Associations between adherence, depressive symptoms and health-related quality of life in young adults with cystic fibrosis

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

K. B. Knudsen, T. Pressler, L. H. Mortensen, M. Jarden, M. Skov, A. L. Quittner, T. Katzenstein, K.A. Boisen

Background: Cystic fibrosis (CF) is a life shortening disease, however prognosis has improved and the adult population is growing. Most adults with cystic fibrosis live independent lives and balance the demands of work and family life with a significant treatment burden. The aim of this study was to examine the relationships among treatment adherence, symptoms of depression and health-related quality of life (HRQoL) in a population of young adults with CF.Methods: We administered three standardized questionnaires to 67 patients with CF aged 18–30 years; Morisky Medication Adherence Scale, Major Depression Inventory, and Cystic Fibrosis Questionnaire-Revised.Results: There was a response rate of 77 % and a majority of the young adults (84 %) were employed or in an education program. Most participants (74 %) reported low adherence to medications. One third (32.8 %) of the participants reported symptoms of depression. HRQoL scores were especially low on Vitality and Treatment Burden, and symptoms of depression were associated with low HRQoL scores (p < 0.01) with medium to large deficits across on all HRQoL domains (Cohen’s d 0.60–1.72) except for the domain treatment burden. High depression symptom scores were associated with low adherence (r = −0.412, p < 0.001).Conclusions: Despite improved physical health, many patients with CF report poor adherence, as well as impaired mental wellbeing and HRQoL. Thus, more attention to mental health issues is needed.
OriginalsprogEngelsk
Artikelnummer1216
TidsskriftSpringerPlus
Vol/bind5
Antal sider8
ISSN2193-1801
DOI
StatusUdgivet - 2016

Bibliografisk note

Erratum to: Associations between adherence, depressive symptoms and health-related quality of life in young adults with cystic fibrosis. DOI: 10.1186/s40064-017-3789-1

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