Literature DB >> 12794409

Opinions about surrogate designation: a population survey in France.

Elie Azoulay1, Frédéric Pochard, Sylvie Chevret, Christophe Adrie, Pierre-Edouard Bollaert, Frédéric Brun, Didier Dreyfuss, Maité Garrouste-Orgeas, Dany Goldgran-Toledano, Mercé Jourdain, Michel Wolff, Jean-Roger Le Gall, Benoît Schlemmer.   

Abstract

OBJECTIVE: Many patients go through periods when they are too ill to give consent or to participate in decisions. When this occurs, patient autonomy is best maintained when a surrogate designated by the patient and familiar with his or her values can speak for the patient. The objective of this study was to determine whether people who are not yet ill are ready to accept surrogate designation. Attitudes toward family participation in care were explored also.
DESIGN: Population survey by telephone. Because refusal of life-sustaining treatment is a dramatic example of patient autonomy, the survey used questions about ICU admission.
SETTING: General population in France.
SUBJECTS: Representative random sample of 8000 residents of France aged 18 yrs or more.
INTERVENTIONS: None. MAIN OUTCOME MEASURES: The survey investigated attitudes.
RESULTS: Most respondents said they would like to designate a surrogate (7205 [90%]) and to have their family share in their care (6691 [84%] for bathing, 5629 [70%] for feeding, and 4139 [52%] for tracheal suctioning) and in decisions about their management (6120 [76%]). Among respondents with a spouse, 79% said they would designate the spouse to speak for them. The attitudes were not influenced by ethnicity, religion or education level.
CONCLUSIONS: Most people living in France would want a surrogate to represent them should they be incompetent and admitted to an ICU. Primary care physicians should inform their patients about the benefits of discussing illness-related issues among friends and family.

Entities:  

Keywords:  Death and Euthanasia; Empirical Approach

Mesh:

Year:  2003        PMID: 12794409     DOI: 10.1097/01.CCM.0000069828.15555.09

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  15 in total

1.  It is time for a gender specific discussion on advanced directives with female patients during routine health visits.

Authors:  Pascal J de Caprariis; Sarah Thompson; Nicole Lippman; Claudia Lyon
Journal:  J Community Health       Date:  2013-12

Review 2.  What are the ethical issues in relation to the role of the family in intensive care?

Authors:  Jean-Pierre Quenot; Fiona Ecarnot; Nicolas Meunier-Beillard; Auguste Dargent; Audrey Large; Pascal Andreu; Jean-Philippe Rigaud
Journal:  Ann Transl Med       Date:  2017-12

3.  Ethical challenges involved in obtaining consent for research from patients hospitalized in the intensive care unit.

Authors:  Fiona Ecarnot; Jean-Pierre Quenot; Guillaume Besch; Gaël Piton
Journal:  Ann Transl Med       Date:  2017-12

4.  Brief report: identifying a proxy for health care as part of routine medical inquiry.

Authors:  K Michael Lipkin
Journal:  J Gen Intern Med       Date:  2006-11       Impact factor: 5.128

5.  Prehospital withholding and withdrawal of life-sustaining treatments. The French LATASAMU survey.

Authors:  Edouard Ferrand; Jean Marty
Journal:  Intensive Care Med       Date:  2006-08-02       Impact factor: 17.440

6.  Do Patients Want their Families or their Doctors to Make Treatment Decisions in the Event of Incapacity, and Why?

Authors:  David Wendler; Robert Wesley; Mark Pavlick; Annette Rid
Journal:  AJOB Empir Bioeth       Date:  2016-04-26

7.  The acceptability of ending a patient's life.

Authors:  M Guedj; M Gibert; A Maudet; M T Muñoz Sastre; E Mullet; P C Sorum
Journal:  J Med Ethics       Date:  2005-06       Impact factor: 2.903

8.  Difference in reported pre-morbid health-related quality of life between ARDS survivors and their substitute decision makers.

Authors:  Damon C Scales; Catherine M Tansey; Andrea Matte; Margaret S Herridge
Journal:  Intensive Care Med       Date:  2006-09-07       Impact factor: 17.440

9.  Substitute consent for research involving the elderly: a comparison between Quebec and France.

Authors:  Gina Bravo; Anne-Marie Duguet; Marie-France Dubois; Cyrille Delpierre; Bruno Vellas
Journal:  J Cross Cult Gerontol       Date:  2008-09

10.  Quality of life in patients aged 80 or over after ICU discharge.

Authors:  Alexis Tabah; Francois Philippart; Jean Francois Timsit; Vincent Willems; Adrien Français; Alain Leplège; Jean Carlet; Cédric Bruel; Benoit Misset; Maité Garrouste-Orgeas
Journal:  Crit Care       Date:  2010-01-08       Impact factor: 9.097

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