Literature DB >> 20937485

Ethical, legal and social issues for personal health records and applications.

Reid Cushman1, A Michael Froomkin2, Anita Cava3, Patricia Abril3, Kenneth W Goodman4.   

Abstract

Robert Wood Johnson Foundation's Project HealthDesign included funding of an ethical, legal and social issues (ELSI) team, to serve in an advisory capacity to the nine design projects. In that capacity, the authors had the opportunity to analyze the personal health record (PHR) and personal health application (PHA) implementations for recurring themes. PHRs and PHAs invert the long-standing paradigm of health care institutions as the authoritative data-holders and data-processors in the system. With PHRs and PHAs, the individual is the center of his or her own health data universe, a position that brings new benefits but also entails new responsibilities for patients and other parties in the health information infrastructure. Implications for law, policy and practice follow from this shift. This article summarizes the issues raised by the first phase of Project HealthDesign projects, categorizing them into four topics: privacy and confidentiality, data security, decision support, and HIPAA and related legal-regulatory requirements. Discussion and resolution of these issues will be critical to successful PHR/PHA implementations in the years to come.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20937485     DOI: 10.1016/j.jbi.2010.05.003

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  7 in total

1.  Transformation of the Doctor-Patient Relationship: Big Data, Accountable Care, and Predictive Health Analytics.

Authors:  Seuli Bose Brill; Karen O Moss; Laura Prater
Journal:  HEC Forum       Date:  2019-12

2.  Adoption of Electronic Personal Health Records in Canada: Perceptions of Stakeholders.

Authors:  Marie-Pierre Gagnon; Julie Payne-Gagnon; Erik Breton; Jean-Paul Fortin; Lara Khoury; Lisa Dolovich; David Price; David Wiljer; Gillian Bartlett; Norman Archer
Journal:  Int J Health Policy Manag       Date:  2016-07-01

3.  Attitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal Genomics.

Authors:  Sandra Soo-Jin Lee; Simone L Vernez; K E Ormond; Mark Granovetter
Journal:  J Pers Med       Date:  2013-10-14

4.  Understanding Parent Perspectives Concerning Adolescents' Online Access to Personal Health Information.

Authors:  Gregory L Gaskin; Janine Bruce; Arash Anoshiravani
Journal:  J Particip Med       Date:  2016-03-14

5.  Technological Health Intervention in Population Aging to Assist People to Work Smarter not Harder: Qualitative Study.

Authors:  Sonia Chien-I Chen
Journal:  J Med Internet Res       Date:  2018-01-04       Impact factor: 5.428

6.  Public Attitudes Regarding Trade-offs Between the Functional Aspects of a Contact-Confirming App for COVID-19 Infection Control and the Benefits to Individuals and Public Health: Cross-sectional Survey.

Authors:  Seiji Bito; Yachie Hayashi; Takanori Fujita; Shigeto Yonemura
Journal:  JMIR Form Res       Date:  2022-07-20

7.  The personal health record paradox: health care professionals' perspectives and the information ecology of personal health record systems in organizational and clinical settings.

Authors:  Kim M Nazi
Journal:  J Med Internet Res       Date:  2013-04-04       Impact factor: 5.428

  7 in total

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