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Introduction: The issue of end-of-life care is the subject of a sensitive debate in French society, particularly regarding the possibility for certain patients to have access to medical assistance in dying. The aim of this study was to assess the knowledge and opinion of healthcare providers on the care practices for patients at the end of life, as well as to highlight any specificities in their discourse.
Method: A survey of healthcare providers' opinions, composed of closed and open questions, that were analyzed using a lexicometric approach, was distributed in a cancer center.
Results: The results of the study reveal a good knowledge of the different procedures. Professionals considered that advance directives should be systematically collected; a majority of them differentiated euthanasia from deep continuous sedation and perceived the latter as a means of relieving patients' suffering without inducing death. The different procedures related to the active assistance in dying were known by a majority of professionals and the survey did not identify a dominant trend concerning the will to practice euthanasia if the legal framework allowed it. Half of the participants considered their training insufficient, indicating the need to fill this gap.
Discussion: This survey underlines the importance of training and support for the professionals caring for patients in palliative situation and their relatives in France.
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http://dx.doi.org/10.1016/j.bulcan.2023.12.009 | DOI Listing |
Palliat Support Care
September 2025
IMPACCT, Faculty of Health, University of Technology Sydney, Sydney, NSW, Australia.
Objectives: Carers are critical to support discharge home from hospital at end of life yet remain under-represented in health service initiatives to assist this transition. A carer-focused intervention embedded into practice may facilitate hospital discharge. This open-labeled, single-arm phase 2 study aimed to determine the feasibility of (1) delivering a multi-staged intervention (CARENET) to carers of advanced cancer patients in a hospital setting and (2) the study design to inform a phase 3 trial.
View Article and Find Full Text PDFPalliat Support Care
September 2025
School of Medicine, The University of Sydney, Camperdown, NSW, Australia.
Objectives: This study explored Australian palliative care clinicians' perspectives on the legalization of voluntary assisted dying (VAD), aiming to identify variables associated with clinicians' views and understand challenges of its implementation.
Methods: An online survey exploring support for legalization of VAD was sent to palliative care clinicians in Queensland and New South Wales and followed up with semi-structured interviews. Support was categorized as positive, uncertain, or negative.
Am J Crit Care
September 2025
Jennifer M. Snaman is an attending physician, Department of Supportive Oncology, Dana-Farber Cancer Institute, and an assistant professor, Department of Pediatrics, Harvard Medical School.
Background: Parents who report feeling prepared for symptoms and circumstances around their child's end of life report less adverse bereavement outcomes. Yet, the actions that bedside clinicians can initiate to help families feel prepared for a child's death remain unclear.
Objectives: To identify actions that nurses engage in to prepare families for the dying process.