4.7 Article

Survival After Implantable Cardioverter-Defibrillator Shocks

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 77, Issue 20, Pages 2453-2462

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2021.03.329

Keywords

KEY WORDS heart failure; ICD shock; inappropriate ICD shock; mortality; ventricular fibrillation; ventricular tachycardia

Funding

  1. Boston Scientific
  2. National Institutes of Health [U01HL096607]
  3. Medtronic
  4. Biotronik
  5. ZOLL
  6. Spire
  7. Abbott
  8. Biosense-Webster

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The study found that a first appropriate ICD shock was associated with increased risk of subsequent mortality, but an inappropriate shock alone was not. Additionally, therapy for ventricular tachycardia or ventricular fibrillation was linked to higher risk of death, while therapy for slower ventricular tachycardia or inappropriate therapy was not. Data also showed that appropriate shocks for VF, shocks for fast VT without prior ATP, and shocks for fast VT after failed ATP were associated with the highest risk of subsequent death.
BACKGROUND There are conflicting data on the impact of implantable cardioverter-defibrillator (ICD) shocks on subsequent mortality. OBJECTIVES The aim of this study was to determine whether the arrhythmic substrate leading to ICD therapy or the therapy itself increases mortality. METHODS The study cohort included 5,516 ICD recipients who were enrolled in 5 landmark ICD trials (MADIT-II, MADITRISK, MADIT-CRT, MADIT-RIT, RAID). The authors evaluated the association of device therapy with subsequent mortality in 4 separate time-dependent models: model I, type of ICD therapy; model II, type of arrhythmia for which ICD therapy was delivered; model III, combined assessment of all arrhythmia and therapy types during follow-up; and model IV, incremental risk associated with repeated ICD shocks. RESULTS When analyzed by the type of ICD therapy (model I), a first appropriate ICD shock was associated with increased risk of subsequent mortality with or without concomitant occurrence of inappropriate shock during follow-up (hazard ratio [HR]: 2.78 and 2.31; p < 0.001 and p = 0.12), whereas inappropriate shock alone was not associated with mortality risk (HR: 1.23; p = 0.42). Similarly, ICD therapy for ventricular tachycardia (VT) $200 beats/min or ventricular fibrillation (VF) (model II) was associated with increased risk of death with or without concomitant therapy for VT <200 beats/min (HRs: 2.25 and 2.62; both p < 0.001), whereas appropriate therapy for VT <200 beats/min or inappropriate therapy (regardless of etiology) did not reach statistical significance (all p > 0.10). Combined assessment of all therapy and arrhythmia types during follow-up (model III) showed that appropriate ICD shocks for VF, shocks for fast VT ($200 beats/min) without prior antitachycardia pacing (ATP), as well as shocks for fast VT delivered after failed ATP, were associated with the highest risk of subsequent death (HR: all >2.8; p < 0.001). Finally, 2 or more ICD appropriate shocks were not associated with incremental risk to the first appropriate ICD shock (model IV). CONCLUSION The combined data from 5 landmark ICD trials suggest that the underlying arrhythmic substrate rather than the ICD therapy is the more important determinant of mortality in ICD recipients. (J Am Coll Cardiol 2021;77:2453-62) (c) 2021 by the American College of Cardiology Foundation.

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