Activation Mapping Of Ventricular Tachycardia Research Articles

Manifestation of conduction block zones by substrate mapping evaluated under multidirectional pacing during ventricular tachycardia ablation

Abstract Introduction Catheter ablation (CA) has proven to be effective therapy for ventricular tachycardia (VT) in patients with structural heart disease. However, activation mapping during VT is often limited in case of non-inducible, non-sustained or hemodynamically tolerable. It has been reported that a substrate-based approach for identifying conduction block and slow-conducting sites during sinus rhythm and ventricular pacing is promising strategies for CA. However, detailed analysis on the effectiveness of substrate mapping with multidirectional pacing to identify critical isthmus in unmappable VT have been lacking. Purpose The purpose of the present study was to evaluate the effectiveness of substrate mapping with multidirectional pacing in VT ablation. Methods From April 2022 to July 2023, 7 consecutive patients (4 men, age 62±9years) who underwent CA of VTs at our institute were enrolled. Isochronal late activation mapping (ILAM) was performed during sinus rhythm, right ventricular (RV) and left ventricular (LV) pacing. Cardiovascular magnetic resonance were performed in 3 of 7 cases to assess the distribution of myocardial late gadolinium enhancement. For catheter ablation, 2Fr electrode catheter was inserted into the anterior interventricular vein (AIV) at the distal site of the coronary sinus. LV pacing was performed using an electrode catheter placed in the AIV. ILAM were constructed by annotating the last deflection of each electrogram. Results In the 7 patients, 5 had ischemic cardiomyopathy and 2 had non-ischemic cardiomyopathy (Figure 1). During sinus rhythm, a deceleration zone (DZ) was identified in only 1 of 7 cases, consistent with linear conduction block. RV pacing demonstrated DZ in 3 of 7 cases. LV pacing revealed DZ in 6 of 7 cases, all of which had conduction blocks. U-shaped conduction blocks, which was not detectable in activation mapping during sinus rhythm, was newly identified in 29% of RV pacing, 71% of LV pacing. Combined RV and LV pacing unmasked the U-shaped conduction block in 86% of the cases. Only in case 7, activation mapping of VT with a cycle length of 470ms could be performed, and VT isthmus activation was observed in the area surrounded by the U-shaped conduction block (Figure 2). In other cases, the clinical VTs were unmappable because of the hemodynamic instability with tachycardia cycle length of approximately 300 milliseconds. Eventually, VTs became non-inducible in 3 of 5 cases in which induction was performed after the CA. During the follow-up period of 7±5 months, 6 of 7 cases remained free from any VT episodes. One patient showed small amount of pericardial effusion after CA. However, there were no life-threatening complications in any patients. Conclusion Substrate mapping using several different wavefront vectors in unstable VTs unveiled conduction block zones that might be potential ablation target sites for VT.Figure 1Figure 2

Periaortic ventricular tachycardia in structural heart disease: Evidence of localized reentrant mechanisms

The mechanisms for scar-related ventricular tachycardia (VT) originating from the periaortic region remain incompletely characterized. The purpose of this study was to map the circuits responsible for periaortic VT in high resolution. Cases with periaortic VT (2016-2020) were analyzed to characterize the substrate and mechanisms with multielectrode mapping. Periaortic VT was defined as low-voltage and/or deceleration zones within 2 cm of the left ventriculoaortic junction with a corresponding critical site during VT. Forty-nine periaortic monomorphic VTs were analyzed in 30 patients (25% of all patients with nonischemic cardiomyopathy). Isolated periaortic substrate was observed in 27% of patients, with 73% having concomitant scar, most commonly in the mid-septum (47%). Deceleration zones were equally prevalent on the septal and lateral portions of the periaortic region (87% vs 73%; P = .19). During activation mapping of VT (tachycardia cycle length 392 ± 105 ms), localized reentrant patterns of activation (14 mm [10-17 mm] × 10 mm [7-14 mm]) were demonstrated in 63% and 37% of VTs showed centrifugal activation, consistent with a focal breakout pattern. Ninety-three percent of VTs fulfilled criteria for a reentrant mechanism. Sixty-five percent of reentrant circuits had endocardial activation gaps within the tachycardia cycle length (3-dimensional circuitry), which were associated with higher rates of recurrence as compared with 2-dimensional complete circuits at 1 year (73% vs 37%; P = .028). Periaortic VTs were observed in 25% of patients with nonischemic cardiomyopathy and scar-related VT. For the first time, localized reentry confined to this anatomically challenging region was demonstrated as the predominant mechanism by high-resolution circuit activation mapping.

High-Density Grid Catheter forDetailedMappingofSinusRhythm and Scar-Related Ventricular Tachycardia: Comparison With a Linear Duodecapolar Catheter.

This study aimed to evaluate the feasibility and accuracy of using a novel grid mapping catheter during scar-related ventricular tachycardia (VT) ablation. Ultra-high-density (UHD) mapping improves identification of local abnormal ventricular activities (LAVAs) and characterization of scar substrates. Consecutive patients underwent endocardial and/or epicardial ablation guided by a HD grid mapping catheter. A linear duodecapolar catheter was used in the initial cases for systematic correlation. Isochronal late activation mapping was performed during sinus rhythm to identify deceleration zones, and activation mapping of VT was performed when tolerated. In 38 patients, 51 electroanatomic maps (left ventricle: 26, epicardium: 21, right ventricle: 4) were created using a grid catheter. LAVAs were identified in 98% of cases and deceleration zones were observed in 86%. High-frequency electrograms with diastolic activation were identified during 44 sustained monomorphic VTs, and the critical isthmus was colocalized to deceleration zones during sinus rhythm in 96% of cases. In 17 cases that underwent sequential mapping with both grid and linear catheters, the low voltage area detected using the grid (HD wave) was significantly smaller, with ratios of 0.61 (<0.5mV) and 0.81 (<1.5mV) relative to the duodecapolar catheter. VT ablation guided by a novel HD grid catheter is safe and feasible for clinical use in human scar-related VT via both endocardial and epicardial approaches. Automated selection of larger bipolar amplitudes among orthogonal pairs consistently displayed smaller low voltage areas than a previously validated linear catheter.

Targeted Ablation of Ventricular Tachycardia Guided by Wavefront Discontinuities During Sinus Rhythm

Accurate and expedited identification of scar regions most prone to reentry is needed to guide ventricular tachycardia (VT) ablation. We aimed to prospectively assess outcomes of VT ablation guided primarily by the targeting of deceleration zones (DZ) identified by propagational analysis of ventricular activation during sinus rhythm. Patients with scar-related VT were prospectively enrolled in the University of Chicago VT Ablation Registry between 2016 and 2018. Isochronal late activation maps annotated to the latest local electrogram deflection were created with high-density multielectrode mapping catheters. Targeted ablation of DZ (>3 isochrones within 1cm radius) was performed, prioritizing later activated regions with maximal isochronal crowding. When possible, activation mapping of VT was performed, and successful ablation sites were compared with DZ locations for mechanistic correlation. Patients were prospectively followed for VT recurrence and mortality. One hundred twenty patients (median age 65 years [59-71], 15% female, 50% nonischemic, median ejection fraction 31%) underwent 144 ablation procedures for scar-related VT. 57% of patients had previous ablation and epicardial access was employed in 59% of cases. High-density mapping during baseline rhythm was performed (2518 points [1615-3752] endocardial, 5049±2580 points epicardial) and identified an average of 2±1 DZ, which colocalized to successful termination sites in 95% of cases. The median total radiofrequency application duration was 29 min (21-38 min) to target DZ, representing ablation of 18% of the low-voltage area. At 12±10 months, 70% freedom from VT recurrence (80% in ischemic cardiomyopathy and 63% in nonischemic cardiomyopathy) was achieved. The overall survival rate was 87%. A novel voltage-independent high-density mapping display can identify the functional substrate for VT during sinus rhythm and guide targeted ablation, obviating the need for extensive radiofrequency delivery. Regions with isochronal crowding during the baseline rhythm were predictive of VT termination sites, providing mechanistic evidence that deceleration zones are highly arrhythmogenic, functioning as niduses for reentry.

High-Resolution Mapping of Postinfarction Reentrant Ventricular Tachycardia: Electrophysiological Characterization of the Circuit.

In vivo description of ventricular tachycardia (VT) circuits is limited by insufficient spatiotemporal resolution. We used a novel high-resolution mapping technology to characterize the electrophysiological properties of the postinfarction reentrant VT circuit. In 15 swine, myocardial infarction was induced by left anterior descending artery balloon occlusion. Animals were studied 6 to 8 weeks after myocardial infarction. Activation mapping of VTs was performed by using the Rhythmia mapping system. Activation time was based on a combination of bipolar and unipolar electrograms. The response to overdrive pacing from different zones of the circuit was examined. A total of 56 monomorphic VTs were induced (3.8±2.1 per animal). Among these, 21 (37.5%) were hemodynamically stable and allowed mapping of the circuit. Isthmuses were 16.4±7.2 mm long and 7.4±2.8 mm wide. Conduction velocities were slowest at the inward curvature into the isthmus entrance (0.28±0.2 m/s), slightly faster at the outward curvature exit (0.40±0.3 m/s) and nearly normal at the central isthmus (0.62±0.2 m/s). In 3 animals, 2 VT morphologies with opposite axes sharing the same isthmus were mapped. Conduction velocities within the shared isthmus were dependent on the activation vector, consistently slower at the proximal curvature. Overdrive pacing from isthmus sites determined by activation mapping was consistent with entrainment criteria for isthmus. However, dimensions of the isthmus defined by entrainment exceeded dimensions of the isthmus measured by activation mapping by 32±18%. In postinfarction reentrant VT, conduction velocities are slowest at the proximal and distal curvatures. Entrainment mapping overestimates the true size of the isthmus. High-resolution activation mapping of VT may better guide ablation therapy.

USING TIMING RELATIONSHIPS OF SINGLE DIASTOLIC ELECTROGRAMS DURING RAPID ACTIVATION MAPPING TO DETERMINE CRITICAL SITE DURING VENTRICULAR TACHYCARDIA ABLATION

USING TIMING RELATIONSHIPS OF SINGLE DIASTOLIC ELECTROGRAMS DURING RAPID ACTIVATION MAPPING TO DETERMINE CRITICAL SITE DURING VENTRICULAR TACHYCARDIA ABLATION

Temporal-component analysis of diastolic electrograms in ventricular tachycardia differentiates nonvulnerable regions of the circuit.

Successful activation mapping of ventricular tachycardia (VT) is dependent on the identification of a region of diastolic conduction by use of point-by-point sequential mapping. It is important to identify the site of transition from diastolic conduction to systolic activation of healthy myocardium (exit site) and differentiate this from nonvulnerable regions of the circuit. We sought to determine the temporal and component characteristics of exit-site electrograms using simultaneous multielectrode endocardial mapping and to differentiate them from bystander sites during activation mapping. Sixteen VTs induced in 12 patients with ischemic cardiomyopathy who underwent multielectrode mapping during VT performed with a custom-made 112-bipolar-electrode endocardial array were analyzed retrospectively. The activation sequence in systole and diastole was annotated, and the timing at exit and bystander sites of the near-field component was characterized in relation to surface electrocardiogram activation and to the far-field component. Spectral content of bipolar electrograms recorded at these sites was additionally analyzed to identify the near-field to far-field interval. The mean activation time at exit sites was 60.0 ± 31.5 ms (range 21-113 ms) ahead of surface QRS but was not significantly different from bystander sites (72.0 ± 55.0 ms, P = .63). However, the time delay from local to far-field activity was significantly lower at exit sites than at bystander sites (24.9 ± 15.6 vs. 86.6 ± 92.0 ms, P = .003), which was confirmed by spectral analysis (10.0 ± 13.1 vs. 89.0 ± 64.5 ms, P = .003). Our analysis suggests that temporal-component analysis of diastolic electrograms during activation mapping of VT provides a practical method to differentiate nonvulnerable sites from the exit site without the need for pacing maneuvers.