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Journal of Community Genetics

, Volume 4, Issue 1, pp 59–67

First Online: 07 October 2012Received: 30 April 2012Accepted: 12 September 2012DOI: 10.1007-s12687-012-0118-9

Cite this article as: Forman, J., Coyle, F., Levy-Fisch, J. et al. J Community Genet 2013 4: 59. doi:10.1007-s12687-012-0118-9


Newborn metabolic screening is the most widespread application of screening technology and provides the most comprehensive application of genetics in health services, where the Guthrie blood spot cards allow screening for metabolic diseases in close to 100 % of all newborn babies. Despite over 40 years of use and significant benefits to well in excess of 100,000 children worldwide, there is remarkably little consensus in what conditions should be screened for and response to new advances in medicine relating to programme expansion. In this article, the international criteria for newborn metabolic screening are considered, and we propose that these criteria are poorly developed in relation to the baby, its family and society as a whole. Additionally, the ethical issues that should inform the application of screening criteria are often not developed to a level where a consensus might easily be achieved. We also consider that when family interests are factored in to the decision-making process, they have a significant influence in determining the list of diseases in the panel, with countries or states incorporating family and societal values being the most responsive. Based on our analysis, we propose that decision criteria for metabolic screening in the newborn period should be adapted to specifically include parent and family interests, community values, patients’ rights, duties of government and healthcare providers, and ethical arguments for action in the face of uncertainty.

KeywordsNewborn metabolic screening Decision criteria Family interests  Download fulltext PDF

Autor: John Forman - Fiona Coyle - Jill Levy-Fisch - Pat Roberts - Sharon Terry - Michael Legge


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