Correlation Between Signal-Averaged ECG and the Histologic Evaluation of the Myocardial Substrate in Right Ventricular Outflow Tract Arrhythmias

Author:

Santangeli Pasquale1,Pieroni Maurizio1,Russo Antonio Dello1,Casella Michela1,Pelargonio Gemma1,Biase Luigi Di1,Macchione Andrea1,Burkhardt J. David1,Bellocci Fulvio1,Santarelli Pietro1,Tondo Claudio1,Natale Andrea1

Affiliation:

1. From the Texas Cardiac Arrhythmia Institute, St David’s Medical Center, Austin, TX (P.S., L.D.B., A.M., J.D.B., A.N.); the Department of Biomedical Engineering, University of Texas, Austin (L.D.B., A.N.); the Department of Cardiology, University of Foggia, Italy (P.S.,L.D.B.); Catholic University of the Sacred Heart, Rome, Italy (M.P., G.P., F.B., P.S.); Cardiac Arrhythmia Research Centre, Centro Cardiologico Monzino, Milan, Italy (A.D.R., M.C., C.T.); and the Department of Cardiovascular Diseases,...

Abstract

Background— The differential diagnosis between idiopathic and cardiomyopathy-related right ventricular outflow tract (RVOT) ventricular arrhythmias (VAs) is crucial. Signal-averaged ECG (SAECG) abnormalities are frequent in cardiomyopathy-related RVOT-VAs, although their pathophysiologic basis and diagnostic value in this setting are undefined. We tested the association between SAECG and the myocardial substrate underlying RVOT-VAs. Methods and Results— Twenty-four consecutive patients (median age, 50 years [42–59]; 12 men) with RVOT-VAs (10 with frequent [>1000/24 hours] premature ventricular contractions, 14 with ventricular tachycardias) underwent SAECG with 40-Hz filtering and electroanatomic mapping (EAM) with EAM-guided biopsy for characterization of the RVOT-VAs substrate. A filtered averaged QRS (fQRS) was obtained and analyzed for fQRS duration, low amplitude signal duration <40 mV (LAS40), and root-mean-square voltage in the last 40 ms of the QRS (RMS40). Standard definition of EAM scar was used. EAM-guided biopsy diagnosed ARVC in 11 (46%), myocarditis in 8 (33%), and idiopathic RVOT-VAs in 5 (21%) patients. Patients with cardiomyopathy-related RVOT-VAs had ≥1 EAM scar (median, 2 [1–2]; all with RVOT scar). EAM of patients with idiopathic RVOT-VAs was normal. Patients with cardiomyopathy-related RVOT-VAs had significantly longer fQRS (106 ms [92–132] versus 83 ms [82–84], P =0.01) and LAS40 (39 ms [36–51] versus 19 ms [18–21], P =0.02), and lower RMS40 (18 µV [9–26] versus 33 µV [32–33], P =0.04). A significant linear correlation was found between the extension (cm2) of the RVOT scar and all 3 SAECG parameters (rs=0.76, P <0.001 for the fQRSd; rs=0.73, P <0.001 for the LAS40; and rs=−0.72, P <0.001 for the RMS40). Using the established 2 of 3 criteria (ie, late potentials), SAECG diagnosed cardiomyopathy-related RVOT-VAs with high positive (100%) but low negative (38%) predictive values and missed 7 of 9 (78%) patients with RVOT scar <8 cm 2 . Conclusions— In patients with RVOT-VAs, abnormal SAECG parameters reflect the presence of extensive cardiomyopathic involvement of the RVOT. However, a negative SAECG does not reliably rule out cardiomyopathy-related RVOT-VAs in the presence of a small RVOT scar.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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