Literature DB >> 31633828

Being a burden to others and wishes to die: The importance of the sociopolitical context.

Bernadette Roest1, Margo Trappenburg1, Carlo Leget1.   

Abstract

All articles in May 2019's special issue of Bioethics offer profound insights into the issue of "being a burden to others" in relation to wishes to die, which are highly relevant for ethical debates about end-of-life care and physician-assisted dying. In this reply, we wish to stress the importance of acknowledging and analyzing the sociopolitical context of the phenomenon "being a burden" in relation to wishes to die and we will show how this analysis could benefit from a care ethical approach. As discussions in care ethics have made clear, caring practices are both social and political practices. An empirical and ethical analysis of "being a burden" therefore needs to take institutional and societal norms and structures into account, in addition to first-person experiences and concepts such as caring needs, relational autonomy, and interdependency. Besides the relevance of the sociopolitical context for the phenomenon "being a burden" as such, the sociopolitical context also seems relevant for the investigation of the phenomenon, which we will illustrate by reflecting on "being a burden" in relation to the practice of physician-assisted dying in the Netherlands.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  being a burden; care ethics; physician-assisted dying; sociopolitical context; wish to die

Year:  2019        PMID: 31633828     DOI: 10.1111/bioe.12688

Source DB:  PubMed          Journal:  Bioethics        ISSN: 0269-9702            Impact factor:   1.898


  3 in total

1.  Relational autonomy in end-of-life care ethics: a contextualized approach to real-life complexities.

Authors:  Carlos Gómez-Vírseda; Yves de Maeseneer; Chris Gastmans
Journal:  BMC Med Ethics       Date:  2020-06-30       Impact factor: 2.652

2.  Perceived Burdensomeness and the Wish for Hastened Death in Persons With Severe and Persistent Mental Illness.

Authors:  Julia Stoll; Christopher James Ryan; Manuel Trachsel
Journal:  Front Psychiatry       Date:  2021-01-12       Impact factor: 4.157

3.  How can we improve the experiences of patients and families who request medical assistance in dying? A multi-centre qualitative study.

Authors:  Simon J W Oczkowski; Diane E Crawshaw; Peggy Austin; Donald Versluis; Gaelen Kalles-Chan; Michael Kekewich; Dorothyann Curran; Paul Miller; Michaela Kelly; Ellen Wiebe; Andrea Frolic
Journal:  BMC Palliat Care       Date:  2021-12-08       Impact factor: 3.234

  3 in total

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