Literature DB >> 29288877

Family Caregivers' Reflections on Experiences of Assisted Suicide in Switzerland: A Qualitative Interview Study.

C Gamondi1, Murielle Pott2, Nancy Preston3, Sheila Payne3.   

Abstract

CONTEXT: Thousands of family members worldwide are annually involved in assisted dying. Family participation in assisted dying has rarely been investigated and families' needs typically are not considered in assisted dying legislation and clinical guidelines.
OBJECTIVES: To explore family caregivers' reflections on experiences of assisted suicide in Switzerland.
METHODS: A cross-sectional qualitative interview study conducted in the Italian- and French-speaking regions of Switzerland. Interpretation and analysis were performed using qualitative content analysis.
RESULTS: Twenty-eight close relatives and family carers of 18 patients who died by assisted suicide in Switzerland were interviewed. Family members perceived their involvement in assisted suicide as characterized by five phases; 1) contemplation, 2) gaining acceptance, 3) gaining permission, 4) organization, and 5) aftermath. Families can participate in these phases at diverse levels and with varying degrees of involvement. Important triggers for families and patients for transition between phases include patients' experiences of their life-threatening illnesses and related treatments, their increasing awareness of approaching death, and family member recognition of their loved one's unbearable suffering. Participating in assisted suicide created further demanding tasks for families in addition to their role of caregivers.
CONCLUSION: Families appeared to be involved in the preparation of assisted suicide along with patients, irrespective of their personal values regarding assisted dying. Support for family members is essential if they are involved in tasks preparatory to assisted suicide. Clinical guidelines and policies concerning assisted dying should acknowledge and address family needs.
Copyright © 2017 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Assisted suicide; assisted dying; decision making; euthanasia; families' experiences; family relations; palliative care; qualitative research

Mesh:

Year:  2017        PMID: 29288877     DOI: 10.1016/j.jpainsymman.2017.12.482

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  5 in total

1.  In-hospital care prior to assisted and unassisted suicide in swiss older people: a state-level retrospective study.

Authors:  Nathalie Dieudonné-Rahm; Sandra Burkhardt; Sophie Pautex
Journal:  BMC Geriatr       Date:  2019-11-06       Impact factor: 3.921

2.  Comparison of the experience of caregiving at end of life or in hastened death: a narrative synthesis review.

Authors:  Jane Lowers; Melissa Scardaville; Sean Hughes; Nancy J Preston
Journal:  BMC Palliat Care       Date:  2020-10-08       Impact factor: 3.234

3.  Assisted Suicide in Parkinsonian Disorders.

Authors:  Georg S Nuebling; Elisabeth Butzhammer; Stefan Lorenzl
Journal:  Front Neurol       Date:  2021-03-15       Impact factor: 4.003

4.  Travelling to die: views, attitudes and end-of-life preferences of Israeli considering receiving aid-in-dying in Switzerland.

Authors:  Daniel Sperling
Journal:  BMC Med Ethics       Date:  2022-04-30       Impact factor: 2.834

5.  A Race to the End: Family Caregivers' Experience of Medical Assistance in Dying (MAiD)-a Qualitative Study.

Authors:  Tharshika Thangarasa; Sarah Hales; Eryn Tong; Ekaterina An; Debbie Selby; Elie Isenberg-Grzeda; Madeline Li; Gary Rodin; Sally Bean; Jennifer A H Bell; Rinat Nissim
Journal:  J Gen Intern Med       Date:  2021-07-21       Impact factor: 5.128

  5 in total

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