Quantification of fragmented QRS complex using intrinsic time-scale decomposition

被引:14
作者
Jin, Feng [1 ]
Sugavaneswaran, Lakshmi [1 ,2 ]
Krishnan, Sridhar [1 ]
Chauhan, Vijay S. [2 ]
机构
[1] Ryerson Univ, Dept Elect & Comp Engn, 350 Victoria St, Toronto, ON M5B 2K3, Canada
[2] Univ Hlth Network, Div Cardiol, Toronto, ON M5G 2C4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Fragmented QRS (fQRS); Intrinsic time-scale decomposition (ITD); Instantaneous morphology feature extraction; Electrocardiogram (ECG); Sudden cardiac death; Risk assessment; HIGH-FREQUENCY COMPONENTS; ECG; ELECTROCARDIOGRAM; NOISE; MARKER;
D O I
10.1016/j.bspc.2016.09.015
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The QRS complex recorded from the surface electrocardiograrm (ECG) arises from electrical activation of the ventricular myocardium through the normal conduction system. The presence of a fragmented QRS (fQRS) complex reflects abnormal electrical activation and has, been recently shown to identify patients with heart disease at risk of sudden cardiac death (SCD). The evaluation of fQRS is currently performed qualitatively by visual inspection which can be time consuming and subject to interpretation. Moreover; qualitative assessment of QRS for fragmentation may be insensitive to more subtle deflections in the QRS complex that may be equally prognostic. This study proposes an automated method to quantify QRS fractionation using intrinsic time-scale decomposition (ITD). Instantaneous morphology features are extracted from the decomposed QRS signal to index variations in its shapes. Our quantitative fQRS metric was found to be significantly greater in QRS complexes with fragmentation compared to normal QRS complexes derived from real-world ECGs in the Physikalisch-Technische Bundesanstalt (PTB) database. ROC analysis showed an area under the curve of 0.96 when fQRS was quantified from the precordial ECG leads, V1-V6. Thus, quantification of fQRS using the proposed ITD-based method can accurately identify fQRS. Our approach shows tremendous potential and could be investigated further for SCD risk assessment in patients with heart disease by improving the identification of fQRS that may or may not be visually apparent. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:513 / 523
页数:11
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