dc.creator | Kielstein, Rita | en |
dc.creator | Sass, Hans-Martin | en |
dc.date.accessioned | 2015-05-05T18:48:40Z | en |
dc.date.available | 2015-05-05T18:48:40Z | en |
dc.date.created | 1993-09 | en |
dc.date.issued | 1993-09 | en |
dc.identifier | 10.1353/ken.0.0247 | en |
dc.identifier.bibliographicCitation | Kennedy Institute of Ethics Journal. 1993 Sep; 3(3): 303-325. | en |
dc.identifier.issn | 1054-6863 | 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=Using+Stories+to+Assess+Values+and+Establish+Medical+Directives&title=Kennedy+Institute+of+Ethics+Journal.++&volume=3&issue=3&pages=303-325&date=1993&au=Kielstein,+Rita | en |
dc.identifier.uri | http://dx.doi.org/10.1353/ken.0.0247 | en |
dc.identifier.uri | http://hdl.handle.net/10822/743042 | en |
dc.description.abstract | While still developing in Germany, a consensus has emerged in the
United States on the use of advance directives for guiding future medical
decision making. This article outlines three phases in the evolution of
advance directive forms -- the legal phase, the checklist phase, and the story
phase. The story-based approach is discussed as the best method for assessing
patient values and incorporating them into advance directives, and a
story-based advance directive form, which has been developed and tested during
the past two years, is presented. | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:KIE/40711 | en |
dc.subject | Advance Directives | en |
dc.subject | Allowing to Die | en |
dc.subject | Attitudes | en |
dc.subject | Attitudes to Death | en |
dc.subject | Autonomy | en |
dc.subject | Case Studies | en |
dc.subject | Communication | en |
dc.subject | Competence | en |
dc.subject | Consensus | en |
dc.subject | Consent | en |
dc.subject | Death | en |
dc.subject | Decision Making | en |
dc.subject | Evaluation | en |
dc.subject | Evolution | en |
dc.subject | Forms | en |
dc.subject | Health | en |
dc.subject | Health Care | en |
dc.subject | International Aspects | en |
dc.subject | Legal Aspects | en |
dc.subject | Life | en |
dc.subject | Pain | en |
dc.subject | Paternalism | en |
dc.subject | Patients | en |
dc.subject | Physicians | en |
dc.subject | Primary Health Care | en |
dc.subject | Prolongation of Life | en |
dc.subject | Quality of Life | en |
dc.subject | Suffering | en |
dc.subject | Suicide | en |
dc.subject | Terminal Care | en |
dc.subject | Third Party Consent | en |
dc.subject | Values | en |
dc.subject | Withholding Treatment | en |
dc.title | Using Stories to Assess Values and Establish Medical Directives | 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 |