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Published on: June 11, 2012
Clinical benefits of tight glycaemic control: focus on the paediatric patient
Ingeborg van den Heuvel1, Dirk Vlasselaers
1Department of Anaesthesiology and Intensive Care Medicine, University Hospital Muenster, Albert-Schweitzer-Strasse 33, 48149, Muenster, Germany. vandenhe@uni-muenster.de
Insights
Tight glycaemic control (TGC) in critically ill children may reduce inflammation and infections but increases hypoglycemia risk. Further multicenter trials are needed to confirm benefits and determine optimal blood glucose targets.
Area of Science:
- Pediatric critical care medicine
- Endocrinology
- Clinical research
Background:
- Hyperglycemia and glucose variability are common in critically ill children, linked to poorer outcomes.
- The causal relationship between glucose control and outcomes requires investigation through randomized controlled trials (RCTs).
Purpose of the Study:
- To evaluate the efficacy of tight glycaemic control (TGC) using insulin infusion in critically ill children.
- To assess the impact of TGC on morbidity and mortality in this population.
Main Methods:
- The study references a single-center RCT that demonstrated the feasibility of TGC.
- This trial involved intensive insulin infusion to manage blood glucose levels.
Main Results:
- TGC led to reduced inflammation, fewer secondary infections, shorter intensive care stays, and decreased need for hemodynamic support.
- A significant increase in biochemical hypoglycemia was observed as a consequence of TGC.
Conclusions:
- While TGC shows promise in critically ill children, long-term effects on development and optimal glucose targets require further investigation.
- Multicenter prospective RCTs are essential before widespread implementation, with potential benefits from technological advancements in glucose monitoring.
Abstract:
Hyperglycaemia and glucose variability occur frequently during critical illness or after major surgery in children and are associated with worse outcome. Association does not necessarily imply causality however, and the question whether tight glycaemic control (TGC) with insulin infusion improves morbidity and mortality can only be answered by randomised controlled trials (RCTs). Currently, only one single-centre RCT exists, proving the concept of TGC in critically ill children. Attenuation of inflammation and reduction of secondary infections, decreased prolonged stay in intensive care and reduced dependency on haemodynamic support were accomplished, despite a substantial increased incidence of biochemical hypoglycaemia. Before universal implementation in paediatric intensive care both long-term effects on outcome and development and issues regarding optimal levels of blood glucose control need to be cleared in multicentre prospective RCTs. Technological improvement might be helpful in optimising blood glucose control.
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