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Beta-blockade with bucindolol in heart failure caused by ischemic versus idiopathic dilated cardiomyopathy.
Author(s) -
Susan Woodley,
Edward M. Gilbert,
Jeffrey L. Anderson,
John B. OʼConnell,
David Deitchman,
Frank G. Yanowitz,
Patrice C. Mealey,
Kirk Volkman,
Dale G. Renlund,
R L Menlove
Publication year - 1991
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.84.6.2426
Subject(s) - medicine , cardiology , heart failure , ejection fraction , dilated cardiomyopathy , placebo , randomization , hypertensive heart disease , cardiac index , dobutamine , cardiomyopathy , randomized controlled trial , hemodynamics , cardiac output , pathology , alternative medicine
BACKGROUND We investigated the effects of bucindolol, a nonselective, non-ISA beta-blocker with mild-vasodilatory properties, in patients with congestive heart failure from ischemic dilated cardiomyopathy (ISCDC, n = 27) and compared the results with those in subjects with heart failure from idiopathic dilated cardiomyopathy (IDC, n = 22). METHODS AND RESULTS Patients were randomized in a double-blind fashion to receive 12 weeks' treatment with either bucindolol or placebo, with randomization stratified for IDC or ISCDC: Invasive (right heart catheterization) and noninvasive (echo, MUGA, central venous norepinephrine, exercise treadmill studies, and symptom scores) tests of heart failure severity were determined at baseline and end of the study. For all subjects (ISCDC plus IDC), relative to placebo treatment, bucindolol-treated patients had significant improvement in ejection fraction, left ventricular size and filling pressure, stroke work index, symptom score, and central venous norepinephrine. However, most of these differences could be attributed to improvement in the IDC subgroup, as the only parameter with a statistically significant degree of improvement in the bucindolol-treated ISCDC subgroup was left ventricular size. CONCLUSIONS We conclude that beta-blockade may produce quantitatively different degrees of response in different kinds of heart muscle disease.

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