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Digitalis Therapy Is Associated With an Increased Risk of ICD Shock Delivery and Device Revision
Gerrit Frommeyer1, Philipp S Lange1, Thomas Kleemann2
1Clinic for Cardiology II - Electrophysiology, University of Münster, Münster, Germany.
Digitalis therapy in patients with systolic heart failure receiving cardiac implantable electronic devices was not associated with increased mortality. However, digitalis use correlated with higher rates of device revision and ICD shock delivery.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Management
Background:
- Digitalis glycosides are used for atrial fibrillation rate control and heart failure treatment.
- Previous research has indicated potential adverse effects of digitalis therapy.
- The study investigated digitalis use in patients with systolic heart failure undergoing ICD or CRT-ICD implantation.
Purpose of the Study:
- To determine the prevalence of digitalis therapy in patients receiving cardiac implantable electronic devices.
- To assess the impact of digitalis therapy on clinical outcomes in this patient population.
Main Methods:
- Analysis of data from the German Device Registry, a nationwide prospective registry.
- Inclusion of 3826 patients undergoing ICD or CRT system implantation.
- Comparison of outcomes between patients receiving digitalis therapy and those who were not.
Main Results:
- Digitalis-treated patients had more severe left ventricular dysfunction, higher NYHA class, and more left bundle branch block.
- One-year mortality and a composite endpoint of death, myocardial infarction, or stroke did not differ significantly between groups.
- Digitalis therapy was associated with increased ICD shock delivery and a higher risk of device revision.
Conclusions:
- Digitalis therapy in patients with systolic heart failure undergoing ICD or CRT implantation is associated with an increased risk of device revision.
- No significant difference in mortality or major adverse cardiovascular events was observed.
- An elevated risk of ICD shock delivery was noted in patients treated with digitalis.
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