CRT-D vs. CRT-P Reduces Mortality in Nonischemic Cardiomyopathy

Quick Takes

  • In the COMPANION trial, in patients with nonischemic cardiomyopathy, CRT-D versus CRT-P was associated with reduced all-cause mortality (adjusted HR, 0.54), while patients with ischemic cardiomyopathy did not exhibit a between-device reduction in all-cause mortality.
  • This new analysis suggests that patients with nonischemic cardiomyopathy eligible for CRT should undergo CRT-D versus CRT-P when appropriate.

Study Questions:

Do patients with heart failure with reduced ejection fraction due to nonischemic etiology eligible for cardiac resynchronization therapy (CRT) benefit from an implantable cardioverter-defibrillator (ICD)?

Methods:

The authors analyzed the COMPANION (Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure) trial database, using Cox proportional hazards modeling stratified by etiology of nonischemic cardiomyopathy versus ischemic cardiomyopathy. The primary outcome was all-cause mortality, and secondary outcomes were the combination of cardiovascular mortality or heart failure hospitalization and sudden cardiac death.

Results:

Among patients randomized to CRT (n = 1,212), 236 died, 131 and 105 in the CRT-pacemaker (CRT-P) and CRT-defibrillator (CRT-D) arms, respectively. The unadjusted and adjusted hazard ratios (HRs) for CRT-D versus CRT-P were both 0.84 (95% confidence interval [CI], 0.65-1.09) for all-cause mortality, with a significant device-etiology interaction. In patients with nonischemic cardiomyopathy, CRT-D versus CRT-P was associated with reduced all-cause mortality (adjusted HR, 0.54; 95% CI, 0.34-0.86), while patients with ischemic cardiomyopathy did not exhibit a between-device reduction in all-cause mortality. The effects of CRT-D versus CRT-P on sudden cardiac death (advantage CRT-D) and cardiovascular mortality or heart failure hospitalization (no difference between CRT-P and CRT-D) were similar between the two etiologies.

Conclusions:

COMPANION trial patients with nonischemic cardiomyopathy exhibited a decrease in all-cause mortality associated with CRT-D but not CRT-P treatment, whereas patients with ischemic cardiomyopathy did not.

Perspective:

Despite almost two decades of primary prevention ICD therapy being offered to patients with nonischemic cardiomyopathy, there remains some uncertainty about the magnitude of benefit in these patients, especially those who are also the recipients of the CRT. Most notably, the DANISH trial failed to demonstrate statistically significant improvement in all-cause mortality in patients with nonischemic cardiomyopathy undergoing ICD implantation. The authors of the present study used previously unreleased data from the COMPANION trial and provided an analysis of outcomes of nonischemic patients with CRT-D versus CRT-P. The startling lack of all-cause mortality reduction of CRT-D versus CRT-P in patients with ischemic cardiomyopathy appears to be related to older age and greater number of vascular comorbidities as well as noncardiac deaths in this cohort. The authors of the present analysis explain the differences between DANISH- and COMPANION-derived outcomes by highlighting higher rates of more advanced heart failure in the COMPANION trial. Of course, the standard heart failure regimen of neither DANISH nor COMPANION trial included sacubitril/valsartan and sodium-glucose cotransporter-2 inhibitors, and it is not known how these recent pharmacological advances may differentially affect outcomes of patients with CRT-D versus CRT-P.

Clinical Topics: Arrhythmias and Clinical EP, Geriatric Cardiology, Heart Failure and Cardiomyopathies, Prevention, Implantable Devices, SCD/Ventricular Arrhythmias, Atrial Fibrillation/Supraventricular Arrhythmias, Acute Heart Failure

Keywords: Arrhythmias, Cardiac, Cardiac Resynchronization Therapy, Cardiomyopathies, Death, Sudden, Cardiac, Defibrillators, Implantable, Geriatrics, Heart Failure, Myocardial Ischemia, Pacemaker, Artificial, Primary Prevention, Secondary Prevention, Stroke Volume


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