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Upplevelser av bemötande i vården hos patienter med fibromyalgi- en litteraturöversikt
Dalarna University, School of Education, Health and Social Studies, Caring Science/Nursing.
Dalarna University, School of Education, Health and Social Studies, Caring Science/Nursing.
2016 (Swedish)Independent thesis Basic level (professional degree), 10 credits / 15 HE creditsStudent thesisAlternative title
Patients experiences of treatment, support and attitudes in health care - a literature review (English)
Abstract [sv]

Bakgrund: Fibromyalgi är ett långvarigt kroniskt smärttillstånd som grundar sig på individens subjektiva smärtupplevelse. Syfte: Syftet var att beskriva hur patienter med fibromyalgi upplevt bemötande i vården. Metod: Denna litteraturöversikt baseras på tretton vetenskapliga artiklar. Resultat: Resultatet resulterade i två huvudkategorier "Patienters upplevelser av bemötande" och "Kunskap och stöd från vårdpersonalen". Patienterna med fibromyalgi upplever dåligt bemötande och att vårdpersonal saknar kunskap om både diagnos och behandling av fibromyalgi. I vården upplever dessa patienter misstro och att de blir dåligt bemötta när de söker för sina smärtsymtom. Patienter med fibromyalgidiagnos önskar ett personcentrerat bemötande och mer tid av sina läkare. Slutsatser: Litteraturöversikten visar att patienter med fibromyalgi i stor utsträckning uppger att de upplever dåligt bemötande, okunskap och brist på engagemang i vården. Framtida forskningen bör fokusera på hur vården kan arbeta mer personcentrerat i denna patientgrupp till exempel genom interventionsstudier.

Abstract [en]

Objectives: Fibromyalgia has long been a chronic pain condition that bases itself on the individual's subjective experience of pain. Aim: The aim was to describe how patients with fibromyalgia experience the treatment, support and attitudes by the health care personal. Methods: This study is a literature review based on thirteen articles’. Results: The result resulted in two main categories "Patients experiences of treatment" and "Knowledge and support from the medical staff". The patients experience that the health care personal has a lack of knowledge of both diagnosis and treatment. The patients also experience distrust in their doctors and experience a lack of adequate help when seeking for their painful symptoms. Patients with fibromyalgia diagnosis experience poor treatment in health care, and want a person-centered approach and more time by their doctors. Conclusions: This literature review shows that patients with fibromyalgia report that they experience poor treatment, ignorance and lack of commitment from health care. Research should focus on how services can work more person-centered for this group of patients, for example by intervention studies.

Place, publisher, year, edition, pages
2016.
Keyword [en]
experience, fibromyalgia, health care, patient, person centered care
Keyword [sv]
fibromyalgi, patient, personcentrerad vård, vårdpersonal, upplevelse
National Category
Nursing
Identifiers
URN: urn:nbn:se:du-20938OAI: oai:DiVA.org:du-20938DiVA: diva2:900735
Available from: 2016-02-05 Created: 2016-02-05

Open Access in DiVA

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7122a5a91af4a8a993ca69ad2ee4e3559fac9b716902edca8d1f6aac0cbb2a40970dbe3b9ad949d38a575c3f97faddaa706fef93e99f1b03a5e879597ddf8b58
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CiteExportLink to record
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Citation style
  • apa
  • harvard1
  • ieee
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