Parental Perspectives on Treatment -- Nontreatment Decisions Involving Newborns With Spina Bifida
Barber, Patricia A.
Marquis, Janet G.
Turnbull, H. Rutherford
Allowing to Die; Alternatives; Attitudes; Autonomy; Communication; Consent; Decision Making; Disclosure; Ethics; Ethics Committees; Evaluation; Government; Government Regulation; Infants; Life; Newborns; Parental Consent; Parents; Physicians; Privacy; Prognosis; Prolongation of Life; Quality of Life; Regulation; Rights; Risks and Benefits; Spina Bifida; Surgery; Survey; Withholding Treatment;
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Mason, J.K.; Meyers, David W. (1986-06)Trends in the United Kingdom and the U.S. are compared with regard to the legal rights of parents to accept or refuse treatment for newborns with congenital defects. British law is seen as generally guided by the principle of ...