Xuan Fengqi, Zuo Zhongyin, Zhang Jie, Zhang Shibei, Liu Zichen, Meng Yunfan, Sun Kuo, Han Yaling, Liang Ming, Wang Zulu
Department of Cardiology, General Hospital of Northern Theater Command, Shenyang 110016, China.
Department of Cardiology, Tianjin Chest Hospital, Tianjin 300222, China.
Cardiol Res Pract. 2024 Jan 4;2024:4412758. doi: 10.1155/2024/4412758. eCollection 2024.
Catheter ablation failure poses a clinical challenge for epicardial or intramural ventricular arrhythmia (VA); however, guidewire ablation within the coronary venous system (CVS) may be effective and safe for targeting VAs.
The ex vivo phase included four steps. In step 1, the steam pop incidence rates during guidewire ablation at power settings of 5, 10, 15, 20, and 25 W were analyzed using 10 mm- and 20 mm-tip guidewires. In step 2, guidewire ablation was performed for application durations of 10, 20, 30, 40, 50, 60, and 90 s, and the lesion size was measured. In step 3, the effects of saline infusion (0, 1, 2, 3, and 4 mL/min) on lesion dimensions and steam pop formation were examined. In step 4, an orthogonal array was constructed to obtain the optimal guidewire ablation parameters. In the phase, guidewire ablation within the CVS was performed in three dogs, and the lesion features in 10 days after ablation were observed.
In step 1, the steam pop incidence rates at 5, 10, 15, 20, and 25 W were 0%, 0%, 12.5%, 62.5%, and 100% using the 10 mm-tip guidewires and 0%, 0%, 0%, 25%, and 75% using the 20 mm-tip guidewires, respectively. In step 2, we found that the lesion areas increased with an increase in the ablation duration (the maximum lesion diameters at 30, 60, and 90 s were 4.9 ± 0.4, 7.0 ± 0.8, and 9.2 ± 0.7 mm in the 10 mm group and 3.2 ± 0.5, 4.5 ± 0.4, and 5.3 ± 0.7 mm in the 20 mm-tip group, respectively). In step 3, we observed that saline infusion was negatively correlated with ablation lesions but had a lower risk of steam pop. The optimal parameters for the 20 mm-tip guidewire ablation were 15 W, 50 s, and 2 mL/min or 20 W, 70 s, and 2 mL/min. In the phase, effective ablation lesions with maximum and minimum diameters of 3.2 ± 0.3 and 2.8 ± 0.5 mm, respectively, were created by the guidewires during the 10-day observation period after ablation.
This novel radiofrequency guidewire ablation technique can feasibly create effective lesions within the CVS, which may improve the efficacy of catheter ablation for challenging epicardial or intramural VA.
导管消融失败对心外膜或心室内壁心律失常(VA)构成临床挑战;然而,在冠状静脉系统(CVS)内进行导丝消融可能对靶向VA有效且安全。
体外阶段包括四个步骤。在步骤1中,使用10毫米和20毫米尖端导丝分析在5、10、15、20和25瓦功率设置下导丝消融期间的蒸汽泡发生率。在步骤2中,进行导丝消融,持续时间为10、20、30、40、50、60和90秒,并测量病变大小。在步骤3中,检查生理盐水输注(0、1、2、3和4毫升/分钟)对病变尺寸和蒸汽泡形成的影响。在步骤4中,构建正交阵列以获得最佳导丝消融参数。在体内阶段,对三只犬进行CVS内的导丝消融,并观察消融后10天的病变特征。
在步骤1中,使用10毫米尖端导丝时,5、10、15、20和25瓦的蒸汽泡发生率分别为0%、0%、12.5%、62.5%和100%,使用20毫米尖端导丝时分别为0%、0%、0%、25%和75%。在步骤2中,我们发现病变面积随消融持续时间的增加而增加(10毫米组在30、60和90秒时的最大病变直径分别为4.9±0.4、7.0±0.8和9.2±0.7毫米,20毫米尖端组分别为3.2±0.5、4.5±0.4和5.3±0.7毫米)。在步骤3中,我们观察到生理盐水输注与消融病变呈负相关,但蒸汽泡风险较低。20毫米尖端导丝消融的最佳参数为15瓦、50秒和2毫升/分钟或20瓦、70秒和2毫升/分钟。在体内阶段,在消融后10天的观察期内,导丝产生了有效消融病变,最大和最小直径分别为3.2±0.3和2.8±0.5毫米。
这种新型射频导丝消融技术能够在CVS内切实可行地产生有效病变,这可能提高对具有挑战性的心外膜或心室内壁VA进行导管消融的疗效。