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Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment
PURPOSE: This study aimed to understand the experience of families caring for a child with cancer in New Zealand (NZ) who received nutrition and dietetic support during cancer treatment and their preferences for the delivery, format, and timing of nutrition information. METHODS: Childhood cancer pat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167176/ https://www.ncbi.nlm.nih.gov/pubmed/37154869 http://dx.doi.org/10.1007/s00520-023-07787-3 |
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author | Clarke, Emma Pugh, Gemma van den Heuvel, Eveline Winstanley, Mark Wood, Andrew C. Laughton, Stephen J. Lovell, Amy L. |
author_facet | Clarke, Emma Pugh, Gemma van den Heuvel, Eveline Winstanley, Mark Wood, Andrew C. Laughton, Stephen J. Lovell, Amy L. |
author_sort | Clarke, Emma |
collection | PubMed |
description | PURPOSE: This study aimed to understand the experience of families caring for a child with cancer in New Zealand (NZ) who received nutrition and dietetic support during cancer treatment and their preferences for the delivery, format, and timing of nutrition information. METHODS: Childhood cancer patients and their families (N = 21) participated in a mixed-methods study at a specialist paediatric oncology centre in Auckland, NZ. Before the semi-structured interview, participants completed a questionnaire capturing demographic, disease, and treatment characteristics of their child, their nutrition concerns, and their information needs. Quantitative data were described, and qualitative thematic analysis of the semi-structured interviews was performed using NVivo data analysis software. RESULTS: Eighty-six percent of participants indicated they had concerns about their child’s nutrition during treatment. The most common concerns were anorexia, vomiting, and weight loss. While many were happy with the quality of the nutrition support received, one-third of the patients wanted more support. Four key themes emerged from the interviews: (1) patients experience significant and distressing nutrition challenges; (2) patients and families have mixed perceptions of EN; (3) there are gaps in the current nutrition support system for inpatients; and (4) a desire for more accessible nutrition support. CONCLUSION: Childhood cancer patients and families experience significant and distressing nutrition challenges during treatment. Standardising information given to patients and their families may optimise nutrition support for paediatric oncology patients and reduce the discordance between families and health professionals. Future implementation of a nutrition decision aid in this population is warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-023-07787-3. |
format | Online Article Text |
id | pubmed-10167176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101671762023-05-10 Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment Clarke, Emma Pugh, Gemma van den Heuvel, Eveline Winstanley, Mark Wood, Andrew C. Laughton, Stephen J. Lovell, Amy L. Support Care Cancer Research PURPOSE: This study aimed to understand the experience of families caring for a child with cancer in New Zealand (NZ) who received nutrition and dietetic support during cancer treatment and their preferences for the delivery, format, and timing of nutrition information. METHODS: Childhood cancer patients and their families (N = 21) participated in a mixed-methods study at a specialist paediatric oncology centre in Auckland, NZ. Before the semi-structured interview, participants completed a questionnaire capturing demographic, disease, and treatment characteristics of their child, their nutrition concerns, and their information needs. Quantitative data were described, and qualitative thematic analysis of the semi-structured interviews was performed using NVivo data analysis software. RESULTS: Eighty-six percent of participants indicated they had concerns about their child’s nutrition during treatment. The most common concerns were anorexia, vomiting, and weight loss. While many were happy with the quality of the nutrition support received, one-third of the patients wanted more support. Four key themes emerged from the interviews: (1) patients experience significant and distressing nutrition challenges; (2) patients and families have mixed perceptions of EN; (3) there are gaps in the current nutrition support system for inpatients; and (4) a desire for more accessible nutrition support. CONCLUSION: Childhood cancer patients and families experience significant and distressing nutrition challenges during treatment. Standardising information given to patients and their families may optimise nutrition support for paediatric oncology patients and reduce the discordance between families and health professionals. Future implementation of a nutrition decision aid in this population is warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-023-07787-3. Springer Berlin Heidelberg 2023-05-08 2023 /pmc/articles/PMC10167176/ /pubmed/37154869 http://dx.doi.org/10.1007/s00520-023-07787-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Clarke, Emma Pugh, Gemma van den Heuvel, Eveline Winstanley, Mark Wood, Andrew C. Laughton, Stephen J. Lovell, Amy L. Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title | Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title_full | Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title_fullStr | Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title_full_unstemmed | Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title_short | Understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
title_sort | understanding the patient and family experience of nutrition and dietetic support during childhood cancer treatment |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167176/ https://www.ncbi.nlm.nih.gov/pubmed/37154869 http://dx.doi.org/10.1007/s00520-023-07787-3 |
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