Littérature scientifique sur le sujet « Refus de soins de la part du patient »
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Articles de revues sur le sujet "Refus de soins de la part du patient"
Bernheim, Emmanuelle. « Le refus de soins psychiatriques est-il possible au Québec ? Discussion à la lumière du cas de l’autorisation de soins ». McGill Law Journal 57, no 3 (4 mai 2012) : 553–94. http://dx.doi.org/10.7202/1009067ar.
Texte intégralSun, Guang, Manon Lemonde et Dominique Tremblay. « Expérience des infirmières en oncologie accompagnant les survivants au cancer pendant la transition du traitement actif vers les soins primaires ». Canadian Oncology Nursing Journal 33, no 3 (14 juillet 2023) : 342–47. http://dx.doi.org/10.5737/23688076333342.
Texte intégralBéguin, Patrick. « Du refus de soins du patient ». Kinésithérapie, la Revue 14, no 152-153 (août 2014) : 36–37. http://dx.doi.org/10.1016/j.kine.2014.06.012.
Texte intégralTournebise, H., J. Bérenguier, F. Picchi, A. Brémond, C. Dupont et MH Boucand. « Refus de soins chez un patient récemment atteint de tétraplégie ». Annales de Réadaptation et de Médecine Physique 39, no 6 (janvier 1996) : 339. http://dx.doi.org/10.1016/0168-6054(96)86888-7.
Texte intégralJean-Louis, Éric. « Le refus de soins d’hygiène chez un patient atteint de schizophrénie ». L'Aide-Soignante 30, no 177 (mai 2016) : 31–32. http://dx.doi.org/10.1016/j.aidsoi.2016.03.012.
Texte intégralRougé-Maillart, C., T. Gaches, N. Jousset et M. Penneau. « Refus de soins du patient, le problème épineux des témoins de Jéhovah ». La Presse Médicale 33, no 4 (février 2004) : 223–27. http://dx.doi.org/10.1016/s0755-4982(04)98541-7.
Texte intégralTardif, Charles, et Christine Dallaire. « La satisfaction des patients francophones de l’Est de l’Ontario traités en réadaptation à domicile ». Francophonies d'Amérique, no 30 (22 septembre 2011) : 61–88. http://dx.doi.org/10.7202/1005881ar.
Texte intégralRemondière, Remi. « La mécanothérapie au temps de la Grande Guerre ». Revue Historique des Armées 274, no 1 (1 janvier 2014) : 78–86. http://dx.doi.org/10.3917/rha.274.0078.
Texte intégralMoore, Katherine N. « Compliance or Collaboration ? the Meaning for the Patient ». Nursing Ethics 2, no 1 (mars 1995) : 71–77. http://dx.doi.org/10.1177/096973309500200109.
Texte intégralBonnemaizon, Audrey, Abdelmajid Amine et Margaret Josion-Portail. « La participation des patients âgés à la relation de soins en question(s) ! » Revue Française de Gestion 46, no 290 (juin 2020) : 107–27. http://dx.doi.org/10.3166/rfg.2020.00458.
Texte intégralThèses sur le sujet "Refus de soins de la part du patient"
El, Amine Dana. « La responsabilité du fait du refus de se soumettre à un acte médical à l'épreuve du concept de responsabilisation : une contribution à l'étude du droit de consentir à l'acte médical ». Electronic Thesis or Diss., Paris 12, 2024. http://www.theses.fr/2024PA120002.
Texte intégralThe study of the concept of empowerment in the context of medical consent, for which we propose a new definition, leads to the assertion that empowerment is part of a logic of encouraging virtuous behaviors in light of a recognized standard. In a society centered on individualism, empowerment through the right to consent has primarily emerged as a process of emancipation, aiming for empowerment and safeguarding individual rights such as, notably, the right to health protection and the right to respect for human dignity. However, the right to consent to medical acts is not merely an individual matter: its exercise can have repercussions on third parties and society as a whole. Beyond the terminological similarities between the notions of responsibility and empowerment, this vision of the free and, as a corollary, fundamentally responsible individual, which is the essence of our study, implies a normative conception of law : the objective is to safeguard essential, if not foundational, principles of our legal system, including the principle of not harming others. This approach entails that we invoke responsibility mechanisms, which present themselves as powerful instruments for regulating harmful behaviors. Through the dual nature of the empowerment concept, the question of consent to medical care is to be transformed from an individual choice to an altruistic one. This study aims to demonstrate the means through which the concept of empowerment, embedded in a strategy of encouragement and submission, contributes to establishing a common foundation of principles allowing a rationalized transition from autonomy to responsibility, acting as a safeguard against the excesses of autonomy in medical decision-making. Embedded in a utilitarian approach, the study aims to demonstrate, in certain hypotheses, the possible and necessary existence of liability for refusing to undergo a medical act without ignoring the foundational principles of medical law that impose, at most, regulating the right to consent without denaturing it. In this context, the study is animated by the desire to balance the need to protect individual interests and those of third parties and society that may be harmed by non-virtuous exercise of individual freedom in medical consent. In any case, the question of sanctioning the refusal to undergo a medical act within the framework of responsibility directly challenges the status of the patient entitled to refuse any medical act. The admission of liability, underlying autonomy, is only possible if it does not entail excessive and disproportionate consequences towards the right to consent. Therefore, the thesis proposes to analyze the right to consent in its relation to classical mechanisms of civil and criminal liability, allowing for the rationalization of the exercise of the right to consent when it threatens third parties and society
Guyon, Gaëlle. « Le refus de soins anticipé : une décision impossible ? » Thesis, Université de Lorraine, 2015. http://www.theses.fr/2015LORR0280.
Texte intégralContext: The current debates concerning the end of life deal with legal, judicial and social issues. What is clear is they all highlight some serious social, ethical and political concerns in France and in the world. The case « Vincent Lambert » shows exactly the difficulties of medical situations between the life and the death of patients, which puts in evidence the limits of the legal framework. Indeed, several judicial reversals happened in this case and illustrate well how difficult it is to make a right medical decision when the patient, their relatives and medical staff have conflicting views. Objective: The objective of our research was to identify which are the difficulties when medical staff has to make a decision applying an anticipated refusal of treatment. As a consequence, the challenge was to answer the following question: is an anticipated refusal of treatment an impossible decision? Methods: Our work was divided into three parts. The first part aimed at asking patients’ opinions as well as assessing their knowledge of the different ways to express their will in advance. Then, the second part had to determine which criteria ensure a good application of advance directives. This study was based on an analysis of the scientific literature and a work in Comparative Law. In the end, the third part presents both practical and judicial problems regarding the application of a decision whose the goal is to withhold and withdraw a life-sustaining treatment Conclusion: This research has raised several issues and it draws our attention on the need to devise effective ways to give an anticipated consent about the end of life. If people want to write advance directives, they should have the possibility to do so and make sure their right to refuse a treatment is respected. In addition, even though someone is unable to give their consent because of their condition or disease, they should be able to use the same right to refuse a treatment and should be sure their decision is respected
Berdah, Daniel Bianchi Christian. « Maladie incurable, imaginaire et refus de soins vers une nouvelle éthique de la relation médecin-malade / ». Créteil : Université de Paris-Val-de-Marne, 2006. http://doxa.scd.univ-paris12.fr:80/theses/th0242787.pdf.
Texte intégralJeanmart, Caroline. « Médecins généralistes et usagers de drogues : analyse des pratiques de part et d'autre d'une frontière (Belgique-France) ». Lille 1, 2007. https://pepite-depot.univ-lille.fr/LIBRE/Th_Num/2007/50377-2007-Jeanmart.pdf.
Texte intégralBouton, Xavier. « Personne diminuée et personne à part entière : de la mise en oeuvre d'un agir distribué avec le patient atteint de déficience motrice dans un service de Médecine Physique et Réadaptation ». Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE2140.
Texte intégralThe doctoral thesis focuses on the assistance of functional impaired patients passing throug a personal self experience following a severe physical injury. It is based on an ethnographic inquiry, combining observations and interviews that have been conducted in two hospital services of Saint-Etienne’s UH. The first service is the functional rehabilitation recovery service and, for the major part, the other is the physical medecine and rehabilitation service. In presenting the « recapacitation » work of a person experimenting a new « non autonomous » body, the thesis explores relations between the medical professionals and patients, during the care and functional rehabilitation activities, but also the way in which relatives are included, in order to impact the perception of the handicap situation and to build collectively an acceptable life project after the hospital stay. This perspective reveals how to confront strong constraints of personal self experience by sharing words, this last become as a ressource to bring into the interactions and thus to engage the patient in an intrasubjective reappropriation of his body and an intersubjective continuity of his being. An important place is given to the hospitalization of quadriplegic patients, which is an extreme case and apart in the patient’s care in the physical medecine and rehabilitation service. The thesis presents a chronicle of a lived experience of these particular patients and thus shows the specificity of the process taken place in order to structure the experience of non autonomous body and to the one who has become dependent, and included in a collective composed of human actors medical professionals, relatives but also technical objects in which his act is distribued. The narrative takes into consideration the time and the moments experienced by these patients in this collective, during the care which can be counted by months and sometimes by years, by describing the ordinary activities in the rooms, those of the technical installations, those of professional’s meetings, finally and exceptionally a meeting’s structure where a group of former patients come with their spouses and a quadriplegic patient accompanied by his partner, to finalize the project of his return to an ordinary social environment
Bocquier, Aurélie. « Contribution à la compréhension des liens entre statut socio-économique et comportements de santé ». Thesis, Aix-Marseille, 2018. http://www.theses.fr/2018AIXM0713.
Texte intégralThis thesis aimed to contribute to current scientific knowledge about the social differentiation of health behaviours in France and to a better understanding of the mechanisms underlying this differentiation. We focused on the role of specific sociocognitive factors (perceptions and beliefs) based on theories derived from the sociology of risk and the sociology of deviance. This work used data from the 2010 Baromètre cancer survey and the 2016 Baromètre santé survey to examine health behaviours related to primary prevention of some cancers (alcohol consumption and sun protection) and infectious diseases (childhood vaccinations). People of low socioeconomic status were more prone to relativize the alcohol-related risks of cancer and to have substantially less knowledge about sun health and more “false beliefs” about sun protection than people of high socioeconomic status. This knowledge and these false beliefs were significant mediators of the positive association between socioeconomic status and sun-protection behaviours. In the field of vaccination, we found a higher prevalence of vaccine hesitancy among parents who had at least passed the “bac”. This association was partly explained by their lower level of trust in health authorities and mainstream medicine than among the least educated group and by their greater commitment to making “good” health-related decisions. From a public health perspective, these results furnish avenues for designing health promotion interventions that take into account the social context in which people’s health behaviours are embedded to improve both effectiveness and equity
Livres sur le sujet "Refus de soins de la part du patient"
Tännsjö, Torbjörn. Coercive care : The ethics of choice in health and medicine. London : Routledge, 1999.
Trouver le texte intégralChapitres de livres sur le sujet "Refus de soins de la part du patient"
Bernard, Michel. « Refus de soin de la part du patient ». Dans 160 questions en responsabilité médicale, 53–56. Elsevier, 2010. http://dx.doi.org/10.1016/b978-2-294-70887-9.00020-8.
Texte intégralBernard, Michel. « Refus de soins de la part du médecin ». Dans 160 questions en responsabilité médicale, 51–52. Elsevier, 2010. http://dx.doi.org/10.1016/b978-2-294-70887-9.00019-1.
Texte intégralArticle collectif. « Mieux situer la place de l’Approche Patient Partenaire de Soins en Grande Région ». Dans Pratiques et interventions en psychologie de la santé, 181–93. Editions des archives contemporaines, 2020. http://dx.doi.org/10.17184/eac.3195.
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