Electrocortical Activity at 7 Days of Life is Affected in Extremely Premature Infants with Patent Ductus Arteriosus

N Bruns1, B Metze2, C Bührer2

  • 1Department of Pediatrics I, University Hospital Essen, Essen, Germany.

Klinische Padiatrie
|April 16, 2015
PubMed

Insights

A patent ductus arteriosus (PDA) negatively impacts the brain activity scores of extremely preterm infants at seven days old. These findings suggest reduced cerebral perfusion due to PDA may cause electrocortical disturbances.

Area of Science:

  • Neonatal neurology
  • Neurophysiology
  • Perinatal medicine

Background:

  • Extremely low gestational age preterm infants (<28 weeks) are at high risk for neurological complications.
  • A patent ductus arteriosus (PDA) is common in this population and may affect cerebral hemodynamics.
  • Assessing brain activity using amplitude-integrated electroencephalography (aEEG) can identify neurological dysfunction.

Purpose of the Study:

  • To investigate the influence of PDA on aEEG in non-sedated preterm infants at 7 days of life.
  • To determine the relationship between gestational age (GA), PDA, and aEEG parameters.

Main Methods:

  • Prospective cohort study of infants born <28 weeks gestation.
  • aEEG recordings at 7 days of life, assessed using Burdjalov score and electronically assessed lower border (eLBA).
  • Statistical analysis included Kruskal-Wallis test and linear regression to evaluate GA and PDA effects.

Main Results:

  • 44 infants were recruited (GA 26.5 weeks).
  • Higher GA correlated with higher aEEG scores and improved continuity.
  • Infants with a PDA had lower total Burdjalov scores and reduced continuity compared to those without a PDA.

Conclusions:

  • PDA negatively affects the total Burdjalov score and continuity of brain activity at 7 days in extremely preterm infants.
  • These electrocortical disturbances may result from diminished cerebral perfusion associated with PDA.
  • aEEG is a valuable tool for monitoring neurological status in preterm infants with PDA.
Abstract