Beta-blocker therapy for heart failure has gained popularity as a resu
lt of recent growing evidence that this group of drugs can reverse or
slow the progressive left ventricular dilation that characterizes hear
t failure. Although the mechanism of this favourable effect on remodel
ling remains unclear, the present evidence indicates that at least a p
ortion of the long-term benefit of these drugs is mediated through the
ir beta-blocking action. A direct effect on myocyte and interstitial g
rowth may be a key factor in their ability to inhibit the remodelling
process. The growing database will eventually raise the possibility th
at all patients with left ventricular dilation should take one of thes
e drugs. A better understanding of differing mechanisms in individual
patients would ideally provide selectivity in the therapeutic approach
.