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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
Implantable cardioverter-defibrillator efficacy in patients with heart failure and left ventricular dysfunction (from
Wojciech Zareba1, Katarzyna Piotrowicz, Scott McNitt
1Heart Research Follow-up Program, Cardiology Unit, Department of Medicine, University of Rochester Medical Center, Rochester, New York 14642-8653, USA. wojciech_zareba@urmc.rochester.edu
Insights
Patients with advanced heart failure (higher NYHA class, BUN) face greater mortality and arrhythmic event risks. However, implantable cardioverter-defibrillator (ICD) therapy benefits all patients regardless of heart failure severity.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Management
Background:
- The Multicenter Automatic Defibrillator Implantation Trial II (MADIT-II) showed implantable cardioverter-defibrillators (ICDs) reduce mortality in postinfarction patients with low ejection fraction (EF).
- Sudden Death in Heart Failure Trial (SCD-HeFT) suggested reduced ICD benefit in patients with New York Heart Association (NYHA) class III heart failure.
Purpose of the Study:
- To evaluate the association between NYHA class, EF, and blood urea nitrogen (BUN) levels with ICD benefit in reducing mortality.
- To assess the relationship of these parameters with ICD therapy for ventricular tachyarrhythmias.
Main Methods:
- Analysis of patient data from the Multicenter Automatic Defibrillator Implantation Trial II.
- Stratification of patients based on NYHA class (I, II, III), EF (< or =20%, 21-25%, 26-30%), and BUN levels (< or =25 mg/dl, >25 mg/dl).
Main Results:
- Higher NYHA class and BUN levels were associated with increased mortality (34%) and arrhythmic event risk (33-35%) compared to lower functional groups (16-20%).
- Ejection fraction (EF) did not significantly differentiate mortality or arrhythmic event risk.
- No significant interactions were found between mortality, ICD therapy, and the tested parameters (NYHA, EF, BUN).
Conclusions:
- Patients with more advanced heart failure (higher NYHA class, BUN) exhibit higher risks of mortality and arrhythmic events.
- Despite increased risk, there is no significant difference in the mortality benefit of ICD therapy across different subgroups of heart failure severity in the MADIT-II trial.
Abstract:
The Multicenter Automatic Defibrillator Implantation Trial II demonstrated a significant 31% reduction in the risk of mortality in postinfarction patients with low ejection fraction (EF < or =30%). Recently, results from the Sudden Death in Heart Failure Trial indicated that a subgroup of patients with New York Heart Association (NYHA) class III heart failure had less benefit from an implantable cardioverter-defibrillator (ICD) than patients with less advanced heart failure. This study evaluates the association between NYHA class, EF, and blood urea nitrogen (BUN) levels as measures of heart failure and left ventricular dysfunction, and ICD benefit in reducing mortality as well as the association of these parameters with ICD therapy for ventricular tachyarrhythmias. NYHA class I was identified in 442 patients (36%), class II in 425 (35%), and class III in 350 patients (29%). EF < or =20% was present in 472 patients (38%), EF of 21% to 25% in 359 patients (29%), and EF of 26% to 30% in 401 patients (33%). BUN < or =25 mg/dl was present in 850 patients (70%) and >25 mg/dl in 368 patients (30%). Patients with higher NYHA class and BUN had higher mortality (34%) and a higher risk of arrhythmic events (33% to 35%) than patients in lower functional groups (16% to 20%). EF did not differentiate the risk. There was no evidence for significant interactions between mortality, ICD therapy, and tested parameters. In conclusion, patients with more advanced heart failure have a higher risk of mortality and arrhythmic events than patients with less severe disease. However, there is no significant difference in the benefit from ICD therapy among the above subgroups of patients in the Multicenter Automatic Defibrillator Implantation Trial.
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