Parental experiences of end of life care decision-making for children with life-limiting conditions in the paediatric intensive care unit: a qualitative interview study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
09 05 2019
Historique:
entrez: 11 5 2019
pubmed: 11 5 2019
medline: 2 6 2020
Statut: epublish

Résumé

To provide an in-depth insight into the experience and perceptions of bereaved parents who have experienced end of life care decision-making for children with life-limiting or life-threatening conditions in the paediatric intensive care unit (PICU). An in-depth qualitative interview study with a sample of parents of children with life-limiting or life-threatening conditions who had died in PICU within the previous 12 months. A thematic analysis was conducted on the interview transcripts. A PICU in a large National Health Service (NHS) tertiary children's hospital in the West Midlands, UK. 17 parents of 11 children who had died in the PICU. Five interconnected themes were identified related to end of life care decision-making:(1) parents have significant knowledge and experiences that influence the decision-making process.(2) Trusted relationships with healthcare professionals are key to supporting parents making end of life decisions.(3) Verbal and non-verbal communication with healthcare professionals impacts on the family experience.(4) Engaging with end of life care decision-making can be emotionally overwhelming, but becomes possible if parents reach a 'place of acceptance'.(5) Families perceive benefits to receiving end of life care for their child in a PICU. The death of a child is an intensely emotional experience for all involved. This study adds to the limited evidence base related to parental experiences of end of life care decision-making and provides findings that have international relevance, particularly related to place of care and introduction of end of life care discussions. The expertise and previous experience of parents is highly relevant and should be acknowledged. End of life care decision-making is a complex and nuanced process; the information needs and preferences of each family are individual and need to be understood by the professionals involved in their care.

Identifiants

pubmed: 31072863
pii: bmjopen-2018-028548
doi: 10.1136/bmjopen-2018-028548
pmc: PMC6528052
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e028548

Subventions

Organisme : Department of Health
ID : DRF-2014-07-065
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Sarah Mitchell (S)

Warwick Medical School, University of Warwick, Coventry, West Midlands, UK.

Jenna L Spry (JL)

Paediatric Intensive Care Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, Birmingham, UK.

Emma Hill (E)

Paediatric Intensive Care Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, Birmingham, UK.

Jane Coad (J)

School of Health Sciences, University of Nottingham, Nottingham, Nottinghamshire, UK.

Jeremy Dale (J)

Warwick Medical School, University of Warwick, Coventry, West Midlands, UK.

Adrian Plunkett (A)

Paediatric Intensive Care Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, Birmingham, UK.

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