Accelerated Variant of an EMD-Based-R Peaks Detection Algorithm Involving FFT-Based Time-Domain Down-Sampling and up-Sampling

IF 0.5 Q4 ENGINEERING, BIOMEDICAL
A. Harkat, R. Benzid, N. Athamena
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引用次数: 0

Abstract

As most of developed empirical mode decomposition (EMD) based R-peaks detection algorithms consume a considerable time of calculation caused by the large length of the input ECG signal, the design of a new technique that allows the acceleration of such methods becomes necessary. Accordingly, a new variant of an EMD-based strategy for R-peaks localization is presented. The new accelerated variant is constituted of three essential parts. The first step is the length reduction of the input signal by means of the truncation in the Fast Fourier Transform (FFT) domain followed by the application of the inverse FFT guaranteeing a suitable time-domain down-sampling. Consequently, the new input signal of a reduced length preserves all medical information contained initially in the original lengthy signal. The second part is dedicated to identify the QRS complex using EMD-based R-peaks detection. This latter comprises a low-pass filter, Empirical Mode Decomposition (EMD) and the Hilbert transform, Finally, the third phase is the time-domain up-sampling using the FFT, the zero padding and the Inverse Fast Fourier Transform (IFFT) to obtain a resulting processed signal which has the same length as the original signal. Next, as a post-processing step, final R-peaks refined localization is achieved. It is noticeable that the new variant ensures same results, in term of accuracy, as the standard method; however, a significant speed-up ratio of 6.95:1 is reported. Additionally, to more prove the effectiveness of the suggested strategy, it has been applied to accelerate two other efficient algorithms and satisfactory speed up ratios of, 7.20:1 and 4.23:1, respectively have been reached.
基于emd的r峰值检测算法的加速变体,包括基于fft的时域下采样和上采样
由于大多数开发的基于经验模式分解(EMD)的R峰值检测算法由于输入ECG信号的大长度而消耗了相当长的计算时间,因此设计一种允许加速这种方法的新技术变得必要。因此,提出了一种基于EMD的R峰定位策略的新变体。新的加速变体由三个重要部分组成。第一步是通过在快速傅立叶变换(FFT)域中的截断来减少输入信号的长度,然后应用逆FFT来保证合适的时域下采样。因此,长度减小的新输入信号保留了最初包含在原始长信号中的所有医疗信息。第二部分致力于使用基于EMD的R峰检测来识别QRS复合物。后者包括低通滤波器、经验模式分解(EMD)和希尔伯特变换。最后,第三阶段是使用FFT、零填充和快速傅立叶逆变换(IFFT)的时域上采样,以获得与原始信号具有相同长度的最终处理信号。接下来,作为后处理步骤,实现最终的R峰精细定位。值得注意的是,新的变体在准确性方面确保了与标准方法相同的结果;然而,据报道,有6.95:1的显著加速比。此外,为了进一步证明所提出的策略的有效性,它已被应用于另外两种有效算法的加速,并分别达到了7.20:1和4.23:1的令人满意的加速比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
14.30%
发文量
73
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