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Quality of Life and...
Quality of Life and Coping with Ulcerative colitis and Crohn's disease
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- Larsson, Kjerstin, 1952- (författare)
- Uppsala universitet,Institutionen för folkhälso- och vårdvetenskap
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- Nordin, Karin, Docent (preses)
- Uppsala universitet,Institutionen för folkhälso- och vårdvetenskap
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- Lööf, Lars, Professor (preses)
- Uppsala universitet,Centrum för klinisk forskning, Västerås
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- Wredling, Regina, Professor (opponent)
- Karolinska Institutet, Institutionen för neurobiologi, vårdvetenskap och samhälle
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(creator_code:org_t)
- ISBN 9789155470005
- Uppsala : Universitetsbiblioteket, 2007
- Engelska 71 s.
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Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Social Sciences, 1652-9030 ; 31
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Abstract
Ämnesord
Stäng
- The aim of this thesis was to investigate health-related quality of life (HRQoL) and coping strategies for individuals with ulcerative colitis (UC) or Crohn’s disease (CD), and to study the effect of a group-based patient information on anxiety/depression and HRQoL. HRQoL and anxiety/depression were investigated (n=492) (Study I). In Study II, anxiety/depression, HRQoL, satisfaction with information and evaluation of the patient information were studied (n=49). Coping with disease activity was investigated in 166 patients reporting current exacerbation (Study III). Fifteen patients were interviewed about disease-related stress, how this is managed and the need of support from the health care (Study IV). Patients with UC reported better HRQoL and less anxiety/depression than did patients with CD during both remission and exacerbation. Satisfaction with information had increased at follow-up 6 months after patient information. The information and the possibility to discuss with lecturers and group members were valued as most important. No change was found in anxiety/depression or HRQoL at follow-up. Both problem-focused and emotion-focused strategies were employed to cope with disease activity, with no difference between patients with UC or CD. The urgent need of toilet availability and stress associated to social situations were the major disease-related stressors. This stress was managed by finding out the location of toilets, bringing toilet paper and extra underwear and emptying bowel before an activity. The patients wanted information and possibilities to talk to experienced staff and to other patients about how to live with the disease. This thesis shows that HRQoL for some patients with UC, and primarily for patients with CD, is impaired. Thus medical staff should be observant of the psychosocial well-being of patients with CD and also of patients with relapse. Methods to identify and support patients with anxiety/depression and poor HRQoL need to be developed. Interventions should target the patient’s specific problems and at appropriate times.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Hälsovetenskap -- Omvårdnad (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Health Sciences -- Nursing (hsv//eng)
Nyckelord
- anxiety
- coping
- Crohn's disease
- depression
- exacerbation
- health-related quality of life
- ulcerative colitis
- Caring sciences
- Vårdvetenskap
Publikations- och innehållstyp
- vet (ämneskategori)
- dok (ämneskategori)
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