Literature DB >> 27113470

Supporting older people with cancer and life-limiting conditions dying at home: a qualitative study of patient and family caregiver experiences of Hospice at Home care.

Barbara A Jack1, Tracy K Mitchell1, Louise C Cope2, Mary R O'Brien1.   

Abstract

AIM: To explore patients' and family caregivers' experiences and perceptions of Hospice at Home care.
BACKGROUND: The public indicate a preference to be cared for and to die at home. This has inherent challenges, with a key factor being the family caregiver. Supporting end-of-life care at home has resulted in the expansion of Hospice at Home services. A wide configuration of services exists with a lack of robust evidence as to what is valued by recipients, particularly those who are older people.
DESIGN: A prospective descriptive qualitative study.
METHODS: Recruitment was purposive. Eligible participants were in receipt of Hospice at Home service on at least three occasions and were deemed to have a life expectancy measured in weeks rather than days. Digitally recorded semistructured interviews with 41 participants (16 patients and 25 family caregivers) were undertaken between October 2014 - July 2015. Data were analysed and organized thematically.
RESULTS: Several subthemes: 'Talking about'; 'Knowing and Doing'; 'Caring for the Caregivers'; and 'Promoting Choice' contributed to the overall theme of Embracing Holism. A positive impact on emotional, psychological, social and physical well-being was apparent.
CONCLUSIONS: This study has provided additional insights as to the value of Hospice at Home care where Hospice Nurses are helping to bring Hospice care into the home. This is helping to support older people who are dying and their caregivers, to live as well as possible and facilitate their wish to be cared for and die in their own home.
© 2016 The Authors. Journal of Advanced Nursing Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Hospice at Home; caregivers; nursing; older people; qualitative research; supportive and palliative care

Mesh:

Year:  2016        PMID: 27113470     DOI: 10.1111/jan.12983

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  14 in total

1.  Caregivers' Perceptions Managing Functional Needs Among Older Adults Receiving Post-Acute Home Health Care.

Authors:  Jo-Ana D Chase; David Russell; Meridith Rice; Carmen Abbott; Kathryn H Bowles; David R Mehr
Journal:  Res Gerontol Nurs       Date:  2019-03-25       Impact factor: 1.571

Review 2.  Informal caregivers' quality of life and management strategies following the transformation of their cancer caregiving role: A qualitative systematic review.

Authors:  Yingying Cai; Alison Simons; Samantha Toland; Junfeng Zhang; Kexin Zheng
Journal:  Int J Nurs Sci       Date:  2021-03-24

3.  What are families most grateful for after receiving palliative care? Content analysis of written documents received: a chance to improve the quality of care.

Authors:  María Aparicio; Carlos Centeno; José Miguel Carrasco; Antonio Barbosa; María Arantzamendi
Journal:  BMC Palliat Care       Date:  2017-09-06       Impact factor: 3.234

4.  A drive for structure: A longitudinal qualitative study of the implementation of the Carer Support Needs Assessment Tool (CSNAT) intervention during hospital discharge at end of life.

Authors:  Alex Hall; Gail Ewing; Christine Rowland; Gunn Grande
Journal:  Palliat Med       Date:  2020-06-03       Impact factor: 4.762

5.  "Non-palliative care" - a qualitative study of older cancer patients' and their family members' experiences with the health care system.

Authors:  Marianne Fjose; Grethe Eilertsen; Marit Kirkevold; Ellen Karine Grov
Journal:  BMC Health Serv Res       Date:  2018-09-29       Impact factor: 2.655

6.  Impact of informational and relational continuity for people with palliative care needs: a mixed methods rapid review.

Authors:  Briony F Hudson; Sabine Best; Patrick Stone; Thomas Bill Noble
Journal:  BMJ Open       Date:  2019-05-29       Impact factor: 2.692

7.  What do patients and family-caregivers value from hospice care? A systematic mixed studies review.

Authors:  Nicole Marie Hughes; Jane Noyes; Lindsay Eckley; Trystan Pritchard
Journal:  BMC Palliat Care       Date:  2019-02-08       Impact factor: 3.234

8.  Development of the Readiness for Home-Based Palliative Care Scale (RHBPCS) for Primary Family Caregivers.

Authors:  Meng-Ping Wu; Lee-Ing Tsao; Sheng-Jean Huang; Chieh-Yu Liu
Journal:  Healthcare (Basel)       Date:  2021-05-19

9.  Optimum hospice at home services for end-of-life care: protocol of a mixed-methods study employing realist evaluation.

Authors:  Claire Butler; Charlotte Brigden; Heather Gage; Peter Williams; Laura Holdsworth; Kay Greene; Bee Wee; Stephen Barclay; Patricia Wilson
Journal:  BMJ Open       Date:  2018-05-16       Impact factor: 2.692

10.  The roles, responsibilities and practices of healthcare assistants in out-of-hours community palliative care: A systematic scoping review.

Authors:  Anne Fee; Deborah Muldrew; Paul Slater; Sheila Payne; Sonja McIlfatrick; Tracey McConnell; Dori-Anne Finlay; Felicity Hasson
Journal:  Palliat Med       Date:  2020-06-15       Impact factor: 4.762

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