Suppr超能文献

单剂量口服地塞米松治疗轻度喉炎的随机试验。

A randomized trial of a single dose of oral dexamethasone for mild croup.

作者信息

Bjornson Candice L, Klassen Terry P, Williamson Janielee, Brant Rollin, Mitton Craig, Plint Amy, Bulloch Blake, Evered Lisa, Johnson David W

机构信息

Department of Pediatrics, University of Calgary, Calgary, Alta, Canada.

出版信息

N Engl J Med. 2004 Sep 23;351(13):1306-13. doi: 10.1056/NEJMoa033534.

Abstract

BACKGROUND

The benefits of dexamethasone treatment for moderate-to-severe croup are well established. However, most children with croup have mild symptoms, and it is unknown whether they would derive the same degree of benefit from dexamethasone treatment as children with more severe disease.

METHODS

We conducted a double-blind trial at four pediatric emergency departments in which 720 children with mild croup were randomly assigned to receive one oral dose of either dexamethasone (0.6 mg per kilogram of body weight) or placebo. The children had mild croup, as defined by a score of < or =2 on the croup scoring system of Westley et al. The primary outcome was a return to a medical care provider for croup within seven days after treatment. The secondary outcome was the presence of ongoing symptoms of croup on days 1, 2, and 3 after treatment. Other outcomes included economic costs, hours of sleep lost by the child, and stress on the part of the parent in relation to the child's illness.

RESULTS

Baseline clinical characteristics were similar in the two groups. Return to medical care was significantly lower in the dexamethasone group (7.3 percent vs. 15.3 percent, P<0.001). In the dexamethasone group, there was quicker resolution of croup symptoms (P=0.003), less lost sleep (P<0.001), and less stress on the part of the parent (P<0.001).

CONCLUSIONS

For children with mild croup, dexamethasone is an effective treatment that results in consistent and small but important clinical and economic benefits. Although the long-term effects of this treatment are not known, our data support the use of dexamethasone in most, if not all, children with croup.

摘要

背景

地塞米松治疗中重度哮吼的益处已得到充分证实。然而,大多数患哮吼的儿童症状较轻,尚不清楚他们是否能从地塞米松治疗中获得与病情较重的儿童相同程度的益处。

方法

我们在四个儿科急诊科进行了一项双盲试验,将720名轻度哮吼患儿随机分为两组,分别口服一剂地塞米松(0.6毫克/千克体重)或安慰剂。这些患儿符合Westley等人哮吼评分系统中评分为≤2分的轻度哮吼标准。主要结局是治疗后7天内因哮吼返回医疗机构就诊。次要结局是治疗后第1、2和3天哮吼持续症状的存在情况。其他结局包括经济成本、患儿睡眠缺失小时数以及家长因患儿疾病所承受的压力。

结果

两组的基线临床特征相似。地塞米松组返回医疗机构就诊的比例显著更低(7.3%对15.3%,P<0.001)。地塞米松组哮吼症状缓解更快(P=0.003),睡眠缺失更少(P<0.001),家长所承受的压力也更小(P<0.001)。

结论

对于轻度哮吼患儿,地塞米松是一种有效的治疗方法,能带来持续且虽小但重要的临床和经济效益。尽管这种治疗的长期效果尚不清楚,但我们的数据支持在大多数(即便不是全部)患哮吼的儿童中使用地塞米松。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验