Date
Location
Presenters
Amy Gutmann, Ph.D.
Commission Chair
James Wagner, Ph.D.
Commission Vice-Chair
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Transcript
DR. GUTMANN: Alas, because of time, and I
know we're pressed for time, I'm going to wrap this up
and ask Jim to make some concluding comments, as well.
Our discussion was sobering to say the least
but necessary to bring facts to light and what we're planning on putting forward publicly as our report.
Let me try and not in any way comprehensive
way but to outline some of the things on the ethical
analysis side that we have agreed upon as a commission
and you'll see that in the report we do this in a much
more detailed way, drawing upon some of the historical
facts that we've just in a very summary way have just
brought to light.
So a civilization, we've said, can be judged
by the way it treats its most vulnerable individuals
and it is our moral responsibility to care for those
who cannot protect themselves and clearly in this
history, we failed to keep that covenant.
The research specifically included populations
that were vulnerable and thereby deserving of
additional safeguards to ensure their adequate
protection. The researchers knew that that was the
case, as indicated in the Terre Haute experiments.
Prison inmates in Guatemala, institutionalized and
mentally-disabled individuals and children were among
the groups most frequently included in the Guatemala
experiments.
Federal regulation, international codes and
the ethics literature all acknowledge that research
involving these groups raises unique issues requiring
additional attention.
That said, many of the institutional codes and
federal regulations that exist today did not exist at
the time, although the Nuremberg Code had
contemporaneously come out, and I'll say something more
about three of the standards that were articulated in
that Code which are not unique to Nuremberg but are
really ethical standards that have been with us for
centuries.
The research team in Guatemala and their
immediate supervisors appear to have had considerable
latitude in the design and conduct of individual
experiments with no evidence of substantive independent
review of the conduct of the research. Again, as Raju
has pointed out, there could have been more review than
there was.
On the contrary, substantial evidence reflects
efforts by the researchers to limit knowledge of the
Guatemala activities as much as possible outside of those conducting it or directly authorizing it.
The experimenters in Guatemala, both the
Americans and their local colleagues, consistently
failed to act in accordance with minimal respect for
human rights and morality in the conduct of research.
It's even more disturbing for us as a commission to
find that the blame lies with medical doctors and
scientists who hold professional positions that carry
with them special privileges and responsibilities,
expected to do no harm, and to abide by the highest
professional standards of ethics.
In the Commission's view, the Guatemala
experiments involved basic violations of ethics, even
as judged against the researchers' own recognition of
the requirements of the medical ethics of the day,
although some of those researchers clearly rejected
those requirements.
Many of their actions violated principles
widely accepted as applicable at the time as well as
the standards of our own time that are embodied in the
ethics and regulation of biomedical research today.
These standards include the following:
First, treating people fairly and with
respect. The voluntary consent of human subjects is
absolutely essential. That is the first sentence of
the Nuremberg Code.
Second, one ought not to subject people to
harm or risk of harm, even with their consent, unless
the risk is reasonable and there is a proportionate
humanitarian benefit to be obtained. Careful and
scientifically-sound research is an essential condition
for medical ethics.
And third, one ought not to treat people as
mere means to the ends of others. Subjects must not
only give informed consent but they also must be free
to withdraw and they certainly ought not to be deceived
unless they have been informed of possible deception
and consented to that.
The Guatemala experiments could not be
approved under current human research protections for
U.S.-funded research. That is clear. Widely-discussed
cases in the post-World War II era with some similar
features have led to a greater appreciation and
articulation of the moral principles underlying medical research.
We hasten to add that in judging and assessing
these experiments as morally wrong and assigning blame
to the individuals, we in no means, by no means mean to
say this was the only example, far from it, of
unethical experiments and blameworthiness not only in
the 1940s but in the '50s, '60s and forward.
A clear consensus has emerged that medical
research must not violate human dignity or undermine
the very human flourishing it seeks to advance in
future patients. The Guatemala experiments and other
troubling violations of this norm that have come to
light in the last 60 years shock the conscience. They
should shock the conscience, not in spite of their
medical context but precisely because of it.
It is clear that many of the actions
undertaken in the Guatemala experiments were grievously
wrong and that the individuals who approved, conducted,
facilitated, and funded these experiments are morally
culpable to various degrees for these wrongs.
Although some individuals are more blameworthy
than others, the blame for this episode cannot be said
to fall solely on the shoulders of one or two
individuals. The unconscionable events that unfolded
in Guatemala in the years 1946 to 1948 also represented
an institutional failure of the sort that modern
requirements of transparency and accountability are
designed to prevent.
In the final analysis, institutions are
comprised of individuals who are expected to exercise
sound judgment in the pursuit of their institutional
mission. This is all the more important when those
individuals hold privileged and powerful roles as
professionals and public officials.
One lesson, just one lesson of the Guatemala
experiments is never to take ethics for granted, let
alone confine ethical principles, confuse ethical
principles with burdensome obstacles to be overcome or
evaded.
This lesson should be a sobering one for our
own and all subsequent human research experiments. We
all know of rules that feel burdensome to comply with
and we all believe that rules shouldn't be any more
burdensome than they need to be to protect us from
unethical experiments, but we should be ever vigilant
to ensure that such reprehensible exploitation of our
fellow human beings is never repeated.
In the charge to the Commission last November,
President Obama said, and I quote, "While I believe the
research community has made tremendous progress in the
area of human subjects research protection, what took
place in Guatemala is a sobering reminder of past
abuses. It is especially important for this Commission
to use its vast expertise, spanning the fields of
science, medicine, policy, ethics, and moral and
religious values to carry out this mission. We owe it
to the people of Guatemala, to future generations of
volunteers at home and all around the world who
participate in medical research."
As a commission, we shall report back to the
President with our findings on the research and our
analysis of the ethics of this shameful piece of
medical history.
That's all I have to say for now and I would
like to turn the floor over to Jim Wagner for some
concluding comments before we adjourn.
DR. WAGNER: Amy, there's very little that
needs to be added to that statement. Thank you so
much. But maybe to highlight one point or two.
The purpose for doing this was not simply to
put a moment of history to bed so that it could be
sealed with some form of sealing wax that says we've done it, we
understand it, and we condemn it, but, rather, it's to
inform what we need to do going forward and what we
recommend going forward, and, of course, that will be
the purpose of our conversations tomorrow.
The challenge, of course, is how to implement
the kinds of principles that you spoke about, Amy, in
such a way that they are for the well-intentioned
researcher seeking how to pursue viable research, that
they are an illuminating aid and not, as you said, some
sort of onerous burden.
On the other hand, for the other kind of
individual or group of individuals, who understand
somehow intrinsically that the value of their work is
so meritorious that it is to be -- it can rise above
restraints and restrictions and ethics, these do need
to be horribly burdensome, in fact impenetrable, if
possible, and how do you do all of this without unduly
restricting the imperative that we have to pursue
biomedical research in the service of humanity, I
think, is the big challenge.
And I'm pleased to be working with this group,
to roll up our sleeves and take that as our next move
going forward.
So thank you very much.
DR. GUTMANN: Thank you. I would like to ask
the staff members of the Presidential Commission for
the Study of Bioethical Issues who have worked on the
historical report and they've worked assiduously, the
125,000 pages of documents doesn't even come close to
capturing all of the work and the drafts which we are
still refining but will soon be put out there for the
public to read, if you would all stand up so we can
thank you for your work, I'd really appreciate it.
(Applause.)
DR. GUTMANN: Tomorrow, we will reconvene and
we will discuss contemporary human subjects protections
standards. This will be our third meeting addressing
this subject and we will look forward to a full day of
speakers and discussion.
I want to thank everyone who's attended again
and we will reconvene tomorrow at 9 a.m.
Thank you very much.
(Whereupon, at 3:13 p.m., the meeting was
adjourned, to reconvene tomorrow morning, Tuesday,
August 30th, 2011, at 9:00 a.m.)
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