Literature DB >> 22742736

The end of life and the family: hospice patients' views on dying as relational.

Alex Broom1, Emma Kirby.   

Abstract

The end of life is a highly emotive and critical period in the life course and families often play a central role during this time. Despite significant sociological work on dying as a relational experience, there has been little exploration of the significance of contemporary family structures and relations. In this article, drawing on the accounts of twenty hospice in-patients, we explore how the end of life (in this case within an in-patient unit) is mediated by family dynamics and expectations. Participants' accounts reveal a range of interpersonal experiences, including: pressures and strains on families and patients; differentiation in family responses to and involvement in the dying process; and tensions between individual and family preferences/desires. We argue that family dynamics strongly influence individual experiences near death and that the focus on individual preferences and the management of disease in palliative care contexts must be augmented with sophisticated and nuanced understandings of the family context. We suggest that sociological conceptual explanations of shifts in social and family life, such as individualisation and ontological security, may also help us better understand the ways families approach and respond to the dying process.
© 2012 The Authors. Sociology of Health & Illness © 2012 Foundation for the Sociology of Health & Illness/Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2012        PMID: 22742736     DOI: 10.1111/j.1467-9566.2012.01497.x

Source DB:  PubMed          Journal:  Sociol Health Illn        ISSN: 0141-9889


  12 in total

1.  Expanded definitions of the 'good death'? Race, ethnicity and medical aid in dying.

Authors:  Cindy L Cain; Sara McCleskey
Journal:  Sociol Health Illn       Date:  2019-04-04

Review 2.  Sociological contributions to race and health: Diversifying the ontological and methodological agenda.

Authors:  Hyeyoung Oh Nelson; Karen Lutfey Spencer
Journal:  Sociol Health Illn       Date:  2021-08-26

Review 3.  Dealing with Family Conflicts in Decision-making in End-of-Life Care of Advanced Cancer Patients.

Authors:  Katsiaryna Laryionava; Eva Caroline Winkler
Journal:  Curr Oncol Rep       Date:  2021-08-27       Impact factor: 5.075

4.  Influences on Care Preferences of Older People with Advanced Illness: A Systematic Review and Thematic Synthesis.

Authors:  Simon N Etkind; Anna E Bone; Natasha Lovell; Irene J Higginson; Fliss E M Murtagh
Journal:  J Am Geriatr Soc       Date:  2018-03-07       Impact factor: 5.562

5.  Family food practices: relationships, materiality and the everyday at the end of life.

Authors:  Julie Ellis
Journal:  Sociol Health Illn       Date:  2018-02

6.  Relational Autonomy, the Right to Reject Treatment, and Advance Directives in Japan.

Authors:  Anri Asagumo
Journal:  Asian Bioeth Rev       Date:  2021-10-09

7.  "It doesn't exist…": negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective.

Authors:  Emma Kirby; Zarnie Lwin; Katherine Kenny; Alex Broom; Holi Birman; Phillip Good
Journal:  BMC Palliat Care       Date:  2018-07-02       Impact factor: 3.234

8.  Palliative care utilization in oncology and hemato-oncology: a systematic review of cognitive barriers and facilitators from the perspective of healthcare professionals, adult patients, and their families.

Authors:  Marco Bennardi; Nicola Diviani; Claudia Gamondi; Georg Stüssi; Piercarlo Saletti; Ivan Cinesi; Sara Rubinelli
Journal:  BMC Palliat Care       Date:  2020-04-13       Impact factor: 3.234

9.  Relational autonomy: what does it mean and how is it used in end-of-life care? A systematic review of argument-based ethics literature.

Authors:  Carlos Gómez-Vírseda; Yves de Maeseneer; Chris Gastmans
Journal:  BMC Med Ethics       Date:  2019-10-26       Impact factor: 2.652

10.  Introducing the trajectory Touchpoint technique: a systematic methodology for capturing the service experiences of palliative care patients and their families.

Authors:  Lynn Sudbury-Riley; Philippa Hunter-Jones; Ahmed Al-Abdin
Journal:  BMC Palliat Care       Date:  2020-07-10       Impact factor: 3.234

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