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How children with juvenile idiopathic arthritis view participation and communication in healthcare encounters: a qualitative study
Umeå universitet, Medicinska fakulteten, Institutionen för samhällsmedicin och rehabilitering, Avdelningen för fysioterapi. Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Pediatrik.
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Pediatrik. Umeå universitet, Medicinska fakulteten, Institutionen för folkhälsa och klinisk medicin, Reumatologi.
Umeå universitet, Medicinska fakulteten, Institutionen för klinisk vetenskap, Pediatrik.ORCID-id: 0000-0001-6328-1098
School of Nursing & Midwifery, Trinity College Dublin, Dublin, Ireland.
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2021 (Engelska)Ingår i: Pediatric Rheumatology, E-ISSN 1546-0096, Vol. 19, nr 1, artikel-id 156Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

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.

Ort, förlag, år, upplaga, sidor
BioMed Central (BMC), 2021. Vol. 19, nr 1, artikel-id 156
Nyckelord [en]
Adolescent, Child, Juvenile idiopathic arthritis, Parent, Participation, Qualitative, Young adults
Nationell ämneskategori
Pediatrik
Identifikatorer
URN: urn:nbn:se:umu:diva-189614DOI: 10.1186/s12969-021-00642-xISI: 000714021400001PubMedID: 34727931Scopus ID: 2-s2.0-85118717334OAI: oai:DiVA.org:umu-189614DiVA, id: diva2:1612223
Forskningsfinansiär
ReumatikerförbundetNorrbacka-EugeniastiftelsenTillgänglig från: 2021-11-17 Skapad: 2021-11-17 Senast uppdaterad: 2024-02-19Bibliografiskt granskad

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Eriksson, CatharinaLind, TorbjörnFjellman-Wiklund, Anncristine

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Lundberg, VeronicaEriksson, CatharinaLind, TorbjörnFjellman-Wiklund, Anncristine
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Avdelningen för fysioterapiPediatrikReumatologi
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