It’s 10am on the morning of 25 June, and I am in the
auditorium of The Canberra Hospital (TCH) listening to Associate Professor MarkYates of the Ballarat Health Services Dementia
Care in Hospitals Program explain what this program is about to the
assembled TCH staff. He’s clearly practised at it, which might be expected,
since the program has been embedded in no less than 25 Victorian health care
providers to date. It’s been so successful at improving the experience of treatment
in hospital for patients with cognitive impairment that it’s pretty much
standard in Victoria. Mark is here today
to kick off the program’s national rollout. TCH is one of four pilot sites
across Australia selected to introduce the program and 18 months later,
comprehensively evaluate its effect.
Prior to Mark Yates, we hear from Jane Allen, the CEO of Alzheimer’sAustralia ACT. She tells us that ‘dementia’ is a catch-all term for a range of
symptoms and types of cognitive impairment, of which the most common is Alzheimer’s,
but it is only one of over one hundred possible diagnoses. It’s most common in
the over-65 age group, but its prevalence is increasing amongst younger people,
although no one is sure why. It’s the single greatest cause of disability for
older Australians. While people don’t often present to hospital with dementia
as their primary issue, people with dementia are prone to a range of injuries
and illnesses, and therefore more likely than those without dementia to be in
hospital. For these people, the busy hospital environment is a confusing and
stressful place, and can cause challenging behaviours as they try to cope.
Dr Anil Paramadhathil is the Director of Geriatric Medicine at TCH, and the man leading the introduction of the Dementia Care program here.
He shows us data from some research he did recently, which looked at the
proportion of the total people admitted to TCH over 6 months who had some form
of cognitive impairment noted on their record. He had expected 20-30%, a
proportion which would be in line with what the Ballarat team’s research has
found. He found less than 1% had this
information on their record. This backs Mark Yate’s assertion, that 1 in 5 families feel that the hospital has
no idea that they are caring for someone with cognitive impairment.
This morning session is about what the program does and how
it helps. It’s a simple program with three main elements. The first, and to my
mind most radical, is that all adult patients admitted to hospital are screened
for cognitive impairment. It’s not as onerous as it sounds, because it’s not a
diagnosis, but one or more simple tests of function. For example, request the patient to draw a clock face,
and then draw on the hands of the clock to show ten past eleven. I learn
that the ability to carry out this apparently simple task says a lot about the absence
or presence of cognitive impairment.
Step two, once cognitive impairment is found, is placing a
symbol at the patient’s bedside to alert staff, in much the same way as a hearing
or sight impairment would be identified. The beauty of a simple, visible symbol
is that any of the staff approaching the bedside, from the food service staff
to the clinical team, will receive the same message, and providing they have
been effectively trained in caring for people with cognitive impairment, a
systemic dementia-appropriate response should occur. Mark shows us the symbol,
which was developed with a consumer focus group. To me it looks like someone
radiating superpowers, but apparently explaining what the abstract symbol means
has become an opportunity for staff education, and that’s got to be a good
thing. Mark assures us that when this program is in full swing, we’ll see that
symbol above one in three of all
adult beds in TCH.
The last part of this program is staff training in how to
care for and communicate with patients with a cognitive impairment and their
carers, so that staff know how to modify their own behaviour and responses in
these circumstances.
The afternoon session of staff training begins with the
story of Joan, whose husband Kyle was hospitalised at an unnamed hospital for a minor operation.
Kyle suffered from Alzheimer’s, and when he was hospitalised Joan asked that
this information was clearly marked on his notes. The information seemed to
have gone missing fairly soon after admission however, and things went downhill
from there. Kyle’s Alzheimer’s wasn’t necessarily obvious to a casual observer,
and when Joan witnessed, among other things, a nurse presenting Kyle with his
medication, asking him to take it and then leaving him to it, she realised that
although she hadn’t planned to stay, she would have to, as there was no way he
could follow such instructions by himself.
Things came to a head when a family member noticed that Kyle had removed
his patient ID band because it was bothering him. Joan advised the hospital
that he needed another one but before this was done, and in one of Joan’s
absences, he disappeared. I’m sure I wasn’t imagining the discomfited seat
shifting in the nursing staff around me as we listened to this tale.
Fortunately the situation resolved without further drama, as Kyle turned up on
foot at his son’s house 3km away, but not before the police were involved and a
procedural hole a mile wide was clear for all to see.
I have a different perspective when I leave the auditorium.
As I emerge into the foyer I am momentarily disorientated and it takes a few
seconds to see which way I need to go. I notice it is noisy, and those bright artificial lights are a bit stressful. All around me are strangers dashing, limping,
wheeling hither and yon. I’m OK though; I know where I am and I’m pretty sure I
can still draw a clock face and place the time on it. It’d be good if I could
also remember where I parked the car though.
Kate Gorman
Consumer Representatives Program
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