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Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol

BACKGROUND: Neonatal hypoglycaemia is common, affecting up to 15 % of newborn babies and 50 % of those with risk factors (preterm, infant of a diabetic, high or low birthweight). Hypoglycaemia can cause brain damage and death, and babies born at risk have an increased risk of developmental delay in...

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Autores principales: Harding, Jane E, Hegarty, Joanne E, Crowther, Caroline A, Edlin, Richard, Gamble, Greg, Alsweiler, Jane M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572621/
https://www.ncbi.nlm.nih.gov/pubmed/26377909
http://dx.doi.org/10.1186/s12887-015-0440-6
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author Harding, Jane E
Hegarty, Joanne E
Crowther, Caroline A
Edlin, Richard
Gamble, Greg
Alsweiler, Jane M
author_facet Harding, Jane E
Hegarty, Joanne E
Crowther, Caroline A
Edlin, Richard
Gamble, Greg
Alsweiler, Jane M
author_sort Harding, Jane E
collection PubMed
description BACKGROUND: Neonatal hypoglycaemia is common, affecting up to 15 % of newborn babies and 50 % of those with risk factors (preterm, infant of a diabetic, high or low birthweight). Hypoglycaemia can cause brain damage and death, and babies born at risk have an increased risk of developmental delay in later life. Treatment of hypoglycaemia usually involves additional feeding, often with infant formula, and admission to Neonatal Intensive Care for intravenous dextrose. This can be costly and inhibit the establishment of breast feeding. Prevention of neonatal hypoglycaemia would be desirable, but there are currently no strategies, beyond early feeding, for prevention of neonatal hypoglycaemia. Buccal dextrose gel is safe and effective in treatment of hypoglycaemia. The aim of this trial is to determine whether 40 % dextrose gel given to babies at risk prevents neonatal hypoglycaemia and hence reduces admission to Neonatal Intensive Care. METHODS/DESIGN: Design: Randomised, multicentre, placebo controlled trial. Inclusion criteria: Babies at risk of hypoglycaemia (preterm, infant of a diabetic, small or large), less than 1 h old, with no apparent indication for Neonatal Intensive Care Unit admission and mother intends to breastfeed. Trial entry & randomisation: Eligible babies of consenting parents will be allocated by online randomisation to the dextrose gel group or placebo group, using a study number and corresponding trial intervention pack. Study groups: Babies will receive a single dose of 0.5 ml/kg study gel at 1 h after birth; either 40 % dextrose gel (200 mg/kg) or 2 % hydroxymethylcellulose placebo. Gel will be massaged into the buccal mucosal and followed by a breast feed. Primary study outcome: Admission to Neonatal Intensive Care. Sample size: 2,129 babies are required to detect a decrease in admission to Neonatal Intensive Care from 10–6 % (two-sided alpha 0.05, 90 % power, 5 % drop-out rate). DISCUSSION: This study will investigate whether admission to Neonatal Intensive Care can be prevented by prophylactic oral dextrose gel; a simple, cheap and painless intervention that requires no special expertise or equipment and hence is applicable in almost any birth setting. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry - ACTRN 12614001263684.
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spelling pubmed-45726212015-09-18 Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol Harding, Jane E Hegarty, Joanne E Crowther, Caroline A Edlin, Richard Gamble, Greg Alsweiler, Jane M BMC Pediatr Study Protocol BACKGROUND: Neonatal hypoglycaemia is common, affecting up to 15 % of newborn babies and 50 % of those with risk factors (preterm, infant of a diabetic, high or low birthweight). Hypoglycaemia can cause brain damage and death, and babies born at risk have an increased risk of developmental delay in later life. Treatment of hypoglycaemia usually involves additional feeding, often with infant formula, and admission to Neonatal Intensive Care for intravenous dextrose. This can be costly and inhibit the establishment of breast feeding. Prevention of neonatal hypoglycaemia would be desirable, but there are currently no strategies, beyond early feeding, for prevention of neonatal hypoglycaemia. Buccal dextrose gel is safe and effective in treatment of hypoglycaemia. The aim of this trial is to determine whether 40 % dextrose gel given to babies at risk prevents neonatal hypoglycaemia and hence reduces admission to Neonatal Intensive Care. METHODS/DESIGN: Design: Randomised, multicentre, placebo controlled trial. Inclusion criteria: Babies at risk of hypoglycaemia (preterm, infant of a diabetic, small or large), less than 1 h old, with no apparent indication for Neonatal Intensive Care Unit admission and mother intends to breastfeed. Trial entry & randomisation: Eligible babies of consenting parents will be allocated by online randomisation to the dextrose gel group or placebo group, using a study number and corresponding trial intervention pack. Study groups: Babies will receive a single dose of 0.5 ml/kg study gel at 1 h after birth; either 40 % dextrose gel (200 mg/kg) or 2 % hydroxymethylcellulose placebo. Gel will be massaged into the buccal mucosal and followed by a breast feed. Primary study outcome: Admission to Neonatal Intensive Care. Sample size: 2,129 babies are required to detect a decrease in admission to Neonatal Intensive Care from 10–6 % (two-sided alpha 0.05, 90 % power, 5 % drop-out rate). DISCUSSION: This study will investigate whether admission to Neonatal Intensive Care can be prevented by prophylactic oral dextrose gel; a simple, cheap and painless intervention that requires no special expertise or equipment and hence is applicable in almost any birth setting. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry - ACTRN 12614001263684. BioMed Central 2015-09-16 /pmc/articles/PMC4572621/ /pubmed/26377909 http://dx.doi.org/10.1186/s12887-015-0440-6 Text en © Harding et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Harding, Jane E
Hegarty, Joanne E
Crowther, Caroline A
Edlin, Richard
Gamble, Greg
Alsweiler, Jane M
Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title_full Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title_fullStr Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title_full_unstemmed Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title_short Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol
title_sort randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hpod): study protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572621/
https://www.ncbi.nlm.nih.gov/pubmed/26377909
http://dx.doi.org/10.1186/s12887-015-0440-6
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