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(2) PLACEBO
CONTROLLED TRIALS "A MORAL
ISSUE"
(3) THE
ENGLISH PATIENT � FACING COVERT
PRIVATISATION
OF THE NHS
(4) HERBAL
REMEDIES: DO THEIR BENEFITS
OUTWEIGH THE
RISKS?
(Influence of maternal age at delivery
and birth order on risk
of type 1 diabetes in childhood:
prospective population based
family study)
http://bmj.com/cgi/content/full/321/7258/420
Children of older mothers have an increased
risk of diabetes
according a new study published in this
week's BMJ. The
risk is highest among first born children
of mothers who start
their families late.
Professor Edwin Gale and colleagues at
Southmead Hospital
in Bristol looked at 1375 families in
the Oxford area in which
one or more child had diabetes. They found
that the mother's
age at delivery was strongly related to
risk of type 1 (insulin
dependent) diabetes. The risk increased
by 25% for each five
year band of maternal age, so that a 45
year old mother was
more than three times likely to have a
child who developed
diabetes than a 20 year old mother. To
a lesser extent the
risk of diabetes was also linked to older
fathers.
Risk of type 1 diabetes was highest among
first born children
of older parents. Second children and
their younger brothers
or sisters were progressively less at
risk of developing the
condition.
Throughout the country women are in general
having their
children at an older age: between 1970
and 1996 the
proportion of children born to mothers
aged 30-34 years
increased from 15% to 28%. The authors
of the BMJ paper
say: "The increase in maternal age at
delivery in the UK over
the past two decades could partly account
for the increase in
incidence of childhood diabetes over this
period."
Contact:
Dr Polly Bingley Diabetes & Metabolism,
Div of Medicine,
University of Bristol Southmead Hospital,
UK
Email: polly.bingley{at}bristol.ac.uk
(2) PLACEBO CONTROLLED
TRIALS "A MORAL
ISSUE"
(Education and Debate: Declaration
of Helsinki should be
strengthened � For and against)
http://bmj.com/cgi/content/full/321/7258/442
The World Medical Association is debating
the next revision
of the Declaration of Helsinki which covers
issues
surrounding using patients in medical
trials. This week's
Education and Debate section in the BMJ
carries for and
against arguments over the morality of
carrying out placebo
controlled trials when there is an existing
accepted treatment
for a condition.
In a placebo controlled trial involving
patients, some
individuals receive the treatment under
test, and others are
given a placebo � a chemically inert substance
given in place
of a drug. Professors Kenneth Rothman
and Karin Michels of
Boston USA argue that placebo comparisons
are unethical if
there is a demonstrably effective treatment
as they would be
denying this treatment to people in need
of it. They write:
"The Declaration of Helsinki explicitly
forbids the use of a
placebo group if an accepted treatment
exists."
Professors Rothman and Michels argue that
the World
Medical Association is under pressure
from the US Food and
Drugs Administration (FDA) to revise the
Declaration. The
FDA, they write, requires many trials
to include a placebo
group. "The most glaring defect in the
FDA's position is that
scientific arguments, right or wrong,
are placed ahead of
ethical concerns" say the two Boston authors.
They want to
see the Helsinki Declaration strengthened
and become
universally acknowledged as "the inviolable
standard for
ethical conduct of human experiments."
Professor Michael Baum of University College
London
criticises the Boston authors for taking
such an absolutist
stance and suggests the issues are not
as simple as they have
suggested.
Contacts:
Professor Kenneth Rothman Dept Epidemiology
& Statistics,
Boston University Medical centre, US
Email: kRothman{at}bu.edu
Professor Michael Baum Department of Surgery,
University
College London, UK
(3) THE ENGLISH
PATIENT � FACING COVERT
PRIVATISATION OF THE NHS
(Editorial: Will intermediate care
be the undoing of the
NHS?)
http://bmj.com/cgi/content/full/321/7258/393
Government proposals to allow NHS bodies
to levy charges
for the personal elements of care will
fundamentally change
the way some English patients receive
health care, says an
editorial in this week's BMJ. Proposals
in the NHS Plan to
extend NHS provision to the private sector
will further erode
the goals of the NHS as a universal comprehensive
service
writes Professor Allyson Pollock.
Under the plan, new care trusts will be
able to commission
and deliver both primary and community
care as well as
social care. They will define what is
NHS care and what is
social care, with the social care elements
subject to local
authority charging policies. Because they
can levy charges for
personal care in the private sector, primary
care trusts will
have clear financial incentives to shift
intermediate care into
non NHS settings, says the BMJ editorial.
The NHS Plan announced 7000 extra NHS beds
by 2004 of
which 5000 will be intermediate care beds,
building "a bridge
between hospital and home". Cottage hospitals,
private
nursing homes and domiciliary and community
settings will
form the heart of the new intermediate
sector. Professor
Pollock says some of the 300,000 NHS patients
expected to
move annually from hospitals into intermediate
care in nursing
and domiciliary settings may have to pay
for their personal
care.
From October 2001 the NHS is committed
to meet only the
costs of nursing care for nursing home
residents; personal
care will be charged for. Professor Pollock
says this will
mean some patients in nursing homes may
be financially
worse off if the NHS switches some intermediate
care to this
sector.
The funding mechanism governing the payment
of care
providers will be critical, says Professor
Pollock. A
Government committed to a universal comprehensive
high
quality NHS would restore the risk-pooling
model of
universal provision by bringing the nursing
elements of the
workforce in the private sector under
NHS control, she
writes.
Contact:
Professor Allyson Pollock School of Public
Policy, University
College London, UK
Email: allyson.pollock{at}ucl.ac.uk
(4) HERBAL REMEDIES:
DO THEIR BENEFITS
OUTWEIGH THE RISKS?
(Herbal medicines: where is the evidence?)
http://bmj.com/cgi/content/full/321/7258/395
With the market for herbal supplements
now approaching
$4bn a year in the United States alone,
what evidence is there
to show that these treatments actually
work, asks Professor
Ernst of Exeter University's Department
of Complimentary
Medicine in a BMJ editorial this week.
An increasing body of evidence is now emerging
that suggest
some herbal medicines are effective �
and often have fewer
adverse effects than standard treatments,
says the author. For
instance, more than 30 clinical trials
show St John's Wort to
be as effective as conventional antidepressants
and ginkgo
biloba has been shown to be more effective
than placebo in
delaying the clinical course of dementia.
Despite these positive results, we should
be aware of the
risks, warns the author. We do not fully
understand how
many of these medicines work and, as many
herbal remedies
are sold as food supplements, they evade
the quality and
safety regulations required for conventional
treatments. Two
recent cases of severe kidney damage caused
by Chinese
herbal tea taken to treat eczema illustrate
the need for a
quality standard for all herbal preparations.
Potential
herb-drug interactions and the cost-effectiveness
of herbal
medicines must also be explored, suggests
the author
As more people turn towards herbal medicines,
health
professionals need access to reliable
information in order to
advise their patients responsibly, concludes
the author. The
UK's minister for public health recently
called for better
protection and information for the public
on herbal medicines
and doctors should take an active part
in this process, he
adds.
Contact:
Professor E Ernst, Department of Complimentary
Medicine,
School of Postgraduate Medicine and Health
Sciences,
University of Exeter, UK
Email: E.Ernst{at}exeter.ac.uk
FOR ACCREDITED JOURNALISTS
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London WC1H 9JR
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Advancement of Science
(http://www.eurekalert.org)