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Original Article
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Volume 359:1873-1884 October 30, 2008 Number 18
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Early Insulin Therapy in Very-Low-Birth-Weight Infants
Kathryn Beardsall, M.R.C.P., Sophie Vanhaesebrouck, M.D., Amanda L. Ogilvy-Stuart, D.M., Christine Vanhole, Ph.D., Christopher R. Palmer, Ph.D., Mirjam van Weissenbruch, Ph.D., Paula Midgley, M.D., Michael Thompson, F.R.C.P., Marta Thio, M.D., Luc Cornette, M.D., Iviano Ossuetta, M.R.C.P., Isabel Iglesias, M.D., Claire Theyskens, M.D., Miranda de Jong, M.D., Jag S. Ahluwalia, F.R.C.P.C.H., Francis de Zegher, Ph.D., and David B. Dunger, M.D.

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ABSTRACT

Background Studies involving adults and children being treated in intensive care units indicate that insulin therapy and glucose control may influence survival. Hyperglycemia in very-low-birth-weight infants is also associated with morbidity and mortality. This international randomized, controlled trial aimed to determine whether early insulin replacement reduced hyperglycemia and affected outcomes in such neonates.

Methods In this multicenter trial, we assigned 195 infants to continuous infusion of insulin at a dose of 0.05 U per kilogram of body weight per hour with 20% dextrose support and 194 to standard neonatal care on days 1 to 7. The efficacy of glucose control was assessed by continuous glucose monitoring. The primary outcome was mortality at the expected date of delivery. The study was discontinued early because of concerns about futility with regard to the primary outcome and potential harm.

Results As compared with infants in the control group, infants in the early-insulin group had lower mean (±SD) glucose levels (6.2±1.4 vs. 6.7±2.2 mmol per liter [112±25 vs. 121±40 mg per deciliter], P=0.007). Fewer infants in the early-insulin group had hyperglycemia for more than 10% of the first week of life (21% vs. 33%, P=0.008). The early-insulin group had significantly more carbohydrate infused (51±13 vs. 43±10 kcal per kilogram per day, P<0.001) and less weight loss in the first week (standard-deviation score for change in weight, –0.55±0.52 vs. –0.70±0.47; P=0.006). More infants in the early-insulin group had episodes of hypoglycemia (defined as a blood glucose level of <2.6 mmol per liter [47 mg per deciliter] for >1 hour) (29% in the early-insulin group vs. 17% in the control group, P=0.005), and the increase in hypoglycemia was significant in infants with birth weights of more than 1 kg. There were no differences in the intention-to-treat analyses for the primary outcome (mortality at the expected date of delivery) and the secondary outcome (morbidity). In the intention-to-treat analysis, mortality at 28 days was higher in the early-insulin group than in the control group (P=0.04).

Conclusions Early insulin therapy offers little clinical benefit in very-low-birth-weight infants. It reduces hyperglycemia but may increase hypoglycemia (Current Controlled Trials number, ISRCTN78428828 [controlled-trials.com] .)


Source Information

From the University of Cambridge (K.B., C.R.P., D.B.D.), Cambridge University Hospitals National Health Service Foundation Trust (K.B., A.L.O.-S., J.S.A.), and the Centre for Applied Medical Statistics (C.R.P.), Cambridge; the Simpson Centre for Reproductive Health, Royal Infirmary of Edinburgh, Edinburgh (P.M.); Luton and Dunstable Hospital, Luton (M. Thompson, I.O.); and Leeds General Infirmary, Leeds (L.C.) — all in the United Kingdom; University of Leuven, Leuven (S.V., C.V., F.Z.), and Ziekenhuis Oost-Limburg, Genk (C.T.) — both in Belgium; VU University Medical Center, Amsterdam (M.W., M.J.); and Hospital Universitari Sant Joan de Déu, Barcelona (M. Thio, I.I.).

Address reprint requests to Dr. Dunger at the Department of Paediatrics, University of Cambridge, Box 116, Level 8, Addenbrooke's Hospital, Hills Rd., Cambridge CB2 0QQ, United Kingdom, or at dbd25{at}cam.ac.uk.

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Related Letters:

Insulin Therapy in Very-Low-Birth-Weight Infants
Van den Berghe G., Vlasselaers D., Vanhorebeek I., Fendler W. M., Mlynarski W. M., Beardsall K., de Zegher F., Dunger D. B., the NIRTURE Investigators , Kashyap S., Polin R. A.
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N Engl J Med 2009; 360:535-537, Jan 29, 2009. Correspondence

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