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Archives of Disease in Childhood - Fetal and Neonatal Edition 2003;88:F308-F311; doi:10.1136/fn.88.4.F308
Copyright © 2003 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Archives of Disease in Childhood Fetal and Neonatal Edition 2003;88:F308
© 2003 Archives of Disease in Childhood Fetal and Neonatal Edition

ORIGINAL ARTICLE

Naloxone for narcotic exposed newborn infants: systematic review

W McGuire and P W Fowlie

Tayside Institute of Child Health, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, UK

Correspondence to:
Correspondence to:
Dr McGuire, Tayside Institute of Child Health, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, UK;
w.mcguire{at}dundee.ac.uk

Background: Naloxone, a specific opiate antagonist, is available for the treatment of newborn infants with respiratory depression that may be due to transplacentally acquired opiates.

Aims: To determine if this treatment has any clinically important benefits, and whether there are any harmful effects.

Methods: Randomised controlled trials that compared naloxone with placebo or no drug for newborn infants with transplacental exposure to narcotics were systematically reviewed. The Cochrane Controlled Trials Register (CCTR; 2002, Issue 3), Medline (1966 to June 2002), and Embase (1988 to June 2002) were searched. Data were extracted, analysed, and synthesised using the standard methods of the Cochrane Neonatal Collaborative Review Group.

Results: Nine trials were found that fulfilled the specified inclusion criteria. Although there was evidence that naloxone increased alveolar ventilation, no data were found on the specified primary outcomes of this review: the need for assisted ventilation or admission to a neonatal unit.

Conclusions: There is a need for a randomised controlled trial to determine if naloxone confers any clinically important benefits on newborn infants with respiratory depression that may be due to transplacentally acquired narcotic.

Keywords: naloxone; narcotic exposure; opiates


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