Switch to: References

Add citations

You must login to add citations.
  1. “Brain Death,” “Dead,” and Parental Denial.John J. Paris, Brian M. Cummings & M. Patrick Moore - 2014 - Cambridge Quarterly of Healthcare Ethics 23 (4):371-382.
    Download  
     
    Export citation  
     
    Bookmark   9 citations  
  • Autonomy and informed consent: A mistaken association? [REVIEW]Sigurdur Kristinsson - 2007 - Medicine, Health Care and Philosophy 10 (3):253-264.
    For decades, the greater part of efforts to improve regulatory frameworks for research ethics has focused on informed consent procedures; their design, codification and regulation. Why is informed consent thought to be so important? Since the publication of the Belmont Report in 1979, the standard response has been that obtaining informed consent is a way of treating individuals as autonomous agents. Despite its political success, the philosophical validity of this Belmont view cannot be taken for granted. If the Belmont view (...)
    Download  
     
    Export citation  
     
    Bookmark   14 citations  
  • Default options and neonatal resuscitation decisions.Marlyse Frieda Haward, Ryan O. Murphy & John M. Lorenz - 2012 - Journal of Medical Ethics 38 (12):713-718.
    Objective To determine whether presenting delivery room management options as defaults influences decisions to resuscitate extremely premature infants. Materials and methods Adult volunteers recruited from the world wide web were randomised to receive either resuscitation or comfort care as the delivery room management default option for a hypothetical delivery of a 23-week gestation infant. Participants were required to check a box to opt out of the default. The primary outcome measure was the proportion of respondents electing resuscitation. Data were analysed (...)
    Download  
     
    Export citation  
     
    Bookmark   5 citations