Departments of Population Health Sciences and Pediatrics, Weill Cornell Medicine, New York, NY, USA.
Division of Neurology, Nationwide Children's Hospital, Columbus, OH, USA.
Epilepsia. 2021 Jan;62(1):198-216. doi: 10.1111/epi.16733. Epub 2020 Dec 24.
Common data elements (CDEs) are standardized questions and answer choices that allow aggregation, analysis, and comparison of observations from multiple sources. Clinical CDEs are foundational for learning health care systems, a data-driven approach to health care focused on continuous improvement of outcomes. We aimed to create clinical CDEs for pediatric epilepsy.
A multiple stakeholder group (clinicians, researchers, parents, caregivers, advocates, and electronic health record [EHR] vendors) developed clinical CDEs for routine care of children with epilepsy. Initial drafts drew from clinical epilepsy note templates, CDEs created for clinical research, items in existing registries, consensus documents and guidelines, quality metrics, and outcomes needed for demonstration projects. The CDEs were refined through discussion and field testing. We describe the development process, rationale for CDE selection, findings from piloting, and the CDEs themselves. We also describe early implementation, including experience with EHR systems and compatibility with the International League Against Epilepsy classification of seizure types.
Common data elements were drafted in August 2017 and finalized in January 2020. Prioritized outcomes included seizure control, seizure freedom, American Academy of Neurology quality measures, presence of common comorbidities, and quality of life. The CDEs were piloted at 224 visits at 10 centers. The final CDEs included 36 questions in nine sections (number of questions): diagnosis (1), seizure frequency (9), quality of life (2), epilepsy history (6), etiology (8), comorbidities (2), treatment (2), process measures (5), and longitudinal history notes (1). Seizures are categorized as generalized tonic-clonic (regardless of onset), motor, nonmotor, and epileptic spasms. Focality is collected as epilepsy type rather than seizure type. Seizure frequency is measured in nine levels (all used during piloting). The CDEs were implemented in three vendor systems. Early clinical adoption included 1294 encounters at one center.
We created, piloted, refined, finalized, and implemented a novel set of clinical CDEs for pediatric epilepsy.
通用数据元素(CDE)是标准化的问题和答案选择,可用于从多个来源聚合、分析和比较观察结果。临床 CDE 是学习型医疗保健系统的基础,这是一种以数据为导向的医疗保健方法,侧重于不断改善结果。我们旨在为儿科癫痫创建临床 CDE。
一个多利益相关者小组(临床医生、研究人员、家长、护理人员、拥护者和电子健康记录 [EHR] 供应商)为癫痫儿童的常规护理制定了临床 CDE。最初的草稿取自临床癫痫笔记模板、为临床研究创建的 CDE、现有登记处的项目、共识文件和指南、质量指标以及示范项目所需的结果。通过讨论和现场测试对 CDE 进行了改进。我们描述了开发过程、CDE 选择的基本原理、试点结果以及 CDE 本身。我们还描述了早期实施情况,包括对 EHR 系统的经验以及与国际抗癫痫联盟癫痫发作类型分类的兼容性。
通用数据元素于 2017 年 8 月起草,并于 2020 年 1 月定稿。优先考虑的结果包括癫痫控制、癫痫无发作、美国神经病学学会质量指标、常见合并症的存在以及生活质量。CDE 在 10 个中心的 224 次就诊中进行了试点。最终的 CDE 包括九个部分的 36 个问题(问题数量):诊断(1)、发作频率(9)、生活质量(2)、癫痫病史(6)、病因(8)、合并症(2)、治疗(2)、过程测量(5)和纵向病史记录(1)。癫痫发作分为全面强直阵挛发作(无论发作起始如何)、运动性、非运动性和癫痫性痉挛。局灶性作为癫痫类型而不是发作类型进行收集。癫痫发作频率以九个级别进行测量(所有级别均在试点中使用)。CDE 在三个供应商系统中得到实施。早期临床应用包括一个中心的 1294 次就诊。
我们创建、试点、改进、定稿并实施了一套新颖的儿科癫痫临床 CDE。