C James
Fordham University, 20 Grasmere Ave, Fairfield, CT, 06824, United States, (212) 280-1600.
J Particip Med. 2025 Aug 1;17:e68261. doi: 10.2196/68261.
Humanity stands at the threshold of a new era in biological understanding, disease treatment, and overall wellness. The convergence of evolving patient and caregiver (consumer) behaviors, increased data collection, advancements in health technology and standards, federal policies, and the rise of artificial intelligence (AI) is driving one of the most significant transformations in human history. To achieve transformative health care insights, AI must have access to comprehensive longitudinal health records (LHRs) that span clinical, genomic, nonclinical, wearable, and patient-generated data. Despite the extensive use of electronic medical records and widespread interoperability efforts, current health care organizations, electronic medical record vendors, and public agencies are not incentivized to develop and maintain complete LHRs. This paper explores the new paradigm of consumers as the common provenance and singular custodian of LHRs. With fully aligned intentions and ample time to dedicate to optimizing their health outcomes, patients and caregivers must assume the sole responsibility to manage or delegate aggregation of complete, accurate, and real-time LHRs. Significant gaps persist in empowering consumers to act as primary custodians of their health data and to aggregate their complete LHRs, a foundational requirement for the effective application of AI. Rare disease communities, leaders in participatory care, offer a compelling model for demonstrating how consumer-driven data aggregation can be achieved and underscore the need for improved policy frameworks and technological tools. The convergence of AI and LHRs promises to transform medicine by enhancing clinical decision-making, accelerating accurate diagnoses, and dramatically advancing our ability to understand and treat disease at an unprecedented pace.
人类正站在生物认知、疾病治疗和整体健康新时代的门槛上。不断演变的患者和护理者(消费者)行为、数据收集的增加、健康技术与标准的进步、联邦政策以及人工智能(AI)的兴起,共同推动着人类历史上最重大的变革之一。为了获得具有变革性的医疗见解,人工智能必须能够获取涵盖临床、基因组、非临床、可穿戴设备以及患者生成数据的全面纵向健康记录(LHR)。尽管电子病历得到了广泛应用且人们在广泛开展互操作性工作,但当前的医疗保健机构、电子病历供应商和公共机构并没有动力去开发和维护完整的LHR。本文探讨了消费者作为LHR的共同来源和唯一保管者这一新范式。患者和护理者有着完全一致的意图,并有充足的时间致力于优化他们的健康结果,因此必须承担起管理或委托汇总完整、准确和实时LHR的唯一责任。在赋予消费者权力使其成为自身健康数据的主要保管者并汇总其完整的LHR方面,仍然存在重大差距,而这是有效应用人工智能的一项基本要求。罕见病群体作为参与式护理的领导者,提供了一个引人注目的模式,展示了如何实现消费者驱动的数据汇总,并强调了改进政策框架和技术工具的必要性。人工智能与LHR的融合有望通过增强临床决策、加速准确诊断以及以前所未有的速度大幅提升我们理解和治疗疾病的能力来变革医学。