在数字时代重新定义罕见病护理:以增强罕见病社区能力为重点的数字健康研讨会的见解和主要收获

Biomedicine hub Pub Date : 2024-04-10 DOI:10.1159/000536274
Emily Lewis, Anuradha Dayal, Ron Li
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引用次数: 0

摘要

摘要 在 2023 年 9 月 8 日于加利福尼亚州斯坦福大学举行的斯坦福大学-加州大学伯克利分校罕见病数字健康研讨会上,研究人员、临床医生、付款人、思想领袖以及罕见病护理人员和倡导者讨论了罕见病患者群体的护理服务现状和数字化护理的未来前景。数字医疗旨在通过新颖的方式改善医疗服务,为罕见病患者提供更精确的诊断、疾病进展监测、治疗、预后和护理管理。会议重点强调了挑战和未满足的需求、数据基础设施和分析、对有针对性和有效的个性化疗法的需求,以及数字医疗转型的重要性。会议还讨论了获得以患者为中心的数字化医疗服务所带来的社会和伦理影响,以及对实施、患者自主权和赋权的看法。
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Redefining Rare Disease Care in the Digital Age: Insights and Key Takeaways from a Digital Health Symposium Focused on Empowering Rare Disease Communities
Abstract At the Stanford-UCB Rare Disease Digital Health Symposium held in Stanford, California, on September 8, 2023, researchers, clinicians, payers, thought leaders, and rare disease caregivers and advocates discussed the current state of care delivery and future perspectives of digitally-enabled care for rare disease patient populations. Digital health aims to improve healthcare delivery through novel ways of providing access to more precise diagnosis, monitoring of disease progression, treatment, prognosis, and care management for rare disease patients. The meeting focused on highlighting challenges and unmet needs, data infrastructure and analytics, the need for targeted and effective personalized therapies, and the importance of digital care transformation. The meeting also covered the social and ethical impact of access to digitally delivered, patient-centered care, as well as views on implementation and patient autonomy and empowerment.
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