“…Although an improvement of LVEF after CS can be observed in a considerable number of patients following coronary revascularization, recovery from severe inflammation, volume optimization, and introduction of HF drugs, adverse clinical events may occur as a consequence of adverse cardiac remodeling, residual ischemia, incomplete LVEF recovery, or progression of the baseline diseases, 6 , 24 , 25 , 26 which all can be targeted by beta blockers, RASI, and MRA, which compose the triple GDMT. 6 , 24 , 27 Although there has been no randomized clinical trial that investigated the effects of HF drugs at the recovery phase of patients with CS, the recent STRONG‐HF (Safety, Tolerability and Efficacy of Rapid Optimization, Helped by NT‐proBNP Testing, of Heart Failure Therapies) trial demonstrated that rapid titration of GDMT using beta blockers, RASI, and MRA reduced the risk of 180‐day all‐cause death or HF hospitalization in patients with acute HF without shock.…”