Literature DB >> 35876830

21st Century Cures Act: ethical recommendations for new patient-facing products.

Brigitte N Durieux1, Matthew DeCamp2, Charlotta Lindvall1,3.   

Abstract

BACKGROUND: Recent legislation ensuring patient access to their electronic health records represents a promising national commitment to patient empowerment. Access and interoperability rules seek to empower individuals as well as increase opportunities for data sharing by hospitals, apps, and other parties for research and innovation. However, there are trade-offs between data accessibility and oversight. Some third-party apps may not be covered by federal regulations, and receiving records directly from individuals may render some services in possession of health data. To promote consumer trust, these services should follow ethical standards regardless of regulatory status. ACTIONABLE PRINCIPLES: This Perspective proposes 3 actionable principles, grounded in medical ethics, for services making use of health data: services should (1) provide informed, dynamic, regular consent, including control over data sharing, (2) promote inclusivity and equity, and (3) intentionally focus on consumer trust and the perception of value in the service provided.
© The Author(s) 2022. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  data privacy; ethics; informed consent; patient data

Mesh:

Year:  2022        PMID: 35876830      PMCID: PMC9471700          DOI: 10.1093/jamia/ocac112

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   7.942


  25 in total

1.  Good intentions are not enough: how informatics interventions can worsen inequality.

Authors:  Tiffany C Veinot; Hannah Mitchell; Jessica S Ancker
Journal:  J Am Med Inform Assoc       Date:  2018-08-01       Impact factor: 4.497

2.  The stigma of obesity in customer service: a mechanism for remediation and bottom-line consequences of interpersonal discrimination.

Authors:  Eden B King; Jenessa R Shapiro; Michelle R Hebl; Sarah L Singletary; Stacey Turner
Journal:  J Appl Psychol       Date:  2006-05

3.  Sharing Patient Data Without Exploiting Patients.

Authors:  Matthew S McCoy; Steven Joffe; Ezekiel J Emanuel
Journal:  JAMA       Date:  2020-01-16       Impact factor: 56.272

Review 4.  Privacy protections to encourage use of health-relevant digital data in a learning health system.

Authors:  Deven McGraw; Kenneth D Mandl
Journal:  NPJ Digit Med       Date:  2021-01-04

5.  A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.

Authors:  Nanibaa' A Garrison; Nila A Sathe; Armand H Matheny Antommaria; Ingrid A Holm; Saskia C Sanderson; Maureen E Smith; Melissa L McPheeters; Ellen W Clayton
Journal:  Genet Med       Date:  2015-11-19       Impact factor: 8.822

Review 6.  The Academic Viewpoint on Patient Data Ownership in the Context of Big Data: Scoping Review.

Authors:  Martin Mirchev; Iskra Mircheva; Albena Kerekovska
Journal:  J Med Internet Res       Date:  2020-08-18       Impact factor: 5.428

7.  The FDA MyStudies app: a reusable platform for distributed clinical trials and real-world evidence studies.

Authors:  Zachary Wyner; Sascha Dublin; Christina Chambers; Shyam Deval; Chayim Herzig-Marx; Shanthala Rao; Adam Rauch; Juliane Reynolds; Jeffrey S Brown; David Martin
Journal:  JAMIA Open       Date:  2020-12-11

8.  A Policy and Practice Review of Consumer Protections and Their Application to Hospital-Sourced Data Aggregation and Analytics by Third-Party Companies.

Authors:  Vasiliki Rahimzadeh
Journal:  Front Big Data       Date:  2021-02-12

9.  The public's comfort with sharing health data with third-party commercial companies.

Authors:  M Grace Trinidad; Jodyn Platt; Sharon L R Kardia
Journal:  Humanit Soc Sci Commun       Date:  2020-11-11

Review 10.  Patients' and public views and attitudes towards the sharing of health data for research: a narrative review of the empirical evidence.

Authors:  Shona Kalkman; Johannes van Delden; Amitava Banerjee; Benoît Tyl; Menno Mostert; Ghislaine van Thiel
Journal:  J Med Ethics       Date:  2019-11-12       Impact factor: 2.903

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