dc.creator | Campbell, A.G.M. | en |
dc.date.accessioned | 2015-05-05T18:13:26Z | en |
dc.date.available | 2015-05-05T18:13:26Z | en |
dc.date.created | 1983-09 | en |
dc.date.issued | 1983-09 | en |
dc.identifier | 10.1136/jme.9.3.136 | en |
dc.identifier.bibliographicCitation | Journal of Medical Ethics. 1983 Sep; 9(3): 136-140. | en |
dc.identifier.issn | 0306-6800 | en |
dc.identifier.uri | http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=The+Right+to+Be+Allowed+to+Die&title=Journal+of+Medical+Ethics.+&volume=9&issue=3&pages=136-140&date=1983&au=Campbell,+A.G.M. | en |
dc.identifier.uri | http://dx.doi.org/10.1136/jme.9.3.136 | en |
dc.identifier.uri | http://hdl.handle.net/10822/724220 | en |
dc.description.abstract | This review of several recent U.S. court decisions in "right to die"
cases was presented at the London Medical Group's 1983 annual conference,
"Human Rights in Medicine." Campbell deplores, as contrary to "natural
justice," the American predilection to involve the legal system in decisions
on withholding treatment from incompetent terminally ill adults and defective
newborns. He maintains that, while society should determine general policies
to guide life and death decisions, the interests of the patient will be best
served if these decisions are usually based on the judgment of physicians and
family members. (KIE abstract) | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:KIE/16094 | en |
dc.subject | Adults | en |
dc.subject | Allowing to Die | en |
dc.subject | Autonomy | en |
dc.subject | Competence | en |
dc.subject | Congenital Disorders | en |
dc.subject | Death | en |
dc.subject | Decision Making | en |
dc.subject | Family Members | en |
dc.subject | Guardians | en |
dc.subject | Human Rights | en |
dc.subject | Infants | en |
dc.subject | Justice | en |
dc.subject | Judicial Action | en |
dc.subject | Legal Aspects | en |
dc.subject | Legal Guardians | en |
dc.subject | Life | en |
dc.subject | Living Wills | en |
dc.subject | Medicine | en |
dc.subject | Newborns | en |
dc.subject | Parents | en |
dc.subject | Physicians | en |
dc.subject | Quality of Life | en |
dc.subject | Review | en |
dc.subject | Right to Die | en |
dc.subject | Rights | en |
dc.subject | Social Control | en |
dc.subject | Terminally Ill | en |
dc.subject | Treatment Refusal | en |
dc.subject | Twins | en |
dc.subject | Value of Life | en |
dc.subject | Withholding Treatment | en |
dc.subject | Wills | en |
dc.title | The Right to Be Allowed to Die | en |
dc.provenance | Digital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine. | en |
dc.provenance | Digital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University. | en |