Assessment of Bereaved Caregiver Experiences of Advance Care Planning for Children With Medical Complexity.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 07 2020
Historique:
entrez: 29 7 2020
pubmed: 29 7 2020
medline: 29 12 2020
Statut: epublish

Résumé

Advance care planning (ACP) is the process of discussing values and preferences for care to help inform medical decision-making. Children with medical complexity (CMC) often have a shortened life span with an unpredictable clinical course and timing of death; however, there is a paucity of literature that describes the experience of ACP from the perspective of bereaved family caregivers of CMC. To explore the experiences of bereaved family caregivers with ACP for CMC. This qualitative study included 12 interviews with 13 bereaved family caregivers of CMC whose deaths had occurred in the 5 years before study commencement (2013-2018). Participants were recruited at a single tertiary care pediatric center; CMC were treated by the Complex Care or Long-term Ventilation clinic in Toronto, Ontario, Canada. Data were collected from July to October 2018. Thematic analysis with an inductive approach was used. Qualitative interviews were conducted using purposive sampling of bereaved family caregivers using semistructured interviews that were recorded and transcribed. Interviews were conducted until saturation was reached. Transcripts were analyzed to create themes that characterized caregiver experiences with ACP. A total of 13 family caregivers were interviewed in 12 interviews, all of whom were parents (12 [92%] women, 1 [8%] man) of a deceased child (aged 7 months to 12 years). Themes were divided in the 3 following categories, which align with the Donabedian model for health service quality: (1) structure of care, (2) ACP process, and (3) end-of-life experience. Notable subthemes for this population included the importance of accounting for parental expertise in the child's care, recurrent experiences with life-threatening events, relative shock of the timing of death, and the multiple losses that caregivers experienced. In this study, parental experiences revealed that there are key aspects of the structure of the child's care, process around ACP, and end-of-life care experiences that provide important reflections on ACP that warrant future study.

Identifiants

pubmed: 32721029
pii: 2768725
doi: 10.1001/jamanetworkopen.2020.10337
pmc: PMC7388020
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2010337

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Auteurs

Sarah Lord (S)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.

Clara Moore (C)

Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.

Madison Beatty (M)

Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.

Eyal Cohen (E)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.
Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Adam Rapoport (A)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Emily's House Children's Hospice, Toronto, Ontario, Canada.

Jonathan Hellmann (J)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.

Kathy Netten (K)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.

Reshma Amin (R)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.

Julia Orkin (J)

Division of Paediatric Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.

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