Incidence, Intrapartum Risk Factors, and Prognosis of Neonatal Hypoxic-Ischemic Encephalopathy Among Infants Born at 35 Weeks Gestation or More

J Obstet Gynaecol Can. 2020 Dec;42(12):1489-1497. doi: 10.1016/j.jogc.2020.04.020. Epub 2020 Jun 13.

Abstract

Introduction: Neonatal hypoxic-ischemic encephalopathy (HIE) is associated with neonatal mortality, acute neurological injury, and long-term neurodevelopmental disabilities; however, the association between intrapartum factors and HIE remains unclear.

Methods: This population-based cohort study used linked obstetrical and newborn data derived from the Nova Scotia Atlee Perinatal Database (NSAPD, 1988-2015) and the AC Allen Perinatal Follow-Up Program Database (2006-2015) for all pregnancies with live, non-anomalous newborns ≥35 weeks gestation, not delivered by pre-labour cesarean section. Temporal trends in HIE incidence were described, and logistic regression estimated odds ratios (OR) with 95% confidence intervals (CI) for the association of intrapartum factors with HIE.

Results: The NSAPD identified 227 HIE cases in the population of 226 711 deliveries from 1988 to 2015. Women with clinical chorioamnionitis in labour (OR 8.0; 95% CI 3.9-16), emergency cesarean delivery (OR 10; 95% CI 7.6-14), shoulder dystocia (OR 3.5; 95% CI 2.1-5.7), placental abruption (OR 18; 95% CI 11-29), and cord prolapse (OR 30; 95% CI 15-61) were more likely to have newborns with HIE. Two-thirds of newborns with HIE had an abnormal intrapartum fetal heart rate tracing. The mortality rate among infants with HIE was 27% by 3 years of age. Neurodevelopmental outcomes in the surviving infants were normal in 43% and showed severe developmental delay in 40%.

Conclusion: Overall, the rate of HIE was low in infants born at ≥35 weeks gestation. The identification of associated intrapartum factors should promote increased surveillance in these clinical situations and emphasize the importance of careful management to optimize newborn outcomes.

Keywords: hypoxic-ischemic encephalopathy; parturition; perinatal death; pregnancy outcome.

MeSH terms

  • Cesarean Section
  • Cohort Studies
  • Female
  • Humans
  • Hypoxia-Ischemia, Brain / epidemiology*
  • Hypoxia-Ischemia, Brain / etiology*
  • Incidence
  • Infant
  • Infant, Newborn
  • Nova Scotia / epidemiology
  • Obstetric Labor Complications
  • Perinatal Death*
  • Pregnancy
  • Pregnancy Outcome / epidemiology
  • Prognosis
  • Risk Factors