Experimentation on children and proxy consent
Journal of Medicine and Philosophy 6 (3):281-294 (1981)
| Abstract | This essay explores the plausibility of attempting to justify the imposition of risk on young children, in the course of therapeutic treatment or nontherapeutic research, by an appeal to proxy consent. In particular, Richard McCormick's reliance on this type of defense is examined and rejected, and an alternative basis for determining the justifiability of such treatment is partially sketched – one which avoids any attempt to ‘construct’ consent on the part of the child. CiteULike Connotea Del.icio.us What's this? | |||||||||
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Garrath Williams (2012). Children as Means and Ends in Large-Scale Medical Research. Bioethics 26 (8):422-430.
G. Bravo (2003). Knowledge of the Legislation Governing Proxy Consent to Treatment and Research. Journal of Medical Ethics 29 (1):44-50.
Victoria A. Miller, Dennis Drotar & Eric Kodish (2004). Children's Competence for Assent and Consent: A Review of Empirical Findings. [REVIEW] Ethics and Behavior 14 (3):255 – 295.
Ferdinand Schoeman (1985). Parental Discretion and Children's Rights: Background and Implications for Medical Decision-Making. Journal of Medicine and Philosophy 10 (1):45-62.
Susan E. Zinner (1995). The Elusive Goal of Informed Consent by Adolescents. Theoretical Medicine and Bioethics 16 (4).
J. Blustein (1978). On Children and Proxy Consent. Journal of Medical Ethics 4 (3):138-140.
T. M. Wilkinson (2001). Parental Consent and the Use of Dead Children's Bodies. Kennedy Institute of Ethics Journal 11 (4):337-358.
Richard O'Neil (1983). Determining Proxy Consent. Journal of Medicine and Philosophy 8 (4):389-403.
Edward Wierenga (1983). Proxy Consent and Counterfactual Wishes. Journal of Medicine and Philosophy 8 (4):405-416.
Sonja Grover (2003). On the Limits of Parental Proxy Consent: Children's Right to Non-Participation in Non-Therapeutic Research. Journal of Academic Ethics 1 (4):349-383.
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