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  1. Maintaining Trust in Newborn Screening.Simone van der Burg & Marcel Verweij - 2012 - Hastings Center Report 42 (5):41-47.
    Newborn screening consists of taking a few drops of blood from a baby's heel in the first week of life and testing it for a list of disorders. In the United States and most countries in Europe, newborn screening programs began in the 1960s and 1970s with screening for phenylketonuria (PKU), a rare metabolic disease that causes severe and irreversible mental retardation unless treated before problems arise. As knowledge about rare diseases expanded and new screening technologies were introduced—such as the (...)
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  • Proceduralisation, choice and parental reflections on decisions to accept newborn bloodspot screening.Stuart G. Nicholls - 2012 - Journal of Medical Ethics 38 (5):299-303.
    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. (...)
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