Phase synchronization in electroencephalographic recordings prognosticates outcome in paediatric coma

Vera Nenadovic1, Jose Luis Perez Velazquez2, James Saunders Hutchison3

  • 1Division of Neurology Sick Kids, Toronto, Ontario, Canada; Brain and Mental Health, Toronto, Ontario, Canada.

Plos One
|April 23, 2014
PubMed

Insights

Brain injury in children can be predicted by analyzing brain signal variability using electroencephalography (EEG). Lower EEG variability indicates a poorer patient outcome, aiding in early prognosis and intervention strategies.

Area of Science:

  • Neuroscience
  • Paediatric Critical Care
  • Biomedical Engineering

Background:

  • Brain injury is a leading cause of death and disability in children.
  • Accurate outcome prediction is crucial for timely interventions but lacks a clinical model.
  • Physiological signal variability, seen in heart rate, may apply to brain signals.

Purpose of the Study:

  • To investigate the correlation between brain signal variability and patient outcomes after paediatric brain injury.
  • To determine if electroencephalographic (EEG) phase synchrony variability can predict prognosis in children.

Main Methods:

  • Retrospective analysis of scalp EEGs from children (1 month–17 years) in coma (GCS <8) post-brain injury (2000-2010).
  • EEG phase synchrony evaluated using Hilbert transform; variability calculated.
  • Patient outcome assessed via Paediatric Performance Category Score (PCPC) at discharge, dichotomized to good (1-3) or poor (4-6).

Main Results:

  • Children with poor outcomes exhibited higher synchrony magnitude (R index) compared to those with good outcomes.
  • Poor outcome group showed lower spatial complexity of synchrony patterns.
  • Lower temporal variability of synchrony index values at 15 Hz was observed in children with poor outcomes.

Conclusions:

  • EEG phase synchrony variability is a potential biomarker for predicting outcomes in paediatric brain injury.
  • Reduced brain signal variability correlates with poorer prognosis after TBI, cardiac arrest, or stroke in children.
  • This finding may inform the development of novel clinical models for early risk stratification.