Academics
at Northumbria University, Newcastle, are evaluating Rapid Response Services to
improve end-of-life care in new research funded by Marie Curie.
When people
reach the end of their lives, it is important that they can choose their place
of death. This could be at home, surrounded by friends and family, in a hospice
or perhaps in hospital.
However, consistent
evidence has shown that there is a mismatch between people’s preferences for
where they would like to die and their actual place of death.
Research
indicates that the majority of people would prefer to die at home; yet, prior to the pandemic, nearly half of deaths took place in hospitals.
Fulfilling
patient preferences for dying at home depends on the appropriate support and
care being available in the community. Rapid Response Services are one way of
enabling people to die at home – but there has been very little research about
their effectiveness for patients, carers and the cost implications of these services.
There is
therefore a need to better understand what people require at the end of their
lives, when they need it and how health and social services can support them.
To address some of the gaps in research, academics from Northumbria University
are conducting a much-needed study to evaluate Rapid Response Services.
Funded by
Marie Curie, the two-year project will enable the team to make recommendations
regarding further implementation of Rapid Response Services. This will help to
influence policy and the ways in which end-of-life care is commissioned, planned and delivered.
Professor of Nursing Amanda Clarke, who is co-leading the research,
said: “It is essential that the services delivering end-of-life care are
available at a time and place when the patient and their family need support.
Contributing to the evidence that shows us how best to do this is of great
importance; we have just one chance to get it right at the end of people’s
lives.”
Sabine Best, Head of Research at Marie Curie said: “For every person we care for at the end of their life, there are
many more missing out on the conversations, support and care they rightly
deserve. We know that the most important knowledge gap in palliative and end of
life research is about how to best provide palliative care outside of working
hours, avoiding crises, and helping people stay in their place of choice. This
research will help us gain a better understanding of the part Rapid Response
Services play in end of life care and enable us to make recommendations and
influence change where it is so vitally needed.
“For those who die within the community, we must ensure there is
suitable care and support available and sadly the pandemic has indicated this
isn’t always the case. We know that a negative end of life experience has a
detrimental impact to those left behind and can make an already challenging
time in someone’s life, even harder to get through.”
Gaining a
better understanding
As part of
the new study, the team will evaluate two different Rapid Response Services in
the North of England, to find out if and how each service helps patients and
their families, how they work with other community teams and the costs of the
services for the NHS.
By looking
at contrasting approaches to these services, the team will be able to highlight
what works best, for who, in what circumstances and why.
The
researchers will conduct interviews and focus groups to ask staff involved in
delivering end-of-life care how the service supports people and, importantly,
they will speak to carers and patients about their experiences of using the
service and whether it has made a difference to them and, if so, in what way.
A growing
need, intensified by the pandemic
The demand
for palliative and end-of-life care was already set to increase rapidly, with the
country’s ageing population meaning more people are living for longer with
multiple and complex conditions, but the Covid-19 pandemic has exacerbated the need
for evidence-based solutions for end-of-life care.
While the
number of people dying at home has increased significantly since the onset of
the pandemic, survey results published by Marie Curie in April 2021 suggested
that as many as 76% of people whose loved one died at home during the pandemic felt
they were not offered all the care and support they needed as carers.
In addition,
recent research by Public Health England shows that existing health and social inequalities
have continued or even worsened during the pandemic, for example amongst people
over the age of 80, men and certain ethnic groups.
The research
team will therefore also examine the impacts of the Covid-19 pandemic on Rapid
Response Services. The findings should enable a better understanding about how
to develop Rapid Response Services to support patients and their carers during the
pandemic and beyond.
Project
Co-lead Dr Joanne Atkinson, Head of the Department of Social Work, Education
and Community Wellbeing,
said: “Covid-19 has seen death and dying placed at the forefront of our
consciousness. We need to make a difference in meaningful ways, evaluating
Rapid Response Teams in end-of-life care allows us to explore how we support
people to die in their own homes in familiar surroundings, beside the people
that matter to them.”
