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A qualitative study of health care professionals’ views and experiences of paediatric advance care planning
BACKGROUND: Good end-of-life care planning is vital to ensure optimal care is provided for patients and their families. Two key factors are open and honest advance care planning conversations between the patient (where possible), family, and health care professionals, focusing on exploring what thei...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044078/ https://www.ncbi.nlm.nih.gov/pubmed/30005657 http://dx.doi.org/10.1186/s12904-018-0347-8 |
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author | Jack, Barbara A. Mitchell, Tracy K. O’Brien, Mary R. Silverio, Sergio A. Knighting, Katherine |
author_facet | Jack, Barbara A. Mitchell, Tracy K. O’Brien, Mary R. Silverio, Sergio A. Knighting, Katherine |
author_sort | Jack, Barbara A. |
collection | PubMed |
description | BACKGROUND: Good end-of-life care planning is vital to ensure optimal care is provided for patients and their families. Two key factors are open and honest advance care planning conversations between the patient (where possible), family, and health care professionals, focusing on exploring what their future wishes are; and the development of an advance care plan document. However, in paediatric and neonatal settings, there has been little research to demonstrate how advance care planning conversations take place. This study explored health care professionals’ views and experiences of paediatric advance care planning in hospitals, community settings and hospices. METHODS: A qualitative methodology was employed using purposive sampling of health care professionals involved in the end-of-life care for children aged 0–18 years known to the hospital palliative care team, and had died at least three months before, but less than 18 months prior to the study. Ethics committee approval was obtained for the study. Located in the North of England, the study involved three hospitals, a children’s hospice, and community services. Data were collected using semi-structured, digitally recorded, telephone interviews. All interviews were transcribed verbatim and subjected to thematic analysis. RESULTS: Twenty-one health care professionals participated, including generalist paediatric staff as well as specialist palliative care staff. Two themes were generated from the study: The timing of planning conversations, including waiting for the relationship with the family to form; the introduction of parallel planning; avoiding a crisis situation. Secondly, supporting effective conversations around advance care planning, including where to have the conversation; introducing the conversation; and how to approach the topic encompassing the value of advance care planning and documentation for families. CONCLUSION: The timing of when to start the advance care planning conversations remains an issue for health care professionals. The value of doing it in stages and considering the environment where the conversations are held was noted. Timely planning was seen as vital to avoid difficult conversations at a crisis point and for co-ordination of care. Good advance care planning is to provide the best person-centred care for the child and experience for the family. |
format | Online Article Text |
id | pubmed-6044078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60440782018-07-16 A qualitative study of health care professionals’ views and experiences of paediatric advance care planning Jack, Barbara A. Mitchell, Tracy K. O’Brien, Mary R. Silverio, Sergio A. Knighting, Katherine BMC Palliat Care Research Article BACKGROUND: Good end-of-life care planning is vital to ensure optimal care is provided for patients and their families. Two key factors are open and honest advance care planning conversations between the patient (where possible), family, and health care professionals, focusing on exploring what their future wishes are; and the development of an advance care plan document. However, in paediatric and neonatal settings, there has been little research to demonstrate how advance care planning conversations take place. This study explored health care professionals’ views and experiences of paediatric advance care planning in hospitals, community settings and hospices. METHODS: A qualitative methodology was employed using purposive sampling of health care professionals involved in the end-of-life care for children aged 0–18 years known to the hospital palliative care team, and had died at least three months before, but less than 18 months prior to the study. Ethics committee approval was obtained for the study. Located in the North of England, the study involved three hospitals, a children’s hospice, and community services. Data were collected using semi-structured, digitally recorded, telephone interviews. All interviews were transcribed verbatim and subjected to thematic analysis. RESULTS: Twenty-one health care professionals participated, including generalist paediatric staff as well as specialist palliative care staff. Two themes were generated from the study: The timing of planning conversations, including waiting for the relationship with the family to form; the introduction of parallel planning; avoiding a crisis situation. Secondly, supporting effective conversations around advance care planning, including where to have the conversation; introducing the conversation; and how to approach the topic encompassing the value of advance care planning and documentation for families. CONCLUSION: The timing of when to start the advance care planning conversations remains an issue for health care professionals. The value of doing it in stages and considering the environment where the conversations are held was noted. Timely planning was seen as vital to avoid difficult conversations at a crisis point and for co-ordination of care. Good advance care planning is to provide the best person-centred care for the child and experience for the family. BioMed Central 2018-07-13 /pmc/articles/PMC6044078/ /pubmed/30005657 http://dx.doi.org/10.1186/s12904-018-0347-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Jack, Barbara A. Mitchell, Tracy K. O’Brien, Mary R. Silverio, Sergio A. Knighting, Katherine A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title | A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title_full | A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title_fullStr | A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title_full_unstemmed | A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title_short | A qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
title_sort | qualitative study of health care professionals’ views and experiences of paediatric advance care planning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044078/ https://www.ncbi.nlm.nih.gov/pubmed/30005657 http://dx.doi.org/10.1186/s12904-018-0347-8 |
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