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      Effects of Tau and Sampling Frequency on the Regularity Analysis of ECG and EEG Signals Using ApEn and SampEn Entropy Estimators

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          Abstract

          Electrocardiography (ECG) and electroencephalography (EEG) signals provide clinical information relevant to determine a patient’s health status. The nonlinear analysis of ECG and EEG signals allows for discovering characteristics that could not be found with traditional methods based on amplitude and frequency. Approximate entropy (ApEn) and sampling entropy (SampEn) are nonlinear data analysis algorithms that measure the data’s regularity, and these are used to classify different electrophysiological signals as normal or pathological. Entropy calculation requires setting the parameters r (tolerance threshold), m (immersion dimension), and τ (time delay), with the last one being related to how the time series is downsampled. In this study, we showed the dependence of ApEn and SampEn on different values of τ, for ECG and EEG signals with different sampling frequencies ( F s ), extracted from a digital repository. We considered four values of F s (128, 256, 384, and 512 Hz for the ECG signals, and 160, 320, 480, and 640 Hz for the EEG signals) and five values of τ (from 1 to 5). We performed parametric and nonparametric statistical tests to confirm that the groups of normal and pathological ECG and EEG signals were significantly different ( p < 0.05) for each F and τ value. The separation between the entropy values of regular and irregular signals was variable, demonstrating the dependence of ApEn and SampEn with F s and τ. For ECG signals, the separation between the conditions was more robust when using SampEn, the lowest value of F s , and τ larger than 1. For EEG signals, the separation between the conditions was more robust when using SampEn with large values of F s and τ larger than 1. Therefore, adjusting τ may be convenient for signals that were acquired with different F s to ensure a reliable clinical classification. Furthermore, it is useful to set τ to values larger than 1 to reduce the computational cost.

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          PhysioBank, PhysioToolkit, and PhysioNet

          Circulation, 101(23)
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            Approximate entropy as a measure of system complexity.

            Techniques to determine changing system complexity from data are evaluated. Convergence of a frequently used correlation dimension algorithm to a finite value does not necessarily imply an underlying deterministic model or chaos. Analysis of a recently developed family of formulas and statistics, approximate entropy (ApEn), suggests that ApEn can classify complex systems, given at least 1000 data values in diverse settings that include both deterministic chaotic and stochastic processes. The capability to discern changing complexity from such a relatively small amount of data holds promise for applications of ApEn in a variety of contexts.
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              Physiological time-series analysis using approximate entropy and sample entropy.

              Entropy, as it relates to dynamical systems, is the rate of information production. Methods for estimation of the entropy of a system represented by a time series are not, however, well suited to analysis of the short and noisy data sets encountered in cardiovascular and other biological studies. Pincus introduced approximate entropy (ApEn), a set of measures of system complexity closely related to entropy, which is easily applied to clinical cardiovascular and other time series. ApEn statistics, however, lead to inconsistent results. We have developed a new and related complexity measure, sample entropy (SampEn), and have compared ApEn and SampEn by using them to analyze sets of random numbers with known probabilistic character. We have also evaluated cross-ApEn and cross-SampEn, which use cardiovascular data sets to measure the similarity of two distinct time series. SampEn agreed with theory much more closely than ApEn over a broad range of conditions. The improved accuracy of SampEn statistics should make them useful in the study of experimental clinical cardiovascular and other biological time series.
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                Author and article information

                Journal
                Entropy (Basel)
                Entropy (Basel)
                entropy
                Entropy
                MDPI
                1099-4300
                14 November 2020
                November 2020
                : 22
                : 11
                : 1298
                Affiliations
                [1 ]Department of Biomedical Engineering, Universidad ECCI, Biomedical Applications EMB-IEEE, Bogotá 111311, Colombia; jesical.talerom@ 123456ecci.edu.co
                [2 ]Center of Research and Development in Health Engineering, Valparaiso University, Valparaíso 2362905, Chile; alejandro.weinstein@ 123456uv.cl
                Author notes
                Author information
                https://orcid.org/0000-0002-7941-0138
                https://orcid.org/0000-0003-2771-2115
                Article
                entropy-22-01298
                10.3390/e22111298
                7711820
                33287066
                4cf953c8-9694-4d13-8eee-f44055a67b98
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 30 October 2020
                : 10 November 2020
                Categories
                Article

                electrophysiological signals,nonlinear signals,entropy,sampling frequencies,time delay

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