Literature DB >> 32854581

Care Considerations in a Patient- and Family-Centered Medical Assistance in Dying Program.

Janine Brown1,2, Donna Goodridge3, Averi Harrison3, Jordan Kemp3, Lilian Thorpe4,5, Robert Weiler6,7.   

Abstract

Objective: Medical Assistance in Dying (MAID) became legal in Canada in June 2016. As part of a project designed to improve end-of-life care for those requesting MAID, qualitative data from patients, families, and providers were used to assess opportunities to enhance patient-and family-centered care (PFCC) in this program.
Methods: Thirty interviews were conducted with patients, families, and healthcare providers. Five patients who requested an assessment for MAID, 11 family members, and 14 healthcare providers were interviewed about their experiences in 2017. Comparative coding and thematic analysis were completed with the support of NVivo12.
Results: Emotional PFCC considerations included: exploring and validating the emotional journey, navigating the uncertain, judgmental experiences, and the emotional impact on families and the care team. Physical PFCC considerations included: sensitivity in eligibility assessments, weaving in interdisciplinary care, provision of anticipatory guidance, and death location. Spiritual PFCC considerations included: honoring choice, listening to life stories, supporting spiritual needs, and acknowledging loss. Relational PFCC considerations included: defining the circle of support, supporting the circle, and relational investments.
Conclusion: Fundamental to a PFCC MAID program, practitioners must be afforded time to provide holistic care. Program-related suggestions include incorporating interdisciplinary care early, and throughout the illness trajectory, consistency in care providers, appropriate anticipatory guidance, and bereavement supports for family, and dedicate space for MAID provisions. Patients and families must be included in the ongoing development and re-evaluation of MAID programs to ensure continued focus on quality end-of-life care.

Entities:  

Keywords:  end-of-life care; interdisciplinary care; medical assistance in dying; patient-and-family centered care; qualitative research; quality improvement

Mesh:

Year:  2020        PMID: 32854581     DOI: 10.1177/0825859720951661

Source DB:  PubMed          Journal:  J Palliat Care        ISSN: 0825-8597            Impact factor:   1.980


  3 in total

1.  Health care providers' ethical perspectives on waiver of final consent for Medical Assistance in Dying (MAiD): a qualitative study.

Authors:  Caroline Variath; Elizabeth Peter; Lisa Cranley; Dianne Godkin
Journal:  BMC Med Ethics       Date:  2022-01-30       Impact factor: 2.652

2.  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.  Experiences of healthcare providers with eligible patients' loss of decision-making capacity while awaiting medical assistance in dying.

Authors:  Caroline Variath; Elizabeth Peter; Lisa Cranley; Dianne Godkin
Journal:  Palliat Care Soc Pract       Date:  2022-10-14
  3 in total

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