• norsk
    • English
  • norsk 
    • norsk
    • English
  • Logg inn
Vis innførsel 
  •   Hjem
  • University of Bergen Library
  • Registrations from Cristin
  • Vis innførsel
  •   Hjem
  • University of Bergen Library
  • Registrations from Cristin
  • Vis innførsel
JavaScript is disabled for your browser. Some features of this site may not work without it.

Forced treatment and care in home-dwelling persons with dementia

Gjellestad, Åshild; Oksholm, Trine; Bruvik, Frøydis Kristine
Journal article, Peer reviewed
Accepted version
Thumbnail
Åpne
accepted version (838.9Kb)
Permanent lenke
https://hdl.handle.net/11250/2753295
Utgivelsesdato
2020
Metadata
Vis full innførsel
Samlinger
  • Department of Global Public Health and Primary Care [2508]
  • Registrations from Cristin [5248]
Originalversjon
Nursing Ethics. 2020.   10.1177/0969733020948107
Sammendrag
Background: The use of forced treatment and care of home-dwelling persons with dementia is a universally important topic. These patients are completely dependent on care from others to continue living at home.

Aim: This study aimed to gain insights into formal decisions related to the forced treatment and care of home-dwelling persons with dementia.

Design and sample: This is a cross-sectional study, based on formal decisions of forced treatment and care of home-dwelling persons with dementia in Norway between 1 January 2015 and 31 December 2016.

Methods: Descriptive statistical analysis. Statistically significant associations suitable for binary logistic regression were presented as odds ratios with 95% confidence intervals.

Ethical considerations: Approved by The Regional Committee for Medical and Health Research Ethics, and by the Norwegian Center for Research.

Results: We found 108 formal decisions of forced treatment and care of persons with dementia. Decisions of admission represented 57% of the data, other medical and safety decisions 27%, and assistance with activities of daily living 16%. In most cases, physicians were responsible for the decisions (77%), but nurses and family members were often involved.

Discussion and conclusion: This study demonstrated a prevalence rate of formally documented decisions of forced treatment and care much lower than findings in previous studies. Poor documentation may constitute a risk for the safety and wellbeing of persons with dementia. Although physicians were usually responsible for the decisions, nurses and family members were often involved in the process. Family participation in forced treatment and care raises ethical dilemmas. More research on the experiences of nurses, persons with dementia and family members with forced treatment and care is needed to aid ethical, legal, and clinically challenging decision-making processes.
Utgiver
SAGE
Tidsskrift
Nursing Ethics
Opphavsrett
Copyright the authors 2020.

Kontakt oss | Gi tilbakemelding

Personvernerklæring
DSpace software copyright © 2002-2019  DuraSpace

Levert av  Unit
 

 

Bla i

Hele arkivetDelarkiv og samlingerUtgivelsesdatoForfattereTitlerEmneordDokumenttyperTidsskrifterDenne samlingenUtgivelsesdatoForfattereTitlerEmneordDokumenttyperTidsskrifter

Min side

Logg inn

Statistikk

Besøksstatistikk

Kontakt oss | Gi tilbakemelding

Personvernerklæring
DSpace software copyright © 2002-2019  DuraSpace

Levert av  Unit