用于心率变异性分析的心跳间隔序列的自动近实时异常点检测和校正:基于奇异谱分析的方法

M. Lang
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引用次数: 4

摘要

背景:心率变异性(HRV)是从心电图(ECG)测量中提取的一系列R-R间隔中得出的。理想情况下,R-R系列的所有组成部分都是窦房结去极化的结果。然而,实际的R-R系列由于异位搏动等心律紊乱而受到异常值的污染,应在HRV分析之前检测并适当纠正。目的:我们介绍了一种基于奇异谱分析(SSA)的新颖、轻量级、接近实时的方法来检测和纠正R-R序列中的异常。本研究旨在从以下几个方面评估该方法的性能:(1)检测性能(灵敏度、特异性和准确性);(2)实际N-N序列与近似的剔除离群值的R-R序列之间的均方根误差(RMSE);(3)在相对均方根误差方面,它如何与竞争对手进行基准测试。方法:一个轻量级的基于ssa的变化点检测程序,通过使用具有自适应阈值的累积和控制图来改进以减少检测延迟,实时监测R-R区间的序列。一旦检测到异常,损坏的部分被替换为使用循环SSA预测获得的相应的异常值清洗近似。接下来,从MIT-BIH正常窦性心律数据库中的18条记录中提取5分钟心电图段的N-N个间隔。然后,对于每个这样的序列,在序列中的随机位置插入一个数字(随机抽取1到6之间的整数)模拟异位心跳,并在1000次蒙特卡罗运行中对结果进行平均。因此,使用与5分钟心电段相对应的18,000条R-R记录来评估检测性能,而使用另外180,000条(每条记录10,000条)来评估校正步骤中引入的误差。本研究共使用了198,000个R-R系列。结果:基于ssa的算法可靠地检测出R-R序列中的异常值,总体灵敏度为96.6%,特异性为98.4%,准确率为98.4%。此外,在清洗后的R-R序列与实际的N-N序列的差异方面,该方法比现有的校正方法平均高出近30%。结论:该算法利用SSA的功能和多功能性自动检测和纠正R-R系列中的伪影,提供了一种有效和高效的补充方法,并可能替代当前的手动编辑金标准。该方法的其他重要特征包括接近实时的操作能力、框架几乎完全无模型的特性(不需要历史训练数据)以及总体上较低的计算复杂度。[j] . JMIR Biomed Eng 2019;4(1):e10740) doi: 10.2196/107401 | e10740 | p. 1 https://biomedeng.jmir.org/2019/1/e10740/(页码不用于引用目的)Lang JMIR BIOMEDICAL ENGINEERING
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Automatic Near Real-Time Outlier Detection and Correction in Cardiac Interbeat Interval Series for Heart Rate Variability Analysis: Singular Spectrum Analysis-Based Approach
Background: Heart rate variability (HRV) is derived from the series of R-R intervals extracted from an electrocardiographic (ECG) measurement. Ideally all components of the R-R series are the result of sinoatrial node depolarization. However, the actual R-R series are contaminated by outliers due to heart rhythm disturbances such as ectopic beats, which ought to be detected and corrected appropriately before HRV analysis. Objective: We have introduced a novel, lightweight, and near real-time method to detect and correct anomalies in the R-R series based on the singular spectrum analysis (SSA). This study aimed to assess the performance of the proposed method in terms of (1) detection performance (sensitivity, specificity, and accuracy); (2) root mean square error (RMSE) between the actual N-N series and the approximated outlier-cleaned R-R series; and (3) how it benchmarks against a competitor in terms of the relative RMSE. Methods: A lightweight SSA-based change-point detection procedure, improved through the use of a cumulative sum control chart with adaptive thresholds to reduce detection delays, monitored the series of R-R intervals in real time. Upon detection of an anomaly, the corrupted segment was substituted with the respective outlier-cleaned approximation obtained using recurrent SSA forecasting. Next, N-N intervals from a 5-minute ECG segment were extracted from each of the 18 records in the MIT-BIH Normal Sinus Rhythm Database. Then, for each such series, a number (randomly drawn integer between 1 and 6) of simulated ectopic beats were inserted at random positions within the series and results were averaged over 1000 Monte Carlo runs. Accordingly, 18,000 R-R records corresponding to 5-minute ECG segments were used to assess the detection performance whereas another 180,000 (10,000 for each record) were used to assess the error introduced in the correction step. Overall 198,000 R-R series were used in this study. Results: The proposed SSA-based algorithm reliably detected outliers in the R-R series and achieved an overall sensitivity of 96.6%, specificity of 98.4% and accuracy of 98.4%. Furthermore, it compared favorably in terms of discrepancies of the cleaned R-R series compared with the actual N-N series, outperforming an established correction method on average by almost 30%. Conclusions: The proposed algorithm, which leverages the power and versatility of the SSA to both automatically detect and correct artifacts in the R-R series, provides an effective and efficient complementary method and a potential alternative to the current manual-editing gold standard. Other important characteristics of the proposed method include the ability to operate in near real-time, the almost entirely model-free nature of the framework which does not require historical training data, and its overall low computational complexity. (JMIR Biomed Eng 2019;4(1):e10740) doi: 10.2196/10740 JMIR Biomed Eng 2019 | vol. 4 | iss. 1 | e10740 | p. 1 https://biomedeng.jmir.org/2019/1/e10740/ (page number not for citation purposes) Lang JMIR BIOMEDICAL ENGINEERING
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