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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.
Objectives:
Patterns and outcomes of multiple organ dysfunction syndrome are unknown in critically ill children with hyperglycemia. We aimed to determine whether tight glycemic control to a lower vs. higher range influenced timing, duration, or resolution of multiple organ dysfunction syndrome as well as characterize the clinical outcomes of subgroups of multiple organ dysfunction syndrome in children enrolled in the Heart And Lung Failure-Pediatric INsulin Titration trial.
Design:
Planned secondary analysis of the multicenter Heart And Lung Failure-Pediatric INsulin Titration trial.
Setting:
Thirty-five PICUs.
Patients:
Critically ill children with hyperglycemia who received the Heart And Lung Failure-Pediatric INsulin Titration protocol from 2012 to 2016.
Interventions:
Randomization to a lower versus higher glucose target group.
Measurements And Main Results:
Of 698 patients analyzed, 48 (7%) never developed multiple organ dysfunction syndrome, 549 (79%) had multiple organ dysfunction syndrome without progression, 32 (5%) developed new multiple organ dysfunction syndrome, and 69 (10%) developed progressive multiple organ dysfunction syndrome. Of those whose multiple organ dysfunction syndrome resolved, 192 (34%) experienced recurrent multiple organ dysfunction syndrome. There were no significant differences in the proportion of multiple organ dysfunction syndrome subgroups between Heart And Lung Failure-Pediatric INsulin Titration glucose target groups. However, patients with new or progressive multiple organ dys function syndrome had fewer ICU-free days through day 28 than those without new or progressive multiple organ dysfunction syndrome, and progressive multiple organ dysfunction syndrome patients had fewer ICU-free days than those with new multiple organ dysfunction syndrome: median 25.1 days for never multiple organ dysfunction syndrome, 20.2 days for multiple organ dysfunction syndrome without progression, 18.6 days for new multiple organ dysfunction syndrome, and 0 days for progressive multiple organ dysfunction syndrome (all comparisons p < 0.001). Patients with recurrent multiple organ dysfunction syndrome experienced fewer ICU-free days than those without recurrence (median, 11.2 vs 22.8 d; p < 0.001).
Conclusions:
Tight glycemic control target range was not associated with differences in the proportion of new, progressive, or recurrent multiple organ dysfunction syndrome. New or progressive multiple organ dysfunction syndrome was associated with poor clinical outcomes, and progressive multiple organ dysfunction syndrome was associated with worse outcomes than new multiple organ dysfunction syndrome. In future studies, new multiple organ dysfunction syndrome and progressive multiple organ dysfunction syndrome may need to be considered separately, as they represent distinct subgroups with different, potentially modifiable risk factors. Patients with recurrent multiple organ dysfunction syndrome represent a newly characterized, high-risk group which warrants attention in future research.
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