Literature DB >> 10663280

Patients' preferences concerning medical information and surrogacy: results of a prospective study in a French emergency department.

E Roupie1, A Santin, R Boulme, J S Wartel, E Lepage, F Lemaire, J L Lejonc, O Montagne.   

Abstract

OBJECTIVE: To study the wishes of a sample of French patients about medical information and surrogacy, at a time when the French Ministry of Health is supporting increased patient autonomy.
DESIGN: A cohort of competent patients with non-critical illnesses or injuries completed an intention-to-act questionnaire on the amount of medical information they would want to receive should they be hospitalized or in a life-threatening situation. The percentage of patients who would want to have a surrogate if they were in a coma was determined, as well as the identity of the preferred surrogate. The subgroup of patients who were married or living with a partner was evaluated separately to determine how often the spouse/partner was the preferred surrogate. Associations were looked for between patients' wishes and age, sex, educational level, occupation, hierarchical order in the family, and level of confidence in medicine.
SETTING: The emergency room of a teaching hospital in the Paris area (France).
RESULTS: Of the 1089 patients included in the study, 5. 5 % reported that they would not want any information, 25.3 % that they would want to participate actively in all decisions about their care, and 87.3 % that they would want to be fully informed if they were in a life-threatening situation. Slightly less than one-third of the patients (29.6 %) believed they would not want a surrogate if they developed a coma. Among the patients living with a spouse/partner, 40.6 % (229/561) indicated they would want their spouse/partner to be their surrogate. A significant correlation was observed between wanting more information and wanting a surrogate. Younger patients with a higher educational level were significantly more likely to predict a desire for information and for a surrogate than the other patients.
CONCLUSION: Our patients expressed a strong desire to receive extensive information should they become seriously ill, and two-thirds of them reported they would want a surrogate. However, only 40.6 % of the patients living with a spouse/partner would want their spouse/partner to be their surrogate. These data suggest that the time has probably come to propose a nation-wide public hearing on medical information and surrogacy in France.

Entities:  

Keywords:  Empirical Approach; Professional Patient Relationship

Mesh:

Year:  2000        PMID: 10663280     DOI: 10.1007/s001340050011

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN: 0342-4642            Impact factor:   17.440


  7 in total

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

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

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Review 4.  Challenges in end-of-life care in the ICU. Statement of the 5th International Consensus Conference in Critical Care: Brussels, Belgium, April 2003.

Authors:  Jean Carlet; Lambertus G Thijs; Massimo Antonelli; Joan Cassell; Peter Cox; Nicholas Hill; Charles Hinds; Jorge Manuel Pimentel; Konrad Reinhart; Boyd Taylor Thompson
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5.  Evaluating our end-of-life practice.

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Review 6.  Medical research in emergency research in the European Union member states: tensions between theory and practice.

Authors:  Erwin J O Kompanje; Andrew I R Maas; David K Menon; Jozef Kesecioglu
Journal:  Intensive Care Med       Date:  2014-02-26       Impact factor: 17.440

7.  'No Time to be Lost!' Ethical considerations on consent for inclusion in emergency pharmacological research in severe traumatic brain injury in the European Union.

Authors:  Erwin J O Kompanje
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  7 in total

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