Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2249
Title: Child and caregiver perspectives on access to psychosocial and educational support in pediatric chronic kidney disease: a focus group study
Authors: Zimmerman, C. T.
Winkelmayer, W. C.
McTaggart, S.
Walker, A.
Ralph, A. F.
Hanson, C. S.
James, L. J.
Ju, A.
Zhang, Y.
Gutman, T.
Tong, A.
Craig, J. C.
Sinha, A.
Dart, A.
Eddy, A. A.
Gipson, D. S.
Bockenhauer, D.
Yap, H. K.
Groothoff, J.
Zappitelli, M.
N, J. A. Webb
Alexander, S. I.
Furth, S.
Samuel, S.
Blydt-Hansen, T. D.
Dionne, J.
Michael, M.
Wenderfer, S. E.
Issue Date: 2022
Source: Apr 26 , 2022
Journal: Pediatr Nephrol
Abstract: BACKGROUND: Children with chronic kidney disease (CKD) generally have worse educational and psychosocial outcomes compared with their healthy peers. This can impair their ability to manage their treatment, which in turn can have long-term health consequences through to adulthood. We attempted to capture the experiences of children with CKD and to describe the perspectives of their parents and caregivers on access to educational and psychosocial support. METHODS: Children with CKD (n = 34) and their caregivers (n = 62) were sampled via focus groups from pediatric hospitals in Australia, Canada, and the USA. Sixteen focus groups were convened and the transcripts were analyzed thematically. RESULTS: We identified four themes: disruption to self-esteem and identity (emotional turmoil of adolescence, wrestling with the sick self, powerlessness to alleviate child's suffering, balancing normality and protection); disadvantaged by lack of empathy and acceptance (alienated by ignorance, bearing the burden alone); a hidden and inaccessible support system (excluded from formal psychological support, falling behind due to being denied special considerations); and building resilience (finding partners in the journey, moving towards acceptance of the illness, re-establishing childhood). CONCLUSIONS: Children with CKD and their caregivers encountered many barriers in accessing psychosocial and educational support and felt extremely disempowered and isolated as a consequence. Improved availability and access to psychosocial and educational interventions are needed to improve the wellbeing and educational advancement of children with CKD. A higher resolution version of the Graphical abstract is available as Supplementary information.1432-198xZhang, Yifan
Orcid: 0000-0003-0716-4246
Gutman, Talia
Tong, Allison
Craig, Jonathan C
Sinha, Aditi
Dart, Allison
Eddy, Allison A
Gipson, Debbie S
Bockenhauer, Detlef
Yap, Hui-Kim
Groothoff, Jaap
Zappitelli, Michael
J A Webb, Nicholas
Alexander, Stephen I
Furth, Susan
Samuel, Susan
Blydt-Hansen, Tom D
Dionne, Janis
Michael, Mini
Wenderfer, Scott E
Winkelmayer, Wolfgang C
McTaggart, Steven
Walker, Amanda
Zimmerman, Cortney T
Ralph, Angelique F
Ju, Angela
James, Laura J
Hanson, Camilla S
ID1197324/National Health and Medical Research Council/
ID1092957/National Health and Medical Research Council/
ID1169149/National Health and Medical Research Council/
Robinson Fellowship/The University of Sydney/
Journal Article
Germany
Pediatr Nephrol. 2022 Apr 26. doi: 10.1007/s00467-022-05551-z.
DOI: 10.1007/s00467-022-05551-z
Keywords: Psychosocial;Mental health;Education;AdolescenceChronic kidney disease
Type: Article
Appears in Sites:Children's Health Queensland Publications

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