Inclusion criteria | |
 • Myocardial infarction within 14 days according to the Universal ESC definition of MI: Detection of a rise and/or fall of cardiac biomarker values with at least one value above the 99th percentile upper reference limit and with at least one of the following: | |
  • Symptoms of ischemia | |
  • New or presumed new significant ST-segment–T wave changes or new left bundle branch block | |
  • Development of pathological Q waves in the ECG | |
  • Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality | |
 • Age > 18 years | |
 • LVEF > 40% by any imaging technique during hospitalization | |
Exclusion criteria | |
 • Any condition that requires beta-blocker treatment according to the treating physician, including but not limited to: | |
  • Beta-blocker-treated arrhythmias | |
  • Beta-blocker-treated hypertension | |
  • Reduced left ventricular ejection fraction | |
  • Cardiomyopathies | |
 • Any condition in which beta-blocker treatment is contraindicated according to the treating physician, including but not limited to: | |
  • Hypotension | |
  • Brady-arrhythmias | |
  • Severe peripheral artery disease | |
  • History of not able to tolerate beta-blocker therapy | |
  • Severe chronic obstructive pulmonary disease or asthma | |
  • Severe valvular heart disease | |
  • Any condition (i.e., dementia) that could lead to increased risk for the patient when treated with beta-blockers | |
 • Clinical evidence of heart failure at the time of randomization | |
 • Lack of signed informed consent and expected cooperation during follow-up | |
 • Pregnancy or of child bearing age not using safe contraception throughout the study period |