Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/40730
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: The Magpie Trial follow up study: outcome after discharge from hospital for women and children recruited to a trial comparing magnesium sulphate with placebo for pre-eclampsia
Author: Magpie Trial Follow Up Study Management Group
Citation: BMC Pregnancy and Childbirth, 2004; 4:5
Publisher: BioMed Central
Issue Date: 2004
ISSN: 1471-2393
School/Discipline: School of Paediatrics and Reproductive Health : Obstetrics and Gynaecology
Contributor: Crowther, Caroline Anne
Abstract: BACKGROUND: The Magpie Trial compared magnesium sulphate with placebo for women with pre-eclampsia. 10,141 women were recruited, 8804 before delivery. Overall, 9024 children were included in the analysis of outcome at discharge from hospital. Magnesium sulphate more than halved the risk of eclampsia, and probably reduced the risk of maternal death. There did not appear to be any substantive harmful effects on the baby, in the short term. It is now important to assess whether these benefits persist, and to provide adequate reassurance about longer term safety. The main objective of the Magpie Trial Follow Up Study is to assess whether in utero exposure to magnesium sulphate has a clinically important effect on the child's chance of surviving without major neurosensory disability. Other objectives are to assess long term outcome for the mother, and to develop and assess appropriate strategies for following up large numbers of children in perinatal trials. STUDY DESIGN: Follow up is only feasible in selected centres. We therefore anticipate contacting 2800–3350 families, for 2435–2915 of whom the woman was randomised before delivery. A further 280–335 children would have been eligible for follow up if they had survived. The total sample size for the children is therefore 3080–3685, 2680–3210 of whom will have been born to women randomised before delivery. Families eligible for the follow up will be contacted, and surviving children screened using the Ages and Stages Questionnaires. Children who screen positive, and a sample of those who screen negative, will whenever possible have a paediatric and neurodevelopmental assessment. When women are contacted to ask how their child is, they will also be asked about their own health. The primary outcome is a composite measure of death or neurosensory disability for the child at 18 months. DISCUSSION: The Follow Up Study began in 2002, and now involves collaborators in 19 countries. Data collection will close at the end of 2003.
Description: Contributing member: Caroline Crowther is listed as a member of the Magpie Trial Follow Up Study Collaborative Group
Rights: © 2004 The Magpie Trial Follow Up Study Management Group and The Magpie Trial Follow Up Study Collaborative Group; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
DOI: 10.1186/1471-2393-4-5
Published version: http://www.biomedcentral.com/1471-2393/4/5
Appears in Collections:Obstetrics and Gynaecology publications

Files in This Item:
File SizeFormat 
hdl_40730.pdf248.75 kBAdobe PDFView/Open


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