Literature DB >> 25326601

Organizational strategies for promoting patient and provider uptake of personal health records.

Susan Wells1, Ronen Rozenblum2, Andrea Park2, Marie Dunn3, David W Bates4.   

Abstract

OBJECTIVE: To investigate organizational strategies to promote personal health records (PHRs) adoption with a focus on patients with chronic disease.
METHODS: Using semi-structured interviews and a web-based survey, we sampled US health delivery organizations which had implemented PHRs for at least 12 months, were recognized as PHR innovators, and had scored highly in national patient satisfaction surveys. Respondents had lead positions for clinical information systems or high-risk population management. Using grounded theory approach, thematic categories were derived from interviews and coupled with data from the survey.
RESULTS: Interviews were conducted with 30 informants from 16 identified organizations. Organizational strategies were directed towards raising patient awareness via multimedia communications, and provider acceptance and uptake. Strategies for providers were grouped into six main themes: organizational vision, governance and policies, work process redesign, staff training, information technology (IT) support, and monitoring and incentives. Successful organizations actively communicated their vision, engaged leaders at all levels, had clear governance, planning, and protocols, set targets, and celebrated achievement. The most effective strategy for patient uptake was through health professional encouragement. No specific outreach efforts targeted patients with chronic disease. Registration and PHR activity was routinely measured but without reference to a denominator population or high risk subpopulations. DISCUSSION AND
CONCLUSION: Successful PHR implementation represents a social change and operational project catalyzed by a technical solution. The key to clinician acceptance is making their work easier. However, organizations will likely not achieve the value they want from PHRs unless they target specific populations and monitor their uptake.
© The Author 2014. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For Permissions, please email: journals.permissions@oup.comFor numbered affiliations see end of article.

Entities:  

Keywords:  adoption; chronic disease; electronic health records; personal health records; quality

Mesh:

Year:  2014        PMID: 25326601      PMCID: PMC4433381          DOI: 10.1136/amiajnl-2014-003055

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  26 in total

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Journal:  Am J Kidney Dis       Date:  2012-11-21       Impact factor: 8.860

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Authors:  Anuj K Dalal; Patricia C Dykes; Sarah Collins; Lisa Soleymani Lehmann; Kumiko Ohashi; Ronen Rozenblum; Diana Stade; Kelly McNally; Constance R C Morrison; Sucheta Ravindran; Eli Mlaver; John Hanna; Frank Chang; Ravali Kandala; George Getty; David W Bates
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5.  Lessons learned implementing a complex and innovative patient safety learning laboratory project in a large academic medical center.

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6.  Personal health records in the Netherlands: potential user preferences quantified by a discrete choice experiment.

Authors:  Domino Determann; Mattijs S Lambooij; Dorte Gyrd-Hansen; Esther W de Bekker-Grob; Ewout W Steyerberg; Marcel Heldoorn; Line Bjørnskov Pedersen; G Ardine de Wit
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10.  The organizational dynamics enabling patient portal impacts upon organizational performance and patient health: a qualitative study of Kaiser Permanente.

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