Search for dissertations about: "patient preference"

Showing result 1 - 5 of 48 swedish dissertations containing the words patient preference.

  1. 1. Patient participation in clinical decsion making : A collaborative effort between patients and nurses

    Author : Jan Florin; Högskolan Dalarna; []
    Keywords : clinical decision making; patient participation; patient needs; nursing diagnosis; needs assessment; control preference scale;

    Abstract : The overall aim of the thesis was to study clinical decision making in nursing. This was performed by evaluation of the quality of nurses’ diagnostic statements and comparison of the concordance between nurses and patients’ perceptions of the patients’ nursing needs, as well as patient preferences for participation in clinical decision making. READ MORE

  2. 2. Patient participation in clinical decision making in nursing : a collaborative effort between patients and nurses

    Author : Jan Florin; Anna Ehrenberg; Margareta Ehnfors; Cornelia Ruland; Örebro universitet; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Clinical decision making; patient participation; nursing diagnosis; patient needs; nursing assessment; control preference scale; Caring sciences; Vårdvetenskap; Vårdvetenskap; Nursing Science;

    Abstract : The overall aim of the thesis was to study clinical decision making in nursing. This was performed by evaluation of the quality of nurses’ diagnostic statements and comparison of the concordance between nurses and patients’ perceptions of the patients’ nursing needs, as well as patient preferences for participation in clinical decision making. READ MORE

  3. 3. Patient Participation in Kidney Care : Patients’ and professionals’ perspectives

    Author : Caroline Hurtig; Ann Catrine Eldh; Fredrik Uhlin; Liselott Årestedt; Axel Wolf; Linköpings universitet; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; chronic kidney failure; long-term condition; mixedmethods; patient participation; person-centred care; qualitative research; quantitative research.;

    Abstract : Background: Patient participation is central to modern healthcare, known to enhance both physical health and well-being. However, the way in which a person prefers to engage can vary depending on their condition, knowledge, and healthcare context. READ MORE

  4. 4. Preference Effects in the Treatment of Panic Disorder

    Author : Martin Svensson; Institutionen för psykologi; []
    Keywords : SAMHÄLLSVETENSKAP; SOCIAL SCIENCES; Preference effects; Doubly randomised controlled preference trial; ; Panic disorder; Cognitive behavioural therapy; Psychodynamic therapy;

    Abstract : Patient preferences have drawn considerable attention as a potential moderator of treatment outcome. The Doubly Randomised Controlled Preference Trial (DRCPT) in which patients are randomised to a choice between two or more treatments or random assignment to one of these same treatments is considered one of the most rigorous tests of the effects of patient preferences on outcomes. READ MORE

  5. 5. Ethical Issues in Cardiology Patients' views of information and decision-making

    Author : Anders Ågård; Medicinsk etik; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Praktisk filosofi; estetik; metafysik; kunskapsteori; ideologi; ideology; decision-making; information disclosure; aesthetics; metaphysics; epistemology; ethics; Kardiovaskulära systemet; Systematic philosophy; Cardiovascular system; interview; atypical chest pain; acute myocardial infarction; cardiopulmonary resuscitation; implantable cardioverter defibrillator; heart failure; patient-caregiver communication; patient preference; informed consent;

    Abstract : The over-riding aim of this thesis was to obtain a deeper understanding of the way patients with cardiac problems view both information related to their health and medical decisions and their role in decision-making processes. An important objective was to identify reasons why patients do not ask for or assimilate information or why they do not want or feel that they are able to influence medical decisions. READ MORE