Literature DB >> 11992303

Strategies for culturally effective end-of-life care.

LaVera M Crawley1, Patricia A Marshall, Bernard Lo, Barbara A Koenig.   

Abstract

As a result of profound worldwide demographic change, physicians will increasingly care for patients from cultural backgrounds other than their own. Differences in beliefs, values, and traditional health care practices are of particular relevance at the end of life. Health care providers and patients and families may not have shared understandings of the meaning of illness or death and may not agree on the best strategies to plan for the end of life or to alleviate pain and suffering. Good end-of-life care may be complicated by disagreements between physicians and patients, difficult interactions, or decisions the physician does not understand. Challenges may result from cultural differences between the patient's background and traditional medical practice. Values so ingrained in physicians as to be unquestioned may be alien to patients from different backgrounds. Physicians need to be sensitive to cultural differences and to develop the skills necessary to work with patients from diverse backgrounds. Community and cultural ties provide a source of great comfort as patients and families prepare for death. This paper describes two cases that raise issues about cross-cultural end-of-life practice and suggests strategies for negotiating common problems. Physicians should assess the cultural background of each patient and inquire about values that may affect care at the end of life. They should become aware of the specific beliefs and practices of the populations they serve, always remembering to inquire whether an individual patient adheres to these cultural beliefs. Attention to cultural difference enables the physician to provide comprehensive and compassionate palliative care at the end of life.

Entities:  

Keywords:  Death and Euthanasia; Professional Patient Relationship

Mesh:

Year:  2002        PMID: 11992303     DOI: 10.7326/0003-4819-136-9-200205070-00010

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  35 in total

1.  Longitudinal Pediatric Palliative Care: Quality of Life & Spiritual Struggle (FACE): design and methods.

Authors:  Ronald H Dallas; Megan L Wilkins; Jichuan Wang; Ana Garcia; Maureen E Lyon
Journal:  Contemp Clin Trials       Date:  2012-06-01       Impact factor: 2.226

2.  Breaking difficult news in a cross-cultural setting: a qualitative study about Latina mothers of children with down syndrome.

Authors:  Kayla M Sheets; Bonnie J Baty; Juan Carlos Vázquez; John C Carey; Wendy L Hobson
Journal:  J Genet Couns       Date:  2011-12-07       Impact factor: 2.537

3.  "Her husband doesn't speak much English": conducting a family meeting with an interpreter.

Authors:  Yael Schenker; Alexander K Smith; Robert M Arnold; Alicia Fernandez
Journal:  J Palliat Med       Date:  2011-11-22       Impact factor: 2.947

4.  Hospice knowledge and intentions among Latinos using safety-net clinics.

Authors:  Claire Selsky; Barbara Kreling; Gheorghe Luta; Solomon B Makgoeng; Jessika Gomez-Duarte; Andrea Gabriela A Barbo; Jeanne S Mandelblatt
Journal:  J Palliat Med       Date:  2012-06-25       Impact factor: 2.947

5.  Interpretation for discussions about end-of-life issues: results from a National Survey of Health Care Interpreters.

Authors:  Yael Schenker; Alicia Fernandez; Kathleen Kerr; David O'Riordan; Steven Z Pantilat
Journal:  J Palliat Med       Date:  2012-07-12       Impact factor: 2.947

6.  An exploratory survey of end-of-life attitudes, beliefs, and experiences of adolescents with HIV/AIDS and their families.

Authors:  Patricia A Garvie; Jianping He; Jichuan Wang; Lawrence J D'Angelo; Maureen E Lyon
Journal:  J Pain Symptom Manage       Date:  2012-07-07       Impact factor: 3.612

7.  'The worst thing about hospice is that they talk about death': contrasting hospice decisions and experience among immigrant Central and South American Latinos with US-born White, non-Latino cancer caregivers.

Authors:  Barbara Kreling; Claire Selsky; Monique Perret-Gentil; Elmer E Huerta; Jeanne S Mandelblatt
Journal:  Palliat Med       Date:  2010-06       Impact factor: 4.762

8.  Ethical aspects of determining and communicating prognosis in critical care.

Authors:  James L Bernat
Journal:  Neurocrit Care       Date:  2004       Impact factor: 3.210

Review 9.  Control and end-of-life care: does ethnicity matter?

Authors:  Deborah L Volker
Journal:  Am J Hosp Palliat Care       Date:  2005 Nov-Dec       Impact factor: 2.500

10.  To die, to sleep: US physicians' religious and other objections to physician-assisted suicide, terminal sedation, and withdrawal of life support.

Authors:  Farr A Curlin; Chinyere Nwodim; Jennifer L Vance; Marshall H Chin; John D Lantos
Journal:  Am J Hosp Palliat Care       Date:  2008-01-15       Impact factor: 2.500

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.