Abstract

At least 44 randomized trials of β blockade in acute myocardial infarction have been reported. All of these trials excluded patients with moderate-to-severe clinical signs of acute left ventricular dysfunction (LVD). Several of the larger trials did include high-risk patients with a history of compensated heart failure or with symptoms and signs suggesting mild LVD. Data from these trials indicate that β-blocker treatment was well tolerated by patients with LVD, both in the acute phase of myocardial infarction and during longterm follow-up treatment. Further, data for LVD patients indicate that mortality in the β-blocker group was reduced by 20–30% when compared wtth the placebo group. A similar mortality reduction was obtained for the entire patient population in the trials. Because of the high mortality among patients wtth mild LVD, the absolute gain in numbers of lives saved per 100 patients treated wtth β blockers is even larger than that in patients without LVD. Data from two long-term trials indicate marked (47% and 43%) reductions in the likelihood of sudden death among LVD patients treated wtth β blockers. These results suggest that all patients wtth LVD who can tolerate β blockade may benefit from treatment wtth these agents.

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