Medicine, Health Care and Philosophy 16 (3):357-364 (2013)

Dagmar Schmitz
Aachen University of Technology
Prenatal care and the practice of prenatal genetic testing are about to be changed fundamentally. Due to several ground-breaking technological developments prenatal screening and diagnosis (PND) will soon be offered earlier in gestation, with less procedure-related risks and for a profoundly enlarged variety of targets. In this paper it is argued that the existing normative framework for prenatal screening and diagnosis cannot answer adequately to these new developments. In concentrating on issues of informed consent and the reproductive autonomy of the pregnant women the ethical debate misses problems related to the clinical pathway as a whole and to implicit normative attributions to clinical actions or the function of health care professionals. If, however, ethical debate would focus on the clinical context and on the ends of PND to a larger extent, it would be able to provide a more comprehensive analysis of the ethical challenges especially of the new technologies in order to be more adequately prepared for their implementation
Keywords Prenatal testing  Non-invasive prenatal diagnosis  Philosophy of medicine  Physician–patient-interaction
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DOI 10.1007/s11019-012-9411-y
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References found in this work BETA

Autonomy and Trust in Bioethics.Onora O'Neill - 2002 - Cambridge University Press.
The Theory and Practice of Autonomy.Gerald Dworkin - 1988 - Cambridge University Press.
Rethinking Informed Consent in Bioethics.Neil C. Manson - 2007 - Cambridge University Press.

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