减少沙丁胺醇雾化器溶液在急诊科治疗哮喘加重中的应用

IF 1.2 Q3 PEDIATRICS
Pediatric quality & safety Pub Date : 2025-05-22 eCollection Date: 2025-05-01 DOI:10.1097/pq9.0000000000000814
Adjoa A Andoh, Charles Hardy, Laura Evans, Amber Milem, Courtney Whitacre, Laura Rust, Amberley Masa, Gregory Stewart
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引用次数: 0

摘要

在2022年秋季全国哮喘发作激增期间,沙丁胺醇雾化器溶液严重短缺,要求我们的机构探索保存雾化沙丁胺醇的方法。计量吸入器(MDI)和振动网状雾化器(VMN)提供了更有效的沙丁胺醇给药方法。我们的目的是在我们的急诊科(ED)纳入替代沙丁胺醇给药方法,以减少雾化沙丁胺醇溶液对哮喘加重的剂量。方法:我们在干预前28个月评估每位患者的平均累积沙丁胺醇剂量。我们的多学科团队使用QI方法开发了干预措施,修改了ED哮喘临床实践指南和相关的电子命令集,以纳入MDI和VMN。主要结果是减少每位患者雾化沙丁胺醇的平均累积剂量。平衡措施包括急诊科住院时间(LOS)、住院率和24小时内的重访率。结果:该项目于2023年5月启动,项目实施后16个月共纳入2781例患者。我们发现了沙丁胺醇雾化的平均剂量从17.42毫克下降到11.57毫克的特殊原因,这种变化在干预后持续存在。虽然我们看到出院患者的急诊科LOS降低,但总体急诊科LOS、入院率或重访率没有变化。结论:临床实践指南和处方的改变,包括替代沙丁胺醇给药方法,导致每位患者雾化沙丁胺醇的平均剂量持续下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decreasing the Use of Albuterol Nebulizer Solution in the Management of Asthma Exacerbations in the Emergency Department.

Introduction: During a nationwide surge in asthma exacerbations in the fall of 2022, there was a critical shortage of albuterol nebulizer solution, requiring our institution to explore ways to conserve nebulized albuterol. The metered-dose inhaler (MDI) and vibrating mesh nebulizer (VMN) offer more efficient methods of albuterol administration. We aimed to incorporate alternative albuterol administration methods within our emergency department (ED) to decrease the amount of nebulized albuterol solution administered for asthma exacerbations.

Methods: We assessed the average cumulative albuterol dose per patient encounter 28 months before our interventions. Our multidisciplinary team developed interventions using QI methods, modifying the ED asthma clinical practice guideline and associated electronic order set to incorporate the MDI and VMN. The primary outcome was decreasing the average cumulative dose of nebulized albuterol per patient encounter. Balancing measures include ED length of stay (LOS), hospital admissions, and revisit rates within 24 hours.

Results: This project began in May 2023, with 2,781 patients included in the subsequent 16 months postproject implementation. We identified special cause variation in the average dose of albuterol nebulization decreasing from 17.42 to 11.57 mg per encounter, which was sustained postintervention. Although we saw decreased ED LOS for discharged patients, there were no changes in overall ED LOS, admissions, or revisit rates.

Conclusions: Changes to the clinical practice guidelines and order set incorporating alternative albuterol administration methods led to a sustained decrease in the average dose of nebulized albuterol used per patient encounter.

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CiteScore
2.20
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