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Utilizing a Prototype Patient-Controlled Electronic Health Record in Germany: Qualitative Analysis of User-Reported Perceptions and Perspectives

机译:利用原型患者控制的电子病历在德国:用户报告的感知和观点的定性分析

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摘要

BackgroundPersonal electronic health records (PHR) are considered instrumental in improving health care quality and efficiency, enhancing communication between all parties involved and strengthening the patient’s role. Technical architectures, data privacy, and applicability issues have been discussed for many years. Nevertheless, nationwide implementation of a PHR is still pending in Germany despite legal regulations provided by the eHealth Act passed in 2015. Within the information technology for patient-oriented care project funded by the Federal Ministry of Education and Research (2012-2017), a Web-based personal electronic health record prototype (PEPA) was developed enabling patient-controlled information exchange across different care settings. Gastrointestinal cancer patients and general practitioners utilized PEPA during a 3-month trial period. Both patients and physicians authorized by them could view PEPA content online and upload or download files.
机译:背景个人电子健康记录(PHR)被认为有助于提高医疗质量和效率,加强所有相关方之间的沟通并增强患者的作用。技术架构,数据隐私和适用性问题已经讨论了很多年。尽管如此,尽管2015年通过了《电子卫生法案》所规定的法律法规,但德国仍在全国范围内实施PHR。在联邦教育与研究部(2012-2017)资助的面向患者的信息技术项目中,开发了基于网络的个人电子健康记录原型(PEPA),可以在不同的护理环境之间交换患者控制的信息。胃肠道癌症患者和全科医生在3个月的试用期内使用了PEPA。他们授权的患者和医生都可以在线查看PEPA内容并上传或下载文件。

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