Narrative Accounts of Youth and Their Mothers With Chronic Headache: Application of a Socio-narratology Framework to Pain Narratives.


Journal

The Clinical journal of pain
ISSN: 1536-5409
Titre abrégé: Clin J Pain
Pays: United States
ID NLM: 8507389

Informations de publication

Date de publication:
01 Oct 2024
Historique:
received: 06 09 2023
accepted: 06 08 2024
medline: 13 9 2024
pubmed: 13 9 2024
entrez: 13 9 2024
Statut: epublish

Résumé

This study was the first to apply a socio-narratology framework to the narratives about child pain as told by youth with chronic pain and their parents, all of whom experience chronic headaches. Storytelling is a powerful social transaction that occurs within systems (eg, families, clinical encounters) and is both shaped by, and can shape, the pain experience. Narrative can be harnessed as a clinical tool to aid in the ability to listen, understand, and improve clinical encounters. Twenty-six youth (aged 11 to 18 y) and their mothers, both with chronic headaches, recruited from a tertiary level pediatric pain clinic separately completed in-depth interviews about children's pain journey narratives. Data were analyzed using narrative analysis, which incorporated elements of socio-narratology to compare similarities and differences between and within dyads' narratives. Five narrative types were generated: (1) The trauma origin story-parents, but not youth, positing traumatic events as the causal link to children's pain; (2) mistreated by the medical system-neglect, harm, and broken promises resulting in learned hopelessness or relying on the family system; (3) the invalidated-invalidation of pain permeated youth's lives, with mothers as empathic buffers; (4) washed away by the pain-challenges perceived as insurmountable and letting the pain take over; and (5) taking power back from pain-youth's ability to live life and accomplish goals despite the pain. Findings support the clinical utility of narrative in pediatric pain, including both parents' and youths' narrative accounts to improve clinical encounters and cocreate more youth-centred, empowering narratives.

Sections du résumé

OBJECTIVES OBJECTIVE
This study was the first to apply a socio-narratology framework to the narratives about child pain as told by youth with chronic pain and their parents, all of whom experience chronic headaches.
BACKGROUND BACKGROUND
Storytelling is a powerful social transaction that occurs within systems (eg, families, clinical encounters) and is both shaped by, and can shape, the pain experience. Narrative can be harnessed as a clinical tool to aid in the ability to listen, understand, and improve clinical encounters.
METHODS METHODS
Twenty-six youth (aged 11 to 18 y) and their mothers, both with chronic headaches, recruited from a tertiary level pediatric pain clinic separately completed in-depth interviews about children's pain journey narratives. Data were analyzed using narrative analysis, which incorporated elements of socio-narratology to compare similarities and differences between and within dyads' narratives.
RESULTS RESULTS
Five narrative types were generated: (1) The trauma origin story-parents, but not youth, positing traumatic events as the causal link to children's pain; (2) mistreated by the medical system-neglect, harm, and broken promises resulting in learned hopelessness or relying on the family system; (3) the invalidated-invalidation of pain permeated youth's lives, with mothers as empathic buffers; (4) washed away by the pain-challenges perceived as insurmountable and letting the pain take over; and (5) taking power back from pain-youth's ability to live life and accomplish goals despite the pain.
CONCLUSION CONCLUSIONS
Findings support the clinical utility of narrative in pediatric pain, including both parents' and youths' narrative accounts to improve clinical encounters and cocreate more youth-centred, empowering narratives.

Identifiants

pubmed: 39268725
doi: 10.1097/AJP.0000000000001238
pii: 00002508-202410000-00003
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

588-600

Informations de copyright

Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

This work was supported by research funding awarded to M.N. from the Vi Riddell Pediatric Pain Initiative, Alberta Children’s Hospital Foundation and Alberta Children’s Hospital Research Institute (Calgary, AB, Canada), and the Canadian Institutes of Health Research Strategy for Patient-Oriented Research “Chronic Pain Network” (Hamilton, ON, Canada). T.L. was supported by a graduate award from the Canadian Institutes of Health Research. The remaining authors declare no conflict of interest.

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Auteurs

Tatiana Lund (T)

Department of Psychology, University of Calgary, Calgary, Canada.

Alexandra Neville (A)

Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University, Stanford.

Abbie Jordan (A)

Department of Psychology and Centre for Pain Research, University of Bath, Bath, UK.

Bernie Carter (B)

Faculty of Health, Social Care and Medicine, Edge Hill University, Ormskirk, UK.

Janice Sumpton (J)

Department of Pharmacy, London Sciences Health Centre, Person With Lived Experience, London, UK.

Melanie Noel (M)

Department of Psychology, University of Calgary, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, Owerko Centre, Calgary, Canada.

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