Impact of Pulmonary Valve Replacement on Ventricular Arrhythmias in Patients With Tetralogy of Fallot and Implantable Cardioverter-Defibrillator.


Journal

JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995

Informations de publication

Date de publication:
10 2021
Historique:
received: 30 11 2020
revised: 22 02 2021
accepted: 24 02 2021
pubmed: 3 5 2021
medline: 29 10 2021
entrez: 2 5 2021
Statut: ppublish

Résumé

This study aimed to assess the impact of pulmonary valve replacement (PVR) on ventricular arrhythmias burden in a population of tetralogy of Fallot (TOF) patients with continuous cardiac monitoring by implantable cardioverter-defibrillators (ICDs). Sudden cardiac death is a major cause of death in TOF, and right ventricular overload is commonly considered to be a potential trigger for ventricular arrhythmias. Data were analyzed from a nationwide French ongoing study (DAI-T4F) including all TOF patients with an ICD since 2000. Survival data with recurrent events were used to compare the burden of appropriate ICD therapies before and after PVR in patients who underwent PVR over the study period. A total of 165 patients (mean age 42.2 ± 13.3 years, 70.1% male) were included from 40 centers. Over a median follow-up period of 6.8 (interquartile range: 2.5 to 11.4) years, 26 patients (15.8%) underwent PVR. Among those patients, 18 (69.2%) experienced at least 1 appropriate ICD therapy. When considering all ICD therapies delivered before (n = 62) and after (n = 16) PVR, the burden of appropriate ICD therapies was significantly lower after PVR (HR: 0.21; 95% confidence interval [CI]: 0.08 to 0.56; p = 0.002). Respective appropriate ICD therapies rates per 100 person-years were 44.0 (95% CI: 35.7 to 52.5) before and 13.2 (95% CI: 7.7 to 20.5) after PVR (p < 0.001). In the overall cohort, PVR before ICD implantation was also independently associated with a lower risk of appropriate ICD therapy in primary prevention patients (HR: 0.29 [95% CI: 0.10 to 0.89]; p = 0.031). In this cohort of high-risk TOF patients implanted with an ICD, the burden of appropriate ICD therapies was significantly reduced after PVR. While optimal indications and timing for PVR are debated, these findings suggest the importance of considering ventricular arrhythmias in the overall decision-making process. (French National Registry of Patients With Tetralogy of Fallot and Implantable Cardioverter Defibrillator [DAI-T4F]; NCT03837574).

Sections du résumé

OBJECTIVES
This study aimed to assess the impact of pulmonary valve replacement (PVR) on ventricular arrhythmias burden in a population of tetralogy of Fallot (TOF) patients with continuous cardiac monitoring by implantable cardioverter-defibrillators (ICDs).
BACKGROUND
Sudden cardiac death is a major cause of death in TOF, and right ventricular overload is commonly considered to be a potential trigger for ventricular arrhythmias.
METHODS
Data were analyzed from a nationwide French ongoing study (DAI-T4F) including all TOF patients with an ICD since 2000. Survival data with recurrent events were used to compare the burden of appropriate ICD therapies before and after PVR in patients who underwent PVR over the study period.
RESULTS
A total of 165 patients (mean age 42.2 ± 13.3 years, 70.1% male) were included from 40 centers. Over a median follow-up period of 6.8 (interquartile range: 2.5 to 11.4) years, 26 patients (15.8%) underwent PVR. Among those patients, 18 (69.2%) experienced at least 1 appropriate ICD therapy. When considering all ICD therapies delivered before (n = 62) and after (n = 16) PVR, the burden of appropriate ICD therapies was significantly lower after PVR (HR: 0.21; 95% confidence interval [CI]: 0.08 to 0.56; p = 0.002). Respective appropriate ICD therapies rates per 100 person-years were 44.0 (95% CI: 35.7 to 52.5) before and 13.2 (95% CI: 7.7 to 20.5) after PVR (p < 0.001). In the overall cohort, PVR before ICD implantation was also independently associated with a lower risk of appropriate ICD therapy in primary prevention patients (HR: 0.29 [95% CI: 0.10 to 0.89]; p = 0.031).
CONCLUSIONS
In this cohort of high-risk TOF patients implanted with an ICD, the burden of appropriate ICD therapies was significantly reduced after PVR. While optimal indications and timing for PVR are debated, these findings suggest the importance of considering ventricular arrhythmias in the overall decision-making process. (French National Registry of Patients With Tetralogy of Fallot and Implantable Cardioverter Defibrillator [DAI-T4F]; NCT03837574).

Identifiants

pubmed: 33933408
pii: S2405-500X(21)00220-6
doi: 10.1016/j.jacep.2021.02.022
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03837574']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1285-1293

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures The Paris-Sudden Death Expertise Center activities are supported by the Institut National de la Santé et de la Recherche Médicale (INSERM), University of Paris, Assistance Publique-Hôpitaux de Paris, Fondation Coeur et Artères, Global Heart Watch, Fédération Française de Cardiologie, Société Française de Cardiologie, Fondation Recherche Medicale, as well as unrestricted grants from industrial partners (Abbott, Biotronik, Boston Scientific, Medtronic, MicroPort, Schiller and Zoll). SDEC Executive Committee is part of the ESCAPE-NET project (Horizon2020 programme). The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Francis Bessière (F)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Kévin Gardey (K)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Abdeslam Bouzeman (A)

Parly II Private Hospital, Le Chesnay, France.

Guillaume Duthoit (G)

La Pitié-Salpêtrière University Hospital, Paris, France.

Linda Koutbi (L)

La Timone Hospital, Marseille, France.

Fabien Labombarda (F)

Caen University Hospital, Caen, France.

Christelle Marquié (C)

Lille University Hospital, Lille, France.

Jean Baptiste Gourraud (JB)

Nantes University Hospital, Nantes, France.

Pierre Mondoly (P)

Toulouse University Hospital, Toulouse, France.

Jean Marc Sellal (JM)

Nancy University Hospital, Nancy, France.

Pierre Bordachar (P)

Bordeaux University Hospital, Bordeaux, France.

Alexis Hermida (A)

Amiens University Hospital, Amiens, France.

Frédéric Anselme (F)

Rouen University Hospital, Rouen, France.

Anouk Asselin (A)

Université de Paris, PARCC, INSERM, Paris, France.

Caroline Audinet (C)

Bretagne Sud Hospital, Lorient, France.

Yvette Bernard (Y)

Besançon University Hospital, Besançon, France.

Serge Boveda (S)

Pasteur Clinic, Toulouse, France.

Philippe Chevalier (P)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Gael Clerici (G)

Saint Pierre University Hospital, La Réunion, France.

Antoine da Costa (A)

Saint Etienne University Hospital, Saint Etienne, France.

Maxime de Guillebon (M)

Pau Hospital, Pau, France.

Pascal Defaye (P)

Grenoble University Hospital, Grenoble, France.

Romain Eschalier (R)

Clermont-Ferrand University Hospital, Clermont-Ferrand, France.

Rodrigue Garcia (R)

Poitiers University Hospital, Poitiers, France.

Charles Guenancia (C)

Dijon University Hospital, Dijon, France.

Benoit Guy-Moyat (B)

Limoges University Hospital, Limoges, France.

Roland Henaine (R)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Didier Irles (D)

Annecy Hospital, Annecy, France.

Laurence Iserin (L)

Adult Congenital Heart Disease Medico-Surgical Unit, European Georges Pompidou Hospital, Paris, France.

François Jourda (F)

Auxerre Hospital, Auxerre, France.

Magalie Ladouceur (M)

Université de Paris, PARCC, INSERM, Paris, France; Adult Congenital Heart Disease Medico-Surgical Unit, European Georges Pompidou Hospital, Paris, France.

Philippe Lagrange (P)

Saint-Pierre Clinic, Perpignan, France.

Mikael Laredo (M)

La Pitié-Salpêtrière University Hospital, Paris, France.

Jacques Mansourati (J)

Brest University Hospital, Brest, France.

Grégoire Massoulié (G)

Clermont-Ferrand University Hospital, Clermont-Ferrand, France.

Amel Mathiron (A)

Amiens University Hospital, Amiens, France.

Philippe Maury (P)

Toulouse University Hospital, Toulouse, France.

Cédric Nguyen (C)

Chalon sur Saône Hospital, Chalon sur Saône, France.

Sandro Ninni (S)

Lille University Hospital, Lille, France.

Marie-Cécile Perier (MC)

Université de Paris, PARCC, INSERM, Paris, France.

Bertrand Pierre (B)

Tours University Hospital, Tours, France.

Frédéric Sacher (F)

Bordeaux University Hospital, Bordeaux, France.

Camille Walton (C)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Pierre Winum (P)

Nîmes University Hospital, Nîmes, France.

Raphaël Martins (R)

Rennes University Hospital, Rennes, France.

Jean Luc Pasquié (JL)

Montpellier University Hospital, Montpellier, France.

Jean Benoit Thambo (JB)

Bordeaux University Hospital, Bordeaux, France.

Xavier Jouven (X)

Université de Paris, PARCC, INSERM, Paris, France; Cardiac Electrophysiology Unit, European Georges Pompidou Hospital, Paris, France.

Nicolas Combes (N)

Université de Paris, PARCC, INSERM, Paris, France; Pasteur Clinic, Toulouse, France.

Sylvie Di Filippo (S)

Louis Pradel Hospital, Hospices civils de Lyon, Lyon, France.

Eloi Marijon (E)

Université de Paris, PARCC, INSERM, Paris, France; Cardiac Electrophysiology Unit, European Georges Pompidou Hospital, Paris, France. Electronic address: https://twitter.com/EloiMarijon.

Victor Waldmann (V)

Université de Paris, PARCC, INSERM, Paris, France; Adult Congenital Heart Disease Medico-Surgical Unit, European Georges Pompidou Hospital, Paris, France; Cardiac Electrophysiology Unit, European Georges Pompidou Hospital, Paris, France. Electronic address: victor.waldmann@gmail.com.

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