Title: A randomised controlled trial of early insulin therapy in very low birth weight infants, "NIRTURE" (neonatal insulin replacement therapy in Europe)
Authors: Beardsall, Kathryn
Vanhaesebrouck, Sophie
Ogilvy-Stuart, Amanda L
Ahluwalia, Jagit
Vanhole, Christine
Palmer, Chris
Midgley, Paula
Thompson, Michael
Cornette, Luc
VanWeissenbruch, Mirjam
Thio, Marta
de Zegher, Francis
Dunger, David B
Issue Date: 10-Aug-2007
Citation: BMC Pediatrics 2007, 7:29
Abstract: Abstract Background Studies in adult intensive care have highlighted the importance of insulin and improved glucose control on survival, with 32% reduction in mortality, 22% reduction in intensive care stay and halving of the incidence of bacteraemia. Very low birth weight infants requiring intensive care also have relative insulin deficiency often leading to hyperglycaemia during the first week of life. The physiological influences on insulin secretion and sensitivity, and the potential importance of glucose control at this time are not well established. However there is increasing evidence that the early postnatal period is critical for pancreatic development. At this time a complex set of signals appears to influence pancreatic development and β cell survival. This has implications both in terms of acute glucose control but also relative insulin deficiency is likely to play a role in poor postnatal growth, which has been associated with later motor and cognitive impairment, and fewer β cells are linked to risk of type 2 diabetes later in life. Methods A multi-centre, randomised controlled trial of early insulin replacement in very low birth weight babies (VLBW, birth weight < 1500 g). 500 infants will be recruited from 10 centres in the UK and Europe. Babies will be randomised to receive a continuous insulin infusion (0.05 units/kg/h) or to receive standard neonatal care from the first day of life and for the next 7 days. If blood glucose (BG) levels fall infants will receive 20% dextrose titrated to maintain normoglycaemia (4–8 mmol/l). If BG is consistently above 10 mmol/l babies will receive standard treatment with additional insulin infusion. The primary end point will be mortality on or before expected date of delivery, secondary end points will be markers of morbidity and include episodes of sepsis, severity of retinopathy, chronic lung disease and growth. Trial Registration Current Controlled Trials ISRCTN78428828. EUDRACT Number 2004-002170-34
URI: http://www.dspace.cam.ac.uk/handle/1810/237667
http://dx.doi.org/10.1186/1471-2431-7-29
Appears in Collections:Scholarly works - Paediatrics

Files in This Item:

File Description SizeFormat
1471-2431-7-29.xml101.81 kBXMLView/Open
1471-2431-7-29.pdf337.73 kBAdobe PDFThumbnail
View/Open
Additional resources for this item
search for alternative versions in eresources@cambridge
retrieve citation metadata in EndNote format

This item has been accessed 240 times.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.