Journal of Medical Ethics 38 (5):299-303 (2012)
Abstract |
Newborn screening is the programme through which newborn babies are screened for a variety of conditions shortly after birth. Programmes such as this are individually oriented but resemble traditional public health programmes because they are targeted at large groups of the population and they are offered as preventive interventions to a population considered healthy. As such, an ethical tension exists between the goals of promoting the high uptake of supposedly ‘effective’ population-oriented programmes and the goal of promoting genuinely informed decision-making. There is, however, a lack of understanding with regard to how parents experience the tension between promoting uptake and facilitating informed choice. This paper addresses this issue, and data are presented to show how aspects of the timing, presentation of information and procedural routinisation of newborn screening serves to impact on the decisions made by parents
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DOI | 10.1136/medethics-2011-100040 |
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References found in this work BETA
Population Screening.Ainsley J. Newson & A. Dawson - forthcoming - Public Health Ethics. Key Concepts and Issues in Policy and Practice:118--42.
How Should We Measure Informed Choice? The Case of Cancer Screening.R. G. Jepson - 2005 - Journal of Medical Ethics 31 (4):192-196.
Knowledge or Understanding? Informed Choice in the Context of Newborn Bloodspot Screening.S. G. Nicholls - 2010 - Public Health Ethics 3 (2):128-136.
New Mothers' Awareness of Newborn Screening, and Their Attitudes to the Retention and Use of Screening Samples for Research Purposes.Angela Davey, Davina French, Hugh Dawkins & Peter O'Leary - 2005 - Genomics, Society and Policy 1 (3):41-51.
Citations of this work BETA
The Ethics of Krabbe Newborn Screening.R. H. Dees & J. M. Kwon - 2013 - Public Health Ethics 6 (1):114-128.
What is in a Name? Parent, Professional and Policy-Maker Conceptions of Consent-Related Language in the Context of Newborn Screening.Stuart G. Nicholls, Holly Etchegary, Laure Tessier, Charlene Simmonds, Beth K. Potter, Jamie C. Brehaut, Daryl Pullman, Robin Z. Hayeems, Sari Zelenietz, Monica Lamoureux, Jennifer Milburn, Lesley Turner, Pranesh Chakraborty & Brenda J. Wilson - 2019 - Public Health Ethics 12 (2):158-175.
What Ethical and Legal Principles Should Guide the Genotyping of Children as Part of a Personalised Screening Programme for Common Cancer?N. Hallowell, S. Chowdhury, A. E. Hall, P. Pharoah, H. Burton & N. Pashayan - 2014 - Journal of Medical Ethics 40 (3):163-167.
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