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1995 IEEE-EMBC and CMBEC

Theme 1: Cardiovascular System

FETAL ECG EXTRACTION FROMSINGLE CHANNEL MATERNAL ECG


USING SVD AND SVR SPECTRUM

P.P. Kanjilal and Goutam Saha


Dept. of Electronics & ECE, I.I.T. Kharagpur, INDIA 721302

ABSTRACT The perioidic segments of CM-ECG data are


Singular Value Decomposition (SVD) and ana- aligned into the successive rows of matrix
lysis based on Singular Value Ratio (SVR) A. A is SV-decomposed and the most dominant
Spectrum have been used f o r the extraction mode A, = ulslvl is separated from A,
of f e t a l ECG (F-ECG) from a single channel forming ARl=A-A,. The extracted component
composite maternal ECG (CM-ECG) signal. The represents the maternal ECG component.
maternal and the f e t a l ECG components are The time series formed from the suc-
identified in terms of the SV-decomposed cessive rows of the residual matrix AR1
modes of the the appropriately configured will contain the F-ECG component along with
d a t a matrices, and the desired F-ECG is the noise. The residual series is rearran-
obtained through selective separation of ged into a matrix B, with each row contain-
SV-decomposed components. ing 1 fetal ECG cycle. The component ulslvT
of B gives the desired F-ECG component.
1 INTRODUCTION
4 RESULTS
There has been different approaches f o r the
extraction of F-ECG from multiple CM-ECG The bidirectionally filtered (with filter
signals [1,21. Proposed is the use of pole at 0.88) CM-ECG signal (Fig.1) is
single channel CM-ECG signal, from which shown in Fig.2. The SVR spectrum (Fig.5) of
F-ECG is extracted through SVR-aided this signal showed a periodicity of 81
SV-decompositio domain separation. time-samples. On separation of the M-ECG
component (Fig.31, the residual series
2 PRELIMINARIES showed presence of a periodic component of
49 in i t s SVR spectrum (Fig.6). The extrac-
SVDTof an mxn matrix A i s given by [31 A = ted F-ECG component is shown in Fig.4.
USV , where U, V are orthogonal matrices, S
= [diag {si, ..,sp):Ol, slz..~s$O with max 5 CONCLUSIONS
Rank(A)=p= min(m,n). If an n-periodic sig-
nal {x(k)) occupies successive rows of A, Here, the 2 unique features are (i) use of
p=1. The most dominant pefiodic component a single CM-ECG signal and (ii) use of a
in {x(k)) is given by slulvl,where u1 and successive extraction in algebraically
vi are the 1st. columns of U and V respec- orthogonal transf o m domain, instead of the
tively. If Rank(A)=l, s1/s2 = infinity; if conventional frequency domain, with due
Rank(A)>l, sl/sz drops.1f {x(k)}+ A, f o r consideration of the nearly repetitive na-
varying n, the corresponding spectrum of ture of the signals of interest. The low-
s1/s2 will exhibit repeating peaks at the frequency interference on the CM-ECG signal
dominant periodicity; this spectrum is as well as the variations in the period
called the SVR spectrum [4,51. In this lengths of the M-ECG and the F-ECG compo-
work, the M-ECG and F-ECG period-lengths nents are taken care of. The tool used is
are determined using SVR spectrum. SVD which i s remarkably robust numerically.

3 OUTLINE OF F-ECG EXTRACTION PROCEDURE REFERENCES


The CM-ECG signa1 is f i r s t bidirectionally [ll Longini, R:L., T.A. Reichert et a1
low-pass filtered t o eliminate trend [SI. (1977): ‘Near-orthogonal basis functions; a

0-7803-2475-7197$1 0.00 01 997 IEEE 187


real time fetal ECG technique', IEEE Trans.
I41 Kanjilal, P.P., and S. Palit 11995):
multiple pattern extraction using
, D., B. De alue decomposition', I E E E Trans.
(1990): 'Comparison of SVD June, t o appear.
e x t r a c t the foetal electrocardiogram from [51 Kanjilal, P.P. (1995): Adaptive Pre-
cutaneous electrode signals', diction and Predictive Control: Principles
Biol. Eng. and Comp., 28, 217- and Applications, Peter Peregrinus (IEE
G.H., and C.F. V Publication), Stevenage, in press.
Matrix Computations, The Johns Hopkins
Univ. Press, Baltimore.

200

0 100
Signal a1
magnitude magnitude
-200 0

-400
800 0
"100 '
o
I

200
I

400
I I

800
I
1000
Fig. I , Fig. 2. Time samples

-100 -60
0 200 400 600 800 1000 0 200 400 600 800 1000
Fig. 3. Time samples Fig. 4. Time samples

ratio
1

0
0 50 100 150 200 250
Fig. 5. Period lengths

188

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