Kawamura Iwanari, Miyazaki Shinsuke, Kato Ryosuke, Takahashi Ken, Negishi Miho, Honda Masaki, Tateishi Ryo, Goto Kentaro, Nishimura Takuro, Yamao Kazuya, Takahashi Kentaro, Ihara Kensuke, Tao Susumu, Takigawa Masateru, Sasano Tetsuo
Department of Cardiovascular Medicine, Institute of Science Tokyo, Tokyo, Japan.
Department of Cardiovascular Medicine, Institute of Science Tokyo, Tokyo, Japan.
Heart Rhythm. 2025 Jun 4. doi: 10.1016/j.hrthm.2025.05.072.
Hemolysis is one of the unique complications of pulsed field ablation (PFA), but the differences in hemolysis between the different PFA systems are not well understood.
This study aimed to investigate the differences in hemolysis between 2 PFA systems.
We included patients who underwent PFA of atrial fibrillation (PulseSelect, 38; Farapulse, 38) and those who underwent cryoballoon ablation (14 patients) as a control. The free hemoglobin levels before and after the procedure, as well as the postprocedure hemolysis and myocardial injury biomarkers within 24 hours, were measured.
There was no significant difference in the total number of applications between PulseSelect and Farapulse (median 53 [50-58] vs median 53 [46-60], P = .868). The free hemoglobin increased from a median of 0.01 (0.00-0.01) to 0.03 (0.02-0.03) in the PulseSelect group and from 0.01 (0.01-0.02) to 0.06 (0.05-0.06) in the Farapulse group. Farapulse had significantly higher levels of hemolysis biomarkers, including lactate dehydrogenase, total bilirubin, and free hemoglobin, than PulseSelect, and a greater number of patients with low-level haptoglobin was observed with Farapulse than PulseSelect (P < .001). No significant difference in the hemolysis biomarkers was observed between PulseSelect and cryoballoon ablation. Myocardial injury biomarkers exhibited significantly higher creatine kinase levels for both PulseSelect and Farapulse than cryoballoon, but no differences were observed between the 2 PFA systems. No patients experienced acute kidney injury in any cohort.
The degree of hemolysis may differ between the PFA systems. Further investigation might be necessary to determine the safe number of PFA applications for each PFA system.
溶血是脉冲场消融(PFA)的独特并发症之一,但不同PFA系统之间溶血的差异尚不清楚。
本研究旨在探讨两种PFA系统之间溶血的差异。
我们纳入了接受房颤PFA治疗的患者(PulseSelect组38例;Farapulse组38例),以及接受冷冻球囊消融治疗的患者(14例)作为对照。测量了术前和术后的游离血红蛋白水平,以及术后24小时内的溶血和心肌损伤生物标志物。
PulseSelect和Farapulse的总应用次数无显著差异(中位数53 [50 - 58] 对中位数53 [46 - 60],P = 0.868)。PulseSelect组的游离血红蛋白从中位数0.01(0.00 - 0.01)增加到0.03(0.02 - 0.03),Farapulse组从0.01(0.01 - 0.02)增加到0.06(0.05 - 0.06)。Farapulse的溶血生物标志物水平显著高于PulseSelect,包括乳酸脱氢酶、总胆红素和游离血红蛋白,且Farapulse组中低水平触珠蛋白的患者数量多于PulseSelect组(P < 0.001)。PulseSelect与冷冻球囊消融之间的溶血生物标志物无显著差异。PulseSelect和Farapulse的心肌损伤生物标志物肌酸激酶水平均显著高于冷冻球囊消融,但两种PFA系统之间未观察到差异。任何队列中均无患者发生急性肾损伤。
PFA系统之间的溶血程度可能不同。可能需要进一步研究以确定每种PFA系统安全的PFA应用次数。