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Published on: July 7, 2016
Digitalis Today: From Doctrine to Disrepute to Disciplined Reconsideration.
Mandeep R Mehra1, Milica Vukicevic2, Akshay S Desai1
1Cardiology Division, Mass General Brigham Heart and Vascular Institute and Harvard Medical School, Boston, Massachusetts.
Low-dose digitalis glycosides can reduce worsening heart failure events without increasing mortality when serum concentrations are controlled. This cardiac glycoside therapy offers a complementary role for selected patients with persistent heart failure risks.
Area of Science:
- Cardiovascular Therapeutics
- Pharmacology
- Heart Failure Management
Background:
- Cardiac glycosides, once foundational heart failure therapy, fell into disuse due to toxicity concerns and lack of mortality benefit shown in the DIG trial.
- Toxicity was often linked to excessive serum concentrations, particularly in women, leading to therapeutic disrepute.
Purpose of the Study:
- To reassess the role of low-dose digitalis glycosides in contemporary cardiovascular therapeutics.
- To evaluate the safety and efficacy of digitalis therapy in selected heart failure patients with persistent residual risk.
Main Methods:
- Review of recent randomized trials (DIGIT-HF, DECISION) and a contemporary meta-analysis.
- Analysis of outcomes related to low-dose digitalis therapy with controlled serum concentrations.
Main Results:
- Consistent directional reductions in worsening heart failure events were observed with low-dose digitalis.
- No excess mortality was found when serum concentrations were carefully controlled.
- Findings suggest historical toxicity was related to excessive exposure, not intrinsic hazard.
Conclusions:
- Digitalis glycosides are not mortality-reducing foundational therapy but serve as complementary agents.
- Recommended for selected patients with persistent heart failure despite optimized therapy, especially those with recurrent decompensation or atrial fibrillation.
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