Insulin therapy in very-low-birth-weight infants.

To the Editor: Beardsall et al. (Oct. 30 issue)1 report the results of the Neonatal Insulin Replacement Therapy in Europe (NIRTURE) trial, which investigated the effects of a fixed-dose insulin (0.05 U per kilogram of body weight per hour) and glucose (20% dextrose) infusion as compared with usual care in very-low-birth-weight infants in the neonatal intensive care unit (ICU). Beardsall and colleagues, as well as Kashyap and Polin, in their accompanying editorial,2 interpret the negative results of this study as evidence against blood glucose control in premature babies. We do not agree with this interpretation. Pronounced hyperglycemia was present in the two study groups (average glucose level, 6.2 mmol per liter [112 mg per deciliter], despite insulin infusion, in the intervention group, and 6.7 mmol per liter [121 mg per deciliter] in the control group), as compared with the much lower normal (fasting) glucose levels in healthy newborns who are less than 4 weeks old (1.7 to 3.3 mmol per liter [31 to 59 mg per deciliter]) or in infants who are 4 weeks to 1 year old (2.2 to 5.0 mmol per liter [40 to 90 mg per deciliter]). Hence, the study intervention actually increased the glucose load and concomitant hyperinsulinemia in the presence of hyperglycemia, a combination that has been shown to be deleterious in patients as well as in animal models of critical illness.3-6 In contrast, achieving strict (ageadjusted) normoglycemia throughout an ICU stay, both in adults and in pediatric patients, has been shown to lower mortality in the ICU and to prevent severe infections and organ damage.3,5,6

[1]  P. Thureen Early aggressive nutrition in very preterm infants. , 2007, Nestle Nutrition workshop series. Paediatric programme.

[2]  T. Cole,et al.  Adverse neurodevelopmental outcome of moderate neonatal hypoglycaemia. , 1988, BMJ.

[3]  J. Magny,et al.  Both relative insulin resistance and defective islet beta-cell processing of proinsulin are responsible for transient hyperglycemia in extremely preterm infants. , 2004, Pediatrics.

[4]  Heather Van Duker,et al.  Alterations in glucose homeostasis in the pediatric intensive care unit: Hyperglycemia and glucose variability are associated with increased mortality and morbidity* , 2008, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

[5]  G. Van den Berghe,et al.  Survival benefits of intensive insulin therapy in critical illness: impact of maintaining normoglycemia versus glycemia-independent actions of insulin. , 2006, Diabetes.

[6]  Christopher R Palmer,et al.  Early insulin therapy in very-low-birth-weight infants. , 2008, The New England journal of medicine.

[7]  R. Polin,et al.  Insulin infusions in very-low-birth-weight infants. , 2008, The New England journal of medicine.

[8]  E. Parton,et al.  Glucose sensor evaluation of glycemic instability in pediatric type 1 diabetes mellitus. , 2003, Diabetes technology & therapeutics.

[9]  W. Hay Intravenous nutrition of the very preterm neonate. , 2005, Acta paediatrica (Oslo, Norway : 1992). Supplement.

[10]  M Schetz,et al.  Intensive insulin therapy in critically ill patients. , 2001, The New England journal of medicine.

[11]  K. Nicolaides,et al.  Blood glucose and oxygen tension levels in small-for-gestational-age fetuses. , 1989, American journal of obstetrics and gynecology.

[12]  A. Williams,et al.  Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. , 2000, Pediatrics.

[13]  C. Wolf‐peeters,et al.  Protection of hepatocyte mitochondrial ultrastructure and function by strict blood glucose control with insulin in critically ill patients , 2005, The Lancet.

[14]  J. Krinsley,et al.  Glycemic variability: A strong independent predictor of mortality in critically ill patients* , 2008, Critical care medicine.