Next Article in Journal
Resection of Calcified and Giant Thoracic Disc Herniation Through Bilateral Postero-Lateral Approach and 360° Cord Release: A Technical Note
Previous Article in Journal
Use of Intravascular Micro-Axial Left Ventricular Assist Devices as a Bridging Strategy for Cardiogenic Shock: Mid-Term Outcomes
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Perspective

Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives

Second Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2024, 13(22), 6805; https://doi.org/10.3390/jcm13226805
Submission received: 24 September 2024 / Revised: 9 November 2024 / Accepted: 10 November 2024 / Published: 12 November 2024
(This article belongs to the Section Cardiology)

Abstract

:
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.

Graphical Abstract

1. Introduction

Catheter ablation for ventricular tachycardias (VTs), especially in scar-related VTs, in patients with heart failure and reduced ejection fraction is a key area of focus within non-pharmacological heart failure therapies. While several randomized controlled trials have demonstrated favorable prognostic outcomes for atrial fibrillation, evidence regarding the efficacy of catheter ablation in reducing cardiac mortality in patients with VTs remains inconclusive (Figure 1) [1,2,3,4,5,6,7,8]. Of course, differences in clinical conditions, as reflected by the PAINESD score (atrial fibrillation is often ablated during the compensated phase, whereas VT is frequently associated with hemodynamic instability during an electrical storm), influence prognosis [9]. Therefore, it is not appropriate to directly compare clinical outcomes following AF and VT ablation. In terms of procedural considerations, a major factor contributing to this uncertainty is the lack of well-established ablation strategies for VTs, including the optimal timing of ablation, procedural endpoints, and methods for visualizing ablation targets.
The principal challenges associated with VT ablation include (1) the difficulty in identifying suitable ablation targets and (2) the deep location of these targets within the myocardial tissue [10]. Concerning the first challenge, ablation strategies have been developed that focus on low-voltage areas, channels identified by delayed potentials, decremental evoked potentials, or local abnormal ventricular activities (LAVAs), defined as sharp, high-frequency ventricular potentials [11,12]. However, these techniques pose several challenges, including the requirement for prolonged procedural times to map these abnormal potentials throughout the entire ventricles and to achieve homogenization of the low-voltage areas [13]. Most importantly, if the VT presents with a focal pattern, which is more characteristic of non-ischemic cardiomyopathy rather than scar-related reentry, identifying the VT origin using these substrate mapping techniques becomes challenging [14]. In the context of scar-related VT, current three-dimensional mapping systems can identify areas of conduction delay during baseline rhythm, represented as zones of isochronal crowding, as demonstrated by isochronal late activation mapping (ILAM) [15]. However, these ablation methods targeting functional substrate abnormalities have still been demonstrating a recurrence rate of approximately 30% for VTs [16]. One of the major reasons for these residual VTs is the presence of critical isthmuses within the intramural layer. To address the second challenge, further investigation into needle ablation or pulsed-field ablation (PFA) is warranted [17,18].
This paper aims to review the current status of the technical challenges associated with catheter ablation for VTs and to highlight the latest promising technologies.

2. Current Status of Arrhythmogenic Substrate Mappings

Although activation mapping during tachycardia is the fundamental method for identifying reentrant circuits, most VTs cannot be sustained due to hemodynamic instability, particularly in patients with heart failure and reduced ejection fraction. While mechanical hemodynamic support, such as percutaneous left ventricular assist devices, can provide hemodynamic stability in these cases, evidence is lacking regarding the improvement of VT recurrence following the procedures [19,20]. Consequently, attention has shifted to functional substrate mapping during baseline rhythm, as these techniques can be performed without concern for worsening heart failure.
The currently accepted method for identifying arrhythmogenic substrates is voltage mapping, which utilizes bipolar potentials to indicate near-field scar areas and unipolar potentials to indicate far-field scar areas. Commonly accepted cut-off values for scar border zone are bipolar voltages of less than 1.5 mV and unipolar voltages of less than 8.3 mV in the left ventricle and less than 5.5 mV in the right ventricle [21,22]. The greatest advantage of these methods is their ease of acquisition and analysis. Dynamic voltage mapping has been reported as a useful tool for identifying the VT isthmus in regions where the voltage is recognized as <0.5 mV and classified as scar tissue. However, the widespread distribution of bystander areas remains a commonly acknowledged disadvantage. LAVAs or late potentials necessitate manual labeling with mapping tags; however, a recent study demonstrated that employing a frequency cut-off value of 220 Hz achieves high sensitivity and specificity for identifying late potentials or LAVAs [23,24]. Although pace mapping may assist in excluding bystander areas, technical issues related to pacing rates and coupling intervals still persist [25]. Scar area homogenization, achieved through scar dechanneling, may also serve as a potential resolution to bystander issues; however, the difficulty of completely eliminating all conducting channels has been reported, which can lead to VT recurrence [26].
Given these challenges, functionally guided substrate mapping has been the focus for improving the efficiency of VT mapping. Tung R. and colleagues reported the utility of ILAM in identifying critical isthmuses. Deceleration zones (DZs), defined as areas of the slowest conduction velocity, are characterized by the isochronal crowding of propagation within a scar, specifically where there is a clustering of isochrones (more than two isochrones within a 1 cm radius) [15]. Hattori M. and colleagues also demonstrated the significance of isochronal crowding within the VT isthmus, further reporting that the rotational activation pattern of propagation facilitates the identification of ablation targets [27]. These methods depend on bipolar potentials, which poses a limitation in identifying the region of interest if the VT isthmus is not located within the ventricular surface layers. Given the frequent presence of three-dimensional circuits in cardiomyopathies, it is necessary to develop functional substrate mapping techniques that utilize the relatively extensive information provided by unipolar potentials [28].

3. Prominent Mapping Techniques Using Unipolar Potentials

As described above, unipolar voltage mapping is well known for relatively reflecting extensive electrophysiological characteristics compared to bipolar mapping; however, functional analyses using unipolar potentials have not been previously assessed [29]. Furthermore, it is well established that two electrophysiological characteristics—conduction abnormalities and heterogeneity of refractoriness—are essential for the establishment of reentrant circuits [30]. However, previous functional substrate mappings, such as ILAM and the rotational activation pattern, have focused on conduction abnormalities but have not adequately addressed repolarization abnormalities. To address these issues, two similar yet distinct techniques utilizing unipolar leads have been reported in recent years.
The reentry vulnerability index reported by Orini M. and colleagues is proposed as a method for identifying VT circuits, reflecting activation time, activation–recovery interval (ARI), and repolarization time using unipolar potentials [31]. They reported that the index accurately localized 72% of VT origins, which is comparable to the DZs identified by ILAM [15,31]. Furthermore, Trayanova N. and colleagues reported efficient ablation outcomes characterized by fewer ablation sites and smaller ablation areas compared to conventional techniques [32]. However, this method has a significant drawback in that it does not clearly define the high-pass filter settings when using unipolar potentials. Commercially available mapping systems typically use a nominal high-pass filter setting of 2 Hz to cancel baseline drift. However, setting the filter at 2 Hz has been reported to critically impact the measurement of the ARI, which is essential for evaluating the ST-T segment [33]. In fact, we also observed distinct ARI measurements between the high-pass filter set at 2 Hz and at 0.05 Hz, which is consistent with the settings used for surface electrocardiograms [34].
It is well established that the refractory period of the ventricular myocardium correlates closely with the ARI measured using the Wyatt method on electrocardiograms recorded with the high-pass filter setting of 0.05 Hz [35]. Nagase S. and colleagues have consistently reported the utility of assessing unipolar potentials recorded with a high-pass filter setting of 0.05 Hz while setting the indifferent electrode to the inferior vena cava [34]. Localized J-ST elevation with a negative T-wave in unipolar potentials, such as the coved type J-ST segment in surface electrocardiograms, can be identified on the epicardium in cases of Brugada syndrome [36]. They concluded that the area exhibiting localized coved type J-ST segments indicates arrhythmogenic substrates associated with Brugada syndrome or J-wave syndrome [37]. Moreover, we reported the utility of unipolar potentials in identifying the trigger area of ventricular fibrillation in a case of Brugada syndrome [38]. Furthermore, recent analyses have revealed that delayed potentials in bipolar potentials, typically interpreted as conduction abnormalities, may actually have different underlying mechanisms in cardiomyopathies and Brugada syndrome [39]. Based on these findings, we have proposed a novel method for visualizing ARI heterogeneities in the ventricles [34]. This method automatically calculates the ARI from the start, defined as the end of the QRS complex, to the end, defined as the point of maximal dV/dt of the unipolar potentials automatically, which is consistent with the Wyatt method (Figure 2).
This novel mapping technique, using the Advisor HD Grid Mapping Catheter (Abbott, MN, USA) with the EnSite system, can be automatically constructed by utilizing unipolar potential morphologies obtained during sinus rhythm or consistent ventricular pacing. Our feasibility study demonstrated that regions with a short refractory period identified using this method exhibited a comparable probability of identifying VT origins to the DZs identified by ILAM. Notably, this approach successfully identified VT origins in approximately 70% of cases where ILAM failed to do so. The findings may be influenced by differences in electrode types: ILAM, derived from bipolar potentials, primarily reflects near-field information and thus has limitations in detecting three-dimensional VT circuits with intramural isthmuses. In contrast, ARI mapping, based on unipolar potentials, may capture far-field information, offering an advantage in cases with intramural VT isthmuses. Based on this speculation, the ARI mapping technique may be effective for cases in which the VT origin cannot be identified using conventional techniques focused on conduction delay. Although several imaging techniques, including computed tomography and magnetic resonance imaging, can provide supportive information for identifying the ventricular tachycardia isthmus prior to the procedure, direct contact mapping remains a crucial method for identifying arrhythmogenic substrates [40]. Imaging quality, particularly in patients with cardiac implantable electronic devices such as implantable cardioverter defibrillators, will be a critical limitation in accurately identifying the details of VT origins [41]. These new technologies focusing on repolarization abnormalities will enhance our understanding of the reentrant circuits of VTs, complementing the widely accepted methods that concentrate on conduction delays, such as the DZs identified by ILAM.

4. Current Status and Future Perspectives of Ablation Sources

Although some of the above-described mapping techniques have been adapted for procedures, VT recurrences remain significant in both ischemic and non-ischemic patients. The primary reason for this is the complexity of the three-dimensional circuit, which includes subendocardial, subepicardial, intramural, and transmural components. In general, radiofrequency ablation creates scar tissue within 4 mm of the electrode, leading to incomplete transmural scarring [42].
For addressing this issue, new treatment approaches such as bipolar ablation, ultra-low temperature cryoablation, needle-tipped electrode ablation, radiation therapy, or PFA have been proposed. Bipolar ablation utilizes two ablation catheters connected to a radiofrequency generator, with one catheter attached to the output terminal and the other to the ground reference. The two catheters are positioned on opposite surfaces of the myocardial layers, particularly across the ventricular septum [43]. The ultra-low temperature cryoablation system utilizes a 15 mm cryoablation element and is considered well suited for papillary muscle and moderator band-related VTs, as it adheres to the tissue and can create deeper and larger lesions compared to conventional cryoablation systems [44,45]. Needle ablation has evidence in humans showing that it typically creates lesions ranging from 5 to 20 mm in size, with a low incidence of complications and a procedural success rate of 97% [17]. Stereotactic ablative radiotherapy is recognized as a noninvasive method for VT ablation using ionizing radiation, which induces DNA breaks in the tissues leading to cell death. Target zones are created within a three-dimensional coordinate system based on computed tomography [46].
Among these cutting-edge innovations, PFA is anticipated to be one of the most versatile techniques available. The concept of PFA involves creating irreversible pores in the cell membrane through the application of a direct external current, resulting in the selective death of cardiac myocytes [47]. This technique has already been widely adopted for atrial ablation in various countries across Europe and North America; however, attempts at VT ablation have only just begun [48,49]. PFA enables extensive ablation in a short duration; however, it has been noted that the depth of lesions may be shallower compared to conventional radiofrequency ablation, which could represent a significant disadvantage, particularly in the context of VT [49]. Conversely, experimental studies have demonstrated lesion depths in the ventricles ranging from 4 to 8 mm with PFA, suggesting that this technique may be comparable to, or even deeper than, radiofrequency ablation [50]. Previous case series have demonstrated a procedural success rate of over 80% with no recurrence of VTs [51]. Notably, contact force, which was once deemed to be of limited importance in the early days of PFA, is now recognized as essential for creating deep and large lesions with this technique [52]. The uniquely shaped 9 mm focal spherical lattice tip catheter, AFFERA (Medtronic, Minneapolis, MN), may enhance the contact force of the tip compared to that of other ringed or flower-shaped catheters. A critical consideration when adapting PFA for the outflow tract area is the reported occurrence of transient ST-segment depressions in surface electrocardiograms [53]. Therefore, coronary evaluations may be necessary prior to procedures that target the outflow tract.
These novel sources for ablation may aid in suppressing VT recurrence and contribute to reducing the necessity for implantable cardioverter defibrillator therapy and cardiac mortality (Figure 3).
Several complications following VT ablation continue to be a concern in the current era. A recent study reported that the procedure-related mortality rate within 30 days following VT ablation in patients with reduced ejection fraction was 0.4%, with complications including stroke due to thromboembolism, cardiac tamponade, pericardial effusion, hematoma, and pericarditis, the most frequent of which was hematoma [54]. To prevent hemorrhage at the puncture sites, vascular closure devices can serve as effective tools when used in conjunction with an echo-guided puncture technique [55]. The safety of PFA in cases of atrial fibrillation has been established; thus, there are strong expectations for enhanced safety in its application for VT ablation as well [56].

5. Conclusions

The procedural and prognostic outcomes of VT ablation remain suboptimal. In recent years, functional substrate mapping has advanced to assess not only conduction abnormalities but also repolarization heterogeneity, ushering in a new era in identifying arrhythmic substrates. To achieve deeper and more durable lesions, various ablation technologies have been developed. The innovations discussed in this paper are expected to significantly enhance treatment efficacy.

Author Contributions

Conceptualization, N.K. and T.I.; writing—original draft preparation, N.K.; writing—review and editing, T.I. All authors have read and agreed to the published version of the manuscript.

Funding

This work was partly supported by a grant from the Yomiuri Television Charity Fund.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

ARIactivation–recovery interval
DZdeceleration zone
ILAMisochronal late activation map
LAVAlocal abnormal ventricular activities
PFApulsed-field ablation
VTventricular tachycardia

References

  1. Sapp, J.L.; Wells, G.A.; Parkash, R.; Stevenson, W.G.; Blier, L.; Sarrazin, J.F.; Thibault, B.; Rivard, L.; Gula, L.; Leong-Sit, P.; et al. Ventricular Tachycardia Ablation versus Escalation of Antiarrhythmic Drugs. N. Engl. J. Med. 2016, 375, 111–121. [Google Scholar] [CrossRef] [PubMed]
  2. Della Bella, P.; Baratto, F.; Vergara, P.; Bertocchi, P.; Santamaria, M.; Notarstefano, P.; Calo, L.; Orsida, D.; Tomasi, L.; Piacenti, M.; et al. Does Timing of Ventricular Tachycardia Ablation Affect Prognosis in Patients With an Implantable Cardioverter Defibrillator? Results From the Multicenter Randomized PARTITA Trial. Circulation 2022, 145, 1829–1838. [Google Scholar] [CrossRef] [PubMed]
  3. Tung, R.; Xue, Y.; Chen, M.; Jiang, C.; Shatz, D.Y.; Besser, S.A.; Hu, H.; Chung, F.P.; Nakahara, S.; Kim, Y.H.; et al. First-Line Catheter Ablation of Monomorphic Ventricular Tachycardia in Cardiomyopathy Concurrent With Defibrillator Implantation: The PAUSE-SCD Randomized Trial. Circulation 2022, 145, 1839–1849. [Google Scholar] [CrossRef] [PubMed]
  4. Reddy, V.Y.; Reynolds, M.R.; Neuzil, P.; Richardson, A.W.; Taborsky, M.; Jongnarangsin, K.; Kralovec, S.; Sediva, L.; Ruskin, J.N.; Josephson, M.E. Prophylactic catheter ablation for the prevention of defibrillator therapy. N. Engl. J. Med. 2007, 357, 2657–2665. [Google Scholar] [CrossRef]
  5. Kuck, K.H.; Schaumann, A.; Eckardt, L.; Willems, S.; Ventura, R.; Delacrétaz, E.; Pitschner, H.F.; Kautzner, J.; Schumacher, B.; Hansen, P.S.; et al. Catheter ablation of stable ventricular tachycardia before defibrillator implantation in patients with coronary heart disease (VTACH): A multicentre randomised controlled trial. Lancet 2010, 375, 31–40. [Google Scholar] [CrossRef]
  6. Kuck, K.H.; Tilz, R.R.; Deneke, T.; Hoffmann, B.A.; Ventura, R.; Hansen, P.S.; Zarse, M.; Hohnloser, S.H.; Kautzner, J.; Willems, S.; et al. Radiofrequency Versus Cryoballoon Catheter Ablation for Paroxysmal Atrial Fibrillation: Durability of Pulmonary Vein Isolation and Effect on Atrial Fibrillation Burden: The RACE-AF Randomized Controlled Trial. Circ. Arrhythm. Electrophysiol. 2017, 10, e004422. [Google Scholar] [CrossRef]
  7. Willems, S.; Tilz, R.R.; Steven, D.; Kääb, S.; Wegscheider, K.; Gellér, L.; Meyer, C.; Heeger, C.H.; Metzner, A.; Sinner, M.F.; et al. Preventive or Deferred Ablation of Ventricular Tachycardia in Patients With Ischemic Cardiomyopathy and Implantable Defibrillator (BERLIN VT): A Multicenter Randomized Trial. Circulation 2020, 141, 1057–1067. [Google Scholar] [CrossRef]
  8. Arenal, Á.; Ávila, P.; Jiménez-Candil, J.; Tercedor, L.; Calvo, D.; Arribas, F.; Fernández-Portales, J.; Merino, J.L.; Hernández-Madrid, A.; Fernández-Avilés, F.J.; et al. Substrate Ablation vs Antiarrhythmic Drug Therapy for Symptomatic Ventricular Tachycardia. J. Am. Coll. Cardiol. 2022, 79, 1441–1453. [Google Scholar] [CrossRef]
  9. Uetake, S.; Hasegawa, K.; Kurata, M.; Davogustto, G.E.; Hu, T.Y.; Siergrist, K.K.; Yoneda, Z.; Richardson, T.D.; Kanagasundram, A.N.; Stevenson, W.G.; et al. Emergent Ablation for Ventricular Tachycardia: Predictors of Prolonged Hospitalization and Mortality. JACC Clin. Electrophysiol. 2024; Online ahead of print. [Google Scholar]
  10. Guandalini, G.S.; Liang, J.J.; Marchlinski, F.E. Ventricular Tachycardia Ablation: Past, Present, and Future Perspectives. JACC Clin. Electrophysiol. 2019, 5, 1363–1383. [Google Scholar] [CrossRef]
  11. Jaïs, P.; Maury, P.; Khairy, P.; Sacher, F.; Nault, I.; Komatsu, Y.; Hocini, M.; Forclaz, A.; Jadidi, A.S.; Weerasooryia, R.; et al. Elimination of local abnormal ventricular activities: A new end point for substrate modification in patients with scar-related ventricular tachycardia. Circulation 2012, 125, 2184–2196. [Google Scholar] [CrossRef] [PubMed]
  12. Porta-Sánchez, A.; Jackson, N.; Lukac, P.; Kristiansen, S.B.; Nielsen, J.M.; Gizurarson, S.; Massé, S.; Labos, C.; Viswanathan, K.; King, B.; et al. Multicenter Study of Ischemic Ventricular Tachycardia Ablation With Decrement-Evoked Potential (DEEP) Mapping With Extra Stimulus. JACC Clin. Electrophysiol. 2018, 4, 307–315. [Google Scholar] [CrossRef] [PubMed]
  13. Fernández-Armenta, J.; Andreu, D.; Penela, D.; Trucco, E.; Cipolletta, L.; Arbelo, E.; Berne, P.; María Tolosana, J.; Pedrote, A.; Brugada, J.; et al. Sinus rhythm detection of conducting channels and ventricular tachycardia isthmus in arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm 2014, 11, 747–754. [Google Scholar] [CrossRef] [PubMed]
  14. Pogwizd, S.M.; McKenzie, J.P.; Cain, M.E. Mechanisms underlying spontaneous and induced ventricular arrhythmias in patients with idiopathic dilated cardiomyopathy. Circulation 1998, 98, 2404–2414. [Google Scholar] [CrossRef]
  15. Irie, T.; Yu, R.; Bradfield, J.S.; Vaseghi, M.; Buch, E.F.; Ajijola, O.; Macias, C.; Fujimura, O.; Mandapati, R.; Boyle, N.G.; et al. Relationship between sinus rhythm late activation zones and critical sites for scar-related ventricular tachycardia: Systematic analysis of isochronal late activation mapping. Circ. Arrhythm. Electrophysiol. 2015, 8, 390–399. [Google Scholar] [CrossRef]
  16. Aziz, Z.; Shatz, D.; Raiman, M.; Upadhyay, G.A.; Beaser, A.D.; Besser, S.A.; Shatz, N.A.; Fu, Z.; Jiang, R.; Nishimura, T.; et al. Targeted Ablation of Ventricular Tachycardia Guided by Wavefront Discontinuities During Sinus Rhythm: A New Functional Substrate Mapping Strategy. Circulation 2019, 140, 1383–1397. [Google Scholar] [CrossRef]
  17. Packer, D.L.; Wilber, D.J.; Kapa, S.; Dyrda, K.; Nault, I.; Killu, A.M.; Kanagasundram, A.; Richardson, T.; Stevenson, W.; Verma, A.; et al. Ablation of Refractory Ventricular Tachycardia Using Intramyocardial Needle Delivered Heated Saline-Enhanced Radiofrequency Energy: A First-in-Man Feasibility Trial. Circ. Arrhythm. Electrophysiol. 2022, 15, e010347. [Google Scholar] [CrossRef]
  18. Nies, M.; Watanabe, K.; Kawamura, I.; Santos-Gallego, C.G.; Reddy, V.Y.; Koruth, J.S. Preclinical Study of Pulsed Field Ablation of Difficult Ventricular Targets: Intracavitary Mobile Structures, Interventricular Septum, and Left Ventricular Free Wall. Circ. Arrhythm. Electrophysiol. 2024, 17, e012734. [Google Scholar] [CrossRef]
  19. Kataoka, N.; Imamura, T.; Uchida, K.; Koi, T.; Nakamura, M.; Kinugawa, K. Urgent catheter ablation in Japanese patients with mechanical circulatory supports suffering from refractory ventricular electrical storm. J. Cardiol. 2023, 81, 229–235. [Google Scholar] [CrossRef]
  20. Sroubek, J.; Vajapey, R.; Sipko, J.J.; Soltesz, E.G.; Weiss, A.J.; Bhargava, M.; Hussein, A.A.; Kanj, M.; Saliba, W.I.; Taigen, T.L.; et al. First-in-Human Experience With Impella 5.0/5.5 for High-Risk Patients With Advanced Heart Failure Undergoing VT Ablation. J. Am. Coll. Cardiol. 2023, 82, 469–471. [Google Scholar] [CrossRef]
  21. Polin, G.M.; Haqqani, H.; Tzou, W.; Hutchinson, M.D.; Garcia, F.C.; Callans, D.J.; Zado, E.S.; Marchlinski, F.E. Endocardial unipolar voltage mapping to identify epicardial substrate in arrhythmogenic right ventricular cardiomyopathy/dysplasia. Heart Rhythm 2011, 8, 76–83. [Google Scholar] [CrossRef] [PubMed]
  22. Hutchinson, M.D.; Gerstenfeld, E.P.; Desjardins, B.; Bala, R.; Riley, M.P.; Garcia, F.C.; Dixit, S.; Lin, D.; Tzou, W.S.; Cooper, J.M.; et al. Endocardial unipolar voltage mapping to detect epicardial ventricular tachycardia substrate in patients with nonischemic left ventricular cardiomyopathy. Circ. Arrhythm. Electrophysiol. 2011, 4, 49–55. [Google Scholar] [CrossRef] [PubMed]
  23. Vlachos, K.; Letsas, K.P.; Srinivasan, N.T.; Frontera, A.; Efremidis, M.; Dragasis, S.; Martin, C.A.; Martin, R.; Nakashima, T.; Bazoukis, G.; et al. The value of functional substrate mapping in ventricular tachycardia ablation. Heart Rhythm O2 2023, 4, 134–146. [Google Scholar] [CrossRef] [PubMed]
  24. Payne, J.E.; Woods, C.; Elshazly, M.B.; Matthews, A.; Kroman, A.; Feng, Z.; Rabinkova, A.; Ghadban, R.; Dhakal, B.; Winterfield, J. A novel automated peak frequency annotation algorithm for identifying deceleration zones and ventricular tachycardia ablation sites. Heart Rhythm 2024, 21, 27–33. [Google Scholar] [CrossRef]
  25. Shinoda, Y.; Jameria, Z.A.; Sahara, N.; Upadhyay, G.A.; Liao, Y.; Martinez, J.; Katrapati, P.; Bai, R.; Zawaneh, M.; Weiss, J.P.; et al. Rate-Dependent Pacemap Matching in Scar-Related Ventricular Tachycardia: Impact of “TR Fusion” Phenomenon. JACC Clin. Electrophysiol. 2024, 10, 2132–2144. [Google Scholar] [CrossRef]
  26. Berruezo, A.; Fernández-Armenta, J.; Andreu, D.; Penela, D.; Herczku, C.; Evertz, R.; Cipolletta, L.; Acosta, J.; Borràs, R.; Arbelo, E.; et al. Scar dechanneling: New method for scar-related left ventricular tachycardia substrate ablation. Circ. Arrhythm. Electrophysiol. 2015, 8, 326–336. [Google Scholar] [CrossRef]
  27. Hattori, M.; Komatsu, Y.; Naeemah, Q.J.; Hanaki, Y.; Ichihara, N.; Ota, C.; Machino, T.; Kuroki, K.; Yamasaki, H.; Igarashi, M.; et al. Rotational Activation Pattern During Functional Substrate Mapping: Novel Target for Catheter Ablation of Scar-Related Ventricular Tachycardia. Circ. Arrhythm. Electrophysiol. 2022, 15, e010308. [Google Scholar] [CrossRef]
  28. Nishimura, T.; Shatz, N.; Weiss, J.P.; Zawaneh, M.; Bai, R.; Beaser, A.D.; Upadhyay, G.A.; Aziz, Z.A.; Nayak, H.M.; Shatz, D.Y.; et al. Identification of Human Ventricular Tachycardia Demarcated by Fixed Lines of Conduction Block in a 3-Dimensional Hyperboloid Circuit. Circulation 2023, 148, 1354–1367. [Google Scholar] [CrossRef]
  29. Qian, P.C.; Oberfeld, B.; Schaeffer, B.; Nakamura, T.; John, R.M.; Sapp, J.L.; Stevenson, W.G.; Tedrow, U.B. Frequency Content of Unipolar Electrograms May Predict Deep Intramural Excitable Substrate: Insights From Intramural Needle Catheter Ablation of Ventricular Tachycardia. JACC Clin. Electrophysiol. 2020, 6, 760–769. [Google Scholar] [CrossRef]
  30. Amoni, M.; Vermoortele, D.; Ekhteraei-Tousi, S.; Donate Puertas, R.; Gilbert, G.; Youness, M.; Thienpont, B.; Willems, R.; Roderick, H.L.; Claus, P.; et al. Heterogeneity of Repolarization and Cell-Cell Variability of Cardiomyocyte Remodeling Within the Myocardial Infarction Border Zone Contribute to Arrhythmia Susceptibility. Circ. Arrhythm. Electrophysiol. 2023, 16, e011677. [Google Scholar] [CrossRef]
  31. Orini, M.; Graham, A.J.; Srinivasan, N.T.; Campos, F.O.; Hanson, B.M.; Chow, A.; Hunter, R.J.; Schilling, R.J.; Finlay, M.; Earley, M.J.; et al. Evaluation of the reentry vulnerability index to predict ventricular tachycardia circuits using high-density contact mapping. Heart Rhythm 2020, 17, 576–583. [Google Scholar] [CrossRef] [PubMed]
  32. Jelvehgaran, P.; O’Hara, R.; Prakosa, A.; Chrispin, J.; Boink, G.J.J.; Trayanova, N.; Coronel, R.; Oostendorp, T. Computational Re-Entry Vulnerability Index Mapping to Guide Ablation in Patients With Postmyocardial Infarction Ventricular Tachycardia. JACC Clin. Electrophysiol. 2023, 9, 301–310. [Google Scholar] [CrossRef] [PubMed]
  33. Stoks, J.; Langfield, P.; Cluitmans, M.J.M. Methodological and Mechanistic Considerations in Local Repolarization Mapping. JACC Clin. Electrophysiol. 2024, 10, 376–377. [Google Scholar] [CrossRef] [PubMed]
  34. Kataoka, N.; Imamura, T.; Uchida, K.; Koi, T.; Kinugawa, K. Unipolar morphology–guided critical isthmus emphasis in a patient with scar-related ventricular tachycardia. Hear. Case Rep. 2024, 10, 656–660. [Google Scholar] [CrossRef]
  35. Chen, P.S.; Moser, K.M.; Dembitsky, W.P.; Auger, W.R.; Daily, P.O.; Calisi, C.M.; Jamieson, S.W.; Feld, G.K. Epicardial activation and repolarization patterns in patients with right ventricular hypertrophy. Circulation 1991, 83, 104–118. [Google Scholar] [CrossRef]
  36. Nagase, S.; Kusano, K.F.; Morita, H.; Nishii, N.; Banba, K.; Watanabe, A.; Hiramatsu, S.; Nakamura, K.; Sakuragi, S.; Ohe, T. Longer repolarization in the epicardium at the right ventricular outflow tract causes type 1 electrocardiogram in patients with Brugada syndrome. J. Am. Coll. Cardiol. 2008, 51, 1154–1161. [Google Scholar] [CrossRef]
  37. Kataoka, N.; Nagase, S.; Kamakura, T.; Noda, T.; Aiba, T.; Kusano, K. Local activation delay exacerbates local J-ST elevation in the epicardium: Electrophysiological substrate in Brugada syndrome. Hear. Case Rep. 2017, 3, 595–598. [Google Scholar] [CrossRef]
  38. Kataoka, N.; Imamura, T. Brugada Syndrome: A Comprehensive Review of Fundamental and Electrophysiological New Findings. J. Clin. Med. 2023, 12, 6590. [Google Scholar] [CrossRef]
  39. Nagase, S.; Kataoka, N.; Morita, H.; Kamakura, T.; Ueoka, A.; Nakamura, T.; Oka, S.; Miyazaki, Y.; Wakamiya, A.; Nakajima, K.; et al. Demonstration of Arrhythmia Substrate-Associated Dispersion of Repolarization by Epicardial Unipolar Mapping in Brugada Syndrome. JACC Clin. Electrophysiol. 2024, 10, 1576–1588. [Google Scholar] [CrossRef]
  40. Chery, G.; Khoshknab, M.; Nazarian, S. Imaging to Facilitate Ventricular Tachycardia Ablation: Intracardiac Echocardiography, Computed Tomography, Magnetic Resonance, and Positron Emission Tomography. JACC Clin. Electrophysiol. 2024, 10, 2277–2292. [Google Scholar] [CrossRef]
  41. Bhuva, A.N.; Kellman, P.; Graham, A.; Ramlall, M.; Boubertakh, R.; Feuchter, P.; Hawkins, A.; Lowe, M.; Lambiase, P.D.; Sekhri, N.; et al. Clinical impact of cardiovascular magnetic resonance with optimized myocardial scar detection in patients with cardiac implantable devices. Int. J. Cardiol. 2019, 279, 72–78. [Google Scholar] [CrossRef] [PubMed]
  42. Masnok, K.; Watanabe, N. Catheter contact area strongly correlates with lesion area in radiofrequency cardiac ablation: An ex vivo porcine heart study. J. Interv. Card. Electrophysiol. 2022, 63, 561–572. [Google Scholar] [CrossRef] [PubMed]
  43. Koruth, J.S.; Dukkipati, S.; Miller, M.A.; Neuzil, P.; d’Avila, A.; Reddy, V.Y. Bipolar irrigated radiofrequency ablation: A therapeutic option for refractory intramural atrial and ventricular tachycardia circuits. Heart Rhythm 2012, 9, 1932–1941. [Google Scholar] [CrossRef] [PubMed]
  44. Rivera, S.; de la Paz Ricapito, M.; Espinoza, J.; Belardi, D.; Albina, G.; Giniger, A.; Roux, J.F.; Ayala-Paredes, F.; Scazzuso, F. Cryoablation for Ventricular Arrhythmias Arising From the Papillary Muscles of the Left Ventricle Guided by Intracardiac Echocardiography and Image Integration. JACC Clin. Electrophysiol. 2015, 1, 509–516. [Google Scholar] [CrossRef]
  45. Whitaker, J.; Batnyam, U.; Kapur, S.; Sauer, W.H.; Tedrow, U. Safety and Efficacy of Cryoablation for Right Ventricular Moderator Band-Papillary Muscle Complex Ventricular Arrhythmias. JACC Clin. Electrophysiol. 2022, 8, 857–868. [Google Scholar] [CrossRef]
  46. Lee, J.; Bates, M.; Shepherd, E.; Riley, S.; Henshaw, M.; Metherall, P.; Daniel, J.; Blower, A.; Scoones, D.; Wilkinson, M.; et al. Cardiac stereotactic ablative radiotherapy for control of refractory ventricular tachycardia: Initial UK multicentre experience. Open Heart 2021, 8, e001770. [Google Scholar] [CrossRef]
  47. Füting, A.; Reinsch, N.; Höwel, D.; Brokkaar, L.; Rahe, G.; Neven, K. First experience with pulsed field ablation as routine treatment for paroxysmal atrial fibrillation. Europace 2022, 24, 1084–1092. [Google Scholar] [CrossRef]
  48. Reddy, V.Y.; Gerstenfeld, E.P.; Natale, A.; Whang, W.; Cuoco, F.A.; Patel, C.; Mountantonakis, S.E.; Gibson, D.N.; Harding, J.D.; Ellis, C.R.; et al. Pulsed Field or Conventional Thermal Ablation for Paroxysmal Atrial Fibrillation. N. Engl. J. Med. 2023, 389, 1660–1671. [Google Scholar] [CrossRef]
  49. Lozano-Granero, C.; Hirokami, J.; Franco, E.; Tohoku, S.; Matía-Francés, R.; Schmidt, B.; Hernández-Madrid, A.; Zamorano Gómez, J.L.; Moreno, J.; Chun, J. Case Series of Ventricular Tachycardia Ablation With Pulsed-Field Ablation: Pushing Technology Further (Into the Ventricle). JACC Clin. Electrophysiol. 2023, 9, 1990–1994. [Google Scholar] [CrossRef]
  50. Im, S.I.; Higuchi, S.; Lee, A.; Stillson, C.; Buck, E.; Morrow, B.; Schenider, K.; Speltz, M.; Gerstenfeld, E.P. Pulsed Field Ablation of Left Ventricular Myocardium in a Swine Infarct Model. JACC Clin. Electrophysiol. 2022, 8, 722–731. [Google Scholar] [CrossRef]
  51. Askarinejad, A.; Kohansal, E.; Sabahizadeh, A.; Hesami, H.; Adimi, S.; Haghjoo, M. Pulsed-Field Ablation in Management of Ventricular Tachycardia: A Systematic Review of Case Reports and Clinical Outcomes. Clin. Cardiol. 2024, 47, e70018. [Google Scholar] [CrossRef] [PubMed]
  52. Nakagawa, H.; Castellvi, Q.; Neal, R.; Girouard, S.; Laughner, J.; Ikeda, A.; Sugawara, M.; An, Y.; Hussein, A.A.; Nakhla, S.; et al. Effects of Contact Force on Lesion Size During Pulsed Field Catheter Ablation: Histochemical Characterization of Ventricular Lesion Boundaries. Circ. Arrhythm. Electrophysiol. 2024, 17, e012026. [Google Scholar] [CrossRef] [PubMed]
  53. Della Rocca, D.G.; Cespón-Fernández, M.; Keelani, A.; Raffa, S.; Pannone, L.; Almorad, A.; Ströker, E.; Borisov, G.; Bala, G.; Sieira, J.; et al. Focal Pulsed Field Ablation for Premature Ventricular Contractions: A Multicenter Experience. Circ. Arrhythm. Electrophysiol. 2024, 17, e012826. [Google Scholar] [CrossRef] [PubMed]
  54. Lee, J.Z.; Tan, M.C.; Karikalan, S.; Deshmukh, A.J.; Srivathsan, K.; Shen, W.K.; El-Masry, H.; Scott, L.; Asirvatham, S.J.; Cha, Y.M.; et al. Causes of Early Mortality After Ventricular Tachycardia Ablation in Patients With Reduced Ejection Fraction. JACC Clin. Electrophysiol. 2023, 9, 824–832. [Google Scholar] [CrossRef] [PubMed]
  55. Van Wiechen, M.P.; Tchétché, D.; Ooms, J.F.; Hokken, T.W.; Kroon, H.; Ziviello, F.; Ghattas, A.; Siddiqui, S.; Laperche, C.; Spitzer, E.; et al. Suture- or Plug-Based Large-Bore Arteriotomy Closure: A Pilot Randomized Controlled Trial. JACC Cardiovasc. Interv. 2021, 14, 149–157. [Google Scholar] [CrossRef]
  56. Ekanem, E.; Neuzil, P.; Reichlin, T.; Kautzner, J.; van der Voort, P.; Jais, P.; Chierchia, G.B.; Bulava, A.; Blaauw, Y.; Skala, T.; et al. Safety of pulsed field ablation in more than 17,000 patients with atrial fibrillation in the MANIFEST-17K study. Nat. Med. 2024, 30, 2020–2029. [Google Scholar] [CrossRef]
Figure 1. The history of large-scale clinical trials of catheter ablation for systolic heart failure. ABL indicates ablation; HF, heart failure; LVEF, left ventricular ejection fraction; VF; ventricular fibrillation; VT; ventricular tachycardia.
Figure 1. The history of large-scale clinical trials of catheter ablation for systolic heart failure. ABL indicates ablation; HF, heart failure; LVEF, left ventricular ejection fraction; VF; ventricular fibrillation; VT; ventricular tachycardia.
Jcm 13 06805 g001
Figure 2. (A) Comparison of the bipolar voltage map, isochronal late activation map (ILAM), and activation–recovery interval (ARI) map of the epicardium in a case of ventricular tachycardia (VT). White circles indicate areas where diastolic potentials were recorded during VT. While both the voltage map and ILAM did not accurately identify regions with recorded diastolic potentials, the ARI map effectively identified the area. (B) Unipolar potentials of the epicardium from regions with shorter and longer ARI are shown. Local ARI can be automatically measured by aligning the starting point with the S-wave in lead I and defining the endpoint as the point of maximal dV/dt of the unipolar potentials, with a blanking period set to extend until the termination of the QRS complex. Point A represents the shortest ARI on the ARI map, while Point B represents the longest ARI. White arrows indicate the automatically documented endpoints.
Figure 2. (A) Comparison of the bipolar voltage map, isochronal late activation map (ILAM), and activation–recovery interval (ARI) map of the epicardium in a case of ventricular tachycardia (VT). White circles indicate areas where diastolic potentials were recorded during VT. While both the voltage map and ILAM did not accurately identify regions with recorded diastolic potentials, the ARI map effectively identified the area. (B) Unipolar potentials of the epicardium from regions with shorter and longer ARI are shown. Local ARI can be automatically measured by aligning the starting point with the S-wave in lead I and defining the endpoint as the point of maximal dV/dt of the unipolar potentials, with a blanking period set to extend until the termination of the QRS complex. Point A represents the shortest ARI on the ARI map, while Point B represents the longest ARI. White arrows indicate the automatically documented endpoints.
Jcm 13 06805 g002
Figure 3. Current status and future perspectives of ventricular tachycardia ablation. The ARI map represents epicardial surface mapping in a case of VT. The encircled area on the ARI map highlights the critical isthmus of the VT circuit. ARI indicates the activation–recovery interval; ILAM, isochronal late activation map; LAVA, local abnormal ventricular activities; RAP, rotational activation pattern. The right figure indicates complications associated with ablation procedures.
Figure 3. Current status and future perspectives of ventricular tachycardia ablation. The ARI map represents epicardial surface mapping in a case of VT. The encircled area on the ARI map highlights the critical isthmus of the VT circuit. ARI indicates the activation–recovery interval; ILAM, isochronal late activation map; LAVA, local abnormal ventricular activities; RAP, rotational activation pattern. The right figure indicates complications associated with ablation procedures.
Jcm 13 06805 g003
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Kataoka, N.; Imamura, T. Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives. J. Clin. Med. 2024, 13, 6805. https://doi.org/10.3390/jcm13226805

AMA Style

Kataoka N, Imamura T. Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives. Journal of Clinical Medicine. 2024; 13(22):6805. https://doi.org/10.3390/jcm13226805

Chicago/Turabian Style

Kataoka, Naoya, and Teruhiko Imamura. 2024. "Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives" Journal of Clinical Medicine 13, no. 22: 6805. https://doi.org/10.3390/jcm13226805

APA Style

Kataoka, N., & Imamura, T. (2024). Catheter Ablation for Ventricular Tachycardias: Current Status and Future Perspectives. Journal of Clinical Medicine, 13(22), 6805. https://doi.org/10.3390/jcm13226805

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop