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National electronic health records and the digital disruption of moral orders

Author

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  • Garrety, Karin
  • McLoughlin, Ian
  • Wilson, Rob
  • Zelle, Gregor
  • Martin, Mike

Abstract

The digitalisation of patient health data to provide national electronic health record systems (NEHRS) is a major objective of many governments. Proponents claim that NEHRS will streamline care, reduce mistakes and cut costs. However, building these systems has proved highly problematic. Using recent developments in Australia as an example, we argue that a hitherto unexamined source of difficulty concerns the way NEHRS disrupt the moral orders governing the production, ownership, use of and responsibility for health records. Policies that pursue digitalisation as a self-evident ‘solution’ to problems in healthcare without due regard to these disruptions risk alienating key stakeholders. We propose a more emergent approach to the development and implementation of NEHRS that supports moral re-ordering around rights and responsibilities appropriate to the intentions of those involved in healthcare relationships.

Suggested Citation

  • Garrety, Karin & McLoughlin, Ian & Wilson, Rob & Zelle, Gregor & Martin, Mike, 2014. "National electronic health records and the digital disruption of moral orders," Social Science & Medicine, Elsevier, vol. 101(C), pages 70-77.
  • Handle: RePEc:eee:socmed:v:101:y:2014:i:c:p:70-77
    DOI: 10.1016/j.socscimed.2013.11.029
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    References listed on IDEAS

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    1. Wei-Chih Lu & I-Ching Tsai & Kuan-Chung Wang & Te-Ai Tang & Kuan-Chen Li & Ya-Ci Ke & Peng-Ting Chen, 2021. "Innovation Resistance and Resource Allocation Strategy of Medical Information Digitalization," Sustainability, MDPI, vol. 13(14), pages 1-20, July.
    2. Assing Hvidt, Elisabeth & Grønning, Anette & Nisbeth Brøgger, Matilde & Møller, Jane Ege & Fage-Butler, Antoinette, 2021. "Multilevel structures and human agency in relation to email consultations: A strong structuration theory analysis of the Danish general practice setting," Social Science & Medicine, Elsevier, vol. 282(C).
    3. Kirsikka Grön, 2021. "Common good in the era of data-intensive healthcare," Palgrave Communications, Palgrave Macmillan, vol. 8(1), pages 1-10, December.
    4. Cherif, Emna & Bezaz, Nora & Mzoughi, Manel, 2021. "Do personal health concerns and trust in healthcare providers mitigate privacy concerns? Effects on patients’ intention to share personal health data on electronic health records," Social Science & Medicine, Elsevier, vol. 283(C).
    5. John Grin & Jan Hassink & Vanja Karadzic & Ellen H.M. Moors, 2018. "Transformative Leadership and Contextual Change," Sustainability, MDPI, vol. 10(7), pages 1-14, June.
    6. Vale, Mira D. & Perkins, Denise White, 2022. "Discuss and remember: Clinician strategies for integrating social determinants of health in patient records and care," Social Science & Medicine, Elsevier, vol. 315(C).

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