Patients’ rights and the end of life in France: Where do we stand in 2024? (notice n° 506058)

détails MARC
000 -LEADER
fixed length control field 01448cam a2200157 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250121084630.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Bretonnière, Sandrine
Relator term author
245 00 - TITLE STATEMENT
Title Patients’ rights and the end of life in France: Where do we stand in 2024?
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2024.<br/>
500 ## - GENERAL NOTE
General note 19
520 ## - SUMMARY, ETC.
Summary, etc. The scope of patients’ rights has been expanding since the mid-twentieth century. Their founding principle is the individual’s consent to medical research, treatment, and care. Part of the movement for patients’ rights, access to medical aid in dying is a long-standing concern of citizens. This article presents a historical and sociological perspective allowing us to trace the genealogy of patients’ rights in the second half of the twentieth century. It analyzes the emergence and consolidation of the political and citizen engagement toward new patients’ rights in medical aid in dying, most notably illustrated by the Citizens’ Convention on End of Life in 2022–2023. Further, I aim to demonstrate that a rebalancing of the doctor-patient relationship is underway, based on an assertive patient autonomy. This dynamic is strengthened by an emphasis on consent and patients’ rights.
786 0# - DATA SOURCE ENTRY
Note L'information psychiatrique | 100 | 10 | 2024-12-31 | p. 785-790 | 0020-0204
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/journal-l-information-psychiatrique-2024-10-page-785?lang=en&redirect-ssocas=7080">https://shs.cairn.info/journal-l-information-psychiatrique-2024-10-page-785?lang=en&redirect-ssocas=7080</a>

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