No good choices, only hard decisions : the delicate nature of team family communication in pompe disease

Detalhes bibliográficos
Autor(a) principal: Neis, Míriam
Data de Publicação: 2024
Outros Autores: Silva, Camila Neves da, Motta, Maria da Graça Corso da, Issi, Helena Becker, Rocha, Cristianne Maria Famer, Ferreira, Anali Martegani, Carvalho, Paulo Roberto Antonacci
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/279998
Resumo: Objective: To describe the experience of a family going through the palliative care decision-making for a child with Pompe disease. Method: Qualitative research, case study design, approved by Ethics Committee (CAAE: 58643816400005327), conducted between 2017/2018. The setting was the Pediatric Intensive Care Unit of a university hospital in Brazil. Participants were family members of children admitted to the Intensive Care Unit and referred for palliative care. Results: The case study relates the decision-making on palliative care for a child with Pompe disease. The parents, surrounded by the palliative care available for the situation, experience the existential reality of the decision-making process to adopt palliative care for their child, together with the multi-professional team. Conclusions: Understanding the concept of quality of life that each family develops when faced with the seriousness of their child’s illness, when the possibilities of cure have been exhausted, is fundamental to the decision making process for adopting palliative care. It is essential to include the participation of the child’s or adolescent’s parents and other family members in the palliative care decision-making process, in order to give the family a voice, minimising their doubts and suffering, as well as offering shelter in a situation of extreme existential vulnerability.
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spelling Neis, MíriamSilva, Camila Neves daMotta, Maria da Graça Corso daIssi, Helena BeckerRocha, Cristianne Maria FamerFerreira, Anali MarteganiCarvalho, Paulo Roberto Antonacci2024-10-15T06:41:17Z20242577-8269http://hdl.handle.net/10183/279998001200117Objective: To describe the experience of a family going through the palliative care decision-making for a child with Pompe disease. Method: Qualitative research, case study design, approved by Ethics Committee (CAAE: 58643816400005327), conducted between 2017/2018. The setting was the Pediatric Intensive Care Unit of a university hospital in Brazil. Participants were family members of children admitted to the Intensive Care Unit and referred for palliative care. Results: The case study relates the decision-making on palliative care for a child with Pompe disease. The parents, surrounded by the palliative care available for the situation, experience the existential reality of the decision-making process to adopt palliative care for their child, together with the multi-professional team. Conclusions: Understanding the concept of quality of life that each family develops when faced with the seriousness of their child’s illness, when the possibilities of cure have been exhausted, is fundamental to the decision making process for adopting palliative care. It is essential to include the participation of the child’s or adolescent’s parents and other family members in the palliative care decision-making process, in order to give the family a voice, minimising their doubts and suffering, as well as offering shelter in a situation of extreme existential vulnerability.application/pdfengInternational Journal of Family & Community Medicine. Budapest: MedCrave, 2017-. Vol. 8, n. 1 (2024), p. 33‒37CriançaFamíliaDoença de depósito de glicogênio tipo IICuidados paliativos integrativosEnfermagem pediátricaChildFamilyGlycogen storage disease type IIIntegrative palliative carePediatric nursingNo good choices, only hard decisions : the delicate nature of team family communication in pompe diseaseEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001200117.pdf.txt001200117.pdf.txtExtracted Texttext/plain36890http://www.lume.ufrgs.br/bitstream/10183/279998/2/001200117.pdf.txt12568d3ff8d0006f8d08ab0cb1771aa9MD52ORIGINAL001200117.pdfTexto completo (inglês)application/pdf525749http://www.lume.ufrgs.br/bitstream/10183/279998/1/001200117.pdf81b2588c0e6804a3370b82ff694887b4MD5110183/2799982024-10-16 06:57:25.58641oai:www.lume.ufrgs.br:10183/279998Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-10-16T09:57:25Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
title No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
spellingShingle No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
Neis, Míriam
Criança
Família
Doença de depósito de glicogênio tipo II
Cuidados paliativos integrativos
Enfermagem pediátrica
Child
Family
Glycogen storage disease type II
Integrative palliative care
Pediatric nursing
title_short No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
title_full No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
title_fullStr No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
title_full_unstemmed No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
title_sort No good choices, only hard decisions : the delicate nature of team family communication in pompe disease
author Neis, Míriam
author_facet Neis, Míriam
Silva, Camila Neves da
Motta, Maria da Graça Corso da
Issi, Helena Becker
Rocha, Cristianne Maria Famer
Ferreira, Anali Martegani
Carvalho, Paulo Roberto Antonacci
author_role author
author2 Silva, Camila Neves da
Motta, Maria da Graça Corso da
Issi, Helena Becker
Rocha, Cristianne Maria Famer
Ferreira, Anali Martegani
Carvalho, Paulo Roberto Antonacci
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Neis, Míriam
Silva, Camila Neves da
Motta, Maria da Graça Corso da
Issi, Helena Becker
Rocha, Cristianne Maria Famer
Ferreira, Anali Martegani
Carvalho, Paulo Roberto Antonacci
dc.subject.por.fl_str_mv Criança
Família
Doença de depósito de glicogênio tipo II
Cuidados paliativos integrativos
Enfermagem pediátrica
topic Criança
Família
Doença de depósito de glicogênio tipo II
Cuidados paliativos integrativos
Enfermagem pediátrica
Child
Family
Glycogen storage disease type II
Integrative palliative care
Pediatric nursing
dc.subject.eng.fl_str_mv Child
Family
Glycogen storage disease type II
Integrative palliative care
Pediatric nursing
description Objective: To describe the experience of a family going through the palliative care decision-making for a child with Pompe disease. Method: Qualitative research, case study design, approved by Ethics Committee (CAAE: 58643816400005327), conducted between 2017/2018. The setting was the Pediatric Intensive Care Unit of a university hospital in Brazil. Participants were family members of children admitted to the Intensive Care Unit and referred for palliative care. Results: The case study relates the decision-making on palliative care for a child with Pompe disease. The parents, surrounded by the palliative care available for the situation, experience the existential reality of the decision-making process to adopt palliative care for their child, together with the multi-professional team. Conclusions: Understanding the concept of quality of life that each family develops when faced with the seriousness of their child’s illness, when the possibilities of cure have been exhausted, is fundamental to the decision making process for adopting palliative care. It is essential to include the participation of the child’s or adolescent’s parents and other family members in the palliative care decision-making process, in order to give the family a voice, minimising their doubts and suffering, as well as offering shelter in a situation of extreme existential vulnerability.
publishDate 2024
dc.date.accessioned.fl_str_mv 2024-10-15T06:41:17Z
dc.date.issued.fl_str_mv 2024
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv International Journal of Family & Community Medicine. Budapest: MedCrave, 2017-. Vol. 8, n. 1 (2024), p. 33‒37
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