Am J Perinatol 2005; 22(1): 19-23
DOI: 10.1055/s-2004-837272
Copyright © 2005 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Predictive Value of Late Decelerations for Fetal Acidemia in Unselective Low-Risk Pregnancies

Hiroshi Sameshima1 , Tsuyomu Ikenoue1
  • 1Perinatal Center and Department of Obstetrics and Gynecology, Miyazaki Medical College, University of Miyazaki, Miyazaki, Japan
Further Information

Publication History

Publication Date:
11 January 2005 (online)

ABSTRACT

We evaluated the clinical significance of late decelerations (LD) of intrapartum fetal heart rate (FHR) monitoring to detect low pH (< 7.1) in low-risk pregnancies. We selected two secondary and two tertiary-level institutions where 10,030 women delivered. Among them, 5522 were low-risk pregnancies. The last 2 hours of FHR patterns before delivery were interpreted according to the guidelines of the National Institute of Child Health and Human Development. The correlation between the incidence of LD (occasional, < 50%; recurrent, ≥ 50%) and severity (reduced baseline FHR accelerations and variability) of LD, and low pH (< 7.1) were evaluated. Statistical analyses included a contingency table with χ2 and the Fisher test, and one-way analysis of variance with the Bonferroni/Dunn test. In the 5522 low-risk pregnancies, 301 showed occasional LD and 99 showed recurrent LD. Blood gases and pH values deteriorated as the incidence of LD increased and as baseline accelerations or variability was decreased. Positive predictive value for low pH (< 7.1) was exponentially elevated from 0% at no deceleration, 1% in occasional LD, and > 50% in recurrent LD with no baseline FHR accelerations and reduced variability. In low-risk pregnancies, information on LD combined with acceleration and baseline variability enables us to predict the potential incidence of fetal acidemia.

REFERENCES

  • 1 Murata Y, Martin Jr C B, Ikenoue T et al.. Fetal heart rate accelerations and late decelerations during the course of intrauterine death in chronically catheterized rhesus monkeys.  Am J Obstet Gynecol. 1982;  144 218-223
  • 2 Martin Jr C B, de Haan J, van der Wildt B, Jongsma H W, Dieleman A, Arts T HM. Mechanisms of alte decelerations in the fetal heart rate. A study with autonomic blocking agensts in fetal lambs.  Eur J Obstet Gynecol Reprod Biol. 1979;  9 361-373
  • 3 Kubli F W, Hon E H, Khazin A F, Takemura H. Observation on heart rate and pH in the human fetus during labor.  Am J Obstet Gynecol. 1969;  104 1190-1206
  • 4 Paul R H, Suidan A K, Yeh S Y, Shifrin B S, Hon E H. Clinical fetal monitoring. VII. The evaluation and clinical significance of intrapartum baseline FHR variability.  Am J Obstet Gynecol. 1975;  123 206-210
  • 5 Clark S L, Gimovsky M L, Miller F C. The scalp stimulation test: a clinical alternative to fetal scalp sampling.  Am J Obstet Gynecol. 1984;  148 274-277
  • 6 Lin C C, Schulman H, Saldana L R. Deceleration/contraction ratios as an index of fetal health during labor.  Obstet Gynecol. 1978;  51 666-670
  • 7 National Institute of Child Health and Human Development Research Planning Workshop . Electronic fetal heart rate monitoring: research guidelines for interpretation.  Am J Obstet Gynecol. 1997;  177 1385-1390
  • 8 Sameshima H, Ikenooue T, Ikeda T, Kamitomo M, Ibara S. Unselected low-risk pregnancies and the effect of continuous intrapartum fetal heart rate monitoring on umbilical blood gases and cerebral palsy.  Am J Obstet Gynecol. 2004;  190 118-123

Hiroshi SameshimaM.D. 

Department of Obstetrics and Gynecology, Miyazaki Medical College, University of Miyazaki

5200 Kihara, Kiyotake

Miyazaki 892-1692, Japan