Mapping the progress and impacts of public health approaches to palliative care: a scoping review protocol
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Date
2016-07-14
Citation
Archibald, D., Patterson, R., Haraldsdottir, E., Hazelwood, M., Fife, S. and Murray, S.A. (2016) ‘Mapping the progress and impacts of public health approaches to palliative care: a scoping review protocol’, BMJ Open, 6(7), p. e012058. Available at: https://doi.org/10.1136/bmjopen-2016-012058.
Abstract
Introduction: Public health palliative care is a term
that can be used to encompass a variety of approaches
that involve working with communities to improve
people's experience of death, dying and bereavement.
Recently, public health palliative care approaches have
gained recognition and momentum within UK health
policy and palliative care services. There is general
consensus that public health palliative care approaches
can complement and go beyond the scope of formal
service models of palliative care. However, there is no
clarity about how these approaches can be undertaken
in practice or how evidence can be gathered relating to
their effectiveness. Here we outline a scoping review
protocol that will systematically map and categorise the
variety of activities and programmes that could be
classified under the umbrella term 'public health
palliative care' and highlight the impact of these
activities where measured.
Methods and analysis: This review will be guided
by Arksey and O'Malley's scoping review methodology
and incorporate insights from more recent innovations
in scoping review methodology. Sensitive searches of
9 electronic databases from 1999 to 2016 will be
supplemented by grey literature searches. Eligible
studies will be screened independently by two
reviewers using a data charting tool developed for this
scoping review.
Ethics and dissemination: This scoping review will
undertake a secondary analysis of data already
collected and does not require ethical approval. The
results will facilitate better understanding of the
practical application of public health approaches to
palliative care, the impacts these activities can have and
how to build the evidence base for this work in future.
The results will be disseminated through traditional
academic routes such as conferences and journals and
also policy and third sector seminars.