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Evaluating the Placebo Status of Nebulized Normal Saline in Patients With Acute Viral Bronchiolitis A Systematic Review and Meta-analysis

机译:评估急性病毒性支气管炎患者雾化生理盐水的安慰剂状态,系统评价和荟萃分析

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摘要

Importance 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. Objective 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. Data Sources 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. Study Selection 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 Extraction and Synthesis Data abstraction was performed per PRISMA guidelines. Fixed- and random-effects, variance-weighted meta-analytic models were used. Main Outcomes and Measures 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. Results 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; I-2 = 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; I-2 = 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; I-2 = 24%). The weighted mean difference in oxygen saturation (23 studies) after nebulized NS was -0.4% (95% CI, -0.6% to -0.2%; I-2 = 79%). Conclusions and Relevance Nebulized NS may be an active treatment for acute viral bronchiolitis. Further evaluation should occur to establish whether it is a true placebo.
机译:作为安慰剂接受雾化的正常盐水(NS)的组的治疗性试验中的重要性,一致的临床改善,作为安慰剂的问题提出了雾化NS是否作为治疗而不是安慰剂的问题。目的通过分析使用雾化NS的使用与雾化NS治疗前后改变和雾化NS治疗前后改变,衡量与支气管炎儿童呼吸状况的呼吸状况的呼吸状况短期协会数据来源MEDLINE和SCOPUS于2019年3月搜索,与所包括的研究和相关系统评论的书目,随机临床试验评估了支气管炎中的雾化疗法的随机临床试验。包括研究选择,将儿童与雾化NS治疗的患儿童比较儿童的随机临床试验。注册接受替代安慰剂的治疗组的研究被包括与其他安慰剂的比较。每个PRISMA指南执行数据提取和合成数据抽象。固定和随机效应,使用方差加权元分析模型。对于呼吸评分,呼吸率和氧饱和度的主要结果和措施汇总估计在治疗的60分钟内,为雾化NS产生了另一种安慰剂和接受雾化Ns之前和之后的改变。结果共有29项研究,包括1583名患者。雾化NS的呼吸评分的标准化平均差异与其他安慰剂(3项研究)在处理后60分钟后用-0.9点(95%CI,-1.2至-0.6分)有利的雾化Ns(p <.001)。呼吸速率或氧饱和度没有差异与其他安慰剂的雾化NS比较。雾化Ns后呼吸评分(25研究)的标准化平均差异为-0.7(95%CI,-0.7至-0.6; I-2 = 62%)。雾化NS后使用一致规模(13项研究)的呼吸评分的加权平均差异为-1.6点(95%CI,-1.9至-1.3点; I-2 = 72%)。雾化Ns后呼吸速率(17项研究)的加权平均差异为-5.5呼吸每分钟(95%CI,每分钟-6.3至-4.6呼吸; I-2 = 24%)。雾化NS后的氧饱和度(23研究)的加权平均差异为-0.4%(95%CI,-0.6%至-0.2%; I-2 = 79%)。结论和相关性NS可能是急性病毒性支气管炎的活性处理。应该发生进一步的评估,以确定它是真正的安慰剂。

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  • 来源
    《JAMA pediatrics》 |2020年第3期|共10页
  • 作者单位

    Dartmouth Hitchcock Med Ctr Childrens Hosp Dept Pediat Lebanon NH 03766 USA;

    Bassett Med Ctr Res Inst Cooperstown NY USA;

    Johns Hopkins Med Sch Dept Pediat 1800 Orleans Ave Bloomberg 8470 Baltimore MD 21287 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
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