研究目的
To study the feasibility and effectiveness of AI‐guided CTI for AFL.
研究成果
AI‐guided ablation of CTI line appeared feasible with similar ablation time and fewer RF applications. Compared to CF guidance, the use of different regional AI values for CTI ablation guidance yielded a higher rate of first‐pass conduction block and no additional complications.
研究不足
This is a retrospective single‐center study with relatively small sample size. The AI values used were empirically chosen based on CTI and left atrial thickness and left atrial AI values in the literature. The follow‐up duration was 6 months which might have overestimated success rates.
1:Experimental Design and Method Selection:
Retrospective comparison of procedural and 6‐month outcomes of ablation for AFL between consecutive patients undergoing either AI‐guided ablation of CTI or CF‐guided ablation at a single center.
2:Sample Selection and Data Sources:
Consecutive patients who underwent first‐time RF of CTI for symptomatic drug‐refractory AFL with CF guidance from March 2016 to May 2017 before AI was used as an ablation method and with AI guidance from June 2017 to July
3:List of Experimental Equipment and Materials:
20 SmartTouch catheter, CARTO 3 V4 system, VisiTag module.
4:Experimental Procedures and Operational Workflow:
RF ablation of CTI was performed under conscious sedation and uninterrupted oral anticoagulation. The procedures were guided by AI or CF.
5:Data Analysis Methods:
Each Visitag dataset, including ablation time, mean CF, impedance drop, FTI, and AI in each group underwent retrospective analyses.
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