UK Drug Utilisation Research Group
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More multidisciplinary working but increased prescribing costs are predicted once the new GMS contract begins. Dawn
Connelly (on the staff of The Journal) reports
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The 15th annual scientific meeting of the UK Drug Utilisation Research Group (now called DURG [UK and Ireland]) took place in Nottingham on 29 January
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Why the new GMS contract will lead to a culture change in primary care

Linda Dodds: budgetary implications |
Primary
care will be changed beyond recognition by the introduction of the new
general medical services contract, according to Linda Dodds,
pharmaceutical adviser, Ashford Primary Care Trust. “It is very
exciting, but I think there are going to be some real problems for primary
care organisations and for the health economy as a whole in England,” she
said.
Ms Dodds told participants about the PRICCE (primary care clinical effectiveness)
project, a quality improvement programme designed by East Kent Health
Authority to increase the quality of care for 14 chronic conditions.
The project sets standards that must be met by GP practices, which are
above those normally expected. Participating GPs receive payment providing
the practice continues to meet the agreed outcomes. The results of the
PRICCE project give a foretaste of the prescribing implications of the
new GMS contract.
Benefits and drawbacks of the new GMS contract
Benefits
Promotes evidence-based practice
Promotes standardised care
Changes the way GPs work
Provides opportunities for improving prescribing quality
Drawbacks
Increased prescribing costs
Increased use of secondary care resources
Opportunities for the pharmaceutical industry |
Ms Dodds pointed out that in cardiovascular prescribing, a key area,
prescribing costs are not slowing much. “As you get an evidence-based
culture, if good evidence comes out that people should be treated more
aggressively and more groups of people should be treated for individual
things, and you have disease registers, and you are seeing these people
on a regular basis, you implement the evidence.”
She said that prescribing does not stop when the target is reached, new
evidence is implemented. “You are driving quality fantastically,
it is a wonderful thing for patients but it is not going to be good for
the budgetary implications to the NHS,” she warned.
The new contract will make practices systematically identify and treat
patients, she said. “It changes the way a practice works. To do
this you have to have your multidisciplinary teams. This is not something
that GPs can achieve on their own. Most of our practices have nurse-led
chronic disease management clinics, and are starting to have pharmacist-led
ones.”
Ms Dodds went on to talk about disease registers. “What you will
find in a quality-based culture is that once you have geared everybody
up to be much more adept at finding patients ... what you see is your
disease prevalence is going up.” In East Kent, over the past three
years there has been an increase of 4,500 in the number of diabetes patients.
This has implications for workload, prescribing, laboratory tests and
referrals. “It has a whole systems effect on what is going to happen
in primary care,” she said. It is great for patients but it does
make a difference to your commissioning, she added.
Ms Dodds pointed out that although disease registers provide a great
tool for PCOs and GPs, they can also benefit the pharmaceutical industry.
Companies could recommend switching to a product that might not fit with
local PCT policies, or implementing an evidence base that the PCT might
not have otherwise supported, and a disease register would facilitate
the switch.
Supplementary prescribing update
Paul Robinson, Department of Health, told participants that work has
already started on extending supplementary prescribing to physiotherapists,
podiatrists, radiographers and optometrists. “We expect that it
will be 2005 before training programmes are in place. But it might well
be early 2005 and we may well have another consultation that begins about
April or May, which should cover the principle of supplementary prescribing
by these four other professions,” he said.
New primary care trusts commonly lack some of the infrastructure to put
[supplementary prescribing] in place,” said Beth Taylor, specialist
principal pharmacist, London Pharmacy Services. “We are going to
have these accredited new prescribers in our organisations very soon
and less than half the organisations [in London] are ready to do that,” she
said during a presentation in which she described her experiences of
implementing supplementary prescribing for
pharmacists.
Another area that the London supplementary prescribing support team has
identified it needs to work on is the promotion of supplementary prescribing
to doctors at a local and national level. “Many doctors have been
extremely supportive ... but sometimes the doctors have said to candidates
that they are delighted that they are doing this, but they have been
less interested in the process, in terms of getting a clinical management
plan in place.”
Prize winning research
Caroline Morris, University of Manchester, and colleagues conducted
a retrospective review of 49,658 electronic patient records in nine GP
practices. They identified indicators for preventable drug-related
morbidity and found that four indicators accounted for almost 60 per
cent of the total number of potential events (302/507). These were
the use of non-steroidal anti-inflammatory drugs in patients with congestive
heart failure or hypertension, lack of monitoring of creatinine and
potassium levels in patients prescribed
angiotensin-converting enzyme inhibitors and the use of hypnotic/anxiolytic
agents. These data can be used to generate feedback via facilitated,
multidisciplinary discussion groups at each practice in order to prevent
future events.
The researchers were awarded the McGavock bursary (£500 to further
their research) for the best abstract submitted. |