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Clinical/general
Date: 29 Dec 2009
Topic: Response to 'Practitioners’ views on managing childhood
obesity in primary care: a qualitative study’
Comments by: Professor Peter Schwarz, TU University,
Dresden, Germany; Anne-Marie Felton, President, Federation of
European Nurses in Diabetes; Dr Michael Hall, International
Diabetes Federation – Europe
Turner et al showed that primary care practitioners are
unaware of guidance provided by the department of health and NICE
on the management of childhood obesity.1 Even if GPs and
practice nurses believed primary care was an appropriate treatment
setting for childhood obesity, they questioned the extent, to which
they could effectively intervene. Furthermore they felt unprepared
to manage childhood obesity and perceived their efforts as
ineffective.
The study raises important issues shared by other
non-communicable disease (NCD) prevention/management initiatives.
As a part of the European funded IMAGE project (Development and
Implementation of a European Guideline and Training Standards for
Diabetes Prevention - IMAGE), a European evidence-based and
practice guideline for the prevention of type 2 diabetes including
obesity will be prepared and will be freely available online and
printed. Parallel to this, a curriculum for the training of
prevention managers will be released in April next year. The IMAGE
concept is that appropriately trained personnel can deliver
efficient and effective prevention strategies to those at risk of
diabetes. A similar approach may be effective for other NCDs,
including obesity.
We are involved with IMAGE, a major EU sponsored
multidisciplinary multinational project, which aims to address the
prevention of diabetes through evidence-based guidelines which
recommend interventions implemented by trained prevention managers.
The project is reaching completion, courses for prevention managers
are currently being piloted in several European centres, and a full
report on the whole IMAGE project will be given at the World
Diabetes Prevention Conference in Dresden in April 2010. Details
can be found at http://www.image-project.eu/
Reference
1. Turner KM, Shield JPH, Salisbury
C. Practitioners’ views on managing childhood obesity in primary
care: a qualitative study. Br J Gen Pract 2009; 59(568): 856-862.
View abstract online
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Date: 29 Dec 2009
Topic: Response to ‘The present state
and future direction of primary care: a qualitative study of GPs’
views’
Comments by: Jim Newmark
As a former senior partner of twenty years and
a salaried doctor of four, the conclusions of this rather
interesting piece of research1 are no surprise. We are
left with the impression of smug partners and embittered salaried
GPs. My sympathies are with the latter.
My plea is for those partners who are perhaps
half a decade, or even a decade, away from retirement, to make the
brave step of changing directions. Perhaps it is time to
voluntarily step down to a salaried position? Why not act as a
grandparent to our younger colleagues? To be happy to hold the baby
while your sons/daughters are out shopping, but to be even happier
handing him/her back at the end of the day for them to go through
those sleepless nights. We are still there for advice, and are
still going to be paid more than the vast majority of people in
this country. We still have our savings, our paid-for house, our
comfortable living. And now perhaps a chance to expand to do what
we always wanted to do – hobbies or another field of medicine. What
are you waiting for?
I know this because I did it. I have never
regretted a second of leaving my well-established and increasingly
successful practice. I love watching it expand and I think I
actually would have held it back if I remained. We remain on
friendly terms, and perhaps there is a bit of a feeling that it was
my child, but it now needs to grow up. Meanwhile, I am learning and
working in other areas of medicine that I never really knew
existed.
Reference
1. Lester H, Campbell S, McDonald R. The
present state and future direction of primary care: a qualitative
study of GPs’ views. Br J Gen Pract 2009; 59(569): 908-915.
View abstract online
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Date: 19 Nov 2009
Topic: Response to ‘Genes, gender, sport, and justice’
Comments by: Edoardo Cervoni
I totally share Peter Toon’s question on how
should we judge athletes. Should this be based on the effort or
performance? In fact, he quite correctly adds: ‘It’s not just
genes carried on the XY chromosomes that affect performance; people
with particular body types as a result of their genetic inheritance
perform very differently in many sports ... Why should we accept
these differences but not chromosomal anomalies?’.
We may argue that assessing effort is almost impossible and most
certainly people are generally more interested in performances.
Thus, performace should be the answer.
But then, it is also true what Peter says: ‘If stronger
muscles result from an anomaly we can describe and name, we might
consider this unfair and exclude the athlete; if it comes from a
fortuitous combination of many genes, not all well understood, we
may not’.
Overall, I think it would be fair assessing people based on
performances and looking at their wellbeing above all. Ultimately,
I am sure that performaces would drop should their wellbeing be
compromised.
Reference
1. Toon PD. Genes,
gender, sport, and justice. Br J Gen Pract 2009; 59(568): 871.
View title page online
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Date: 18 Nov 2009
Topic: Response to 'GPs' views on the practice of
physician-assisted suicide and their role in proposed UK
legalisation: a qualitative study'
Comments by: Mr B Cosway, Mr D Arnold, Intercalated BSc
medical students; Dr Iain J Robbé, Clinical Senior Lecturer, School
of Medicine, Cardiff University
We would like to congratulate Hussain and White1 for
their paper regarding the views of general practitioners on
physician-assisted suicide. We agree that this qualitative approach
has filled what was previously a void in current understanding.
However, we do have concerns regarding the inclusion of only GPs
who had a specific interest in medical ethics or terminal care.
While we agree that a higher quality of data may come from GPs with
these special interests than those who may have given the topic
less thought, we question whether those without an interest in
these fields have not considered their opinions regarding this
current and controversial topic. Furthermore, if a revised bill is
passed in to law then it seems likely that all GPs will play some
role in the implementation. We therefore suggest a more typical
sample of GPs would be required for a true representation of
views.
We hope that research into this topic continues and we propose a
quantitative analysis of the proportion of GPs willing to support
the bill and the extent to which they would involve themselves in
assisted suicide. This could then be expanded to other healthcare
professionals that may be affected.
Reference
1. Hussain T, White P. GPs’ views
on the practice of physician-assisted suicide and their role in
proposed UK legislation: a qualitative study. Br J Gen Pract 2009;
59(568): 844-849.
View abstract online
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Date: 8 Nov 2009
Topic: Response to ‘Health inequalities in the UK: remedy requires
action beyond redistribution of wealth’
Comments by: Dr Fergus Dignan, Frampton Mansell,
Gloucestershire
I read with great interest the article on health inequalities in
the UK by Edin Lakasing1 in the October edition of the
BJGP, but I was surprised that no reference was made to 'The Spirit
Level: Why more equal societies almost always do
better'.2
Lakasing emphasises the main ailment of our society, that is the
obscene wealth divide between the top 20% and bottom 20%, and he is
right in saying that: ‘It is clear that there are limits to what
medicine can achieve in redressing health inequalities’.
The Spirit Level describes the effect of widening wealth gaps in
western societies. The UK and the USA have a 10-fold difference in
income between the top 20% and bottom 20% and also have some of the
worst parameters in the western world. Interestingly, the
Scandinavian countries and Japan have the narrowest income gap and
also the best health and social statistics.
What is this connection between income gap and societal health? The
clue is in the title of the book. It is what happens to people’s
spirits when they exist in an unequal society. I am not talking on
a supernatural or religious level. I am talking about feelings of
well being and personal contentment. One can imagine how someone on
a sink estate in a major city feels when looking at the lives of
the very wealthy. No chance of ever aspiring to that life, so why
bother making any effort at all?
The solution therefore is to dramatically narrow the income divide
in our society. No easy task, I know! I would commend all GPs, and
other health care workers for that matter, to read 'The Spirit
Level'.
References
1. Lakasing E. Health inequalities in the UK: remedy requires
action beyond redistribution of wealth. Br J Gen Pract 2009;
59(567): 782-784.
View title page online
2. Wilkinson R, Pickett K. The Spirit Level: Why more equal
societies almost always do better. Penguin, 2009.
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Date: 8 Oct 2009
Topic: Response to ‘The Commercialisation of GP services’
Comments by: Tim Parkin
This interesting paper1 discusses
the award of GP service contracts to commercial organisations and
the lack of evidence of the impact of this on value for money and
quality of service. We believe our paper ‘Quality of care in a
franchised GP group’2 does present such evidence as
applied to the awarding of contracts to existing local GPs. We
would invite the authors to consider this information.
References
1. Heins Elke, Pollock AE, Price
D. The commercialisation of GP services: a survey of APMS contracts
and new GP ownership. Br J Gen Pract 2009; 59(567):
e339-e343.
View abstract online
2. Parkin T, Orchard J, Parkin T. Quality of care in a
franchised GP group. Br J Healthc Manag 2008; 14(11):
492–499.
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Date: 7 Oct 2009
Topic: Response to ‘London Allergy Show 2009: an exhibition of
black magic’
Comments by Lindsey McManus, Education Executive, Allergy
UK
I would like to add my comment to this discussion on the London Allergy
Show. I work for Allergy UK, we are a Patient Information
Organisation, a charity, backed by some of the leading experts in
the field of allergy, and we cover all aspects of allergy.
When the Allergy Show first started we had stands there
ourselves. Sadly after a couple of years we chose not to
continue, for exactly this reason. Although we may have been the
'voice of reason' at the show we did not feel comfortable being
associated with the kind of exhibitors that you have
mentioned. We now know however that the show is in new hands
and we have been in talks with them. Hopefully this will make a
difference to future show.
What I would like to say is that if there are any GPs who would
like any help or advice on Allergy please do not hesitate in
contacting me at Allergy UK. We do have an excellent
education programme for Health Care Professionals alongside a
wealth of information for members of the public.
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Date: 22 September 2009
Topic: Response to ‘James Mackenzie
lecture: Practice, politics, and
possibilities’1
Comments by: Dr Victoria
Hartnell
Where is all the discussion? If ever there was
a rallying call to the apathetic and apolitical, this is it. Is
there any discussion between the RCGP leadership and the BMA
leadership to co-ordinate ‘marketing’ of generalists? I am
convinced perhaps by the humour as much as the clarity of the
arguments, that Martin Marshall does the same job as me; not always
a familiar feeling in this august publication.
Reference
1. Marshall M. Practice, politics, and
possibilities. Br J Gen Pract 59(565): 605–612.
View abstract online
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Date: 27 August 2009
Topic: Quo Vadis? Point of care testing: a patient’s
perspective
Comments by: Francis FitzGibbon, Lisburn, County
Antrim
UK government policy in recent years has been advocating and
encouraging patients to take a more active role in managing their
own healthcare. The outcome of the recent Lord Darzi review, High
Quality Care for All, 2008 together with various other NHS policies
like the IT initiative Connecting for Health, has supported the
introduction of new technologies known as Point of Care Testing
(POCT).
Many of these devices can now be purchased by patients over the
counter for home testing in high street pharmacies and even
supermarkets. Whilst in the hands of a trained physician these
devices may be useful in assisting a GP to perform a patient
diagnosis faster, as a patient I am concerned that their use by
untrained lay users may lead to more harm than good.
Interestingly, when I last visited my GP, I asked him whether
the practice itself would use POCT more widely, apart from the
usual dipstick tests, such glucose, cholesterol coagulation, and
urine testing. He explained that POCT would not be further used in
primary care for the following reasons:
- Primary Care Trusts already have an arrangement with their
local hospital based Pathology Service for carrying out patient
test requests.
- There is no available funding in primary care to cover the
additional cost of POCT.
- Due to the daily patient workload here is no available staff or
time to carry out POCT more widely.
- For more advanced testing and diagnosis GPs prefer to refer
patients on to specialists outpatients clinics.
As a patient I can see the obvious benefit of having an earlier
test result by POCT instead of having to telephone the GP clinic, a
week later. If patients could be told their test results on the
same day of their appointment they would prefer it, also presumably
GPs would be able to make an earlier decision regarding their
treatment. In the light of these constraints, I wonder
whether POCT will ever reach its maximum beneficial potential.
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Date: 12 August 2009
Topic: Response to ‘Do the Quality and Outcomes Framework patient
experience indicators reward practices that offer improved
access?’
Comments by: Dr John Orchard
This paper asks the wrong question.1 The correct
question is why do patient surveys not reflect improved access.
Since 2003 we have taken over the management of two local failing
practices. Despite achieving maximum clinical QOF points, providing
instant access, myriad increased services, including increasing the
medical and nursing staff by 500%, we cannot change patient
perception sufficiently to reach target patient satisfaction
scores.
A nearby practice has done nothing to change its attitude or
accessibility but has moved into a LIFT centre: result, increased
patient satisfaction. Patient surveys measure perception not
performance and should be scrapped. Practices in deprived areas
that require most funding to improve health care will be penalised
by illiterate and uninformed patients: the same patients who fail
to attend same day appointments in practice, urgent hospital
out-patients, and who are verbally and physically aggressive to
staff.
Reference
1. Baker R, Bankart MJ, Murtagh GM. Do the Quality and Outcomes
Framework patient experience indicators reward practices that offer
improved access?
Br J Gen Pract 2009; 59(565): e267–e272.
View abstract online
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Date: 15 June 2009
Topic: London Allergy Show 2009: an exhibition of black magic
Comments by: David J Jackson, BSc MBBS MRCP, Department of
Respiratory Medicine, Imperial College London
The 6th annual ‘Allergy and Gluten Free Show’ took place this
weekend at the Olympia hall in London. Unfortunately, the majority
of stands selling allergy tests and treatments were promoting
products with as much in common with allergy as flying pigs has
with swine flu.
For a small fortune members of the public were ‘tested’ for a
range of allergies with machines measuring muscle energy levels,
and told that spraying your skin with oxygen reduces an allergic
reaction. Others were sold home blood test kits for measuring their
Immunoglobulin G levels despite the fact that Immunoglobulin E is
the most important marker of allergy.
Asthma sufferers were shown ways to cure their asthma through a
series of manoeuvres with their thumb and finger described as
‘identical’ to the value of salbutamol. Thousands of the general
public parted with their hard earned money on tests that have no
biologic plausibility let alone an evidence base to them.
There was a deafening silence from the Department of Health who
failed to provide a representative and in so doing ignored a
fantastic opportunity to educate the public on a group of diseases
that affects about 20 million of them. Instead the public
were educated by individuals with no understanding
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Date: 8 Jun 2009
Topic: Fairy Fabric Care advertorial
Comments by: Dr Nigel Walsh MRCGP
I am writing to you in regard to the ‘article’ by Dr David
Atherton which appeared in the BJGP dated June 2009.* Dr Atherton
is stated to be Consultant Paediatric Dermatologist at Great Ormond
St. Hospital and is skincare advisor to Fairy Non Bio and Fabric
Softener.
The ‘article’ seems to be an advertisement endorsing the use of
Fairy Fabric Care products which he states have been evaluated for
skin safety but have also been shown by the manufacturer to be as
‘gentle next to skin as clothes washed in water alone’.
Dr Atherton’s article includes a colour photograph of himself. I
could hardly believe to read that an eminent physician at a
teaching hospital would descend to promoting a commercial product
in this fashion. The general advice on baby skin care is most
informative but the juxtaposition of the product photographs is
objectionable.
I note that the article is not stated to be an advertisement,
that the products are not therapeutic substances (and therefore not
subject to government regulations) but unlike other opinions in the
journal there is no reference as to funding or competing
interests.
I would be most grateful to receive your views on the ethics of
such an article and whether Fairy Products paid the journal for
this ‘advertisement’.
* Web Editor's note: the advertorial appeared on the back
cover of the June 2009 issue of the BJGP.
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Date: 8 Jun 2009
Topic: Response to ‘The end of
practice-based research?’ — craft innovation versus practice-based
research
Comments by: Nigel Masters,
GP, Highfield Surgery, High Wycombe, Buckinghamshire
I would like to contribute to the debate in
the letters section about modern day practice based
research.1 As full-time general medical practitioner
over 27 years I have been generating ideas and ways to help
patients at the frontline of primary care. Some of these ideas
which I refer to as a craft innovation have been used throughout
the world to improve patient care, and some have been published in
peer review journals. It may help to describe some of this work as
it can slip across academic borders from time to time and so could
then be considered proper clinical research.
While doing my GP training I developed the
foot pump nebuliser2 which has been widely used in the
UK and world and it is still manufactured 27 years
later.3 I wrote an article in Modern Medicine (now
defunct) which resulted in an article in the Observer Business news
and eventually a peer reviewed journal.4
Later I explored nebulised opiate
delivery5 and the myth of medication caries.6
These papers explored issues of affecting everyday work: safety in
drug delivery and whether medicines prescribing was causing tooth
decay. Admittedly, at this time I was a part time lecturer in an
academic department and this was helpful in providing some support
for these papers. Further research explored housing design and
mental ill health and this was published in the Journal of
Psychiatry.7 Later I tracked the spread of hepatitis
carriage through my Vietnamese patients which resulted in an
editorial in the British Medical Journal.8
After I left my inner city environment and
went for a normal shire county practice where I continued to try
and innovate and improve patient care. In 2004 I won the national
GP enterprise award and the BUPA communication prize for clinical
indications on prescription. This work has never been peer reviewed
but can be seen on the web9 and is widely used by many
practices to inform modern medicine delivery. Our practice won a
national award for holistic care of chronic obstructive pulmonary
disease (COPD) patients in 200610 and is delivering a
COPD disease strategy across a collaborative of 33 practices.
New tools have been developed which include
the world’s first smoking pack year calculator.11 This
website was launched in June 2007 and has over 200,000 calculations
performed! The websites have been funded from prize money and are
free to view. Just recently I have become once again a finalist in
the GP enterprise awards for the croup calculator12 a
new exemplar for dose prescribing in children by increasing
confidence and safety in prescribing dexamethasone for croup in
young children. This dexamethasone calculator is free from me by
contacting me at my email address.
This work is really a hobby and I have never
received any academic funding which in any case might be difficult
to obtain as I am not linked to any university department! Thus
although my work is practice based it cannot be considered academic
but at times and with support it can reach peer reviewed journals.
I consider that this innovative craft seam at the primary care coal
face is under threat and needs to be nurtured and I am grateful for
competitions such as the GP enterprise award that try to highlight
these hidden nuggets that can really benefit patients.
References
1. Murdoch JC. The end of
practice-based research? Br J Gen Pract 2009; 59(558): 52.
View abstract online
2. RCGP occasional paper
29. Trainee projects 1985: 42.
3. http://www.asthmarelief.co.uk/
4. Dunn AM, Darvell F, Wilson RSE. An
evaluation of the foot pump as a driving source for nebuliser
solutions. Br J Dis Chest 1985; (79): 172-176.
5. Masters NJ, Bennet MRD, Wedley
JR. Nebulised morphine a new delivery method for pain relief. The
Practitioner 1985; (229): 649-653.
6. Masters NJ. The Practitioner
Medication Caries: a dental myth. 1987;(231): 56-64.
7. Birtchnell J, Masters N,
Deahl M. Depression and the physical environment. A study of
young married woman on a housing estate. Br J Psych 1988; (153):
56-64.
8. Masters N, Livingstone A,
Cencora V. Hepatitis B :prevention in primary care. BMJ 1989;
(298): 908.
9. http://www.clinicalindications.com/
10. Tutt C, Masters N. Recording
‘pack years‘ aids assessment of risk and diagnosis of COPD.
http://www.eguidelines.co.uk/
11. http://www.smokingpackyears.com/
12. RCGP News, June 2009.
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Date: 29 May 2009
Topic: Response to ‘Frailty: an emerging concept for general
practice’
Comments by: Avril Danczak, GP, Manchester
Jan De Lepeleire et al1 have highlighted a very
important area in the assessment of older patients. I fully endorse
their emphasis on the ways that frailty may be reversed. However,
frailty can be a prognostic indicator that should alert us to other
issues, such as effective planning for end-of-life care. Frailty
can be useful as a component in the identification of an
irreversible decline.
Patients and relatives often need clear information about this
state, which is also crucial for carers (professional or
laypersons). At the end of life, frailty increases and may alert us
to:
* the need to stop active or inappropriate interventions,
* to plan the place of end of life care,
* to ensure proper symptom control,
* to stop the revolving door cycle of fruitless admissions that can
mar the final days/weeks of some elderly patients,
* to prepare relatives and carers that death is approaching,
and
* to help relatives/carers prepare for death and appropriate
grieving.
I was a little disappointed that the paper did not discuss this
area in more detail. We are already moving away from the idea that
palliative care/terminal care only applies to malignant conditions.
Death is, at some point, inevitable. Part of our duty to patients
and carers is to ensure that death is managed appropriately and
with dignity. We need better understanding of when frailty is
irreversible as well as an optimistic and rehabilitative approach
to reversible factors.
Reference
1. De Lepeleire J, Iliffe S,
Mann E, Degryse JM. Frailty: an emerging concept for general
practice. Br J Gen Pract 2009; 59(562): e177-e182.
View abstract online
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Date: 6 May 2009
Topic: Website for GPs with colour vision deficiency
Comments by: J Anthony B Spalding, formerly a GP, UK. Barry H
Cole, Emeritus Professor of Optometry, University of Melbourne,
Australia. Fraz A Mir, Consultant Physician, Addenbrooke’s
Hospital, Cambridge, UK.
It remains a common opinion in the medical profession that colour
vision deficiency has little or no effect on the work of the
doctor. In fact this is not true. There is now much evidence that
doctors with this deficiency can misread colour codes and physical
signs that involve colour and that they can be unaware at the time
that an error has been made.
Advice is needed to avoid this situation. But the problem
remains that there are few teachers with the knowledge to advise in
the necessary detail. Advice is frequently inadequate or is not
given. Some doctors may find their own way to adapt and, of course,
those with a mild deficiency will be little affected
However, a website is now available that gives the evidence that
confirms the above statements and this includes the previously
unpublished comments of medical students with the deficiency. It
offers advice to doctors, medical students, and prospective medical
students who have colour vision deficiency. It aims is to explain
how to be aware of the difficulties, how to respond to them, and
how to make an informed choice of specialty. Access to the website
is via: www.colourmed.com
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Date: 20 April 2009
Topic: The patient–doctor relationship: a synthesis of the
qualitative literature on patients' perspectives
Comments by: Sarah Ryan
I am currently a sixth form student, interested in the issue of
what patients consider to be a good doctor. In February this year I
produced a questionnaire administered in a highly-regarded local
general practice, to about 80 patients over 3 days, specifying that
patients be selected for the questionnaire only if they had
requested to see a particular doctor, and asking them to rate the
attributes of that doctor and comment on what they valued in their
relationship with the doctor.
The findings of my research broadly confirmed the conclusions of
the Ridd et al article in the April BJGP.1 However, in
this area of research a finite conclusion is hard to come by. This
may be due to humans’ intrinsic nature, as patients will always
have their own opinions. The study of doctor–patient relationships
is really a study of the way human beings interact, and although
there are obvious professional boundaries, many of characteristics
that the research concludes deepen this relationship (such as
trust, understanding, equal participation, and loyalty) are
congruent with any relationship. Maybe the key to a having a
healthy patient–doctor relationship is for both sides to view each
other how they would view any other person.
Reference
1. Ridd M, Shaw A, Lewis G, Salisbury C. The patient-doctor
relationship: a synthesis of the qualitative literature on
patients' perspectives. Br J Gen Pract 2009; 59(561):
e116-e133.
View abstract online
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Date: 3 April 2009
Topic: Response to: ‘Ordering blood tests for patients with
unexplained fatigue in general practice: what does it yield?
Results of the VAMPIRE trial’
Comments by: Jacqui Footman BA(Hons) PGCE, Information
Officer, South Molton ME Support Group, North Devon
I am concerned that this article by Koch et al1 may
discourage GPs from thorough testing for patients with CFS/ME. At
the ME Research UK conference in 2008 Dr Gavin Spickett, consultant
leading one of the NHS specialist CFS/ME services, stated that
significant numbers of patients referred to the service in fact
turned out to have other (more treatable) conditions.
I have a particular and personal interest in this topic in so
far as I languished under a diagnosis of CFS/ME for 4 years without
further medical testing. I did receive what could be considered the
best NHS care currently available for ‘CFS/ME’ but nevertheless in
my prime at age 43 waved goodbye to a promising teaching/management
career. I was subsequently found (sort of by accident) to have
Crohn's disease, which had clearly gone undiagnosed for many
years.
When lupus tests had come back negative, raised plasma viscosity
tests had been ignored as unexplainable and few further tests done
for several years. Now, some months on from an ileal resection (but
after 5 years on Incapacity Benefit) I am eventually less disabled
by fatigue. With testing, I recently discovered I also have
osteoporosis and low Vitamin D. Many patients with chronic pain are
being found to have low vitamin D, and what a simple thing to
resolve once the test is done! How much better would my bone
density now be if I had been tested and treated 5 years sooner?
I write to urge GPs to take testing and investigation more
seriously and to avoid jumping to conclusions of somatoform
illness, particularly when fatigue extends to CFS/ME, in order to
help prevent further tragic and possibly avoidable losses. Most
patient support groups recommend Health Canada's Clinical Guideline
for help with this.2
References
1. Koch H, van Bokhoven M, ter
Riet G, van Alphen-Jager JMT, van der Weijden T, Dinant G-J,
Bindels P. Ordering blood tests for patients with unexplained
fatigue in general practice: what does it yield? Results of the
VAMPIRE trial. Br J Gen Pract 2009; 59(561):e93-e100.
View abstract online.
2. Carruthers et al. Myalgic Encephalomyelitis/Chronic Fatigue
Syndrome: Clinical Working Case Definition, Diagnostic and
Treatment Protocols. J Chronic Fatigue Syndrome 2003; 11(1).
Overview available at
http://www.mefmaction.net/Patients/Overviews/tabid/122/Default.aspx
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Date: 1 Apr 2009
Topic: Response to ‘The contraceptive revolution’: slow progress in
provision of modern contraception
Comments by: David Metson, Easthampstead
Surgery, Bracknell, Berkshire
In Hannaford and Belfield’s recent editorial on 'The
contraceptive revolution', they state that there has been some
excellent progress but there was 'work still to be done'.
1 One aspect of this is surely the implementation of the
2005 NICE guidelines which recommend greater provision of
long-acting reversible contraception (LARC). 2
NICE stated that LARC methods were more cost effective than the
combined pill and increased intake would reduce the number of
unintended pregnancies. Action is needed to reduce the figure of
30% of births being unplanned and 200,000 terminations of pregnancy
occurring annually in England and Wales.3
How are we doing? A Family Planning Association (FPA) survey in
2006/7 found that only 14% of women using contraceptives chose LARC
methods.4 In contrast, the use of LARC is greater
elsewhere; for example, in France 32% of contractive users choose
coils.
In 2008, 90 randomly selected GP practices in the Thames Valley
were asked whether they fitted LARC. Thirty-two (36%) practices
replied. The number fitting IUCDs, IUSs, and implants was 14 (44%).
A further nine (28%) practices fitted only IUCDs and IUSs, and
5 (16%) of practices fitted only IUCDs or only implants. Four
practices (13%) fitted no LARC.
It is disappointing that 3 years after the NICE guidelines were
published, less than half of the practices who responded to the
survey were fitting the full range of LARC. Reasons given for
not fitting LARC include 'the high risk of problems and
complications' and one practice said they would stop fitting if
funding was withdrawn.
It is surprising that fewer practices fitted implants than coils
when implants need less skill to fit than coils. The new QOF points
may increase provision of LARC but GPs will be rewarded for merely
suggesting these methods and not actually fitting them.
This small study suggests that while there has been some
progress in implementing the NICE guidelines, there is much work
still to be done.
Reference
1. Hannaford P, Belfied T. The contraceptive revolution: some
excellent progress but work still to be done. Br J Gen Pract 2009;
59 (558): 4-6.
View abstract online
2. National Institute for Health and Clinical Excellence. NICE
clinical guideline 30. Long acting reversible contraception: the
effective and appropriate use of long-acting reversible
contraception, 2005. http://www.nice.org.uk/CG030
3. National Collaborating Centre for Women's and Children's
Health. Long-acting reversible contraception - the effective and
appropriate use of long-acting reversible contraception. London:
RCOG Press, 2005.
4. Family Planning Association. Newsletter Nov 07.
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Date: 3 Jul 2008
Topic: Response to ‘Top Tips in 2 minutes: Consulting with
children’
Comments by: Dr Chris Godwin, Blaina Medical Practice,
Blaenau Gwent
Tim Caroe1 in a piece on communication with children
refers to a child’s mother as ‘mum’ as in “That’s fine” said
mum’. Many paediatricians do the same (for example,
‘Mum says the child is better’). The immediate impression is
of Dr Caroe’s or the paediatrician’s mother sitting sweetly in the
corner of the consulting room giving advice to her nearly grown-up
son. The second impression is of a presumptive doctor arrogantly
giving a pet name to the child’s mother, who may never be referred
to as ‘mum’ at home. The third is of a curmudgeonly son-of-a-camel
allowing himself to be needled by trivia and writing to journals
about it in metaphorical green ink.
Reference
1. Caroe T. Top Tips in 2
minutes. Br J Gen Pract 2008; 58(552): 520-521.
View abstract online
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Date: 11 Jun 2008
Topic: A cautionary tale highlighting problems that can occur when
prescribing analgesic patches in older people
Comments by: Mr JW Hobman, Senior House Officer Elderly
Medicine, GP; Dr Ian R Craig, Consultant in
Elderly Medicine, Department of Medicine for the Elderly Dewsbury
District Hospital, Dewsbury
We report the case of a 79 year old lady which highlights the care
required in the prescribing of analgesic patches in older people.
Our patient was known to have osteoporosis and presented to her GP
with increasing back pain that was unresponsive to co-codamol. In
conjunction with the patient’s family a trial of buprenorphine
patches was commenced. Her past history included long-term warfarin
for atrial fibrillation. Because of difficulty establishing stable
anticoagulation over the preceding months a 1mg/day warfarin dose
with a view to achieving benefit without risk was instituted. This
is an appealing theory which is however unlikely to be
efficacious.1
When her family arrived to change the patch after 3 days our
patient was found non- specifically unwell. An out of hours (OOH)
GP diagnosed a urinary tract infection and prescribed cephalexin.
No patches were seen on the patient at the visit. When the clinical
condition worsened the OOH doctor was recalled. He found an empty
patch box in the bin. An ambulance was called.
In the emergency department five patches were found on the
patient’s flank. These were only obvious with the patient
completely undressed. The patches were removed and naloxone given.
Initial progress was good. However the patient later developed new
and unrelated cardiac problems from which she died 8 days after
admission.
Patches are now an established method of prescribing. Without
careful examination patches have the potential to remain hidden
from carers and health care professionals. This is particularly
important when visiting unfamiliar patients out of hours when the
complete medication history may not be immediately available.
The case highlights the risks of prescribing patches
particularly in patients with impaired cognition. Our patient’s
cognitive impairment was relatively recent and only apparent on
direct questioning. The previous problem with warfarin compliance
was perhaps a subtle early sign of cognitive decline.
Analgesic patches can be useful in patients when poor compliance
is an issue. Carers must be made aware that external heat sources
such as heat pads and hot water bottles will increase absorption of
the active ingredient. Carers must also be advised to keep the
medicine out of reach of their confused dependant.
Reference
1. Stroke Prevention in
Atrial Fibrillation Investigators. Adjusted-dose warfarin versus
low-intensity fixed dose warfarin plus aspirin for high risk
patients with atrial fibrillation: Stroke Prevention in Atrial
Fibrillation III randomised clinical trial. Lancet. 1996;348:
633–638
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Date: 5 May 2008 11:56
Topic: Triage of febrile children
Comments by: Ben Essex
I think it is essential to ask if the child
has been to a malaria area in the previous few weeks. There is no
mention of this critical question in the paper by Monteny et
al.1 This is an important omission.
Reference
Monteny M, Berger MY, van der
Wouden JC, Broekman BJ, Koes BW. Triage of febrile children at a GP
cooperative: determinants of a consultation. Br J Gen Pract 2008;
58(549):242–247.
View abstract online
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Date: 17 Mar 2008
Topic: Headache
classification
Comments by: DP Kernick
Ninety-five per cent of headaches that we see
are classified as primary, i.e. an underlying pathology cannot be
demonstrated. In the April issue of the journal, Dr
Jackson1 highlights a number of important points in
describing her approach to primary headache that are equally
relevant to many other areas of medicine. The fundamental starting
point is that when presented with the unknown, we need to make
sense of the situation and act. With headache we construct a
taxonomy based on clinical description and response to treatment,
an exercise undertaken by committee.2 As our knowledge
increases, classifications change accordingly.
However, the maps we construct are only an
approximation of the terrain we seek to navigate. As Dr Jackson
says, there are benefits of a clear diagnosis and explanation even
if the pathophysiology is inaccurate. Her important observation
with which I concur is the importance of creating a story that
makes sense to both physician and patient helping them to ‘go on
together’.
My own perspective is that far greater
insights into the pathogenesis of headache can be obtained by
studying the non-linear dynamics of the underlying neural processes
rather than a reductionist approach which focuses on an artificial
static.3 But that’s just an alternative map that seems
to make sense for me.
References
1. Jackson A. Management of headache. Br J Gen
Pract 2008; 58(549): 282–283.
View title page online.
2. The International Classification of
Headache Disorders. 2nd edition. Cephalalgia
2004; 24:(Suppl 1).
3. Kernick D. Migraine – new perspectives from chaos theory.
Cephalalgia 2005;25: 561-566.
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Date: 14 Feb 2008 14:58
Topic: Yogurt and antibiotic-associated diarrhoea
Comments by: Jeremy
Hamilton-Miller
The conclusion drawn by Conway et a1 as a result of
their recent study is: ‘Overall, this study failed to demonstrate
that yogurt has any effect on antibiotic-associated diarrhoea’. I
am concerned that this gives the wrong message, as readers will
take this to mean that this conclusion applies to all brands of
bioyoghurt, when only one brand (Yeo Valley) had been tested. It is
highly likely that each different brand of yoghurt will vary, in
that the precise strains of the so-called ‘probiotic’ organisms
used in their manufacture are separate, distinct biological
entities, each with differing properties.
Conway et al state that ‘Yoghurt is a probiotic’, citing a paper by
Guarner et al2; however, the latter paper refers
specifically to ordinary yoghurt (made using Lactobacillus
delbrueckii subsp. bulgaricus and Streptococcus thermophilus) and
not bioyoghurt, in respect to its ability to relieve lactose
intolerance. A product cannot be assumed to be a probiotic unless
and until the specific strains therein have been shown to exert a
health benefit in humans, in order to fulfil the generally accepted
definition. Some bioyoghurts do fulfil these criteria.
Conway et al do not tell readers the precise strains present in
the Yeo Valley product tested here, merely that they belong to the
species Lactobacillus acidophilus and Bifidobacterium animalis
subsp lactis. There are thousands of different strains within these
two species, each of which is different; only a very few strains
will have been shown to possess probiotic properties. I have been
informed by Neil Lewis of Yeo Valley that these strains are,
respectively, LA5 and BB12, both of which are well-known.
Unfortunately, most suppliers of probiotics, whether in the form of
yoghurts or supplements, give no information on the label as to
either the precise strains present or any indication of numbers of
viable bacteria present in their marketed products. These two
factors – lack of precise strain identification and no information
as to bacterial numbers – thus make it impossible for the consumer
or the practitioner to make an informed choice.
The question also arises as to which antibiotics were taken in
the three groups. Different antibiotics vary in their propensity to
cause diarrhoea – for example, trimethoprim is rarely responsible
for this, while the incidence for cefixime may be as high as
30%.
References
1. Conway S, Hart A, Clark A, Harvey I. Does eating yogurt prevent
antibiotic-associated diarrhoea? A placebo-controlled randomised
controlled trial in general practice. Br J Gen Pract 2007; 57(545):
953-959.
View abstract online
2. Guarner F, Perdigon G, Corthier G et al. Should yoghurt
cultures be considered probiotic? Br J Nutr 2005; 93: 783-786.
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Date: 2 Feb 2008
Topic: Easing the pain: challenges and opportunities in headache
management
Comments by: Ian K Campbell
What a missed opportunity! In his otherwise balanced editorial,
Dr David Watson1 fails to mention several of the most
common causes of headache seen in general practice: (1) chronic
mild unrecognised dehydration, (how any of us drink enough?); (2)
caffeine excess in one form or another; and (3) referred pain from
musculo-skeletal trigger points over one or both occipital
processes (acupuncture points GB 20-ALWAYS examine these
areas!)
As Dr Watson suggests, tension headaches form a significant
percentage of generalised headaches; in my experience also, sinus
pain is over-diagnosed, as is headache due to refractive error!
Reference
1. Watson DPB. Easing the pain: challenges and opportunities in
headache management. Br J Gen Pract 2008; 58 (547): 77-78.
View title page online
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Date: 26 Jan 2008
Topic: Management of ear wax in primary care
Comments by: Matthew Weller, SpR ENT, Heart of England
Foundation Trust, Birmingham
As a specialist registrar in ENT surgery, I read with interest
the recent article by Coppin et al on the management of earwax in
primary care.1 It would certainly seem from this
randomised controlled trial that the use of a bulb syringe as a
first line treatment for patients at home would be a suitable
alternative to formal ear syringing. If problems were to persist,
then syringing could be considered as a second line of treatment.
It should be noted as well that the most important endpoint would
be the alleviation of symptoms, rather than complete clearance of
wax from the ear canal. Wax in the ear canal is a normal
occurrence, and does not need removing unless the patient is
symptomatic, or examination of the tympanic membrane is
required.
I do have a couple of points to raise. Firstly, the paper states
that it is not known which wax softening drops are most effective,
and references a systematic review published in the BJGP in 2004.
In these days of evidence-based medicine, systematic reviews are
the gold standard in assessing the available literature on a
subject. The Cochrane database provides rigorous assessment of the
current literature, and the Cochrane review of cerumen softening
agents published in 2003 concluded that use of wax softening agents
was more effective than no treatment, but that there was no
significant difference in the different types of over-the-counter
softening agents.2 Based on current evidence the use of
water as a softening agent would be as effective, but cheaper, than
sodium bicarbonate.
Secondly, the study concludes that patient satisfaction was
slightly lower in the group using the bulb compared with the
irrigation group. I would suggest that the satisfaction of the bulb
group would increase if this treatment were available as an
over-the-counter option at the pharmacy, thus removing the need for
a visit to the GP. This could bring the level of patient
satisfaction in line with the satisfaction of those undergoing
formal irrigation.
References
1. Coppin R, Wicke D, Little P. Managing earwax in primary care:
efficacy of self-treatment using a bulb syringe. Br J Gen Pract
2008; 58 (546): 44-49.
View abstract online
2. Burton MJ, Doree CJ. Ear drops for the removal of ear wax.
Cochrane Database of Systematic Reviews 2003, Issue 3. Art. No.:
CD004326. DOI: 10.1002/14651858.CD004326
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Date: Jan 2008
Topic: Forge water, folklore, and warts
Comments by: D Deeny
I note, from reading both local and international medical
journals, that there is no evidence that current treatment of
cutaneous warts is effective1, 2 This is particularly
true for the use of liquid nitrogen.
I have been in general practice for 15 years. I can only concur
with the evidence. I have spent money buying liquid nitrogen
equipment and getting supplies of it delivered. I have not found it
of much use when treating cutaneous warts.
Forge water, the water the blacksmith uses to cool hot irons,
has being used by the Irish as a ‘wart cure’ for
centuries.3-5 As a boy, I remember dipping my hands in
forge water; my warts went without trace, within weeks. I had
multiple hand warts for 3 years, several treatments had been tried,
to no avail, from surgery to salicylic acid pastes.
There is a Farrier School in Kildare Town. The organiser of this
school allowed me access to their forge water. Recently, five
patients used the forge water. In four out of five patients, all
their warts disappeared with 3 months, including a 4-year-old with
15 hand warts! Needless to say they were pleased with the results,
as some had many warts for years. Forge water treatment was
painless and a non destructive treatment for their warts. It worked
for both plantar and hand warts.
It may be that water, high in iron concentration, is effective.
Who knows?, there maybe science in the myth. If forge water is
truly effective, GPs can use their expensive liquid nitrogen
containers to store blacksmiths’ ‘Wart Cure’!
References
1. Gibbs S, Harvey I. Topical treatments for cutaneous warts.
Cochrane Database Syst Rev. 2006, 3: CD001781.
2. Bourke J. Treatment of cutaneous warts. Modern Medicine
Ireland, Oct 2006.
3. O Hogan D. Irish Superstitions, page 88.
4. Vaughan P. The Last Blacksmith of Lissmore, page 74.
5. O Farrell P. Superstitions of the Irish country people,
page 41.
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Date: 2 Jan 2008, 13:56:49
Topic: Bulb syringing for earwax
Comments by: Dr Judith A Langfield
I was fascinated to read this article. My parents used to syringe
their own ears using a rubber bulb syringe. They did so because
before 1948 they had to pay to see the doctor. This obviously
encouraged self-treatment. It would be intriguing to see this come
back into general use again.
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Date: 4 Oct 2007
Topic: 'Connected care in a fragmented world'
Comments by: Dr Jane Wilcock,
GP, The Lowry Medical Practice
Pendlebury Health Centre, Swinton,
Manchester
I would like to hug Jane Farmer for a
wonderful clear, bold article1 stating the
real values of general practice both to patients and GPs!
After years of feeling that I am out of
date and old fashioned in my GP values and unfashionably remaining
in the same practice for 20 years I have read a supportive
article. The political society we read about subscribes to
portfolio careers and valuing fame, choice and change but
here’s to all those GPs who are quietly going about
their careers trying to offer consistency and high quality
health care across the UK.
Reference
1. Farmer J. Connected care in a
fragmented world: lessons from rural health care. Br J Gen Pract
2007; 57(536): 225-230.
View abstract online.
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Date: 16 Aug 2007
Topic: NICE fever advice
Comments by: Wouter Havinga
The NICE guidelines for ‘Feverish illness in young children’ is
a document that contains useful practical advice on fever care. It
illustrates that when dealing with a child with fever, the issue is
to exclude an underlying dangerous infection rather than treating
the fever with antipyretic interventions. This gives the
opportunity for every clinician to give the same
confidence-building message to the public.
- Antipyretic agents (paracetamol and ibuprofen) should not be
used routinely with the sole aim of reducing body temperature in
children with fever who are otherwise well.
- Antipyretic agents do not prevent febrile convulsions and
should not be used specifically for this purpose.
- Paracetamol and ibuprofen should not routinely be given
alternately to children with fever.
- Tepid sponging is not recommended for the treatment of
fever.
- Children with fever should not be under dressed or over
wrapped.
- The use of antipyretic agents should be considered in children
with fever who appear distressed or unwell. Either paracetamol or
ibuprofen can be used to reduce temperature in children with
fever. Paracetamol and ibuprofen should not be administered
at the same time to children with fever.1
To build confidence in parents who are caring for feverish
children, it is essential that health professionals stop
maintaining two medical myths, the first that fevers can get too
high and death ensues; and second, that febrile convulsions happen
when the temperature gets too high. These two myths are the cause
for the widespread anxiety about fever. Furthermore, doctors
believe that reducing the temperature makes the child feel more
comfortable.
The result of the advice ‘to manage the fever’ gives parents the
impression that the temperature should be reduced and is often
advised as such by clinicians. However, the above bullet points
illustrate otherwise. This is important because every practicing
doctor in the out-of-hours service is aware of phone calls from
parents who ring in a panic because they realise that they ‘cannot
control the temperature’.
This iatrogenic fever phobia is a frequent cause for distress in
parents, which has its effects on the child, and the health
professionals who deal with the caller.
Due to the frequency of these type of calls, it puts pressure on
the out-of-hours service. The outdated advice ‘to manage the fever’
or ‘to control the fever’ is potentially resulting in a second call
during the same shift when the temperature is not responding, and
this again is the cause for attendances to the primary care centres
and subsequent contacts with the paediatric departments and
admissions.
Rather than advising to fear and fight a fever, doctors can give
advice that supports the fever process and, as such, build
confidence in parents caring for their feverish child. Implementing
this NICE advice and organising a public awareness campaign to
support the fever process has the potential to create health gains
for all involved and financial gains for the PCTs due to less
pressure on the services.
Reference
1. http://guidance.nice.org.uk/CG47/quickrefguide/pdf/English
(page 14)
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Date: 16 Aug 2007
Topic: Defined daily dose for topical NSAID use –
clinical update
Comments by: D Carnes, PL Cross, and M
Underwood
For the purposes of a randomised controlled trial (RCT) comparing
the effectiveness of topical versus oral ibuprofen for chronic knee
pain in primary care, we needed a defined daily dose of topical
ibuprofen required to treat one knee (TOIB study ISRCTN
7935305).
With the exception of diclofenac in dimethyl sulfoxide cutaneous
solution, the dosage regimens for topical non-steroidal
anti-inflammatory drugs (NSAIDs) given in the BNF and patient
information sheets are vague. A maximum daily amount of 15g
is suggested for ketoprofen gel, and 25g for one preparation of
felbinac gel, but these are total daily doses, not per joint. No
specific amount is given for ibuprofen gel. Nor were the
manufacturers able to give advice on a normal dose for one
knee.
Some ex vivo studies of the penetration of ibuprofen into the
knee joint and peri-articular structures have specified a daily
dose of topical ibuprofen. However, the amount used in these
studies was substantially larger than the dose one might expect to
use in routine practice: 7.5g of 5% ibuprofen gel three times
daily, which provides 1125 mg of ibuprofen per day from 22.5g of
gel. This dosage regimen would mean that a 100g tube of gel would
last just 4.4 days, which would be unrealistic for routine use. To
establish a realistic defined daily dose for topical NSAID use for
knee pain we used two approaches:
1. A typical loading dose for topical preparations is 2mg
vehicle/cm2 of skin (personal communication Marie Miller, Dermal
Laboratories.) We were unable to identify any previous estimates
for the surface area of the skin over the knee or those parts of
the knee to which patients typically apply topical preparations.
Therefore we estimated the knee surface by considering the knee as
a cylinder. One of our research team (DC) measured the knees of 15
members of the public, all over 35 years of age. Measurements were
taken of the circumference of the extended knee at three levels:
the superior aspect of the lateral and medial condyles of the
femur, the joint line, and the tibial tuberosity. The mean of these
values was taken to be the circumference.
We also measured the vertical height of the extended knee from the
superior border of the patella to the insertion of the patella
tendon at the tibial tuberosity. Mean circumference was 39.4cm and
height 13.9cm giving a surface area of 548cm2. We then halved this
figure because in our clinical experience topical NSAIDs are
generally applied to the anterior aspect of the knee only, giving
an area of 274 cm2, which was multiplied by 2mg to provide an
estimate of a single application (0.55g). Although the surface area
of the knees measured may not be completely representative of the
population with chronic knee pain, and the surface area of the knee
varies slightly according to the degree of flexion;4 these
results are likely to be sufficiently accurate for our purpose.
2. The fingertip unit of creams and ointments was developed as a
guide for the use of topical steroid preparations for
dermatological practice. It is used to help patients assess how
much topical steroid to use. The unit equates to approximately 2.5
cm of cream or ointment, the length of the distal phalanx of the
index finger; it weighs approximately 0.5g and covers
approximately 312cm2, an area similar to that of the
anterior aspect of the knee. This approach suggests that a single
application of ointment is 0.5 gram.
Both approaches came up with a similar value. We therefore
defined a single application as 0.5g. Manufacturers typically
recommend topical ibuprofen application three or four times per
day. We standardised a three times daily regimen for all
preparations. This made a defined daily application of a topical
NSAID cream, gel, or ointment for one knee 1.5 g, which for
ibuprofen 5% equates to 75mg ibuprofen per day (a 10% preparation
concentration would equate to 150mg).
These doses of ibuprofen are substantially less than the
1125mg/day used in ex vivo penetration studies: 7% of that used by
Dominkus.3 Few prescriptions for oral NSAIDs are for more
than 200g;6 and, according to the pharmaceutical company estimate
of 2mg/cm2, to rub in the 7.5g of vehicle used for one dose by
Dominkus a skin area of 3750cm2 would be required. We
recognise that the amount of active ingredient absorbed will vary,
depending on the concentration of the preparation. However, the
actual amount of vehicle applied is likely to be unaffected by the
concentration of any active ingredients. We feel confident
that 1.5g is a realistic defined daily dose of topical NSAID for
one knee.
This calculation will serve to inform clinicians and researchers
on the appropriate dosage for topical NSAIDs.
References
1. Cross PL, Ashby D, Harding G, et al; TOIB Study Team. TOIB
Study. Are topical or oral ibuprofen equally effective for the
treatment of chronic knee pain presenting in primary care: a
randomised controlled trial with patient preference study. BMC
Musculoskeletal Disord. 2005; 6: 55.
2. British Medical Association and Royal Pharmaceutical Society,
London. British National Formulary 51. London; March 2006. p
531.
3. Dominkus M, Nicolakis M, Kotz R, et al. Comparison if tissue and
plasma levels of ibuprofen after oral and topical administration.
Artzneim-Forsch/Drug Res: 46(11):1138–1143.
4. Finlay AY, Edwards PH, Harding KG. ‘Fingertip unit’ in
dermatology. Lancet 1989; 2(8655): 155.
5. Long CC, Finlay AY, Averill RW. The rule of hand: 4 hand
areas=2FTU=1g. Arch Dermatol 1992; 128(8): 1129–1130.
6. http://www.ic.nhs.uk/pubs/prescostanalysis2005/pcaexcel/file
(accessed 18 Sept 2006).
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_______________
Physical health
Date: Jun 2009
Topic: Is it time to say farewell to oxytetracycline and
tetracycline?
Comments by: Angus Thompson, a former Prescribing Advisor
from Somerset with an interest in antimicrobial prescribing;
recently joined the Unit for Medication Outcomes Research and
Education (UMORE), University of Tasmania, Australia.
For decades oxytetracycline and tetracycline have been part of many
prescribers’ armamentarium in the fight against infection, but do
they still have a role today?
Most often prescribed in 4 times a day regimes, requiring dosing
on an empty stomach, away from milk, indigestion remedies, iron,
and zinc which may impair their absorption — let’s face it, they
are hardly the simplest of drugs to take effectively! In an era
when promoting best practice in the use of antibiotics is a
priority, continuing to use drugs where there is a high probability
of poor compliance and consequently a risk of sub-optimally
effective therapy seems rather irrational.
So if we do not use oxytetracycline or tetracycline, what would
be used instead? If a member of the tetracycline family is
indicated specifically, for example in acne or certain respiratory
tract infections, then doxycycline is the clear alternative. With
no need to take on an empty stomach or avoid milk, and its
patient-friendly, concordance promoting, once-daily dosing; surely
it’s a closed case?
But what about the budget some may ask? The implication being
that as oxytetracycline and tetracycline have been around for
decades they must be inexpensive. Certainly at just £1 for a week
long course oxytetracycline is; but the same cannot be said of
tetracycline which costs around £9 for the same quantity. This
makes it significantly more costly than virtually any other oral
antibiotic used in primary care these days, including doxycycline
which is now similarly priced to oxytetracycline.1
And what about microbiological appropriateness? The current
version of the Health Protection Agency antibiotic prescribing
guidance for primary care includes doxycycline in all those
scenarios where a tetracycline is indicated.2 Consistent
with this is the statement in the British National Formulary that
‘microbiologically there is little to choose between the various
tetracyclines…’.3
A further potential advantage of doxycycline is that, unlike
oxytetracycline and tetracycline, it is not prone to accumulation
in renal impairment and can therefore be used, with care, in this
significant group of patients.
It would seem the only potential down sides to the use of
doxycycline when compared to oxytetracycline and tetracycline are
possible photosensitivity reactions and the need to swallow the
capsules with plenty of water to reduce the risk of oesophageal
irritation. But when considered against the other arguments to make
doxycycline the tetracycline of choice, these are of modest
significance.
In other areas of prescribing long established drugs have stood
the test of time and in some cases found new niches, but in the
case of the older tetracyclines, there would now seem to be a good
case to drop them from our primary care formularies.
References
1. NHS Business Services
Authority. Drug Tariff, January 2009. NHS Business Services
Authority, Newcastle.
2. Health Protection Agency, London. Management of infection
guidance for primary care, 2001 (reviewed June 2008).
3. BMJ Group and RPS Publishing, London. British National
Formulary, Edition 56; September 2008.
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Discussion.
Date: 7 Jul 2008
Topic: Response to ‘Magic bullets for insomnia?’
Comments by: John S Dowden, Medical Editor, Australian
Prescriber
The article ‘Magic bullets for insomnia?’1 was of
interest because of recent concerns in Australia about the adverse
effects of z drugs, particularly zolpidem. Adverse reactions such
as hallucinations and amnesia appeared soon after zolpidem was
marketed in Australia,2 but there have been increasing
reports of bizarre behaviour in patients taking the drug.
These bizarre adverse events include painting while sleeping,
eating while asleep, and sleepwalking.2,3
Approximately 10% of all reports mention sleep driving. This can be
considered with the 1.4% of the English patients who associated z
drugs with road traffic accidents.1
The concerns about patient safety prompted Australian drug
regulatory authorities to consider rescheduling zolpidem as a
controlled drug. That option was not pursued, but a black box
warning has been added to the product information. This includes
the recommendation to limit the use of zolpidem to a maximum of 4
weeks.3 A similar warning has been included in the
information for patients.
References
1. Siriwardena AN, Quershi MZ, Dyas JV, Middleton H, Orner R.
Magic bullets for insomnia? Patients’ use and experiences of newer
(Z drugs) versus older (benzodiazepine) hypnotics for sleep
problems in primary care. Br J Gen Pract 2008; 58(551): 417-422.
View abstract online
2. Adverse Drug Reactions Advisory
Committee (ADRAC). Seeing things with zolpidem. Australian Adverse
Drug Reactions Bulletin 2002; 21 (1). http://www.tga.gov.au/adr/aadrb/aadr0202.htm#zolpi
3. Zolpidem ("Stilnox") - updated information – February 2008.
Department of Health and Ageing 2008 http://www.tga.gov.au/alerts/stilnox2.htm
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Date: 25 Nov 2007 21:56
Topic: Primary Care Spirometry: Coordinated
efforts needed to enhance spirometry quality and interpretation in
primary care
Comments by: Poels PJP MD, Schermer TRJ PhD, I Smeele
PhD
In the September issue of this journal, White et al.1
reported on the feasibility and usefulness of remote electronic
reporting (by e-mail) of primary care based spirometry. They
conclude that the quality of spirometry tests was low and the
agreement between specialists and GPs on acceptability was slight,
and on diagnosis was fair. The authors’ advice to investigate next
if quality of spirometry testing and interpretation in primary care
can be improved by remote electronic reporting.
Although the paper provides some interesting new information,
there is also much that the authors do not report. For instance,
the paper only reports on the acceptability of spirometry tests in
terms of agreement between the GP and the respiratory specialist.
More details about the actual quality of the submitted spirometry
tests would be required to be able to verify the authors’
conclusion that the ‘quality of the spirometry done in primary care
was unsatisfactory’.
Despite these shortcomings in the study methods used, we agree
with the authors that some kind of continuous support for GPs is
necessary to improve test quality as well as interpretation of the
test results.2 We recently reported that the use of a
computerized expert system for the interpretation of the spirometry
test results had no benefit for the acuity of GPs’ diagnosis and
subsequent management changes.3 From another study we
know that chest physicians can give valid interpretations of lung
function when they just receive written information without
actually seeing the patient.4
So what need to happen next? There is an increased awareness by
government authorities, insurance companies, and healthcare
professionals that primary care spirometry testing needs to be
accredited in some way.5 Therefore, in the Netherlands
the COPD and asthma general practice advisory group (www.cahag.nl) and all other disciplines
involved in primary care spirometry (i.e. lung function
technicians, chest physicians, GPs, practice nurses) will soon
start unfolding a nationwide programme to enhance the quality
of primary care spirometry.
This programme consist of three elements: (1) improving training
(e.g. clarifying the minimum requirements of a spirometry training
like has previously been done in New Zealand,6 use of
standardised educational materials like CD-ROM Spirometry
Fundamentals7); (2) improving organisation (e.g.
describing standards for minimum practice organisation and
protocols for cooperation with secondary care); and (3) improving
quality assurance (e.g. periodic outreach visit by lung function
technicians,8 incorporation of spirometry quality
indicators in practice accreditation, and a system of registration
of the spirometry driver license).
We believe that only with such coordinated efforts spirometry
performance and interpretation in primary care can be enhanced
structurally.
References
1. White P, Wong W, Fleming T, Gray B. Primary care spirometry:
test quality and the feasibility and usefulness of specialist
reporting.
Br J Gen Pract, 2007; 57 (542): 701-705.
View abstract online.
2. Poels PJ, Schermer TR, van Weel C, Calverley PM.
Spirometry in chronic obstructive pulmonary disease. BMJ 2006;
333(7574):870-871.
3. Poels PJP, Schermer TRJ, Schellekens DPA, Akkermans RP, de
Vries Robbe PF, Kaplan A et al. Impact of a spirometry expert
system on general practitioners' decision-making. Eur Respir J
2007; Published ahead of print June 27, 2007,
10.1183/09031936.00012007.
4. Lucas A, Smeenk F, Smeele I. Interpretation of the results
of spirometry and anamnesis into a diagnose and advice for
treatment: validity and reliability. Eur Resp J 2004;
24(48):87s.
5. Gruffydd-Jones K, Stephenson P, Levy M, GPIAG Working
party. What standards and terms of employment should respiratory
practitioners with a special interest expect from an employing
organisation? Prim Care Respir J. 2007 Jun;16(3):182-7.
6. Spirometry training courses. A Position Paper of The
Australian and New Zealand Society of Respiratory Science & The
Thoracic Society of Australia and New Zealand. http://www.anzsrs.org.au/spirotrainingposition.pdf February
2004.
7. Spirometry Fundamentals. http://www.spirofun.org/.
8. Thuyns V, Schermer J, Jacobs E, Folgering M, Bottema M, van
Weel C. Effect of periodic outreach visits by lung function
technicians on the validity of general practice spirometry. Eur
Respir J 2003; 22(45):439s.
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Date: 4 Oct 2007
Topic: Primary care spirometry
Comments by: Paul J Nicholson OBE FRCP FFOM MRCGP,
London
Guidelines for the care of patients with chronic obstructive
pulmonary disease (COPD)1 and those for
asthma2 encourage the objective assessment of lung
function at all levels of health care. However, limited data are
available on the quality of spirometry performed in primary care.
Since spirometry is incentivised by the Quality Outcomes Framework,
the study by White et al3 in this journal (Sept 07
issue) is important, as is a coincidental study in the US that
shows that of 368 tests completed in primary care over 6 months,
71% were technically adequate for interpretation and that family
physician and pulmonary expert interpretations were concordant in
76% of tests.4
White et al challenge an ‘unstated assumption’ that the
professionalism of primary care clinicians will ensure that
spirometry is performed to an acceptable standard.3
Wherever this assumption might exist, it must be purged actively.
Spirometry is among the most useful and accurate measures of
respiratory health, however, when not performed correctly, it can
lead to misdiagnosis and mismanagement. Like many health
measurements, spirometry is subject to measurement error.
Measurements of the same quantity can vary in the same individual,
from one day to another, in different hands, with different
equipment, at different centres. Error may arise in the subject,
the observer and/or the measurement process. In spirometry, the
most common cause of erroneous results is sub-optimal patient
coaching.5 Thus spirometry requires specific training
over and above basic professional training. NICE guidelines
emphasise the need for appropriate training and for competence in
the interpretation of spirometry results.1
White et al state that there is currently no standard for the
training and conduct of primary care spirometry. As an occupational
physician responsible for spirometry programmes in a non-hospital
setting, I argue that the competence of clinicians performing
spirometry and interpreting results are identical, irrespective of
the clinical setting. Of note, the Association for Respiratory
Technology and Physiology (ARTP) with the British Thoracic Society
(BTS) provide a competence qualification in spirometry. The
certificate in spirometry incorporates competence assessment via a
training course run at over 20 centres nationwide, a written
assignment, a portfolio of examples and a short practical exam and
viva. The certificate is noted to be useful for nurses in both
primary and secondary care.6
The authors methodology required practices to perform spirometry
according to the 1994 update of the American Thoracic Society (ATS)
guidelines.7 However, these were superseded in 2005 by
joint ATS and European Respiratory Society (ERS) guidelines that
are available for free online.8
The authors point out that the quality of spirometry is likely
to be determined by several factors including the quality and
length of spirometry training, the aptitude of the spirometry
technician, supervision after completion of training, and the
quality of test interpretation. The ATS and ERS also published
guidelines on interpretative strategies for lung function tests in
2005.9 These too are available for free online.
Eaton et al’s study of spirometry in primary care practice
demonstrated that non-acceptability of results was largely
ascribable to failure to satisfy end-of-test criteria.10
Failure to use appropriately calibrated/prepared equipment is
another concern.11 These issues emphasise the importance
not only of effective training but also of effective quality
assurance programmes. The ARTP, BTS, and British Lung Foundation
want the mandatory implementation of quality assurance measures for
all NHS personnel performing spirometry within by
2010.10 Given that standards do exist, spirometry in
primary care is instantly amenable to clinical audit, peer review
and therefore quality improvement. Specialist reporting of
spirometry conducted in primary care, as studied by White et al,
could prove to be a useful quality improvement tool, but adequate
training of those performing spirometry must to be the primary
corrective measure to correct this quality non-conformance.
References
1. Chronic Obstructive Pulmonary Disease. Management of
chronic obstructive pulmonary disease in adults in primary and
secondary care. NICE. London. 2004. http://www.nice.org.uk/pdf/CG012_niceguideline.pdf
2. British Thoracic Society; Scottish Intercollegiate
Guidelines Network. British guideline on the management of asthma.
SIGN, Edinburgh 2007; 2007.
http://www.sign.ac.uk/guidelines/published/support/guideline63/download.html
3. White P, Wong W, Fleming T, Gray B. Primary care
spirometry: test quality and the feasibility and usefulness of
specialist reporting.
Br J Gen Pract, 2007; 57 (542): 701-705.
View abstract online.
4. Yawn BP, Enright PL, Lemanske RF, et al. Spirometry can
be done in family physicians' offices and alters clinical decisions
in management of asthma and COPD. Chest, 2007 Jun 5 [Epub ahead of
print].
5. Enright PL. How to make sure your spirometry tests are
of good quality.
Respir Care, 2003;48:773-776.
6. http://www.artp.org.uk/
7. American Thoracic Society. Standardization of
spirometry: 1994 update. Am J Respir Crit Care Med, 1995; 152:
1107-1136.
8. Miller MR, Hankinson J, Brusasco V, et al.
Standardisation of spirometry. Eur Respir J, 2005;26:319-338.
http://erj.ersjournals.com/cgi/content/full/26/2/319
9. Interpretative strategies for lung function tests.
Eur Respir J, 2005;26:948-968.
http://erj.ersjournals.com/cgi/content/full/26/5/948
10. Eaton T, Withy S, Garrett JE, et al. Spirometry in
primary care practice: the importance of quality assurance and the
impact of spirometry workshops. Chest, 1999;116:276-277.
11. Joint Statement from the Association for Respiratory
Technology & Physiology (ARTP), the British Thoracic Society
(BTS) and the British Lung Foundation (BLF) for World COPD Day
2005. http://www.brit-thoracic.org.uk/article9.html
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Date: 16 Aug 2007
Topic: Are pneumococci also the most frequent germs in
exacerbations of chronic bronchitis?
Comments by: Carl Llor, Primary
Healthcare Centre Jaume I, Tarragona; Josep Maria
Cots, Primary Healthcare Centre La Marina, Barcelona,
Spain
We read the article recently published by Holm et al1
on the aetiology of lower respiratory tract infections with
interest. In this article, the authors only reported 16.8% of
bacterial aetiology among the patients with non-pneumonic
infections of the lower respiratory tract. In this study
Streptococcus pneumoniae was the most frequent among the bacterial
agents observed, being isolated in one third of the bacterial
infections followed by Haemophilus influenzae in 21.7% of the total
number of bacterial infections.
The authors comment that expectoration was more frequent among
the patients without pneumonia than among those with radiologically
confirmed pneumonia. Among the 316 patients with non-pneumonic
infections, many were probably exacerbations of chronic bronchitis
or even with spirometric diagnosis of COPD. It would therefore be
interesting to know the aetiology of these patients since hospital
series indicate H. influenzae as the most frequent aetiological
agent.
However, in a study carried out by our group in primary care
patients (n = 1947) with exacerbations of chronic bronchitis, the
most frequently isolated agent was pneumococcus with almost 35% of
all the bacterial causes.2 On the other hand, in this
study H. influenzae, was only responsible for 12.6% of all the
exacerbations, being third by order of frequency. If the results
obtained by Holm et al were similar in patients with chronic
bronchitis, this would further support the different aetiology of
the patients within the community setting compared with that of the
hospital, which would be explained by the lesser severity of the
patients attending our consultation offices.
Since a microbiologic study was performed, it would also be
interesting to know, if possible, what diagnoses the respiratory
infections by H. influenzae corresponded to and whether there was a
correlation between the different aetiological agents and the
concentrations of C-reactive protein and procalcitonin, taking into
account that in other studies the highest values of these
inflammatory markers seemed to be more associated with pneumococcal
infection.3
References
1. Holm A, Nexoe J, Bistrup LA, et al. Aetiology and
prediction of pneumonia in lower respiratory tract infection in
primary care. Br J Gen Pract 2007; 57(540): 547–554.
View abstract online.
2. Llor C, Cots JM, Herreras A. Bacterial etiology of chronic
bronchitis exacerbations treated by primary care physicians. Arch
Bronconeumol 2006; 42: 388–393.
3. Almirall J, Bolíbar I, Torán P, et al. Community-acquired
pneumonia Maresme study group. Contribution of C-reactive protein
to the diagnosis and assessment of severity of community-acquired
pneumonia. Chest 2004; 125: 1335–1342.
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Date: 16 Aug 2007
Topic: Chronic musculoskeletal pain
Comment by: Dr Anna Alexander, FY2 Department of
Medicine, Hammersmith Hospital, London
It was interesting to read the systematic review on prognostic
factors for musculoskeletal pain in primary care by Mallen et al
and the editorial by Carnes and Underwood (BJGP August 2007).
It is very clear that we need more research on chronic
musculoskeletal pain before we could come to any definite
conclusion. Cervicogenic headache is a highly controversial issue
and had been through much debate. Research has shown that
interleukin beta (IL-β) and Tumour Necorosis Factor alpha (TNF-α)
have a role in cervicogenic headache. It is possible that a similar
mechanism may exist in low back pain and in other musculoskeletal
pains. Until we find the biomolecular markers of this condition, it
will be misunderstood and treatment will continue to be
contaminated by non-scientific practice.
Reference
1. Martelletti P. Proonflammaotry pathways in cervicogenic
headache. Clin Exp Rheumatology 2000, 18(Suppl 19): S33–S38.
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_______________
Service organisation
Date: 7 Jul 2008
Topic: Response to ‘Death certification post Shipman’
Comments by: David Church, GP, Machynlleth
I do not agree with Messrs Holden and Cox that the current
system for death certification is seriously flawed.1
After all, I understand that Dr Shipman’s case was detected by the
current system not less than twice! The failure was not in the
death certification system, but in lack of action by those to whom
the discrepancies were reported. The problem is that the tone of
the inquiry was directed towards finding someone to blame ‘outside’
of the official authorities. It therefore fell to blaming GPs,
despite a complete opposite truth in the evidence, which just
happened to be convenient to the government anyway, who were in the
midst of trying to discredit GPs in any way possible so that
various other changes in the NHS could be forced through.
It is no surprise that there have been no concrete actions to
change the existing system of certification of cause of death: no
failings were detected within the system, and consequently no-one
has come up with any way of doing any part of it better. Plus, the
aims of the inquiry were achieved without improving the system
criticized – the Government’s aims were not to improve death
certification, but to lay a smear on GPs, which was achieved quite
readily due to lack of effective counterspin by the profession’s
representatives.
Reference
1. Holden J, Cox S. Death
certification post Shipman. Br J Gen Pract 2008; 58(552): 510.
View title page online
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Date: 6 Jul 2008
Topic: Response to ‘The NHS at 60’
Comments by: Alan Keith, GP, Rotherham, South
Yorkshire
I was interested and not a little surprised to read in Prof.
Graham Watt's leading article1 that the QOF has ‘largely
ironed out social gradients in incentivised quality markers’. If
Prof. Watt cared to look down from his ivory tower for a moment he
would realize that it has done nothing of the sort. It certainly
could have been used to this end and it is a tragedy that it has
not.
The reason of course is that in calculating quality payments it
is the square root of the prevalence of a chronic disease rather
than the prevalence, which can be safely assumed to correlate with
the actual workload involved, that is used to calculate the
payments. The effect of this is to take money out of practices in
which there are a great proportion of deprived, elderly or ethnic
minority patients (We have all three) and put in the pockets of GPs
in some of the most prosperous and desirable parts of the
country.
The GPC who negotiated this egregious deal have proved
extraordinarily resistant to any attempt to change, or even discuss
it, in spite of the fact that it was roundly condemned at this
year's LMC conference.
Furthermore, it was not discussed at last year's ARM of the BMA;
the reason being that although I had proposed the motion and it had
been quite properly put forward by the Rotherham division of the
BMA, it was unaccountably omitted from the agenda by the staff at
BMA house. This year however I was luckier, the motion actually
made it onto the agenda but unfortunately in a position in which it
is most unlikely to be debated.
It is not as if this would be difficult to rectify. It could be
done by a stroke of the pen and would be entirely revenue neutral.
Indeed, one wonders what on earth inspired the civil servants from
the Department of Health to allow it in the first place. If the
government are to be believed they are whole hearted in favour of
supporting general practice in deprived areas. Unless of course
this is part of the softening up process for the advent of APMS
practices.
It could of course be claimed that, in spite of all thi,s QOF
does deliver extra funding where there was none before and perhaps
we should be grateful for these crumbs from the rich man's
table.
Reference
1. Watt G. The NHS at 60: time to
end the fairy tale. Br J Gen Pract 2008; 58(552): 459-460.
View title page online
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Date: 6 Jul 2008
Topic: Response to ‘Alsfords’s theoretical political
framework’
Comments by: Dr Mark Freeman, Churchwood Medical Practice,
St Leonards-on-sea, East Sussex
Charlotte Williamson’s piece on Alsford’s theoretical political
model1 provides a seductive analysis which she is
applying to the flux happening now within health service
organisation in the UK. However it should be acknowledged that this
is a political theory. By describing clinician’s interests as
‘dominant’, the use of language alone implies that their interest
should be moderated or brought down.
Alsford developed his theory to effect change in 1970s US health
care, when many could agree clinicians’ interests may be entrenched
for financial reasons. However I would argue that what motivates
clinicians who have grown up in, been trained in, and who work in
the NHS of the UK is quite different. Williamson alludes to
professional monopolists believing altruism as a motivator. I would
argue this is a truth rather than a belief. Going the extra mile
for the patient, or staying on the extra hour to sort out a
problem, demonstrates the beneficence of the clinician and nurtures
the relationship for the patient. This is a marker of quality that
I have yet to see quantified or put into the equation when it comes
to advocating change. It is integral with a sense of
ownership of the system by the clinician. Clinicians know it is in
the best interests of the patient (and indeed a silent majority of
patients know this also).
When clinicians are seen as resistant to change it needs to be
borne in mind they are so when they can see a system that works
being eroded. The type of personality that is attracted to medicine
is not the same as the businessman. When describing our interest as
‘dominant’, it is not the money that it is making us resist change,
it is the preservation of a system whereby we can feel good about
doing good. Individual patients see the benefit of this every
day. Politicians need to understand how fundamental this is
to the whole business of doctors treating patients to the
satisfaction of all concerned. And when doctors are seen as
resisting change, we need to shout loudly that it is not because of
conservatism (with which so may find convenient to label us), but
because we are and always have been radical advocates of out
patients’ interests.
Reference
Williamson C. Alford's theoretical political framework and its
application to interests in health care now. Br J Gen Pract 2008;
58(552): 512-516.
View abstract online
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Date: 4 Mar 2008 11:36:43
Topic: Complementary medicine
Comments by: Dr Andrew Sikorski
Ernst is a left brain
analyst.1 We GPs have to make sense of convoluted
individual histories in snapshot opportunities and assist these
individuals to the best of our ability while ticking QoF boxes and
attempting to stick to 'Primo non Nocere'. Unsurprisingly not all
the answers were presented during the education we received at
medical school nor are they all contained within the BNF. Anyone
trying to stick to the rigid guidelines is calling down the known
ills of our vocation on their shoulders – burn out, depression,
drink, drugs, divorce and suicide.
Fortunately we have a corpus callosum linking between our right
and left brains.
Hence doing our best with our patients can lead to some amazing
stories of recovery or coping in the face of unanswerable
adversity. We all realize Ernst hasn't the answers for us – let’ s
ensure he leaves us some hope. Dismissing complementary therapeutic
techniques is like throwing the baby out with the bath water and by
now I would be mad, bad or dead without them.
Reference
Edzard E. Complementary and alternative medicine: what the NHS
should be funding? Br J Gen Pract 2008; 58(548): 208-209.
View title page online
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Date: Jan 2008
Topic: GP burnout
Comments by: Francesco Carelli, Professor F.M.
University of Milan, EURACT Council Director of Communications
Anders Brondt with Frede Olesen and Danish
colleagues1 demonstrate that burnout is affecting many
GPs. The paper reports a study of Italian GPs which found higher
levels of emotional exhaustion and depersonalisation, but lower
values on personal accomplishment compared with the Danish
research.2
In Italy I co-ordinated the European Research on Burn Out in
General Practice sponsored by EGORN. The results were presented at
EGPRN meetings and WONCA Congresses in Amsterdam, Kos, Florence,
and Paris.3 The study confirmed that burnout syndrome
among GPs is becoming an international and widespread problem.
Apart from high workload and lack of a portfolio career, one of the
most important reasons is the high (and intolerable) pressure from
governments, mainly in terms of budget rationing. Furthermore, in
Italy there is the emergence of groups in the public who are more
demanding and less deferential, and there is the feeling that the
media has become more hostile towards the medical
profession.4
The public has begun to have higher (and sometimes unrealistic)
expectations of public services. Politicians have responded by
opening up a debate about the size of public spending, but often
they appear to be too hasty in blaming the medical profession when
things go wrong.4 Guidelines, protocols, regulations,
and inspections are perceived by many doctors as eroding their
control over their own professional lives.
In Italy, as in other 12 European countries, we used the Maslach
questionnaire and a modified questionnaire to investigate some
aspects of GPs’ working lives. Over 30% declared they were thinking
of changing jobs. This was mainly regarding 47-55 years olds who
were working in urban settings. GPs expressed feeling: (a)
emotionally drained from work; (b) used at the end of the workday;
and c) frustrated with the job. A relevant number of GPs,
regardless of whether they live in urban, rural, or mixed settings,
are having marriage problems.
This situation about job satisfaction and burnout is clearly
increasing because of bureaucracy, progressive loss of role, and
uncertainty regarding the future for the National Health System and
contrasting interests in the political field.
References
1. Brøndt A, Sokolowski I, Olesen F, Vedsted P. Continuing
medical education and burnout among Danish GPs. Br J Gen
Pract. 2008; 58(546): 15-19.
View abstract online
2. Grassi I, Magnani K. Psychiatric morbidity and burnout in
the medical profession: an Italian study of general practitioners
and hospital physicians. Psychother Psychosom 2000; 69(6):
329-334.
3. Carelli F, Petrazzuoli F, Lionis C, Soler K. A particular
aspect of GPs’ burn-out syndrome: the intolerable bureaucratic
pressure felt as an institutional mobbing, WONCA Europe Conference,
Florence, August 2006.
4. Carelli F. Where job satisfaction is dying. BMJ, 2003; 326:
22.
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Date: 19 Nov 2007
Topic: Personal and public health care
Comments by: David Church, GP, Machynlleth, Powys
I would tend to disagree with Prof. Abholz’s1 view
that it is only within the last few years that GPs have seen a
shift from personal to public health roles. And as a result or
implemented by QOF or EBM.
It may be true of GPs in other countries, but British GPs have had
a strong duty and role in public health as well as personal care
for centuries, possibly longer, depending on one’s view of the
origin date of general practice.
At medical schools in the 1980s there was good grounding in
public health for all of us, not just GPs, from departments as
diverse as ‘Man in Society’, ‘Infection Control’, and Microbiology,
for a start. Indeed, the Leeds School (and no doubt others) was set
up partly around and involving the staff of the Public Dispensary.
However, going back further, there were huge contributions to
social medicine by local authorities under the Poor Laws (when
properly discharged), and their predecessors, the Parish Wardens,
using general medical manpower when needed.
Certain instances of historical public medicine are rightly
famous in Britain – the Broad Street Pump, for example, and William
Pickles. Going back even further, there is evidence that roman
military forces in Britain were served by attached medical staff
who, being part of the military establishment would have had
loyalties to the Legion as well as the individual, and so were
taking public health into consideration.
I think it is an integral part of medical tradition in Britain to
be aware of the public health effects of individual illness and
treatment, and one of which we can and should be proud.
Reference
1. Abholz H-H. Conflicts between personal and public health care:
can one GP serve two masters? Br J Gen Pract 2007; 57(542):
693-694.
View abstract online.
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Date: 19 Nov 2007
Topic: Death certification
Comments by: Dr M G Bamber and Dr A McKechnie, The
Surgery, Back Lane, Colsterworth, Grantham, Lincs
I read your paper in the Back Pages of the
BJGP1 with increasing sadness. The purpose of a
death certificate is primarily to state the cause of death, while
the other two functions you cite are soft accompaniments.
Your example where you state that there was ‘… no doubt at all
that death was from natural causes’ depressed me in a journal
designed to educate its readers. My increasingly unfashionable view
is that the doctor should try to find the cause of every death. How
can you expect the state of the nation’s health to be assessed from
guesses and kind words on death certificates designed to be
‘acceptable to both the registrar and the family’?
The reluctance to both variously request and finance autopsies
has now produced the situation that a doctor can train as a
histopathologist in the UK without ever having done an autopsy.
Many young doctors have not seen, let alone performed, an
autopsy.
Some conditions identified after death may have real relevance
to surviving relatives and medical and nursing attendants. My
anecdotal favourites in my career to date have been aortic
aneurysms and tuberculosis.
Peter Davies elsewhere in the same edition of the
Journal2 quotes Raymond Tallis referring to ‘sessional
functionaries robotically following guidelines’.
Please be more inspiring and reactionary, if only for the sake
of younger colleagues alone, so that Tallis’ observation can be
reversed.
References
1. Jewell D. Viewpoint - Death certification. Br J Gen Pract
2007; 57(540): 583.
View article in full.
2. Davies P. Mangin on QOF. Br J Gen Pract 2007; 57(540):
580–581.
View abstract online.
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Date: 4 Oct 2007
Topic: Advanced Access
Comments by: Terry Kemple, Horfield Health Centre,
Horfield, Bristol
Is it difficult to get a fast, convenient or personalized
appointment with a GP?
Chris Salisbury et al's two papers1,2 in the August
BJGP investigated the effects of the introduction of the ‘Advance
Access’ scheme. The scheme was meant to fix the perceived problem
that patients couldn’t get to consult a GP quickly. The studies
showed that in reality Advance Access was not needed, fixed
nothing, and produced only marginal changes.
The Department of Health’s national access survey3
investigated but did not confirm the perception that getting an
appointment with a GP was difficult. In some areas there may be
problems. In my own practice the survey reported that 18% of
patients felt they couldn't get an appointment within 48 hours, but
we think we have plenty of unbooked appointments at the start of
each day and if there is no additional unbooked appointment
available we will always see patients the same day if they want.
These gaps between perception and reality need acknowledging and
addressing.
Primary health care services are being compared with services
like supermarkets that seem to be open to sell all things, to all
people, all of the time, almost everywhere. GPs feel under pressure
to copy the supermarket example but if GPs do provide enough
appointment then the problem might be the public’s perception of
what‘s on offer.
Patients want a choice of appointments2 that includes
a fast service (that is, same day), a convenient service (at a day
and time of the patient’s choice), and a personalized service (with
a doctor of their choice within a few working days). GPs can never
guarantee that an appointment is fast, convenient, and personalized
but they can make the choice between these services (and their
consequences) clearer for patients. If GPs do under provide, poorly
describe, or badly explain their services, it’s like supermarkets
failing to stock their shelves with plainly labeled products and
with no instructions on how to use the products.
The stock of appointments needs to be relabeled in terms that
the patients understand like fast, convenient or personalized
appointments. Clear instructions on how to use the fast ‘same day’,
convenient appointment with any GP and the personalized appointment
with a named GP can help patients choose what they want, and know
what they can expect in that appointment.
Unlike supermarkets, primary health care in the UK really is
accessible for all people, all of the time, almost everywhere.
Patients will soon enjoy even more choice about who, when, where,
and how they access and use primary health care as the patient’s
NHS summary care record becomes widely available.
If it is easy to get a fast, convenient or personalized
appointment with a GP then the gap between perception and reality
is a marketing failure that the NHS needs to fix with better
advertising of its GP services.
References
1. Salisbury C, Montgomery AA, Simons L, et al. Impact of
Advanced Access on access, workload, and continuity: controlled
before-and-after and simulated-patient study. Br J Gen Pract 2007;
57(541): 608-614.
View abstract online.
2. Salisbury C, Goodall S, Montgomery AA, et al. Does Advanced
Access improve access to primary health care? Questionnaire survey
of patients. Br J Gen Pract 2007; 57(541): 615-621.
View abstract online.
3. National GP Patient Surveys on Access and Choice
Summary Report 2006/2007
http://www.dh.gov.uk/en/Publicationsandstatistics/Publications/PublicationsPolicyAndGuidance/DH_075455
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Date: 9 Aug 2007 21:36
Topic : 10 Downing Street Petition Against 0844 NEG Surgery Line
Doctors Numbers
Comments by: a concerned
patient
As many GPs will be aware, as the results of the activities of a
company called Network Europe Group (NEG) and their activities in
marketing a telephone switchboard service solution for doctors’
practices (Surgery Line), many GPs have ditched their conventional
local priced 01/02 numbers in favour of 0844 numbers provided by
NEG along with the so called ‘free’ new switchboard and call
queuing equipment.
However, there is a growing movement against the use of these
numbers by patients who are wholly opposed to their adoption by
their local doctors’ surgeries.
Some of these discontented patients have now started a petition
against the use of the 0844 NEG numbers by doctors surgeries on the
10 Downing Street petitions website at:
http://petitions.pm.gov.uk/NGN-use-by-GPs/
Many patients oppose the use of these 0844 NEG Surgery Line
numbers for the following reasons:
- They are excluded from flat-rate landline calling plans like BT
Option 3 where customers pay a fixed price such as £7.99 per month
for unlimited 01/02 calls. Instead, 0844 numbers are charged at £3
per hour and are not even the same price as a local rate call
(£1.80 per hour) for callers who do not subscribe to a fixed price
calling plan.
- They are excluded from bundled minutes on practically all
mobile phone contract bundled minutes plans and also cost extra on
pay as you go phones too. Some mobile phone providers charge up to
40p per minute to call an 0844 NEG number.
- The 0844 numbers are charged at 13p per minute from BT
Payphones compared to 1p per minute for 01/02 numbers from the same
BT Payphone.
- Calls to 0844 numbers from overseas are usually barred as are
calls to the 0870 number which is the only one NEG allows doctors
using their service to quote as a replacement number. Where the
numbers can be called from overseas the cost is often 10 times
higher, or more, than calling a UK 01/02 number.
The overall view of patients is that, by getting these numbers
doctors are putting their own commercial interests first in cutting
the budget their practice has to spend on advanced telephone
equipment by getting it subsidised through the calls, whereas
patients believe doctors should pay for the equipment out of their
own budgets and continue to charge their patients for normal priced
01/02 calls.
I would be interested to hear the views of GPs on this
matter.
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Date: 2 Aug 2007 15:17
Topic: Interpersonal continuity article
Comments by: Kerr L. White
M.D.
The BJGP is the best GP/FP by all measures! The piece in the RJGP
(July 2007) by Barbara Starfield (the first colleague I appointed
when I started the new Department of Health Care Organization at
Johns Hopkins in 1965) and John Horder (a long-time friend who I
first met in 1959) is a classic! They have boiled down in two-and a
half pages the essential contribution of primary care to
compassionate and scientifically-informed medical responses to the
population's diverse health problems, but also its fundamental role
in underpinning any balanced, safe, and cost-effective health care
'system'. The list of references is superb. It is a true classic
and copies should be sent to all U.K. MPs and all U.S. Congress
Members.
Reference
1. Starfield B, Horder J.
Interpersonal continuity: old and new perspectives. Br J Gen Pract
2007; 57(540): 527-529.
View abstract online.
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_______________
Patient groups
Date: 24 Dec 2007
Topic: Denial of primary care to vulnerable migrants
Comments by: Tom Yates, 5th year Medical
Student, Cambridge; Virginia Leggatt, Physician,
Medical Foundation for the Care of Victims of Torture,
London
The Department of Health and Home Office are reviewing access to
NHS services for foreign nationals and are due to report shortly.
If, as expected,1, 2 rules governing access to primary
care are aligned with those governing hospital care, victims of
trafficking, undocumented migrants, and refused asylum seekers will
lose the right to access freely many NHS primary care services.
This group includes those unable to return to their country
of origin because this is deemed unsafe, either on medical grounds
or for reasons of security. As these individuals are entitled to
claim National Asylum Support Service assistance, it seems
inconsistent to deny them access to primary care.
Clearly, the majority of this group are unable to pay private
healthcare costs3 so if these proposals are implemented,
they will be denied access to almost all health care. Evidence is
growing4 that the 2004 hospital charging regulations
have led to care being denied not only to refused asylum seekers,
but also to other vulnerable individuals with every right to free
NHS care. It seems likely that, if the rules governing access to
primary care are changed, similar errors will occur.
Migrant children denied primary care would be unlikely to
receive childhood vaccinations, reducing herd immunity and
endangering their peers. In addition, many migrants with worrying
symptoms who are denied investigation in primary care will appear
in accident and emergency departments, where care is significantly
more expensive. Delayed diagnosis of communicable diseases could
have implications not only for the individuals concerned but also
for the whole community. Managing advanced illness once treatment
has been deemed ‘immediate and necessary’ will be much more
costly.
Without increased funding for administration, charging in
primary care is unlikely to be workable.5 The only
health impact assessment of such charging suggested that, even in
areas accepting large numbers of migrants, foreign nationals are
unlikely to place significant burdens upon primary care services
and that the costs of administering any charging regime are
unlikely to be recouped.5 There are other practical
considerations, including liability when harm accrues to
patients.
We consider it unethical to use the deliberate denial of health
care to enforce immigration policy. We do not believe that it is
the role of GPs to police such policies and urge those who agree to
make submissions to the Department of Health consultation that
will follow the publication of the review.
Reference
1. Medact. Proposals to exclude
overseas visitors from eligibility to free NHS Primary
Medical
Services: impact on vulnerable migrant groups. London: Medact,
2007. Available from
www.medact.org/content/refugees/Briefing%20V1%20agreed.pdf
(accessed 23 Dec
2007).
2. Yates T, Crane RJ, Rushby M. Charging vulnerable migrants for
health care. Student BMJ 2007; 15: 433.
3. Refugee Action. The destitution trap: research into
destitution among refused asylum
seekers in the UK. London: Refugee Action, 2006.
www.refugee-action.org.uk/campaigns/documents/RA_DestReport_Final_LR.pdf
(accessed 23 Dec 2007).
4. Kelley N, Stevenson J. First do no harm: denying healthcare
to people whose asylum
claims have failed. London: Refugee Council, 2006.
www.refugeecouncil.org.uk/policy/position/2006/healthcare.htm
(accessed 23 Dec 2007).
5. Hargreaves S, Friedland JS, Holmes A. The Identification and
charging of Overseas Visitors at the NHS Services in Newham: a
Consultation. London: Newham Primary Care Trust, 2006.
www.newhampct.nhs.uk/docs/publications/IHUEntitlementReport06.pdf
(accessed 23 Dec 2007).
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