TY - JOUR
T1 - Automated estimation of fetal cardiac timing events from doppler ultrasound signal using hybrid models
AU - Marzbanrad, Faezeh
AU - Kimura, Yoshitaka
AU - Funamoto, Kiyoe
AU - Sugibayashi, Rika
AU - Endo, Miyuki
AU - Ito, Takuya
AU - Palaniswami, Marimuthu
AU - Khandoker, Ahsan H.
PY - 2014/7
Y1 - 2014/7
N2 - In this paper, a new noninvasive method is proposed for automated estimation of fetal cardiac intervals from Doppler Ultrasound (DUS) signal. This method is based on a novel combination of empirical mode decomposition (EMD) and hybrid support vector machines - hidden Markov models (SVM/HMM). EMD was used for feature extraction by decomposing the DUS signal into different components (IMFs), one of which is linked to the cardiac valve motions, i.e. opening (o) and closing (c) of the Aortic (A) and Mitral (M) valves. The noninvasive fetal electrocardiogram (fECG) was used as a reference for the segmentation of the IMF into cardiac cycles. The hybrid SVM/HMM was then applied to identify the cardiac events, based on the amplitude and timing of the IMF peaks as well as the sequence of the events. The estimated timings were verified using pulsed doppler images. Results show that this automated method can continuously evaluate beat-to-beat valve motion timings and identify more than 91% of total events which is higher than previous methods. Moreover, the changes of the cardiac intervals were analyzed for three fetal age groups: 16-29, 30-35, and 36-41 weeks. The time intervals from Q-wave of fECG to Ac (Systolic Time Interval, STI), Ac to Mo (Isovolumic Relaxation Time, IRT), Q-wave to Ao (Preejection Period, PEP) and Ao to Ac (Ventricular Ejection Time, VET) were found to change significantly (p < 0.05) across these age groups. In particular, STI, IRT, and PEP of the fetuses with 36-41 week were significantly (p < 0.05) different from other age groups. These findings can be used as sensitive markers for evaluating the fetal cardiac performance.
AB - In this paper, a new noninvasive method is proposed for automated estimation of fetal cardiac intervals from Doppler Ultrasound (DUS) signal. This method is based on a novel combination of empirical mode decomposition (EMD) and hybrid support vector machines - hidden Markov models (SVM/HMM). EMD was used for feature extraction by decomposing the DUS signal into different components (IMFs), one of which is linked to the cardiac valve motions, i.e. opening (o) and closing (c) of the Aortic (A) and Mitral (M) valves. The noninvasive fetal electrocardiogram (fECG) was used as a reference for the segmentation of the IMF into cardiac cycles. The hybrid SVM/HMM was then applied to identify the cardiac events, based on the amplitude and timing of the IMF peaks as well as the sequence of the events. The estimated timings were verified using pulsed doppler images. Results show that this automated method can continuously evaluate beat-to-beat valve motion timings and identify more than 91% of total events which is higher than previous methods. Moreover, the changes of the cardiac intervals were analyzed for three fetal age groups: 16-29, 30-35, and 36-41 weeks. The time intervals from Q-wave of fECG to Ac (Systolic Time Interval, STI), Ac to Mo (Isovolumic Relaxation Time, IRT), Q-wave to Ao (Preejection Period, PEP) and Ao to Ac (Ventricular Ejection Time, VET) were found to change significantly (p < 0.05) across these age groups. In particular, STI, IRT, and PEP of the fetuses with 36-41 week were significantly (p < 0.05) different from other age groups. These findings can be used as sensitive markers for evaluating the fetal cardiac performance.
KW - Doppler ultrasound (DUS)
KW - empirical mode decomposition (EMD)
KW - fetal cardiac intervals
KW - fetal monitoring
KW - hidden Markov models (HMM)
KW - hybrid SVM/HMM
KW - support vector machine (SVM)
UR - http://www.scopus.com/inward/record.url?scp=84904333155&partnerID=8YFLogxK
U2 - 10.1109/JBHI.2013.2286155
DO - 10.1109/JBHI.2013.2286155
M3 - Article
C2 - 24144677
AN - SCOPUS:84904333155
SN - 2168-2194
VL - 18
SP - 1169
EP - 1177
JO - IEEE Journal of Biomedical and Health Informatics
JF - IEEE Journal of Biomedical and Health Informatics
IS - 4
M1 - 6636069
ER -