesterase
inhibitor with positive inotropic and vasodilator properties, to 73
pretransplantation patients with end-stage heart failure who exhibited a
clinical requirement for additional inotropic support. The clinical course
and myocardial beta-adrenergic receptor status in the explanted hearts of
these 73 patients was compared with results in 113 concurrently listed
pretransplantation patients not requiring additional inotropic support.
Only three patients required cessation of enoximone because of adverse
effects, all from exacerbation of ventricular arrhythmias. Sixty-six of 73
(90.4%) enoximone-treated patients ultimately underwent cardiac
transplantation a mean of 39.2 +/- 6.6 days (range 1 to 221 days) after
starting enoximone, whereas seven patients (9.6%) died awaiting cardiac
transplantation. The respective 1- , 3-, and 6-month pretransplantation
survival rates of patients treated with enoximone calculated from their
time on the waiting list for transplantation were 88.0%, 82.5%, and 82.5%
compared with 92.1%, 83.8%, and 76.2% in control patients not receiving
enoximone (all p = not significant). In 25 patients who received enoximone,
ventricular myocardial beta-adrenergic receptors were measured at the time
of transplantation and compared with values in failing ventricles from 52
pretransplantation patients not exposed to enoximone. Compared with
ventricular myocardium of patients not given enoximone or intravenous
beta-adrenergic agonists, total beta-adrenergic receptor (beta 1 plus beta
2) density was not decreased in patients treated with enoximone or
enoximone plus intravenous beta-adrenergic agonists, but was decreased by
31% (p less than 0.05) in patients given intravenous beta-adrenergic
agonists alone. Additionally, patients treated with enoximone had higher
myocardial beta 2-adrenergic receptor densities than respective subgroups
treated without (28% higher, p less than 0.01) or with (65% higher, p less
than 0.01) intravenous beta-adrenergic agonists. Finally, isoproterenol- or
calcium-mediated contractile responses in isolated right ventricular
preparations from 14 patients treated with enoximone were similar to values
in control patients not exposed to enoximone or intravenous beta-adrenergic
agonists, suggesting that enoximone-related beta-adrenergic subsensitivity
or damage to the contractile apparatus does not occur.
ARTICLES
Low-dose enoximone in subjects awaiting cardiac transplantation. Clinical results and effects on beta-adrenergic receptors
Cardiology Division, University of Utah School of Medicine, Salt Lake City.
This article has been cited by other articles:
![]() |
M. R. Costanzo, S. Augustine, R. Bourge, M. Bristow, J. B. O'Connell, D. Driscoll, and E. Rose Selection and Treatment of Candidates for Heart Transplantation : A Statement for Health Professionals From the Committee on Heart Failure and Cardiac Transplantation of the Council on Clinical Cardiology, American Heart Association Circulation, December 15, 1995; 92(12): 3593 - 3612. [Abstract] [Full Text] |
||||
![]() |
A. M. Feldman, M. R. Bristow, W. W. Parmley, P. E. Carson, C. J. Pepine, E. M. Gilbert, J. E. Strobeck, G. H. Hendrix, E. R. Powers, R. P. Bain, et al. Effects of Vesnarinone on Morbidity and Mortality in Patients with Heart Failure N. Engl. J. Med., July 15, 1993; 329(3): 149 - 155. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |