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      Importance of the heart vector origin point definition for an ECG analysis: The Atherosclerosis Risk in Communities (ARIC) study

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          Abstract

          —Our goal was to investigate the effect of a global XYZ median beat construction and the heart vector origin point definition on predictive accuracy of ECG biomarkers of sudden cardiac death (SCD). —Atherosclerosis Risk In Community study participants with analyzable digital ECGs were included (n=15,768; 55% female, 73% white, mean age 54.2±5.8 y). We developed an algorithm to automatically detect the heart vector origin point on a median beat. Three different approaches to construct a global XYZ beat and two methods to locate origin point were compared. Global electrical heterogeneity was measured by sum absolute QRST integral (SAI QRST), spatial QRS-T angle, and spatial ventricular gradient (SVG) magnitude, azimuth, and elevation. Adjudicated SCD served as the primary outcome. —There was high intra-observer (kappa 0.972) and inter-observer (kappa 0.984) agreement in a heart vector origin definition between an automated algorithm and a human. QRS was wider in a median beat that was constructed using R-peak alignment than in time-coherent beat (88.1±16.7 vs. 83.7±15.9 ms; P<0.0001), and on a median beat constructed using QRS-onset as a zeroed baseline, vs. isoelectric origin point (86.7±15.9 vs. 83.7±15.9 ms; P<0.0001). ROC AUC was significantly larger for QRS, QT, peak QRS-T angle, SVG elevation, and SAI QRST if measured on a time-coherent median beat, and for SAI QRST and SVG magnitude if measured on a median beat using isoelectric origin point. —Time-coherent global XYZ median beat with physiologically meaningful definition of the heart vector’s origin point improved predictive accuracy of SCD biomarkers.

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          Author and article information

          Journal
          Computers in Biology and Medicine
          Computers in Biology and Medicine
          Elsevier BV
          00104825
          January 2019
          January 2019
          : 104
          : 127-138
          Article
          10.1016/j.compbiomed.2018.11.013
          6400224
          30472495
          60250649-6d33-48c7-a171-63b81426a6fb
          © 2019

          https://www.elsevier.com/tdm/userlicense/1.0/

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