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Estimation of Complexity of Sampled Biomedical Continuous Time Signals Using Approximate Entropy

机译:使用近似熵估计采样生物医学连续时间信号的复杂度

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摘要

Non-linear analysis found many applications in biomedicine. Approximate entropy (ApEn) is a popular index of complexity often applied to biomedical data, as it provides quite stable indications when processing short and noisy epochs. However, ApEn strongly depends on parameters, which were chosen in the literature in wide ranges. This paper points out that ApEn depends on sampling rate of continuous time signals, embedding dimension, tolerance (under which a match is identified), epoch duration and low frequency trends. Moreover, contradicting results can be obtained changing parameters. This was found both in simulations and in experimental EEG. These limitations of ApEn suggest the introduction of an alternative index, here called modified ApEn, which is based on the following principles: oversampling is compensated, self-recurrences are ignored, a fixed percentage of recurrences is selected and low frequency trends are removed. The modified index allows to get more stable measurements of the complexity of the tested simulated data and EEG. The final conclusions are that, in order to get a reliable estimation of complexity using ApEn, parameters should be chosen within specific ranges, data must be sampled close to the Nyquist limit and low frequency trends should be removed. Following these indications, different studies could be more easily compared, interpreted and replicated. Moreover, the modified ApEn can be an interesting alternative, which extends the range of parameters for which stable indications can be achieved.
机译:非线性分析发现了在生物医学中的许多应用。近似熵(ApEn)是一种经常用于生物医学数据的复杂性流行指标,因为在处理短而嘈杂的时期时,它提供了相当稳定的指示。但是,ApEn强烈依赖于在文献中广泛选择的参数。本文指出,ApEn取决于连续时间信号的采样率,嵌入尺寸,容差(在此之下可以识别匹配项),历时长短和低频趋势。而且,改变参数可以获得矛盾的结果。在模拟和实验性脑电图中均发现了这一点。 ApEn的这些局限性建议引入一个替代索引,这里称为修改后的ApEn,它基于以下原则:补偿过采样,忽略自递归,选择固定百分比的递归并消除低频趋势。修改后的索引可以对测试的模拟数据和EEG的复杂性进行更稳定的测量。最终结论是,为了使用ApEn获得可靠的复杂度估计,应在特定范围内选择参数,必须在接近奈奎斯特极限的范围内采样数据,并应消除低频趋势。遵循这些指示,可以更轻松地比较,解释和复制不同的研究。此外,修改后的ApEn可能是一个有趣的选择,它扩展了可以实现稳定指示的参数范围。

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