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德国消费者对国家电子健康记录的看法及其采用的障碍:卫生政策是否需要改变沟通方式?

Consumer perspectives on the national electronic health record and barriers to its adoption in Germany: does health policy require a change in communication?

作者信息

Kröner Saskia, Schreiweis Björn, Strotbaum Veronika, Brandl Lea Christine, Pobiruchin Monika, Wiesner Martin

机构信息

Health Informatics Research Group, University AS Osnabrück, Osnabrück, Germany.

Institute for Medical Informatics and Statistics, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.

出版信息

BMC Health Serv Res. 2025 Jan 7;25(1):33. doi: 10.1186/s12913-024-12175-6.

Abstract

BACKGROUND

The national health record (ePA) was introduced January 1, 2021 in Germany and is available to every person insured under statutory health insurance. This study investigated the acceptance and expectations of the national health record in Germany, focusing on consumer perspectives, expectations, barriers, information needs, and communication aspects.

METHODS

An exploratory, observational, cross-sectional online survey was conducted one year after ePA introduction, followed by descriptive statistical analysis.

RESULTS

The top three ePA use cases were medical document collection, simplified data exchange between medical institutions, and emergency medical information. Adoption barriers included lack of information and access, privacy concerns, and perceived lack of necessity. Participants that felt informed about the ePA, reported they received information primarily from health insurances, the media, and educational or professional sources, mainly through printed brochures, social media, or via emails. Most participants (86.5%) preferred being informed through conversations, particularly with health insurance providers (81.5%) and doctors (61.0%). Written information was highly desired (94.5%), preferably via email or information letters/flyers. However, more than half of the participants (55.6%) reported being uninformed about the ePA introduction.

CONCLUSION

The study revealed a communication gap between providers and consumers, leading to a low acceptance rate of digital health technologies. Comparisons with other countries showed low adoption rates for opt-in systems. The authors suggest changing communication strategies, given users prefer direct information from doctors or health insurance companies. Adopting an opt-out system with professional social media and marketing campaigns could increase nationwide ePA adoption.

摘要

背景

德国于2021年1月1日引入了国家健康记录(电子患者档案,ePA),法定医疗保险的每位参保人员均可使用。本研究调查了德国对国家健康记录的接受度和期望,重点关注消费者的观点、期望、障碍、信息需求及沟通方面。

方法

在电子患者档案引入一年后开展了一项探索性、观察性横断面在线调查,随后进行描述性统计分析。

结果

电子患者档案的前三大用例是医疗文件收集、医疗机构间简化的数据交换以及紧急医疗信息。采用障碍包括信息缺乏和获取途径不足、隐私担忧以及认为缺乏必要性。那些感觉了解电子患者档案的参与者报告称,他们主要从健康保险公司、媒体以及教育或专业来源获取信息,主要是通过印刷手册、社交媒体或电子邮件。大多数参与者(86.5%)更喜欢通过对话获取信息,尤其是与健康保险公司(81.5%)和医生(61.0%)对话。非常希望获得书面信息(94.5%),最好是通过电子邮件或信息信函/传单。然而,超过一半的参与者(55.6%)报告称对电子患者档案的引入不知情。

结论

该研究揭示了提供者与消费者之间的沟通差距,导致数字健康技术的接受率较低。与其他国家的比较显示,选择加入系统的采用率较低。作者建议改变沟通策略,因为用户更喜欢来自医生或健康保险公司的直接信息。采用带有专业社交媒体和营销活动的选择退出系统可能会提高全国范围内电子患者档案的采用率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7a7/11706193/0fc2d69aabc0/12913_2024_12175_Fig1_HTML.jpg

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