AI Article Synopsis

  • The study analyzed insulin use in critically ill infants with stress-induced hyperglycemia, involving 302 patients in pediatric intensive care units.
  • Insulin therapy was compared to conventional treatment and a control group, focusing on outcomes like PICU stay length, organ dysfunction, and mortality rates.
  • Findings showed that insulin therapy had no significant benefits on these outcomes, and blood glucose levels normalized without insulin, without increased risk of complications.

Article Abstract

The aim of the present study was to examine the benefits of insulin use and non-use in critically ill infants with stress-induced hyperglycemia. The present retrospective study used clinical data from 302 critically ill infants with stress hyperglycemia admitted to pediatric intensive care units (PICUs). The patients were recruited randomly and divided into three groups: The tight glycemic control, conventional insulin therapy and control groups. Correlations between insulin therapy and improved clinical outcomes were assessed according to key parameters (length of PICU stay, total length of stay, occurrence of organ dysfunction and mortality). Correlations between blood glucose level and these parameters in the three groups were also examined. Blood glucose levels following insulin therapy were not correlated with the length of PICU stay, total length of stay, mortality, secondary coma, or secondary hepatic or renal dysfunction in the three groups. At 96 h following PICU admission, blood glucose levels were statistically similar (5.0±1.2, 4.9±1.3 and 5.1±0.9 mmol/l, respectively; P>0.05). Insulin therapy was revealed to have no benefit on the length of hospitalization, the occurrence of organ dysfunction or mortality in critically ill pediatric patients with stress hyperglycemia. Even with no insulin use, the blood glucose level could spontaneously return to normal, with no associated risk of organ dysfunction or fatality.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566070PMC
http://dx.doi.org/10.3892/etm.2019.7537DOI Listing

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