TY - GEN
T1 - Quantification of cardiac motion using in vivo fiducial markers for beam ablation of cardiac arrhythmias
AU - Rettmann, M. E.
AU - Hohmann, S.
AU - Konishi, H.
AU - Newman, L. K.
AU - Deisher, A. J.
AU - Kruse, J. J.
AU - Merrell, K.
AU - Foote, Robert
AU - Herman, M. G.
AU - Packer, D. L.
N1 - Funding Information:
Dr. D. Packer in the past 12 months has provided consulting services for Abbott, AtriFix, Biosense Webster, Inc., Cardio Syntax, EBAmed, Johnson & Johnson, MediaSphere Medical, LLC, MedLumics, Medtronic, NeuCures, St. Jude Medical, Siemens, Spectrum Dynamics, Centrix, Thermedical, and Xenter, Inc.. Dr. Packer received no personal compensation for these consulting activities, unless noted. Dr. Packer receives research funding from the Abbott, Biosense Webster, Boston Scientific/EPT, CardioInsight, EBAmed, Medtronic, Inc, NeuCures, Siemens, St. Jude Medical, Inc, Thermedical, Inc., NIH, Robertson Foundation, Vital Project Funds, Inc., Xenter, Inc., Mr. and Mrs. J. Michael Cook/Fund. Mayo Clinic and Dr. Packer have a financial interest in Analyze-AVW technology that may have been used to analyze some of the heart images in this research. In accordance with the Bayh-Dole Act, this technology has been licensed to commercial entities, and both Mayo Clinic and Dr. Packer have received royalties greater than $10,000, the federal threshold for significant financial interest. In addition, Mayo Clinic holds an equity position in the company to which the AVW technology has been licensed. Dr. Packer and Mayo Clinic jointly have equity in a privately held company, EBAmed. Royalties from Wiley & Sons, Oxford, and St. Jude Medical. Dr. Packer has a licensing agreement with the American Heart Association for the Mayo AF Symptom Inventory (MAFSI) Survey and has contractual rights to receive future royalties under this license.
Publisher Copyright:
© 2022 SPIE.
PY - 2022
Y1 - 2022
N2 - External beam ablation therapy has the potential to treat cardiac arrhythmias non-invasively by targeting arrhythmogenic myocardial tissue; however, a challenge of treating cardiac tissue with beam ablation therapy is cardiac motion. Currently, cardiac motion is typically compensated by expansion of the target volume which can potentially lead to collateral damage of surrounding healthy tissue. This collateral damage could be minimized by gating the beam delivery to a portion of the cardiac cycle. In prior work, we evaluated cardiac motion using anatomic landmarks in multi-phase cardiac computed tomography volumes of swine hearts across the left atria and ventricles. Other work evaluated left atrial motion using implanted fiducial clips. In the current work, we extend this prior work by quantifying cardiac motion using gold standard implanted fiducial clips across all four chambers of the heart. Cardiac motion varied by chamber, ranging from 2.1 to 7.2 mm in the x direction, 7.2 to 8.1 mm in the y direction, and 3.1 to 9.7 mm in the z direction. In addition, we quantify the reduction in motion if delivery were gated to phases 40% to 90% of the cardiac cycle, which corresponds to treating across 50% of the cardiac cycle. Cardiac motion across 50% of the cardiac cycle ranged from 1.1 to 5.3 mm in the x direction, 4.5 to 5.2 mm in the y direction, and 1.2 to 7.8 mm in the z direction. Percentage reduction in motion for treating during 50% of the cardiac cycle ranged from 18% to 47% in the x direction, 31% to 43% in the y direction, and 11% to 61% in the z direction. These results demonstrate that a substantial improvement in target localization could be achieved by gating the beam to 50% of the cardiac cycle.
AB - External beam ablation therapy has the potential to treat cardiac arrhythmias non-invasively by targeting arrhythmogenic myocardial tissue; however, a challenge of treating cardiac tissue with beam ablation therapy is cardiac motion. Currently, cardiac motion is typically compensated by expansion of the target volume which can potentially lead to collateral damage of surrounding healthy tissue. This collateral damage could be minimized by gating the beam delivery to a portion of the cardiac cycle. In prior work, we evaluated cardiac motion using anatomic landmarks in multi-phase cardiac computed tomography volumes of swine hearts across the left atria and ventricles. Other work evaluated left atrial motion using implanted fiducial clips. In the current work, we extend this prior work by quantifying cardiac motion using gold standard implanted fiducial clips across all four chambers of the heart. Cardiac motion varied by chamber, ranging from 2.1 to 7.2 mm in the x direction, 7.2 to 8.1 mm in the y direction, and 3.1 to 9.7 mm in the z direction. In addition, we quantify the reduction in motion if delivery were gated to phases 40% to 90% of the cardiac cycle, which corresponds to treating across 50% of the cardiac cycle. Cardiac motion across 50% of the cardiac cycle ranged from 1.1 to 5.3 mm in the x direction, 4.5 to 5.2 mm in the y direction, and 1.2 to 7.8 mm in the z direction. Percentage reduction in motion for treating during 50% of the cardiac cycle ranged from 18% to 47% in the x direction, 31% to 43% in the y direction, and 11% to 61% in the z direction. These results demonstrate that a substantial improvement in target localization could be achieved by gating the beam to 50% of the cardiac cycle.
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UR - http://www.scopus.com/inward/citedby.url?scp=85131959744&partnerID=8YFLogxK
U2 - 10.1117/12.2613484
DO - 10.1117/12.2613484
M3 - Conference contribution
AN - SCOPUS:85131959744
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2022
A2 - Linte, Cristian A.
A2 - Siewerdsen, Jeffrey H.
PB - SPIE
T2 - Medical Imaging 2022: Image-Guided Procedures, Robotic Interventions, and Modeling
Y2 - 21 March 2022 through 27 March 2022
ER -