Survivors with bad outcome after hypoxic-ischaemic encephalopathy: full-term neonates compare unfavourably with

J Pfenninger1, D Bachmann, B P Wagner

  • 1Paediatric Intensive Care Unit, University Children's Hospital, Inselspital, Bern, Switzerland.

Swiss Medical Weekly
|July 17, 2001
PubMed

Insights

Hypoxic-ischaemic encephalopathy (HIE) affects neonates and children, with similar overall outcomes. However, neonates had more survivors with poor outcomes, potentially due to developmental differences.

Area of Science:

  • Neonatal Intensive Care
  • Pediatric Intensive Care
  • Neurology

Background:

  • Hypoxic-ischaemic encephalopathy (HIE) is a critical condition in neonatal and pediatric intensive care, leading to significant mortality and long-term morbidity.
  • Understanding factors influencing outcomes in HIE is crucial for improving patient management.

Purpose of the Study:

  • To analyze outcomes in full-term neonates and children with HIE.
  • To specifically investigate the impact of life support withdrawal on patient outcomes.

Main Methods:

  • Retrospective analysis of HIE patients admitted between 1992-1996.
  • HIE severity assessed using Sarnat stages (neonates) and coma duration (children).
  • Outcomes evaluated using the Glasgow Outcome Scale; bad outcome defined as death or severe disability.

Main Results:

  • In neonates (n=38), Sarnat stage, convulsions, EEG, cardiovascular failure, and MOD were associated with bad outcomes (27 cases, 14 deaths).
  • In children (n=45), persistent coma, EEG, cardiovascular failure, liver dysfunction, and MOD predicted bad outcomes (36 cases, 33 deaths).
  • Life support withdrawal preceded death in 9/14 neonates and 15/15 children.

Conclusions:

  • Overall good and bad outcomes did not significantly differ between neonates and older children with HIE.
  • Neonatal HIE cases showed a higher proportion of survivors with bad outcomes, even after life support withdrawal.
  • Potential reasons for this difference include maturational and metabolic variations, and anatomical differences in the neonatal skull.
Abstract