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The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study

BACKGROUND: The children’s agency and that exercised by parents and health professionals in palliative care, along with structural limitations imposed by the conditions of inequality, will provide a new perspective from medical anthropology and biomedicine to improve pediatric palliative care in com...

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Autores principales: Fay, Martina, Guadarrama, Jessica, Colmenares-Roa, Tirsa, Moreno-Licona, Iraís, Cruz-Martin, Ana Gabriela, Peláez-Ballestas, Ingris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863456/
https://www.ncbi.nlm.nih.gov/pubmed/33541339
http://dx.doi.org/10.1186/s12904-021-00723-4
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author Fay, Martina
Guadarrama, Jessica
Colmenares-Roa, Tirsa
Moreno-Licona, Iraís
Cruz-Martin, Ana Gabriela
Peláez-Ballestas, Ingris
author_facet Fay, Martina
Guadarrama, Jessica
Colmenares-Roa, Tirsa
Moreno-Licona, Iraís
Cruz-Martin, Ana Gabriela
Peláez-Ballestas, Ingris
author_sort Fay, Martina
collection PubMed
description BACKGROUND: The children’s agency and that exercised by parents and health professionals in palliative care, along with structural limitations imposed by the conditions of inequality, will provide a new perspective from medical anthropology and biomedicine to improve pediatric palliative care in complex therapeutic scenarios. The main purpose of the study was to analyze the ways in which pediatric patients have agency in relation to their parents and palliative care (PC) professionals within the hospital setting, as well as the structural circumstances that constrain said agency. METHOD: A hospital ethnography (by means of non-participant observation and interviews) of the palliative care (PC) unit in a children’s hospital was conducted over the course of six months. A thematic analysis was performed using the ATLAS.ti software . RESULTS: Thirteen cases were reconstructed of underage patients of both sexes patients together with their families; five health professionals were interviewed. The analysis identified the following 6 thematic axes, around which this article is organized: 1. The relationship between the exercise of proxy agency and the medical decisions concerning underage patients. 2. Negotiating agency and support in decision-making. 3. Child autonomy. 4. The experiences of health professionals. 5. Limitations of palliative care. 6. Bureaucratization of palliative care. CONCLUSIONS: In pediatric palliative care, agency is a process whereby different agencies intertwine: lack of pediatric patients ‘agency, the parents’ agency, the parents’ agency as representatives of their children (proxy agency), and the agency of health professionals. The concept of relational agency is proposed, defined as a set of group actions and decision-making centered around the pediatric patients’s agency and the proxy agency. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12904-021-00723-4.
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spelling pubmed-78634562021-02-05 The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study Fay, Martina Guadarrama, Jessica Colmenares-Roa, Tirsa Moreno-Licona, Iraís Cruz-Martin, Ana Gabriela Peláez-Ballestas, Ingris BMC Palliat Care Research Article BACKGROUND: The children’s agency and that exercised by parents and health professionals in palliative care, along with structural limitations imposed by the conditions of inequality, will provide a new perspective from medical anthropology and biomedicine to improve pediatric palliative care in complex therapeutic scenarios. The main purpose of the study was to analyze the ways in which pediatric patients have agency in relation to their parents and palliative care (PC) professionals within the hospital setting, as well as the structural circumstances that constrain said agency. METHOD: A hospital ethnography (by means of non-participant observation and interviews) of the palliative care (PC) unit in a children’s hospital was conducted over the course of six months. A thematic analysis was performed using the ATLAS.ti software . RESULTS: Thirteen cases were reconstructed of underage patients of both sexes patients together with their families; five health professionals were interviewed. The analysis identified the following 6 thematic axes, around which this article is organized: 1. The relationship between the exercise of proxy agency and the medical decisions concerning underage patients. 2. Negotiating agency and support in decision-making. 3. Child autonomy. 4. The experiences of health professionals. 5. Limitations of palliative care. 6. Bureaucratization of palliative care. CONCLUSIONS: In pediatric palliative care, agency is a process whereby different agencies intertwine: lack of pediatric patients ‘agency, the parents’ agency, the parents’ agency as representatives of their children (proxy agency), and the agency of health professionals. The concept of relational agency is proposed, defined as a set of group actions and decision-making centered around the pediatric patients’s agency and the proxy agency. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12904-021-00723-4. BioMed Central 2021-02-04 /pmc/articles/PMC7863456/ /pubmed/33541339 http://dx.doi.org/10.1186/s12904-021-00723-4 Text en © The Author(s) 2021 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/. 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 in a credit line to the data.
spellingShingle Research Article
Fay, Martina
Guadarrama, Jessica
Colmenares-Roa, Tirsa
Moreno-Licona, Iraís
Cruz-Martin, Ana Gabriela
Peláez-Ballestas, Ingris
The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title_full The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title_fullStr The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title_full_unstemmed The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title_short The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
title_sort relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863456/
https://www.ncbi.nlm.nih.gov/pubmed/33541339
http://dx.doi.org/10.1186/s12904-021-00723-4
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