Enduring disturbances in regional cerebral blood flow and brain oxygenation at 24 h after asphyxial cardiac arrest in

Lesley M Foley1, Robert S B Clark2,3,4, Alberto L Vazquez1,5

  • 1Animal Imaging Center, University of Pittsburgh, Pittsburgh, Pennsylvania.

Pediatric Research
|September 17, 2016
PubMed

Insights

Persistent disturbances in cerebral blood flow (CBF) and brain oxygenation (PbO2) occur 24 hours after pediatric cardiac arrest (CA). These findings suggest a need for clinical monitoring of CBF and PbO2 in pediatric CA survivors.

Area of Science:

  • Neuroscience
  • Cardiovascular Science
  • Pediatric Critical Care

Background:

  • Cerebral blood flow (CBF) and brain oxygenation (PbO2) disturbances are early complications of pediatric cardiac arrest (CA).
  • Previous studies in a CA model showed that CBF-targeted therapies improve neurological outcomes.
  • The therapeutic window for interventions targeting CBF and PbO2 requires further investigation.

Purpose of the Study:

  • To determine if disturbances in CBF and PbO2 persist 24 hours after experimental pediatric CA.
  • To assess the potential therapeutic window for CBF- and PbO2-targeted therapies in pediatric CA survivors.

Main Methods:

  • Regional CBF and PbO2 were measured 24 hours post-asphyxial CA in immature rats.
  • Arterial spin label MRI was used to measure CBF.
  • Tissue electrodes were employed to measure PbO2.

Main Results:

  • Cerebral blood flow (CBF) returned to sham levels in most brain regions by 24 hours, except for the thalamus, which showed a >32% increase in CBF post-CA.
  • Brain oxygenation (PbO2) levels in the cortex and thalamus were comparable to sham values in rats receiving supplemental oxygen.
  • In rats breathing room air, cortical PbO2 was significantly lower 24 hours after CA compared to sham controls.

Conclusions:

  • Sustained increases in thalamic CBF and decreased cortical PbO2 (hypoxia) persist 24 hours post-CA in rats not receiving supplemental oxygen.
  • These enduring physiological disturbances highlight the need for clinical correlation and monitoring of CBF and PbO2 in pediatric CA patients.
  • The findings suggest that therapeutic interventions targeting CBF and PbO2 may be beneficial beyond the acute phase of pediatric CA.
Abstract

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