Literature DB >> 20697469

A patient survey assessing the awareness and acceptability of the emergency care summary and its consent model in Scotland.

Chris Johnstone1, Gerry McCartney.   

Abstract

BACKGROUND: The Emergency Care Summary (ECS) was introduced in 2006 to allow aspects of the general practitioner (GP; family doctor, equivalent to primary care physician) medical record to be viewed in hospitals and out-of-hours centers in Scotland. Records were automatically uploaded unless patients actively opted out. This study investigated patient awareness and acceptance of this process.
METHODS: This was a questionnaire survey of patients in a GP surgery (office) in Paisley, Scotland.
RESULTS: Survey results indicated that 42 percent of patients were aware of the ECS, and 16 percent said that they recognized the leaflet posted to households. Of those who recognized the leaflet, 92 percent said they were happy for their record to be part of the system, while the others did not realize their record was to be included. Having read the leaflet, 97 percent said that they were happy for their record to be included in the ECS.
CONCLUSIONS: This study shows that most patients were not aware of the Emergency Care Summary or did not remember seeing the leaflet posted to households. Having read the leaflet, the vast majority of patients were happy for their records to be included in the system. The low awareness of the ECS calls into question the validity of an implied consent model using an information leaflet distributed by post.

Entities:  

Keywords:  Emergency Care Summary; Summary Care Record; confidentiality; consent; electronic care summary; implied consent; informed consent

Mesh:

Year:  2010        PMID: 20697469      PMCID: PMC2889371     

Source DB:  PubMed          Journal:  Perspect Health Inf Manag        ISSN: 1559-4122


  3 in total

1.  Informed consent and the security of the electronic health record (EHR): some policy considerations.

Authors:  Eike-Henner W Kluge
Journal:  Int J Med Inform       Date:  2004-03-31       Impact factor: 4.046

2.  Lessons from the central Hampshire electronic health record pilot project: issues of data protection and consent.

Authors:  Trina Adams; Martin Budden; Chris Hoare; Hugh Sanderson
Journal:  BMJ       Date:  2004-04-10

3.  Computer records.

Authors:  A Gordon Baird; C Mary Donnelly
Journal:  Br J Gen Pract       Date:  2007-06       Impact factor: 5.386

  3 in total
  3 in total

1.  Consumer support for health information exchange and personal health records: a regional health information organization survey.

Authors:  Vaishali N Patel; Rina V Dhopeshwarkar; Alison Edwards; Yolanda Barrón; Jeffrey Sparenborg; Rainu Kaushal
Journal:  J Med Syst       Date:  2010-07-29       Impact factor: 4.460

2.  Patient consent and opting-out.

Authors:  A Gordon Baird
Journal:  Br J Gen Pract       Date:  2015-11       Impact factor: 5.386

3.  A novel metadata management model to capture consent for record linkage in longitudinal research studies.

Authors:  Christiana McMahon; Spiros Denaxas
Journal:  Inform Health Soc Care       Date:  2017-11-06       Impact factor: 2.439

  3 in total

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