Literature DB >> 24503882

How outcomes are achieved through patient portals: a realist review.

Terese Otte-Trojel1, Antoinette de Bont1, Thomas G Rundall2, Joris van de Klundert1.   

Abstract

OBJECTIVE: To examine how patient portals contribute to health service delivery and patient outcomes. The specific aims were to examine how outcomes are produced, and how variations in outcomes can be explained.
METHODS: We used a realist review method, which aims to describe how 'an intervention works, for whom, and in what circumstances' by analyzing patterns between context, mechanism, and outcomes. We reviewed 32 evaluation studies of patient portals published since 2003.
RESULTS: The reviewed evaluations indicate that as a complement to existing health services, patient portals can lead to improvements in clinical outcomes, patient behavior, and experiences. Four different mechanisms are reported to yield the reported outcome improvements. These are patient insight into personal health information, activation of information, interpersonal continuity of care, and service convenience. The vast majority of evaluations were conducted in integrated health service networks in the USA, and we detected no substantial variation in outcomes across these networks. DISCUSSION AND
CONCLUSIONS: Patient portals may impact clinical outcomes and health service delivery through multiple mechanisms. Given the relative uniformity of evaluation contexts, we were not able to detect patterns in how patient portals work in different contexts. Nonetheless, it appears from the overwhelming proportion of patient portal evaluations coming from integrated health service networks, that these networks provide more fertile contexts for patient portals to be effective. To improve the understanding of how patient portals work, future evaluations of patient portals should capture information about mechanisms and context that influence their outcomes. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

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Year:  2014        PMID: 24503882      PMCID: PMC4078283          DOI: 10.1136/amiajnl-2013-002501

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


  35 in total

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8.  A research agenda for personal health records (PHRs).

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  62 in total

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Review 4.  Family Caregivers and Consumer Health Information Technology.

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Journal:  J Gen Intern Med       Date:  2015-08-27       Impact factor: 5.128

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7.  Identifying unmet informational needs in the inpatient setting to increase patient and caregiver engagement in the context of pediatric hematopoietic stem cell transplantation.

Authors:  Elizabeth Kaziunas; David A Hanauer; Mark S Ackerman; Sung Won Choi
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8.  Seeking health information online: does limited healthcare access matter?

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9.  A Model of Organizational Context and Shared Decision Making: Application to LGBT Racial and Ethnic Minority Patients.

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