Department of Pediatrics, Children's Hospital at Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
JAMA Pediatr. 2020 Mar 1;174(3):250-259. doi: 10.1001/jamapediatrics.2019.5195.
In therapeutic trials for acute viral bronchiolitis, consistent clinical improvement in groups that received nebulized normal saline (NS) as placebo raises the question of whether nebulized NS acts as a treatment rather than a placebo.
To measure the short-term association of nebulized NS with physiologic measures of respiratory status in children with bronchiolitis by analyzing the changes in these measures between the use of nebulized NS and the use of other placebos and the changes before and after nebulized NS treatment.
MEDLINE and Scopus were searched through March 2019, as were bibliographies of included studies and relevant systematic reviews, for randomized clinical trials evaluating nebulized therapies in bronchiolitis.
Randomized clinical trials comparing children 2 years or younger with bronchiolitis who were treated with nebulized NS were included. Studies enrolling a treatment group receiving an alternative placebo were included for comparison of NS with other placebos.
Data abstraction was performed per PRISMA guidelines. Fixed- and random-effects, variance-weighted meta-analytic models were used.
Pooled estimates of the association with respiratory scores, respiratory rates, and oxygen saturation within 60 minutes of treatment were generated for nebulized NS vs another placebo and for change before and after receiving nebulized NS.
A total of 29 studies including 1583 patients were included. Standardized mean differences in respiratory scores for nebulized NS vs other placebo (3 studies) favored nebulized NS by -0.9 points (95% CI, -1.2 to -0.6 points) at 60 minutes after treatment (P < .001). There were no differences in respiratory rate or oxygen saturation comparing nebulized NS with other placebo. The standardized mean difference in respiratory score (25 studies) after nebulized NS was -0.7 (95% CI, -0.7 to -0.6; I2 = 62%). The weighted mean difference in respiratory scores using a consistent scale (13 studies) after nebulized NS was -1.6 points (95% CI, -1.9 to -1.3 points; I2 = 72%). The weighted mean difference in respiratory rate (17 studies) after nebulized NS was -5.5 breaths per minute (95% CI, -6.3 to -4.6 breaths per minute; I2 = 24%). The weighted mean difference in oxygen saturation (23 studies) after nebulized NS was -0.4% (95% CI, -0.6% to -0.2%; I2 = 79%).
Nebulized NS may be an active treatment for acute viral bronchiolitis. Further evaluation should occur to establish whether it is a true placebo.
在急性病毒性细支气管炎的治疗试验中,接受雾化生理盐水(NS)作为安慰剂的组中一致的临床改善提出了一个问题,即雾化 NS 是否作为治疗而不是安慰剂起作用。
通过分析在使用雾化 NS 和其他安慰剂之间以及在使用雾化 NS 治疗前后这些测量值的变化,测量雾化 NS 对细支气管炎患儿呼吸状态的生理测量值的短期关联。
通过 MEDLINE 和 Scopus 检索了截至 2019 年 3 月的文献,还检索了纳入研究的参考文献和相关系统评价,以评估细支气管炎中雾化治疗的随机临床试验。
纳入了比较 2 岁或以下患有细支气管炎并接受雾化 NS 治疗的儿童的随机临床试验。纳入了比较接受替代安慰剂的治疗组的研究,以比较 NS 与其他安慰剂。
按照 PRISMA 指南进行数据提取。使用固定效应和随机效应、方差加权的荟萃分析模型。
生成了雾化 NS 与另一种安慰剂以及在接受雾化 NS 前后的呼吸评分、呼吸频率和氧饱和度的 60 分钟内的关联的汇总估计值。
共纳入了 29 项研究,包括 1583 名患者。雾化 NS 与其他安慰剂(3 项研究)的呼吸评分标准化均值差有利于雾化 NS,在治疗后 60 分钟时为 -0.9 分(95%CI,-1.2 至 -0.6 分)(P<0.001)。比较雾化 NS 与其他安慰剂时,呼吸率或氧饱和度没有差异。雾化 NS 后呼吸评分的标准化均值差(25 项研究)为 -0.7(95%CI,-0.7 至 -0.6;I2=62%)。使用一致量表(13 项研究)雾化 NS 后呼吸评分的加权平均差异为 -1.6 分(95%CI,-1.9 至 -1.3 分;I2=72%)。雾化 NS 后呼吸率的加权平均差异(17 项研究)为 -5.5 次/分钟(95%CI,-6.3 至 -4.6 次/分钟;I2=24%)。雾化 NS 后氧饱和度的加权平均差异(23 项研究)为 -0.4%(95%CI,-0.6%至 -0.2%;I2=79%)。
雾化 NS 可能是急性病毒性细支气管炎的一种有效治疗方法。应进一步评估以确定其是否为真正的安慰剂。