Permutation entropy improves fetal behavioural state classification based on heart rate analysis from biomagnetic recordings in near term fetuses

被引:113
作者
Frank, B. [1 ]
Pompe, B.
Schneider, U.
Hoyer, D.
机构
[1] Univ Jena, Dept Neurol, Inst Pathophysiol & Pathobiochem, D-6900 Jena, Germany
[2] Univ Jena, Dept Neurol, Biomagnet Ctr, D-6900 Jena, Germany
[3] Univ Greifswald, Inst Phys, Greifswald, Germany
[4] Univ Jena, Dept Obstet & Gynaecol, D-6900 Jena, Germany
关键词
fetal behavioural states; heart rate variability; biomagnetic recording; permutation entropy; Kullback-Leibler entropy;
D O I
10.1007/s11517-005-0015-z
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
The relevance of the complexity of fetal heart rate fluctuations with regard to the classification of fetal behavioural states has not been satisfyingly clarified so far. Because of the short behavioural states, the permutation entropy provides an advantageous complexity estimation leading to the Kullback-Leibler entropy (KLE). We test the hypothesis that parameters derived from KLE can improve the classification of fetal behaviour states based on classical heart rate fluctuation parameters (SDNN, RMSSD, ln(LF), ln(HF)). From measured heartbeat sequences ( 35 healthy fetuses at a gestational age between 35 and 40 completed weeks) representative intervals of 256 heartbeats were visually preclassified into fetal behavioural states. Employing discriminant analysis to separate the states 1F, 2F and 4F, the best classification result by classical parameters was 80.0% ( SDNN). After additionally considering KLE parameters it was improved significantly (p < 0.0005) to 94.3% (ln(LF), KLE_Mean). It could be confirmed that KLE can improve the state classification. This might reflect the consideration of different physiological aspects by classical and complexity measures.
引用
收藏
页码:179 / 187
页数:9
相关论文
共 41 条
[31]  
*SPSS INC, 2002, SPSS WIND R
[32]  
Stinstra J, 2002, BJOG-INT J OBSTET GY, V109, P1235
[33]   Multi-channel magnetocardiography for detecting beat morphology variations in fetal arrhythmias [J].
Sturm, R ;
Müller, HP ;
Pasquarelli, A ;
Demelis, M ;
Erné, SN ;
Terinde, R ;
Lang, D .
PRENATAL DIAGNOSIS, 2004, 24 (01) :1-9
[34]  
Teukolsky SA, 1992, NUMERICAL RECIPES C, VSecond
[35]   Fetal heart rate variability and complexity in the course of pregnancy [J].
Van Leeuwen, P ;
Lange, S ;
Bettermann, H ;
Grönemeyer, D ;
Hatzmann, W .
EARLY HUMAN DEVELOPMENT, 1999, 54 (03) :259-269
[36]  
Van Leeuwen Peter, 2003, BMC Physiol, V3, P2, DOI 10.1186/1472-6793-3-2
[37]  
Voss A, 1996, CARDIOVASC RES, V31, P419
[38]   Assessment of fetal neurodevelopment via fetal magnetocardiography [J].
Wakai, RT .
EXPERIMENTAL NEUROLOGY, 2004, 190 :S65-S71
[39]   SPATIOTEMPORAL PROPERTIES OF THE FETAL MAGNETOCARDIOGRAM [J].
WAKAI, RT ;
WANG, MH ;
MARTIN, CB .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1994, 170 (03) :770-776
[40]   SPECTRAL-ANALYSIS OF ANTEPARTUM FETAL HEART-RATE-VARIABILITY FROM FETAL MAGNETOCARDIOGRAM RECORDINGS [J].
WAKAI, RT ;
WANG, MH ;
PEDRON, SL ;
REID, DL ;
MARTIN, CB .
EARLY HUMAN DEVELOPMENT, 1993, 35 (01) :15-24