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Updated: Aug 24, 2026

Improving IV Insulin Administration in a Community Hospital
Published on: June 11, 2012
Intravenous insulin decreases protein breakdown in infants on extracorporeal membrane oxygenation
Michael S D Agus1, Patrick J Javid, Daniel P Ryan
1Department of Medicine, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.
Insights
Infants on extracorporeal membrane oxygenation (ECMO) experience severe protein breakdown. Insulin therapy significantly reduced this protein degradation, offering a potential new treatment for critically ill infants.
Area of Science:
- Biochemistry
- Pediatric Critical Care
Background:
- Infants requiring extracorporeal membrane oxygenation (ECMO) exhibit extreme protein catabolism.
- Conventional nutritional support is often ineffective in managing this severe protein breakdown.
Purpose of the Study:
- To investigate the efficacy of the anabolic hormone insulin in reducing protein degradation in infants on ECMO.
Main Methods:
- A prospective, randomized, crossover trial involving four parenterally fed infants on ECMO.
- Utilized a 4-hour hyperinsulinemic euglycemic clamp followed by a saline control infusion.
- Quantified whole-body protein flux and breakdown using stable isotope L-[1-13C]leucine infusion.
Main Results:
- Insulin infusion increased serum insulin levels 15-fold compared to saline control.
- Insulin significantly decreased total leucine flux and leucine flux from protein breakdown.
- Insulin administration resulted in a 32% reduction in protein breakdown.
Conclusions:
- The anabolic hormone insulin effectively reduced protein breakdown in critically ill infants on ECMO.
- Intravenous insulin may offer significant benefits for metabolic management in critically ill infants, potentially improving outcomes.
Background/Purpose:
Infants requiring extracorporeal membrane oxygenation (ECMO) have the highest rates of protein catabolism ever reported. Recent investigations have found that such extreme protein breakdown is refractory to conventional nutritional management. In this pilot study, the authors sought to use the anabolic hormone insulin to reduce the profound protein degradation in this cohort.
Methods:
Four parenterally fed infants on ECMO were enrolled in a prospective, randomized, crossover trial. Subjects were administered an insulin infusion using a 4-hour hyperinsulinemic euglycemic clamp followed by a control saline infusion on consecutive days in random order. Whole-body protein flux and breakdown were quantified using a primed continuous infusion of the stable isotope L-[1-13C]leucine. Statistical analyses were performed using paired t tests.
Results:
Serum insulin levels were increased 15-fold during the insulin clamp compared with the saline control (407 +/- 103 v 26 +/- 12 microU/mL; P <.05). During the insulin infusion, infants had decreased rates of total leucine flux (214 +/- 25 v 298 +/- 38 micromol/kg/h; P <.05) and leucine flux derived from protein breakdown (156 +/- 40 v 227 +/- 54 micromol/kg/h; P <.05) when compared with saline control. Overall, insulin administration produced a 32% reduction in protein breakdown (P <.05).
Conclusions:
In this pilot study, the anabolic hormone insulin markedly reduced protein breakdown in critically ill infants on ECMO. Because elevated protein breakdown correlates with mortality and morbidity, the administration of intravenous insulin may ultimately have broad applicability to the metabolic management of critically ill infants.
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