Abstract

PurposeSignal-averaged ECG (SAECG) can detect inhomogeneous myocardial conduction in patients presenting with ventricular tachycardia (VT) after myocardial infarction. Radiofrequency ablation (RFCA) aims at elimination of the endocardial late potentials and non-inducibility of VT. Previously, we demonstrated that abnormal SAECG at baseline can return to normal after a successful VT ablation. The present research investigates the post-ablation changes in SAECG after RFCA of VT and their relation to the procedural long-term outcomes.MethodsThirty-three patients (31 male; age 68 ± 9 years; EF 36 ± 12%) with ischemic VT were prospectively enrolled to receive RFCA. One VT (range 1–7) per patient was ablated using substrate-guided RFCA and complete success was achieved in 28 (85%) cases. SAECG was performed before (t1), immediately after (t2), and at least 6 months (t3) after the RFCA.ResultsAfter RFCA, the amount of patients showing abnormal SAECG decreased from 82% initially (t1) to 57.6% post-interventionally (t2); P = 0.008; and remained unchanged thereafter in 57% (t3). Patients who experienced VT recurrence (VT+) during the follow-up period had broader averaged QRS (t2): (VT+) 150 ± 26 vs. (VT−) 129 ± 21 ms; P = 0.015, as well as longer LAS40 (t2): (VT+) 60 ± 26 vs. (VT−) 43 ± 18 ms; P = 0.03. Abnormal SAECG (t2) was a strong predictor for VT recurrence: HR 5.4; 95% CI 1.5–21. SAECG detected more late potentials in patients with inferior than in those with anterior scars: 95% vs. 58%; P = 0.016.ConclusionsRFCA of VT in the left ventricle can improve an abnormal SAECG in some patients after myocardial infarction. Normal SAECG after RFCA of VT is associated with a lower risk for VT recurrence and death.

Highlights

  • Survivors of myocardial infarction (MI) are at higher risk for sudden cardiac death (SCD) caused by fast ventricularBorislav Dinov and Lisa Schramm contributed to this work

  • The signalaveraged ECG (SAECG) is a non-invasive tool for SCD risk assessment which was extensively studied in patients with ischemic cardiomyopathy [1,2,3]

  • The time domain SAECG relies on the prolongation of the averaged QRS and the presence of low-voltage, high-frequency signals at the end of the QRS complex to identify individuals who are at risk of malignant arrhythmias

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Summary

Introduction

Borislav Dinov and Lisa Schramm contributed to this work. The time domain SAECG relies on the prolongation of the averaged QRS and the presence of low-voltage, high-frequency signals at the end of the QRS complex to identify individuals who are at risk of malignant arrhythmias. These abnormal findings are considered as a representation of inhomogeneous slow intraventricular conduction through areas of infarct scars and may predispose to occurrence of re-entry VT. Their crucial role was demonstrated in several recent studies showing that extensive scar homogenization was associated with better outcomes than limited mapping and ablation of the clinical VT only [5, 6]

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