Literature DB >> 21521585

Information infrastructure for consumer health: a health information exchange stakeholder study.

Judah Thornewill1, Alan F Dowling, Barbara A Cox, Robert J Esterhay.   

Abstract

BACKGROUND: An enabling infrastructure for population-wide health information capture and transfer is beginning to emerge in the U.S. However, the essential infrastructure component that is still missing is effective health information exchange (HIE). Health record banks (HRBs) are one of several possible approaches to achieving HIE. Is the approach viable? If so, what requirements must be satisfied in order for it to succeed?
PURPOSE: The research, conducted in 2007-2008, explored HRB-related interests, concerns, benefits, payment preferences, design requirements, value propositions, and challenges for 12 healthcare stakeholder groups and the consumers they serve in a U.S. metropolitan area of 1.3 million people.
METHODS: A mixed-methods design was developed in a community action research context. Data were gathered and analyzed through 23 focus groups, 13 web surveys, a consumer phone survey (nonstratified random sample) and follow-up meetings. Recruiting goals for leaders representing targeted groups were achieved using a multi-channel communications strategy. Key themes were identified through data triangulation. Then, requirements, value propositions and challenges were developed through iterative processes of interaction with community members.
RESULTS: Results include key themes, design requirements, value propositions, and challenges for 12 stakeholder groups and consumers.
CONCLUSIONS: The research provides a framework for developing a consumer permission-driven, financially sustainable, community HRB model. However, for such a model to flourish, it will need to be part of a nationwide network of HIEs with compatible HRB approaches able to overcome a number of challenges.
Copyright © 2011 American Journal of Preventive Medicine. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21521585     DOI: 10.1016/j.amepre.2011.01.010

Source DB:  PubMed          Journal:  Am J Prev Med        ISSN: 0749-3797            Impact factor:   5.043


  4 in total

1.  Disclosing Genetic Risk for Coronary Heart Disease: Attitudes Toward Personal Information in Health Records.

Authors:  Sherry-Ann Brown; Hayan Jouni; Tariq S Marroush; Iftikhar J Kullo
Journal:  Am J Prev Med       Date:  2017-01-03       Impact factor: 5.043

2.  Sustainability considerations for health research and analytic data infrastructures.

Authors:  Adam Wilcox; Gurvaneet Randhawa; Peter Embi; Hui Cao; Gilad J Kuperman
Journal:  EGEMS (Wash DC)       Date:  2014-09-17

3.  Health information exchange policies of 11 diverse health systems and the associated impact on volume of exchange.

Authors:  N Lance Downing; Julia Adler-Milstein; Jonathan P Palma; Steven Lane; Matthew Eisenberg; Christopher Sharp; Christopher A Longhurst
Journal:  J Am Med Inform Assoc       Date:  2016-06-14       Impact factor: 4.497

4.  Geographical distribution of patients visiting a health information exchange in New York City.

Authors:  Arit Onyile; Sandip R Vaidya; Gilad Kuperman; Jason S Shapiro
Journal:  J Am Med Inform Assoc       Date:  2012-10-27       Impact factor: 4.497

  4 in total

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