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Published on: December 11, 2017
Chronic right coronary artery changes after cavotricuspid isthmus ablation using a small-basket pentaspline pulsed
Taiki Masuyama1, Takehito Sasaki1, Kohki Nakamura1
1Division of Cardiology, Gunma Prefectural Cardiovascular Center, Maebashi City, Gunma, Japan.
Background:
Pulsed field ablation (PFA) is increasingly used for atrial fibrillation ablation; however, its safety for cavotricuspid isthmus (CTI) ablation, particularly regarding the right coronary artery (RCA), remains unclear.
Objective:
This study aimed to evaluate the acute and chronic effects of PFA-based CTI ablation on the RCA and to compare procedural outcomes with radiofrequency ablation (RFA).
Methods:
We retrospectively analyzed 96 patients who underwent an initial CTI ablation during atrial fibrillation ablation and had paired preablation and approximately 6-month follow-up coronary computed tomographic angiography (CCTA) data available from routine clinical care. CTI ablation was performed using a small-basket pentaspline PFA catheter (PFA group n = 55) or an RFA catheter (RFA group n = 41). We assessed RCA stenosis progression using the Coronary Artery Disease Reporting and Data System category and minimal luminal area and also evaluated periprocedural safety and efficacy.
Results:
In the PFA group, 54 patients (98.2%) showed no stenosis progression. The Coronary Artery Disease Reporting and Data System category and minimal luminal area did not significantly change between preablation and follow-up CCTA (median [interquartile range] 0 [0-1] vs 0 [0-1], P = .317; 11.3 [8.4-15.1] vs 11.0 [8.0-15.1] mm2, P = .828). 1 patient (1.8%) developed a transient RCA spasm, whereas no spasms occurred in the RFA group. In a propensity score-matched analysis, PFA was associated with a shorter procedure time, shorter time to CTI block, and higher first-pass success.
Conclusion:
Small-basket PFA for CTI ablation was associated with no major CCTA-detectable progression in the distal RCA in most patients and favorable procedural characteristics compared with RFA. Further prospective studies are needed to confirm long-term safety and efficacy.
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