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UiS Brage
Bachelor thesis . 2023
Data sources: UiS Brage
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
UiS Brage
Bachelor thesis . 2023
Data sources: UiS Brage
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Demens og brukermedvirkning

Authors: Eike, Anne; Kalvatn, Peter Tinnesen;

Demens og brukermedvirkning

Abstract

Abstract Background Patients with dementia often have communication challenges to a lesser og greater extent, and this makes them prone that their possibility for user participation weakens, both in the home when they receive home care, in transition from home to care home, and in the care home. It can exert stress for the patient, and the patient's right of user participation often gets violated. Examples of situations where the right of participation gets violated is by the use of coercion, or when the next of kin or nurses make choices on behalf of the patient. Aim The aim of the assignment is to find and describe measures to fulfil the patient's right of user participation when their possibilities of communication weakens. Method A literature analysis has been made with six chosen scientific articles in a form, in addition to other relevant literature and our own experiences and reflections. Results Good documentation and involvement of the next of kin and cooperating personell is important when arranging participation for people with dementia in situations that revolve around everyday life, in the transition phase between home and care home, and in care home. Key words: Dementia, dignity, user participation, coercion, integrity, competence, autonomy

Sammendrag Bakgrunn Pasienter med demens har som regel kommunikasjonsutfordringer i større eller mindre grad, og dette gjør at de er utsatt for at deres mulighet til medvirkning blir svekket, både i hjemmet når de mottar hjemmesykepleie, i overgangen mellom hjem og institusjon, og på institusjon. Det kan være belastende for pasientene, og pasientenes rett til medvirkning blir ofte krenket. Eksempler på situasjoner der retten til medvirkning blir krenket er ved bruk av tvang, eller når pårørende eller sykepleiere tar valg på vegne av pasienten. Hensikt Hensikten med oppgaven er å finne og beskrive aktuelle tiltak for å innfri pasientens rett til medvirkning når deres mulighet til å kommunisere svikter. Metode Det har blitt foretatt en litteraturstudie med seks utvalgte vitenskapelige forskningsartikler i en litteraturoversikt, i tillegg til annen relevant litteratur og egne erfaringer og refleksjoner. Resultater God dokumentasjon og involvering av pårørende og samarbeidende personell står sentralt for å legge til rette for at personer med demens kan medvirke i situasjoner som omhandler hverdagslivet til pasienten i overgang til institusjon og i institusjon. Nøkkelord: Demens, verdighet, medbestemmelse, medvirkning, tvang, integritet, kompetanse, autonomi

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average
Green
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