Literature DB >> 10606831

The rational use of beta-adrenoceptor blockers in the treatment of heart failure. The changing face of an old therapy.

I B Squire1, D B Barnett.   

Abstract

Heart failure is one of the commonest debilitating conditions of industrialized society, with mortality and morbidity comparable with that of the common neoplastic diseases. The role of antagonists of the adrenergic beta-receptor (beta-blockers) in heart failure has been the subject of debate for many years. Data from studies of the therapeutic use of beta-blockers in patients following acute myocardial infarction suggest that in this circumstance these agents confer at least as much benefit to patients with heart failure as they do to those without. Similarly retrospective analysis of a number of the studies of angiotensin converting enzyme (ACE) inhibitors in heart failure suggest a greater effect of the combination of beta-blocker with ACE inhibitor compared with ACE inhibitor alone. The results of recent prospective, placebo-controlled studies of the addition of beta-blocker to standard therapy in patients with chronic heart failure have confirmed a significant beneficial effect. beta-blocker therapy in these studies was well tolerated and in addition to improved mortality, beta-blocker therapy is associated with improved morbidity in terms of progressive heart failure and numbers of hospitalizations. Initiation of beta-blocker therapy in heart failure may be associated with deterioration of cardiac function in the short term. Treatment should be started at a low dose of beta-blocker with slow up-titration in a number of steps over several weeks. In spite of the established benefits of ACE inhibition in patients with heart failure, this treatment is under-utilized. Part of this shortfall is due to physicians' perceptions regarding potential unwanted effects of ACE inhibition. Perceptions regarding unwanted effects of beta-adrenoceptor blocker therapy are likely to be at least as great. While beta-blockade represents a welcome addition to the therapeutic armoury of physicians caring for patients with heart failure, initiation and stabilization of beta-adrenoceptor blocker therapy should be undertaken under specialist supervision.

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Year:  2000        PMID: 10606831      PMCID: PMC2014889          DOI: 10.1046/j.1365-2125.2000.00112.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  45 in total

Review 1.  Nonuniformity: a physiologic modulator of contraction and relaxation of the normal heart.

Authors:  D L Brutsaert
Journal:  J Am Coll Cardiol       Date:  1987-02       Impact factor: 24.094

Review 2.  Cardiovascular injury induced by sympathetic catecholamines.

Authors:  J I Haft
Journal:  Prog Cardiovasc Dis       Date:  1974 Jul-Aug       Impact factor: 8.194

3.  Effect of propranolol after acute myocardial infarction in patients with congestive heart failure.

Authors:  K Chadda; S Goldstein; R Byington; J D Curb
Journal:  Circulation       Date:  1986-03       Impact factor: 29.690

4.  Adverse effects of beta-blockade withdrawal in patients with congestive cardiomyopathy.

Authors:  K Swedberg; A Hjalmarson; F Waagstein; I Wallentin
Journal:  Br Heart J       Date:  1980-08

5.  Beta blockade during and after myocardial infarction: an overview of the randomized trials.

Authors:  S Yusuf; R Peto; J Lewis; R Collins; P Sleight
Journal:  Prog Cardiovasc Dis       Date:  1985 Mar-Apr       Impact factor: 8.194

6.  Metoprolol in acute myocardial infarction (MIAMI). A randomised placebo-controlled international trial. The MIAMI Trial Research Group.

Authors: 
Journal:  Eur Heart J       Date:  1985-03       Impact factor: 29.983

7.  Effects of enalapril on mortality in severe congestive heart failure. Results of the Cooperative North Scandinavian Enalapril Survival Study (CONSENSUS).

Authors: 
Journal:  N Engl J Med       Date:  1987-06-04       Impact factor: 91.245

8.  A randomized trial of low-dose beta-blockade therapy for idiopathic dilated cardiomyopathy.

Authors:  J L Anderson; J R Lutz; E M Gilbert; S G Sorensen; F G Yanowitz; R L Menlove; M Bartholomew
Journal:  Am J Cardiol       Date:  1985-02-01       Impact factor: 2.778

9.  A randomized trial of propranolol in patients with acute myocardial infarction. II. Morbidity results.

Authors: 
Journal:  JAMA       Date:  1983-11-25       Impact factor: 56.272

10.  Regional distribution of beta-adrenoceptors in the human heart: coexistence of functional beta 1- and beta 2-adrenoceptors in both atria and ventricles in severe congestive cardiomyopathy.

Authors:  O E Brodde; S Schüler; R Kretsch; M Brinkmann; H G Borst; R Hetzer; J C Reidemeister; H Warnecke; H R Zerkowski
Journal:  J Cardiovasc Pharmacol       Date:  1986 Nov-Dec       Impact factor: 3.105

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  2 in total

Review 1.  Impact of GPCRs in clinical medicine: monogenic diseases, genetic variants and drug targets.

Authors:  Paul A Insel; Chih-Min Tang; Ines Hahntow; Martin C Michel
Journal:  Biochim Biophys Acta       Date:  2006-10-05

2.  Plasma membrane-associated nucleoside diphosphate kinase (nm23) in the heart is regulated by beta-adrenergic signaling.

Authors:  Susanne Lutz; Roman A Mura; Hans Joerg Hippe; Christiane Tiefenbacher; Feraydoon Niroomand
Journal:  Br J Pharmacol       Date:  2003-10-14       Impact factor: 8.739

  2 in total

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