Autonomic Dysfunction in Neonates with Hypoxic Ischemic Encephalopathy Undergoing Therapeutic Hypothermia Impairs

Heather Campbell1, Rathinaswamy B Govindan2, Srinivas Kota3

  • 1Pediatric Residency Program, Children's National Health System, Washington, DC.

Insights

Infants with impaired autonomic nervous systems (ANS) show abnormal physiological responses to routine care, indicating a risk for brain injury. Heart rate variability can identify these high-risk newborns for tailored neuroprotective strategies.

Area of Science:

  • Neonatal neurology
  • Autonomic nervous system function
  • Physiological monitoring

Background:

  • Hypoxic-ischemic encephalopathy (HIE) is a major cause of neonatal brain injury.
  • Autonomic dysfunction is common in HIE infants and may exacerbate brain injury.
  • Caregiving events can trigger physiological stress in vulnerable newborns.

Purpose of the Study:

  • To determine if infants with HIE and autonomic dysfunction exhibit aberrant physiological responses to care events.
  • To assess if these aberrant responses contribute to ongoing brain injury.
  • To explore the utility of heart rate variability (HRV) in identifying such infants.

Main Methods:

  • Continuous monitoring of heart rate (HR), blood pressure (BP), cerebral near-infrared spectroscopy (NIRS), and video electroencephalogram (EEG) in HIE infants treated with hypothermia.
  • Identification of 99 care events (stimulating and vagal) between 16-24 hours of age.
  • Stratification of infants into impaired vs. intact autonomic nervous system (ANS) groups based on pre-event HRV.

Main Results:

  • Infants with intact ANS showed expected HR/BP increases to stimuli, while impaired ANS infants had blunted responses.
  • Vagal stimuli caused HR decrease in intact ANS infants, but minimal change in impaired ANS infants.
  • Cerebral blood flow/volume increased in impaired ANS infants during diaper changes, unlike intact ANS infants.

Conclusions:

  • HRV metrics effectively identify HIE infants with impaired ANS function at risk for maladaptive responses to care.
  • These findings support HRV as a real-time biomarker for guiding neuroprotective care in high-risk newborns.
Abstract

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