Is Bioethics Ethical?
	The Weekly Standard, 
	28 May, 2000.
	Reproduced with the permission. For more information on subscribing 
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	Decision making has been 
							quietly co-opted by bioethics, a genre of 
							philosophical discourse practiced by an elite group 
							of academics, philosophers, lawyers, and physicians, 
							many of whom are openly hostile to the sanctity of 
							life and the Hippocratic traditions that most people 
							still take for granted.
	The case of James H. Armstrong, M.D. v. The State 
							of Montana should have been merely a skirmish in the 
							never-ending national struggle over abortion. 
							Instead, relying on the reasoning of certain experts 
							in the moral choices surrounding health care, the 
							Montana Supreme Court issued in October 1999 a 
							sweeping decision that could make huge changes in 
							the way Montanans live and the way they die.
	What happened in Montana is happening across the 
							country, usually less dramatically but nonetheless 
							steadily. The United States has a bad case of 
							expertitis, and for many years we have been ceding 
							to experts control over our public decisions. Now 
							the most important questions about health care have 
							been added to the list. Decision making has been 
							quietly co-opted by bioethics, a genre of 
							philosophical discourse practiced by an elite group 
							of academics, philosophers, lawyers, and physicians, 
							many of whom are openly hostile to the sanctity of 
							life and the Hippocratic traditions that most people 
							still take for granted.
	Bioethicists spend much of their time arguing 
							with one another, beneath or, more accurately, above 
							the public radar, in arcane academic journals, 
							books, university symposia, and government-appointed 
							commissions. This is no empty intellectual 
							enterprise, but a project aimed at changing America. 
							In the course of their arguments, bioethicists are 
							arriving at a consensus about the course of our 
							medical future, and they are slowly succeeding at 
							transforming the laws of public health and the 
							ethics of clinical medicine in their own image.
	At issue in the Montana case was a state law 
							requiring that doctors (as opposed to 
							physician-assistants) perform all abortions. This 
							the court unanimously overturned; but it didn't stop 
							there. Writing for a 6-2 majority, Justice James C. 
							Nelson went on to impose a radical philosophical 
							imperative on the people of Montana, unwarranted by 
							the facts of the case and 
unnecessary to its prudent adjudication. Indeed, 
							Nelson's audacious opinion will be grist for 
							litigation in Montana for many years to come.
	Its essential holding is this: The Montana 
							Constitution broadly guarantees each individual the 
							right to make medical judgments affecting her or his 
							bodily integrity and health in partnership with a 
							chosen health care provider free from government 
							interference. As the two justices who objected to 
							the scope of the ruling, Karla M. Gray and Chief 
							Justice J.A. Turnage, warned, the Court's opinion 
							sweeps so broadly as to encompass and decide such 
							issues as the right to physician-assisted suicide 
							and other important health and medical-related 
							issues which simply were not litigated in this case.
	Gray and Turnage's trepidation is abundantly 
							warranted. If the ruling means that virtually 
							anything goes medically in Montana so long as a 
							patient requests it and a health care professional 
							is willing to provide it, then patients can ask 
							doctors to kill them for organ-donation purposes, 
							parents or guardians can secure the killing of 
							disabled infants, and people can volunteer to be 
							experimented on in dangerous ways that are currently 
							illegal, all this as a result not of a considered 
							decision by the people of Montana but of a 
							little-noticed ruling by the state supreme court.
	As it happens, the Montana constitutional 
							convention that created the state right to privacy 
							in 1972 explicitly refused to include abortion and 
							other medical issues in the privacy guarantee. So, 
							to justify its ruling, the court looked to 
							precedents like Roe v. Wade, the 1973 U.S. Supreme 
							Court decision that legalized abortion nationwide. 
							Even more than on case law, however, the Montana 
							court relied on philosophical treatises. In 
							particular, the authority it cited most frequently 
							is the book Life's Dominion: An Argument About 
							Abortion, Euthanasia, and Individual Freedom (1993), 
							by the attorney and bioethicist Ronald Dworkin.
	Dworkin's thesis is that true adherence to a 
							modern understanding of the sanctity-of-life ethic 
							requires that all of us be permitted to decide for 
							ourselves about abortion and euthanasia and that our 
							decisions be accepted by society and tolerated by 
							those who disagree. Otherwise society is 
							totalitarian. The majority opinion in Armstrong 
							cites Life's Dominion so many times and applies its 
							reasoning so enthusiastically that Ronald Dworkin's 
							philosophy may now be considered the court-mandated 
							health care creed of the state of Montana.
	Dworkin's triumph in Armstrong v. Montana 
							illustrates the growing influence of bioethics. To 
							become a bioethicist isn't hard. No tests have to be 
							passed; practitioners are not licensed, like 
							attorneys, physicians, real estate agents, and 
							hairdressers; and, while more than 30 universities 
							offer degrees in bioethics, there are no standards 
							of excellence that generally apply. A Catholic 
							priest may be a bioethicist, as may an atheist 
							college professor. Health care professionals such as 
							nurses and community ombudsmen may get appointed to 
							hospital ethics committees, take a few training 
							courses, and call themselves bioethicists. Indeed, I 
							could say that I am a bioethicist, having written 
							and lectured extensively on the ethics of assisted 
							suicide and the withholding of medical treatment 
							from dying and disabled people.
	The mere designation, however, does not give one 
							influence within the bioethics movement. That is to 
							say, there is a very big difference between being a 
							bioethicist and subscribing to the ideology of 
							mainstream bioethics. It is the adherents of the 
							ideology who matter and who hold a steadily 
							increasing sway over the laws of public health, the 
							application of medical ethics, and the protocols 
							that govern hospital care.
	This phenomenon is relatively new. It began about 
							30 years ago as an intellectual exchange among 
							medical ethicists, philosophers, and theologians 
							with widely varying views about how to resolve the 
							dilemmas presented by the growth of technological 
							medicine. In the early years, there was a robust 
							contest for the heart and soul of the movement. 
							Adherents of human equality and the sanctity of 
							life, such as the late Paul Ramsey, were pitted 
							against utilitarians who emphasize the quality of 
							life, such as the late Joseph Fletcher, the 
							patriarch of modern bioethics. Over the years, the 
							Ramsey school made crucial contributions, most 
							notably, helping promote the right to refuse 
							unwanted medical treatment, but steadily lost 
							influence. Today, mainstream bioethics is 
							substantially homogeneous in outlook, and the 
							primary differences among bioethicists concern the 
							proper ways to apply generally agreed-upon values to 
							health care policy and individual medical decisions. 
							It is in this sense that bioethics has become an 
							ideology, albeit one that not every bioethicist 
							shares.
	In order to have clout within the bioethics 
							movement and seriously affect the discourse that is 
							its hallmark, one must subscribe to its intellectual 
							underpinnings. Pro-lifers have no influence, by 
							definition, and those whose advocacy is rooted in 
							religion are usually ignored. Mainstream bioethics 
							reached a consensus long ago that religious values 
							are divisive in a pluralistic society and thus have 
							little place in the formulation of public policy. 
							Those who believe in abortion rights but also hold 
							that all born humans are equally endowed with moral 
							worth, along with those who subscribe to the do no 
							harm ethos of the Hippocratic oath, have little 
							impact, since mainstream bioethics rejects 
							Hippocratic medicine as paternalistic and shrugs off 
							equal human moral worth as a relic of the West's 
							religious past.
	In mainstream bioethics, human beings per se have 
							no special rights or moral value. The movement as a 
							whole no longer thinks in that idiom. Instead, it 
							overwhelmingly embraces a quality-of-life ethic that 
							requires individual humans to earn their moral and 
							legal rights by displaying certain cognitive 
							capacities. This is usually described as achieving 
							the status of a person. As we shall see, the 
							criteria for personhood are still a matter of debate 
							among bioethicists. But the notion that personhood 
							rather than humanness is what counts in determining 
							moral worth and legal rights is nearly universally 
							accepted within the mainstream movement and has been 
							taught in American universities and colleges to a 
							whole generation of students. Bioethics ideology 
							rejects person status for newborns, people with 
							severe brain damage, and those with dementia, all of 
							whom it regards as beings of lesser worth than those 
							with more developed frontal lobes. There is serious 
							debate within bioethics, however, whether to extend 
							personhood to some animals (nonhuman animals, in 
							bioethics parlance), even as it is being stripped 
							from some humans.
	Part of what makes this alarming is that the 
							values and presumptions of bioethics ideology are 
							not shared generally throughout society. Unlike 
							adherents to this ideology, most people believe that 
							being human in and of itself confers a special moral 
							status. Most people view a newborn infant as having 
							the same moral worth as all other humans and want 
							their doctors to subscribe to the Hippocratic oath. 
							This means that, as the government, the law, and 
							organized medicine rely increasingly on expert 
							bioethicists to supply the answers to public policy 
							dilemmas in areas such as cloning, stem cell 
							research, health care rationing, and organ 
							procurement for transplantation, those answers are 
							likely to be based on beliefs not generally shared 
							by the people affected. More and more, public 
							policies and medical protocols are likely to 
							conflict with, rather than reflect, the values of 
							the citizenry.
	If bioethics ideology is out of step with 
							mainstream American thinking, however, it is 
							entirely consistent with the mindset of the elite. 
							As Daniel Callahan, one of the movement's pioneers, 
							wrote in the Hastings Center Report in 1993, the 
							final factor of great importance in bioethics' 
							success was the emergence ideologically of a form of 
							bioethics that dovetailed nicely with the reigning 
							political liberalism of the educated classes in 
							America.
	It is not surprising, then, that movement 
							bioethicists have become among society's most 
							powerful members or that their work affects American 
							culture from top to bottom: They serve on federal 
							and state public policy commissions. They write 
							health legislation. They teach the next generation 
							of doctors, lawyers, business executives, and 
							government policy makers in our institutions of 
							higher learning. They are paid by HMOs to consult on 
							issues such as when desired medical treatment can be 
							withheld or withdrawn unilaterally. They direct 
							hospital and nursing-home ethics committees that 
							make or influence decisions ranging from whether to 
							withhold treatment from premature infants to whether 
							to pull feeding tubes from stroke patients who are 
							not dying. They testify as expert witnesses in court 
							cases and submit friend of the court briefs in legal 
							cases of major significance, thereby affecting the 
							evolution of law. They serve on institutional review 
							boards that oversee the ethics of medical 
							experiments using human subjects. They help write 
							protocols governing organ procurement. Occasionally, 
							their work leads to startling lurches in the law, as 
							in Montana. More typically, their advocacy erodes 
							ethical standards and values slowly, as waves 
							transform shorelines, through a succession of subtle 
							changes in public policy and medical ethics, a 
							process known within the movement as policy creep.
	What makes this especially worrisome is that once 
							a policy is formally adopted or embedded in law, it 
							has the power to modify the beliefs of the people it 
							affects. Thus, the patriarch, Joseph Fletcher, 
							viewed the field expansively, as determining how we 
							are to live and act, a wisdom he deemed specially 
							appropriate to the medical sciences and medical 
							arts. Some bioethicists see themselves as the 
							creators of a new moral paradigm that will replace 
							the archaic Judeo-Christian order as the 
							philosophical underpinning of society.
	To appreciate fully the mindset of bioethics and 
							the consequences that will flow from its growing 
							influence on public policy, one need only look to 
							the journals in which its leading thinkers 
							communicate with one another and with their 
							colleagues in the trenches of American medicine in 
							physicians' offices, on hospital ethics committees, 
							at consultancies advising nursing homes where 
							bioethics values affect everyday decisions. Two of 
							the most prominent journals devoted exclusively to 
							bioethics are the Hastings Center Report, a 
							bimonthly published by the bioethics think tank the 
							Hastings Center, of Garrison, New York, and the 
							Kennedy Institute of Ethics Journal, a quarterly 
							published by Georgetown University. Although not 
							every article in these publications embraces 
							bioethics ideology, the vast majority do. These 
							journals channel the discussion in a definite 
							direction.
	The December 1999 issue of the Kennedy Institute 
							of Ethics Journal is a case in point. It 
							concentrates on the continuing debate over 
							personhood. A person, the journal's introduction 
							says, is someone morally considerable who is the 
							subject of moral rights and merits moral protection. 
							Most people would say that all human beings qualify. 
							The authors of several articles disagree.
	The lead author, John Harris, the Sir David 
							Alliance professor of bioethics at the University of 
							Manchester, in England, claims that it is necessary 
							to establish the criteria for personhood so as to 
							identify those sorts of individuals who have the 
							ëhighest' moral value or importance. It is not life 
							per se that is dispositive, but life of such quality 
							as to bring [individuals] into the same moral 
							categories as ourselves. Being human alone does not 
							do the trick: Personhood theory creates castes of us 
							and them, in an explicit hierarchy of human worth.
	Harris makes a rather astonishing assertion, 
							considering the brouhaha over abortion. He baldly 
							states that human life begins at conception. This, 
							of course, does not mean he opposes abortion to the 
							contrary. Remember, it is not human life that 
							matters in personhood theory; human beings do not 
							deserve special status merely because of their 
							species. Harris blandly denigrates unborn human 
							life: The human embryo and fetus, he writes, in all 
							stages of its development from conception to birth 
							is no more interesting or complex than the embryos 
							of other creatures and indeed no more interesting 
							than the adult forms of other creatures, for example 
							cats and canaries.
	Harris next opines that the exploration of who is 
							a person must include animals, because the exclusion 
							of fauna from personhood deliberations would be 
							arbitrary and an act of speciesism, a claim of 
							superiority based on species, which Harris considers 
							as disreputable as an assertion of superiority based 
							on race, gender, nationality, religion, or any other 
							nonmoral characteristic.
	So, who (or what) should duly be deemed a person? 
							To Harris, a person is a being that can value 
							existence. This means persons might, in principle, 
							be members of any species, or indeed machines. He 
							explicitly states that fetuses and newborn infants 
							are not persons, nor are people with significant 
							cognitive disability or dementia.
	The ultimate purpose of personhood analysis is to 
							determine whom we can kill and still get a good 
							night's sleep. Harris writes, "Persons who want to 
							live are wronged by being killed. Nonpersons or 
							potential persons cannot be wronged in this way 
							because death does not deprive them of something 
							they value. If they cannot wish to live, they cannot 
							have that wish frustrated by being killed." So much 
							for the moral wrongness of murdering newborns and 
							throwing them into trash dumpsters.
	In the same issue of the Kennedy Institute of 
							Ethics Journal, Georgetown's Tom L. Beauchamp, 
							co-author with James F. Childress of one of the most 
							influential bioethics textbooks, Principles of 
							Biomedical Ethics, also writes about personhood, 
							taking a different route to essentially the same 
							destination as Harris. Beauchamp asserts that the 
							key to determining personhood is analyzing whether a 
							being enjoys moral personhood, which he calls both a 
							cognitive and moral-capacity criterion for 
							possession of moral rights. He writes, "It is safe 
							to assume that a creature is a moral person if (1) 
							it is capable of making moral judgments about the 
							rightness and wrongness of actions and (2) it has 
							motives that can be judged morally."
	Beauchamp, like Harris, asserts that under his 
							theory, unprotected persons would presumably include 
							fetuses, newborns, psychopaths, severely 
							brain-damaged patients, and various demented 
							patients. Beauchamp does not believe that moral 
							personhood should be the sole basis for moral rights 
							or that animals can be moral persons, but he does 
							assert that humans who are not moral persons may be 
							treated with the same levels of respect or 
							exploitation as animals are now; some humans are 
							equal or inferior in moral standing to some 
							nonhumans. If this conclusion is defensible, he 
							writes, we will need to rethink our traditional view 
							that these unlucky humans cannot be treated in the 
							ways we treat relevantly similar nonhumans. For 
							example, they might be aggressively used as human 
							research subjects and sources of organs. In other 
							words, Beauchamp holds out the prospect that we may 
							someday exploit living infants and cognitively 
							disabled human beings as if they were mere natural 
							resources.
	The November-December 1999 Hastings Center Report 
							focuses on the ethics of expanding organ procurement 
							from non-heart-beating cadaver donors, that is, 
							people who have died from cardiac arrest instead of 
							brain death. Much of the discussion has to do with 
							how long doctors should have to wait after a heart 
							stops beating before judging the donor dead for 
							purposes of organ procurement and still be in 
							compliance with the dead donor rule, which requires 
							that donors of vital and non-paired organs be dead 
							before having their organs procured. (Many 
							bioethicists want to discard the dead donor rule, to 
							increase organ availability, but that argument is 
							not made here.) Some organ centers currently wait 
							only two minutes after the cessation of the 
							heartbeat to procure organs; a recent bioethics 
							panel recommended five minutes. The arguments are 
							important, but arcane, and would take too long to 
							explain here.
	That said, the ultimately utilitarian approach of 
							mainstream bioethics is much in evidence. John A. 
							Robertson, holder of the Vinson Elkins chair at the 
							University of Texas Law School, where he teaches 
							criminal law, constitutional law, and bioethics, 
							makes an audacious proposal. He notes that until and 
							unless law and medical ethics discard the dead donor 
							rule, as many bioethicists urge, it will be 
							impossible to use such people as anencephalic 
							infants (babies born with most of their brains 
							missing) or unconscious people as vital-organ 
							donors. Even with the dead donor rule in place, 
							however, Robertson suggests that single kidneys and 
							some other body tissues could be harvested from such 
							people, who would not be directly harmed by such 
							use. 
	Again, the proposal is to use cognitively 
							disabled people as mere natural resources. One 
							wonders whether the New Mexico woman who recently 
							woke up after being unconscious for 16 years would 
							have objected had she awakened to learn that one of 
							her kidneys and her corneas had been taken from her 
							on the theory that the loss of them could not harm 
							her.
	Like ruminating cows, bioethicists earnestly chew 
							and rechew their ideas until they have explored 
							every nuance, considered every implication, and the 
							movers and shakers of the movement have achieved 
							consensus about a particular approach. When that 
							point comes, public policy often changes fast: 
							Notice the speed with which removing feeding tubes 
							from unconscious, cognitively disabled people became 
							ethical and legal throughout the country once 
							bioethicists agreed it was no different morally from 
							withdrawing antibiotics.
	If mainstream bioethicists tread gingerly in 
							pushing their agenda into policy, it is for fear of 
							a public backlash, provoked by what bioethicists 
							jokingly call the yuck factor. For those of us who 
							believe that bioethics is directing us down immoral 
							and dangerous paths, this fear of the light offers 
							the best hope of an antidote. Since it is almost 
							surely too late to transform the movement's 
							utilitarian assumptions from within, keeping the 
							movement contained inside the academy appears to be 
							the most promising strategy to prevent our society 
							from being remade in bioethics' image. To do this 
							will require heightened media scrutiny and public 
							awareness of what ideological bioethics is, what it 
							stands for, why it matters, and what consequences 
							will befall us all if the new medicine becomes our 
							future.
	That is easier said than done, of course. But 
							there are ways. The ideology could be engaged 
							vigorously, from the grass roots to the academy to 
							the halls of Congress. Philanthropists could be 
							persuaded to endow academic chairs dedicated to 
							exploring human equality as the basis for health 
							care law and policy, much as bioethics chairs are 
							used to promote the quality-of-life agenda. 
							Politicians, devoted to their constituents' welfare, 
							could resist the bioethics tide. Nonprofit groups 
							could be formed to follow the bioethics movement, 
							publish journals, engage the proponents in public 
							debate, and alert the media to particularly noxious 
							developments. The popular media, especially 
							television and radio talk shows, could recognize the 
							urgency of covering bioethics as seriously as they 
							cover politics. After all, are not issues like 
							personhood and the harvesting of organs from living 
							people as compelling as tax policy and welfare 
							reform?
	Beyond the media, a counter-bioethics movement 
							could be created by those who believe that the only 
							truly moral way to resolve the dilemmas with which 
							bioethics grapples is by strict adherence to 
							universal human equality. 
	Perhaps this new, ethical bioethics could be 
							called human-rights bioethics. It would boldly 
							promote the proposition that there is no them and 
							us; only us. Surely, an abundance of academics, 
							physicians, lawyers, disability rights activists, 
							patient advocates, theologians, and just plain 
							people would be willing to stand up proudly for the 
							equal moral worth of all living people. For now, 
							their rallying cry could be: No more Montanas.