Ventricular Tachycardia Isthmus Research Articles

Dispersion of Activation in Single-Beat Global Maps During Programmed Ventricular Stimulation Identifies Infarct-Related Ventricular Tachycardia Isthmus Sites.

Electrophysiological characterization of ventricular tachycardia (VT) isthmus sites is complex and time-consuming. We aimed at developing and validating a global mapping strategy during programmed ventricular stimulation (PVS) to reveal the underlying electrophysiological properties of the infarct-related substrate and to enable identification of highly heterogeneous activation sites associated with protected VT isthmus sites. Experimental study that included 22 pigs with established myocardial infarction undergoing invivo characterization of the anatomical and functional myocardial substrate associated with potential arrhythmogenicity. High-density sequential activation maps during ventricular pacing and VT were compared with single-beat maps using a 64-pole basket catheter positioned in the left ventricle. Further analyses were performed using a novel local activation time-dispersion score to identify regional activation time heterogeneities on both baseline drive pacing and each of the extrastimuli of the PVS protocol. Basket catheter splines covered a median of 81.2% of the endocardial surface of the left ventricle. Basket-catheter-derived single-beat activation maps (N=16) during pacing showed a linear relationship with high-density sequential activation maps. Induction of ventricular arrhythmias was associated with higher local activation time-dispersion score values on single-beat global maps during PVS (N=6, 46 arrhythmia induction attempts). Single-beat-derived local activation time-dispersion score maps during successive coupled extrastimuli of the PVS showed a progressive increase in the predictive performance to identify monomorphic VT isthmus sites within the scar region (area under the curve = 0.779 in S2, area under the curve = 0.859 in S4; N=7). Sixty-four-pole-derived single-beat local activation time-dispersion score global maps during PVS identify infarct-related endocardial regions with highly heterogeneous activation times that are associated with protected VT isthmus sites.

Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives.

Catheter ablation for ventricular tachycardia (VT) in patients with systolic heart failure remains a critical yet challenging area of non-pharmacological therapy. Despite positive outcomes in atrial fibrillation, evidence for the efficacy of VT ablation in reducing cardiac mortality is inconclusive due to the absence of standardized ablation strategies. The primary challenges include difficulties in identifying suitable ablation targets and their deep locations within myocardial tissue. Current techniques, such as voltage mapping, provide valuable insights; however, they are limited by the presence of numerous bystander areas and the occurrence of incomplete transmural scarring. Recent advancements in functional substrate mapping have focused on identifying critical isthmuses without requiring hemodynamic stabilization during VT, thereby shifting the emphasis to the analysis of potentials during baseline rhythm. While methods like isochronal late activation mapping have improved target identification, they primarily address conduction abnormalities without adequately considering repolarization heterogeneity. This review highlights emerging technologies that utilize unipolar potentials to assess repolarization heterogeneities and identify VT isthmuses. Furthermore, novel ablation sources such as pulsed-field ablation, bipolar ablation, and ultra-low temperature cryoablation are being explored to create deeper and more durable lesions, addressing the limitations of traditional radiofrequency ablation. These advancements aim to reduce VT recurrence and improve overall treatment efficacy. Ultimately, understanding these innovative strategies is expected to optimize procedural outcomes and significantly enhance the management of patients with scar-related VT.

3D-targeted, electrocardiographic imaging-aided stereotactic radioablation for ventricular tachycardia storm: a case report

Abstract Background Stereotactic arrhythmia radioablation (STAR) is a promising non-invasive therapy for patients with ventricular tachycardia (VT). Accurate identification of the arrhythmogenic volume, or clinical target volume (CTV), on the radiotherapy (RT) 4D planning computed tomography (CT) scan is key for STAR efficacy and safety. This case report illustrates our workflow of electro-structural image integration for CTV delineation. Case summary A 72-year-old man with ischaemic cardiomyopathy and VT storm, despite two (endocardial and epicardial) catheter-based ablations, was consented for STAR. A 3D electro-structural arrhythmia model was generated from co-registered electroanatomical voltage and activation maps, electrocardiographic (ECG) imaging, and the cardiac CT angiography scan (in ADAS 3D), pinpointing the VT isthmus and inferoapical VT exit. At this location, an area with short recovery times was found with ECG imaging. A multidisciplinary team delineated the CTV on the transmural ventricular myocardium, which was fused with the 4D planning CT scan using a digital images and communication in medicine (DICOM) radiotherapy file. The CTV was 63% smaller compared with using the conventional American Heart Association 17-segment approach (11 vs. 24 cm3). A single fraction of 25 Gy was delivered to the internal target volume. After an 8-week blanking period, no VT recurrences or radiation-related side-effects were noted. Eight months later, the patient died from end-stage heart failure. Discussion We report a novel workflow for 3D-targeted and ECG imaging-aided CTV delineation for STAR, resulting in a smaller irradiated volume compared with segmental approaches. Acute and intermediate outcome and safety were favourable. Non-invasive ECG imaging at baseline and during induced VT holds promise for STAR guidance.

Detailed analysis of electrogram peak frequency to guide ventricular tachycardia substrate mapping.

Differentiating near-field (NF) and far-field (FF) electrograms (EGMs) is crucial in identifying critical arrhythmogenic substrate during ventricular tachycardia (VT) ablation. A novel algorithm annotates NF-fractionated signals enabling EGM peak frequency (PF) determination using wavelet transformation. This study evaluated the algorithms' effectiveness in identifying critical components of the VT circuit during substrate mapping. A multicentre, international cohort undergoing VT ablation was investigated. VT activation maps were used to demarcate the isthmus zone (IZ). Offline analysis was performed to evaluate the diagnostic performance of low-voltage area (LVA) PF substrate mapping. A total of 30 patients encompassing 198 935 EGMs were included. The IZ PF was significantly higher in sinus rhythm (SR) compared to right ventricular paced (RVp) substrate maps (234 Hz (195-294) vs. 197 Hz (166-220); P = 0.010). Compared to LVA PF, the IZ PF was significantly higher in both SR and RVp substrate maps (area under curve, AUC: 0.74 and 0.70, respectively). The LVA PF threshold of ≥200 Hz was optimal in SR maps (sensitivity 69%; specificity 64%) and RVp maps (sensitivity 60%; specificity 64%) in identifying the VT isthmus. In amiodarone-treated patients (n = 20), the SR substrate map IZ PF was significantly lower (222 Hz (186-257) vs. 303 Hz (244-375), P = 0.009) compared to amiodarone-naïve patients (n = 10). The ≥200 Hz LVA PF threshold resulted in an 80% freedom from VT with a trend towards reduced ablation lesions and radiofrequency times. LVA PF substrate mapping identifies critical components of the VT circuit with an optimal threshold of ≥200 Hz. Isthmus PF is influenced by chronic amiodarone therapy with lower values observed during RV pacing.

Novel systematic processing of cardiac magnetic resonance imaging identifies target regions associated with infarct-related ventricular tachycardia.

There is lack of agreement on late gadolinium enhancement cardiac magnetic resonance (LGE-CMR) imaging processing for guiding ventricular tachycardia (VT) ablation. We aim at developing and validating a systematic processing approach on LGE-CMR images to identify VT corridors that contain critical VT isthmus sites. This is a translational study including 18 pigs with established myocardial infarction and inducible VT undergoing in vivo characterization of the anatomical and functional myocardial substrate associated with VT maintenance. Clinical validation was conducted in a multicentre series of 33 patients with ischaemic cardiomyopathy undergoing VT ablation. Three-dimensional LGE-CMR images were processed using systematic scanning of 15 signal intensity (SI) cut-off ranges to obtain surface visualization of all potential VT corridors. Analysis and comparisons of imaging and electrophysiological data were performed in individuals with full electrophysiological characterization of the isthmus sites of at least one VT morphology. In both the experimental pig model and patients undergoing VT ablation, all the electrophysiologically defined isthmus sites (n = 11 and n = 19, respectively) showed overlapping regions with CMR-based potential VT corridors. Such imaging-based VT corridors were less specific than electrophysiologically guided ablation lesions at critical isthmus sites. However, an optimized strategy using the 7 most relevant SI cut-off ranges among patients showed an increase in specificity compared to using 15 SI cut-off ranges (70 vs. 62%, respectively), without diminishing the capability to detect VT isthmus sites (sensitivity 100%). Systematic imaging processing of LGE-CMR sequences using several SI cut-off ranges may improve and standardize procedure planning to identify VT isthmus sites.

Near-field detection and peak frequency metric for substrate and activation mapping of ventricular tachycardias in two- and three-dimensional circuits.

Successful ventricular arrhythmia (VA) ablation requires identification of functionally critical sites during contact mapping. Estimation of the peak frequency (PF) component of the electrogram (EGM) may improve correct near-field (NF) annotation to identify circuit segments on the mapped surface. In turn, assessment of NF and far-field (FF) EGMs may delineate the three-dimensional path of a ventricular tachycardia (VT) circuit. A proprietary NF detection algorithm was applied retrospectively to scar-related re-entry VT maps and compared with manually reviewed maps employing first deflection (FDcorr) for VT activation maps and last deflection (LD) for substrate maps. Ventricular tachycardia isthmus location and characteristics mapped with FDcorr vs. NF were compared. Omnipolar low-voltage areas, late activating areas, and deceleration zones (DZ) in LD vs. NF substrate maps were compared. On substrate maps, PF estimation was compared between isthmus and bystander sites. Activation mapping with entrainment and/or VT termination with radiofrequency (RF) ablation confirmed critical sites. Eighteen patients with high-density VT activation and substrate maps (55.6% ischaemic) were included. Near-field detection correctly located critical parts of the circuit in 77.7% of the cases compared with manually reviewed VT maps as reference. In substrate maps, NF detection identified deceleration zones in 88.8% of cases, which overlapped with FDcorr VT isthmus in 72.2% compared with 83.3% overlap of DZ assessed by LD. Applied to substrate maps, PF as a stand-alone feature did not differentiate VT isthmus sites from low-voltage bystander sites. Omnipolar voltage was significantly higher at isthmus sites with longer EGM durations compared with low-voltage bystander sites. The NF algorithm may enable rapid high-density activation mapping of VT circuits in the NF of the mapped surface. Integrated assessment and combined analysis of NF and FF EGM-components could support characterization of three-dimensional VT circuits with intramural segments. For scar-related substrate mapping, PF as a stand-alone EGM feature did not enable the differentiation of functionally critical sites of the dominant VT from low-voltage bystander sites in this cohort.

Wavefront curvature analysis derived from preprocedural imaging can identify the critical isthmus in patients with postinfarcted ventricular tachycardia

BackgroundWhere activation wavefront curvature is convexly shaped, functional conduction block can occur. ObjectiveThe purpose of this study was to determine whether left ventricular (LV) wall thickness determined from contrast-enhanced computed tomography (CT) is useful in localizing such areas in clinical postinfarction reentrant ventricular tachycardia (VT). MethodsWe evaluated data from 6 patients who underwent catheter ablation for postinfarction VT. CT imaging with inHEART processing was conducted 1–3 days before electrophysiological (EP) study to determine LV wall thickness (T). Activation wavefront curvature was approximated as ΔT/T, where ΔT represents wall thickness change. During EP study, bipolar LV VT electrograms were acquired using a high-density mapping catheter, and activation times were determined. Maps of T, ΔT/T, and VT activation were subsequently compared using statistical analyses. ResultsTwo of 6 cases exhibited dual circuit morphologies, resulting in a total of 8 VT morphologies analyzed. The LV wall near the VT isthmus location tended to be thin, on the order of a few hundred micrometers. Regions of largest ΔT/T partially coincided with the lateral isthmus boundaries where electrical conduction block occurred during VT. ΔT/T at the boundaries, measured from imaging, was significantly larger compared to values at the isthmus midline and to the global LV mean value (P <.001). ConclusionWavefront curvature measured by ΔT/T and caused by source–sink mismatch is dependent on ventricular wall thickness. Areas of high wavefront curvature partly coincide with and may be helpful in locating the VT isthmus in infarct border zones using preprocedural imaging analysis.

Single-beat mapping during programmed ventricular stimulation identifies infarct-related ventricular tachycardia isthmus sites

Abstract Introduction Complete characterization of reentrant ventricular tachycardia (VT) circuits using classical electrophysiological criteria and high-density mapping during VT is complex. Often, VT episodes cannot be fully characterized because of hemodynamic instability during the mapping procedure. This common limitation has motivated the implementation of mapping strategies during sinus rhythm or ventricular pacing aiming to identify scar regions associated with VT isthmuses or potential arrhythmogenicity. However, these strategies still require time-consuming catheter-based mapping. Purpose We aimed to develop and validate a single-beat mapping strategy during programmed ventricular stimulation (PVS) to identify scar regions associated with VT isthmus sites. We hypothesize that protected VT isthmuses within scar regions are characterized by larger activation time dispersion than surrounding scar areas not related to critical isthmus sites. Methods Experimental study including 16 pigs with established myocardial infarction (MI) in the anterior wall. Ten-to-twelve weeks after MI, pigs underwent left ventricular characterization using 3D late-gadolinium enhancement cardiac magnetic resonance imaging, and further invasive electroanatomical mapping to obtain high-density sequential activation maps during ventricular pacing and VT. High-density maps were compared with single-beat maps using a 64-pole basket catheter positioned in the left ventricle. After VT induction, high-density activation maps in well-tolerated VT episodes were used to identify VT isthmus sites. Simultaneous activation data from the 64-pole basket catheter were also obtained during PVS and VT. Off-line analysis was performed to: (i) validate single-beat activation maps during the baseline drive pacing cycle length (S1), and (ii) identify basket-catheter electrodes with the larger local activation time-dispersion score (LAT-DS) during PVS including up to 4 coupled extrastimuli (S2, S3, S4, S5) (Figure 1). LAT-DS was defined as the normalized product of the LAT of each electrode and the activation dispersion among its neighboring electrodes. Results Basket-catheter based single-beat activation maps during S1 pacing showed high correlation values with high-density sequential activation maps (N=16. R²=0.91). In 7 pigs, the VT isthmus site was fully characterized using high-density activation maps. During any of the coupled extrastimuli of the PVS protocol, basket catheter electrodes colocalizing with documented VT isthmus sites on high-density maps showed higher LAT-DS values compared to surrounding electrodes located on scar or healthy regions. Conversely, LAT values alone could not differentiate scar regions relevant for VT maintenance during PVS protocol (Figure 2). Conclusions Sixty-four pole single-beat activation maps during PVS identify left ventricular scar areas with higher than surrounding LAT-DS values that are associated with VT isthmus sites.Figure 1.Experimental modelFigure 2.A-Example. B-C-Full results

The evaluation of the efficacy of automated peak frequency annotation algorithm for the identification of critical isthmus of ventricular tachycardia and deceleration zones

Abstract Background Substrate modification techniques have widely been adopted due to hemodynamic instability and non-inducibility of clinical ventricular tachycardia (VT). Accurate annotation of local near field EGMs is paramount to better evaluate the ventricular substrate. Furthermore, annotation of late potentials (LP) necessitates substantial manual input and isochronal late activation mapping (ILAM) involves constant sensitivity adjustments, potentially affecting the accuracy of local ventricular signal representation. Objective This study aims to assess the utility of novel automated peak frequency (PF), which aims to determine near field local activity in low voltage regions in the prediction of the CI of scar related reentrant VTs. Furthermore, the effectiveness of automated PF annotation of near field EGMs to identify deceleration zone (DZ) during ILAM was also evaluated. Methods A total of 18 patients with scar-related VT were analyzed. In all patients, VT isthmuses were identified based on activation maps and acute termination achieved during radiofrequency ablation. Automated PF annotation using Ensite X system (Abbott) was retrospectively performed in all cases specifically in areas of low voltage with fractioned signals. The accuracy of applying the PF value and automated ILAM map for detecting VT isthmus was also assessed. Results Among the study group, 12 (66.7%) had ischemic cardiomyopathy, while 6 (33.3%) had nonischemic cardiomyopathy [3 (16.7%) with arrhythmogenic right ventricular cardiomyopathy, 2 (11.1%) with idiopathic dilated cardiomyopathy, and 1 (5.6%) with hypertrophic cardiomyopathy]. All identified isthmuses were located in areas exhibiting bipolar voltage below 0.5 mV and a PF of 250 Hz with fractionated EGMs Automated NF DZ annotation predicted the VT isthmus in 16/18 (88.9%) of the cases similar to the conventional ILAM with manual adjustment (88.9%). Conclusion Using high-density electroanatomical mapping with near field algorithm, a PF cutoff of 250 Hz accurately identified the low voltage regions to predict the CI of VT. In addition, automated annotation of EGMs during ILAM similarly identified the DZs compared with conventional last deflection algorithm with manual adjustments, which were colocalized with CI of VTs.

Tissue composition underlying local impedance in chronic infarction: an histological study

Abstract Background Local impedance (LI) mapping is feasible and provides additional tissue characterization of the ventricular tachycardia (VT) substrate. VT isthmuses are usually located in areas of intermediate LI while low LI regions did not actively participate in the VT circuit. Histological studies evaluating the tissue composition underlying different LI values are lacking. Purpose To describe the tissue composition underling different LI subtypes in a chronic myocardial infarction (MI) swine model. Methods One-month after a non-reperfused anterior MI, five Landrace X Large White pigs underwent endocardial LI mapping (figure 1). LI thresholds were set using the blood-pool LI value to define low, intermediate, and high tissue resistance subtypes. A navigated needle-catheter was used to inject methylene-blue at sites with intermediate and low LI to guide the ex vivo tissue localization. Tissue was obtained for further histological analysis. Low and intermediate LI zones were analysed. Results A total of six and eight samples were analysed for low and intermediate LI, respectively. Compared to low LI zones, intermediate LI tissue displayed less Collagen I (1.03±0.26 vs. 0.34±0.35%, p=0.0082), Collagen III (9.92±2.98 vs. 6.47±1.80%, p=0.0380) and Collagen Volume Fraction (10.92±2.77 vs. 6.81±1.92, p=0.0163), without differences in the overall fibrotic and adipocytic deposition (figure 2). No significant differences in the Cx43, CTnI and SERCA2 expression were observed. Conclusion LI subtypes showed distinctive histological composition. Intermediate LI sites displayed less collagen content (I, III and collagen volume fraction) compared to those with low LI.Endocardial LI mappingHystological analysis: Collagen Content

Novel systematic processing of cardiac magnetic resonance imaging identifies target regions associated with infarct-related ventricular tachycardia

Abstract Introduction In the clinic, complete characterization of reentrant ventricular tachycardia (VT) circuits using classical electrophysiological criteria and state-of-the-art high density mapping during VT is complex, and often cannot be completed because of hemodynamic instability. This common limitation has motivated the implementation of mapping strategies during sinus rhythm or ventricular pacing aiming to identify scar regions associated with VT isthmuses or potential arrhythmogenicity. Complementary imaging-based strategies including advanced analyses of scar tissue characteristics have been also proposed for procedure planning and identification of potential arrhythmogenic regions. However, the most recent expert consensus report on catheter ablation of ventricular arrhythmia highlights the lack of agreement on the preferable signal intensity (SI) cut-off values for assessment of tissue heterogeneity and scar areas on late gadolinium enhancement cardiac magnetic resonance (LGE-CMR) images. The latter makes LGE-CMR imaging processing highly operator-dependent and potentially sensitive to selection bias. Purpose We aimed at developing and validating a systematic processing approach on LGE-CMR images to identify potential VT corridors that may include protected isthmuses associated with VT maintenance. Methods Translational study including 18 pigs with established myocardial infarction and inducible VT undergoing in vivo characterization of the anatomical and functional myocardial substrate associated with VT maintenance. Clinical validation was conducted in a multicenter series of 33 patients with ischemic cardiomyopathy undergoing VT ablation. Three-dimensional CMR-LGE images were processed using systematic scanning of 15 signal intensity cut-off ranges to obtain surface visualization of all potential VT corridors. Analysis and comparisons of imaging and electrophysiological data were performed in individuals with full electrophysiological characterization of the isthmus sites of at least one VT morphology. Results In both the experimental pig model and patients undergoing VT ablation, all the electrophysiologically-defined isthmus sites (n=11 and n=19, respectively) showed overlapping regions with CMR-based potential VT corridors. Such imaging-based VT corridors were less specific than electrophysiologically-guided ablation lesions at functionally relevant isthmus sites (Figure). However, in patients, decreasing from 15 to 7 the number of signal intensity cut-off ranges for systematic imaging processing significantly reduced the area of imaging-based potential VT corridors, without diminishing the capability to detect functionally relevant VT isthmus sites. Conclusions Systematic processing of 3D LGE-CMR images provides unbiased identification of imaging based potential VT corridors that contain functionally relevant protected isthmus sites.

Predictors of decremental conduction after extrastimulus in post-infarction ventricular tachycardia substrate maps

Abstract Introduction Ventricular tachycardia (VT) substrate ablation techniques attempt to identify areas of decremental conduction (DC) within the scar, given their close relationship with VT isthmuses. DC identification requires the systematic use of extrastimuli during substrate mapping. This can be time consuming and induce ventricular arrhythmias during mapping. Objective This study aims to identify predictors of decremental response after extastimulus that allow recognizing areas with higher probability of DC conduction in order to focus functional mapping of the substrate on them. Methods Sixteen consecutive ischemic patients (93.8% male, 66.3±12.4 years) undergoing VT substrate ablation were included. A detailed substrate map during right ventricular (RV) pacing was obtained in all of them. Systematic analysis of electrograms (EGMs) recorded from the infarct area was performed during RV pacing at 600-500 ms, and during a short-coupled RV extrastimulus. Electrograms during RV pacing exhibiting decremental evoked conduction delay after an extrastimulus (DECD-AE) were compared to those not showing DECD-AE. Results Mean low voltage (&amp;lt;1.5 mV) area was 45±18.6 cm2. A total of 1744 EGMs were analyzed. Of them, 453 (26%) showed DECD-AE. Bipolar EGMs showing DECD-AE exhibited a higher number of deflections [4(interquartile range 3-5) vs 2(1-3); p&amp;lt;0.0001], a higher amplitude [0.52(0.27-1) vs 0.3(0.14-0.7) mV; p=0.003] and similar duration [114(102-135) vs 117(100-133 ms); p=0.492] compared to EGMs without DECD-AE. The area under curve was 0.64 for bipolar voltage and 0.8 for number of bipolar deflections. The presence of &amp;lt;3 bipolar deflections excluded DECD-AE with a negative predictive value of 98.5%. Conclusions In areas of myocardial scar, bipolar EGMs with &amp;lt;3 deflections are unlikely to present DECD-AE. Focusing functional mapping on signals with ≥3 deflections could simplify procedures and save time.

Dynamic voltage mapping of the ventricular tachycardia substrate

Abstract Background Substrate mapping techniques that predict ventricular tachycardia (VT) isthmus components in sinus or paced rhythm are necessary as mapping during VT is often not possible. Voltage maps lack accuracy in differentiating scar, traditionally displayed as tissue &amp;lt;0.50mV, from bordering arrhythmogenic substrate. We developed a practical technique aiming to improve the utility of a voltage map during VT ablation, termed ‘Dynamic Voltage Mapping’ (DVM). Methods Consecutive patients with post-infarct VT at our centre underwent left ventricle (LV) voltage mapping (mean 4762 points) with Carto3 v.7® and a PentaRay®, or Ensite X® and a HD Grid mapping catheter. Both mapping systems offer algorithms that allow substrate activation maps to be superimposed and analysed on the surface of a voltage display (i.e. Carto Ripple Maps, or Ensite X activation vectors). DVM is a process that sequentially adjusts the voltage display to highlight scar tissue in areas devoid of Ripple bars, or in areas where activation vectors point in multiple unfathomable directions (‘vector disarray’). This approach is summarised in Figures 1 &amp; 2 and was retrospectively performed in all cases. This alternative scar voltage limit was termed the ‘DVM scar threshold’ (mV). Tissue below this threshold was termed ‘DVM-scar’, and tissue immediately surrounding (up to 0.5mV) was termed "DVM-Borderzone (BZ)". Results Twenty-five patients (mean age 64.4±11.0 years, 88% male, LV ejection fraction 31.8±6.9%, 16.4±8.5 years since infarct) were studied (n=15 Carto; n=10 EnSite). Across all cases, the mean shell area with voltage &amp;lt;0.50 mV was 36.8±20.3 cm2. The mean DVM scar threshold was 0.24±0.07 mV (Carto: 0.22±0.07 mV [range 0.12–0.35 mV]; EnSite: 0.26±0.08 [range 0.18–0.50 mV]). The mean DVM-scar area was 18.4±14.3 cm2, significantly smaller than the traditional 0.50mV value (p=0.0002). In the 8 patients where stable VT was mapped, the VT isthmus sites co-located within the DVM-BZ in all cases, exemplified in the figures. Pace-mapping at the DVM-BZ matched the remaining unmappable VT morphologies. Ablation lesions were retrospectively superimposed onto the DVM map and generally co-located within the DVM-BZ. No ablation was delivered in tissues &amp;gt;0.5mV. At median follow-up of 8.8 months, VT burden significantly reduced (median 3 episodes in 3-months pre vs. 0 post; p&amp;lt;0.001), with 76% of patients VT-free. Conclusion DVM appears to improve the delineation of the post-infarct VT substrate, and is feasible using two commercially-available mapping systems. The mean voltage threshold that differentiated DVM-Scar from BZ tissue was significantly lower than the traditional 0.50 mV scar definition, at 0.24mV, though ranged widely, suggesting that scar thresholds require individualised substrate definition. Targeted ablation of DVM-BZ may be effective at reducing future VT, though requires prospective validation.Figure 1Figure 2

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

Neural network for automatic ICD-EGMs matching in pace-mapping and ablation of ventricular arrhythmias

Abstract Background Mapping of the ventricular arrhythmias (VA) is often not possible due to the non-inducibility of the electrophysiological study (EPS). Since twelve-lead electrocardiograms (ECG) of the clinical ventricular tachycardia (VT) are also often not available, therefore stored implantable cardioverter-defibrillator (ICD) electrograms (EGMs) of the clinical VT are often the only documentation. The pace mapping matching to the stored ICD-EGM template of the clinical VT can help to identify the VT exit site. Automatic objective computing of similarity scores between EGMs is impossible because ICD programmer devices do not have any interface allowing the export of digital EGMs. Therefore, images can only be accessed for similarity by subjective eyeballing. The MatcherNet Siamese neural network takes a pair of EGM images and predicts their similarity. Purpose This study aimed to assess the feasibility of the automatic ICD-EGMs matching by MatcherNet neural network for pace mapping of VT/premature ventricular contraction (PVC) exit site. Methods Consecutive patients undergoing VT ablation or ablation of ventricular fibrillation, triggered by PVC were included in the study, if the clinical VT/PVC was not inducible during EPS but ICD-EGMs of clinical VT/PVC were stored in the device. Electro-anatomical mapping was performed to reveal substrates (low-voltage areas, abnormal potentials, DEEP-potentials, conduction crowding). Subsequently, the low-output pacing from various locations tagged on the 3D map of LV was performed, and the paced ICD-EGM images were stored from the ICD programmer device for offline analysis and calculation of the similarity. RF ablation was conducted based on the substrate map findings, including the area of the most remarkable similarity between paced ICD-EGMs and clinical ICD-EGM templates assessed by eyeballing. The ICD-EGMs similarity scores (Manhattan similarity and Pearson correlation) were predicted by MatcherNet for each pacing site offline and transferred to the 3D map for the assessment of similarity distribution (Figure 1). Results We included 7 patients with VA episodes registered and stored by their ICD. The clinical characteristics are presented in Table1. In all patients, we were able to find the sites of highest ICD-EGM similarity to the clinical template with gradual decrementing of the similarity score at the increasingly distant pacing areas. The site of the highest similarity was collocated with VT substrate and ablation areas in all patients. Abrupt change of the similarity score at the adjacent pacing sites was detected in the 2 cases, indicating the possible protected VT isthmus. After ablation procedure only one patient with DCM experienced VA recurrence. Conclusion This technology opens new possibilities for the utilization of ICD-EGMs during the pace mapping of ventricular tachycardia, especially in the cases of non-inducibility during electrophysiological study.Figure 1Table 1

Non-invasive assessment of the ventricular tachycardia isthmus during sinus rhythm

Abstract Background The ablation of ventricular tachycardias (VT) presents significant challenges due to the complex and time-consuming approaches involved in identifying arrhythmogenic regions. Combining non-invasive electrocardiographic imaging (ECGI) with endocardial mapping could potentially enhance the efficacy of interventions. Objective To evaluate the capability of ECGI in guiding operators towards areas of VT isthmuses during sinus rhythm. Methods Patients with scar-related VT, confirmed by late gadolinium enhancement cardiac magnetic resonance, were prospectively enrolled. We compared the areas of slowed conduction identified by ECGI with the VT sustaining regions identified endocardially. Simultaneous Electroanatomical Mapping (EAM) and ECGI mapping were performed during VT ablation procedures. In patients in whom a hemodynamically stable VT was maintained, the reentry circuit was mapped endocardially, and the ablation target was identified. The left ventricle was segmented into 9 regions, categorized as either VT-isthmus or non-VT isthmus based on EAM findings. Prior to ablation, local activation times (LAT) and conduction velocity (CV) ECGI sinus maps were computed. Slow conduction was quantified non-invasively by computing different ECGI metrics per region, including the mean and the standard deviation (SD) of LAT and CV, the regional Total Activation Time (rTAT) – time span between the earliest and latest activated nodes–, and the Slow Conduction Velocity (SCV) – the percentage of nodes where velocity falls below 60 cm/s -. Results The study included 20 consecutive patients with ischemic cardiomyopathy who were referred for VT ablation. A total of 21 regions linked to the VT isthmus were identified endocardially in 17 patients (age: 66.1±8.8 years, 94.1% male, left ventricular ejection fraction: 26.4±7.3%). Figure 1 illustrates the correlation between the VT circuit and the ECGI sinus map in two patients with extensive left ventricular fibrosis. ECGI metrics related to VT isthmuses exhibited a higher standard deviation in both LAT (18.1±2.0 vs 9.8±1.2 ms; p=0.001), and CV (50.4±4.7 vs 37.1±2.8 cm/s; p=0.011), and a greater percentage of nodes with slowed conduction (13.7±2.7 vs 7.4±1.6 %; p=0.029), compared to non-VT isthmus regions, Figure 2. Multivariate logistic regression analysis revealed that SD-LAT was the strongest predictor of VT isthmus localization. Conclusion ECGI has demonstrated the capability to pinpoint slowed conduction areas responsible for VT in sinus rhythm, showing promise in planning and guiding VT ablation strategies. This advancement paves the way for further research into using this non-invasive tool to improve risk stratification methods for ventricular arrhythmias.

Substrate Mapping for Ventricular Tachycardia Ablation Through High-Density Whole-Chamber Double Extra Stimuli: The S3 Protocol

BackgroundA partial delineation of targets for ablation of ventricular tachycardia (VT) during a stable rhythm is likely responsible for a suboptimal success rate. The abnormal low-voltage near-field functional components may be hidden within the high-amplitude far-field signal. ObjectivesThe aim of this study was to evaluate the benefit and feasibility of functional substrate mapping using a full-ventricle S3 protocol and to assess its colocalization with arrhythmogenic conducting channels (CCs) on late gadolinium enhancement cardiac magnetic resonance. MethodsAn S3 mapping protocol with a drive train of S1 followed by S2 (effective refractory period + 30 ms) and S3 (effective refractory period + 50 ms) from the right ventricular apex was performed in 40 consecutive patients undergoing scar-related VT ablation. Deceleration zones (DZs) and areas of late potentials (LPs) were identified for all maps. A preprocedural noninvasive substrate assessment was done using late gadolinium enhancement cardiac magnetic resonance and postprocessing with automated CC identification. ResultsThe S3 protocol was completed in 34 of the 40 procedures (85.0%). The S3 protocol enhanced the identification of VT isthmus on the basis of DZ (89% vs 62%; P < 0.01) and LP (93% vs 78%; P = 0.04) assessment. The percentage of CCs unmasked by DZs and LPs using S3 maps was significantly higher than the ones using S2 and S1 maps (78%, 65%, and 48% [P < 0.001] and 88%, 81%, and 68% [P < 0.01], respectively). The functional substrate identified during S3 activation mapping was significantly more extensive than the one identified using S2 and S1, including a greater number of DZs (2.94, 2.47, and 1.82, respectively; P < 0.001) and a wider area of LPs (44.1, 38.2, and 29.4 cm2, respectively; P < 0.001). After VT ablation, 77.9% of patients have been VT free during a median follow-up period of 13.6 months. ConclusionsThe S3 protocol was feasible in 85% of patients, allows a better identification of targets for ablation, and might improve VT ablation results.

Personalized voltage maps guided by cardiac magnetic resonance in the era of high-density mapping

BackgroundVoltage mapping could identify the conducting channels potentially responsible for ventricular tachycardia (VT). Standard thresholds (0.5–1.5 mV) were established using bipolar catheters. No thresholds have been analyzed with high-density mapping catheters. In addition, channels identified by cardiac magnetic resonance (CMR) has been proven to be related with VT. ObjectiveThe purpose of this study was to analyze the diagnostic yield of a personalized voltage map using CMR to guide the adjustment of voltage thresholds. MethodsAll consecutive patients with scar-related VT undergoing ablation after CMR (from October 2018 to December 2020) were included. First, personalized CMR-guided voltage thresholds were defined systematically according to the distribution of the scar and channels. Second, to validate these new thresholds, a comparison with standard thresholds (0.5–1.5 mV) was performed. Tissue characteristics of areas identified as deceleration zones (DZs) were recorded for each pair of thresholds. In addition, the relation of VT circuits with voltage channels was analyzed for both maps. ResultsThirty-two patients were included [mean age 66.6 ± 11.2 years; 25 (78.1%) ischemic cardiomyopathy]. Overall, 52 DZs were observed: 44.2% were identified as border zone tissue with standard cutoffs vs 75.0% using personalized voltage thresholds (P = .003). Of the 31 VT isthmuses detected, only 35.5% correlated with a voltage channel with standard thresholds vs 74.2% using adjusted thresholds (P = .005). Adjusted cutoff bipolar voltages that better matched CMR images were 0.51 ± 0.32 and 1.79 ± 0.71 mV with high interindividual variability (from 0.14–1.68 to 0.7–3.21 mV). ConclusionPersonalized voltage CMR-guided personalized voltage maps enable a better identification of the substrate with a higher correlation with both DZs and VT isthmuses than do conventional voltage maps using fixed thresholds.

Sinus rhythm activation signature indicates reentrant ventricular tachycardia inducibility and approximate isthmus location

BackgroundSinus rhythm activation time is useful to assess infarct border zone substrate. ObjectiveWe sought to further investigate sinus activation in ventricular tachycardia (VT). MethodsCanine postinfarction data were analyzed retrospectively. In each experiment, an infarct was created in the left ventricular wall by left anterior descending coronary artery ligation. At 3 to 5 days after ligation, 196–312 bipolar electrograms were recorded from the anterior left ventricular epicardium overlapping the infarct border zone. Sustained monomorphic VT was induced by premature electrical stimulation in 50 experiments and was noninducible in 43 experiments. Acquired sinus rhythm and VT electrograms were marked for electrical activation time, and activation maps of representative sinus rhythm and VT cycles were constructed. The sinus rhythm activation signature was defined as the cumulative number of multielectrode recording sites that had activated per time epoch, and its derivative was used to predict VT inducibility and to define the sinus rhythm slow/late activation sequence. ResultsPlotting mean activation signature derivative, a best cutoff value was useful to separate experiments with reentrant VT inducibility (sensitivity, 42/50) vs noninducibility (specificity, 39/43), with an accuracy of 81 of 93. For the 50 experiments with inducible VT, recording sites overlying a segment of isochrone encompassing the sinus rhythm slow/late activation sequence spanned the VT isthmus location in 32 cases (64%), partially spanned it in 15 cases (30%), but did not span it in 3 cases (6%). ConclusionThe sinus rhythm activation signature derivative is assistive to differentiate substrate supporting reentrant VT inducibility vs noninducibility and to identify slow/late activation for targeting isthmus location.

Experimental demonstration of real-time cardiac physiology-based radiotherapy gating for improved cardiac radioablation on an MR-linac.

Cardiac radioablation is a noninvasive stereotactic body radiation therapy (SBRT) technique to treat patients with refractory ventricular tachycardia (VT) by delivering a single high-dose fraction to the VT isthmus. Cardiorespiratory motion induces position uncertainties resulting in decreased dose conformality. Electocardiograms (ECG) are typically used during cardiac MRI (CMR) to acquire images in a predefined cardiac phase, thus mitigating cardiac motion during image acquisition. We demonstrate real-time cardiac physiology-based radiotherapy beam gating within a preset cardiac phase on anMR-linac. MR images were acquired in healthy volunteers (n = 5, mean age = 29.6 years, mean heart-rate (HR) = 56.2 bpm) on the 1.5 T Unity MR-linac (Elekta AB, Stockholm, Sweden) after obtaining written informed consent. The images were acquired using a single-slice balance steady-state free precession (bSSFP) sequence in the coronal or sagittal plane (TR/TE = 3/1.48 ms, flip angle = 48 , SENSE = 1.5, , voxel size = , partial Fourier factor = 0.65, frame rate = 13.3 Hz). In parallel, a 4-lead ECG-signal was acquired using MR-compatible equipment. The feasibility of ECG-based beam gating was demonstrated with a prototype gating workflow using a Quasar MRI4D motion phantom (IBA Quasar, London, ON, Canada), which was deployed in the bore of the MR-linac. Two volunteer-derived combined ECG-motion traces (n = 2, mean age = 26 years, mean HR = 57.4 bpm, peak-to-peak amplitude = 14.7 mm) were programmed into the phantom to mimic dose delivery on a cardiac target in breath-hold. Clinical ECG-equipment was connected to the phantom for ECG-voltage-streaming in real-time using research software. Treatment beam gating was performed in the quiescent phase (end-diastole). System latencies were compensated by delay time correction. A previously developed MRI-based gating workflow was used as a benchmark in this study. A 15-beam intensity-modulated radiotherapy (IMRT) plan ( Gy) was delivered for different motion scenarios onto radiochromic films. Next, cardiac motion was then estimated at the basal anterolateral myocardial wall via normalized cross-correlation-based template matching. The estimated motion signal was temporally aligned with the ECG-signal, which were then used for position- and ECG-based gating simulations in the cranial-caudal (CC), anterior-posterior (AP), and right-left (RL) directions. The effect of gating was investigated by analyzing the differences in residual motion at 30, 50, and 70% treatment beam duty cycles. ECG-based (MRI-based) beam gating was performed with effective duty cycles of 60.5% (68.8%) and 47.7% (50.4%) with residual motion reductions of 62.5% (44.7%) and 43.9% (59.3%). Local gamma analyses (1%/1 mm) returned pass rates of 97.6% (94.1%) and 90.5% (98.3%) for gated scenarios, which exceed the pass rates of 70.3% and 82.0% for nongated scenarios, respectively. In average, the gating simulations returned maximum residual motion reductions of 88%, 74%, and 81% at 30%, 50%, and 70% duty cycles, respectively, in favor of MRI-basedgating. Real-time ECG-based beam gating is a feasible alternative to MRI-based gating, resulting in improved dose delivery in terms of high rates, decreased dose deposition outside the PTV and residual motion reduction, while by-passing cardiac MRIchallenges.