Literature DB >> 29039375

DataWell: Public Involvement in the Development of a Federated Platform for Shared Patient Records in Greater Manchester, U.K.

Gary Leeming1, Sarah Thew1.   

Abstract

Sharing personal health data for direct care, health improvement, planning and research is recognised as important to improving the quality and safety of care. However, the complexities of sharing data, including technology, information governance and consent issues, means that many projects have difficulty communicating with the public about why they wish to share data, or what the benefits might be. Great Manchester Academic Health Science Network has established a Public Experience Group to help co-design the requirements for a health information exchange, called DataWell, across over 30 health and care organisations in Greater Manchester. This group has allowed the programme to uniquely respond to questions of how consent and data sharing should work with DataWell for direct care, as well as exploring other uses of the data, including planning and research.

Entities:  

Keywords:  Public involvement; co-production; health information exchange; user centred design

Mesh:

Year:  2017        PMID: 29039375

Source DB:  PubMed          Journal:  Stud Health Technol Inform        ISSN: 0926-9630


  1 in total

1.  A Prerequisite for Patient Centred Care is Empowering and Engaging Patients in the Digital Health: Report from EFMI Special Topic Conference (STC) 2017.

Authors:  Simon de Lusignan
Journal:  Acta Inform Med       Date:  2017-12
  1 in total

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