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1.
JONAS Healthc Law Ethics Regul ; 9(4): 125-31, quiz 132-3, 2007.
Article in English | MEDLINE | ID: mdl-18043329

ABSTRACT

The Patient Self-determination Act requires that patients be informed in writing of their right to accept or refuse treatment and the right to an advance directive. For the past 15 years, hospitals have been providing these written materials, yet advance directives are still not adequately directing end-of-life care. Barriers and facilitators to implementation of this law are discussed, as well as the role of nursing management in meeting its true intent.


Subject(s)
Advance Care Planning/organization & administration , Informed Consent/legislation & jurisprudence , Patient Rights/legislation & jurisprudence , Patient Self-Determination Act/organization & administration , Advance Care Planning/ethics , Attitude of Health Personnel , Attitude to Health , Cultural Characteristics , Health Knowledge, Attitudes, Practice , Health Services Needs and Demand , Humans , Informed Consent/ethics , Informed Consent/psychology , Medicaid/legislation & jurisprudence , Medicare/legislation & jurisprudence , Nurse's Role , Organizational Innovation , Patient Rights/ethics , Patient Self-Determination Act/ethics , Religion , Socioeconomic Factors , Treatment Refusal/legislation & jurisprudence , United States , Western World
4.
J Cult Divers ; 13(1): 3-9, 2006.
Article in English | MEDLINE | ID: mdl-16696539

ABSTRACT

Attention to culturally specific rituals germane to end-of-life rituals are important for the nurse who is delivering culturally competent care. The Patient Self-Determination Act implemented in the United States in 1991 brought with it some specific assumptions of values related to end-of-life care involving patient autonomy, informed decision making, truth telling and control over the dying process (USC, 1990). The assumptions and values assumed in this act are not necessarily shared by persons in the United States who are from a minority culture, particularly one other than White of European descent. This manuscript considers the values of the Patient Self-Determination Act passed in the United States and specific cultural beliefs which may pose a conflict for the care giver in the delivery of culturally competent care. The Giger and Davdihizar (2004) Transcultural Assessment Model is used as a way to assess patient and the family in an effort to plan culturally appropriate care that recognizes the uniqueness of each individual at the end of life.


Subject(s)
Advance Directives/ethnology , Clinical Competence , Cultural Diversity , Terminal Care/psychology , Transcultural Nursing/organization & administration , Advance Directives/legislation & jurisprudence , Attitude to Death/ethnology , Attitude to Health/ethnology , Clinical Competence/standards , Cultural Characteristics , Decision Making , Health Knowledge, Attitudes, Practice , Humans , Informed Consent/legislation & jurisprudence , Informed Consent/psychology , Minority Groups/legislation & jurisprudence , Minority Groups/psychology , Models, Nursing , Negotiating/psychology , Nurse-Patient Relations , Nursing Assessment/organization & administration , Patient Care Planning/organization & administration , Patient Self-Determination Act/organization & administration , Personal Autonomy , Social Values , Terminal Care/organization & administration , Truth Disclosure , United States
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