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How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study

BACKGROUND: Children report that they do not participate in their healthcare as much as they want, despite having the lawful right to form their own views and the right to express those views freely in all matters affecting them. Children and parents appeared to be more satisfied when healthcare pro...

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Autores principales: Lundberg, Veronica, Eriksson, Catharina, Lind, Torbjörn, Coyne, Imelda, Fjellman-Wiklund, Anncristine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561993/
https://www.ncbi.nlm.nih.gov/pubmed/34727931
http://dx.doi.org/10.1186/s12969-021-00642-x
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author Lundberg, Veronica
Eriksson, Catharina
Lind, Torbjörn
Coyne, Imelda
Fjellman-Wiklund, Anncristine
author_facet Lundberg, Veronica
Eriksson, Catharina
Lind, Torbjörn
Coyne, Imelda
Fjellman-Wiklund, Anncristine
author_sort Lundberg, Veronica
collection PubMed
description BACKGROUND: Children report that they do not participate in their healthcare as much as they want, despite having the lawful right to form their own views and the right to express those views freely in all matters affecting them. Children and parents appeared to be more satisfied when healthcare professionals (HCP) use a participatory style in healthcare encounters. AIM: To explore how children, adolescents and young adults with Juvenile Idiopathic Arthritis (JIA) and parents of children with JIA view their participation and communication in healthcare encounters with healthcare professionals. METHODS: Using a qualitative study design, participatory workshops were held separately for children and young adults with JIA and parents of children with JIA. The workshop data were analysed with Graneheim and Lundman’s Qualitative Content Analysis resulting in one main theme and two subthemes. RESULTS: The theme “Feeling alienated or familiar with healthcare encounters” illuminates how children felt alienated at healthcare encounters if they found the encounters emotionally distressing. Children could withhold information regarding their health and function from both HCPs and their family and friends. The subtheme “Distancing oneself from healthcare” describe why children felt reluctant to engage in the healthcare encounters and experienced difficulty expressing how they really felt. The subtheme “Being a normal event in life” describe how children felt more comfortable over time engaging with HCPs when they knew what would happen, and felt that HCPs gave them the necessary support they needed to participate. CONCLUSIONS: Children’s participation in healthcare encounters varied depending if children felt alienated or familiar to the healthcare situations. Children distance themselves and are reluctant to engage in healthcare encounters if they find them emotionally distressing and feel disregarded. Over time, children can become more familiar and at ease with healthcare situations when they feel safe and experience personal and positive encounters. When the children are prepared for the encounter, provided with the space and support they want and receive tailored help they are more enabled to participate.
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spelling pubmed-85619932021-11-03 How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study Lundberg, Veronica Eriksson, Catharina Lind, Torbjörn Coyne, Imelda Fjellman-Wiklund, Anncristine Pediatr Rheumatol Online J Research Article BACKGROUND: Children report that they do not participate in their healthcare as much as they want, despite having the lawful right to form their own views and the right to express those views freely in all matters affecting them. Children and parents appeared to be more satisfied when healthcare professionals (HCP) use a participatory style in healthcare encounters. AIM: To explore how children, adolescents and young adults with Juvenile Idiopathic Arthritis (JIA) and parents of children with JIA view their participation and communication in healthcare encounters with healthcare professionals. METHODS: Using a qualitative study design, participatory workshops were held separately for children and young adults with JIA and parents of children with JIA. The workshop data were analysed with Graneheim and Lundman’s Qualitative Content Analysis resulting in one main theme and two subthemes. RESULTS: The theme “Feeling alienated or familiar with healthcare encounters” illuminates how children felt alienated at healthcare encounters if they found the encounters emotionally distressing. Children could withhold information regarding their health and function from both HCPs and their family and friends. The subtheme “Distancing oneself from healthcare” describe why children felt reluctant to engage in the healthcare encounters and experienced difficulty expressing how they really felt. The subtheme “Being a normal event in life” describe how children felt more comfortable over time engaging with HCPs when they knew what would happen, and felt that HCPs gave them the necessary support they needed to participate. CONCLUSIONS: Children’s participation in healthcare encounters varied depending if children felt alienated or familiar to the healthcare situations. Children distance themselves and are reluctant to engage in healthcare encounters if they find them emotionally distressing and feel disregarded. Over time, children can become more familiar and at ease with healthcare situations when they feel safe and experience personal and positive encounters. When the children are prepared for the encounter, provided with the space and support they want and receive tailored help they are more enabled to participate. BioMed Central 2021-11-02 /pmc/articles/PMC8561993/ /pubmed/34727931 http://dx.doi.org/10.1186/s12969-021-00642-x Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Lundberg, Veronica
Eriksson, Catharina
Lind, Torbjörn
Coyne, Imelda
Fjellman-Wiklund, Anncristine
How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title_full How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title_fullStr How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title_full_unstemmed How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title_short How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
title_sort how children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561993/
https://www.ncbi.nlm.nih.gov/pubmed/34727931
http://dx.doi.org/10.1186/s12969-021-00642-x
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