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Long-term treatment with metoprolol after myocardial infarction: effect on 3 year mortality and morbidity
Insights
Metoprolol treatment significantly reduced cardiac deaths, sudden death, and nonfatal reinfarction in patients after myocardial infarction. Benefits were most pronounced in those with large infarcts.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute myocardial infarction survivors require effective treatments to reduce mortality and reinfarction.
- Beta-blockers, like metoprolol, are commonly used post-myocardial infarction.
- Long-term effects of metoprolol in specific patient subgroups remain an area of investigation.
Purpose of the Study:
- To evaluate the long-term efficacy of metoprolol in reducing mortality and reinfarction after acute myocardial infarction.
- To assess the impact of metoprolol on cardiac death, sudden death, and nonfatal reinfarction.
- To identify patient subgroups that benefit most from metoprolol treatment.
Main Methods:
- A double-blind, randomized study comparing metoprolol (100 mg twice daily) with placebo.
- Patients stratified by age, infarct size, and ventricular arrhythmias.
- Follow-up duration of 36 months.
Main Results:
- Metoprolol significantly reduced overall nonfatal reinfarction (11.7% vs. 21.1%) and sudden death (5.8% vs. 14.7%).
- Cardiac death was significantly reduced in patients with large infarcts (12.5% vs. 32.1%).
- Cerebrovascular events were less frequent in the metoprolol group.
Conclusions:
- Metoprolol treatment after myocardial infarction significantly reduces nonfatal reinfarction and sudden death in all patients.
- A significant reduction in cardiac death was observed in patients with large infarcts.
- Metoprolol demonstrates a favorable long-term safety and efficacy profile post-myocardial infarction.
Abstract:
The effects of metoprolol treatment in patients surviving acute myocardial infarction have been investigated in a double-blind randomized study. The patients were stratified according to age, infarct size and type of ventricular arrhythmias before administration of metoprolol, 100 mg twice daily (n = 154), or placebo (n = 147). All patients were followed up for 36 months. There were 31 (29 cardiac) and 25 (20 cardiac) deaths in the placebo and metoprolol groups, respectively. Subgroup analyses showed a significant reduction of cardiac death in patients with a large infarct (32.1% with placebo versus 12.5% with metoprolol, p less than 0.05) as a result of active treatment. Sudden death rates were 14.7% in the placebo versus 5.8% in the metoprolol group (p less than 0.05). The incidence of nonfatal reinfarction was 21.1% in the placebo versus 11.7% in the metoprolol group (p less than 0.05). The reduction in nonfatal reinfarction was similar in all pretreatment risk strata. The difference between the two groups in cumulative number of cardiac deaths and patients experiencing nonfatal reinfarction increased throughout the study. Furthermore, cerebrovascular events (p less than 0.05) and coronary bypass surgery (p = 0.058) were more frequent in the placebo group. In conclusion, after 36 months of metoprolol treatment after myocardial infarction, there was a significant reduction of nonfatal reinfarction and sudden death in all patients and a reduction of cardiac death in those with a large infarct.
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