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Neurocognitive development of children 4 years after critical illness and treatment with tight glucose control: a
Dieter Mesotten1, Marijke Gielen, Caroline Sterken
1Department of Intensive Care Medicine, Catholic University of Leuven, Leuven, Belgium.
Insights
Tight glucose control (TGC) in pediatric intensive care did not harm long-term neurodevelopment. This approach, while increasing hypoglycemia, showed no adverse effects on intelligence or overall outcomes in children.
Area of Science:
- Pediatric Intensive Care Medicine
- Neurodevelopmental Outcomes
- Glucose Management
Background:
- Tight glucose control (TGC) in pediatric intensive care reduced morbidity and mortality but increased hypoglycemia.
- Concerns existed regarding potential adverse effects of both hyperglycemia and hypoglycemia on developing brains.
Purpose of the Study:
- To assess long-term neurodevelopmental outcomes in children treated with TGC in the ICU.
- To validate the short-term benefits of TGC and exclude potential harm.
Main Methods:
- A prospective, randomized controlled trial involving 700 pediatric ICU patients.
- Long-term follow-up at 3 years, assessing intelligence (IQ), visual-motor integration, attention, motor coordination, executive functions, memory, and behavior.
- Comparison with healthy siblings and unrelated children.
Main Results:
- TGC did not affect full-scale IQ scores or increase the incidence of poor outcomes (death or severe disability).
- No differences were observed in intelligence, visual-motor integration, or memory between TGC and usual care (UC) groups.
- TGC significantly improved motor coordination and cognitive flexibility.
Conclusions:
- Children treated with TGC in the ICU did not exhibit worse intelligence measures at follow-up compared to those receiving UC.
- Brief hypoglycemia induced by TGC was not associated with adverse neurocognitive outcomes.
Context:
A large randomized controlled trial revealed that tight glucose control (TGC) to age-adjusted normoglycemia (50-80 mg/dL at age <1 year and 70-100 mg/dL at age 1-16 years) reduced intensive care morbidity and mortality compared with usual care (UC), but increased hypoglycemia (≤40 mg/dL) (25% vs 1%).
Objective:
As both hyperglycemia and hypoglycemia may adversely affect the developing brain, long-term follow-up was required to exclude harm and validate short-term benefits of TGC.
Design, Setting, And Patients:
A prospective, randomized controlled trial of 700 patients aged 16 years or younger who were admitted to the pediatric intensive care unit (ICU) of the University Hospitals in Leuven, Belgium, between October 2004 and December 2007. Follow-up was scheduled after 3 years with infants assessed at 4 years old between August 2008 and January 2012. Assessment was performed blinded for treatment allocation, in-hospital (83%) or at home/school (17%). For comparison, 216 healthy siblings and unrelated children were tested.
Main Outcome Measures:
Intelligence (full-scale intelligence quotient [IQ]), as assessed with age-adjusted tests (Wechsler IQ scales). Further neurodevelopmental testing encompassed tests for visual-motor integration (Beery-Buktenica Developmental Test of Visual-Motor Integration); attention, motor coordination, and executive functions (Amsterdam Neuropsychological Tasks); memory (Children's Memory Scale); and behavior (Child Behavior Checklist).
Results:
Sixteen percent of patients declined participation or could not be reached (n = 113), resulting in 569 patients being alive and testable at follow-up. At a median (interquartile range [IQR]) of 3.9 (3.8-4.1) years after randomization, TGC in the ICU did not affect full-scale IQ score (median [IQR], 88.0 [74.0-100.0] vs 88.5 [74.3-99.0] for UC; P = .73) and had not increased incidence of poor outcomes (death or severe disability precluding neurocognitive testing: 19% [68/349] vs 18% [63/351] with UC; risk-adjusted odds ratio, 0.93; 95% CI, 0.60-1.46; P = .72). Other scores for intelligence, visual-motor integration, and memory also did not differ between groups. Tight glucose control improved motor coordination (9% [95% CI, 0%-18%] to 20% [95% CI, 5%-35%] better, all P ≤ .03) and cognitive flexibility (19% [95% CI, 5%-33%] better, P = .02). Brief hypoglycemia evoked by TGC was not associated with worse neurocognitive outcome.
Conclusion:
At follow-up, children who had been treated with TGC during an ICU admission did not have a worse measure of intelligence than those who had received UC.
Trial Registration:
clinicaltrials.gov Identifier NCT00214916.
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