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信任的影响以及退出机制在德国通过电子健康记录共享健康数据意愿中的作用:电话调查研究

The Impact of Trust and the Role of the Opt-Out Mechanism in Willingness to Share Health Data via Electronic Health Records in Germany: Telephone Survey Study.

作者信息

Wilke Felix

机构信息

Department of Social Work, University of Applied Sciences Jena, Carl-Zeiss-Promenade 2, Jena, 07745, Germany, 49 3641205815.

出版信息

JMIR Hum Factors. 2025 Apr 15;12:e65718. doi: 10.2196/65718.

DOI:10.2196/65718
PMID:40233172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12013774/
Abstract

BACKGROUND

Electronic health records (EHRs) offer a valuable resource for research and health care improvement. However, public acceptance of sharing personal health data is critical to the success of such initiatives. In Germany, automatic data sharing via EHRs will be implemented unless people opt out.

OBJECTIVE

This study aims to assess the willingness of the German population to share health data via EHRs and to explore the role of trust in influencing these attitudes.

METHODS

A computer-assisted telephone interview study was conducted in December 2023, with 1004 respondents aged 18 years and older, representative of the German population. Descriptive statistics and multivariate linear regression models were used to analyze the data.

RESULTS

The survey shows that 43.4% (n=432) of respondents would be willing to share their health data via EHR, and a significant 34% (n=338) remain undecided. While the population is open to adoption of the EHR for personal health issues (n=483, 53% show interest in using it), the opt-out model for data sharing is viewed critically, with 44.7% (n=438) of respondents rejecting it. Socioeconomic status significantly influences the willingness to share data, with higher income, education, and digital literacy being associated with greater openness to data sharing. However, trust emerged as the most significant factor. Additionally, experiences with digital technologies increase the willingness to share personal health data.

CONCLUSIONS

The German population shows general openness toward EHRs and data sharing. Trust plays a critical role in promoting willingness to share health data. The findings highlight challenges in Germany's transition to an opt-out system.

摘要

背景

电子健康记录(EHRs)为研究和医疗保健改善提供了宝贵资源。然而,公众对共享个人健康数据的接受程度对于此类举措的成功至关重要。在德国,除非人们选择退出,否则将通过电子健康记录实现自动数据共享。

目的

本研究旨在评估德国民众通过电子健康记录共享健康数据的意愿,并探讨信任在影响这些态度方面的作用。

方法

2023年12月进行了一项计算机辅助电话访谈研究,有1004名18岁及以上的受访者,代表德国人口。使用描述性统计和多元线性回归模型分析数据。

结果

调查显示,43.4%(n = 432)的受访者愿意通过电子健康记录共享他们的健康数据,另有34%(n = 338)的人尚未决定。虽然民众对采用电子健康记录处理个人健康问题持开放态度(n = 483,53%表示有兴趣使用),但对数据共享的退出模式持批评态度,44.7%(n = 438)的受访者拒绝这种模式。社会经济地位显著影响数据共享意愿,收入、教育程度和数字素养较高与对数据共享的更大开放性相关。然而,信任是最显著的因素。此外,数字技术体验增加了共享个人健康数据的意愿。

结论

德国民众对电子健康记录和数据共享总体持开放态度。信任在促进健康数据共享意愿方面起着关键作用。研究结果凸显了德国向退出系统过渡中的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fd/12013774/86b2c00d6451/humanfactors-v12-e65718-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fd/12013774/116f8b6ac43d/humanfactors-v12-e65718-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fd/12013774/86b2c00d6451/humanfactors-v12-e65718-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fd/12013774/116f8b6ac43d/humanfactors-v12-e65718-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fd/12013774/86b2c00d6451/humanfactors-v12-e65718-g002.jpg

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本文引用的文献

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2
Attitude towards consent-free research use of personal medical data in the general German population.德国普通民众对个人医疗数据无同意使用研究的态度。
Heliyon. 2024 Mar 11;10(6):e27933. doi: 10.1016/j.heliyon.2024.e27933. eCollection 2024 Mar 30.
3
[Knowledge and attitudes towards sharing of health data: Results of a population survey].
[关于健康数据共享的知识与态度:一项人口调查的结果]
Z Evid Fortbild Qual Gesundhwes. 2024 Mar;184:50-58. doi: 10.1016/j.zefq.2023.11.001. Epub 2023 Dec 23.
4
Measuring the willingness to share personal health information: a systematic review.测量个人健康信息共享意愿:系统评价。
Front Public Health. 2023 Jul 20;11:1213615. doi: 10.3389/fpubh.2023.1213615. eCollection 2023.
5
Understanding Public Attitudes and Willingness to Share Commercial Data for Health Research: Survey Study in the United Kingdom.理解公众对健康研究中商业数据共享的态度和意愿:英国的调查研究。
JMIR Public Health Surveill. 2023 Mar 23;9:e40814. doi: 10.2196/40814.
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A Process Related View on the Usage of Electronic Health Records from the Patients' Perspective: A Systematic Review.从患者角度看电子健康记录的使用:一个过程相关的观点:系统评价。
J Med Syst. 2022 Dec 29;47(1):2. doi: 10.1007/s10916-022-01886-0.
7
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Digit Health. 2022 Jul 6;8:20552076221112840. doi: 10.1177/20552076221112840. eCollection 2022 Jan-Dec.
8
Complexities of health and acceptance of electronic health records for the Austrian elderly population.奥地利老年人群体的健康复杂性与电子健康记录的接受程度。
Eur J Health Econ. 2023 Feb;24(1):53-66. doi: 10.1007/s10198-022-01451-z. Epub 2022 Mar 14.
9
Secondary research use of personal medical data: patient attitudes towards data donation.个人医疗数据的二次研究利用:患者对数据捐赠的态度。
BMC Med Ethics. 2021 Dec 15;22(1):164. doi: 10.1186/s12910-021-00728-x.
10
Motives for withdrawal of participation in biobanking and participants' willingness to allow linkages of their data.参与生物银行研究的退出动机及参与者允许其数据关联的意愿。
Eur J Hum Genet. 2022 Mar;30(3):367-377. doi: 10.1038/s41431-021-00997-5. Epub 2021 Nov 22.