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Identifying experiences of supportive care of children and young people affected by kidney failure: a qualitative systematic review.

Paterson, C.; Turner, M.; Hooper, M.‐E.; Ladbrook, E.; Macauley, L.; McKie, A.

Authors

C. Paterson

M. Turner

M.‐E. Hooper

E. Ladbrook

L. Macauley

A. McKie



Abstract

Children and young people affected by kidney failure experience complexities in their care. Little is known about the unique needs of this young patient population group living with a long-term condition. A meta-aggregation of all qualitative studies was conducted to identify experiences of supportive care among children and young people living with kidney failure. A systematic review of qualitative studies was conducted following the Joanna Briggs Institute meta-aggregation method. This review has been reported according to the PRISMA statement guidelines. Six electronic databases (CINAHL, Cochrane Library, MEDLINE, Proquest, PsycINFO, and Scopus) were comprehensively searched by an expert systematic review librarian using keywords and subject headings, from inception to September 2022. All studies were accessed using a predetermined inclusion and exclusion criteria. Methodological quality assessment and data extraction performed. Qualitative findings accompanied by illustrative quotes from included studies were extracted and grouped into categories which created the overall synthesised findings. A total of 34 studies were included in this review representing a total of 613 children and young people affected by kidney failure. There was a total of 190 findings which created 13 categories representing experiences of supportive care. The meta-aggregation developed five synthesised findings namely: 'physical needs', 'information and technology', 'treatment and healthcare', 'social needs' and 'psychological impacts'. This systematic review identified that children and young people affected by kidney failure can experience a range of unmet supportive care needs in routine clinical services. Kidney failure impacted children and young people's self-identify, social and peer networks, introduced daily practical needs because of inherent physical and psychological burden due to the failure and associated treatments. Despite improvements in the medical management of kidney failure in children and young people, further attention is needed to optimise supported self-management in this young patient group.

Citation

PATERSON, C., TURNER, M., HOOPER, M.-E., LADBROOK, E., MACAULEY, L. and MCKIE, A. 2024. Identifying experiences of supportive care of children and young people affected by kidney failure: a qualitative systematic review. Journal of renal care [online], 50(3), pages 252-274. Available from: https://doi.org/10.1111/jorc.12484

Journal Article Type Review
Acceptance Date Nov 19, 2023
Online Publication Date Dec 20, 2023
Publication Date Sep 30, 2024
Deposit Date Jan 8, 2024
Publicly Available Date Jan 8, 2024
Journal Journal of renal care
Print ISSN 1755-6678
Electronic ISSN 1755-6686
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 50
Issue 3
Pages 252-274
DOI https://doi.org/10.1111/jorc.12484
Keywords Qualitative; Systematic review; Supportive care; Young adults; Children; Renal failure
Public URL https://rgu-repository.worktribe.com/output/2188294
Additional Information This article has been published with separate supporting information. This supporting information has been incorporated into a single file on this repository and can be found at the end of the file associated with this output.

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Copyright Statement
© 2023 The Authors. Journal of Renal Care published by John Wiley & Sons Ltd on behalf of European Dialysis & Transplant Nurses Association/European Renal Care Association. This is an open access
article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.





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