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‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study

OBJECTIVES: Persons with advanced chronic kidney disease (CKD) have unique support needs associated with managing a chronic yet often silent condition, complex treatment-related decisions and care transitions. The aim of this study was to explore perspectives on how peer support could address CKD su...

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Autores principales: Elliott, Meghan J, Love, Shannan, Fox, Danielle E, Verdin, Nancy, Donald, Maoliosa, Manns, Kate, Cunningham, David, Goth, Jill, Hemmelgarn, Brenda R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109100/
https://www.ncbi.nlm.nih.gov/pubmed/35551080
http://dx.doi.org/10.1136/bmjopen-2021-057518
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author Elliott, Meghan J
Love, Shannan
Fox, Danielle E
Verdin, Nancy
Donald, Maoliosa
Manns, Kate
Cunningham, David
Goth, Jill
Hemmelgarn, Brenda R
author_facet Elliott, Meghan J
Love, Shannan
Fox, Danielle E
Verdin, Nancy
Donald, Maoliosa
Manns, Kate
Cunningham, David
Goth, Jill
Hemmelgarn, Brenda R
author_sort Elliott, Meghan J
collection PubMed
description OBJECTIVES: Persons with advanced chronic kidney disease (CKD) have unique support needs associated with managing a chronic yet often silent condition, complex treatment-related decisions and care transitions. The aim of this study was to explore perspectives on how peer support could address CKD support needs and augment care. DESIGN: This study employed a qualitative descriptive methodology. Data were collected through focus groups (cofacilitated by patient partners) and semistructured interviews. SETTING: Four multidisciplinary CKD clinics across Southern Alberta, Canada. PARTICIPANTS: We purposively sampled among adult patients with advanced, non-dialysis CKD and their caregivers, as well as trained peer mentors from The Kidney Foundation of Canada’s Kidney Connect programme. ANALYSIS: Transcripts were coded in duplicate, and themes were generated inductively through a thematic analysis approach. RESULTS: We conducted seven focus groups with a total of 39 patient and caregiver participants. Seven patients and caregivers who were unable to attend a focus group and 13 peer mentors participated in a telephone interview. Although patients and caregivers had limited awareness of peer support, participants acknowledged its central role in affirming their experiences and enabling confidence to live well with kidney disease. We identified four themes related to the anticipated role of peer support in addressing support needs for people with non-dialysis CKD: (1) creating connection; (2) preparing for uncertainty; (3) adapting to new realities; and (4) responsive peer support delivery. Aligning peer support access with patient readiness and existing CKD management supports can promote optimism, community and pragmatic adaptations to challenges. CONCLUSIONS: Patients, caregivers and peer mentors highlighted a unique value in the shared experiences of CKD peers to anticipate and manage disease-related challenges and confidently face a future living with kidney disease.
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spelling pubmed-91091002022-05-27 ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study Elliott, Meghan J Love, Shannan Fox, Danielle E Verdin, Nancy Donald, Maoliosa Manns, Kate Cunningham, David Goth, Jill Hemmelgarn, Brenda R BMJ Open Renal Medicine OBJECTIVES: Persons with advanced chronic kidney disease (CKD) have unique support needs associated with managing a chronic yet often silent condition, complex treatment-related decisions and care transitions. The aim of this study was to explore perspectives on how peer support could address CKD support needs and augment care. DESIGN: This study employed a qualitative descriptive methodology. Data were collected through focus groups (cofacilitated by patient partners) and semistructured interviews. SETTING: Four multidisciplinary CKD clinics across Southern Alberta, Canada. PARTICIPANTS: We purposively sampled among adult patients with advanced, non-dialysis CKD and their caregivers, as well as trained peer mentors from The Kidney Foundation of Canada’s Kidney Connect programme. ANALYSIS: Transcripts were coded in duplicate, and themes were generated inductively through a thematic analysis approach. RESULTS: We conducted seven focus groups with a total of 39 patient and caregiver participants. Seven patients and caregivers who were unable to attend a focus group and 13 peer mentors participated in a telephone interview. Although patients and caregivers had limited awareness of peer support, participants acknowledged its central role in affirming their experiences and enabling confidence to live well with kidney disease. We identified four themes related to the anticipated role of peer support in addressing support needs for people with non-dialysis CKD: (1) creating connection; (2) preparing for uncertainty; (3) adapting to new realities; and (4) responsive peer support delivery. Aligning peer support access with patient readiness and existing CKD management supports can promote optimism, community and pragmatic adaptations to challenges. CONCLUSIONS: Patients, caregivers and peer mentors highlighted a unique value in the shared experiences of CKD peers to anticipate and manage disease-related challenges and confidently face a future living with kidney disease. BMJ Publishing Group 2022-05-12 /pmc/articles/PMC9109100/ /pubmed/35551080 http://dx.doi.org/10.1136/bmjopen-2021-057518 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Renal Medicine
Elliott, Meghan J
Love, Shannan
Fox, Danielle E
Verdin, Nancy
Donald, Maoliosa
Manns, Kate
Cunningham, David
Goth, Jill
Hemmelgarn, Brenda R
‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title_full ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title_fullStr ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title_full_unstemmed ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title_short ‘It’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
title_sort ‘it’s the empathy’—defining a role for peer support among people living with chronic kidney disease: a qualitative study
topic Renal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109100/
https://www.ncbi.nlm.nih.gov/pubmed/35551080
http://dx.doi.org/10.1136/bmjopen-2021-057518
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