"There's So Much More Support We Could Have Provided": Child Life Specialists' Stories of the Challenges Working in Adult Oncology.

challenges child life specialist death narrative oncology palliative care stress systemic barriers

Journal

Qualitative health research
ISSN: 1049-7323
Titre abrégé: Qual Health Res
Pays: United States
ID NLM: 9202144

Informations de publication

Date de publication:
30 Nov 2023
Historique:
medline: 1 12 2023
pubmed: 1 12 2023
entrez: 30 11 2023
Statut: aheadofprint

Résumé

A cancer diagnosis in patients who are parents of minor children is uniquely stressful for both parents and children. Children need developmentally appropriate information and support to help reduce their fears and worries. Child life specialists (CLSs) are health professionals who work in pediatric environments to support children and families with the stress and uncertainty of illnesses. Increasingly, CLSs have been called upon to support children of patients in adult clinical environments. Our objective was to elucidate CLS caregiving narratives related to working with children of adult cancer patients. We used narrative inquiry to interview four CLSs working in adult oncology. Canadian CLSs who have experience providing care for children and families affected by parental cancer were recruited via convenience sampling. We used narrative analysis methods that included multiple close reads of the data, generating narrative themes, and noting conflicts or tensions in the data. CLSs' caregiving stories often highlighted the complexities of working in an adult oncology environment. Their narratives included challenges in providing optimal care to the children, including family-level barriers (such as parental wishes to withhold information from their children) and systemic barriers (such as late referrals and limited options for bereavement support). CLS participants identified several challenges of working with families in adult oncology. The CLSs highlighted a desire for additional institutional support for children of adult oncology patients and for themselves working in these environments in order to achieve what they believed to be optimal care.

Identifiants

pubmed: 38035631
doi: 10.1177/10497323231215950
doi:

Types de publication

Journal Article

Langues

eng

Pagination

10497323231215950

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Shipra Taneja (S)

Department of Family Medicine, McMaster University, Hamilton, ON, Canada.

Meredith Vanstone (M)

Department of Family Medicine, McMaster University, Hamilton, ON, Canada.

David L Lysecki (DL)

Department of Family Medicine, McMaster University, Hamilton, ON, Canada.
Department of Pediatrics, McMaster University, Hamilton, ON, Canada.

Heather McKean (H)

Hamilton Health Sciences, McMaster Children's Hospital, Hamilton, ON, Canada.

Daryl Bainbridge (D)

Department of Oncology, McMaster University, Hamilton, ON, Canada.

Jonathan Sussman (J)

Department of Oncology, McMaster University, Hamilton, ON, Canada.

Monica Molinaro (M)

Department of Family Medicine, McMaster University, Hamilton, ON, Canada.
Institute of Health Sciences Education, McGill University, Montreal, QC, Canada.

Classifications MeSH