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Hur upplever föräldrar vården för barn med ätsvårigheter? En kvalitetssäkring av en mottagning för ätsvårigheter i södra Sverige

Lindholm, Vendela LU and Hassel, Elvira LU (2025) PSPR14 20242
Department of Psychology
Abstract (Swedish)
Föräldrar till barn med ätsvårigheter upplever stor stress. I Sverige finns inga nationella vårdriktlinjer för barn med ätsvårigheter. Mottagningen för ätsvårigheter arbetar med att behandla barn med ätsvårigheter och att stötta familjerna. Mottagningens vård har tidigare aldrig kvalitetsgranskats. Syftet med den här uppsatsen var undersöka hur föräldrar till barn med ätsvårigheter upplevde att vara en del av sitt barns behandling, genom att göra en kvalitetssäkring. Åtta semi-strukturerade intervjuer genomfördes med föräldrar till barn som fick behandling från mottagningen. Intervjuerna analyserades med en reflexiv konventionell innehållsanalys. Analysen resulterade i två huvudkategorier: Behandling och Bemötande. Den första kategorin... (More)
Föräldrar till barn med ätsvårigheter upplever stor stress. I Sverige finns inga nationella vårdriktlinjer för barn med ätsvårigheter. Mottagningen för ätsvårigheter arbetar med att behandla barn med ätsvårigheter och att stötta familjerna. Mottagningens vård har tidigare aldrig kvalitetsgranskats. Syftet med den här uppsatsen var undersöka hur föräldrar till barn med ätsvårigheter upplevde att vara en del av sitt barns behandling, genom att göra en kvalitetssäkring. Åtta semi-strukturerade intervjuer genomfördes med föräldrar till barn som fick behandling från mottagningen. Intervjuerna analyserades med en reflexiv konventionell innehållsanalys. Analysen resulterade i två huvudkategorier: Behandling och Bemötande. Den första kategorin beskrev föräldrarnas erfarenheter av den medicinska behandlingen. Den andra kategorin beskrev stödet och mottagandet från vårdpersonalen. Resultatet belyste både framgångsområden och utvecklingsområden inom varje kategori. De framgångsfaktorer som identifierades var bland annat alliansen med vårdpersonalen, kommunikationen mellan personal och föräldrar, kontinuerlig behandling och konkreta insatser. De utvecklingsområden som identifierades var att behandlingens syfte kunde framstå som otydligt, att skapa möjligheter för föräldrar att dela erfarenheter och ett ökat individfokus och medbestämmande. Framgångsfaktorerna och utvecklingsområdena låg i hög grad i linje med tidigare forskning. Mottagningen bör framöver arbeta med att utveckla vården som barn med ätsvårigheter får, baserat på den här kvalitetssäkringen. (Less)
Abstract
Parents of children with eating difficulties suffer from great distress. In Sweden
there are no national guidelines for the care of children with eating difficulties.
The evaluated pediatric clinic consists of a cross-professional team that treats
children with eating difficulties and supports the children’s families. The care
provided by the clinic has never been evaluated. The purpose of this thesis was to
explore how parents with children with eating difficulties experience being a part
of their child’s treatment through a qualitive assurance. Eight semi-structured
interviews were carried out with parents of children receiving treatment from the
clinic. The interviews were analyzed with a reflexive conventional content
... (More)
Parents of children with eating difficulties suffer from great distress. In Sweden
there are no national guidelines for the care of children with eating difficulties.
The evaluated pediatric clinic consists of a cross-professional team that treats
children with eating difficulties and supports the children’s families. The care
provided by the clinic has never been evaluated. The purpose of this thesis was to
explore how parents with children with eating difficulties experience being a part
of their child’s treatment through a qualitive assurance. Eight semi-structured
interviews were carried out with parents of children receiving treatment from the
clinic. The interviews were analyzed with a reflexive conventional content
analysis. The analysis resulted in two main categories: Medical treatment and
Personal treatment. The first category described the parents’ experiences of the
clinic’s medical treatment. The second category described the parents’
experiences of personal treatment with the healthcare staff. The results
highlighted both strengths and areas for development within each category. The
identified success factors included, among others, the alliance with the healthcare
staff, communication between staff and parents, continuous treatment and
concrete interventions. The areas for development identified were clarifying the
treatment’s purpose, enabling opportunities for parents to share experiences, and
increasing focus on individuality and decision-making. The success factors and
areas for development were largely in line with previous research. Moving
forward, the clinic should strive to further develop the care provided to children
with eating difficulties based on this quality assurance. (Less)
Please use this url to cite or link to this publication:
author
Lindholm, Vendela LU and Hassel, Elvira LU
supervisor
organization
course
PSPR14 20242
year
type
H3 - Professional qualifications (4 Years - )
subject
keywords
Pediatric feeding disorder, ätsvårigheter, kvalitetssäkring, föräldrar, eating difficulties, quality assurance, treatment, parents
language
Swedish
id
9183224
date added to LUP
2025-01-30 08:41:13
date last changed
2025-01-30 08:41:13
@misc{9183224,
  abstract     = {{Parents of children with eating difficulties suffer from great distress. In Sweden
there are no national guidelines for the care of children with eating difficulties.
The evaluated pediatric clinic consists of a cross-professional team that treats
children with eating difficulties and supports the children’s families. The care
provided by the clinic has never been evaluated. The purpose of this thesis was to
explore how parents with children with eating difficulties experience being a part
of their child’s treatment through a qualitive assurance. Eight semi-structured
interviews were carried out with parents of children receiving treatment from the
clinic. The interviews were analyzed with a reflexive conventional content
analysis. The analysis resulted in two main categories: Medical treatment and
Personal treatment. The first category described the parents’ experiences of the
clinic’s medical treatment. The second category described the parents’
experiences of personal treatment with the healthcare staff. The results
highlighted both strengths and areas for development within each category. The
identified success factors included, among others, the alliance with the healthcare
staff, communication between staff and parents, continuous treatment and
concrete interventions. The areas for development identified were clarifying the
treatment’s purpose, enabling opportunities for parents to share experiences, and
increasing focus on individuality and decision-making. The success factors and
areas for development were largely in line with previous research. Moving
forward, the clinic should strive to further develop the care provided to children
with eating difficulties based on this quality assurance.}},
  author       = {{Lindholm, Vendela and Hassel, Elvira}},
  language     = {{swe}},
  note         = {{Student Paper}},
  title        = {{Hur upplever föräldrar vården för barn med ätsvårigheter? En kvalitetssäkring av en mottagning för ätsvårigheter i södra Sverige}},
  year         = {{2025}},
}