Assessment of wave front activation duration and speed across the right ventricular outflow tract using electrocardiographic imaging as predictors of the origin of the premature ventricular contractions: A validation study

• Published in: Journal of electrocardiology Vol. 73; pp. 68 - 75
• Main Authors: Parreira, Leonor, Carmo, Pedro, Marinheiro, Rita, Mesquita, Dinis, Chmelevsky, Mikhail, Ferreira, António, Marques, Lia, Pinho, Joana, Chambel, Duarte, Nunes, Silvia, Amador, Pedro, Gonçalves, Pedro, Marques, Hugo, Caria, Rui, Adragão, Pedro
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.07.2022
• Subjects: Activation duration; Activation speed; Catheter ablation; Catheter Ablation - methods; ECGI; Electrocardiography - methods; Heart Ventricles; Humans; Male; Middle Aged; Non-invasive mapping; Outflow tract; Premature ventricular contractions; Tachycardia, Ventricular; Ventricular Premature Complexes - diagnosis; Ventricular Premature Complexes - surgery; ECGI; Premature ventricular contractions; Activation duration; Catheter ablation; Activation speed; Outflow tract; Non-invasive mapping
• ISSN: 0022-0736; 1532-8430
• DOI: 10.1016/j.jelectrocard.2022.05.005

Evaluate right ventricular outflow tract (RVOT) activation duration (AD) and speed, invasively and with the electrocardiographic imaging (ECGI), as predictors of the origin of the PVCs, validating the ECGI. 18 consecutive patients, 8 males, median age 55 (35–63) years that underwent ablation of PVCs with inferior axis and had ECGI performed before ablation. Isochronal activation maps of the RVOT in PVC were obtained with the ECGI and invasively. Total RVOT AD was measured as the time between earliest and latest activated region, and propagation speed by measuring the area of the first 10 ms of activation. Cut-off values for AD, activation speed and number of 10 ms isochrones to predict the origin of the PVCs, were obtained with the ROC curve analysis. Agreement between methods was done with Pearson correlation test and Bland-Altman plot. PVCs originated from the RVOT in 11 (61%) patients. The stronger predictor of PVC origin was the AD. The median AD in PVCs from RVOT was significantly longer than from outside the RVOT, both with ECGI and invasively, respectively 62 (58–73) vs 37 (33–40) ms, p < 0.0001 and 68 (60–75) vs 35 (29–41) ms, p < 0.0001. Agreement between the two methods was good (r = 0.864, p < 0.0001). The cut-off value of 43 ms for AD measured with ECGI predicted the origin of the PVCs with a sensitivity and specificity of 100%. We found good agreement between ECGI and invasive map. The AD measured with ECGI was the best predictor of the origin of the PVCs.