TY - JOUR
T1 - Intrapulmonary vein ablation without stenosis
T2 - A novel balloon-based direct current electroporation approach
AU - Witt, Chance M.
AU - Sugrue, Alan
AU - Padmanabhan, Deepak
AU - Vaidya, Vaibhav
AU - Gruba, Sarah
AU - Rohl, James
AU - DeSimone, Christopher V.
AU - Killu, Ammar M.
AU - Naksuk, Niyada
AU - Pederson, Joanne
AU - Suddendorf, Scott
AU - Ladewig, Dorothy J.
AU - Maor, Elad
AU - Holmes, David R.
AU - Kapa, Suraj
AU - Asirvatham, Samuel J.
N1 - Publisher Copyright:
© 2018 The Authors.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Background—Current thermal ablation methods for atrial fibrillation, including radiofrequency and cryoablation, have a suboptimal success rate. To avoid pulmonary vein (PV) stenosis, ablation is performed outside of the PV, despite the importance of triggers inside the vein. We previously reported on the acute effects of a novel direct current electroporation approach with a balloon catheter to create lesions inside the PVs in addition to the antrum. In this study, we aimed to determine whether the effects created by this nonthermal ablation method were associated with irreversible lesions and whether PV stenosis or other adverse effects occurred after a survival period. Methods and Results—Initial and survival studies were performed in 5 canines. At the initial study, the balloon catheter was inflated to contact the antrum and interior of the PV. Direct current energy was delivered between 2 electrodes on the catheter in ECG-gated 100 μs pulses. A total of 10 PVs were treated demonstrating significant acute local electrogram diminution (mean amplitude decrease of 61.2±19.8%). After the survival period (mean 27 days), computed tomography imaging showed no PV stenosis. On histologic evaluation, transmural, although not circumferential, lesions were seen in each treated vein. No PV stenosis or esophageal injury was present. Conclusions—Irreversible, transmural lesions can be created inside the PV without evidence of stenosis after a 27-day survival period using this balloon-based direct current ablation approach. These early data show promise for an ablation approach that could directly treat PV triggers in addition to traditional PV antrum ablation.
AB - Background—Current thermal ablation methods for atrial fibrillation, including radiofrequency and cryoablation, have a suboptimal success rate. To avoid pulmonary vein (PV) stenosis, ablation is performed outside of the PV, despite the importance of triggers inside the vein. We previously reported on the acute effects of a novel direct current electroporation approach with a balloon catheter to create lesions inside the PVs in addition to the antrum. In this study, we aimed to determine whether the effects created by this nonthermal ablation method were associated with irreversible lesions and whether PV stenosis or other adverse effects occurred after a survival period. Methods and Results—Initial and survival studies were performed in 5 canines. At the initial study, the balloon catheter was inflated to contact the antrum and interior of the PV. Direct current energy was delivered between 2 electrodes on the catheter in ECG-gated 100 μs pulses. A total of 10 PVs were treated demonstrating significant acute local electrogram diminution (mean amplitude decrease of 61.2±19.8%). After the survival period (mean 27 days), computed tomography imaging showed no PV stenosis. On histologic evaluation, transmural, although not circumferential, lesions were seen in each treated vein. No PV stenosis or esophageal injury was present. Conclusions—Irreversible, transmural lesions can be created inside the PV without evidence of stenosis after a 27-day survival period using this balloon-based direct current ablation approach. These early data show promise for an ablation approach that could directly treat PV triggers in addition to traditional PV antrum ablation.
KW - Animal study
KW - Atrial fibrillation
KW - Direct current ablation
KW - Electroporation
KW - Pulmonary vein stenosis
UR - http://www.scopus.com/inward/record.url?scp=85050493930&partnerID=8YFLogxK
U2 - 10.1161/JAHA.118.009575
DO - 10.1161/JAHA.118.009575
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C2 - 29987121
AN - SCOPUS:85050493930
SN - 2047-9980
VL - 7
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
IS - 14
M1 - e009575
ER -