The partner's perspective of the impact of pituitary disease: Looking beyond the patient.
caregivers
coping strategies
hypopituitarism
partners
pituitary adenomas
quality of life
Journal
Journal of health psychology
ISSN: 1461-7277
Titre abrégé: J Health Psychol
Pays: England
ID NLM: 9703616
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
pubmed:
16
8
2017
medline:
1
9
2020
entrez:
17
8
2017
Statut:
ppublish
Résumé
People with pituitary disease report impairments in quality of life. The aim of this study was to elucidate the impact of the pituitary condition on the lives of partners. Four focus groups of partners of people with pituitary disease (Cushing's disease, non-functioning adenoma, acromegaly, prolactinoma) were conducted. Partners mentioned worries related to the pituitary disease and negative beliefs about medication, coping challenges, relationship issues, social issues and unmet needs regarding care. This study emphasizes the importance of not only paying attention to psychosocial well-being of people with pituitary disease but also to their partners.
Identifiants
pubmed: 28810427
doi: 10.1177/1359105317695427
pmc: PMC6749171
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1687-1697Références
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