Young adults' perspectives on living with kidney failure: a systematic review and thematic synthesis of qualitative studies.
Author
Bailey, P. K.
Hamilton, A. J.
Clissold, Rhian L.
Inward, C. D.
Caskey, F. J.
Ben-Shlomo, Y.
Owen-Smith, A.
Date
2018-01Journal
BMJ openType
Journal ArticlePublisher
BMJDOI
10.1136/bmjopen-2017-019926Rights
Archived with thanks to BMJ open. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/ licenses/by-nc/4.0/Metadata
Show full item recordAbstract
Young adults fare worse than younger adolescents or older adults on a broad range of health indicators. Those with a chronic illness such as renal failure are a particularly vulnerable group, who experience poor outcomes compared with both children and older adults. Understanding how being in receipt of renal replacement therapy (RRT) affects the lives of young adults might help us to better prepare and support these individuals for and on RRT, and improve outcomes. This study aimed to synthesise research describing young adults' experiences of the psychosocial impact of kidney failure and RRT.