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Questioning the consensus: managing carrier status results generated by newborn screening
Fiona Alice Miller1, Jason Scott Robert, Robin Z Hayeems
1Department of Health Policy, Faculty of Medicine, University of Toronto, Toronto, ON, Canada. fiona.miller@utoronto.ca
Abstract:
An apparent consensus governs the management of carrier status information generated incidentally through newborn screening: results cannot be withheld from parents. This normative stance encodes the focus on autonomy and distaste for paternalism that characterize the principles of clinical bioethics. However, newborn screening is a classic public health intervention in which paternalism may trump autonomy and through which parents are-in effect-required to receive carrier information. In truth, the disposition of carrier results generates competing moral infringements: to withhold information or require its possession. Resolving this dilemma demands consideration of a distinctive body of public health ethics to highlight the moral imperatives associated with the exercise of collective authority in the pursuit of public health benefits.

