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Optimizing Radiofrequency Ablation of Paroxysmal and Persistent Atrial Fibrillation by Direct Catheter Force Measurement—A Case‐Matched Comparison in 198 Patients

2014; Wiley; Volume: 38; Issue: 2 Linguagem: Inglês

10.1111/pace.12549

1540-8159

Elisabeth Sigmund, Helmut Püererfellner, Michael Derndorfer, Γεώργιος Κόλλιας, Siegmund Winter, Josef Aichinger, Hans‐Joachim Nesser, Martin Martinek,

Cardiovascular Syncope and Autonomic Disorders

Background Sufficient electrode‐tissue contact is crucial for adequate lesion formation in radiofrequency catheter ablation (RFCA). Objective We assessed the impact of direct catheter force measurement on acute procedural parameters and outcome of RFCA for paroxysmal and persistent atrial fibrillation (AF). Methods Ninety‐nine consecutive patients (70% men) with paroxysmal (63.6%) or persistent AF underwent left atrial RFCA using a 3.5‐mm open‐irrigated‐tip (OIT) catheter with contact force measurement capabilities (group 1). For comparison a case‐matched cohort with standard OIT catheters was used (99 patients; group 2). Case matching included gender, type of AF, number or RFCA procedures, and type of procedure. Results Procedural data showed a significant decline in radiofrequency ablation time from 52 ± 20 to 44 ± 16 minutes (P = 0.003) with a remarkable mean reduction in overall procedure time of 34 minutes (P = 0.0001; 225.8 ± 53.1 vs 191.9 ± 53.3 minutes). In parallel, the total fluoroscopy time could be significantly reduced from 28.5 ± 11.0 to 19.9 ± 9.3 minutes (P = 0.0001) as well as fluoroscopy dose from 74.1 ± 58.0 to 56.7 ± 38.9 Gy/cm 2 (P = 0.016). Periprocedural complications were similar in both groups. Conclusions The use of contact force sensing technology is able to significantly reduce ablation, procedure, and fluoroscopy times as well as dose in RFCA of AF in a mixed case‐matched group of paroxysmal and persistent AF. Energy delivery is substantially reduced by avoiding radiofrequency ablation in positions with insufficient surface contact. Additionally 12‐month outcome data showed increased efficacy. Such time saving and equally safe technology may have a relevant impact on laboratory management and increased cost effectiveness.