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Malignant Purkinje ectopy induced by sodium channel blockers

  • William Escande
  • , Jean-Baptiste Gourraud
  • , Michel Haissaguerre*
  • , Estelle Gandjbakhch
  • , Thomas Lavergne
  • , Raphael Martins
  • , Ghassen Cheniti
  • , Philipp Krisai
  • , Jean Sylvain Hermida
  • , Philippe Maury
  • , Jose-Louis Merino
  • , Jean-Luc Pasquié
  • , Nicolas Combes
  • , Elodie Surget
  • , Josselin Duchateau
  • , Thomas Pambrun
  • , Nicolas Derval
  • , M. lèze Hocini
  • , Pierre Jaïs
  • , Pieter G. Postema
  • Koonlawee Nademanee, Ed Vigmond, Olivier Bernus, Frederic Sacher, Vincent Probst
*Corresponding author for this work
  • French Society of Dermatology and Department of Dermatology, France
  • Electrophysiology and Heart Modeling Institute
  • CNRS
  • Ultrasound and Cardiology Departments, University Hospital, Institut du Thorax, Nantes, France
  • Université de Bordeaux
  • Sorbonne Université
  • Hôpital européen Georges Pompidou
  • CHU de Rennes
  • University of Basel
  • CHU Amiens Picardie
  • Hôpital de Rangueil
  • Universidad Autónoma de Madrid
  • Lapeyronie - CHU of Montpellier, France
  • Clinique Pasteur Toulouse
  • Chulalongkorn University

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: Sodium channel blocker (SCB) infusion is used to unmask the electrocardiographic pattern of Brugada syndrome. The test may also induce premature ventricular complexes (PVCs) in individuals without Brugada pattern, the clinical relevance of which is little known. Objective: The purpose of this study was to describe the prevalence of short-coupled (Sc) PVCs induced by ajmaline or flecainide in patients with suspected or documented severe ventricular arrhythmias. Methods: We reviewed the SCB tests performed in 335 patients with suspected ventricular arrhythmias and structurally normal hearts in 9 centers. ScPVCs were defined as frequent and repetitive PVCs with an R-on-T pattern on SCB tests. Repeated SCB tests were performed in 7 patients and electrophysiological mapping of ScPVCs in 9. Results: Sixteen patients (8 men; mean age 36 ± 11 years) showed ScPVCs and were included. ScPVCs appeared 229 ± 118 seconds after the initiation of infusion and displayed coupling intervals of 288 ± 28 ms. ScPVC patterns were monomorphic in 12 patients, originating from the Purkinje system in mapped patients. Repetitive PVCs were induced in 15 patients (94%) including polymorphic ventricular tachycardias in 9 (56%). SCB infusion was repeated 45 (interquartile range 0.6–46) months later and induced identical ScPVC in all. SCB test was the only mean to reveal the malignant arrhythmia in 6 patients. Catheter ablation was performed in 9 patients, resulting in arrhythmia elimination in 8 with a follow-up of 6 (interquartile range 2–9) years. Conclusion: SCB can induce ScPVC, mostly from Purkinje tissue, in a small subset of patients with idiopathic ventricular arrhythmias. Its high reproducibility suggests a distinct individual mechanism.
Original languageEnglish
Pages (from-to)1595-1603
Number of pages9
JournalHeart rhythm
Volume19
Issue number10
Early online date2022
DOIs
Publication statusPublished - Oct 2022

Keywords

  • Ajmaline
  • Flecainide
  • Idiopathic ventricular fibrillation
  • Premature ventricular complex
  • Purkinje system

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