首页> 外文期刊>British Medical Journal >Randomised, double blind, placebo controlled clinical trial of efficacy of vitamin A treatment in non-measles childhood pneumonia
【24h】

Randomised, double blind, placebo controlled clinical trial of efficacy of vitamin A treatment in non-measles childhood pneumonia

机译:维生素A治疗非麻疹性儿童肺炎疗效的随机,双盲,安慰剂对照临床试验

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: To evaluate the impact on clinical recovery and severity of the addition of large doses of vitamin A to the standard treatment for childhood pneumonia. Design: A randomised, double blind, placebo controlled trial. Setting: Study children were recruited at a public hospital in Recife, north east Brazil, an area of marginal vitamin A deficiency. Subjects: 472 children aged 6 to 59 months with clinical diagnosis of pneumonia. Interventions: 200 000 IU (infants) or 400 000 IU (1-4 year olds) of vitamin A in oil or similar capsules of placebo divided into two daily oral doses, in addition to the standard treatment Main outcome measures: Duration of the episode and incidence of adverse outcomes. Results: The groups were similar with respect to overall duration of pneumonia and incidence of adverse outcomes. Children who received vitamin A, however, were less likely to have fever by day 3 (P = 0.008) and were 29% less likely to fail to respond to the first line antibiotic (P = 0.054). Conclusion: There was little evidence for an effect of vitamin A treatment on the immediate outcome of the pneumonia episode.
机译:目的:评估在儿童肺炎标准治疗中添加大剂量维生素A对临床恢复和严重程度的影响。设计:一项随机,双盲,安慰剂对照试验。地点:研究儿童是在巴西东北部累西腓的一家公共医院招募的,该地区边缘维生素A缺乏。受试者:472名6到59个月大的临床诊断为肺炎的儿童。干预措施:除标准治疗外,将油或类似安慰剂胶囊中的维生素A溶于200,000 IU(婴儿)或400,000 IU(1-4岁),分为每日两次口服剂量,主要疗效指标:发作持续时间和不良后果的发生率。结果:各组在总体肺炎持续时间和不良结局发生率方面相似。然而,接受维生素A的儿童在第3天发烧的可能性较小(P = 0.008),对一线抗生素无效的可能性要低29%(P = 0.054)。结论:几乎没有证据表明维生素A治疗可对肺炎发作的直接结果产生影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号