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基于主成分分析的T波形态参数的可重复性及对T波偏移位置的依赖性。

T-wave morphology parameters based on principal component analysis reproducibility and dependence on T-offset position.

作者信息

Extramiana Fabrice, Haggui Abdeddayem, Maison-Blanche Pierre, Dubois Rémi, Takatsuki Seiji, Beaufils Philippe, Leenhardt Antoine

机构信息

Cardiology Department, Lariboisière Hospital, APHP, Paris 7 University, France.

出版信息

Ann Noninvasive Electrocardiol. 2007 Oct;12(4):354-63. doi: 10.1111/j.1542-474X.2007.00185.x.

Abstract

BACKGROUND

T-wave morphology parameters based on principal component analysis (PCA) are candidate to better understand the relation between QT prolongation and torsades de pointes. We aimed to assess the repeatability and to determine the influence of T-end position on PCA parameters.

METHODS

Digital ECGs recorded from 30 subjects were used to assess short term (5 minutes), circadian and long-term (28 days) repeatability of PCA parameters. The T-end cursor position was moved backward and forward (+/- 8 ms) from its optimal position. We calculated QRS-T angle, PCA ratio, and T-wave residuum (TWR).

RESULTS

At long-term evaluation, coefficients of variation were 11.3 +/- 9.9%, 11.7 +/- 7.1%, and 23.0 +/- 22.0% for the QRS-T angle, PCA ratio, TWR, respectively. After moving the T-end cursor, repeatability was 0.42 +/- 0.2%, 1.00 +/- 1.04%, 4.0 +/- 4.2% for the same PCA parameters.

CONCLUSIONS

T-wave morphology parameters based on PCA are reproducible with the exception of TWR and QRS-T angle. In addition, PCA is robust, showing only little dependence on T-end cursor position. These data should be taken into account for safety pharmacology trials.

摘要

背景

基于主成分分析(PCA)的T波形态学参数有望更好地理解QT间期延长与尖端扭转型室速之间的关系。我们旨在评估PCA参数的可重复性,并确定T波终点位置对其的影响。

方法

使用从30名受试者记录的数字心电图来评估PCA参数的短期(5分钟)、昼夜节律和长期(28天)可重复性。将T波终点光标位置从其最佳位置前后移动(±8毫秒)。我们计算了QRS-T夹角、PCA比率和T波残差(TWR)。

结果

在长期评估中,QRS-T夹角、PCA比率、TWR的变异系数分别为11.3±9.9%、11.7±7.1%和23.0±22.0%。移动T波终点光标后,相同PCA参数的可重复性分别为0.42±0.2%、1.00±1.04%、4.0±4.2%。

结论

除TWR和QRS-T夹角外,基于PCA的T波形态学参数具有可重复性。此外,PCA具有稳健性,对T波终点光标位置的依赖性很小。在安全药理学试验中应考虑这些数据。

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