4.2 Article

Segmented independent component analysis for improved separation of fetal cardiac signals from nonstationary fetal magnetocardiograms

Journal

BIOMEDICAL ENGINEERING-BIOMEDIZINISCHE TECHNIK
Volume 60, Issue 3, Pages 235-244

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/bmt-2014-0114

Keywords

fetal magnetocardiography; independent component analysis; signal nonstationarity; signal quality; signal segmentation

Funding

  1. Italian Ministry for Research, INTERLINK Project, New methods to reconstruct and analyze the fetal cardiac signals recorded by magnetocardiography [II04CD8G5A]
  2. National Institutes of Health [R01 HL063174]
  3. CNPq (Brazil) [308604/2013-0, 307941/2010-8]
  4. FAPESP (Brazil) [2010/09921-3]

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Fetal magnetocardiograms (fMCGs) have been successfully processed with independent component analysis (ICA) to separate the fetal cardiac signals, but ICA effectiveness can be limited by signal nonstationarities due to fetal movements. We propose an ICA-based method to improve the quality of fetal signals separated from fMCG affected by fetal movements. This technique (SegICA) includes a procedure to detect signal nonstationarities, according to which the fMCG recordings are divided in stationary segments that are then processed with ICA. The first and second statistical moments and the signal polarity reversal were used at different threshold levels to detect signal transients. SegICA effectiveness was assessed in two fMCG datasets (with and without fetal movements) by comparing the signal-to-noise ratio (SNR) of the signals extracted with ICA and with SegICA. Results showed that the SNR of fetal signals affected by fetal movements improved with SegICA, whereas the SNR gain was negligible elsewhere. The best measure to detect signal nonstationarities of physiological origin was signal polarity reversal at threshold level 0.9. The first statistical moment also provided good results at threshold level 0.6. SegICA seems a promising method to separate fetal cardiac signals of improved quality from nonstationary fMCG recordings affected by fetal movements.

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