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低剂量肾上腺素雾化吸入治疗喘鸣的疗效:一项随机、安慰剂对照、双盲试验。

Efficacy of low-dose nebulized epinephrine as treatment for croup: A randomized, placebo-controlled, double-blind trial.

机构信息

Department of Emergency Medicine, Seoul National University Bundang Hospital, Gyeonggi, Republic of Korea; School of Medicine, Kangwon National University, Chuncheon, Gangwon-do, Republic of Korea.

Department of Emergency Medicine, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

Am J Emerg Med. 2019 Dec;37(12):2171-2176. doi: 10.1016/j.ajem.2019.03.012. Epub 2019 Mar 8.

Abstract

OBJECTIVE

Croup treatment usually involves a single dose of systemic dexamethasone combined with nebulized epinephrine. However, the optimal dose of l-epinephrine remains unclear. We examined whether a low dose (0.1 mg/kg) was inferior to the conventional dose (0.5 mg/kg) of 1:1000 nebulized l-epinephrine in patients with moderate to severe croup.

METHODS

This randomized double-blind clinical non-inferiority trial was conducted in three pediatric emergency departments from May 2015 to October 2017. Children 6 months to 5 years old with moderate to severe croup (Westley scale scores 3-11) were eligible. Subjects were randomly assigned to the conventional dose (0.5 mg/kg: maximum 5 mg) or low dose (0.1 mg/kg; maximum 1 mg) group. All subjects received 0.6 mg/kg dexamethasone. Croup scores and other vital signs were measured before and at 30, 60, 90, and 120 min after nebulized l-epinephrine administration. The primary outcome was the change in croup score after 30 min.

RESULTS

The final analysis included 84 patients. The groups did not differ significantly in terms of demographic parameters. At 30 min after treatment with nebulized l-epinephrine, the croup scores in both groups were significantly reduced from the baseline values (p < 0.05) and did not differ between the two groups (p = 0.42). Neither blood pressure nor heart rate differed between the two groups.

CONCLUSIONS

Low-dose 1:1000 l-epinephrine was not inferior in croup score reduction to the conventional dose in patients with moderate to severe croup. Clinical trial No: NCT01664507, KCT0002318.

摘要

目的

喉炎的治疗通常涉及单次全身给予地塞米松联合雾化肾上腺素。然而,1:1000 雾化 l-肾上腺素的最佳剂量仍不清楚。我们研究了低剂量(0.1mg/kg)是否劣于中重度喉炎患者的常规剂量(0.5mg/kg)。

方法

这是一项于 2015 年 5 月至 2017 年 10 月在三个儿科急诊室进行的随机、双盲、临床非劣效性试验。有中度至重度喉炎(Westley 评分 3-11 分)的 6 个月至 5 岁儿童符合入选条件。患者被随机分为常规剂量(0.5mg/kg:最大 5mg)或低剂量(0.1mg/kg;最大 1mg)组。所有患者均接受 0.6mg/kg 地塞米松。在雾化 l-肾上腺素前和雾化后 30、60、90 和 120 分钟测量喉炎评分和其他生命体征。主要结局为雾化后 30 分钟时喉炎评分的变化。

结果

最终分析包括 84 例患者。两组在人口统计学参数方面无显著差异。雾化 l-肾上腺素后 30 分钟时,两组的喉炎评分均较基线值显著降低(p<0.05),两组之间无差异(p=0.42)。两组的血压和心率均无差异。

结论

在中重度喉炎患者中,低剂量 1:1000 l-肾上腺素在降低喉炎评分方面并不劣于常规剂量。临床试验编号:NCT01664507,KCT0002318。

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