Key result
Digitoxin reduces all-cause mortality or heart failure hospitalization ~18% vs placebo in HFrEF.
Why the study?
No randomised clinical trials had evaluated cardiac glycosides for almost three decades following the DIG trial, leaving conflicting observational evidence regarding their role in the modern era of heart failure therapy.
Does digitoxin reduce the risk of all-cause mortality or heart failure hospitalization in patients with symptomatic HFrEF on contemporary guideline-directed medical therapy?
Does digitoxin reduce the risk of all-cause mortality or heart failure hospitalization in patients with symptomatic HFrEF on contemporary guideline-directed medical therapy?
Hazard Ratio: 0.82 (95% CI 0.69–0.98)
Absolute Risk Reduction: 5%
Number Needed to Treat: 22
p-value: p=0.03
The review of the DIGIT-HF trial suggests digitoxin offers safe and effective adjunctive risk reduction for HFrEF patients already on modern guideline-directed therapies.
May support adjunctive digitoxin in HFrEF on GDMT; leaves open confirmation before practice change.
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.
No takes yet. Share an insight, caveat, or question.
Sciatti et al. (2026) conducted a review in Heart Failure with reduced Ejection Fraction (HFrEF) (n=1,240). Digitoxin vs. Placebo was evaluated on Composite of all-cause mortality or first hospitalization for heart failure (HR 0.82, 95% CI 0.69-0.98, p=0.03). Digitoxin reduced the composite endpoint of all-cause mortality or first heart failure hospitalization by 18% (HR 0.82, p=0.03) compared to placebo in patients with HFrEF on contemporary therapy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: