Literature DB >> 27269277

Use of the My Health Record by people with communication disability in Australia: A review to inform the design and direction of future research.

Bronwyn Hemsley1, Andrew Georgiou2, Rob Carter3, Sophie Hill4, Isabel Higgins5, Paulette van Vliet5, Susan Balandin3.   

Abstract

BACKGROUND: People with communication disability often struggle to convey their health information to multiple service providers and are at increased risk of adverse health outcomes related to the poor exchange of health information.
OBJECTIVE: The purpose of this article was to (a) review the literature informing future research on the Australian personally controlled electronic health record, 'My Health Record' (MyHR), specifically to include people with communication disability and their family members or service providers, and (b) to propose a range of suitable methodologies that might be applied in research to inform training, policy and practice in relation to supporting people with communication disability and their representatives to engage in using MyHR.
METHOD: The authors reviewed the literature and, with a cross-disciplinary perspective, considered ways to apply sociotechnical, health informatics, and inclusive methodologies to research on MyHR use by adults with communication disability. RESEARCH OUTCOMES: This article outlines a range of research methods suitable for investigating the use of MyHR by people who have communication disability associated with a range of acquired or lifelong health conditions, and their family members, and direct support workers.
CONCLUSION: In planning the allocation of funds towards the health and well-being of adults with disabilities, both disability and health service providers must consider the supports needed for people with communication disability to use MyHR. There is an urgent need to focus research efforts on MyHR in populations with communication disability, who struggle to communicate their health information across multiple health and disability service providers. The design of studies and priorities for future research should be set in consultation with people with communication disability and their representatives.
© The Author(s) 2016.

Entities:  

Keywords:  communication; communication disabilities; disability; e-health; electronic health records; health communication; health equity; health information management; methods; personal health records; research

Mesh:

Year:  2016        PMID: 27269277     DOI: 10.1177/1833358316652060

Source DB:  PubMed          Journal:  Health Inf Manag        ISSN: 1833-3583            Impact factor:   3.185


  4 in total

1.  The E-health Literacy Demands of Australia's My Health Record: A Heuristic Evaluation of Usability.

Authors:  Louisa Walsh; Bronwyn Hemsley; Meredith Allan; Natalie Adams; Susan Balandin; Andrew Georgiou; Isabel Higgins; Shaun McCarthy; Sophie Hill
Journal:  Perspect Health Inf Manag       Date:  2017-10-01

Review 2.  Understanding digital health ecosystem from Australian citizens' perspective: A scoping review.

Authors:  Abraham Oshni Alvandi; Chris Bain; Frada Burstein
Journal:  PLoS One       Date:  2021-11-15       Impact factor: 3.240

3.  Energy efficiency in software: A case study on sustainability in personal health records.

Authors:  José A García-Berná; José L Fernández-Alemán; Juan M Carrillo de Gea; Ambrosio Toval; Javier Mancebo; Coral Calero; Félix García
Journal:  J Clean Prod       Date:  2020-09-22       Impact factor: 9.297

4.  Assessing the information quality and usability of My Health Record within a health literacy framework: What's changed since 2016?

Authors:  Louisa Walsh; Bronwyn Hemsley; Meredith Allan; Maria R Dahm; Susan Balandin; Andrew Georgiou; Isabel Higgins; Shaun McCarthy; Sophie Hill
Journal:  Health Inf Manag       Date:  2019-08-01       Impact factor: 3.185

  4 in total

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