McGuire W, Fowlie P W, Evans D J
Tayside Institute of Child Health, Ninewells Hospital and Medical School, Dundee, UK, DD1 9SY.
Cochrane Database Syst Rev. 2004;2004(1):CD003955. doi: 10.1002/14651858.CD003955.pub2.
Studies in animal models have suggested that naloxone, a specific opiate antagonist, may improve outcomes for newborn infants with perinatal asphyxia.
In newborn infants of greater than 34 weeks' gestation with suspected perinatal asphyxia: to assess the effects of naloxone versus placebo or no drug, and of single versus multiple doses of naloxone, on mortality, long term neurological problems, severity of hypoxic-ischaemic encephalopathy, and frequency of neonatal seizures.
We used the standard search strategy of the Cochrane Neonatal Review Group. This included searches of the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 3, 2003), MEDLINE (1966 - August 2003), EMBASE (1980 - August 2003), conference proceedings, and previous reviews.
Randomised or quasi-randomised controlled trials comparing naloxone versus placebo, or no drug, or another dose of naloxone, in newborn infants of greater than 34 weeks' gestation with suspected perinatal asphyxia.
We extracted data using the standard methods of the Cochrane Neonatal Review Group, with separate evaluation of trial quality and data extraction by two authors. The pre-specified outcomes for this review were: death before hospital discharge, severe neurodevelopmental disability, severity of hypoxic-ischaemic encephalopathy, and seizures in the neonatal period.
We identified only one eligible randomised controlled trial. This study compared the use of naloxone with placebo in newborn infants with an Apgar score of six or less at one minute after birth. There were not any data on the pre-specified outcomes for this review.
REVIEWER'S CONCLUSIONS: There are insufficient data available to evaluate the safety and effectiveness of the routine use of naloxone for newborn infants of greater than 34 weeks' gestation with suspected perinatal asphyxia. A further randomised controlled trial is needed to determine if naloxone benefits newborn infants with suspected perinatal asphyxia. Such a trial should assess clinically important outcomes such as mortality, and adverse short and long term neurological outcomes.
动物模型研究表明,纳洛酮(一种特定的阿片类拮抗剂)可能改善围产期窒息新生儿的预后。
在孕周大于34周且疑似围产期窒息的新生儿中:评估纳洛酮与安慰剂或不使用药物相比,以及单剂量与多剂量纳洛酮相比,对死亡率、长期神经问题、缺氧缺血性脑病严重程度和新生儿惊厥发生率的影响。
我们采用了Cochrane新生儿综述小组的标准检索策略。这包括检索Cochrane对照试验中央注册库(CENTRAL,《Cochrane图书馆》,2003年第3期)、MEDLINE(1966年 - 2003年8月)、EMBASE(1980年 - 2003年8月)、会议论文集以及以往的综述。
随机或半随机对照试验,比较纳洛酮与安慰剂、不使用药物或另一剂量纳洛酮,用于孕周大于34周且疑似围产期窒息的新生儿。
我们使用Cochrane新生儿综述小组的标准方法提取数据,由两位作者分别评估试验质量和提取数据。本综述预先设定的结局为:出院前死亡、严重神经发育残疾、缺氧缺血性脑病严重程度和新生儿期惊厥。
我们仅识别出一项符合条件的随机对照试验。该研究比较了纳洛酮与安慰剂在出生后1分钟阿氏评分≤6分的新生儿中的使用情况。对于本综述预先设定的结局没有任何数据。
现有数据不足以评估在孕周大于34周且疑似围产期窒息的新生儿中常规使用纳洛酮的安全性和有效性。需要进一步进行随机对照试验以确定纳洛酮是否对疑似围产期窒息的新生儿有益。这样的试验应评估如死亡率以及短期和长期不良神经结局等临床重要结局。