How fatigue is experienced and handled by female outpatients with inflammatory bowel disease

Bidragets oversatte titel: Hvordan fatigue opleves og håndteres af kvindelige patienter med inflammatoriske tarmlidelser

Anne Beck, Palle Bager, Peter Errboe Jensen, Jens F. Dahlerup

Publikation: Bidrag til tidsskriftTidsskriftsartikelForskningpeer review

Abstract

Background. Fatigue is a significant aspect of everyday life for patients with inflammatory bowel disease (IBD), and it influences their
health-related quality of life. Little is known about fatigue fromthe patient’s perspective. Aim. To investigate howfemale IBDpatients
experience and handle fatigue. Methods. The study included 11 female outpatients. These patients were 40–59 years old and had
IBD ≥ one year and a significantly increased fatigue score. Patients with severe active IBD, anaemia, comorbidity, or pregnancy were
excluded. The included patients agreed to participate in a semistructured interview. The interviews were analysed usingMalterud’s
principles of systematic text condensation. Results. The patients described physical and mental symptoms of fatigue that led to
social-, physical-, andwork-related limitationswith emotional consequences. To handle fatigue, the patients used planning, priority,
acceptance, exercise, and support. Two of the eleven patients used exercise on a regular basis. Surprisingly, some patients indicated
that they did not need to talk with professionals about their fatigue unless a cure was available. Conclusion. Fatigue in IBD includes
physical andmental symptoms that limit the patients’ social-, physical-, andwork-related lives.Despite this, some patients expressed
that they had chosen to accept their fatigue.
Bidragets oversatte titelHvordan fatigue opleves og håndteres af kvindelige patienter med inflammatoriske tarmlidelser
OriginalsprogEngelsk
Artikelnummer153818
TidsskriftGastroenterology Research and Practice
Antal sider8
ISSN1687-6121
StatusUdgivet - 2013

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