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

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.

[1]  Jonathan D. Gold,et al.  Banking on health: Personal records and information exchange. , 2006, Journal of healthcare information management : JHIM.

[2]  R. Esterhay,et al.  Capitalizing the NHIN: a strategy for funding an integrated nationwide network of community HIEs. , 2007, Journal of healthcare information management : JHIM.

[3]  Alan F. Dowling,et al.  CHINs—The Current State , 1997 .

[4]  eHealth Initiative Migrating Toward Meaningful Use: the State of Health Information Exchange , 2009 .

[5]  D. McGraw,et al.  Privacy as an enabler, not an impediment: building trust into health information exchange. , 2009, Health affairs.

[6]  Walter Sujansky,et al.  Retrospective: lessons learned from the Santa Barbara project and their implications for health information exchange. , 2007, Health affairs.

[7]  Andrew P. McAfee,et al.  The state of regional health information organizations: current activities and financing. , 2007, Health affairs.

[8]  Meredith Minkler,et al.  Community-based research partnerships: Challenges and opportunities , 2005, Journal of Urban Health.

[9]  Judah Thornewill,et al.  The consumer's view of the electronic health record: engaging patients in EHR adoption. , 2008, Journal of healthcare information management : JHIM.

[10]  Douglas D. Perkins,et al.  Transdisciplinary, multilevel action research to enhance ecological and psychopolitical validity , 2008 .

[11]  Marion J. Ball,et al.  The Health Record Banking imperative: A conceptual model , 2007, IBM Syst. J..

[12]  R. Steinbrook Health care and the American Recovery and Reinvestment Act. , 2009, The New England journal of medicine.

[13]  B. Fried Gauging the Progress of the National Health Information Technology Initiative: Perspectives from the Field , 2008 .

[14]  P. Brennan,et al.  Information Networks for Community Health , 1997 .

[15]  Janet Marchibroda,et al.  The potential of HIEs as infomediaries. , 2007, Journal of healthcare information management : JHIM.

[16]  Mahesh S. Raisinghani,et al.  Personal health records: key adoption issues and implications for management , 2008, Int. J. Electron. Heal..

[17]  A. Shabo,et al.  A Global Socio-economic-medico-legal Model for the Sustainability of Longitudinal Electronic Health Records , 2006, Methods of Information in Medicine.

[18]  Charles Safran,et al.  Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper. , 2007, Journal of the American Medical Informatics Association : JAMIA.

[19]  David W. Bates,et al.  White Paper: Personal Health Records: Definitions, Benefits, and Strategies for Overcoming Barriers to Adoption , 2006, J. Am. Medical Informatics Assoc..

[20]  P Starr,et al.  Smart technology, stunted policy: developing health information networks. , 1997, Health affairs.

[21]  D. Bates,et al.  Patients’ Attitudes Toward Electronic Health Information Exchange: Qualitative Study , 2009, Journal of medical Internet research.

[22]  R. Steinbrook Personally controlled online health data--the next big thing in medical care? , 2008, The New England journal of medicine.

[23]  D H BYERS,et al.  Occupational Health Information Exchange. , 1957, Public health reports.

[24]  Elizabeth A November,et al.  Creating sustainable local health information exchanges: can barriers to stakeholder participation be overcome? , 2008, Research brief.

[25]  Isaac S Kohane,et al.  Tectonic shifts in the health information economy. , 2008, The New England journal of medicine.

[26]  J. Overhage Health information exchange: 'lex parsimoniae'. , 2007, Health affairs.

[27]  Linda L. Dimitropoulos,et al.  Privacy and Security Solutions for Interoperable Health Information Exchange , 2007 .

[28]  T. Jick Mixing Qualitative and Quantitative Methods: Triangulation in Action. , 1979 .