You are not logged in.

Families as carers-information needs in a cultural context

Nguyen, Lemai and Shanks, Graeme 2007, Families as carers-information needs in a cultural context, in ACIS2007 Toowoomba 5 to 7 December 2007 : proceedings of the 18th Australasian conference on information systems: proceedings of the 18th Australasian conference, University of Southern Queensland, Toowoomba, QLD, pp. 1089-1098.

Attached Files
Name Description MIMEType Size Downloads

Title Families as carers-information needs in a cultural context
Author(s) Nguyen, LemaiORCID iD for Nguyen, Lemai
Shanks, Graeme
Conference name Conference on Information Systems (18th : 2007 : Toowoomba, Qld.)
Conference location Toowoomba, QLD
Conference dates 5-7 December 2007
Title of proceedings ACIS2007 Toowoomba 5 to 7 December 2007 : proceedings of the 18th Australasian conference on information systems: proceedings of the 18th Australasian conference
Editor(s) [Unknown]
Publication date 2007
Conference series Conference on Information Systems
Start page 1089
End page 1098
Publisher University of Southern Queensland
Place of publication Toowoomba, QLD
Keyword(s) health information systems
information needs
Summary While the important role of family as a carer has been increasingly recognised in healthcare service provision, particularly for patients with acute or chronic illnesses, the carer’s information needs have not been well understood and adequately supported by current health information systems. In order to effectively provide continuous and home-based care for the patient, a family relative as the primary carer needs sufficient access to medical knowledge and patient’s health information. There are two challenges. First, being a family relative, the primary carer is often a non-medical practitioner. Second, in Australia, many primary carers are family relatives of patients from a non-English speaking background. They are often seen as interpreters in clinical consultation sessions. Their roles and responsibilities as an interpreter and a carer are often mixed and blurry.
Therefore, their information needs are often seen as secondary to the patient or neglected. The primary carer’s information needs are currently not yet well understood.

This paper reports finding from a case study which examines an on-line diary of a husband-carer who provided support and care for his wife, who at the time of care was a lung cancer patient. The case study examines an ongoing learning process that the husband went through, identifies information needs by the carer and cultural factors which played an important role in the husband’s interpretation of information, decision making and provision of care. The finding extends a current model of the user’s information needs in the literature and suggests implications for further research into developing health information systems to meet information needs by the family carer.
ISBN 9780909756963
Language eng
Field of Research 111711 Health Information Systems (incl Surveillance)
HERDC Research category E1 Full written paper - refereed
Copyright notice ©Lemai Nguyen and Graeme Shanks, 2007
Persistent URL

Connect to link resolver
Unless expressly stated otherwise, the copyright for items in DRO is owned by the author, with all rights reserved.

Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 0 times in TR Web of Science
Scopus Citation Count Cited 3 times in Scopus
Google Scholar Search Google Scholar
Access Statistics: 672 Abstract Views, 0 File Downloads  -  Detailed Statistics
Created: Mon, 29 Sep 2008, 09:04:32 EST

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact