Automated intraprocedural localization of origin of ventricular activation using patient-specific computed tomographic imaging

To facilitate catheter ablation of ventricular tachycardia (VT), we previously developed an automated method to identify sources of left ventricular (LV) activation in real time using 12-lead electrocardiography (ECG), the accuracy of which depends on acquisition of a complete electroanatomic (EA) m...

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Published inHeart rhythm Vol. 17; no. 4; pp. 567 - 575
Main Authors Zhou, Shijie, Sapp, John L., Horáček, B. Milan, Warren, James W., MacInnis, Paul J., Davis, Jason, Elsokkari, Ihab, Choudhury, Rajin, Parkash, Ratika, Gray, Chris, Gardner, Martin, MacIntyre, Ciorsti J., AbdelWahab, Amir
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.04.2020
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Summary:To facilitate catheter ablation of ventricular tachycardia (VT), we previously developed an automated method to identify sources of left ventricular (LV) activation in real time using 12-lead electrocardiography (ECG), the accuracy of which depends on acquisition of a complete electroanatomic (EA) map. The purpose of this study was to assess the feasibility of using a registered cardiac computed tomogram (CT) rather than an EA map to permit real-time localization and avoid errors introduced by incomplete maps. Before LV VT ablation, 10 patients underwent CT imaging and 3-dimensional reconstruction of the cardiac surface to create a triangle mesh surface, which was registered to the EA map during the procedure and imported into custom localization software. The software uses QRS integrals from leads III, V2, and V6; derives personalized regression coefficients from pacing at ≥5 sites with known locations; and estimates the location of unknown activation sites on the 3-dimensional patient-specific LV endocardial surface. Localization accuracy was quantified for VT exit sites in millimeters by comparing the calculated against the known locations. The VT exit site was identified for 20 VTs using activation and entrainment mapping, supplemented by pace-mapping at the scar margin. The automated localization software achieved incremental accuracy with additional pacing sites and had a mean localization error of 6.9 ± 5.7 mm for the 20 VTs. Patient-specific CT geometry is feasible for use in real-time automated localization of ventricular activation and may avoid reliance on a complete EA map.
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ISSN:1547-5271
1556-3871
DOI:10.1016/j.hrthm.2019.10.025