Literature DB >> 35181825

Caregiver perspectives of dialysis initiation for children with kidney disease: a qualitative study.

Taylor R House1, Abby R Rosenberg2, Cortney T Zimmerman3, Krysta S Barton4, Aaron Wightman2.   

Abstract

BACKGROUND: To better support family-centered care surrounding dialysis initiation, greater understanding of caregiver experience is necessary.
METHODS: Using thematic analysis, we conducted a secondary analysis of semi-structured interview data from a qualitative study of caregivers of children receiving dialysis recruited from 3 pediatric centers. Prominent themes in caregiver experience of caring for a child initiating dialysis were identified.
RESULTS: Thirty-five caregivers participated. Three major themes emerged from qualitative analysis: (1) parenting disrupted - caregivers experienced an acute disruption in their parenting role due to the unexpected, emergent circumstances and vast information accompanying their child's diagnosis; (2) redefining parenting - caregivers sought to reestablish their innate parental role and foster their evolving medical provider role through reassurance that their child could survive, communication with the medical team, and engaging in care plan development; and (3) leveraging dual identities - to positively impact their child's experience and enable flourishing, caregivers leveraged their established caregiver role and newly realized medical provider role through voicing their perspectives, watching over their child's care, and preparing for future changes in their child's health. If caregivers' evolution was not nurtured and enabled, acute fluctuations in their child's care could contribute to future disruption and need to restore their parental role. However, if caregiver development was fostered, caregivers acquired increased ability to prepare for vacillations in their child's care.
CONCLUSIONS: Improving delivery of family-centered care and support of caregivers at dialysis initiation will require directed efforts by nephrology care teams to foster caregiver evolution and resilience and respond to the family's changing experience of kidney disease. A higher resolution version of the Graphical abstract is available as Supplementary information.
© 2022. The Author(s), under exclusive licence to International Pediatric Nephrology Association.

Entities:  

Keywords:  Caregiver burden; Dialysis initiation; Family-centered care; Patient-centered care; Pediatric

Mesh:

Year:  2022        PMID: 35181825     DOI: 10.1007/s00467-022-05472-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.651


  22 in total

1.  Generating best evidence from qualitative research: the role of data analysis.

Authors:  Julie Green; Karen Willis; Emma Hughes; Rhonda Small; Nicky Welch; Lisa Gibbs; Jeanne Daly
Journal:  Aust N Z J Public Health       Date:  2007-12       Impact factor: 2.939

Review 2.  In their own words: the value of qualitative research to improve the care of children with chronic kidney disease.

Authors:  Camilla S Hanson; Jonathan C Craig; Allison Tong
Journal:  Pediatr Nephrol       Date:  2016-10-15       Impact factor: 3.714

3.  Taking it day by day: when children undergo hemodialysis and renal transplantation.

Authors:  M R Crittenden; E Waechter; C A Mikklesen
Journal:  Child Today       Date:  1977 May-Jun

Review 4.  Sustaining life or prolonging dying? Appropriate choice of conservative care for children in end-stage renal disease: an ethical framework.

Authors:  Janis M Dionne; Lori d'Agincourt-Canning
Journal:  Pediatr Nephrol       Date:  2014-10-21       Impact factor: 3.714

5.  Child and Parental Perspectives on Communication and Decision Making in Pediatric CKD: A Focus Group Study.

Authors:  Talia Gutman; Camilla S Hanson; Sarah Bernays; Jonathan C Craig; Aditi Sinha; Allison Dart; Allison A Eddy; Debbie S Gipson; Detlef Bockenhauer; Hui-Kim Yap; Jaap Groothoff; Michael Zappitelli; Nicholas J A Webb; Stephen I Alexander; Stuart L Goldstein; Susan Furth; Susan Samuel; Tom Blydt-Hansen; Janis Dionne; Mini Michael; Scott E Wenderfer; Wolfgang C Winkelmayer; Helen Currier; Steven McTaggart; Amanda Walker; Angelique F Ralph; Angela Ju; Laura J James; Simon Carter; Allison Tong
Journal:  Am J Kidney Dis       Date:  2018-07-03       Impact factor: 8.860

6.  Quality of life among siblings of patients with chronic conditions.

Authors:  Jenny Velasco; Verónica Ferraris; Alfredo Eymann; Paula A Coccia; Lidia R Ghezzi; María C Sánchez; Carmen L De Cunto; Daniel D'Agostino; Jorge R Ferraris
Journal:  Arch Argent Pediatr       Date:  2020-08       Impact factor: 0.635

7.  Medical traumatic stress symptoms in pediatric patients on dialysis and their caregivers: a pilot study.

Authors:  Shari K Neul
Journal:  Nephrol Nurs J       Date:  2012 Nov-Dec       Impact factor: 0.959

Review 8.  Promoting resilience among parents and caregivers of children with cancer.

Authors:  Abby R Rosenberg; K Scott Baker; Karen L Syrjala; Anthony L Back; Joanne Wolfe
Journal:  J Palliat Med       Date:  2013-05-06       Impact factor: 2.947

9.  Family-centered care: current applications and future directions in pediatric health care.

Authors:  Dennis Z Kuo; Amy J Houtrow; Polly Arango; Karen A Kuhlthau; Jeffrey M Simmons; John M Neff
Journal:  Matern Child Health J       Date:  2012-02

10.  Perceptions of pediatric nephrologists regarding timing of dialysis initiation in children in Canada.

Authors:  Jeremy A Saban; Michael Zappitelli; Susan M Samuel; Manish M Sood; R Todd Alexander; Steven Arora; Robin L Erickson; Kristine Kroeker; Braden J Manns; Allison B Dart
Journal:  Can J Kidney Health Dis       Date:  2016-07-01
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