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. 2024 May;10(5):916-926.
doi: 10.1016/j.jacep.2024.102334. Epub 2024 Mar 20.

Mortality Benefit Among Primary Prevention Implantable Cardioverter-Defibrillator Recipients on Contemporary Heart Failure Treatment

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Free article

Mortality Benefit Among Primary Prevention Implantable Cardioverter-Defibrillator Recipients on Contemporary Heart Failure Treatment

Aamir Ahmed et al. JACC Clin Electrophysiol. 2024 May.
Free article

Abstract

Background: Past clinical trials have shown the benefit of implantable cardioverter-defibrillators (ICDs) for reducing sudden cardiac death in at-risk patients. However, heart failure management and ICD technology have changed since these trials were first published. An updated assessment of ICD mortality benefit is needed.

Objectives: The purpose of this study was to compare mortality rates between patients with a primary prevention (PP) indication for an ICD who did or did not receive an ICD using a contemporary, real-world data set.

Methods: Data was obtained from a large electronic health record data set covering patients in the United States from 2012 through 2020 who had a PP indication for an ICD and survived at least 1-year postindication.

Results: A total of 25,296 patients were identified as having a PP indication for ICD implantation, of which 2,118 (8.4%) were treated with an ICD within a year. Treated patients were younger than nontreated patients (age 63.4 years vs 66.1 years) with a smaller proportion of women (25.0% vs 36.7%). After 4-to-1 propensity matching, treated patients had similar clinical characteristics to nontreated patients. A Cox proportional hazard model estimated a 24.3% lower risk of all-cause mortality in patients when treated vs not treated with an ICD (HR: 0.757; 95% CI: 0.678-0.835; P <0.001). There was no detectable difference in ICD benefit between patients with ischemic and nonischemic heart disease (P = 0.50).

Conclusions: ICD treatment of patients with a PP indication is associated with improved mortality even in the context of evolving adjunctive HF treatment, consistent with earlier landmark trials.

Keywords: implantable cardioverter-defibrillator; mortality; primary prevention; sudden cardiac arrest; sudden cardiac death.

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Conflict of interest statement

Funding Support and Author Disclosures This work was supported by Medtronic. Dr Ahmed has served as a consultant to Abbott and Medtronic. Dr Auricchio has served as a consultant to Boston Scientific, Cairdac, EP Solutions, Philips, and Radcliffe Publishers; has received speaker fees from Boston Scientific, Medtronic, Microport, and Philips; participates in clinical trials sponsored by Boston Scientific, Medtronic, Philips, and XSpline; and has intellectual properties with Boston Scientific, Biosense Webster, and Microport CRM. Dr Mittal has served as a consultant to Abbott, Boston Scientific, Impulse Dynamics, and Medtronic. Dr Pickett has received honoraria/consultant fees Boston Scientific and Medtronic. Dr Wilkoff had served as a consultant for, speaker for, and performed research for Medtronic, Boston Scientific, Abbott, Biotronik, Impulse Dynamics, Philips, and Cook. Mr Jacobsen, Ms Marti, Mr Holbrook, and Ms Soderlund are employees/shareholders of Medtronic. Dr Curtis has served on the advisory board for and received honoraria for speaking from Medtronic and Abbott; and has served on the advisory board of Janssen Pharmaceuticals, Milestone Pharmaceuticals, and Eagle Pharmaceuticals.

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