TY - JOUR
T1 - Improved local activation time annotation of fractionated atrial electrograms for atrial mapping
AU - Abdi, Bahareh
AU - Hendriks, Richard C.
AU - van der Veen, Alle Jan
AU - de Groot, Natasja M.S.
PY - 2020
Y1 - 2020
N2 - Background: Local activation time (LAT) annotation in unipolar electrograms is complicated by interference from nonlocal atrial activities of neighboring tissue. This happens due to the spatial blurring that is inherent to electrogram recordings. In this study, we aim to exploit multi-electrode electrogram recordings to amplify the local activity in each electrogram and subsequently improve the annotation of LATs. Methods: An electrogram array can be modeled as a spatial convolution of per cell transmembrane currents with an appropriate distance kernel, which depends on the cells’ distances to the electrodes. By deconvolving the effect of the distance kernel from the electrogram array, we undo the blurring and estimate the underlying transmembrane currents as our desired local activities. However, deconvolution problems are typically highly ill-posed and result in unstable solutions. To overcome this issue, we propose to use a regularization term that exploits the sparsity of the first-order time derivative of the transmembrane currents. Results: We perform experiments on simulated two-dimensional tissues, as well as clinically recorded electrograms during paroxysmal atrial fibrillation. The results show that the proposed approach for deconvolution can improve the annotation of the true LAT in the electrograms. We also discuss, in summary, the required electrode array specifications for an appropriate recording and subsequent deconvolution. Conclusion: By ignoring small but local deflections, algorithms based on steepest descent are prone to generate smoother activation maps. However, by exploiting multi-electrode recordings, we can efficiently amplify small but local deflections and reveal new details in the activation maps that were previously missed.
AB - Background: Local activation time (LAT) annotation in unipolar electrograms is complicated by interference from nonlocal atrial activities of neighboring tissue. This happens due to the spatial blurring that is inherent to electrogram recordings. In this study, we aim to exploit multi-electrode electrogram recordings to amplify the local activity in each electrogram and subsequently improve the annotation of LATs. Methods: An electrogram array can be modeled as a spatial convolution of per cell transmembrane currents with an appropriate distance kernel, which depends on the cells’ distances to the electrodes. By deconvolving the effect of the distance kernel from the electrogram array, we undo the blurring and estimate the underlying transmembrane currents as our desired local activities. However, deconvolution problems are typically highly ill-posed and result in unstable solutions. To overcome this issue, we propose to use a regularization term that exploits the sparsity of the first-order time derivative of the transmembrane currents. Results: We perform experiments on simulated two-dimensional tissues, as well as clinically recorded electrograms during paroxysmal atrial fibrillation. The results show that the proposed approach for deconvolution can improve the annotation of the true LAT in the electrograms. We also discuss, in summary, the required electrode array specifications for an appropriate recording and subsequent deconvolution. Conclusion: By ignoring small but local deflections, algorithms based on steepest descent are prone to generate smoother activation maps. However, by exploiting multi-electrode recordings, we can efficiently amplify small but local deflections and reveal new details in the activation maps that were previously missed.
KW - Atrial fibrillation
KW - Atrial mapping
KW - Deconvolution
KW - Electrogram model
KW - Electrograms
KW - Fractionation
KW - Local activation time estimation
KW - Transmembrane current
UR - http://www.scopus.com/inward/record.url?scp=85076888455&partnerID=8YFLogxK
U2 - 10.1016/j.compbiomed.2019.103590
DO - 10.1016/j.compbiomed.2019.103590
M3 - Article
VL - 117
JO - Computers in Biology and Medicine
JF - Computers in Biology and Medicine
SN - 0010-4825
M1 - 103590
ER -