FARAPULSE™ PFA system resulted in a significantly greater reduction in haptoglobin on postoperative day 1 compared to Pulse Select™, but levels recovered by day 2.
Does the FARAPULSE PFA system cause more hemolysis compared to the Pulse Select PFA system in patients undergoing catheter ablation for atrial fibrillation?
100 patients with paroxysmal or persistent atrial fibrillation undergoing primary catheter ablation, mean age 75 ± 9 years, 43 women, at a single center in Japan.
Catheter ablation using the FARAPULSE pulsed-field ablation (PFA) system
Catheter ablation using the Pulse Select pulsed-field ablation (PFA) system
Hemolysis assessed by change in serum haptoglobin levels from baseline (Δ-haptoglobin) on postoperative day 1safety
The FARAPULSE PFA system is associated with greater transient hemolysis on postoperative day 1 compared to the Pulse Select system, but without adverse clinical impact.
Abstract Background Pulsed-field ablation (PFA) is an emerging technology for catheter ablation in atrial fibrillation. Unlike conventional thermal ablation techniques, PFA is associated with a lower risk of complications such as esophageal injury, phrenic nerve palsy and pulmonary vein stenosis.1) However, PFA-specific complications, including hemolysis, have been reported. 2)Given differences in voltage settings and device design, the degree of hemolysis may vary between PFA systems, but this variability remains unclear. Objective This study aimed to compare hemolysis following ablation with the Pulse Select™ (Medtronic) and FARAPULSE™ (Boston Scientific) PFA systems. Methods Patients with paroxysmal or persistent atrial fibrillation who underwent primary catheter ablation using either the Pulse Select™ or FARAPULSE™ PFA system at Osaka Rosai Hospital between October 2024 and January 2025 were included. Hemolysis was assessed by measuring serum haptoglobin levels preoperatively, immediately postoperatively, and on postoperative days 1 and 2. The change in haptoglobin from baseline (Δ-haptoglobin) was calculated, and comparisons between the two groups were performed at each time point. Results A total of 100 patients (75 ± 9 years, 43 women) were included, with 75 undergoing ablation using Pulse Select™ and 25 using FARAPULSE™. The number of applications did not differ significantly between the two groups (FARAPULSE™: 40 ± 10 applications; Pulse Select™: 39 ± 7 applications). In both groups, Δ-haptoglobin was significantly greater (indicating a decrease) on postoperative day 1 compared to baseline (Pulse Select™, p0.0001; FARAPULSE™, p0.0001), with a significantly greater reduction observed in the FARAPULSE™ group (p=0.017). By postoperative day 2, haptoglobin levels had recovered. Transient acute kidney injury (AKI) corresponding to stage 1 of the KDIGO classification was observed in 10 patients, but renal function subsequently improved, with no significant difference between the groups. No cases of prolonged hospitalization due to anemia progression or worsening renal function were observed in either group. Conclusion Hemolysis, as indicated by a reduction in haptoglobin, was significantly greater on postoperative day 1 in patients treated with FARAPULSE™ compared to those treated with Pulse Select™. However, haptoglobin levels recovered by postoperative day 2, and no adverse impact on clinical outcomes was observed.Baseline characteristics Changes in Blood Test Following PFA
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Ayako Sugino
Y E Egami
N K Kobayashi
European Heart Journal
Osaka Rosai Hospital
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Sugino et al. (Sat,) reported a other. FARAPULSE™ PFA system resulted in a significantly greater reduction in haptoglobin on postoperative day 1 compared to Pulse Select™, but levels recovered by day 2.
www.synapsesocial.com/papers/698586238f7c464f2300a0bb — DOI: https://doi.org/10.1093/eurheartj/ehaf784.855