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Published in: BMC Palliative Care 1/2021

Open Access 01-12-2021 | Care | Research article

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

Authors: Martina Fay, Jessica Guadarrama, Tirsa Colmenares-Roa, Iraís Moreno-Licona, Ana Gabriela Cruz-Martin, Ingris Peláez-Ballestas

Published in: BMC Palliative Care | Issue 1/2021

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Abstract

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.
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Literature
2.
go back to reference Mexico Human Rights Watch. Cuidar cuando no es posible curar. Asegurando el derecho a los cuidados paliativos en México. USA: Human Rights Watch; 2014. Mexico Human Rights Watch. Cuidar cuando no es posible curar. Asegurando el derecho a los cuidados paliativos en México. USA: Human Rights Watch; 2014.
4.
go back to reference Santos-Preciado JI, Anaya-Nuñez R, García-Moreno J. El Consejo de Salubridad General (CSG) y los Cuidados Paliativos. Consejo de Salubridad General. www.csg.gob.mx. Accessed 11 Jan 2021. Santos-Preciado JI, Anaya-Nuñez R, García-Moreno J. El Consejo de Salubridad General (CSG) y los Cuidados Paliativos. Consejo de Salubridad General. www.​csg.​gob.​mx. Accessed 11 Jan 2021.
5.
go back to reference Guadarrama-Orozco J, Garduño-Espinosa J, Vargas-Lopez G, Viesca-Treviño C. Informed consent and parental refusal to medical treatment in childhood. The threshold of medical and social tolerance. Part I. Bol Med Infant Mex. 2015;73:208–14. Guadarrama-Orozco J, Garduño-Espinosa J, Vargas-Lopez G, Viesca-Treviño C. Informed consent and parental refusal to medical treatment in childhood. The threshold of medical and social tolerance. Part I. Bol Med Infant Mex. 2015;73:208–14.
6.
go back to reference Ghirotto L, Busani E, Salvati M, Di Marco V, Caldarelli V, Artioli G. Researching children’s perspectives in pediatric palliative care: a systematic review and meta10 summary of qualitative research. Palliative Supportive Care. 2019;17(1):107–18.CrossRef Ghirotto L, Busani E, Salvati M, Di Marco V, Caldarelli V, Artioli G. Researching children’s perspectives in pediatric palliative care: a systematic review and meta10 summary of qualitative research. Palliative Supportive Care. 2019;17(1):107–18.CrossRef
7.
go back to reference Cicero-Oneto CE, Valdez-Martinez E, Bedolla M. Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study. BMC Med Ethics. 2017;18:74.CrossRef Cicero-Oneto CE, Valdez-Martinez E, Bedolla M. Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study. BMC Med Ethics. 2017;18:74.CrossRef
8.
go back to reference Wainer R. Hacia una Antropología del morir-entre-nosotros o cómo entender el afecto en el final de la vida en niñ@s. IX Congreso Argentino de Antropología Social. Posadas: Facultad de Humanidades y Ciencias Sociales - Universidad Nacional de Misiones; 2008. Wainer R. Hacia una Antropología del morir-entre-nosotros o cómo entender el afecto en el final de la vida en niñ@s. IX Congreso Argentino de Antropología Social. Posadas: Facultad de Humanidades y Ciencias Sociales - Universidad Nacional de Misiones; 2008.
9.
go back to reference Magistris G. La construcción del 'niño como sujeto de derechos' y la agencia infantil en cuestión. Journal de Ciencias Sociales. Revista Académica de la Facultad de Ciencias Sociales de la Universidad de Palermo 2018; 6(11):6–28. Magistris G. La construcción del 'niño como sujeto de derechos' y la agencia infantil en cuestión. Journal de Ciencias Sociales. Revista Académica de la Facultad de Ciencias Sociales de la Universidad de Palermo 2018; 6(11):6–28.
10.
go back to reference Pizza G. Antonio Gramsci y la antropología médica contemporánea. Hegemonía, “capacidad de actuar” (agency) y transformaciones de la persona. Revista de Antropología Social. 2005;14:15–32. Pizza G. Antonio Gramsci y la antropología médica contemporánea. Hegemonía, “capacidad de actuar” (agency) y transformaciones de la persona. Revista de Antropología Social. 2005;14:15–32.
11.
go back to reference Giddens A. The constitution of society: outline of the theory of structuration. Oxford: Blackwell; 1984. Giddens A. The constitution of society: outline of the theory of structuration. Oxford: Blackwell; 1984.
12.
go back to reference van der Geest S, Finkler K. Hospital ethnography: introduction. Soc Sci Med. 2004;59(10):1995–2001.CrossRef van der Geest S, Finkler K. Hospital ethnography: introduction. Soc Sci Med. 2004;59(10):1995–2001.CrossRef
13.
go back to reference Finkler K. Biomedicine globalized and localized: western medical practices in an outpatient clinic of a Mexican hospital. Soc Sci Med. 2004;59(10):2051–37.CrossRef Finkler K. Biomedicine globalized and localized: western medical practices in an outpatient clinic of a Mexican hospital. Soc Sci Med. 2004;59(10):2051–37.CrossRef
14.
go back to reference Nowell L, Norris J, White D, Moules N. Thematic analysis: striving to meet the trustworthiness criteria. Int J Qual Methods. 2017;16:1–13.CrossRef Nowell L, Norris J, White D, Moules N. Thematic analysis: striving to meet the trustworthiness criteria. Int J Qual Methods. 2017;16:1–13.CrossRef
15.
go back to reference Martínez A. Departamento de Cuidados Paliativos, una nueva arista en el HIMFG. Ixtlilton La revista del HIMFG. 2019;23:6–7. Martínez A. Departamento de Cuidados Paliativos, una nueva arista en el HIMFG. Ixtlilton La revista del HIMFG. 2019;23:6–7.
16.
go back to reference Heredia CR. ¿Cómo es el dolor? Indagaciones médicas, registros y etiologías del dolor en cuidados paliativos pediátricos. Cuadernos de Antropología Social. 2019;49:147–62. Heredia CR. ¿Cómo es el dolor? Indagaciones médicas, registros y etiologías del dolor en cuidados paliativos pediátricos. Cuadernos de Antropología Social. 2019;49:147–62.
19.
go back to reference Bluebond-Langner M, Belasco JB, De Mesquita Wander M. “I want to live, until I don’t want to live anymore”: involving children with life-threatening and life shortening illnesses in decision making about care and treatment. Nurs Clin N Am. 2010;45(3):329–43.CrossRef Bluebond-Langner M, Belasco JB, De Mesquita Wander M. “I want to live, until I don’t want to live anymore”: involving children with life-threatening and life shortening illnesses in decision making about care and treatment. Nurs Clin N Am. 2010;45(3):329–43.CrossRef
22.
go back to reference Clark JD, Dudzinski DM. The culture of Dysthanasia: attempting CPR in terminal ill children. Pediatrics. 2013;131:572–80.CrossRef Clark JD, Dudzinski DM. The culture of Dysthanasia: attempting CPR in terminal ill children. Pediatrics. 2013;131:572–80.CrossRef
23.
go back to reference Hsiao J, Evan E, Zelter L. Parent and child perspectives on physician communication in pediatric palliative care. Palliative Supportive Care. 2007;5:355–65.CrossRef Hsiao J, Evan E, Zelter L. Parent and child perspectives on physician communication in pediatric palliative care. Palliative Supportive Care. 2007;5:355–65.CrossRef
24.
go back to reference Tates K, Meeuwesen L. Doctor-parent-child communication. A (re) view of the literature. Soc Sci Med. 2001;52(6):839–51.CrossRef Tates K, Meeuwesen L. Doctor-parent-child communication. A (re) view of the literature. Soc Sci Med. 2001;52(6):839–51.CrossRef
25.
go back to reference World Health Organization. Strengthening the doctor–patient relationship. A framework for action. India: World Health Organization; 2013. World Health Organization. Strengthening the doctor–patient relationship. A framework for action. India: World Health Organization; 2013.
Metadata
Title
The relationship between proxy agency and the medical decisions concerning pediatric patients in palliative care: a qualitative study
Authors
Martina Fay
Jessica Guadarrama
Tirsa Colmenares-Roa
Iraís Moreno-Licona
Ana Gabriela Cruz-Martin
Ingris Peláez-Ballestas
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Palliative Care / Issue 1/2021
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/s12904-021-00723-4

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