Andoh Adjoa A, Hardy Charles, Evans Laura, Milem Amber, Whitacre Courtney, Rust Laura, Masa Amberley, Stewart Gregory
From the Division of Emergency Medicine, Department of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio.
Center for Clinical Excellence, Department of Pediatrics, Nationwide Children's Hospital, Columbus, Ohio.
Pediatr Qual Saf. 2025 May 22;10(3):e814. doi: 10.1097/pq9.0000000000000814. eCollection 2025 May-Jun.
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.
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.
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.
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.
在2022年秋季全国范围内哮喘急性加重病例激增期间,沙丁胺醇雾化溶液严重短缺,这要求我们机构探索节约雾化沙丁胺醇的方法。定量吸入器(MDI)和振动网式雾化器(VMN)提供了更有效的沙丁胺醇给药方法。我们旨在将替代沙丁胺醇给药方法纳入我们的急诊科(ED),以减少用于哮喘急性加重的雾化沙丁胺醇溶液的用量。
我们评估了在我们采取干预措施前28个月每位患者每次就诊时的平均累积沙丁胺醇剂量。我们的多学科团队采用质量改进方法制定了干预措施,修改了ED哮喘临床实践指南和相关电子医嘱集,以纳入MDI和VMN。主要结果是减少每位患者每次就诊时雾化沙丁胺醇的平均累积剂量。平衡指标包括ED住院时间(LOS)、住院率和24小时内复诊率。
该项目于2023年5月开始,在项目实施后的16个月内纳入了2781名患者。我们发现沙丁胺醇雾化平均剂量出现特殊原因变异,从每次就诊17.42毫克降至11.57毫克,干预后这一情况持续存在。虽然我们看到出院患者的ED LOS有所下降,但总体ED LOS、住院率或复诊率没有变化。
纳入替代沙丁胺醇给药方法的临床实践指南和医嘱集的改变导致每位患者每次就诊时使用的雾化沙丁胺醇平均剂量持续下降。