RECORD: RELIABLE ELECTRONIC CAPTURE OF RELEVANT DATA

记录：相关数据的可靠电子捕获

• 批准号: 6208216
• 负责人: STEPHEN C PORTER
• 金额: $ 7.68万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-07-01 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/6208216
• 关键词: Internet; automated medical record system; behavioral /social science research tag; case history; clinical research; computer system design /evaluation; data collection methodology /evaluation; diagnosis quality /standard; human subject; interview; parent offspring interaction; parents; preschool child (1-5)

Current use of electronic medical records in health care creates barriers between the patient as a provider of information and the creation of the health record. This proposal will be executed within the NLM-funded PING (Personal Internetworked Notary and Guardian) project. The specific aims are: 1) to design a web- based tool to enable parents' direct report of historical data into the electronic medical record, and 2) to measure the quality of medical histories entered by a parent for his/her child. I will develop and test this informational tool in two stages. First, an iterative process to study the quantity and quality of information gathered from user-interfaces of varying structures will occur. User feedback on the interface will be combined with content analysis of acquired information to produce a comprehensive interview covering five common symptoms experienced by a parent/child dyad in an acute illness visit. The interview will be deployed and tested in stage two. Validity will be measured by percent agreement between the parent-generated record and the final physician-generated record. Item-specific disagreement will be further studied to test the hypothesis that parental report will emphasize a higher level of symptom acuity than that reflected in the physician's charting.

目前在医疗保健中使用电子医疗记录在作为信息提供者的患者与创建健康记录之间产生了障碍。 该提案将在NLM资助的PING（个人互联网公证人和监护人）项目中执行。 具体目标是：1）设计基于网络的工具，以使父母能够将历史数据直接报告到电子医疗记录中，以及2）测量父母为他/她的孩子输入的医疗历史的质量。 我将分两个阶段开发和测试这个信息工具。首先，将出现一个迭代过程来研究从不同结构的用户界面收集的信息的数量和质量。 界面上的用户反馈将与所获取信息的内容分析相结合，以产生一个全面的采访，涵盖五个常见的症状经历的父母/儿童二人组在急性疾病的访问。 面试将在第二阶段进行部署和测试。 有效性将通过父母生成的记录和最终医生生成的记录之间的一致性百分比来衡量。 将进一步研究项目特异性分歧，以检验父母报告将强调比医生图表中反映的更高水平的症状敏锐度的假设。