Literature DB >> 30328125

Institutional non-participation in assisted dying: Changing the conversation.

Philip Shadd1, Joshua Shadd2.   

Abstract

Whether institutions and not just individual doctors have a right to not participate in medical assistance in dying (MAID) is controversial, but there is a tendency to frame the issue of institutional non-participation in a particular way. Conscience is central to this framing. Non-participating health centres are assumed to be religious and full participation is expected unless a centre objects on conscience grounds. In this paper we seek to reframe the issue. Institutional non-participation is plausibly not primarily, let alone exclusively, about conscience. We seek to reframe the issue by making two main points. First, institutional non-participation is primarily a matter of institutional self-governance. We suggest that institutions have a natural right of self-governance which, in the case of health centres such as hospitals or hospices, includes the right to choose whether or not to offer MAID. Second, there are various legitimate reasons unrelated to conscience for which a health centre might not offer MAID. These range from considerations such as institutional capacity and expertise to a potential contradiction with palliative care and a concern to not conflate palliative care and MAID in public consciousness. It is a mistake to frame the conversation simply in terms of conscience-based opposition to MAID or full participation. Our goal is to open up new space in the conversation, for reasons unrelated to conscience as well as for non-religious health centres who might nonetheless have legitimate grounds for not participating in MAID.
© 2018 John Wiley & Sons Ltd.

Keywords:  conscientious objection; institutional non-participation; institutional rights; medical assistance in dying; palliative care

Mesh:

Year:  2018        PMID: 30328125     DOI: 10.1111/bioe.12528

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


  5 in total

1.  Hospice care providers experiences of grappling with medical assistance in dying in a hospice setting: a qualitative descriptive study.

Authors:  Shannon Freeman; Davina Banner; Valerie Ward
Journal:  BMC Palliat Care       Date:  2021-04-12       Impact factor: 3.234

2.  How does Medical Assistance in Dying affect end-of-life care planning discussions? Experiences of Canadian multidisciplinary palliative care providers.

Authors:  Anita Ho; Joshua S Norman; Soodabeh Joolaee; Kristie Serota; Louise Twells; Leeroy William
Journal:  Palliat Care Soc Pract       Date:  2021-09-20

3.  "Respecting our patients' choices": making the organizational decision to participate in voluntary assisted dying provision: findings from semi-structured interviews with a rural community hospice board of management.

Authors:  Kirsten Auret; Terri J Pikora; Kate Gersbach; Robert J Donovan
Journal:  BMC Palliat Care       Date:  2022-09-16       Impact factor: 3.113

4.  The rocks and hard places of MAiD: a qualitative study of nursing practice in the context of legislated assisted death.

Authors:  Barbara Pesut; Sally Thorne; Catharine J Schiller; Madeleine Greig; Josette Roussel
Journal:  BMC Nurs       Date:  2020-02-17

5.  Junior doctors and conscientious objection to voluntary assisted dying: ethical complexity in practice.

Authors:  Rosalind J McDougall; Ben P White; Danielle Ko; Louise Keogh; Lindy Willmott
Journal:  J Med Ethics       Date:  2021-06-14       Impact factor: 5.926

  5 in total

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