Spectral analysis of fetal heart rate variability as a predictor of intrapartum fetal distress

2001 ◽  
Vol 73 (2) ◽  
pp. 109-116 ◽  
Author(s):  
D.Y. Chung ◽  
Y.B. Sim ◽  
K.T. Park ◽  
S.H. Yi ◽  
J.C. Shin ◽  
...  
Author(s):  
Olivier Sibony ◽  
Jean-Pierre Fouillot ◽  
Mokhtar Benaoudia ◽  
Abdelhay Benhalla ◽  
Jean-François Oury ◽  
...  

1993 ◽  
Vol 35 (1) ◽  
pp. 15-24 ◽  
Author(s):  
Ronald T. Wakai ◽  
Minghong Wang ◽  
Stephen L. Pedron ◽  
Deborah L. Reid ◽  
C.B. Martin

2018 ◽  
Vol 39 (2) ◽  
pp. 025008 ◽  
Author(s):  
G J J Warmerdam ◽  
R Vullings ◽  
J O E H Van Laar ◽  
M B Van der Hout-Van der Jagt ◽  
J W M Bergmans ◽  
...  

SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A325-A325
Author(s):  
G Pien ◽  
J Bei ◽  
H Watson ◽  
F Sgambati ◽  
R Raghunathan ◽  
...  

Abstract Introduction While studies have established that SDB during pregnancy increases the risk of adverse maternal outcomes, fetal effects are less well studied. Evidence suggests that fetal heart rate decelerations, an indicator of fetal distress, may be elicited by SDB. We examined the relationship between maternal SDB events and fetal heart rate (FHR) and fetal heart rate variability (FHRV). Methods Obese (BMI≥30kg/m2) non-smoking women carrying singleton fetuses underwent overnight polysomnography (34-37 weeks gestational age), with simultaneous fetal heart rate monitoring. Standard methods were used to score sleep, SDB events (apneas/hypopneas) and to analyze fetal heart rate parameters. Using linear mixed effect models, we examined changes in mean FHR and FHR variability (expressed by FHR SD) between the 10-second period immediately before individual SDB events, during events to the end of the associated oxygen desaturation period, and the 10-second period immediately following the SDB event. Results Valid PSG and FHR data were obtained from 85 third trimester maternal-fetal dyads. Across all participants, there were 2779 maternal SDB events (apneas or hypopneas). Mean AHI for individual subjects was 9.04 (SD 13.75). 39 women had OSA (AHI≥5), which was mostly mild. Mean FHR did not change significantly during and after episodes of SDB episodes compared to pre-event FHR, and did not change afterwards compared to during events, in unadjusted or adjusted (sleep stage, apnea type, degree of desaturation, age) analyses. In unadjusted analyses, FHRV significantly increased during SDB episodes compared to pre-SDB FHRV. After SDB events, FHRV was significantly lower than during SDB events. In fully adjusted models, these findings remained highly significant. FHRV was not significantly different after SDB events compared to pre-SDB event FHRV in unadjusted or adjusted models. Conclusion We observed consistent changes in FHR variability during and after maternal SDB events. Mean FHRV significantly increased during maternal SDB episodes compared to baseline FHRV, and decreased after SDB episodes. In contrast, mean FHR did not change significantly before, during and after SDB episodes. These data demonstrate that the fetus reacts to maternal SDB events, and raise questions about persistent effects of maternal SDB on the developing fetus. Support NIH HD079411


2003 ◽  
Vol 18 (4) ◽  
pp. 284-288 ◽  
Author(s):  
Carolyn Troeger ◽  
Andreas F. Schaub ◽  
Paolo Bernasconi ◽  
Irene Hösli ◽  
Wolfgang Holzgreve

1995 ◽  
Vol 79 (1) ◽  
pp. 63-65 ◽  
Author(s):  
O. Sibony ◽  
J. P. Fouillot ◽  
D. Luton ◽  
J. F. Oury ◽  
P. Blot

Spectral analysis of fetal heart rate variability allows quantitative determination of the main components that affect this variability. The physiological significance of these components is unclear; however, movements appear to contribute to variability. We studied six fetuses in which immobility required for in utero magnetic resonance or invasive fetal procedures was achieved by fetal intravascular injection of curare between 32 and 36 amenorrhea weeks. For each fetus, we compared spectral density parameters of heart rate variability. After curare administration, mean spectrum power was halved. We did not observe a larger significant decrease in any (very low, low, or high) frequency band. The other parameters of spectral analysis of variability were unaltered. Fetal movements accounted for a significant proportion of human fetal heart rate variability but did not constitute a unique frequency component.


Sign in / Sign up

Export Citation Format

Share Document