Three-dimensional cardiac magnetic resonance allows the identification of slow-conducting anatomical isthmuses in tetralogy of Fallot.

Anatomical isthmus Cardiac magnetic resonance Risk stratification Tetralogy of Fallot Ventricular tachycardia

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
15 May 2024
Historique:
received: 14 09 2023
revised: 14 03 2024
accepted: 15 04 2024
medline: 15 5 2024
pubmed: 15 5 2024
entrez: 15 5 2024
Statut: aheadofprint

Résumé

Patients with repaired tetralogy of Fallot remain at risk of life-threatening ventricular tachycardia related to slow-conducting anatomical isthmuses (SCAIs). Preventive ablation of SCAI identified by invasive electroanatomical mapping is increasingly performed. This study aimed to non-invasively identify SCAI using 3D late gadolinium enhancement cardiac magnetic resonance (3D-LGE-CMR). Consecutive tetralogy of Fallot patients who underwent right ventricular electroanatomical mapping (RV-EAM) and 3D-LGE-CMR were included. High signal intensity threshold for abnormal myocardium was determined based on direct comparison of bipolar voltages and signal intensity by co-registration of RV-EAM with 3D-LGE-CMR. The diagnostic performance of 3D-LGE-CMR to non-invasively identify SCAI was determined, validated in a second cohort, and compared with the discriminative ability of proposed risk scores. The derivation cohort consisted of 48 (34 ± 16 years) and the validation cohort of 53 patients (36 ± 18 years). In the derivation cohort, 78 of 107 anatomical isthmuses (AIs) identified by EAM were normal-conducting AI, 22 were SCAI, and 7 blocked AI. High signal intensity threshold was 42% of the maximal signal intensity. The sensitivity and specificity of 3D-LGE-CMR for identifying SCAI or blocked AI were 100% and 90%, respectively. In the validation cohort, 85 of 124 AIs were normal-conducting AI, 36 were SCAI, and 3 blocked AI. The sensitivity and specificity of 3D-LGE-CMR were 95% and 91%, respectively. All risk scores showed an at best modest performance to identify SCAI (area under the curve ≤ .68). 3D late gadolinium enhancement cardiac magnetic resonance can identify SCAI with excellent accuracy and may refine non-invasive risk stratification and patient selection for invasive EAM in tetralogy of Fallot.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Patients with repaired tetralogy of Fallot remain at risk of life-threatening ventricular tachycardia related to slow-conducting anatomical isthmuses (SCAIs). Preventive ablation of SCAI identified by invasive electroanatomical mapping is increasingly performed. This study aimed to non-invasively identify SCAI using 3D late gadolinium enhancement cardiac magnetic resonance (3D-LGE-CMR).
METHODS METHODS
Consecutive tetralogy of Fallot patients who underwent right ventricular electroanatomical mapping (RV-EAM) and 3D-LGE-CMR were included. High signal intensity threshold for abnormal myocardium was determined based on direct comparison of bipolar voltages and signal intensity by co-registration of RV-EAM with 3D-LGE-CMR. The diagnostic performance of 3D-LGE-CMR to non-invasively identify SCAI was determined, validated in a second cohort, and compared with the discriminative ability of proposed risk scores.
RESULTS RESULTS
The derivation cohort consisted of 48 (34 ± 16 years) and the validation cohort of 53 patients (36 ± 18 years). In the derivation cohort, 78 of 107 anatomical isthmuses (AIs) identified by EAM were normal-conducting AI, 22 were SCAI, and 7 blocked AI. High signal intensity threshold was 42% of the maximal signal intensity. The sensitivity and specificity of 3D-LGE-CMR for identifying SCAI or blocked AI were 100% and 90%, respectively. In the validation cohort, 85 of 124 AIs were normal-conducting AI, 36 were SCAI, and 3 blocked AI. The sensitivity and specificity of 3D-LGE-CMR were 95% and 91%, respectively. All risk scores showed an at best modest performance to identify SCAI (area under the curve ≤ .68).
CONCLUSIONS CONCLUSIONS
3D late gadolinium enhancement cardiac magnetic resonance can identify SCAI with excellent accuracy and may refine non-invasive risk stratification and patient selection for invasive EAM in tetralogy of Fallot.

Identifiants

pubmed: 38748258
pii: 7674115
doi: 10.1093/eurheartj/ehae268
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Dutch Heart Foundation

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Yoshitaka Kimura (Y)

Department of Cardiology, Heart-Lung-Center, Leiden University Medical Center (LUMC), P.O. Box 9600, Leiden 2300 RC, The Netherlands.
Willem Einthoven Center of Arrhythmia Research and Management (WECAM), Leiden, The Netherlands, and Aarhus, Denmark.

Justin Wallet (J)

Department of Cardiology, Heart-Lung-Center, Leiden University Medical Center (LUMC), P.O. Box 9600, Leiden 2300 RC, The Netherlands.
Willem Einthoven Center of Arrhythmia Research and Management (WECAM), Leiden, The Netherlands, and Aarhus, Denmark.

Benjamin Bouyer (B)

Department of Cardiac Pacing and Electrophysiology, IHU Liryc, Electrophysiology and Heart Modeling Institute, Bordeaux University Hospital (CHU), Bordeaux, France.

Monique R M Jongbloed (MRM)

Department of Cardiology, Heart-Lung-Center, Leiden University Medical Center (LUMC), P.O. Box 9600, Leiden 2300 RC, The Netherlands.
Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden, The Netherlands.
Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands.

Robin Bertels (R)

Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden, The Netherlands.
Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands.

Mark G Hazekamp (MG)

Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden, The Netherlands.
Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Jean-Benoit Thambo (JB)

Department of Congenital Heart Disease, Bordeaux University Hospital, Bordeaux, France.

Xavier Iriart (X)

Department of Congenital Heart Disease, Bordeaux University Hospital, Bordeaux, France.

Hubert Cochet (H)

Department of Radiology, Bordeaux University Hospital, Bordeaux, France.

Frederic Sacher (F)

Department of Cardiac Pacing and Electrophysiology, IHU Liryc, Electrophysiology and Heart Modeling Institute, Bordeaux University Hospital (CHU), Bordeaux, France.

Hildo J Lamb (HJ)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Nico A Blom (NA)

Center for Congenital Heart Disease Amsterdam-Leiden (CAHAL), Leiden, The Netherlands.
Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands.

Katja Zeppenfeld (K)

Department of Cardiology, Heart-Lung-Center, Leiden University Medical Center (LUMC), P.O. Box 9600, Leiden 2300 RC, The Netherlands.
Willem Einthoven Center of Arrhythmia Research and Management (WECAM), Leiden, The Netherlands, and Aarhus, Denmark.

Classifications MeSH