Abstract
Abstract Introduction Left bundle branch area pacing (LBBAP) provides a more synchronous and physiological ventricular activation than conventional right ventricular pacing (RVP) in LBBB patients. QRS duration (QRSd) is the standard measurement for assessing depolarization synchrony, but it only provides information about the activation time and not about the activation sequence. Purpose Our aim is to assess the activation sequence by precordial activation delay (pAD) using a low-frequency (LF) ECG method comparing baseline and paced ECG in LBBAP and RVP patients. Methods Twelve-lead ECGs recordings were acquired from 29 patients with LBBB (16 LBBAP and 13 RVP) after 24 hours of sequential LBBAP or RVP. LF-ECG was employed for QRS-complex analysis. The activation time for each lead was computed and an activation sequence constructed by linking them. pAD was calculated as the time between the first and the last lead activation. pAD provides information about both, the delay in ventricular depolarization as indicated by its magnitude, and the depolarization direction (as it can take a positive or negative value indicating a left or right ventricle delay, respectively). Results At baseline, both groups (LBBAP and RVP) showed the latest activation at V5-V6, supported by positive median pAD values with no statistically significant differences between both groups (50 (21, 65) vs. 54 (17, 67) ms, p=0.93). LBBAP reduced V6 delay and pAD values compared to the baseline QRS (basal: 50 (21, 65) vs. paced: 2 (-18, 25) ms, p<0.001) while RVP did not exhibit any difference (basal: 54 (17, 67) vs. paced: 36 (19, 53) ms, p=0.33). LBBAP provided lower pAD values when compared to RVP (2 (-18, 25) vs. 36 (19, 53) ms, p<0.01). Conclusions pAD measured using a LF-ECG analysis is a feasible method to evaluate depolarization synchrony and provides complementary information to QRSd. In contrast to RVP, LBBAP generates a physiological ventricular activation sequence in patients with LBBB.Baseline patients characteristicsVentricular activation sequences and pAD
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