Literature DB >> 32584638

The Seismic Shift in End-of-Life Care: Palliative Care Challenges in the Era of Medical Assistance in Dying.

Anita Ho1,2,3, Soodabeh Joolaee3,4,5, Kim Jameson1,6, Christopher Ng7.   

Abstract

Background: Concerns regarding personal, professional, administrative, and institutional implications of medical assistance in dying (MAiD) are of particular interest to palliative and hospice care providers (PHCPs), who may encounter additional moral distress and professional challenges in providing end-of-life (EOL) care in the new legislative and cultural era. Objective: To explore PHCPs' encountered challenges and resource recommendations for caring for patients considering MAiD. Design: Qualitative thematic analysis of audio-recorded semistructured interviews with PHCPs. Setting/Subjects: Multidisciplinary PHCPs in acute, community, residential, and hospice care in Vancouver, Canada, with experience supporting patients who have made MAiD inquiries or requests. Measurements: Interviews were deidentified, transcribed verbatim, and coded by four researchers using a common coding scheme. Key themes were analyzed.
Results: Twenty-six PHCP participants included physicians (n = 7), nurses (n = 12), social workers (n = 5), and spiritual health practitioners (n = 2). Average interview length was 52 minutes (range 35-90). Analysis revealed four broad challenges associated with providing EOL care after MAiD legalization: (1) moral ambiguity and provider distress, (2) family distress, (3) interprofessional team conflict, and (4) impact on palliative care. Participants also recommended three types of resources to support clinicians in delivering quality EOL care to patients contemplating MAiD: (1) education and training, (2) pre- and debriefing for team members, and (3) tailored bereavement support. Conclusions: PHCPs encountered multilevel MAiD-related challenges, but noted improvement in organizational policies and coordination. Resources to enhance training, pre- and debriefing, and tailored bereavement may further support PHCPs in providing high-quality EOL care as they navigate the legislative and cultural shifts.

Entities:  

Keywords:  Canada; bioethics; hospice care; medical assistance in dying; palliative care; qualitative research

Year:  2020        PMID: 32584638     DOI: 10.1089/jpm.2020.0185

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  4 in total

1.  Being a safe place: a qualitative study exploring perceptions as to how a rural community hospice could respond to enactment of voluntary assisted dying legislation.

Authors:  Kirsten Auret; Terri Pikora; Kate Gersbach
Journal:  BMC Palliat Care       Date:  2022-01-04       Impact factor: 3.234

2.  Exploring key stakeholders' attitudes and opinions on medical assistance in dying and palliative care in Canada: a qualitative study protocol.

Authors:  Gilla K Shapiro; Eryn Tong; Rinat Nissim; Camilla Zimmermann; Sara Allin; Jennifer Gibson; Madeline Li; Gary Rodin
Journal:  BMJ Open       Date:  2021-12-03       Impact factor: 2.692

3.  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

4.  Medical assistance in dying legislation: Hospice palliative care providers' perspectives.

Authors:  Soodabeh Joolaee; Anita Ho; Kristie Serota; Matthieu Hubert; Daniel Z Buchman
Journal:  Nurs Ethics       Date:  2021-09-19       Impact factor: 2.874

  4 in total

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