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    <subfield code="a">10.3389/fphys.2021.674223</subfield>
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    <subfield code="a">ART-2021-125674</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Riccio, J</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-6264-4229</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Characterization of Atrial Propagation Patterns and Fibrotic Substrate With a Modified Omnipolar Electrogram Strategy in Multi-Electrode Arrays</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Introduction: The omnipolar electrogram method was recently proposed to try to generate orientation-independent electrograms. It estimates the electric field from the bipolar electrograms of a clique, under the assumption of locally plane and homogeneous propagation. The local electric field evolution over time describes a loop trajectory from which omnipolar signals in the propagation direction, substrate and propagation features, are derived. In this work, we propose substrate and conduction velocity mapping modalities based on a modified version of the omnipolar electrogram method, which aims to reduce orientation-dependent residual components in the standard approach.&lt;/p> &amp; nbsp;&lt;/p> Methods: A simulated electrical propagation in 2D, with a tissue including a circular patch of diffuse fibrosis, was used for validation. Unipolar electrograms were calculated in a multi-electrode array, also deriving bipolar electrograms along the two main directions of the grid. Simulated bipolar electrograms were also contaminated with real noise, to assess the robustness of the mapping strategies against noise. The performance of the maps in identifying fibrosis and in reproducing unipolar reference voltage maps was evaluated. Bipolar voltage maps were also considered for performance comparison.&lt;/p> &amp; nbsp;&lt;/p> Results: Results show that the modified omnipolar mapping strategies are more accurate and robust against noise than bipolar and standard omnipolar maps in fibrosis detection (accuracies higher than 85 vs. 80% and 70%, respectively). They present better correlation with unipolar reference voltage maps than bipolar and original omnipolar maps (Pearson''s correlations higher than 0.75 vs. 0.60 and 0.70, respectively).&lt;/p> &amp; nbsp;&lt;/p> Conclusion: The modified omnipolar method improves fibrosis detection, characterization of substrate and propagation, also reducing the residual sensitivity to directionality over the standard approach and improving robustness against noise. Nevertheless, studies with real electrograms will elucidate its impact in catheter ablation interventions.&lt;/p></subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA-FSE/T39-20R-BSICoS group</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/766082/EU/MultidisciplinarY training network for ATrial fibRillation monItoring, treAtment and progression/MY-ATRIA</subfield>
    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 766082-MY-ATRIA</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN-FEDER/PID2019-105674RB-I00</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2019-104881RB-I00</subfield>
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    <subfield code="a">PHYSIOLOGY</subfield>
    <subfield code="b">20 / 81 = 0.247</subfield>
    <subfield code="c">2021</subfield>
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    <subfield code="a">Physiology (medical)</subfield>
    <subfield code="c">2021</subfield>
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    <subfield code="a">Physiology</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Alcaine, A</subfield>
    <subfield code="0">(orcid)0000-0002-0166-2837</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Rocher, S</subfield>
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    <subfield code="a">Martinez-Mateu, L</subfield>
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    <subfield code="a">Laranjo, S</subfield>
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    <subfield code="a">Saiz, J</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Laguna, P</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3434-9254</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Martinez, JP</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7503-3339</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ingeniería Electrón.Com.</subfield>
    <subfield code="c">Área Teoría Señal y Comunicac.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">12 (2021)</subfield>
    <subfield code="p">Front. physiol.</subfield>
    <subfield code="t">FRONTIERS IN PHYSIOLOGY</subfield>
    <subfield code="x">1664-042X</subfield>
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