Literature DB >> 23510011

Respecting autonomy in the end-of-life care of people with intellectual disabilities: a qualitative multiple-case study.

N Bekkema1, A J E de Veer, C M P M Hertogh, A L Francke.   

Abstract

BACKGROUND: The aim of this article was to describe how caregivers and relatives shape respect for autonomy in the end-of-life care for people with intellectual disabilities (ID) and to discuss to what extent this corresponds with a relational concept of autonomy, such as described in care ethics.
METHOD: This study consisted of a qualitative design in which the cases of 12 recently deceased people with ID were reconstructed by interviewing the caregivers and relatives who were closest to the person at the end of their life. A cyclic process of data collection and analysis was used. Interviews were transcribed verbatim and data were analysed inductively.
RESULTS: Respect for autonomy in the end-of-life care of people with ID was mainly reflected in helping the person with ID familiarise with three transitions: new information on the diagnosis and prognosis, changing care needs and wishes, and important decisions that were at stake. In respecting autonomy, relatives and caregivers encountered several challenges. These concerned ascertaining information needs, communicating about illness and death, inexperience in end-of-life care, eliciting current and hidden last wishes, the dependence of people with ID and conflicting wishes. Several qualities were important for respecting autonomy: attention to information needs, connecting, recognising end-of-life care needs, giving space to show wishes and preferences, and discussing dilemmas.
CONCLUSIONS: If caregivers and relatives embrace autonomy as a relational construct, attained through an open, active and reflective attitude, and have more access to knowledge about communication and how to identify end-of-life care needs, this could lead to improved respect for the ID persons' autonomy at the end of life. We discuss the view that a relational concept of autonomy is useful for describing respect for autonomy in end-of-life care for people with ID, but that more reflection and openness is needed to sufficiently employ relationships and regard autonomy as a product of joint work.
© 2013 The Authors. Journal of Intellectual Disability Research © 2013 John Wiley & Sons Ltd, MENCAP & IASSIDD.

Entities:  

Keywords:  autonomy; decision-making; end-of-life care; ethics; intellectual disabilities; truth-telling

Mesh:

Year:  2013        PMID: 23510011     DOI: 10.1111/jir.12023

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  4 in total

1.  'From activating towards caring': shifts in care approaches at the end of life of people with intellectual disabilities; a qualitative study of the perspectives of relatives, care-staff and physicians.

Authors:  Nienke Bekkema; Anke J E de Veer; Cees M P M Hertogh; Anneke L Francke
Journal:  BMC Palliat Care       Date:  2015-07-25       Impact factor: 3.234

2.  Withholding treatment and intellectual disability: Second survey on end-of-life decisions in Switzerland.

Authors:  Monika T Wicki
Journal:  SAGE Open Med       Date:  2016-06-06

3.  The palliative care needs of adults with intellectual disabilities and their access to palliative care services: A systematic review.

Authors:  Emily Adam; Katherine E Sleeman; Sarah Brearley; Katherine Hunt; Irene Tuffrey-Wijne
Journal:  Palliat Med       Date:  2020-06-17       Impact factor: 4.762

4.  Disability-based arguments against assisted dying laws.

Authors:  Ben Colburn
Journal:  Bioethics       Date:  2022-04-07       Impact factor: 2.512

  4 in total

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