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Статті в журналах з теми "Patient acteur de sa santé"
Raymond, Gérard. "Le patient acteur de sa santé." Bulletin de l'Académie Nationale de Médecine 197, no. 8 (November 2013): 1545–46. http://dx.doi.org/10.1016/s0001-4079(19)31201-4.
Повний текст джерелаDegos, Laurent. "Automédication: le patient acteur de sa santé." Bulletin de l'Académie Nationale de Médecine 191, no. 8 (November 2007): 1503–8. http://dx.doi.org/10.1016/s0001-4079(19)32899-7.
Повний текст джерелаRabiller, Johanna, Nicolas Clere, and Céline Onno. "Rendre le patient transplanté rénal acteur de sa santé." Actualités Pharmaceutiques 58, no. 584 (March 2019): 33–38. http://dx.doi.org/10.1016/j.actpha.2019.01.017.
Повний текст джерелаMalafosse, Victor. "Comment motiver le patient pour le rendre acteur de sa santé." Kinésithérapie, la Revue 18, no. 194 (February 2018): 43. http://dx.doi.org/10.1016/j.kine.2017.12.008.
Повний текст джерелаJullian-Desayes, Ingrid, Marie Joyeux-Faure, Sébastien Baillieul, Rita Guzun, Renaud Tamisier, and Jean-Louis Pepin. "Quelles perspectives pour le syndrome d’apnées du sommeil et la santé connectée ?" L'Orthodontie Française 90, no. 3-4 (September 2019): 435–42. http://dx.doi.org/10.1051/orthodfr/2019019.
Повний текст джерелаRochette, Corinne, Emna Cherif, and Elisabeth Martin-Verdier. "Le site internet institutionnel des établissements de santé : un support de communication au service de l’empowerment des patients ?" Communication & management Vol. 20, no. 2 (February 14, 2024): 7–30. http://dx.doi.org/10.3917/comma.202.0007.
Повний текст джерелаRubin, Sabrina, Solange Franger, Adeline Martin, Régis Lorguilloux, and Farid Kneife. "Le patient acteur de sa santé lors d’une arthroplastie de genou en ambulatoire." La Revue de l'Infirmière 67, no. 238 (February 2018): 32–34. http://dx.doi.org/10.1016/j.revinf.2017.12.004.
Повний текст джерелаPsiuk, Thérèse. "Le concept du patient partenaire, de l’implicite vers l’explicite." Droit, Santé et Société N° 3, no. 3 (February 14, 2024): 3–6. http://dx.doi.org/10.3917/dsso.103.0003.
Повний текст джерелаTourniaire, Nolwenn, Julie Leseur, Agnès Roy, Aurélie de la Motte Rouge, and Dominique Pougheon Bertrand. "Comment intégrer un patient partenaire dans une équipe de soins ?" Santé Publique Vol. 35, no. 3 (October 12, 2023): 285–95. http://dx.doi.org/10.3917/spub.233.0285.
Повний текст джерелаHayar, Said, and Laurent Mériade. "La diffusion des outils et services e-santé auprès de leurs utilisateurs : l’exemple de « Mon espace santé » en France." Gestion et management public Pub. anticipées, no. 5 (April 21, 2050): 1f—21. http://dx.doi.org/10.3917/gmp.pr1.0012.
Повний текст джерелаДисертації з теми "Patient acteur de sa santé"
Godfroid, Tiphaine. "Le patient acteur dans la prise en charge du cancer : attentes normatives et travail du malade." Thesis, Université Grenoble Alpes (ComUE), 2017. http://www.theses.fr/2017GREAH014/document.
Повний текст джерелаThe patient actor in the management of cancer : normative expectations and patient workIn the context of a humanisation of care that enhances the figure of the individual as an actor in his or her health, this thesis questions the positioning of patients affected by cancer and their caregivers and close relatives in the care and experience of this pathology from the point of view of their "becoming actor". It highlights the disease management work done by the affected individuals, notably by analyzing how they deal with the uncertain dimensions of the experience of cancer. It also shows how the ethical considerations of the "right to information", the patient "associated with decisions" or even "at the heart of care" and the fight against cancer policy centered on "health education" contribute to bring to the foreground normative expectations that weigh on the sick. Through four stages of the disease - the discovery and announcement of cancer, the treatment period, the experience of remission and end-of-life trajectories - it more specifically examines the differences between the expected and prescribed roles and the roles effectively endorsed, the strategies of cooperation, negotiation or resistance between the actors and the elements that underpin the decision-making of the patients and their commitment to the actions they take to face cancer on a daily basis. The underlying questioning thus focuses on the actions and strategies undertaken by the actors affected in an attempt to control a trajectory of illness marked by uncertainty and how the latter integrate - or not the expectations of " the individual actor of his health and his disease "
Knitza, Johannes. "Renforcer l'autonomie des patients grâce à la santé digitale - Analyse de symptom checkers, de self-sampling-devices et de collectes électroniques des résultats rapportés par les patients dans le domaine des soins en rhumatologie et de la médecine d'urgence." Electronic Thesis or Diss., Université Grenoble Alpes, 2024. http://www.theses.fr/2024GRALS013.
Повний текст джерелаEnsuring that patients can access medical care promptly and improving the standard of that care are crucial aims for healthcare facilities. Healthcare providers however face the challenge of a decreasing number of physicians across all specialties, complicating the effort to keep up with the rising demand for care. Departments specializing in rheumatology, which manage chronic conditions requiring ongoing care, are especially impacted. Emergency services, too, are frequently overwhelmed due to the suboptimal allocation of their ever-shrinking resources.The ongoing health crisis has intensified existing challenges, leading to a widespread implementation of digital tools to aid both patients and healthcare professionals. Nonetheless, the practicality, effectiveness, and clinical value of many digital solutions remain unverified through scientific research. Against this backdrop, the principal aim of this doctoral research was to investigate the integration and application of three cutting-edge digital health technologies (DHT). The purpose was to empower patients, enhance patient autonomy in daily disease management and to improve professional healthcare monitoring. The technologies examined include: (1) symptom checkers (SC), dedicated software for symptom assessment and care seeking guidance; (2) self-sampling devices (SSD), tools enabling patients to collect biological samples independently at home; and (3) electronic patient-reported outcomes (ePRO), systems for capturing patients' self-reported health status.Three objectives were therefore successively pursued. These were: (1) to evaluate the accuracy, acceptance and usability of SCs in patients seeking rheumatology and emergency care; (2) to evaluate the accuracy, acceptance and usability of SSDs in patients with rheumatic diseases; and (3) to evaluate patient-reported electronic outcomes in patients with rheumatoid arthritis and axial spondyloarthritis.To achieve these objectives, we conducted 12 studies (including six randomized controlled trials) involving a total of 3971 participants (3356 patients presenting with rheumatological complaints, 450 patients admitted to the emergency department and 165 healthcare professionals). These studies have resulted in 20 scientific articles, 18 of which have been published in international peer-reviewed journals and 2 are currently submitted for publication.Our results indicate a high level of patient acceptance of SCs. However, their diagnostic accuracy is still highly inadequate, and their use tends to produce overdiagnosis and omission of certain diagnoses. More worryingly, SCs have failed in a substantial number of cases to diagnose life-threatening emergencies. In addition, our results underline a patient preference for the use of SSDs applied to the upper arm, judged to be less painful than traditional fingerpricking. Ultimately, granting rheumatologists access to patient-generated data from home, merging insights from symptom checkers and self-sampling devices, has markedly enhanced diagnostic accuracy. Employing machine learning algorithms to analyse patient symptom reports, along with the integration of imaging data, has further increased diagnostic accuracy. Moreover, the incorporation of electronic patient-reported outcomes (ePRO) alongside data on inflammatory markers obtained through SSDs has substantially decreased in-person consultations and released new resources.The findings of this doctoral study underscore the viability and promise of a digitally supported patient pathway. This pathway is particularly encouraging for managing individuals with chronic diseases such as rheumatic conditions however also for patients requiring emergency care
Gabriel, Aurélie. "Le mineur, quel acteur de santé ?" Paris 5, 2011. http://www.theses.fr/2011PA05D001.
Повний текст джерелаThe March 4th, 2002 law pertaining to patients’ rights and the quality of health care carved a special status for underage children. Indeed, the law sets up enhanced patient’s rights specifically designed for minors. The minor child is endowed with the right to receive medical information delivered in a manner consistent with his maturity. The child is further endowed with the right of consent consistent with his exercise of free will and ability to partake in the decision process. As a result, the child being under the legal age for majority does not systematically exclude him or her from the decision making process. Whereas the minor was traditionally excluded from the doctor-patient relationship in favor of his parents, he is henceforth granted to right to be an active participant to his own health care decision. To assimilate the minor’s patient right to legal competency would however be inaccurate. Indeed, the child’s own rights evolve with general patient’s rights. While such rights apply to him, the child nevertheless cannot exercise them for lack of legal competence. Exercise of those legal rights usually rests with the parents or legal guardians until such time as the child reaches the age of majority or is emancipated. Two kinds of rights thus show concomitant evolutions : Children specific rights they only can exercise, and general rights to be exercisedby parents or guardians. The entire problem consists then in determining the influence of these own rights on the general rights and to deduct the place from it and the role realities of the minor as actor of health. The challenge therefore consists in determining the influence of specific over general rights in the context of a minor’s health care decisions. As a general rule, the minor remains a decision maker within a framework. In principle, the exercise of parental general rights has priority over that of children specific ones. Yet, the law ensures the minor child’s right to his own health decision making. Children’s access to self-determination in health care does however conflict with the lack of legal competency, so that it allows in fine every minor to become an autonomous health care decision maker. From then on, it seems convenient to introduce a health care decision making authority increasing with age, leading to an early competency to make health care decision. Following the example of foreign legislation, the age of majority for health care could be set to thirteen
Linden, Caroline. "Pharmacien : acteur de santé, implication du pharmacien dans la prise en charge des usagers de drogues substituées." Paris 5, 1999. http://www.theses.fr/1999PA05P017.
Повний текст джерелаRomijn, François. "S’exposer en inquiétude. Le sujet fait et défait avec les médiations nouvelles sur sa santé." Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEH038.
Повний текст джерелаMore than ever before humans have access to new knowledge about their biological life (e.g., genes, biochemical marks influencing phenotypes, neurons, microbiota). This knowledge is progressively transfered out of laboratories and into commercial markets. Then, by means of an ever-increasing number of readily available mediations (e.g. direct-to-consumer (epi)genomic tests (DTC GT), health-related uses of the Internet, direct-to-consumer genomic tests, self-tracking applications on smartphones) layusers are connected to an increasingly diverse array of data (e.g., online diagnostics, genomic predispositions, probabilities, SNP’s). My doctoral thesis develops an investigation of the practices whereby individuals ensure continuity with others/themselves when confronted to new knowledge related to their biology. Knowing the so-called “real” or potential biological endowment of oneself but also of others has tremendous social, political and ethical consequences. These new reflexive technologies grant individuals with an objectifying image of their “identity”. These new objectifying data related to the biological self puts the subject to test. They confront them to inquietudes they have to cope with.Built on three fieldworks located in the field of health (the classic medical examination, health-related information on the Internet, health-related direct-to-consumer genomic tests), this research fosters a better understanding of this social phenomenon. My investigation specifically seeks to clarify the variety of ways that allow individuals to integrate these new data marked with a strong degree of realism. The approach set forth in this research revolves on a specific anthropological question: how human beings find arrangements with situations in which they are not only confronted to others but also with objectifying data related to their biological life? This anthropological problematic invites us to bring at least as much attention to what connects us with others than to the specific ways individuals ensure continuity with themselves in contexts where the “living” raises question. My research demonstrates that the conduct actually adopted by users of the three mediations studied is irreducible to the expected liberal autonomy often promoted in the literature as “management of one’s health”. A careful analysis of the subject’s consistence facing this new knowledge highlights social dynamics that have received little attention in the field of social sciences of health. The fieldworks carried out provide new insights on the human ability to bring together different positions or definitions of what is happening and/or who you are in order to arrange with these discoveries that challenge their subject consistency. Rather than considering the equivocal features and sometimes the outright ambiguity of the conducts as a failure of the analysis, this research effort contributes achieving a better understanding of the pervasiveness of composition in our relationship to our self and the others in social contexts related to biology
Bogaert, Brenda. "Patient Life Empowerment : Toward a Patient Developed Approach : Integrating epistemic contributions of refractory epilepsy patients in France and China through a method with emotions and a method with capabilities." Thesis, Lyon, 2020. http://www.theses.fr/2020LYSE3010.
Повний текст джерелаThe notion of patient empowerment is valued today as both a right and a responsibility. We ask doctors to help the patient participate and the patient to learn about and to manage the disease. However, the doctor-patient relationship continues to be a source of suffering for the patient, the healthcare provider, and for the family. An urgent task for public policymakers today is to create a facilitating environment for all types of patients. We propose two methods in philosophy inspired by American philosopher Martha Nussbaum, a method with emotions and a method with capabilities, to develop our patient empowerment approach. With her contribution, we develop a collaborative approach with our patients, the patient life empowerment approach. We consider the patient’s life holistically, including in relationships with their families, their doctors, and in society. With our approach, we advocate for a larger social responsibility to help patients to flourish
Cognard, Marion. "L'expérience de la parentalité de mères psychotiques : perspective des mères et des professionnels de santé La parentalité des mères psychotiques : une revue des facteurs de risque et de protection facteurs de protection dans les familles où les parents sont en prises avec des problèmes de santé mentale L’expérience de la parentalité de mères psychotiques La parentalité des mères psychotiques et sa prise en charge en psychiatrie vue par les professionnels de santé La perception des professionnels de santé face à la parentalité des mères présentant un trouble psychique." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCB152.
Повний текст джерелаThe parenting of psychotic mothers has become a social reality more frequent since the advent of neuroleptics and the development of extra-hospital care, but it remains little studied. Most research focuses on the risk factors and disabilities of mothers with psychotic disorders. To better understand the experience of parenting psychotic mothers, we conducted a research, combining qualitative and quantitative methods, with 18 mothers diagnosed with psychotic disorder and followed in adult psychiatry. We also interviewed 16 health professionals practicing in psychiatry to know their point of view and their representations on these parenting and their follow-up. We took a new perspective, focusing on the protective factors and the resilient process of psychotic mothers. We wanted to highlight the environmental factors that can help these mothers in their parenting role and explore their specific needs. Psychotic mothers and health professionals responded to a semi-directive interview. 6 scales were also submitted to the mothers to provide additional results to their testimony (SUMD disorder awareness scale, PSI parental stress scale, SSQ6 social support scale, RQ relationship attachment scale, PACOTIS parenting competence scale and RSA resilience scale). The results show that despite difficulties in managing the symptoms and the daily lives of their children, these mothers say they are satisfied with their parenting role. Nevertheless, the score on the parental stress scale is high among all of these mothers interviewed and the majority of mothers feel lonely and stuck in their role, while they all benefit from a particular support (family or professional). Although these aspects may be a negative aspect of their parenthood, it seems to be a protective factor in itself. Indeed, it promotes the search for social support, the monitoring of medical treatment and the feeling of having meaning in their lives. The results also show a strong positive correlation between the resilience score and the impression of being a good parent. The role of the environment is paramount in these situations. Yet many judgments are felt, especially during the announcement of pregnancy and can slow down the demand for help. The testimony of the professionals shows the representations existing around this question. While all professionals perceive the difficulties of these mothers, parenting skills are difficult to identify. This question seems little mentioned by adult psychiatry professionals for lack of interest or knowledge. However, as for the interviewed mothers, the professionals confirm the importance that this problem be treated by the psychiatric services. Specific accompaniments around parenting or training schemes were considered. The confrontation of the experiments also shows the limits related to the organization of the services and representations which make the handling of this problematic complex. These results therefore suggest the importance of an ecosystem approach to these parenting situations in order to foster a process of resilience for these mothers and families. Finally, they highlight the need to question new approaches that focus on the individual rather than the symptom such as empowerment or recovery programs so that mothers can develop their full inner potential
Книги з теми "Patient acteur de sa santé"
Carnet Naturopathies: Permet de Faire un Bilan de Santé Vitalite et Alimentaire de Votre Patient Lors de Sa Première Consultation, Idee de Cadeau de Noel, Femme et Enfant - Grand Format 21,59x27,94 Cm - 200 Pages. Independently Published, 2020.
Знайти повний текст джерелаPress, Healthy. Anamnèse Carnet Pour Naturopathes et Thérapeutes: Permet de Faire un Bilan de Santé Vitalite et Alimentaire de Votre Patient Lors de Sa Première Consultation, Idee de Cadeau de Noel, Femme et Enfant - Grand Format 21,59x27,94 Cm - 200 Pages. Independently Published, 2020.
Знайти повний текст джерелаЧастини книг з теми "Patient acteur de sa santé"
Lajoux, Christian. "Les laboratoires au chevet du patient : du fantasme à la démarche qualité ?" In De l'observance à la gouvernance de sa santé, 81. Presses Universitaires de France, 2007. http://dx.doi.org/10.3917/puf.laud.2007.01.0081.
Повний текст джерелаFOUCHER, S., J. B. LE-LOCH, A. DESBREST, L. GABILLY, H. LEFORT, and K. TAZAROURTE. "Catastrophe avec nombreuses victimes en milieu urbain." In Médecine et Armées Vol. 46 No.3, 213–24. Editions des archives contemporaines, 2018. http://dx.doi.org/10.17184/eac.7336.
Повний текст джерелаLarfouilloux, Julien. "E-santé : de nouveaux enjeux liés à l’émergence du numérique dans le rapport du patient‑citoyen à sa santé." In Santé, numérique et droit-s, 323–30. Presses de l’Université Toulouse 1 Capitole, 2018. http://dx.doi.org/10.4000/books.putc.4915.
Повний текст джерелаPloton, Louis. "Psychogérontologie clinique et pathologique." In Psychogérontologie clinique et pathologique, 35–42. In Press, 2019. http://dx.doi.org/10.3917/pres.menec.2019.02.0036.
Повний текст джерелаDurand, Nadine. "L'optimisation du circuit administratif du patient et sa participation à la performance d'une organisation au profit de l'usager." In Performance et innovation dans les établissements de santé, 207. Dunod, 2015. http://dx.doi.org/10.3917/dunod.fermo.2015.01.0207.
Повний текст джерелаLEBOEUF L’ANTHOËN, Isabelle, Marie DOBIGNIES, and Pascal ANTOINE. "Compassionate Mind Training." In Le patient et son entourage, 41–52. Editions des archives contemporaines, 2023. http://dx.doi.org/10.17184/eac.7536.
Повний текст джерелаCARFANTAN, C., J. P. EVEN, A. ANSELME, E. DULAURENT, J. BOISSI, C. BAYT, and J. BANCAREL. "Médecin inséré dans le poste de commandement interarmées de théâtre «Barkhane»." In Médecine et Armées Vol. 46 No.2, 99–106. Editions des archives contemporaines, 2018. http://dx.doi.org/10.17184/eac.7348.
Повний текст джерелаТези доповідей конференцій з теми "Patient acteur de sa santé"
Maizeray, S., H. Herry, G. Valette, and S. Boisramé. "Innovation dans la communication et la gestion du stress en chirurgie orale : méthode d’analyse ProcessCom®." In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206602003.
Повний текст джерелаRoume, M., S. Azogui-Lévy, G. Lescaille, V. Descroix, and J. Rochefort. "Connaissances, attitudes et pratiques en pathologie de la muqueuse buccale des chirurgiens-dentistes en France, enquête nationale." In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206602010.
Повний текст джерелаOujdad, S., S. Zafad, H. El Attar, and I. Ben Yahya. "Histiocytose langerhansienne de l’adulte : à propos d’un cas." In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206603013.
Повний текст джерела