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应对在临床登记处整合数字健康技术以衡量以患者为中心的结果所面临的挑战。

Addressing the challenges of integrating digital health technologies to measure patient-centred outcomes in clinical registries.

作者信息

Marra Caroline, Chico Tim, Alexandrow April, Dixon Will G, Briffa Norman, Rainaldi Erin, Little Max A, Size Kristin, Tsanas Athanasios, Franklin Joseph B, Kapur Ritu, Grice Helen, Gariban Anwar, Ellery Joy, Sudlow Cathie, Abernethy Amy P, Morris Andrew

机构信息

Verily Life Sciences, South San Francisco, CA, USA.

Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK; British Heart Foundation Data Science Centre, London, UK; Health Data Research, London, UK.

出版信息

Lancet Digit Health. 2025 Mar;7(3):e225-e231. doi: 10.1016/S2589-7500(24)00223-1. Epub 2024 Dec 12.

Abstract

Longitudinal patient registries generate important evidence for advancing clinical care and the regulatory evaluation of health-care products. Most national registries rely on data collected as part of routine clinical encounters, an approach that does not capture real-world, patient-centred outcomes, such as physical activity, fatigue, ability to do daily tasks, and other indicators of quality of life. Digital health technologies that obtain such real-world data could greatly enhance patient registries but unresolved challenges have so far prevented their broad adoption. Based on our experience implementing digital health technologies in registries and observational studies, we propose potential solutions to three practical challenges we have repeatedly encountered: determining what to measure digitally, selecting the appropriate device, and ensuring representativeness and engagement over time. We describe the example of a hypothetical patient registry for valvular heart disease, a condition for which there is substantial variation in treatment selection and postintervention outcomes, and for which patient-centred outcome data are urgently needed to inform clinical care guidelines and health-service commissioning.

摘要

纵向患者登记为推进临床护理和医疗产品的监管评估提供了重要证据。大多数国家登记系统依赖于作为常规临床诊疗一部分收集的数据,这种方法无法获取以患者为中心的真实世界结局,如身体活动、疲劳、日常任务执行能力以及其他生活质量指标。获取此类真实世界数据的数字健康技术可极大地增强患者登记系统,但迄今尚未解决的挑战阻碍了它们的广泛采用。基于我们在登记系统和观察性研究中实施数字健康技术的经验,我们针对反复遇到的三个实际挑战提出了潜在解决方案:确定数字化测量的内容、选择合适的设备以及确保长期的代表性和参与度。我们描述了一个假设的瓣膜性心脏病患者登记系统的示例,对于这种疾病,治疗选择和干预后结局存在很大差异,并且迫切需要以患者为中心的结局数据来为临床护理指南和卫生服务委托提供信息。

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