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Ethical issues arising from the requirement to sign a consent form in palliative care.
Plu I., Purssell-François I., Moutel G., Ellien F., Hervé C.
Journal of Medical Ethics 34, 4 (2008) 279-80 - http://www.hal.inserm.fr/inserm-00270886
 (18375681) 
Ethical issues arising from the requirement to sign a consent form in palliative care.
Isabelle Plu () 1, 2, Irène Purssell-François1, 2, Grégoire Moutel2, Françoise Ellien3, Christian Hervé2
1 :  Service de médecine légale
http://www.chu-dijon.fr/
CHU Dijon
France
2 :  LEM - Laboratoire d'éthique médicale et médecine légale
Université Paris V - Paris Descartes
Faculté de médecine, 45 rue des Saints-Pères, Paris 75006
France
3 :  Réseau SPES
Réseau Soins Palliatifs Essonne Sud
ZA Rue de la Bigotte, 91750 Champcueil
France
French healthcare networks aim to help healthcare workers to take care of patients by improving cooperation, coordination and the continuity of care. When applied to palliative care in the home, they facilitate overall care including medical, social and psychological aspects. French legislation in 2002 required that an information document explaining the functioning of the network should be given to patients when they enter a healthcare network. The law requires that this document be signed. Ethical issues arise from this legislation with regard to the validity of the signature of dying patients. Signature of the consent form by a guardian or trustee, a designated person--the Person of Trust--transforms the doctor-patient relationship into a triangular doctor-patient-third-party relationship.
Sciences du Vivant/Ethique
Anglais
1473-4257

Articles dans des revues avec comité de lecture
10.1136/jme.2006.019075
Journal of Medical Ethics (J Med Ethics)
Publisher BMJ Publishing Group
ISSN 0306-6800 
internationale
04/2008
34
4
279-80

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2006_019075_Sign_a_consent.doc(51.5 KB)
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