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dc.creatorWeiss, Suzanne M.en
dc.date.accessioned2015-05-05T18:30:40Zen
dc.date.available2015-05-05T18:30:40Zen
dc.date.created1991en
dc.date.issued1991en
dc.identifier.bibliographicCitationJournal of Clinical Ethics. 1991 Fall; 2(3): 196-199.en
dc.identifier.issn1046-7890en
dc.identifier.urihttp://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.urihttp://hdl.handle.net/10822/736525en
dc.description.abstractConclusion: 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.formatArticleen
dc.languageenen
dc.sourceBRL:KIE/35846en
dc.subjectAdvance Directivesen
dc.subjectAgeden
dc.subjectAllowing to Dieen
dc.subjectAutonomyen
dc.subjectCompetenceen
dc.subjectComprehensionen
dc.subjectEducationen
dc.subjectFamily Membersen
dc.subjectFederal Governmenten
dc.subjectGovernmenten
dc.subjectGovernment Regulationen
dc.subjectHealthen
dc.subjectInformation Disseminationen
dc.subjectInstitutional Policiesen
dc.subjectLegal Aspectsen
dc.subjectLegislationen
dc.subjectLifeen
dc.subjectLong-Term Careen
dc.subjectNursing Homesen
dc.subjectPatient Admissionen
dc.subjectPatientsen
dc.subjectPatients' Rightsen
dc.subjectPublic Policyen
dc.subjectRegulationen
dc.subjectRight to Dieen
dc.subjectRightsen
dc.titleThe PSDA: A Long-Term Care Viewen
dc.provenanceDigital 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.provenanceDigital 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


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