Clin Res Cardiol (2021). 10.1007/s00392-021-01933-9

Accuracy and acute efficacy of the novel injection-based occlusion algorithm in cryoballoon pulmonary vein isolation guided by dielectric imaging
L. Rottner1, F. Moser1, R. Schleberger2, J. Weimann1, J. Moser2, M. Lemoine2, P. Münkler2, L. Dinshaw2, T. Risius3, P. Kirchhof1, F. Ouyang4, B. Reissmann1, A. Metzner2, A. Rillig2
1Klinik für Kardiologie, Universitäres Herz- und Gefäßzentrum Hamburg GmbH, Hamburg; 2Klinik für Kardiologie mit Schwerpunkt Elektrophysiologie, Universitäres Herz- und Gefäßzentrum Hamburg GmbH, Hamburg; 3Kardiologische Praxis Orchideenstieg, Hamburg; 4Kardiologie, Asklepios Klinik St. Georg, Hamburg;

Background: Cryoballoon (CB)-based pulmonary vein isolation (PVI) currently requires occlusion assessment of each pulmonary vein (PV) using fluoroscopy and dye injection.

Objective:  This study evaluated, whether the novel KODEX-EPD (EPD Solutions, Philips, Netherlands) occlusion tool reliably verifies PV-occlusion according to a novel dye-injection based algorithm.

Methods: A total of 75 patients suffering from AF, who underwent CB-based PVI, were analyzed. Feasibility, acute efficacy, procedure duration and radiation exposure were evaluated for patients in whom KODEX-EPD and its occlusion tool were applied (n=50, EPD-group) and compared to a control group of patients undergoing conventional CB-based PVI (n=25, conventional cryoablation-group). To accurately visualize PV anatomy, selective PV-angiographies were performed in the first half of the patients of the EPD-group (EPD-group A) in addition to a 3D left atrial (LA) KODEX-EPD-based imaging using a spiral mapping catheter (Achieve, SMC1, Medtronic, MN, USA). PV-angiographies were waived in the following patients (EPD-group B). PV-occlusion was confirmed via fluoroscopy in all patients of the EPD-group to validate the accuracy of the novel occlusion tool.

Results: CB-based PVI was successful in 50/50 patients of the EPD-group (mean age 63±11 years, 31 (62%) male, 18 paroxysmal (36%), LA diameter 43±7 mm) and in 25/25 patients of the conventional cryoablation-group (66±10 years, 19 (76%) male, 9 paroxysmal (36%), LA diameter 41±6 mm). In the final evaluation phase (EPD-group B) LA fluoroscopy times and dose area products were comparable to the conventional cryoablation-group (10.5±5 vs 8.8±4 minutes; p=0.23 and 403±425 vs 321±202 cGycm2; p=0.44), while the amount of dye was significantly reduced (EPD-group B: 31±18 ml vs conventional cryoablation-group: 50±20 ml, p<0.0001). Concordance of PV-occlusion angiography with the KODEX-EPD injection-workflow was documented in 237/272 (87%) occlusion-analyses among 198 PVs.

Conclusion: The novel KODEX-EPD occlusion tool allows for accurate PV-occlusion assessment without additional fluoroscopic verification in the majority of PVs and CB-based PVI in conjunction with KODEX-EPD is accompanied with high acute ablation success rates.


https://dgk.org/kongress_programme/ht2021/P768.htm