Literature DB >> 25350215

Preparing for palliative caregiving as a transition in the awareness of death: family carer experiences.

Anna Janze1, Anette Henriksson.   

Abstract

AIM: The aim of this study was to explore family caregivers´ experiences from partners' stories about preparing for caregiving.
METHODS: The study had a descriptive and interpretive design using qualitative interviews and qualitative content analysis.
RESULTS: Preparing for caregiving was described in the two sub-themes: living in uncertainty, focusing on the present and preparing for the future; and preparing for caregiving while transitioning to new roles. One overarching theme 'preparing for caregiving in awareness of death' was seen as a common thread throughout the results. Preparing meant dealing with changes in life, living in uncertainty and transitioning to new roles.
CONCLUSION: Family (partner) caregivers continuously tried to prepare in different ways in response to their partners' illness. Preparing for caregiving meant to willingly or unwillingly prepare for the dying and death of their partner and awareness about this was always present in some way, influencing the whole experience.

Entities:  

Keywords:  Caregiving; Family caregivers; Hospice care; Palliative care; Spouse caregivers

Mesh:

Year:  2014        PMID: 25350215     DOI: 10.12968/ijpn.2014.20.10.494

Source DB:  PubMed          Journal:  Int J Palliat Nurs        ISSN: 1357-6321


  6 in total

1.  Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers.

Authors:  Maja Holm; Ida Carlander; Carl-Johan Fürst; Yvonne Wengström; Kristofer Årestedt; Joakim Öhlen; Anette Henriksson
Journal:  BMC Palliat Care       Date:  2015-04-24       Impact factor: 3.234

2.  Constructing stability - a classic grounded theory of next-of-kin in palliative cancer care.

Authors:  Carina Werkander Harstäde; Anna Sandgren
Journal:  BMC Palliat Care       Date:  2020-06-05       Impact factor: 3.234

3.  What does it mean to be the main caregiver to a terminally ill family member in Lithuania?: A qualitative study.

Authors:  Jolanta Kuznecovienė; Rūta Butkevičienė; W David Harrison; Eimantas Peičius; Gvidas Urbonas; Kristina Astromskė
Journal:  PLoS One       Date:  2022-05-12       Impact factor: 3.752

4.  Adolescents' and young people's needs and preferences for support when living with a parent with life-threatening cancer: a grounded theory study.

Authors:  Emily Bergersen; Maria Larsson; Malin Lövgren; Cecilia Olsson
Journal:  BMC Palliat Care       Date:  2022-09-22       Impact factor: 3.113

5.  Intensity of Predeath Grief and Postdeath Grief of Family Caregivers in Palliative Care in Relation to Preparedness for Caregiving, Caregiver Burden, and Social Support.

Authors:  Lena Axelsson; Anette Alvariza; Maja Holm; Kristofer Årestedt
Journal:  Palliat Med Rep       Date:  2020-09-09

6.  Striving for a balance between leading and following the patient and family - nurses' strategies to facilitate the transition from life-prolonging care to palliative care: an interview study.

Authors:  Ulrika Hilding; Renée Allvin; Karin Blomberg
Journal:  BMC Palliat Care       Date:  2018-04-03       Impact factor: 3.234

  6 in total

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