FC 8.6 Changing Places, Spaces and Faces: A Mixed Methods Study Showing the Changing Preferences about Place of Care at the End-of-Life Since the COVID-19 Pandemic

C. Bailey*, P. Guo, J. MacArtney, A. Finucane, R. Meade, E. Wagstaff, S. Swan

*Corresponding author for this work

Research output: Contribution to journalAbstractpeer-review

Abstract

Background/aims: During the covid-19 pandemic, the number of home deaths increased as people avoided institutionalised settings. The research investigates the changing profile of place of death and the impact it has on the future of hospice services.

Methods: Mixed methods:
(1) systematic review to understand the evidence base around place of care preferences;
(2) analysis of mortality data to show the percentage increase in home deaths and highlight peaks;
(3) interviews with 37 participants (15 carers and 22 hospice staff) to explore reasons behind the decision-making and identify impact on quality of life using the ICECAP-CPM. Results were discussed at two stakeholder roundtable events to draw out policy and practice implications for hospice care.

Results: There was a significant change in place of death towards home deaths for those dying from non-covid related conditions. Increased hospital deaths were more closely linked to the presence of covid on the death certificate. Risk factors associated with hospital deaths included black and minority ethnic groups, lower socio-demographic factors and the presence of an underlying health conditions such as cardiovascular disease and diabetes. Qualitative data analysis reveals that preferences around decision-making to be cared for at home were due to a fear of contracting the virus in institutionalised settings (hospices and hospitals) and visiting restrictions. Quality of life remained high for hospice inpatient and community patients showing good symptom control and communication but concerns were raised about dignity, coping, being with people who care and feeling supported during the main lockdown period. Policy roundtables identified the need for better workforce support and systems of community support for carers.

Conclusions: It is timely to address the future of ’hospice’ and explore how services can better support people in communities who are the main providers of end-of-life care and support the changing hospice workforce.
Original languageEnglish
Pages (from-to)43-43
Number of pages1
JournalPalliative Medicine
Volume37
Issue number1S
DOIs
Publication statusPublished - 7 Jun 2023
Event18th EAPC World Congress - Rotterdam, Netherlands
Duration: 15 Jun 202317 Jun 2023

Bibliographical note

Oral presentation (Free Communication session FC 8.6) at the 18th World Congress of the European Association for Palliative Care in Rotterdam, the Netherlands, 15-17 June, 2023.

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