Literature DB >> 33118991

Needs of caregivers of patients receiving in-home palliative and end-of-life care.

Elizabeth Pepin1, Johanne Hébert2.   

Abstract

Home support for patients receiving in-home palliative and end-of-life care (PELC) is greatly dependent on the daily presence of caregivers and their involvement in care delivery. However, the needs of caregivers throughout the care trajectory of a loved one receiving in-home PELC are still relatively unknown. OBJECTIVES AND
METHODOLOGY: This descriptive qualitative study focuses on the role of caregivers who have cared for a person receiving in-home PELC with the goal of describing their needs throughout the care trajectory. As part of this process, 20 caregivers took part in semi-directed interviews. RESULTS AND DISCUSSION: This study sheds light on the multiple needs of caregivers of loved ones receiving in-home PELC. These informational, emotional, and psychosocial needs show that caregivers experience changes in their relationship with their loved one. Spiritual needs were expressed through the meaning ascribed to the home support experience. And the practical needs expressed by participants highlight the importance of round-the-clock access to PELC services and the essential importance of nursing support.
CONCLUSION: The needs of caregivers of loved ones receiving in-home PELC are not being met to a satisfactory degree. It is important to consider these needs in the care trajectory, alongside the needs of the patients themselves, in order to improve the support experience leading up to the bereavement period.
© 2020 Canadian Association of Nurses in Oncology (CANO).

Entities:  

Keywords:  caregivers; needs; nursing role; palliative and end-of-life care; transition

Year:  2020        PMID: 33118991      PMCID: PMC7586699          DOI: 10.5737/23688076302147152

Source DB:  PubMed          Journal:  Can Oncol Nurs J        ISSN: 1181-912X


  20 in total

1.  An exploration into the palliative and end-of-life experiences of carers of people with Parkinson's disease.

Authors:  Felicity Hasson; W George Kernohan; Marian McLaughlin; Mary Waldron; Dorry McLaughlin; Helen Chambers; Barbara Cochrane
Journal:  Palliat Med       Date:  2010-06-04       Impact factor: 4.762

2.  Caring at home until death: enabled determination.

Authors:  Carole A Robinson; Joan L Bottorff; Erin McFee; Laura J Bissell; Gillian Fyles
Journal:  Support Care Cancer       Date:  2016-12-06       Impact factor: 3.603

3.  'You only have one chance to get it right': A qualitative study of relatives' experiences of caring at home for a family member with terminal cancer.

Authors:  Jonathan Totman; Nancy Pistrang; Susan Smith; Susan Hennessey; Jonathan Martin
Journal:  Palliat Med       Date:  2015-01-29       Impact factor: 4.762

4.  Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool.

Authors:  Samar M Aoun; Kathleen Deas; Linda J Kristjanson; David W Kissane
Journal:  Palliat Support Care       Date:  2016-05-13

5.  Preparedness for caregiving: A phenomenological study of the experiences of rural Australian family palliative carers.

Authors:  Naomi Mason; Suzanne Hodgkin
Journal:  Health Soc Care Community       Date:  2019-02-27

6.  Preparing for family caregiving in specialized palliative home care: an ongoing process.

Authors:  Maja Holm; Anette Henriksson; Ida Carlander; Yvonne Wengström; Joakim Öhlen
Journal:  Palliat Support Care       Date:  2014-06-09

7.  Barriers and facilitators influencing death at home: A meta-ethnography.

Authors:  Abdul Samad Wahid; Meelad Sayma; Shiraz Jamshaid; Doa'a Kerwat; Folashade Oyewole; Dina Saleh; Aaniya Ahmed; Benita Cox; Claire Perry; Sheila Payne
Journal:  Palliat Med       Date:  2017-06-12       Impact factor: 4.762

8.  A model of caregiving through the end of life: seeking normal.

Authors:  Janice Penrod; Judith E Hupcey; Peggy Z Shipley; Susan J Loeb; Brenda Baney
Journal:  West J Nurs Res       Date:  2011-03-14       Impact factor: 1.967

9.  What family caregivers learn when providing care at the end of life: a qualitative secondary analysis of multiple datasets.

Authors:  Laura M Funk; Kelli I Stajduhar; Linda Outcalt
Journal:  Palliat Support Care       Date:  2014-02-13

10.  Dying at home: a qualitative study of family carers' views of support provided by GPs community staff.

Authors:  David Seamark; Susan Blake; Sarah G Brearley; Christine Milligan; Carol Thomas; Mary Turner; Xu Wang; Sheila Payne
Journal:  Br J Gen Pract       Date:  2014-12       Impact factor: 5.386

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