Combining endocardial mapping and electrocardiographic imaging (ECGI) for improving PVC localization: A feasibility study.
Combining endocardial mapping and electrocardiographic imaging (ECGI) for improving PVC localization: A feasibility study.
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DOI:
10.1016/j.jelectrocard.2021.08.013
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发表时间:
2021-11
影响因子:
1.3
通讯作者:
MacLeod, Rob S.
中科院分区:
文献类型:
--
作者:
Good, Wilson W.;Zenger, Brian;Bergquist, Jake A.;Rupp, Lindsay C.;Gillette, Karli;Angel, Nathan;Chou, Derrick;Plank, Gernot;MacLeod, Rob S.
Accurate reconstruction of cardiac activation wavefronts is crucial for clinical diagnosis, management, and treatment of cardiac arrhythmias. Furthermore, reconstruction of activation profiles within the intramural myocardium has long been impossible because electrical mapping was only performed on the endocardial surface. Recent advancements in electrocardiographic imaging (ECGI) have made endocardial and epicardial activation mapping possible. We propose a novel approach to use both endocardial and epicardial mapping in a combined approach to reconstruct intramural activation times. To implement and validate a combined epicardial/endocardial intramural activation time reconstruction technique. We used 11 simulations of ventricular activation paced from sites throughout myocardial wall and extracted endocardial and epicardial activation maps at approximate clinical resolution. From these maps, we interpolated the activation times through the myocardium using thin-plate-spline radial basis functions. We evaluated activation time reconstruction accuracy using root-mean-squared error (RMSE) of activation times and the percent of nodes within 1 ms of the ground truth. Reconstructed intramural activation times showed an RMSE and percentage of nodes within 1 ms of the ground truth simulations of 3 ms and 70%, respectively. In the worst case, the RMSE and percentage of nodes were 4 ms and 60%, respectively. We showed that a simple, yet effective combination of clinical endocardial and epicardial activation maps can accurately reconstruct intramural wavefronts. Furthermore, we showed that this approach provided robust reconstructions across multiple intramural stimulation sites.
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影响因子:
10.9
作者:
Gillette, Karli;Gsell, Matthias A. F.;Plank, Gernot
通讯作者:
Plank, Gernot
影响因子:
82.9
作者:
Ramanathan, C;Ghanem, RN;Rudy, Y
通讯作者:
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影响因子:
8.4
作者:
Hohmann, Stephan;Rettmann, Maryam E.;Packer, Douglas L.
通讯作者:
Packer, Douglas L.
影响因子:
3.2
作者:
Zenger B;Good WW;Bergquist JA;Burton BM;Tate JD;Berkenbile L;Sharma V;MacLeod RS
通讯作者:
MacLeod RS
影响因子:
4
作者:
Cluitmans M;Brooks DH;MacLeod R;Dössel O;Guillem MS;van Dam PM;Svehlikova J;He B;Sapp J;Wang L;Bear L
通讯作者:
Bear L