Improving implementation and team communication by integrating a cystic fibrosis transition readiness (CF R.I.S.E.) program into electronic health records.

IF 2.7 3区 医学 Q1 PEDIATRICS Pediatric Pulmonology Pub Date : 2025-01-01 Epub Date: 2024-10-23 DOI:10.1002/ppul.27326
Catherine Enochs, Amy G Filbrun, Michelle Hjelm, Julie Lehrmann, Lisa Mullen, Rebeca Packard, Jessica Roach, Anna K Saulitis, Samya Z Nasr
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Abstract

Background: The cystic fibrosis (CF) Responsibility. Independence. Self-care. Education. (R.I.S.E.) program was developed to provide assessment and education, supporting transition readiness for people with cystic fibrosis (pwCF). Lack of integration within electronic health records (EHR) was a barrier to implementation of CF R.I.S.E. University of Michigan was able to integrate CF R.I.S.E. into EHR.

Aim: To improve implementation and EHR documentation of CF R.I.S.E. module completion by pwCF across two (CF) programs from baseline (10.5%) to 75% per month in 6 months (January through June 2023).

Methods: Two CF programs utilized quality improvement (QI) methods and tools and ad hoc support by a CF Learning Network (QI) specialist. Eligibility included pwCF ≥16 years old seen in CF clinics who accepted CF R.I.S.E.

Participation: Beginning January 2, 2023, programs met in biweekly, virtual meetings to discuss implementation. Deidentified data were collected monthly tracking modules completed by pwCF and number of team members engaging with CF R.I.S.E. and documenting in EHR. Data timelines were baseline (November-December 2022), project period (January-June 2023), and post-project (July-December 2023).

Results: Completion rates increased from baseline (10.5%) to 48% (range 33% to 81%) through December 2023. During the project, an average 7.7 team members completed an average 19.2 modules per month. Post-project, an average 8 team members completed an average 16.5 modules per month.

Conclusions: This collaboration demonstrated how utilization of EHR allowed for successful CF R.I.S.E. improvement at both programs. Shared software utilization and QI initiatives may be a way to facilitate timely dissemination of best practices through learning health systems.

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将囊性纤维化过渡准备(CF R.I.S.E.)计划整合到电子病历中,改善实施和团队沟通。
背景:囊性纤维化(CF)的责任。独立。自理。教育。(R.I.S.E.)计划旨在为囊性纤维化患者(pwCF)提供评估和教育,帮助他们做好过渡准备。密歇根大学能够将囊性纤维化 R.I.S.E. 集成到电子健康记录(EHR)中。目标:在 6 个月内(2023 年 1 月至 6 月),将两个囊性纤维化计划中囊性纤维化患者完成囊性纤维化 R.I.S.E. 模块的比例从基线(10.5%)提高到每月 75%:方法:两个 CF 计划采用质量改进 (QI) 方法和工具,并由 CF 学习网络 (QI) 专家提供特别支持。参与资格包括在接受 CF R.I.S.E.Participation 的 CF 诊所就诊的年龄≥16 岁的儿童:从 2023 年 1 月 2 日开始,各项目每两周举行一次虚拟会议,讨论实施情况。每月收集去身份化数据,跟踪患者完成的模块以及参与 CF R.I.S.E.并在 EHR 中记录的团队成员人数。数据时间轴为基线(2022 年 11 月至 12 月)、项目期(2023 年 1 月至 6 月)和项目后(2023 年 7 月至 12 月):项目完成率从基线(10.5%)上升至 2023 年 12 月的 48%(范围为 33% 至 81%)。项目期间,平均每月有 7.7 名团队成员完成 19.2 个模块。项目结束后,平均每月有 8 名团队成员完成 16.5 个模块:此次合作展示了电子病历的使用是如何在两个项目中成功改进 CF R.I.S.E.的。共享软件使用和 QI 计划可能是通过学习型医疗系统促进及时传播最佳实践的一种方法。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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