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Published on: June 11, 2012
Glucose control, organ failure, and mortality in pediatric intensive care
Michael Yung1, Barry Wilkins, Lynda Norton
1The Women's and Children's Hospital, Adelaide, South Australia.
Insights
Hyperglycemia is common in pediatric intensive care units (PICUs), affecting 89% of ventilated children and increasing the risk of organ failure and death. However, early hyperglycemia does not predict later organ dysfunction, and insulin use is rare.
Area of Science:
- Pediatric Critical Care Medicine
- Endocrinology
- Clinical Research
Background:
- Hyperglycemia is a frequent complication in critically ill children.
- Understanding its prevalence and impact in pediatric intensive care units (PICUs) is crucial for patient outcomes.
Purpose of the Study:
- To determine the prevalence of hyperglycemia in ventilated children.
- To assess the association between hyperglycemia and organ failure.
- To document glycemic control practices in Australasian PICUs.
Main Methods:
- Prospective inception cohort study conducted in nine specialist PICUs across Australia and New Zealand.
- Included 409 children ventilated for over 12 hours, excluding specific conditions.
- Collected blood glucose measurements, clinical data for PELOD scores, and insulin use for up to 14 days.
Main Results:
- 89% of patients experienced peak blood glucose levels > 6.1 mmol/L, with hyperglycemia identified in 13% of subjects.
- Hyperglycemia was independently associated with a higher Paediatric Logistic Organ Dysfunction (PELOD) score (≥10) and increased mortality.
- Early hyperglycemia (first 48 hours) showed associations with outcomes but not with later or worsening organ failure.
Conclusions:
- Hyperglycemia is prevalent, occurs early, and is linked to organ failure and death in PICU patients.
- Early hyperglycemia is not predictive of subsequent or escalating organ dysfunction.
- Insulin therapy is infrequently utilized in Australasian PICUs.
Objective:
In ventilated children, to determine the prevalence of hyperglycemia, establish whether it is associated with organ failure, and document glycemic control practices in Australasian pediatric intensive care units (PICUs).
Design:
Prospective inception cohort study.
Setting:
All nine specialist PICUs in Australia and New Zealand.
Patients:
Children ventilated > 12 hrs excluding those with diabetic ketoacidosis, on home ventilation, undergoing active cardiopulmonary resuscitation on admission, or with do-not-resuscitate orders.
Interventions:
None.
Measurements And Main Results:
All blood glucose measurements for up to 14 days, clinical and laboratory values needed to calculate Paediatric Logistic Organ Dysfunction (PELOD) scores, and insulin use were recorded in 409 patients. Fifty percent of glucose measurements were > 6.1 mmol/L, with 89% of patients having peak values > 6.1 mmol/L. The median time to peak blood glucose was 7 hrs. Hyperglycemia was defined by area under the glucose-time curve > 6.1 mmol/L above the sample median. Thirteen percent of hyperglycemic subjects died vs. 3% of nonhyperglycemic subjects. There was an independent association between hyperglycemia and a PELOD score > or = 10 (odds ratio 3.41, 95% confidence interval 1.91-6.10) and death (odds ratio 3.31, 95% confidence interval 1.26-7.7). Early hyperglycemia, defined using only glucose data in the first 48 hrs, was also associated with these outcomes but not with PELOD > or = 10 after day 2 or with worsening PELOD after day 1. Five percent of patients received insulin.
Conclusions:
Hyperglycemia is common in PICUs, occurs early, and is independently associated with organ failure and death. However, early hyperglycemia is not associated with later or worsening organ failure. Australasian PICUs seldom use insulin.
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