Abstract
Objective:
The development and evaluation of a labor risk model consisting of a combination of antepartum risk factors and intrapartum fetal heart rate (FHR) characteristics that can reliably identify those infants at risk for adverse neonatal outcome in labor.
Study design:
A nested case–control study of term singleton deliveries at the nine hospitals between March 2007 and December 2009. Eligibility criteria included: gestational age ⩾37.0 weeks; singleton pregnancy; documented continuous FHR monitoring for ⩾2 h before delivery; assessment of FHR tracing at least every 20 min; and, available maternal and neonatal outcomes. Adverse neonatal outcome was defined as nonanomalous infants admitted to the newborn intensive care unit with either a 5 minute Apgar score <7 or an umbilical artery pH<7.1. Initial risk score was determined using data available at 1 h after admission. Patients with an initial risk score between 7 and 15 were considered high risk. Intrapartum risk scores were then created for these patients using FHR tracing data and labor characteristics.
Result:
A total of 51 244 patients were identified meeting study criteria. Of the antepartum variables evaluated (n=31), 10 were associated with an adverse outcome. The high-risk group made up 28% of the population and accounted for 59.8% of the adverse outcomes. Intrapartum characteristics were then evaluated in this high-risk group. Intrapartum evaluation identified the highest risk group with a C/S rate of 40% and adverse outcome rate of 11.3%.
Conclusion:
Incorporation of maternal and antepartum risk factors with FHR analysis can improve the ability to identify the fetus at risk in labor.
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Acknowledgements
This study was supported by grants funded by Deseret Foundation, Salt Lake City, UT, USA, grant 576.
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This study was presented at the 31st Annual Meeting of the Society for Maternal-Fetal Medicine, San Francisco, CA, USA, February 2011.
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Holmgren, C., Esplin, M., Jackson, M. et al. A risk stratification model to predict adverse neonatal outcome in labor. J Perinatol 33, 914–918 (2013). https://doi.org/10.1038/jp.2013.64
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DOI: https://doi.org/10.1038/jp.2013.64