Morris Megan A, Sarmiento Cristina, Eberle Kori
Jt Comm J Qual Patient Saf. 2024 Jan;50(1):16-23. doi: 10.1016/j.jcjq.2023.10.006. Epub 2023 Oct 21.
This qualitative study aimed to understand how early adopting health care organizations (HCOs) implement the documentation of patients' disability status and accommodation needs in the electronic health record (EHR).
The authors conducted qualitative interviews with HCOs that had active or past initiatives to implement systematic collection of disability status in the EHR. The interviews elicited participants' current experiences, desired features of a standard EHR build, and challenges and successes. A team-based analysis approach was used to review and summarize quotations to identify themes and categorize text that exemplified identified themes.
Themes identified from the interviews included "why" organizations collected disability status; of "what" their EHR build consisted, including who collected, how often data were collected, and what data were collected; and "how" organizations were implementing systematic collection. The main purpose for collection of disability status and accommodation needs was to prepare for patients with disabilities. Due to this priority, participants believed collection should (1) occur prior to patients' clinical encounters, (2) be conducted regularly, (3) use standardized language, and (4) be available in a highly visible location in the EHR. Leadership support to integrate collection into existing workflows was essential for success.
Patients with disabilities experience significant disparities in the receipt of equitable health care services. To provide equitable care, HCOs need to systematically collect disability status and accommodation needs in the EHR to ensure that they are prepared to provide equitable care to all patients with disabilities.
本定性研究旨在了解早期采用电子健康记录(EHR)的医疗保健组织(HCO)如何记录患者的残疾状况和便利需求。
作者对那些曾积极开展或过去开展过在EHR中系统收集残疾状况举措的HCO进行了定性访谈。访谈引出了参与者当前的经历、标准EHR构建所需的功能以及挑战与成功经验。采用基于团队的分析方法来审查和总结引述内容,以确定主题并对体现已确定主题的文本进行分类。
从访谈中确定的主题包括组织收集残疾状况的“原因”;其EHR构建的“内容”,包括谁来收集、数据收集的频率以及收集哪些数据;以及组织“如何”实施系统收集。收集残疾状况和便利需求的主要目的是为残疾患者做好准备。基于这一优先事项,参与者认为收集工作应(1)在患者临床就诊之前进行,(2)定期开展,(3)使用标准化语言,(4)在EHR中一个高度显眼的位置可用。将收集工作整合到现有工作流程中的领导支持对于成功至关重要。
残疾患者在获得公平的医疗保健服务方面存在显著差异。为了提供公平的护理,HCO需要在EHR中系统地收集残疾状况和便利需求,以确保他们准备好为所有残疾患者提供公平的护理。