Distinct Substrates of Idiopathic Ventricular Fibrillation Revealed by Arrhythmia Characteristics on Implantable Cardioverter-Defibrillator.

Purkinje cardiomyopathy idiopathic ventricular fibrillation implantable cardioverter-defibrillator sudden cardiac death ventricular fibrillation

Journal

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

Informations de publication

Date de publication:
21 Jun 2024
Historique:
received: 12 01 2024
revised: 25 04 2024
accepted: 27 04 2024
medline: 6 7 2024
pubmed: 6 7 2024
entrez: 6 7 2024
Statut: aheadofprint

Résumé

Idiopathic ventricular fibrillation (IVF) can be associated with undetected distinct conditions such as microstructural cardiomyopathic alterations (MiCM) or Purkinje (Purk) activities with structurally normal hearts. This study sought to evaluate the characteristics of recurrent VF recorded on implantable defibrillator electrograms, associated with these substrates. This was a multicenter collaboration study. At 32 centers, we selected patients with an initial diagnosis of IVF and recurrent arrhythmia at follow-up without antiarrhythmic drugs, in whom mapping demonstrated Purk or MiCM substrate. We analyzed variables related to previous ectopy, sinus rate preceding VF, trigger, and initial VF cycle lengths. Logistic regression with cross validation was used to evaluate the performance of criteria to discriminate Purk or MiCM substrates. Among 95 patients (35 women, age 35 ± 11 years) meeting the inclusion criteria, IVF was associated with MiCM in 41 and Purk in 54 patients. A total of 117 arrhythmia recurrences including 91% VF were recorded on defibrillator. Three variables were mostly discriminant. Sinus tachycardia (≤570 ms) was more frequent in MiCM (35.9% vs 13.4%, P = 0.014) whereas short-coupled (<350 ms) triggers were most frequent in Purk-related VF (95.5% vs 23.1%, P = 0.001), which also had shorter VFCLs (182 ± 15 ms vs 215 ± 24 ms, P < 0.001).The multivariable combination provided the highest prediction (accuracy = 0.93 ± 0.05, range 0.833-1.000), discriminating 81% of IVF substrates with a high probability (>80%). Ectopy were inconsistently present before VF. Characteristics of arrhythmia recurrences on implantable cardioverter- defibrillator provide phenotypic markers of the distinct and hidden substrates underlying IVF. These findings have significant clinical and genetic implications.

Sections du résumé

BACKGROUND BACKGROUND
Idiopathic ventricular fibrillation (IVF) can be associated with undetected distinct conditions such as microstructural cardiomyopathic alterations (MiCM) or Purkinje (Purk) activities with structurally normal hearts.
OBJECTIVE OBJECTIVE
This study sought to evaluate the characteristics of recurrent VF recorded on implantable defibrillator electrograms, associated with these substrates.
METHODS METHODS
This was a multicenter collaboration study. At 32 centers, we selected patients with an initial diagnosis of IVF and recurrent arrhythmia at follow-up without antiarrhythmic drugs, in whom mapping demonstrated Purk or MiCM substrate. We analyzed variables related to previous ectopy, sinus rate preceding VF, trigger, and initial VF cycle lengths. Logistic regression with cross validation was used to evaluate the performance of criteria to discriminate Purk or MiCM substrates.
RESULTS RESULTS
Among 95 patients (35 women, age 35 ± 11 years) meeting the inclusion criteria, IVF was associated with MiCM in 41 and Purk in 54 patients. A total of 117 arrhythmia recurrences including 91% VF were recorded on defibrillator. Three variables were mostly discriminant. Sinus tachycardia (≤570 ms) was more frequent in MiCM (35.9% vs 13.4%, P = 0.014) whereas short-coupled (<350 ms) triggers were most frequent in Purk-related VF (95.5% vs 23.1%, P = 0.001), which also had shorter VFCLs (182 ± 15 ms vs 215 ± 24 ms, P < 0.001).The multivariable combination provided the highest prediction (accuracy = 0.93 ± 0.05, range 0.833-1.000), discriminating 81% of IVF substrates with a high probability (>80%). Ectopy were inconsistently present before VF.
CONCLUSIONS CONCLUSIONS
Characteristics of arrhythmia recurrences on implantable cardioverter- defibrillator provide phenotypic markers of the distinct and hidden substrates underlying IVF. These findings have significant clinical and genetic implications.

Identifiants

pubmed: 38970599
pii: S2405-500X(24)00356-6
doi: 10.1016/j.jacep.2024.04.028
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Haissaguerre has received grant support from Biosense Webster. Dr Marijon has received grant support and consulting fees from Medtronic, Boston Scientific, Abbott, Microport, Biotronik, and Zoll. Pr Gandjbakhch has received lecture fees from Biotronik; and consulting fees from Medtronic, Microport, and Abbott. Dr Tilz is a consultant for Boston Scientific, Biotronik, Biosense Webster, and Abbott Medical; has received speaker honoraria from Boston Scientific, Biotronik, Biosense Webster, Abbott Medical, and Lifetech; and has received research grants from Abbott, Biosense Webster, and Lifetech. Dr Roten has received research grants from Medtronic, the Swiss National Foundation, the Swiss Heart Foundation, the Immanuel and Ilse Straub Foundation, and the Sitem Insel Support Fund, all for work outside the submitted study; and has received speaker/consulting honoraria from Abbott and Medtronic. Dr Reichlin has receivedresearch grants from the Swiss National Science Foundation, the Swiss Heart Foundation, the Sitem Insel support funds, Biotronik, Boston-Scientific, and Medtronic, all for work outside the submitted study; and has received speaker/consulting honoraria or travel support from Abbott/SJM, Biosense-Webster, Biotronik, Boston-Scientific, and Medtronic, all for work outside the submitted study. Support for his institution’s fellowship program from Abbott/SJM, Biosense-Webster, Biotronik, Boston-Scientific, and Medtronic for work outside the submitted study. Dr Sacher has receivedspeaking honorarium from Abbott, Boston Scientific, and Biosense Webster; and equity from InHeart. Dr Nogami has received lecture fees from Abbott; and endowments from Medtronic. Dr Massoullié has received lecture fees from Boston Scientific, Biosense Webster, and Abbot. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Michel Haïssaguerre (M)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France; Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France. Electronic address: michel.haissaguerre@chu-bordeaux.fr.

Jean-Marc Sellal (JM)

Cardiology Department, Nancy University Hospital (CHRU), Nancy, France.

Karim Benali (K)

Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France; Department of Cardiac Electrophysiology, Saint-Etienne University Hospital Center, Jean-Monnet University, Saint-Etienne, France.

Benjamin de Becker (B)

AZ Sint-Jan Brugge AV, Bruges Hospital, Bruges, Belgium.

Pascal Defaye (P)

Rhythmology and Cardiac stimulation Unit, Grenoble University Hospital (CHU), Grenoble, France.

Patrizio Pascale (P)

Cardiology Department, Lausanne University Hospital (CHUV), Lausanne, Switzerland.

Raphael Martins (R)

Cardiology Department, Rennes University Hospital (CHU), Rennes, France.

Philippe Mabo (P)

Cardiology Departement, Namur University Hospital (CHU UCL Namur), Yvoir, Belgium.

Olivier Xhaet (O)

Cardiology Department, APHP Hôpital Bichat, Paris, France.

Fabrice Extramiana (F)

Cardiology Department, Rhythmology Unit, Hôpital Européen Georges Pompidou, Paris, France.

Elodie Surget (E)

Heart Rhythm Centre, Hospital da Luz, Lisbon, Portugal.

Thomas Lavergne (T)

Cardiology Department, Caen Normandie University Hospital (CHU), Caen, France.

Eloi Marijon (E)

Pitié-Salpêtrière University Hospital, Institute of Cardiology, Paris, France.

Pedro Adragao (P)

Department of Medical Sciences, University of Turin, Turin, Italy.

Maria Salomé Carvalho (MS)

Heart Rhythm Centre, Hospital da Luz, Lisbon, Portugal.

Paul-Ursmar Milliez (PU)

Cardiology Department, Caen Normandie University Hospital (CHU), Caen, France.

Mickael Laredo (M)

Pitié-Salpêtrière University Hospital, Institute of Cardiology, Paris, France.

Estelle Gandjbakhch (E)

Pitié-Salpêtrière University Hospital, Institute of Cardiology, Paris, France.

Carla Giustetto (C)

Department of Medical Sciences, University of Turin, Turin, Italy.

Fiorenzo Gaita (F)

Universitätsklinikum Schleswig-Holstein (UKSH), Klinik für Rhythmologie, Lübeck, Germany.

Roland Tilz (R)

Cardiology Department, Strasbourg University Hospital (CHRU), Strasbourg, France.

Laurence Jesel-Morel (L)

Cardiology Department, Strasbourg University Hospital (CHRU), Strasbourg, France.

Johannes Steinfurt (J)

Department of Cardiology, Universitäts-Herzzentrum Freiburg - Bad Krozingen, Freiburg, Germany.

Thomas Arentz (T)

Department of Cardiology, Universitäts-Herzzentrum Freiburg - Bad Krozingen, Freiburg, Germany.

Sebastien Knecht (S)

AZ Sint-Jan Brugge AV, Bruges Hospital, Bruges, Belgium.

Mattias Duytschaever (M)

AZ Sint-Jan Brugge AV, Bruges Hospital, Bruges, Belgium.

Laurent Roten (L)

Inselspital, Bern University Hospital, University Clinic for Cardiology, Bern, Switzerland.

Tobias Reichlin (T)

Inselspital, Bern University Hospital, University Clinic for Cardiology, Bern, Switzerland.

Marjaneh Fatemi (M)

Cardiology Department, Brest University Hospital(CHU), Brest, France.

Jacques Mansourati (J)

Cardiology Department, Brest University Hospital(CHU), Brest, France.

Claude Kouakam (C)

Cardiology Department, Lille University Hospital (CHRU), Lille, France.

Francis Bessière (F)

Cardiac Rhythmology Department, Hôpital cardiologique Louis Pradel, Hospices Civils de Lyon, Lyon, France.

Philippe Chevalier (P)

Cardiac Rhythmology Department, Hôpital cardiologique Louis Pradel, Hospices Civils de Lyon, Lyon, France.

Rafik Tadros (R)

Montreal Heart Institute (ICM), Montréal, Canada.

Laurent Macle (L)

Montreal Heart Institute (ICM), Montréal, Canada.

Francisco Gallego (F)

Montreal Heart Institute (ICM), Montréal, Canada.

Alexios Hadjis (A)

Electrophysiology Unit, Cardiology Department, Sacré-Coeur Hospital of Montréal (HSCM), Montréal, Canada.

Frederic Sacher (F)

Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France; Reference Center for Hereditary Rhythmic Diseases and Sudden Death Prevention (CMARY), Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Dylan Pereira (D)

Cardiology Department, Tours University Hospital (CHU), Tours, France.

Jerome Hourdain (J)

Cardiology Department, Tours University Hospital (CHU), Tours, France.

Jean-Claude Deharo (JC)

Cardiology Department, Marseille University Hospital La Timone (AP-HM), Marseille, France.

Romain Eschalier (R)

Cardiology Department, Marseille University Hospital La Timone (AP-HM), Marseille, France; Cardiology Department, Clermont-Ferrand University Hospital, (CHU), Clermont-Ferrand, France.

Grégoire Massoulié (G)

Cardiology Department, Clermont-Ferrand University Hospital, (CHU), Clermont-Ferrand, France.

Philippe Maury (P)

Cardiology Department, Rangueil University Hospital (CHU), Toulouse, France.

Decebal Gabriel Latcu (DG)

Cardiology Department, Princess Grace Hospital, Monaco.

Frederic Anselme (F)

Cardiology Department, Rouen-Normandie University Hospital (CHU), Rouen, France.

Josselin Duchateau (J)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France; Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Romain Tixier (R)

Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Koonlawee Nademanee (K)

Pacific Rim Electrophysiology Research Institute at Bumrungrad Hospital, Bangkok, Thailand.

Akihiko Nogami (A)

Tokyo Heart Rhythm Hospital, Tokyo, Japan.

Natasja de Groot (N)

Erasmus Medical Center, Rotterdam, the Netherlands.

Edward Vigmond (E)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France.

Olivier Bernus (O)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France.

Marc Strik (M)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France; Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Pierre Bordachar (P)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France; Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Aude Cathala (A)

Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Xavier Bouteiller (X)

Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Remi Dubois (R)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France.

Sylvain Ploux (S)

IHU Liryc, Electrophysiology and Heart Modeling Institute, Foundation Bordeaux Université, Bordeaux, France; Cardiac electrophysiology and stimulation, Cardiology Department, Bordeaux University Hospital (CHU), Pessac, France.

Classifications MeSH