A related editorial notes that despite a primary composite endpoint that included several clinical events (cardiovascular death, heart failure, or sustained ventricular arrhythmia), the REMINDER study should be considered a ‘proof-of-concept’ trial, driven by the ‘surrogate’ endpoint of elevated levels of natriuretic peptides, which accounted for 87% of the primary composite endpoint events.
A larger, adequately powered study with longer follow up is required before a strategy of early mineralocorticoid receptor antagonist administration could be recommended for the broader STEMI population.