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Synopsis
In When Medicine Went Mad, one of the nation's leading bioethicists-and an extraordinary panel of experts and concentration camp survivors-examine problems first raised by Nazi medical experimentation that remain difficult and relevant even today. The importance of these issues to contemporary bioethical disputes-particularly in the thorny areas of medical genetics, human experimentation, and euthanasia-are explored in detail and with sensitivity.
Publishers Weekly
The Nazis performed monstrous biomedical experiments on concentration camp prisoners, compiling racial and other information while slowly killing them. Should the data from these experiments be banned, or mined for their possible potential benefit? This set of papers from a 1989 symposium at the University of Minnesota (where Caplan directs the Center for Biomedical Ethics) opens with the testimonies of camp survivors, who urge that the data be shredded. Another contributor argues that the data are scientifically worthless; others agonize over the issue and conclude that the Nazi data ought to be published. Of broader interest is an essay showing how the science of racial hygiene, which supported forced sterilization of undesirable racial groups, among other policies, took hold in Germany long before the Nazis came to power. One contributor compares Nazi euthanasia to the current practice of withdrawing life-support systems from patients whose continued treatment is not ``costworthy.'' The closing paper thoughtfully looks at ethical dilemmas surrounding the Human Genome Project, an attempt to map human genes which, critics charge, could open the door to Nazi-like abuses. (Sept.)