LSE Health, Department of Health Policy, London School of Economics and Political Science, London, United Kingdom; Department of International Health, Care and Public Health Research Institute (CAPHRI), Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands; Digital Public Health Task Force, Association of School of Public Health in the European Region (ASPHER), Brussels, Belgium.
Department of Medicine, University of Cambridge, United Kingdom.
Int J Med Inform. 2024 Sep;189:105513. doi: 10.1016/j.ijmedinf.2024.105513. Epub 2024 Jun 5.
BACKGROUND: Patient engagement when providing patient access to health data results from an interaction between the available tools and individual capabilities. The recent digital advancements of the healthcare field have altered the manifestation and importance of patient engagement. However, a comprehensive assessment of what factors contribute to patient engagement remain absent. In this review article, we synthesised the most frequently discussed factors that can foster patient engagement with their health data. METHODS: A scoping review was conducted in MEDLINE, Embase, and Google Scholar. Relevant data were synthesized within 7 layers using a thematic analysis: (1) social and demographic factors, (2) patient ability factors, (3) patient motivation factors, (4) factors related to healthcare professionals' attitudes and skills, (5) health system factors, (6) technological factors, and (7) policy factors. RESULTS: We identified 5801 academic and 200 Gy literature records, and included 292 (4.83%) in this review. Overall, 44 factors that can affect patient engagement with their health data were extracted. We extracted 6 social and demographic factors, 6 patient ability factors, 12 patient motivation factors, 7 factors related to healthcare professionals' attitudes and skills, 4 health system factors, 6 technological factors, and 3 policy factors. CONCLUSIONS: Improving patient engagement with their health data enables the development of patient-centered healthcare, though it can also exacerbate existing inequities. While expanding patient access to health data is an important step towards fostering shared decision-making in healthcare and subsequently empowering patients, it is important to ensure that these developments reach all sectors of the community.
背景:在为患者提供获取健康数据的途径时,患者参与源于可用工具和个体能力之间的相互作用。最近医疗保健领域的数字化进步改变了患者参与的表现形式和重要性。然而,对于促成患者参与其健康数据的因素的全面评估仍然缺失。在这篇综述文章中,我们综合了最常讨论的可以促进患者参与其健康数据的因素。
方法:在 MEDLINE、Embase 和 Google Scholar 中进行了范围综述。使用主题分析在 7 个层面内综合相关数据:(1)社会人口因素,(2)患者能力因素,(3)患者动机因素,(4)与医疗保健专业人员态度和技能相关的因素,(5)卫生系统因素,(6)技术因素,(7)政策因素。
结果:我们确定了 5801 篇学术文献和 200 篇灰色文献记录,并将其中的 292 篇纳入本综述。总体而言,提取出了 44 个可能影响患者参与其健康数据的因素。我们提取了 6 个社会人口因素、6 个患者能力因素、12 个患者动机因素、7 个与医疗保健专业人员态度和技能相关的因素、4 个卫生系统因素、6 个技术因素和 3 个政策因素。
结论:提高患者对其健康数据的参与度可以促进以患者为中心的医疗保健的发展,但也可能加剧现有的不平等现象。尽管扩大患者对健康数据的访问权限是促进医疗保健中共同决策并进而赋予患者权力的重要步骤,但确保这些发展惠及社区的所有阶层也很重要。
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