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Facilitating family needs and support at the end of life in hospital: A descriptive study

Bloomer, Melissa, Poon, P, Runacres, F and Hutchinson, Alison 2021, Facilitating family needs and support at the end of life in hospital: A descriptive study, Palliative Medicine, pp. 1-6, doi: 10.1177/02692163211066431.

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Title Facilitating family needs and support at the end of life in hospital: A descriptive study
Author(s) Bloomer, MelissaORCID iD for Bloomer, Melissa orcid.org/0000-0003-1170-3951
Poon, P
Runacres, F
Hutchinson, AlisonORCID iD for Hutchinson, Alison orcid.org/0000-0001-5065-2726
Journal name Palliative Medicine
Article ID 02692163211066431
Start page 1
End page 6
Total pages 6
Publisher Sage Journals
Place of publication London, England
Publication date 2021-12-30
ISSN 0269-2163
1477-030X
Keyword(s) Aged
CARE
communication
culturally competent care
death
decision making
end-of-life care
family
family care
frail elderly
General & Internal Medicine
Health Care Sciences & Services
Life Sciences & Biomedicine
Medicine, General & Internal
palliative care
PATIENT
Public, Environmental & Occupational Health
QUALITY
Science & Technology
UNIT
Summary Background: Caring for family members of dying patients is a vital component of end-of-life care, yet family members’ needs at the end of life may be unmet. Aim: To explore hospital clinician assessment and facilitation of family needs and practices to support families at the end of life. Design: Descriptive study utilising a retrospective medical record audit. Setting and Sample: Undertaken in a large public hospital, the sample included 200 deceased patients from four specialities; general medicine (n = 50), intensive care (n = 50), inpatient palliative care (n = 50) and aged rehabilitation (n = 50). Data were analysed according to age; under 65-years and 65-years or over. Results: Deceased patients’ mean age was 75-years, 60% were Christian and Next-of-Kin were documented in 96% of cases. 79% spoke English, yet interpreters were used in only 6% of cases. Formal family meetings were held in 64% of cases. An assessment of family needs was undertaken in 52% of cases, and more likely for those under 65-years (p = 0.027). Cultural/religious practices were supported/facilitated in only 6% of all cases. Specialist palliative care involvement was more likely for those aged 65-years or over (p = 0.040) and social work involvement more likely for those under 65-years (p = 0.002). Pastoral care and bereavement support was low across the whole sample. Conclusions: Prioritising family needs should be core to end-of-life care. Anticipation of death should trigger routine referral to support personnel/services to ensure practice is guided by family needs. More research is needed to evaluate how family needs assessment can inform end-of-life care, supported by policy.
Language eng
DOI 10.1177/02692163211066431
Field of Research 1117 Public Health and Health Services
1199 Other Medical and Health Sciences
HERDC Research category C1 Refereed article in a scholarly journal
Free to Read? Yes
Persistent URL http://hdl.handle.net/10536/DRO/DU:30161308

Document type: Journal Article
Collections: Faculty of Health
School of Nursing and Midwifery
Open Access Collection
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Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.