Division of Pediatric Emergency Medicine, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
J Pediatr. 2010 Oct;157(4):630-4, 634.e1. doi: 10.1016/j.jpeds.2010.04.074. Epub 2010 Jun 19.
To compare the efficacy and safety of 5%, 3%, and 0.9% saline solution for treating acute bronchiolitis in the prehospital setting.
This was a double-blind trial including consecutive infants aged <18 months treated in an urban urgent care setting. A total of 165 patients were randomized to receive nebulized 5%, 3%, or 0.9% (normal) saline with epinephrine every 4 hours. The primary efficacy outcome was bronchiolitis severity score improvement at 48 hours (chi2 analysis). Scores and oxygen saturation immediately before and after each treatment were recorded to assess safety.
A total of 187 previously healthy infants (median age, 3.1 months) diagnosed with bronchiolitis were enrolled. Positivity for respiratory syncytial virus was similar in the 3 treatment groups (mean, 56%). At 48 hours, the mean severity score for the 5% saline group was 3.69+/-1.09, and that for the 0.9% saline group was 4.12+/-1.11 (P=.04; difference, 0.43, 95% confidence interval for the difference, 0.02-0.88). The mean severity score for the 3% saline group was intermediate at 4.00+/-1.22. Revisit rates after discharge were similar in the 3 treatment groups. No adverse reactions or other safety concerns were identified.
Nebulization with 5% hypertonic saline is safe, can be widely generalizable, and may be superior to current treatment for early outpatient treatment of bronchiolitis.
比较 5%、3%和 0.9%盐水溶液在院前环境中治疗急性细支气管炎的疗效和安全性。
这是一项双盲试验,纳入了在城市急救环境中治疗的连续 18 个月以下的婴儿。共有 165 名患者随机接受雾化 5%、3%或 0.9%(生理盐水)加肾上腺素,每 4 小时一次。主要疗效结局是 48 小时时细支气管炎严重程度评分的改善(卡方分析)。在每次治疗前后记录评分和氧饱和度,以评估安全性。
共纳入了 187 名既往健康的患有细支气管炎的婴儿(中位数年龄为 3.1 个月)。3 种治疗组的呼吸道合胞病毒阳性率相似(平均为 56%)。48 小时时,5%盐水组的平均严重程度评分为 3.69+/-1.09,0.9%盐水组为 4.12+/-1.11(P=.04;差异为 0.43,95%置信区间的差值为 0.02-0.88)。3%盐水组的平均严重程度评分居中,为 4.00+/-1.22。出院后复诊率在 3 个治疗组中相似。未发现不良反应或其他安全问题。
雾化 5%高渗盐水安全、具有广泛的可推广性,并且可能优于目前治疗早期门诊治疗细支气管炎的方法。