Publication | Closed Access
Topology and Random-Walk Network Representation of Cardiac Dynamics for Localization of Myocardial Infarction
42
Citations
21
References
2013
Year
EngineeringMi LocalizationNetwork AnalysisLocalizationBiomedical Signal AnalysisNetwork DynamicElectrophysiological EvaluationData SciencePattern RecognitionBiosignal ProcessingBiological NetworkBiostatisticsNetwork PhysiologyHuman MotionPtb DatabasePublic HealthCardiologyCardiovascular ImagingMyocardial InfarctionRandom-walk Network RepresentationTemporal Pattern RecognitionTopological RepresentationMi LocationsBiomedical ModelingSignal ProcessingCardiac PathologyNetwork ScienceCardiac DynamicsComputational NeuroscienceCardiac ElectrophysiologyElectrophysiologyHigh-dimensional NetworkSystems Biology
While detection of acute cardiac disorders such as myocardial infarction (MI) from electrocardiogram (ECG) and vectorcardiogram (VCG) has been widely reported, identification of MI locations from these signals, pivotal for timely therapeutic and prognostic interventions, remains a standing issue. We present an approach for MI localization based on representing complex spatiotemporal patterns of cardiac dynamics as a random-walk network reconstructed from the evolution of VCG signals across a 3-D state space. Extensive tests with signals from the PTB database of the PhysioNet databank suggest that locations of MI can be determined accurately (sensitivity of ∼88% and specificity of ∼92%) from tracking certain consistently estimated invariants of this random-walk representation.
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