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A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation
Published on: February 28, 2012
A Quarter of a Century Later: What is Dofetilide's Clinical Role Today?
Deborah L Wolbrette1, Sarah Hussain1, Ilir Maraj1
11 Heart and Vascular Institute, Penn State University College of Medicine, The Milton S. Hershey Medical Center, Hershey, PA, USA.
Insights
Dofetilide effectively converts atrial fibrillation and flutter in real-world use, showing higher rates than clinical trials. It is safe and well-tolerated when initiated under hospital monitoring, especially for patients with normal renal function and QT intervals.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Dofetilide is a Class III antiarrhythmic agent.
- Approved for persistent atrial fibrillation/flutter and sinus rhythm maintenance.
- Previous trials indicated neutral mortality in post-MI and heart failure patients.
Purpose of the Study:
- Review postmarket data on dofetilide's real-world efficacy and safety.
- Evaluate off-label use in various arrhythmias.
- Compare real-world conversion rates to clinical trial data.
Main Methods:
- Review of postmarket data.
- Analysis of real-world efficacy and safety in diverse patient populations.
- Assessment of off-label use and conversion rates.
Main Results:
- Real-world acute conversion rates for atrial fibrillation and flutter exceed clinical trial findings.
- Dofetilide demonstrates success in off-label use for paroxysmal atrial fibrillation/flutter, atrial tachycardia, and ventricular tachycardia.
- Acceptable safety profile when initiated with hospital monitoring and appropriate dosing based on creatinine clearance.
Conclusions:
- Dofetilide is well-tolerated and effective for patients with adequate renal function and normal QT intervals.
- It is a suitable option when avoiding atrioventricular nodal blockade is desired.
- Real-world data supports higher efficacy than previously reported in clinical trials.
Abstract:
Dofetilide is a class III antiarrhythmic agent approved by the Food and Drug Administration for the conversion of atrial fibrillation and atrial flutter and maintenance of sinus rhythm in symptomatic patients with persistent arrhythmia. Drug trials showed neutral mortality in post-myocardial infarction patients and those with heart failure. This is a review of postmarket data, including real-world efficacy and safety in a variety of populations. Dofetilide has been used off-label with success in patients with paroxysmal atrial fibrillation and atrial flutter, as well as atrial tachycardia and ventricular tachycardia. The real-world acute conversion rate of atrial fibrillation and atrial flutter is higher than that reported in clinical trials. Dofetilide has an acceptable safety profile when initiated (or reloaded) under hospital monitoring and dosed according to creatinine clearance. Dofetilide is well tolerated and a good choice for patients with acceptable renal function and a normal QT interval, especially if atrioventricular nodal blockade needs to be avoided.
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