Outcomes Associated With Multiple Organ Dysfunction Syndrome in Critically Ill Children With Hyperglycemia

Lauren E Marsillio1,2, Lisa A Asaro3, Vijay Srinivasan4,5

  • 1Division of Pediatric Critical Care Medicine, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.

Insights

Tight glycemic control did not alter multiple organ dysfunction syndrome (MODS) subgroups in critically ill children. However, new, progressive, or recurrent MODS significantly worsened clinical outcomes, highlighting distinct patient groups for future research.

Area of Science:

  • Pediatric critical care medicine
  • Endocrinology
  • Intensive care research

Background:

  • Multiple organ dysfunction syndrome (MODS) is a significant concern in critically ill children, but its patterns and outcomes in those with hyperglycemia remain unclear.
  • Understanding the impact of glycemic control on MODS development and resolution is crucial for optimizing treatment strategies in pediatric intensive care units (PICUs).

Purpose of the Study:

  • To investigate the influence of tight glycemic control (lower vs. higher glucose targets) on the timing, duration, and resolution of MODS in critically ill children with hyperglycemia.
  • To characterize the clinical outcomes associated with different subgroups of MODS in this patient population.

Main Methods:

  • A planned secondary analysis of the multicenter Heart And Lung Failure-Pediatric INsulin Titration (HHF-PINT) trial.
  • Critically ill children with hyperglycemia receiving the HHF-PINT protocol (2012-2016) were randomized to lower or higher glucose target groups.
  • MODS subgroups (never, without progression, new, progressive, recurrent) were identified and analyzed in relation to glycemic control and clinical outcomes, including ICU-free days.

Main Results:

  • No significant differences in MODS subgroups were observed between the lower and higher glucose target groups.
  • Patients experiencing new or progressive MODS had significantly fewer ICU-free days compared to those without MODS or MODS without progression.
  • Progressive MODS was associated with worse outcomes than new MODS, and recurrent MODS represented a high-risk group with fewer ICU-free days.

Conclusions:

  • Tight glycemic control within the tested ranges did not impact the proportion of new, progressive, or recurrent MODS in critically ill children with hyperglycemia.
  • New and progressive MODS are linked to poorer clinical outcomes, suggesting they may represent distinct entities with potentially modifiable risk factors.
  • Recurrent MODS identifies a newly characterized high-risk group requiring further investigation and attention in clinical practice and research.
Abstract

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