dc.creator | Weiss, Suzanne M. | en |
dc.date.accessioned | 2015-05-05T18:30:40Z | en |
dc.date.available | 2015-05-05T18:30:40Z | en |
dc.date.created | 1991 | en |
dc.date.issued | 1991 | en |
dc.identifier.bibliographicCitation | Journal of Clinical Ethics. 1991 Fall; 2(3): 196-199. | en |
dc.identifier.issn | 1046-7890 | 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+Psda:+a+Long-Term+Care+View&title=Journal+of+Clinical+Ethics.++&volume=2&issue=3&pages=196-199&date=1991&au=Weiss,+Suzanne+M. | en |
dc.identifier.uri | http://hdl.handle.net/10822/736525 | en |
dc.description.abstract | Conclusion: The PSDA [Patient Self-Determination Act] is a welcome
development for nursing facilities, as well as residents and families. For
years, many residents, families, and facilities have not confronted the issue
of end-of-life treatment decisions. The result has been a "double blind"
situation for all concerned. Few residents enter a nursing facility having
written advance directives, and many have never discussed their treatment
wishes with family members. At the same time, nursing facilities have failed
to alert entering residents to facility policies concerning requests to
receive (or forgo) treatment at the end of life. In fact, some facilities have
never developed written policies. Implementation of the PSDA will create
dramatic changes in the way many nursing facilities address the subject of
advance directives with their residents. It is hoped that these changes will
help patients and residents communicate their treatment wishes more
comfortably and with confidence that their decisions will be carried out. In
addition, providers will have greater assurance that they understand the
resident's wishes if and when certain treatment contingencies occur.... | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:KIE/35846 | en |
dc.subject | Advance Directives | en |
dc.subject | Aged | en |
dc.subject | Allowing to Die | en |
dc.subject | Autonomy | en |
dc.subject | Competence | en |
dc.subject | Comprehension | en |
dc.subject | Education | en |
dc.subject | Family Members | en |
dc.subject | Federal Government | en |
dc.subject | Government | en |
dc.subject | Government Regulation | en |
dc.subject | Health | en |
dc.subject | Information Dissemination | en |
dc.subject | Institutional Policies | en |
dc.subject | Legal Aspects | en |
dc.subject | Legislation | en |
dc.subject | Life | en |
dc.subject | Long-Term Care | en |
dc.subject | Nursing Homes | en |
dc.subject | Patient Admission | en |
dc.subject | Patients | en |
dc.subject | Patients' Rights | en |
dc.subject | Public Policy | en |
dc.subject | Regulation | en |
dc.subject | Right to Die | en |
dc.subject | Rights | en |
dc.title | The PSDA: A Long-Term Care View | 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 |