Confidence undermined
After heralding the new pharmacy contract introduced nearly three years
ago as the lever to develop a clinically focused community pharmacy sector,
the Pharmaceutical Services Negotiating Committee seems to be developing
a new message over its funding.
For the past two or so years, the tone
from the PSNC has been conciliatory, emphasising that
negotiations with the Department of Health were making progress and
even creating the impression that community pharmacy’s future
was secure and likely to flourish.
Now the tone is different. In a hard-hitting speech due to be given
at the PSNC’s annual dinner after The Journal went to
press, the chairman, Chris Hodges, argues that the Government’s failure to introduce
new advanced services has undermined
pharmacists’ confidence (p295).
So what has prompted the change? In the past month there have been a
number of letters in The Journal critical of the PSNC and its
negotiating skills. Possibly unfairly, the PSNC has been accused of being
primarily
responsible for the Category M reimbursement fiasco — which is
now leaving some pharmacies in a parlous state. (Shadow health minister
Andrew Lansley has joined
the letter writers this week [p305].)
These factors, among others, may have prompted Dr Hodges to go on the
offensive. He was also expected to argue in his speech that, while the
2005 funding arrangements were fair for the 9,750 pharmacies in England
in 2005, as a result of the new control-of-entry regulations, the same
resources are now being shared by 10,300 pharmacies.
Community pharmacies in England are angry, and rightly so. Let us hope
that the PSNC can really deliver the right funding this year. Back to Top
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No black or white answers
With the number of tests being carried out in the NHS annually running into the hundreds of millions and with the recent massive expansion in tests available for the public to buy, concern was raised earlier this week about the lack
of regulation of all these different products (p298).
The problem seems to be two-fold: there is not sound evidence for all these tests
and the results, themselves, do not always give black or white answers — some
may only indicate that an individual has an increased propensity to develop a
disease or condition at some unspecified time in the future.
Individuals using
a DIY test may need help in interpreting the findings (which may be challenging
for GPs and pharmacists unless they have a special knowledge of genetics, for
example) and they also face the unintended consequence of believing they are
ill when they are not.
So what is to be done? Suggestions have been made that a BNF-type guide should
be developed that indicates what evidence there is for a particular test which
would be available for health professionals to consult when faced with a worried
patient.
Gathering the evidence would be labour-intensive but might ensure
that healthy people do not burden the NHS unnecessarily and may prove cost-effective
as a project.
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