Subcutaneous versus transvenous implantable defibrillator in patients with hypertrophic cardiomyopathy.

Antitachycardia pacing Hypertrophic cardiomyopathy Implantable cardioverter-defibrillator Programming Subcutaneous defibrillator Ventricular tachycardia

Journal

Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317

Informations de publication

Date de publication:
05 2022
Historique:
received: 10 11 2021
revised: 05 01 2022
accepted: 10 01 2022
pubmed: 18 1 2022
medline: 6 5 2022
entrez: 17 1 2022
Statut: ppublish

Résumé

Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited cardiomyopathy. The implantable cardioverter-defibrillator (ICD) is important for prevention of sudden cardiac death (SCD) in patients at high risk. In recent years, the subcutaneous implantable cardioverter-defibrillator (S-ICD) has emerged as a viable alternative to the transvenous implantable cardioverter-defibrillator (TV-ICD). The S-ICD does not require intravascular access; however, it cannot provide antitachycardia pacing (ATP) therapy. The purpose of this study was to assess the real-world incidence of ICD therapy in patients with HCM implanted with TV-ICD vs S-ICD. We compared the incidence of ATP and shock therapies among all HCM patients with S-ICD and TV-ICD enrolled in the Boston Scientific ALTITUDE database. Cumulative Kaplan-Meier incidence was used to compare therapy-free survival, and Cox proportional hazard ratios were calculated. We performed unmatched as well as propensity match analyses. We included 2047 patients with TV-ICD and 626 patients with S-ICD, followed for an average of 1650.5 ± 1038.5 days and 933.4 ± 550.6 days, respectively. Patients with HCM and TV-ICD had a significantly higher rate of device therapy compared to those with S-ICD (32.7 vs 14.5 therapies per 100 patient-years, respectively; P <.001), driven by a high incidence of ATP therapy in the TV-ICD group, which accounted for >67% of therapies delivered. Shock incidence was similar between groups, both in the general and the matched cohorts. Patients with HCM and S-ICD had a significantly lower therapy rate than patients with TV-ICD without difference in shock therapy, suggesting potentially unnecessary ATP therapy. Empirical ATP programming in patients with HCM may be unbeneficial.

Sections du résumé

BACKGROUND
Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited cardiomyopathy. The implantable cardioverter-defibrillator (ICD) is important for prevention of sudden cardiac death (SCD) in patients at high risk. In recent years, the subcutaneous implantable cardioverter-defibrillator (S-ICD) has emerged as a viable alternative to the transvenous implantable cardioverter-defibrillator (TV-ICD). The S-ICD does not require intravascular access; however, it cannot provide antitachycardia pacing (ATP) therapy.
OBJECTIVE
The purpose of this study was to assess the real-world incidence of ICD therapy in patients with HCM implanted with TV-ICD vs S-ICD.
METHODS
We compared the incidence of ATP and shock therapies among all HCM patients with S-ICD and TV-ICD enrolled in the Boston Scientific ALTITUDE database. Cumulative Kaplan-Meier incidence was used to compare therapy-free survival, and Cox proportional hazard ratios were calculated. We performed unmatched as well as propensity match analyses.
RESULTS
We included 2047 patients with TV-ICD and 626 patients with S-ICD, followed for an average of 1650.5 ± 1038.5 days and 933.4 ± 550.6 days, respectively. Patients with HCM and TV-ICD had a significantly higher rate of device therapy compared to those with S-ICD (32.7 vs 14.5 therapies per 100 patient-years, respectively; P <.001), driven by a high incidence of ATP therapy in the TV-ICD group, which accounted for >67% of therapies delivered. Shock incidence was similar between groups, both in the general and the matched cohorts.
CONCLUSION
Patients with HCM and S-ICD had a significantly lower therapy rate than patients with TV-ICD without difference in shock therapy, suggesting potentially unnecessary ATP therapy. Empirical ATP programming in patients with HCM may be unbeneficial.

Identifiants

pubmed: 35038570
pii: S1547-5271(22)00028-5
doi: 10.1016/j.hrthm.2022.01.013
pii:
doi:

Substances chimiques

Adenosine Triphosphate 8L70Q75FXE

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

759-767

Informations de copyright

Copyright © 2022 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Lior Jankelson (L)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York. Electronic address: Lior.jankelson@nyulangone.org.

Leonid Garber (L)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Mark Sherrid (M)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Daniele Massera (D)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Paul Jones (P)

Boston Scientific Corporation, St. Paul, Minnesota.

Chirag Barbhaiya (C)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Douglas Holmes (D)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Robert Knotts (R)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Scott Bernstein (S)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Michael Spinelli (M)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

David Park (D)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Anthony Aizer (A)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

Larry Chinitz (L)

Leon H. Charney Division of Cardiology, NYU Langone Health, NYU School of Medicine, New York, New York.

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Classifications MeSH