One of the more interesting figures in
contemporary bioethics is Oxford’s Julian Savulescu. An Australian who is a
former student of Peter Singer, he boldly rides utilitarian theories wherever
they wander, regardless of unsettling this might seem to his readers. As a fan
of eugenics and human enhancement, he is a weathervane for bioethics which is
sceptical of human dignity. So it was interesting to read on his blog that he has
rejected one of the cornerstones of Enlightenment humanism, equality:
“Equality is an ideal born of the vice, or
one of the seven deadly sins, of envy. It has no intrinsic value but panders to
our vicious nature to be envious of others…
“Equality has no intrinsic value. Our
commitment should be to the lives of individual people not to human ideals like
equality.
“Equality is a dominant moral ideal in
contemporary society. Egalitarianism is the stated principle for the [National
Health Service}: equal treatment for equal need. Equality might be a good rule
of thumb but it should not be a final regulative ideal. “ ~ Julian
Savulescu’s blog, June 17
Last year British doctor and philosopher
Raymond Tallis published a cranky article in The New Humanist about
“neurotrash” which complained about the exuberant proliferation of neuros: “If
you come across a new discipline with the prefix ‘neuro’ and it is not to do
with the nervous system itself, switch on your bullshit detector. If it has
society in its sights, reach for your gun. Bring on the neurosceptics.”
Heeding his summons, Eran Klein, of Oregon
Health and Sciences University, has published an article in the journal
Neuroethics entitled “Is There a Need for Clinical Neuroskepticism?”
“It is far from clear that a future world
in which everyone wears neurospectacles is the best one available to us.
Neuroscience has changed the way we understand ourselves and no doubt will
continue to do so, often for the better. But it provides just one way to
encounter the world. Enveloping ourselves in a discourse of the ‘neuro’ —
though perhaps seductive at times — can also crowd out other valuable ways of
talking about and understanding ourselves and our place in the world. Sometimes
talk of neurons, synapses, and circuits must give way to talk of open futures,
distributive justice, and perfectionism. A healthy dose of neuroskepticism may
be just what’s needed for medicine to travel along neurotechnology’s golden
road.” ~ Neuroethics,
Aug 17
German doctors and medical historians have
criticised the German Medical Association’s present and previous presidents for
omitting the Nazi past of another former president in a recent obituary in
Deutsches Ärzteblatt, the German counterpart of the BMJ. The article concluded
by stating that Hans Joachim Sewering "rendered outstanding services to
the protection of ethical values in medical practice".
The German medical community’s considerable
efforts to come to terms with the Nazi past make this omission
incomprehensible, say 81 signatories to an open letter.
The editor countered that a previous short
article had mentioned Sewering’s Nazi past. He also said the German Medical
Association and the Deutsches Ärzteblatt had tried hard to shed light on the
Nazi period by commissioning
independent research projects.
Professor Sewering was a member of both the
Nazi Party and the SS. He began work in a lung hospital for disabled children
near Munich in 1942. Between June 1943 and February 1945 he sent at least nine
children to another hospital known for euthanasia. Five of them died there from
malnutrition. However, witnesses
accused him of involvement in the intentional starvation and drugging of
over
900 mentally and physically disabled patients.
After the war, he became an official in the
German and Bavarian Medical Associations and was president of the German
Medical Association from 1973 to 1978. His Nazi past emerged in 1993 when he
sought to become president of the World Medical Association. He failed but remained
an honoured member of the national association and received many distinctions.
~ BMJ, Aug 16
After a three-year investigation Harvard
University has admitted that a renowned expert on the evolution of morality
has engaged in scientific misconduct. Professor Marc Hauser, a popular
lecturer, and an influential exponent of the neurological basis for human moral
codes, is alleged to have been responsible for “eight instances of scientific
misconduct”.
University authorities cited “problems
involving data acquisition, data analysis, data retention, and the reporting of
research methodologies and results” but gave few details. However, one of his research
assistants told the Cronicle of
Higher Education that “the professor was reporting bogus data and …
aggressively pushed back against those who questioned his findings or asked for
verification”.
Apparently his colleagues complained to the
Universtiy when they noticed that Professor Hauser fabricated responses made by
rhesus monkeys when he tested whether they could recognise speech patterns.
Professor Hauser told The
New York Times, “I acknowledge that I made some significant mistakes”. He
said that he was “deeply sorry for the problems this case had caused to my
students, my colleagues and my university.” ~ New York
Times, Aug 20
Katrina Clark, 21, and Lindsay Greenawalt,
25, were both conceived with donor sperm and raised by single mothers. Katrina
succeeded in finding her biological fathers and Lindsay failed. According to a
report from Associated Press, they are part of an increasingly outspoken
generation of sperm donor offspring. Speaking from experience, they have
advocated publically for the rights of sperm donor children, in particular
their right to know their biological fathers.
“The loss associated with being donor
conceived is something that I will carry for the rest of my life, and that to
deliberately create a human being with that loss is unethical,” Ms Greenwalt
wrote recently on her blog, Confessions
of a Cryokid.
All she knows about her father is that he
is 49, attended college, and has brown hair and greenish eyes. She knows a few
medical details, thanks to a recent update sent by her father to the Xytex
sperm bank in Augusta, Georgia. “He knows I'm looking for him — and he doesn't
want to make contact,” Greenawalt said.
Ms Clark found her father fairly quickly.
However, their communication “has been pretty much nonexistent”, and they have
not met face-to-face. "I still wonder about him," she added.
"There's so much about him I still don't know."
US sperm banks are increasingly offering
identity-release policies, in which donors agree to allow their offspring to
contact them once they reach age 18. However, many donors still choose to
remain anonymous. A past president of the Society for Assisted Reproductive Technologies,
Dr Jamie Grifo of New York University's Fertility Center, told AP that it is
not a good idea. "It may not be a popular point of view, but when these
decisions are made by donor and a parent, the child doesn't have a say,"
he said. "If the contract is for it to be anonymous, it should remain
anonymous, and the child just has to deal with that." ~
AP, Aug 16
The University of California, Berkeley will
not release personal genetic information to incoming students who participated
in an orientation program about genetics. The program “Bring Your Genes to Cal”
was criticised by the California Department of Public Health because state law
prohibits gene testing outside a medical setting.
Mark Schlissel, dean of biological
sciences, said he disagreed with the department’s ruling that advance approval
for testing was required from physicians, and that the testing should be done
in clinical labs with special licences rather than by university technicians.
He also argued that the project should be exempted from the state rules because
it was an educational exercise.
Privacy advocates and ethicists had criticised
the test as a disturbing use of genetic data. Some students felt that they were
being quietly coerced into participating, and that their saliva samples and
resulting personal information would not be sufficiently protected. ~ LA Times,
Aug 13
The US Food and Drug Administration has
embarked upon a legal battle to extend its authority over stem cell treatments.
It has enjoined a Colorado company, Regenerative Sciences, from treating
patients with stem cells from their own bone marrow or synovial fluid. These
are being injected to treat fractures, torn tendons and other ailments. The
clinic charges patients US$7,000–9,000 and does about 20 procedures every
month.
Christopher Centeno, the medical director
of the company, is ready for a fight. He disputes the FDA’s jurisdiction. Since
the company uses a patient’s own cells, as IVF clinics do, it is none of the
FDA’s business.
Both sides realise that the case could be a
landmark decision. Conventional stem cell researchers are wary of shady operators
who claim therapeutic benefits for stem cells without much research. Douglas
Sipp, of the International Society for Stem Cell Research, worries about what
will happen if Centeno’s company wins in the courts. "Companies would
likely feel empowered to ignore requirements for demonstrable safety and
efficacy of autologous medicinal products, creating an 'anything goes'
atmosphere," he told Nature.
And Centeno agrees: "If we win, the
entire regulatory structure for autologous cell processing, with or without
culture, will be rewritten such that any physician using good practices and
treating patients responsibly can use stem cells as part of his or her medical
practice," he says. ~ Nature, Aug 17
Australia may crack down on the
billion-dollar cosmetic surgery industry’s pitch for teenage business.
According to the Sunday Age, a government report recommends that teens have mandatory
psychological examinations and a three-month cooling-off period.
Incentives such as gifts, discounts or
loans would be banned together with advertising using “before and after” shots
of breast enlargements, nose jobs and tummy tucks.
The Australian Health Ministers' Advisory
Council says there is a “disturbing trend” in young people seeking cosmetic
surgery and treatments such as Botox, liposuction and laser therapy. “Demand
for such procedures is fuelled by lifestyle choices to enhance physical
appearance and boost confidence, rather than medical need,” the report states.
At the moment, any registered doctor can advertise
as a cosmetic surgeon. The report recommends that only doctors formally trained
in plastic surgery be allowed to describe themselves as cosmetic surgeons. ~ Sydney
Morning Herald, Aug 15
A spinal fluid tap may be 100% accurate in
predicting whether a patient will develop Alzheimer’s disease, according to a
study published in Archives of Neurology.
According to the New York Times, until now
the presence of the disease could only be confirmed after an autopsy, although
it begins ten or more years before symptoms appear. But a simple spinal tap
could predict whether someone has the progressive and incurable brain disease
and identify them as potential subjects for research into cures. “This is what
everyone is looking for, the bull’s-eye of perfect predictive accuracy,” said
Dr Steven DeKosky, dean of the University
of Virginia medical school.
The news was widely reported in the media
and shot to the top of the most-read articles in the Times. The conumdrums of a
screening test for Alzheimer’s were clear to everyone. Would healthy people
want to know that they have a disease for which there is no cure? How would
they react?
For researchers, the benefits are obvious.
It would be far more efficient to test potential treatments on people in the
initial stage of the disease. In an accompanying editorial, two experts
declared that spinal taps may become a routine “screening test to identify clinically healthy
individuals at risk”. This would be helpful in developing “early application of
treatments to delay onset of symptoms or slow progression of
cognitive impairments”.
Bioethicist
Jonathan Moreno, of the University of Pennsylvania, pointed out in The
New Republic that the existence of an accurate and relatively simple test
creates many policy problems. As many as 5.1 million Americans may have Alzheimer’s.
How will that affect their health insurance? How will it affect families? Will
it lead to suicide or will it encourage people to put their affairs in order? ~
New
York Times, Aug 9
Morality
is a tricky business. If you are an expert in preaching about it, people tend
to hold you to a higher standard of probity. Perhaps this is what has made allegations of
academic misconduct against one of the leading exponents of the “new science of
morality” so disturbing for Bostonians.
Harvard
professor Marc D. Hauser has persuasively argued that no action is inherently
wrong. "We generally do not commit wrong acts because we recognize that
they are wrong and because we do not want to pay the emotional price of doing
something we perceive as wrong," he says. As an evolutionary biologist, he
is fascinated by the idea of evil and thinks that his research can shed light
on its origin and its attraction. “I believe that science, and scientists, have
an important role to play in shaping the moral agenda. We have an obligation to
use facts and reason to guide what we ought to do,” he contended forcefully in a recent essay on The Edge.
Unfortunately,
Professor Hauser has just taken a year-long leave after Harvard found evidence
of faked results in some of his research. What sparked the investigation was a
2002 paper in the journal Cognition on whether monkeys learn rules. It is now
being formally retracted because the data do not support the findings.
This
is not the only paper under a cloud. Last month the prestigious British journal
Proceedings of the Royal Society B published a correction to one of Hauser’s
papers and now Science is looking at a 2007 paper.
“This
retraction creates a quandary for those of us in the field about whether other
results are to be trusted as well, especially since there are other papers
currently being reconsidered by other journals as well,” Michael Tomasello,
co-director of the Max Planck Institute for Evolutionary Anthropology in
Leipzig, Germany, told the Boston Globe.
“If scientists can’t trust published papers, the whole process breaks
down.”
Professor
Hauser has been one of Harvard’s most popular teachers and is currently working
on a new book with the provisional title, “Evilicious: Explaining Our Evolved
Taste for Being Bad.’ ~ Boston Globe, Aug 10
Consequences of the Bio-Medical Revolution
May 1, 2010, Biola University, La Mirada, CA
Helping nurses understand technological advances in health care and their ethical consequences.
Fertility, Infertility and Gender
June 16-18, 2010, Maynooth, Ireland (near Dublin)
Sponsored by the Linacre Centre for Healthcare Ethics, Oxford.
Obama’s Illegal Stem-Cell Policy
Public Discourse
Obama’s stem-cell policy is not only contrary to sound reason and good science, it violates the law.
The hidden story of Britain’s ‘snowbabies’
London Telegraph
There are tens of thousands of 'spare' IVF embryos currently in storage in Britain, but parents face an agonising choice…
Letting Go
New Yorker
What should medicine do when it can’t save your life? asks Atul Gawande