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Releases Saturday 14 June 2003
No 7402 Volume 326

Please remember to credit the BMJ as source when publicising an
article and to tell your readers that they can read its full text on the
journal's web site (http://bmj.com).

If your story is posted on a website please include a link back to
the source BMJ article (URL's are given under titles).


(1)  PATIENTS REMOVED FROM GP LISTS FEEL
VICTIMISED

(2)  SHOULD DRUG COMPANIES BE ALLOWED TO
TALK TO PATIENTS?

(3)  ASSERTIVE PATIENTS ARE "DEEPENING
INEQUALITIES IN HEALTH CARE"

(4)  TREAT ME AS A PERSON NOT JUST A
NUMBER, SAY PATIENTS

(5)  DON'T TAKE YOUR HEALTH FOR GRANTED,
SAYS CHRISTOPHER REEVE

(6)  CAN BEING A PATIENT HELP MAKE A BETTER
DOCTOR?

(7)  RESOLVING THE ETHICAL PITFALLS OF
INTIMATE EXAMINATIONS


 

(1)  PATIENTS REMOVED FROM GP LISTS FEEL
VICTIMISED

(Patients' accounts of being removed from their general
practitioner's list: qualitative study)
http://bmj.com/cgi/content/full/326/7402/1316

Patients who are removed from a general practitioner's
list feel threatened and see their removal as an attack on
their right to be an NHS patient, finds a study in this
week's BMJ.

Researchers interviewed 28 patients who had been
removed from their general practitioner's list. The
interviews were often very emotionally charged, with
patients expressing a range of emotions, including grief,
anger, hatred, alienation, and depression.

Patients viewed their removal as unjustified and showed
that they were "good" patients, who attempted to comply
with the rules they understood to govern the
doctor-patient relationship.

Patients viewed the removing general practitioner as
someone who broke the "lay rules" of the doctor-patient
relationship: that doctors should be caring, polite,
truthful, and clinically competent and should value
personal care. According to the patients, "bad" GPs
broke the "caring" rule by "not being bothered," not
listening to patients, or not acknowledging their
concerns.

Patients experienced removal as deeply distressing and
stigmatising. Some saw their removal as an abuse of
power by GPs, especially as GPs were not required to
justify their actions.

This study shows the negative impact of decisions about
removal on patients, say the authors. They suggest
measures that could help to mitigate some of these
effects, such as a clear practice policy on removal that is
accessible to patients and informing patients of the
reasons for their removal.

However, the circumstances that lead to removal are not
straightforward, and the views and priorities of both
parties—patients and GPs—must be considered in any
moves to reform this area, they conclude.

Rafat Saeed lives in West London and has had
difficulties finding a local GP willing to take him on.
Commenting on the research he says: "Being removed
without knowing why is very distressing and most
upsetting. There should not be any discrimination once a
patient is reallocated, but due to a lack of communication
and help, discrimination takes place. Patients have to
carry the burden of being tagged."

Contacts:

Tim Stokes, Senior Lecturer in General Practice,
Department of General Practice & Primary Health Care,
University of Leicester, UK

Rafat Saeed, Hounslow, West London, UK
Email: ssrafatrr{at}btinternet.com
 

(2)  SHOULD DRUG COMPANIES BE ALLOWED TO
TALK TO PATIENTS?

(Should drug companies be allowed to talk directly to
patients?)
http://bmj.com/cgi/content/full/326/7402/1302

If people are to become more involved in their own
health care, they must be able to gain access to high
quality, balanced, accurate, and up to date information,
but should this information come from drug companies?

In this week's BMJ, Trevor Jones of the Association of
the British Pharmaceutical Industry and Wendy Garlick
of the Consumers' Association go head to head.

Pharmaceutical companies spend 10-12 years
developing a new drug, which gives them unparalleled
knowledge and experience of their products. Yet it
remains the only industry where companies are forbidden
to communicate with individual customers about their
products, argues Trevor Jones.

All stakeholders, including the pharmaceutical industry,
have a part to play in the provision of information to the
public. It is no longer acceptable to keep patients in the
dark and to expect them to be happy relinquishing
control of their health care, he adds.

Informed patients can lead to better health outcomes,
reduction in hospitalisations, and more patients
complying with their medication. In fact, the benefits far
outweigh the risks, he concludes.

People are right to be sceptical about pharmaceutical
companies' ability to be responsible information
providers, argues Wendy Garlick.

A recent survey showed that only 25% of the public
would trust drug companies to provide them with
impartial information, and a recent proposal to lift the
ban on 'direct to consumer advertising' has just been
rejected by European health ministers.

"The decision shows that the MEPs share our and
others' views that advertising does not equate to
education or information."

She believes that there should be one main portal to
independent and impartial information on medicines and
treatments, which is stripped of any commercial or
personal bias. The priority must be to address what
patients and carers need and want, she concludes.

Contacts:

Trevor Jones, Director General, ABPI, Association of
the British Pharmaceutical Industry, London, UK
Email: abpi{at}abpi.org.uk

Jackie Glatter, Consumers' Association, London, UK
 

(3)  ASSERTIVE PATIENTS ARE "DEEPENING
INEQUALITIES IN HEALTH CARE"

(Just how demanding can we get before we blow it?)
http://bmj.com/cgi/content/full/326/7402/1277

Assertive patients who swallow up doctors' time with
lists of questions are increasing health inequalities by
leaving needier patients waiting, according to an article in
this week's BMJ.

As a child, Hilda Bastian remembers learning clearly that
part of being "good" at the doctor's was to say whatever
he or she wanted to hear. But now it worries her that as
the better equipped patients corner more and more of
their doctors' time, the people who need to rely most on
the doctor and find it hard to be assertive could lose out.

Evidence shows that not being liked by doctors and
nurses affects your health care. The patient bringing in
information from the internet has now joined the ranks of
patients who are commonly disliked.

Obviously, this has to change, writes the author. But we
need to consider the question of how to be a "good
patient" in the context of what it will do to the dynamics
of the doctor-patient encounter.

Doctors talk more to the patients they identify with and
like. A lack of rapport has been identified as one of the
major reasons that people from lower socioeconomic
groups or of a different race to their doctor have worse
health outcomes, she adds.

"By 2013, I hope we know how to cultivate more
mutual, trusting relationships between doctors and all
kinds of patients. Just how demanding can we get before
we blow it for ourselves ? not to mention take more than
our fair share?"

Contact:

Hilda Bastian, Managing Editor of the Cochrane
Collaboration consumer website, Victoria, Australia
Email: hilda.bastian{at}cochraneconsumer.com
 

(4)  TREAT ME AS A PERSON NOT JUST A
NUMBER, SAY PATIENTS

(How important is personal care in general practice?)
http://bmj.com/cgi/content/full/326/7402/1310

Not being able to see a doctor who knows you or with
whom you have developed a relationship could have an
impact on your personal care, finds a study in this week's
BMJ.

Researchers interviewed patients, doctors, nurses, and
administrative staff at six general practices in
Leicestershire to explore their experiences of personal
care.

Patients described personal care as involving empathy,
and the perception that health professionals listened and
"had time" for them. One patient said: "Dr O helped me a
lot you see. I find it easier to talk to him cause he listens
really, really well."

Individualised or tailored care was also an important
theme. GPs and nurses talked about tailoring their
management of conditions, while receptionists talked
about tailoring their social talk, as specific ways of
providing personal care.

Patients often referred to the importance of professionals
knowing about them and/or their family history, and a
continuing relationship was central to many accounts of
personal care. One patient said: "I think a one to one
relationship obviously makes the care personal ? and
really that's established over the years."

Practices and individual health professionals can provide
personal care even when patients do not consult a
familiar health professional, say the authors. If GPs and
other practice members wish to provide personal care, it
is important for them to have good communication skills,
and the time to use these skills effectively.

Changes in policy and practice in primary care could
threaten personal care for some patients if it becomes
more difficult for them to see a health professional who
knows them or with whom they have an ongoing
relationship, add the authors.

They recommend that practices should have systems that
enable patients to consult a health professional with
whom they have an ongoing relationship whenever they
prefer to do so.

Contact:

Carolyn Tarrant, Research Associate, Department of
General Practice and Primary Health Care, University of
Leicester, UK
Email:  ccp3{at}le.ac.uk
 

(5)  DON'T TAKE YOUR HEALTH FOR GRANTED,
SAYS CHRISTOPHER REEVE

(Man and superman)
http://bmj.com/cgi/content/full/326/7402/1287

The actor Christopher Reeve was thrust into the limelight
after a riding accident in 1995 left him severely disabled.
In this week's BMJ he talks frankly about life in a
wheelchair, the importance of taking care of your health,
and his campaign work for the Christopher Reeve
Paralysis Foundation.

Reeve decided to use his celebrity status to campaign for
stem cell research that might help find a cure for him and
others like him, but he was stunned to find out just how
controversial it was, particularly in the United States.

"A number of religions think that destroying an embryo,
even one that is already destined to be thrown away as
medical waste is immoral," he says. They have weighed
in on the issue, talking about the sanctity of life."

He insists that he is using his celebrity status responsibly
and believes that his work as a patient advocate has had
a huge benefit on his mental health. "There is a reason to
get up every morning, beyond being here for my family. I
have work to do everyday that may effect the outcomes
for other patients."

Reeve is also a great believer in being proactive over
personal health. "I urge people not to take their health for
granted. To really pay attention to diet and exercise,
particularly as people get older," he says.

So what does he think makes a good doctor and a good
patient? "A good doctor goes the extra mile for his
patients, in spite of the limitations of the healthcare
system," says Reeve. "They need to be independent
thinkers who are full of compassion."

"A good patient should learn everything he can about his
illness or disability and be willing to try reasonable
recommendations and meet challenges that are posed by
doctors or patients. A good patient also needs to
maintain self discipline."

Contacts:

Maggie Goldberg, Christopher Reeve Paralysis
Foundation, USA
Email: media{at}crpf.org

Lynn Eaton, Journalist and guest editor, BMJ, London,
UK
Email: leaton{at}bmj.com
 

(6)  CAN BEING A PATIENT HELP MAKE A BETTER
DOCTOR?

(Doctors' Diagnosis)
http://bmj.com/cgi/content/full/326/7402/1323

What happens when doctors are told they have chronic
conditions? In this week's BMJ three journalists meet
three doctors with similar conditions to discuss the
personal and professional implications of being both one
of "us" and one of "them."

Mike Shooter, president of the Royal College of
Psychiatrists, has suffered bouts of depression
throughout his career. He feels his personal experience
of mental illness has helped his understanding as a
psychiatrist. "I think it has helped knowing what it feels
like from inside ? I do think it has given me a kind of
empathy," he tells Helen Crane, who also suffers with
severe depression.

Derbyshire general practitioner, Stuart Bootle, has had
diabetes for 20 years. His experiences as an NHS
patient have influenced his NHS career, but the fact that
he is a doctor specialising in diabetes does not mean he's
a perfect patient. "I don't always look after myself all the
time — like everyone, I want a balance in my life," he
admits to Paul Smith, who also has type 1 diabetes.

Former general practitioner, Stephen Hempling, had
multiple sclerosis diagnosed at 50. Once his diagnosis
had been made, he found that other general practitioners
would "shunt" patients with MS to him on the grounds
that he could empathise. "The thing was that I liked
seeing them because I liked talking to them," he explains
to Harriet Gaze, who has MS.

Contacts:

Paul Smith, Reporter, Health Service Journal, London,
UK
Email:  paul.smith{at}emap.com

Harriet Gaze, Freelance Journalist, London, UK
Email:  harrietgaze{at}aol.com
 

(7)  RESOLVING THE ETHICAL PITFALLS OF
INTIMATE EXAMINATIONS

(Letters: Please don't touch me there)
http://bmj.com/cgi/content/full/326/7402/1326

Intimate examinations are one of patients' greater
worries. In this week's BMJ, readers respond to a
survey of medical students published earlier this year,
which suggested that many examinations are carried out
without adequate patient consent.

"I was admitted two days before surgery for a hiatus
hernia," says Mary Selby. "During that time 12-20
medical students examined me vaginally. Whilst all asked
permission, and I consented, it never occurred to me that
I was in a position to refuse. I was upset by the
examinations and felt both vulnerable and unclean after
them. Having no advocate on the ward makes it very
difficult for patients to refuse examinations which they
would very much like to avoid. I still wish I had refused."

But how do students acquire clinical skills without
practising on patients? A new approach using manikins
with actors has been developed. This ensures that
students are prepared to deal with contextual challenges
of real work settings, writes Debra Nestel of Monash
University, Australia.

Another training programme has been developed to deal
with these legitimate problems. Students at Antwerp
University in Belgium perform three procedures,
supervised by intimate examination assistants. Attention
is focused on personal attitude, the students' technical
ability and communication skills. Students reported
feeling more secure while performing intimate
examinations, and paid more attention to patients'
feelings, integrity, and privacy.

Contacts:

Mary Selby, Principal General Practitioner, Newmarket,
UK Email: happyselby{at}btinternet.com

Debra Nestel, Lecturer, Centre for Medical and Health
Sciences Education, Monash University, Australia
Email: debra.nestel{at}med.monash.edu.au

Kristin Hendrickx, General Practitioner, University of
Antwerp, Belgium
Email:  kristin.hendrickx{at}pandora.be
 


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