Paul
Allen, Head of Integrated Commissioning (Integrated Care & Frailty) for the Council
and ICB, introduced the report on this item
which summarised issues around dementia, including the process of
how a dementia diagnosis was made. This often started with the GP,
but it was also important to engage with communities and residents
on this as people didn’t necessarily always recognise when
they have cognitive impairment. The report also highlighted the
importance of listening to patients and residents and a number of
areas for improvement that could be made around this.
Post-diagnostic support was another area where improvement efforts
would be made to develop a network of support so that people
didn’t feel isolated after their diagnosis.
Paul Allen also highlighted some specialist areas including the
multi-agency care co-ordination team to support people with
frailty, including dementia, and enhanced support in care homes as
around 70% of care home residents had some form of
dementia.
Paul
Allen then responded to questions from the Panel:
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Asked by Cllr Brennan why a greater proportion of
BAME people suffered from dementia compared to white groups as
stated in the report, Paul Allen explained that there was a genetic
component which impacted on the likelihood of acquiring particular
conditions. There was also less likelihood of people from some
under-served communities coming forward for diagnosis and so a
Dementia Co-ordinator had been funded to work with communities to
raise awareness around cognitive impairment. A bid had also been
put in for a Dementia Facilitator which was a different role
working with GPs on diagnosis rates. Cllr Connor proposed that a
further update should be received by the Panel at a later date on
the progress with these roles. (ACTION) Cllr Brennan asked
whether more details could be provided on the genetic component and
it was agreed that a link to a relevant medical research study
could be circulated. (ACTION)
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Cllr Peacock spoke about her experience of working
with people with dementia suggested that swimming sessions could be
made available for them as she had seen how beneficial this could
be. Paul Allen acknowledged that, while dementia was progressive,
it was possible for people to have a good quality of life for many
years if they were diagnosed early and had access to the right
treatment. This treatment was not just about medication but also
about physical and mental activity and so there had been investment
in community assets to support this. This included activities such
as walking programmes, but he was open to other suggestions in this
area. Helena Kania asked whether this offer on activities had been
connected to social prescribing so that people were aware that
these were available. Paul Allen said that the team were preparing
an Aging Well training and awareness pack, an element of which was
on dementia. An aim was to encourage the more than 170 social
prescribers and community navigators in this space to come forward
and learn more about dementia. This could involve some of them
becoming dementia friends or experts/champions to develop a network
of people who could mutually support each other.
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Cllr Abela referred to the drop in the diagnostic
rate during the pandemic that was described in the report and asked
about the consequences of this and the current status of the
backlog. Paul Allen acknowledged that the consequences were still
being felt, both in terms of workforce issues and of people feeling
isolated. His general sense was that people were coming forward
later than we would want them to, meaning that interventions were
not always as effective. This position was still being recovered
from, which was why there was a strong emphasis on supporting
individuals over the next few months.
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Referring to the underdiagnosis issues, Cllr
Iyngkaran asked how many residents in the borough would be expected
to be diagnosed. Paul Allen responded that the estimated figure was
2,200, as mentioned in the report, and it was thought that around
two-thirds of those had been diagnosed, not all of whom would
necessarily have been diagnosed at an early stage. Camden borough
had diagnosed around 80% of its residents with dementia and so this
was a benchmark to aim for. The key investments to improve this
included the Dementia Co-ordinator, the work with GPs on diagnosis
levels and the work with communities to improve understanding of
cognitive impairment.
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Cllr Iyngkaran highlighted that dementia did not
just affect people over the age of 65 as there were a small
proportion of people with dementia who were younger. Paul Allen
concurred with this point and mentioned that one of the members of
their Dementia Reference Group was a carer for somebody with early
onset dementia. While this was a small group, there were
conversations and strategies around supporting these people, not
least because they would have potentially a long time yet to
live.
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Cllr Peacock commented that the Haynes Centre in
Hornsey provided an excellent service but felt that a similar
service was needed in the east of the Borough as the former Grange
centre in White Hart Lane had closed some years ago. Paul Allen
referred to a slide with the list of current dementia services
across the Borough which included new premises for the Grace
Organisation but agreed that there should not be an overreliance on
one side of the Borough. Beverley Tarka added that the Grange has
been closed as part of the Council’s response to the
austerity measures that had been put in place. She acknowledged
that it was important to have resources in different sections of
the Borough which is why the Cypriot Centre in the Central area and
the Grace Centre in the East area were highlighted on the slide.
Cllr Peacock said that there was a religious element to the Grace
Centre which may not be suitable for all residents. Asked by Cllr
Connor whether a dementia centre for excellence would be
established in the east and whether this would be linked with the
Grace Centre site, Beverley Tarka clarified that this would all be
part of a single service within the former Irish Centre site and
that the refurbishment of the building was being designed to
dementia standards. Conversations were ongoing with the Grace
Organisation in terms of the service delivery. She was not aware of
the religious element described by Cllr Peacock but would be happy
to report back on this point. Cllr Peacock also commented that the
former Irish Centre previously provided a luncheon club which was
attended by a wide cohort of people, including some with dementia
and their carers, and would welcome something similar being
reinstated. Cllr Connor requested that an update be provided on the
expected offer from the Grace Organisation at the Irish Centre.
(ACTION)
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Vicky Murphy noted that there had been a request to
provide information on the number of people accessing dementia
services. However, there was some complexity around this as there
were a full range of services that people could access, including
through direct payments, and not just day services.
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Cllr Connor referred to paragraph 2.13 of the report
which set out key priorities highlighted by patients and carers,
noting that these priorities would be implemented and co-produced
through the Aging Well Board, and asked when a progress update on
this was likely to be available. Paul Allen explained that the
dementia pathway illustrated at the end of the report had been
co-produced. The team would engage with as many people as possible
but the key group in that space was typically the dementia
reference group which had been quite vibrant recently in term of
attracting people. The focus was currently on delivery and so an
update may be possible in approximately six months.
(ACTION)
RESOLVED – That further information be
obtained on the evidence of dementia risk and ethnicity and on the
expected offer from the Grace Organisation.
RESOLVED – That a future update on dementia
issues be added to the work programme.