Key result
Baseline ECG criteria predicted inferolateral scar with 92% sensitivity and 90% specificity in preserved EF, and anteroseptal scar with 92% sensitivity and 81% specificity in dilated cardiomyopathy.
Why the study?
Can baseline 12-lead ECG characteristics predict the location of scar (anteroseptal vs inferolateral) in patients with non-ischaemic cardiomyopathy and ventricular tachycardia?
Observational (n=108)
Can baseline 12-lead ECG characteristics predict the location of scar (anteroseptal vs inferolateral) in patients with non-ischaemic cardiomyopathy and ventricular tachycardia?
Patients with non-ischaemic cardiomyopathy (NICM) and ventricular tachycardia can be categorized as anteroseptal (AS) or inferolateral (IL) scar sub-types based on imaging and voltage mapping studies. The aim of this study was to correlate the baseline electrocardiogram (ECG) with endo-epicardial voltage maps created during ablation procedures and identify the ECG characteristics that may help to distinguish the scar as AS or IL. We assessed 108 baseline ECGs; 72 patients fulfilled criteria for dilated cardiomyopathy whereas 36 showed minimal structural abnormalities. Based on the unipolar low-voltage distribution, the scar pattern was classified as predominantly AS (n = 59) or IL (n = 49). Three ECG criteria (PR interval < 170 ms or QRS voltage in inferior leads <0.6 mV or a lateral q wave) resulted in 92% sensitivity and 90% specificity for predicting an IL pattern in patients with preserved ejection fraction (EF). The four-step algorithm for dilated cardiomyopathy included a paced ventricular rhythm or PR > 230 ms or QRS > 170 ms or an r ≤ 0.3 mV in V3 having 92 and 81% of sensitivity and specificity, respectively, in predicting AS scar pattern. A significant negative correlation was found between the extension of the endocardial unipolar low voltage area and left ventricular EF (rs = −0.719, P < 0.001). The extent of endocardial AS unipolar low voltage was correlated with PR interval and QRS duration (rs = 0.583 and rs = 0.680, P < 0.001, respectively) and the IL epicardial unipolar low voltage with the mean voltage of the limb leads (rs = −0.639, P < 0.001). Baseline ECG features are well correlated with the distribution of unipolar voltage abnormalities in NICM and may help to predict the location of scar in this population.
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Olóriz et al. (2015) conducted an observational in Non-ischaemic cardiomyopathy and ventricular tachycardia (n=108). 12-lead electrocardiogram vs. Endo-epicardial voltage maps was evaluated on Correlation of baseline ECG with endo-epicardial voltage maps to distinguish anteroseptal or inferolateral scar. Baseline ECG criteria predicted inferolateral scar with 92% sensitivity and 90% specificity in preserved EF, and anteroseptal scar with 92% sensitivity and 81% specificity in dilated cardiomyopathy.
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