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  1. Children’s informed signified and voluntary consent to heart surgery: Professionals’ practical perspectives.Priscilla Alderson, Hannah Bellsham-Revell, Joe Brierley, Nathalie Dedieu, Joanna Heath, Mae Johnson, Samantha Johnson, Alexia Katsatis, Romana Kazmi, Liz King, Rosa Mendizabal, Katy Sutcliffe, Judith Trowell, Trisha Vigneswaren, Hugo Wellesley & Jo Wray - 2022 - Nursing Ethics 29 (4):1078-1090.
    Background: The law and literature about children’s consent generally assume that patients aged under-18 cannot consent until around 12 years, and cannot refuse recommended surgery. Children deemed pre-competent do not have automatic rights to information or to protection from unwanted interventions. However, the observed practitioners tend to inform young children s, respect their consent or refusal, and help them to “want” to have the surgery. Refusal of heart transplantation by 6-year-olds is accepted. Research question: What are possible reasons to explain (...)
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  • A critical realist analysis of consent to surgery for children, human nature and dialectic: the pulse of freedom.Priscilla Alderson, Katy Sutcliffe & Rosa Mendizabal - 2020 - Journal of Critical Realism 19 (2):159-178.
    Consent can only be voluntary, freely given and uncoerced. Can this legal adult standard also apply to children? High-risk surgery is seldom a wanted choice, but compared with the dangers of the un...
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  • Children and health-care research: best treatment, best interests and best practice.Hazel Biggs - 2011 - Clinical Ethics 6 (1):15-19.
    In order for children to receive the best possible medical treatment, it is essential that research is conducted to discover safe and effective interventions and dosages. This article focuses on the legal and ethical implications of recruiting into health-care research minors who are not competent to consent. It considers the role played by best interests in obtaining valid parental consent for the participation of children in research, both at common law and under the Regulations that govern clinical trials of medicinal (...)
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  • Children’s consent and the zone of parental discretion.P. Alderson - 2017 - Clinical Ethics 12 (2):55-62.
    This paper briefly reviews highlights from decades of debates in medicine, law, bioethics, psychology and social research about children’s and parents’ views and consent to medical treatment and research. There appears to have been a rise and later a fall in respect for children’s views, illustrated among many examples by a recent book on the zone of parental discretion, which is reviewed. A return to greater respect for children’s views and consent is advocated.
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  • Researching young children’s perception of food in Irish pre-schools: An ethical dilemma.Charlotte Johnston Molloy, Nóirín Hayes, John Kearney, Corina Glennon Slattery & Clare Corish - 2012 - Research Ethics 8 (3):155-164.
    Poor nutrition habits have been reported in the childcare setting. While the literature advocates the need to carry out ‘Voice of the Child’ research, few studies have explored this methodology with regard to children and food, in particular in the pre-school setting. This article aims to outline the ethical issues raised by a research ethics committee and to discuss the impact of these issues on a study that hoped to determine the food perceptions of children (aged three to four years) (...)
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