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Showing result 1 - 5 of 16 swedish dissertations matching the above criteria.
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1. Homecare and technology : old dreams - new means?
Abstract : To meet the demands and to maintain an acceptable level of services in health and homecare, implementation and use of ICT as support for caring work, are increasing. The assumption is that technology will give rise to a large number of improvements, such as effectiveness and ability to follow up and evaluate the performance of the services provided. READ MORE
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2. Building Usability into Health Informatics : Development and Evaluation of Information Systems for Shared Homecare
Abstract : How can we develop usable and work process-oriented ICT systems for shared homecare?Shared homecare involves different professionals, consists of mobile work and requires immediate and ubiquitous access to patient-oriented information, supporting an integrated view on the care process.This thesis presents a new collaborative design method for user needs analysis and requirements specification in the context of health information systems development; the Multi-disciplinary Thematic Seminar (MdTS) method. READ MORE
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3. Sharing is Caring : Integrating Health Information Systems to Support Patient-Centred Shared Homecare
Abstract : In the light of an ageing society with shrinking economic resources, deinstitutionalization of elderly care is a general trend. As a result, homecare is increasing, and increasingly shared between different health and social care organizations. To provide a holistic overview about the patient care process, i.e. READ MORE
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4. Unravelling the duality of Caregivinghood - How informal caregivers describe their situation when salutogenically approached
Abstract : Demographic changes and an emphasis on community care, increase the number of informal caregivers to older adults in most societies. Their willingness to provide care and that they are healthy enough to manage, is essential. READ MORE
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5. Patients' quality of life - Living with incurable cancer in palliative homecare
Abstract : My clinical experience is that living in incurable cancer at the end of life is complex to patients and their families. Patients seem to have a rather good quality of life (QoL) but problems related to the progression of the illness constantly challenges and changes QoL. READ MORE