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孕 30 至 34 周时使用硫酸镁:神经保护试验(MAGENTA)--研究方案。

Magnesium sulphate at 30 to 34 weeks' gestational age: neuroprotection trial (MAGENTA)--study protocol.

机构信息

Australian Research Centre for Health of Women and Babies (ARCH), The Robinson Institute, The University of Adelaide, Adelaide, Australia.

出版信息

BMC Pregnancy Childbirth. 2013 Apr 9;13:91. doi: 10.1186/1471-2393-13-91.

Abstract

BACKGROUND

Magnesium sulphate is currently recommended for neuroprotection of preterm infants for women at risk of preterm birth at less than 30 weeks' gestation, based on high quality evidence of benefit. However there remains uncertainty as to whether these benefits apply at higher gestational ages.The aim of this randomised controlled trial is to assess whether giving magnesium sulphate compared with placebo to women immediately prior to preterm birth between 30 and 34 weeks' gestation reduces the risk of death or cerebral palsy in their children at two years' corrected age.

DESIGN

Randomised, multicentre, placebo controlled trial.

INCLUSION CRITERIA

Women, giving informed consent, at risk of preterm birth between 30 to 34 weeks' gestation, where birth is planned or definitely expected within 24 hours, with a singleton or twin pregnancy and no contraindications to the use of magnesium sulphate.Trial entry & randomisation: Eligible women will be randomly allocated to receive either magnesium sulphate or placebo.Treatment groups: Women in the magnesium sulphate group will be administered 50 ml of a 100 ml infusion bag containing 8 g magnesium sulphate heptahydrate [16 mmol magnesium ions]. Women in the placebo group will be administered 50 ml of a 100 ml infusion bag containing isotonic sodium chloride solution (0.9%). Both treatments will be administered through a dedicated IV infusion line over 30 minutes.Primary study outcome: Death or cerebral palsy measured in children at two years' corrected age.

SAMPLE SIZE

1676 children are required to detect a decrease in the combined outcome of death or cerebral palsy, from 9.6% with placebo to 5.4% with magnesium sulphate (two-sided alpha 0.05, 80% power, 5% loss to follow up, design effect 1.2).

DISCUSSION

Given the magnitude of the protective effect in the systematic review, the ongoing uncertainty about benefits at later gestational ages, the serious health and cost consequences of cerebral palsy for the child, family and society, a trial of magnesium sulphate for women at risk of preterm birth between 30 to 34 weeks' gestation is both important and relevant for clinical practice globally.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry - ACTRN12611000491965.

摘要

背景

基于高质量证据表明镁剂对早产儿有神经保护作用,目前建议对有早产风险(妊娠 30 周前)的孕妇使用硫酸镁治疗。但是否对妊娠 34 周前的孕妇有获益仍然存在不确定性。本随机对照试验旨在评估对妊娠 30-34 周前即将早产的孕妇使用硫酸镁与安慰剂治疗,是否能降低其子女校正年龄 2 岁时的死亡或脑瘫风险。

设计

随机、多中心、安慰剂对照试验。

纳入标准

有早产风险的孕妇,签署知情同意书,妊娠 30-34 周,预计在 24 小时内分娩,单胎或双胎妊娠,无硫酸镁使用禁忌。试验纳入和随机化:符合条件的孕妇随机分配至硫酸镁组或安慰剂组。治疗组:硫酸镁组孕妇给予 50ml 含 8g 七水硫酸镁(16mmol 镁离子)的 100ml 输注袋;安慰剂组孕妇给予 50ml 含等渗氯化钠溶液(0.9%)的 100ml 输注袋。两种治疗方法均通过专用静脉输注管输注 30 分钟。主要研究结局:校正年龄 2 岁时的死亡或脑瘫。

样本量

需要 1676 名儿童才能检测出硫酸镁治疗组与安慰剂组的联合结局(死亡或脑瘫)发生率的降低,从安慰剂组的 9.6%降至硫酸镁组的 5.4%(双侧 α 0.05,80%功效,5%失访率,设计效应 1.2)。

讨论

鉴于系统评价中保护作用的程度、对更晚孕龄时获益的不确定性、脑瘫对儿童、家庭和社会的严重健康和经济后果,对于妊娠 30-34 周前有早产风险的孕妇使用硫酸镁进行试验,无论对于全球临床实践还是对于全球的社会和经济,都是重要且相关的。

试验注册

澳大利亚新西兰临床试验注册中心-ACTRN12611000491965。

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