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Selection of optimal recording sites for limited lead body surface potential mapping: A sequential selection based approach

DOI: 10.1186/1472-6947-6-9

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Abstract:

The study was conducted using a dataset consisting of body surface potential maps (BSPM) recorded from 116 subjects which included 59 normals and 57 subjects exhibiting evidence of old Myocardial Infarction (MI). The performance of the algorithm was evaluated using spatial RMS voltage error and correlation coefficient to compare original and reconstructed map frames.In all, three configurations of the algorithm were evaluated and it was concluded that there was little difference in the performance of the various configurations. In addition to observing the performance of the selection algorithm, several lead subsets of 32 electrodes as chosen by the various configurations of the algorithm were evaluated. The rationale for choosing this number of recording sites was to allow comparison with a previous study that used a different algorithm, where 32 leads were deemed to provide an acceptable level of reconstruction performance.It was observed that although the lead configurations suggested in this study were not identical to that suggested in the previous work, the systems did bear similar characteristics in that recording sites were chosen with greatest density in the precordial region.Body Surface Potential Mapping refers to the process of acquisition and display of temporal and spatial distributions of electrocardiographic potentials recorded from multiple sites on the torso [1]. In contrast to more conventional recording techniques, such as the 12 lead ECG, where scalar traces allow for assessment of wave amplitudes, intervals and morphology, Body surface potential maps (BSPM) are assessed based on the shape of their contours, number and location of extrema and the dynamics of each [2]. As well as providing the ability to locate electrocardiographic events in both space and time, BSPMs yield more diagnostic content by capturing information at anatomical regions not interrogated by the widely utilised 12 lead ECG. This allows for more comprehensive diagnosis of con

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