Circulation, Vol 60, 1201-1207, Copyright © 1979 by American Heart Association
DR Rosing, KM Kent, JS Borer, SF Seides, BJ Maron and SE Epstein
The hemodynamic effects of intravenous verapamil administration were
examined in 27 patients with hypertrophic cardiomyopathy. Increasing doses
of verapamil produced small increases in heart rate and cardiac output and
a significant decrease in systolic blood pressure, but had no significance
effect on mean pulmonary artery wedge pressure or left ventricular
end-diastolic pressure. The highest dose of verapamil increased heart rate
from 72 +/- 3 to 81 +/- 6 beats/min and reduced systolic blood pressure
from 118 +/- 8 to 99 +/- 5 mm Hg (p less than 0.005). This dose decreased
the basal left ventricular outflow tract gradient from 94 +/- 14 to 49 +/-
14 mm Hg and the average left ventricular outflow tract gradient during the
Valsalva maneuver from 76 +/- 5 to 63 +/- 13 mm Hg, during amyl nitrite
inhalation from 69 +/- 15 to 39 +/- 13 mm Hg, and during isoproterenol
infusion from 108 +/- 29 to 70 +/- 21 mm Hg (p less than 0.01). These
results indicate that verapamil can significantly decrease left ventricular
outflow obstruction in patients with hypertrophic cardiomyopathy and thus
may provide an important new therapeutic agent in the treatment of this
disorder.
ARTICLES
Verapamil therapy: a new approach to the pharmacologic treatment of hypertrophic cardiomyopathy. I. Hemodynamic effects
This article has been cited by other articles:
![]() |
M. A. Fifer and G. J. Vlahakes Management of Symptoms in Hypertrophic Cardiomyopathy Circulation, January 22, 2008; 117(3): 429 - 439. [Full Text] [PDF] |
||||
![]() |
M. Ashidagawa, M. Ohara, and Y. Koide An Intraoperative Diagnosis of Dynamic Left Ventricular Outflow Tract Obstruction Using Transesophageal Echocardiography Leads to the Treatment with Intravenous Disopyramide Anesth. Analg., February 1, 2002; 94(2): 310 - 312. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. V. Sherrid, G. Pearle, and D. Z. Gunsburg Mechanism of Benefit of Negative Inotropes in Obstructive Hypertrophic Cardiomyopathy Circulation, January 13, 1998; 97(1): 41 - 47. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hamada, Y. Shigematsu, S. Ikeda, Y. Hara, H. Okayama, K. Kodama, T. Ochi, and K. Hiwada Class Ia Antiarrhythmic Drug Cibenzoline : A New Approach to the Medical Treatment of Hypertrophic Obstructive Cardiomyopathy Circulation, September 2, 1997; 96(5): 1520 - 1524. [Abstract] [Full Text] |
||||
![]() |
E. D. Wigle, H. Rakowski, B. P. Kimball, and W. G. Williams Hypertrophic Cardiomyopathy : Clinical Spectrum and Treatment Circulation, October 1, 1995; 92(7): 1680 - 1692. [Full Text] |
||||
![]() |
B. Heric, B. W. Lytle, D. P. Miller, E. R. Rosenkranz, H. M. Lever, and D. M. Cosgrove Surgical management of hypertrophic obstructive cardiomyopathy:Early and late results J. Thorac. Cardiovasc. Surg., July 1, 1995; 110(1): 195 - 208. [Abstract] [Full Text] |
||||
![]() |
M. D. Winniford, J. T. Willerson, and L. D. Hillis Calcium Antagonists in the Treatment of Individuals with Ischemic Heart Disease Angiology, August 1, 1982; 33(8): 522 - 539. [Abstract] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1979 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |