Navanandan Nidhya, Federico Monica, Mistry Rakesh D
Children's Hospital Colorado, University of Colorado School of Medicine, Section of Pediatric Emergency Medicine, Aurora, CO.
Children's Hospital Colorado, University of Colorado School of Medicine, Section of Pediatric Pulmonary Medicine, Aurora, CO.
J Pediatr. 2017 Jun;185:149-154.e2. doi: 10.1016/j.jpeds.2017.02.032. Epub 2017 Mar 8.
To evaluate the efficacy of brief, single administration of positive expiratory pressure (PEP) therapy in reducing clinical severity and need for additional second-line therapies and hospitalization in children presenting to the emergency department (ED) with acute asthma.
This was a prospective randomized controlled trial of children 2-18 years of age presenting to a tertiary-care academic pediatric ED with moderate-to-severe asthma exacerbations from December 2014 to June 2016. Children who continued to have moderate asthma severity after completion of initial therapies (albuterol/ipratropium bromide and corticosteroids) were randomized to receive PEP therapy or standard of care. The primary outcome was change in pulmonary asthma score before and after intervention, as assessed by a blinded physician. Secondary outcomes included need for additional therapies, ED length of stay, and disposition.
A total of 52 patients were randomized to receive either PEP (n?=?26) or standard therapy (n?=?26). Study groups were similar in demographics and baseline characteristics. There was no significant difference in primary outcome between groups with a mean change in Pulmonary Asthma Score of 0.92 (±1.2) in the PEP group and 0.40 (±1.2) in the standard group (P?=?.12). There also was no significant difference in need for additional therapies, ED length of stay, and disposition. Mild, self-resolving side effects were observed in 3 subjects receiving PEP therapy.
Single, brief, administration of PEP therapy after completion of first-line therapies does not improve clinical severity in children presenting to the ED with acute asthma.
ClinicalTrials.gov: NCT02494076.
评估在急诊科(ED)就诊的急性哮喘儿童中,短期单次给予呼气末正压(PEP)治疗在降低临床严重程度、减少额外二线治疗需求及住院需求方面的疗效。
这是一项前瞻性随机对照试验,研究对象为2014年12月至2016年6月在一家三级医疗学术儿科急诊科就诊的2至18岁中重度哮喘急性加重患儿。在完成初始治疗(沙丁胺醇/异丙托溴铵和皮质类固醇)后仍有中度哮喘严重程度的患儿被随机分为接受PEP治疗组或标准治疗组。主要结局是由一名盲法医生评估的干预前后肺哮喘评分的变化。次要结局包括额外治疗的需求、急诊科住院时间及出院处置。
共有52例患者被随机分为接受PEP治疗组(n = 26)或标准治疗组(n = 26)。研究组在人口统计学和基线特征方面相似。两组的主要结局无显著差异,PEP组的肺哮喘评分平均变化为0.92(±1.2),标准组为0.40(±1.2)(P = 0.12)。在额外治疗需求、急诊科住院时间及出院处置方面也无显著差异。3例接受PEP治疗的受试者出现了轻微的、可自行缓解的副作用。
在一线治疗完成后短期单次给予PEP治疗并不能改善在急诊科就诊的急性哮喘儿童的临床严重程度。
ClinicalTrials.gov:NCT02494076。