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首页> 外文期刊>The journal of asthma >Comparison of a rapid albuterol pathway with a standard pathway for the treatment of children with a moderate to severe asthma exacerbation in the emergency department
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Comparison of a rapid albuterol pathway with a standard pathway for the treatment of children with a moderate to severe asthma exacerbation in the emergency department

机译:快速羟丙酚途径对急转院治疗中度至严重哮喘恶化的儿童的标准途径的比较

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Objective: The objective of this study was to determine if a rapid albuterol delivery pathway with a breath-enhanced nebulizer can reduce emergency department (ED) length of stay (LOS), while maintaining admission rates and side effects, when compared to a traditional asthma pathway with a standard jet nebulizer. Methods: Children aged 3-18 presenting to a large urban pediatric ED for asthma were enrolled if they were determined by pediatric asthma score to have a moderate to severe exacerbation. Subjects were randomized to either a standard treatment arm where they received up to 2 continuous albuterol nebulizations, or a rapid albuterol arm where they received up to 4 rapid albuterol treatments with a breath-enhanced nebulizer, depending on severity scoring. The primary endpoint was ED LOS from enrollment until disposition decision. Asthma scores, albuterol dose, side effects, and return visits were also recorded. Results: A total of 50 subjects were enrolled (25 in each arm). The study LOS was shorter in the rapid albuterol group (118 vs. 163 minutes, p = 0.0002). When total ED LOS was analyzed, the difference was no longer statistically significant (192 vs. 203 minutes, p = 0.65). There were no statistically significant differences with respect to admission rates, asthma score changes, side effects, or return visits. Conclusion: A rapid albuterol treatment pathway that utilizes a breath-enhanced nebulizer is an effective alternative to traditional pathways that utilize continuous nebulizations for children with moderate to severe asthma exacerbations in the ED.
机译:目的:本研究的目的是确定具有呼吸增强雾化器的快速羟丙酚递送途径是否可以减少急诊部(ED)的住宿时间(LOS),同时保持与传统哮喘相比的入学率和副作用。途径与标准喷射雾化器。方法:3-18岁的儿童提出给大型城市儿科的哮喘ED,如果他们被儿科哮喘评分确定,则纳入哮喘的患者,以具有中度至严重的加剧。受试者随机化为标准治疗臂,在那里它们最多可接受2连续的氨基甲醇雾化,或者快速的苯酚臂,其中它们接受高达4种快速的氨基甲醇治疗,其具有呼吸增强的雾化器,具体取决于严重程度评分。主要终点是入学直到处置决策的洛杉矶。还记录了哮喘评分,氨基甲酸剂量,副作用和返回访问。结果:注册了总共50个受试者(每只手臂25个)。 Happical Baluterol组的研究LOS较短(118 vs.163分钟,P = 0.0002)。当分析总ED LOS时,差异不再是统计学意义(192 Vs.203分钟,P = 0.65)。关于入学率没有统计学上显着的差异,哮喘评分变化,副作用或返回访问。结论:利用呼吸增强的雾化器的快速羟基醇治疗途径是对传统途径的有效替代方案,其利用患儿的持续雾化的传统途径,以中度至ED中的严重哮喘恶化。

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