Anna Vaynrub, Subiksha Umakanth, Harry West, Alissa Michel, Jill Dimond, Stephan Constante, Katherine D Crew, Rita Kukafka
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引用次数: 0
Abstract
A critical strategy in limiting breast cancer (BC) mortality is the early identification of high-risk patients and implementation of risk-reducing measures. RealRisks, an online decision aid constructed by our team to provide education on BC risk and personalized risk assessment, allows users the option to connect to their electronic health record (EHR) to extract requisite data to calculate BC risk via Fast Healthcare Interoperability Resources (FHIR). Using data from RealRisks user profiles, baseline questionnaires, and interview transcripts, we sought to understand the differences between the groups of patients who opted to download their data via the EHR vs. those who did not. A higher percentage of those who downloaded data (53.8% vs. 42.3%) identified as Hispanic/Latino compared to those who did not download. Thematic analysis suggested that while data security and privacy concerns may lead to hesitation, it is perhaps technological barriers that most significantly limit EHR download.
限制乳腺癌(BC)死亡率的一个关键策略是早期识别高危患者并实施降低风险的措施。RealRisks是由我们的团队构建的在线决策辅助工具,旨在提供BC风险教育和个性化风险评估,允许用户选择连接到他们的电子健康记录(EHR),以提取必要的数据,通过快速医疗保健互操作性资源(FHIR)计算BC风险。使用来自RealRisks用户档案、基线问卷和访谈记录的数据,我们试图了解选择通过电子病历下载数据的患者组与不选择通过电子病历下载数据的患者组之间的差异。与没有下载数据的人相比,下载数据的人(53.8% vs. 42.3%)中西班牙裔/拉丁裔人的比例更高。专题分析表明,虽然数据安全和隐私问题可能导致犹豫,但技术障碍可能是限制电子病历下载的最重要因素。