PO-02-228 ASSOCIATION BETWEEN SIGNAL-AVERAGED ECG INDICES AND RV STRUCTURAL ABNORMALITIES IN PATIENTS WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY: INSIGHTS FROM NORDIC ARVC REGISTER

Abstract

The value of signal-averaged ECG (SAECG) derived ventricular late potentials (LP) as a minor depolarization criterion of arrhythmogenic right ventricular cardiomyopathy (ARVC) has been debated. Another criterion from the same category, terminal activation duration (TAD>55 ms), is obtained from standard V1 ECG lead, which makes it easier for use. However little data exist regarding the relationship between structural right ventricular (RV) ARVC substrate, LP and TAD. We aimed to explore the association between structural and functional RV abnormalities assessed using cardiac magnetic resonance (CMR), SAECG parameters, and abnormal TAD. Patients with definite ARVC diagnosis or genotype-positive family members who were recruited in the Nordic ARVC Registry with SAECG and CMR were included (n=268, mean age 42±16 years, female 46%, probands 49%). RV end-diastolic volume index (RVEDVI), RV ejection fraction (RVEF), and late gadolinium enhancement (LGE) presence were assessed. RV was defined as enlarged if RVEDVI > 100 ml/m2 for men and 90 ml/m2 for women. RVEF was considered reduced if lower than 45%. SAECG components were assessed using TFC2010 definitions: filtered QRS duration (fQRSd)>114 ms, duration of terminal low-amplitude QRS signal below 40 μV (LAS40)> 38 ms and root-mean-square voltage of the terminal 40 ms (RMS40)< 20 μV. An abnormal value of any one or more of these indexes was considered as the presence of LP. We assessed sensitivity and specificity of the SAECG indexes and TAD for association with abnormal RVEF, LGE and/or RVEDVI. C-statistics was used to assess the association between each of SAECG parameters as continuous variables and RV abnormalities. All 3 SAECG indexes were significantly associated with RV structural abnormalities using c-statistics (Table), each of them characterized by higher specificity and lower sensitivity than LP. TAD demonstrated high specificity but poor sensitivity in prediction of RV structural abnormalities. LP had lower specificity, but much higher sensitivity for association with RV structural and functional abnormalities than TAD. In a large cohort of patients with definite ARVC or genotype-positive family members SAECG indexes appear to have lower specificity for detection of structural and functional RV abnormalities compared to TAD, however its sensitivity far exceeds the one of the TAD and supports SAECG value as an ECG indicator of RV substrate.