Maximizing Data Capture for Race and Ethnicity of Children Admitted to Critical Care Units.

IF 2.7 3区 医学 Q2 CRITICAL CARE MEDICINE
Patricia A Hickey, Jean A Connor, Cheryl Toole, Valerie L Ward
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引用次数: 0

Abstract

Background: Access to complete patient sociodemographic data in a hospital's electronic health record is important for identifying and understanding health inequities and designing interventions to close health care gaps. Through participation in a national safety collaborative, this team identified many patients in intensive care units (ICUs) for whom sociodemographic data (race and ethnicity) were incomplete or missing.

Objectives: To describe the processes the team used to understand how sociodemographic data were being ascertained for children admitted to hospital ICUs; demonstrate how interprofessional care teams can collaborate to create solutions for vulnerable patients; and provide steps that can be used at other hospitals to decrease missing sociodemographic data and deliver equitable care.

Methods: A plan-do-study-act framework guided this initiative to improve collection of data on the race and ethnicity of ICU patients. Via 4 plan-do-study-act cycles, care vulnerabilities and implemented tests of change were evaluated to achieve the goal of capturing sociodemographic data within 72 hours of patient admission.

Results: A new process was developed for patient experience representatives to collect, enter, and track sociodemographic data accurately. Through education and use of a script, documentation rates reached 80% to 100%.

Conclusions: Overcoming barriers in the electronic health record and creating new processes supported the collection of sociodemographic data for children admitted to ICUs. Engaging and acknowledging the value of interprofessional teams was important in this successful groundwork to help deliver equitable care.

最大限度地获取入住重症监护病房的儿童的种族和民族数据。
背景:获取医院电子健康记录中完整的患者社会人口统计数据对于识别和了解卫生不公平现象以及设计干预措施以缩小卫生保健差距非常重要。通过参与国家安全协作,该团队确定了许多重症监护病房(icu)中社会人口统计数据(种族和民族)不完整或缺失的患者。目的:描述该团队用于了解如何确定住院重症监护儿童的社会人口统计数据的过程;展示跨专业护理团队如何合作,为弱势患者创造解决方案;并提供可在其他医院使用的步骤,以减少缺失的社会人口数据并提供公平的护理。方法:计划-研究-行动框架指导该倡议,以改善ICU患者种族和民族数据的收集。通过4个计划-研究-行动周期,评估护理脆弱性和实施的变化测试,以实现在患者入院后72小时内获取社会人口统计数据的目标。结果:为患者体验代表开发了一个新的过程来准确地收集、输入和跟踪社会人口统计数据。通过教育和使用脚本,文档率达到了80%到100%。结论:克服电子健康记录中的障碍和创建新的流程支持了icu入院儿童的社会人口统计数据的收集。在这一成功的基础工作中,参与和承认跨专业团队的价值对于帮助提供公平的护理非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
103
审稿时长
6-12 weeks
期刊介绍: The editors of the American Journal of Critical Care (AJCC) invite authors to submit original manuscripts describing investigations, advances, or observations from all specialties related to the care of critically and acutely ill patients. Papers promoting collaborative practice and research are encouraged. Manuscripts will be considered on the understanding that they have not been published elsewhere and have been submitted solely to AJCC.
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