Key result
Sodium channel blockers induce short-coupled Purkinje PVCs in ~5% of patients with suspected ventricular arrhythmias.
Why the study?
Sodium channel blocker infusion may induce premature ventricular complexes in individuals without a Brugada pattern, but the clinical relevance of this finding is little known.
What is the prevalence and clinical relevance of short-coupled PVCs induced by sodium channel blockers in patients with suspected ventricular arrhythmias?
Observational (n=16)
Yes
What is the prevalence and clinical relevance of short-coupled PVCs induced by sodium channel blockers in patients with suspected ventricular arrhythmias?
Sodium channel blockers can reproducibly induce malignant short-coupled PVCs originating from the Purkinje system in a small subset of patients with idiopathic ventricular arrhythmias.
May identify Purkinje-origin short-coupled PVCs in a minority of suspected ventricular arrhythmia cases; leaves open therapeutic implications pending prospective validation.
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.
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Escande et al. (2022) conducted an observational in Suspected ventricular arrhythmias with structurally normal hearts (n=16). Sodium channel blocker (ajmaline or flecainide) infusion was evaluated on Prevalence and characteristics of short-coupled premature ventricular complexes.
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