Seeing is believing: visualization of pulmonary vein gaps using ultra-high resolution electroanatomic mapping
Editorial

Seeing is believing: visualization of pulmonary vein gaps using ultra-high resolution electroanatomic mapping

Chin-Yu Lin1,2,3, Fa-Po Chung1,2, Yenn-Jiang Lin1,2, Shih-Ann Chen1,2

1Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; 2Institution of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan; 3Department of Medicine, Taipei Veterans General Hospital, Yuan-Shan Branch, Taipei, Taiwan

Correspondence to: Fa-Po Chung, MD. Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Taipei, Taiwan. Email: marxtaiji@gmail.com.

Provenance: This is an invited Editorial commissioned by the Section Editor Fang-Zhou Liu (Guangdong Cardiovascular Institute, Guangdong, China).

Comment on: Masuda M, Fujita M, Iida O, et al. The identification of conduction gaps after pulmonary vein isolation using a new electroanatomic mapping system. Heart Rhythm 2017. [Epub ahead of print].


Submitted Sep 20, 2017. Accepted for publication Oct 16, 2017.

doi: 10.21037/jtd.2017.10.136


Atrial fibrillation (AF) is the most common cardiac arrhythmia. Given the increase in the aging population, the prevalence will potentially double in the coming 5 decades (1). Haissaguerre et al. (2) and Chen et al. (3) firstly reported the dominant and pathologic role of pulmonary vein (PV) triggers as being responsible for the arrhythmogenesis of AF. Owing to the advancement of mapping techniques and understanding of the pathogenesis, catheter ablation has been considered as an effective and alternative treatment option for AF patients, and a complete electrical PV isolation (PVI) is the current Class I recommendation (4). Although numerous techniques and ablation strategies have been explored and investigated to improve the durability of ablation lesions, the recovery of the PV conduction, which accounts for up to 80% of AF recurrences during the second procedure, remains the leading cause of AF recurrences (5,6). Once the PVs are electronically reconnected, ablation by targeting the conduction PV gaps to achieve a complete re-isolation is crucial (4). In spite of the evolution of materials and navigation systems, circular mapping catheters have exclusively been applied to evaluate the left atrium-PV (LA-PV) conduction and PV reconnections for almost the past 20 years. However, the complexity of the scar derived from a previous ablation line and the weak electrogram features can contribute to the interpretation of the PV gaps, and as a consequence, the clinical hurdle during a repeat AF ablation.

In the issue of Heart Rhythm, Masuda et al. (7) prospectively enrolled 31 consecutive patients undergoing a second ablation with identifiably reconnected conduction at any of the four PVs after a prior PVI. The authors postulated the reconnection of the PV gaps could be better recognized by a new ultra-high resolution electroanatomic mapping system [Rhythmia®, Boston Scientific, Marlborough (Cambridge), MA, USA] using the Orion® catheter (Boston Scientific), a 64-pole small basket catheter. The results demonstrated that the new electroanatomic mapping system could facilitate the visualization of 54 reconnected gaps in 39 ipsilateral PV pairs along the previous PVI lines. Of them, 31 (57%) gaps could be visualized directly on the propagation map, while manual electrogram re-annotation was required for the remaining 23 (43%) gaps, which were more frequently located at the anterior and carinal regions than the other regions.

Notably, at the crossover point between the gap pathway and encircling PVI line, the 3.5-mm tip ablation catheter failed to record any local electrograms in 20% of the gaps obtained from ultra-high resolution mapping. The authors used the traditional circular catheter as the gold standard to evaluate a successful PVI. Ablation of these gaps, defined by ultra-high resolution mapping, contributed to either the alteration of the activation sequence or the elimination of the PV potentials, implying neither an overestimation nor underestimation of these gaps. Nevertheless, in spite of an attempt to adjust the lower limit of the voltage threshold by starting with 0.20 mV and a substantial decrement of 0.02 mV, the voltage map could not identify the gap location in the majority (65%) of these gaps.

The efficacy of detecting LA-PV reconnections in this study was better than that of the previous report. Anter et al. (8) demonstrated that PVIs were underestimated by the Orion catheter in 9% of PVs, while the Lasso catheter in conjunction with pacing maneuvers overestimated it in 21% of PVIs. Differing from the present study, patients that underwent an index or repeat procedure were included. The definition of the primary endpoint was based on the comparison between the recorded electrograms and reality of the PV connection through pacing maneuvers, which may explain the diverse effectiveness in these two studies. Moreover, despite the fact that Orion improved the recording of the PV potentials after an incomplete isolation, the false-positive identification of PV-like potentials from nearby structures was increased. Far-field signals in the anterior and carinal regions could be derived from the activations of the left atrial appendage, superior vena cava, ligament of Marshall, and right atrium, and a specific maneuver might be required to differentiate within these areas (9-11). Similar to the study by Kosiuk et al. (12), manual adjustment of the window from an incorrect automatic annotation of a far field signal to a delayed and/or separated local PV potential was necessary for the delineation of the conducting gaps, which might possibly lead to a longer procedural or fluoroscopy time.

There are differences between the Orion and Lasso catheters. The Lasso circular catheter has 20 electrodes with a 1 mm2 surface area, 3 mm interelectrode spacing, and maximal diameter of 25 mm, while the Orion basket has 8 splines with 8 electrodes on each spline (total 64 electrodes), surface area of 0.4 mm2, interelectrode spacing of 2.5 mm, and maximal diameter of 22 mm. The above electrode differences will translate into not only more accurate and higher density electroanatomic maps, but also a higher resolution and better sensitivity to near field signals by the Orion catheter than conventional mapping (13). Through the use of the Orion catheter, the gap could be evaluated by a wavelet propagating into the PVs by ultra-high resolution mapping.

Additionally, there are several additional issues to be addressed in the future investigation of this novel mapping catheter and navigation system. First of all, Bisbal et al. (14) studied the correlation between the electrical PV reconnections and delayed-enhancement cardiac magnetic resonance (DE-CMR)-based PV gap identification. The result demonstrated that the electrical PV reconnection sites identified by a circular catheter were matched with the gaps recognized by the DE-CMR in 79% of PVs. Whether the electrical reconnections identified by the ultra-high resolution map could have better agreement with the DE-CMR findings remains unknown. Second, the authors studied the identification of the PV gaps during repeat procedures in AF patients. Whether the application of the ultra-high resolution map during the index or repeat AF ablation procedure can bring better clinical outcomes and less recurrence needs future investigation.

In summary, the advancement of signal processing systems and mapping catheters, as well as the significant improvement in the mapping density and quality, has led to a pivotal breakthrough in the identification of PV gaps during repeat AF ablation procedures. Future investigation will be warranted regarding AF recurrences through the application of the ultra-high resolution mapping system.


Acknowledgements

Funding: This work was supported by the Center for Dynamical Biomarkers and Translational Medicine, Ministry of Science and Technology (Grant No. MOST104-2314-B-075-089-MY3, MOST103-2911-I-008-001, MOST103-2314-B-075-089-MY3, NSC 102-2314-B-010-056-MY2), Research Foundation of Cardiovascular Medicine (Grant No. RFCM 104-01-012, RFCM 105-02-028, RFCM 105-02-008, and RFCM 105-02-028), TVGH-NTUH Joint Research Program (Grant No. VGHUST105-G7-4-1), Szu-Yuan Research Foundation of Internal Medicine (Grant No. 106003), TVGH-NTUH Joint Research Program (Grant No. VN103-04) and Taipei Veterans General Hospital (Grant No. V103C-042, V104B-018, V104E7-001, V104C-109, V105B-014, V105C-122, V105C-116, V106C-158 and V106B-010).


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Krijthe BP, Kunst A, Benjamin EJ, et al. Projections on the number of individuals with atrial fibrillation in the European Union, from 2000 to 2060. Eur Heart J 2013;34:2746-51. [Crossref] [PubMed]
  2. Haïssaguerre M, Jais P, Shah DC, et al. Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N Engl J Med 1998;339:659-66. [Crossref] [PubMed]
  3. Chen SA, Hsieh MH, Tai CT, et al. Initiation of atrial fibrillation by ectopic beats originating from the pulmonary veins: electrophysiological characteristics, pharmacological responses, and effects of radiofrequency ablation. Circulation 1999;100:1879-86. [Crossref] [PubMed]
  4. Calkins H, Hindricks G, Cappato R, et al. Temporary removal: 2017 hrs/ehra/ecas/aphrs/solaece expert consensus statement on catheter and surgical ablation of atrial fibrillation. Heart Rhythm 2017;14:e275-e444. [Crossref] [PubMed]
  5. Lo LW, Lin YJ, Chang SL, et al. Predictors and Characteristics of Multiple (More Than 2) Catheter Ablation Procedures for Atrial Fibrillation. J Cardiovasc Electrophysiol 2015;26:1048-56. [Crossref] [PubMed]
  6. Ouyang F, Antz M, Ernst S, et al. Recovered pulmonary vein conduction as a dominant factor for recurrent atrial tachyarrhythmias after complete circular isolation of the pulmonary veins: lessons from double Lasso technique. Circulation 2005;111:127-35. [Crossref] [PubMed]
  7. Masuda M, Fujita M, Iida O, et al. The identification of conduction gaps after pulmonary vein isolation using a new electroanatomic mapping system. Heart Rhythm 2017. [Epub ahead of print]. [Crossref] [PubMed]
  8. Anter E, Tschabrunn CM, Contreras-Valdes FM, et al. Pulmonary vein isolation using the Rhythmia mapping system: Verification of intracardiac signals using the Orion mini-basket catheter. Heart Rhythm 2015;12:1927-34. [Crossref] [PubMed]
  9. Shah D, Burri H, Sunthorn H, et al. Identifying far-field superior vena cava potentials within the right superior pulmonary vein. Heart Rhythm 2006;3:898-902. [Crossref] [PubMed]
  10. Shah D, Haissaguerre M, Jais P, et al. Left atrial appendage activity masquerading as pulmonary vein potentials. Circulation 2002;105:2821-5. [Crossref] [PubMed]
  11. Tai CT, Hsieh MH, Tsai CF, et al. Differentiating the ligament of Marshall from the pulmonary vein musculature potentials in patients with paroxysmal atrial fibrillation: electrophysiological characteristics and results of radiofrequency ablation. Pacing Clin Electrophysiol 2000;23:1493-501. [Crossref] [PubMed]
  12. Kosiuk J, Hilbert S, John S, et al. Preliminary experience with high-density electroanatomical mapping for ablation of atrial fibrillation - Comparison of mini-basket and novel open irrigated magnetic ablation catheter in consecutive patients. Int J Cardiol 2017;228:401-5. [Crossref] [PubMed]
  13. Berte B, Relan J, Sacher F, et al. Impact of electrode type on mapping of scar-related VT. J Cardiovasc Electrophysiol 2015. [Epub ahead of print]. [Crossref] [PubMed]
  14. Bisbal F, Guiu E, Cabanas-Grandio P, et al. CMR-guided approach to localize and ablate gaps in repeat AF ablation procedure. JACC Cardiovasc Imaging 2014;7:653-63. [Crossref] [PubMed]
Cite this article as: Lin CY, Chung FP, Lin YJ, Chen SA. Seeing is believing: visualization of pulmonary vein gaps using ultra-high resolution electroanatomic mapping. J Thorac Dis 2017;9(11):4205-4207. doi: 10.21037/jtd.2017.10.136