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Evidence of beta-blockers' benefits after myocardial infarction (MI) is decades old. Now, two open-label randomized trials with blinded endpoint evaluation update the evidence. Each trial randomized patients with acute MI (with or without ST-segment elevation) and a left ventricular ejection fraction ≥40% to receive either a beta-blocker (chosen by the treating physician) within 14 days post-MI or no beta-blocker. Each trial enrolled about 20% women.
In BETAMI-DANBLOCK, involving 5600 patients in Denmark and Norway, 95% of the beta-blocker group received long-acting metoprolol. During a 3.5-year median follow-up, incidence of the primary outcome — all-cause mortality or a major cardiovascular event — was significantly lower in the beta-block…