膈神经对脉冲场消融反应的表征

Brian T. Howard, D. Haines, A. Verma, N. Kirchhof, N. Barka, Birce Onal, M. Stewart, Daniel C. Sigg
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引用次数: 16

摘要

背景:膈神经麻痹是众所周知的心脏消融术的并发症,是由直接热能的应用引起的。新兴的脉冲场消融(PFA)可能降低膈神经损伤的风险,但尚未得到很好的表征。方法:在猪PFA模型分娩过程中使用加速计和连续起搏。在第一个实验阶段,PFA浓度升高(n=12)传递到膈神经,建立了急性剂量反应。在第二阶段,神经以单一消融水平为目标,观察重复消融对神经功能的影响(n=4)。第三个慢性期以消融心脏组织附近神经的组织病理学特征为特征(n=6)。结果:急性时,我们观察到膈神经功能的剂量依赖性反应,包括可逆性休克(R2=0.965, P<0.001)。此外,急性结果表明膈神经功能对不同水平的PFA和导管邻近放置有反应,导致:无效果、有效果或休克。在慢性研究阶段,成功分离上腔静脉的剂量预计不会导致膈神经功能障碍,与4周时膈神经功能和膈神经组织病理学正常相关。结论:导管与膈神经的距离和PFA剂量水平对膈神经反应至关重要。大体和组织病理学评估膈神经和膈在一个慢性时间点没有发现损伤。这些结果为理解PFA对膈神经的易感性和恢复提供了基础,并为在动物模型之外的应用提供了适当的谨慎。
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Characterization of Phrenic Nerve Response to Pulsed Field Ablation
Background: Phrenic nerve palsy is a well-known complication of cardiac ablation, resulting from the application of direct thermal energy. Emerging pulsed field ablation (PFA) may reduce the risk of phrenic nerve injury but has not been well characterized. Methods: Accelerometers and continuous pacing were used during PFA deliveries in a porcine model. Acute dose response was established in a first experimental phase with ascending PFA intensity delivered to the phrenic nerve (n=12). In a second phase, nerves were targeted with a single ablation level to observe the effect of repetitive ablations on nerve function (n=4). A third chronic phase characterized assessed histopathology of nerves adjacent to ablated cardiac tissue (n=6). Results: Acutely, we observed a dose-dependent response in phrenic nerve function including reversible stunning (R2=0.965, P<0.001). Furthermore, acute results demonstrated that phrenic nerve function responded to varying levels of PFA and catheter proximity placements, resulting in either: no effect, effect, or stunning. In the chronic study phase, successful isolation of superior vena cava at a dose not predicted to cause phrenic nerve dysfunction was associated with normal phrenic nerve function and normal phrenic nerve histopathology at 4 weeks. Conclusions: Proximity of the catheter to the phrenic nerve and the PFA dose level were critical for phrenic nerve response. Gross and histopathologic evaluation of phrenic nerves and diaphragms at a chronic time point yielded no injury. These results provide a basis for understanding the susceptibility and recovery of phrenic nerves in response to PFA and a need for appropriate caution in moving beyond animal models.
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