Adams Sarah Nicole, Abel Mary, Fowler Dustin, Braden Jennifer, Ebeling Myla D, Simpson Annie N, Titus M Olivia, Andrews Annie Lintzenich
a Department of Medicine , Vanderbilt University , Nashville , TN , USA.
b Department of Pediatrics , Medical University of South Carolina , Charleston , South Carolina , USA.
J Asthma. 2018 Mar;55(3):252-258. doi: 10.1080/02770903.2017.1323917. Epub 2017 May 26.
To determine if improvement in Inhaled Corticosteroid (ICS) prescribing in the pediatric emergency department (PED) can be sustained after transition from intense intervention to low-intervention phase, and to determine ICS fill rates.
A Quality Improvement (QI) project began in Aug 2012. Results through Feb 2014 were previously published. In Feb 2014 interventions were scaled back to determine the sustainability of QI success. Eligible patients included children aged 2-17 seen in the PED for asthma between Feb 2014 and Sept 2016. The primary change when moving to the low-intervention phase was stopping monthly attending feedback. The primary outcome was the proportion of patients who were prescribed an ICS at the time of PED discharge. The secondary objective of this study was to determine the proportion of patients who filled their ICS prescription in the 6 months following Emergency Department (ED) visit.
The goal rate of ICS prescribing was 75%. After transition to the low-intervention phase, the ICS prescribing rate was maintained at a median of 79% through Sept 2016. ICS fill rate in the first 30 days following ED visit was 89%, although this quickly fell to below 40% for months 2-6.
The ICS prescribing rate remained the goal of 75% over a 2.5-year period after transition to a low-intervention phase. High ICS fill rates immediately after ED visit have been demonstrated. However, rapid decline in these rates over subsequent months suggests a need for future efforts to focus on long-term ICS adherence among children with ED visits for asthma.
确定儿科急诊科(PED)吸入性糖皮质激素(ICS)处方的改善在从强化干预阶段过渡到低干预阶段后是否能够持续,并确定ICS的取药率。
一项质量改进(QI)项目于2012年8月启动。此前已发表了截至2014年2月的结果。2014年2月,干预措施逐步缩减,以确定QI成功的可持续性。符合条件的患者包括2014年2月至2016年9月期间在PED因哮喘就诊的2至17岁儿童。进入低干预阶段的主要变化是停止每月的出勤反馈。主要结局是PED出院时开具ICS处方的患者比例。本研究的次要目的是确定急诊科(ED)就诊后6个月内取到ICS处方的患者比例。
ICS处方的目标率为75%。过渡到低干预阶段后,到2016年9月,ICS处方率中位数维持在79%。ED就诊后前30天的ICS取药率为89%,尽管在第2至6个月迅速降至40%以下。
过渡到低干预阶段后的2.5年期间,ICS处方率保持在75%的目标。已证明ED就诊后立即有较高的ICS取药率。然而,随后几个月这些比率迅速下降,表明未来需要努力关注因哮喘到ED就诊儿童的长期ICS依从性。