Digitoxin treatment was associated with a reduction in all-cause mortality and heart failure hospitalizations in patients with reduced ejection fraction.
Does digitoxin reduce the composite endpoint of all-cause mortality and hospitalisations for heart failure in patients with heart failure with reduced ejection fraction?
The DIGIT-HF trial demonstrates that digitoxin reduces the composite of all-cause mortality and heart failure hospitalizations in HFrEF patients on contemporary guideline-directed medical therapy, potentially reopening its clinical role.
Absolute Event Rate: 0% vs 0%
Abstract Cardiac glycosides represent one of the oldest therapeutic pillars in medicine, although their role has progressively diminished in the modern era of neurohormonal therapy for heart failure (HF). Following publication of the DIG trial in 1997, no randomised clinical trials evaluating this drug class were conducted for almost three decades, while observational studies and meta-analyses accumulated, often yielding conflicting results. The DIGIT-HF randomised clinical trial (2025) addressed a major unmet need by evaluating digitoxin in patients with heart failure with reduced ejection fraction in the contemporary era of guideline-directed medical therapy. Treatment with digitoxin was associated with favourable outcomes, including a reduction in the composite endpoint of all-cause mortality and hospitalisations for heart failure, thereby reopening a long-standing debate on the role of digitalis, which had remained marginal for many years. This article reviews the history of digitalis, the main evidence generated over recent decades, the evolution of clinical guidelines from 1997 to 2022, and the conceptual and clinical implications of the DIGIT-HF trial.
Sciatti et al. (Wed,) reported a other. Digitoxin treatment was associated with a reduction in all-cause mortality and heart failure hospitalizations in patients with reduced ejection fraction.
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