| BMC Pediatrics | |
| Randomised trial of neonatal hypoglycaemia prevention with oral dextrose gel (hPOD): study protocol | |
| Jane M Alsweiler3  Greg Gamble1  Richard Edlin1  Caroline A Crowther1  Joanne E Hegarty2  Jane E Harding1  | |
| [1] Liggins Institute, University of Auckland, Auckland, New Zealand;Newborn Services, Auckland City Hospital, Auckland, New Zealand;Department of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand | |
| 关键词: Randomised controlled trial; Neonate; Oral dextrose gel; Hypoglycaemia; | |
| Others : 1225227 DOI : 10.1186/s12887-015-0440-6 |
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| received in 2015-02-08, accepted in 2015-09-01, 发布年份 2015 | |
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【 摘 要 】
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.
【 授权许可】
2015 Harding et al.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150919020943516.pdf | 385KB |
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