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Artykuły w czasopismach na temat "Gouvernance des données – Aspect médical"
Önen, Melek, Francesco Cremonesi i Marco Lorenzi. "Apprentissage automatique fédéré pour l’IA collaborative dans le secteur de la santé". Revue internationale de droit économique XXXVI, nr 3 (21.04.2023): 95–113. http://dx.doi.org/10.3917/ride.363.0095.
Pełny tekst źródłaAmat, Philippe. "À la recherche d’un équilibre dans les décisions thérapeutiques. L’exemple du traitement des malocclusions de classe II chez l’enfant et l’adolescent". L'Orthodontie Française 87, nr 4 (grudzień 2016): 375–92. http://dx.doi.org/10.1051/orthodfr/2016042.
Pełny tekst źródłaPerrot, S., P. Louis, J. Y. Milon i H. Bismut. "Automédication de la douleur : état des lieux, enjeux et rôle attendu du pharmacien dans le parcours de soins". Douleur et Analgésie 34, nr 2 (19.05.2021): 104–13. http://dx.doi.org/10.3166/dea-2021-0147.
Pełny tekst źródłaUrquijo, Laura Gómez. "La conexión entre política de cohesión y gobernanza económica en la UE: Eficiencia del nuevo marco para abordar las consecuencias de la crisis". Regions and Cohesions 5, nr 3 (1.12.2015): 44–62. http://dx.doi.org/10.3167/reco.2015.050304.
Pełny tekst źródłaLeclerc, Véronique, Alexandre Tremblay i Chani Bonventre. "Anthropologie médicale". Anthropen, 2020. http://dx.doi.org/10.17184/eac.anthropen.125.
Pełny tekst źródłaRozprawy doktorskie na temat "Gouvernance des données – Aspect médical"
Azzi, Rita. "Blockchain Adoption in Healthcare : Toward a Patient Centric Ecosystem". Electronic Thesis or Diss., Institut polytechnique de Paris, 2023. http://www.theses.fr/2023IPPAT053.
Pełny tekst źródłaThe healthcare sector evolves constantly, driven by technological advancement and innovative solutions. From remote patient monitoring to the Internet of Things (IoT), Artificial Intelligence (AI), personalized medicine, mobile health, and electronic records systems, technology has improved patient outcomes and enhanced care delivery. These technologies have shifted the healthcare ecosystem to be more patient-centered, focusing on meeting the patient's needs rather than the needs of the individual organizations within it. However, this transformative shift experienced by the healthcare industry is associated with multiple challenges due to the inherent complexity and fragmentation of the healthcare ecosystem. This dissertation addresses three healthcare ecosystem challenges that significantly impact patients. The first challenge addressed is the problem of counterfeit or falsified drugs that represent a threat to public health, resulting from the vulnerabilities in the pharmaceutical supply chain, notably centralized data management and the lack of transparency. The second challenge addressed is the problem of healthcare data fragmentation that thwarts care coordination and impacts clinical efficiency. This problem results from the dynamic and complex patients' journey in the healthcare system, shaped by their unique health needs and preferences. Patient data are scattered across multiple healthcare organizations within centralized databases and are ruled by policies that hinder data sharing and patients' empowerment over their data. The third challenge addressed is the confidentiality and privacy of healthcare data that, if compromised, shatter the trust relationship between patients and healthcare stakeholders. This challenge results from the healthcare organizations' poor data governance that increases the risk of data breaches and unauthorized access to patient information.The blockchain has emerged as a promising solution to address these critical challenges. It was introduced into the healthcare ecosystem with the promise of enforcing transparency, authentication, security, and trustworthiness. Through comprehensive analysis and case studies, this dissertation assesses the opportunities and addresses the challenges of adopting the blockchain in the healthcare industry. We start with a thorough review of the state of the art covering the blockchain's role in improving supply chain management and enhancing the healthcare delivery chain. Second, we combine theoretical and real-world application studies to develop a guideline that outlines the requirements for building a blockchain-based supply chain. Third, we propose a patient-centric framework that combines blockchain technology with Semantic technologies to help patients manage their health data. Our fourth contribution presents a novel approach to data governance by developing a blockchain-based framework that improves data security and empowers patients to participate actively in their healthcare decisions. In this final contribution, we widen the scope of the proposed framework to include a roadmap for its adoption across diverse domains (banking, education, transportation, and logistics, etc.)
Laboile, Xavier. "Aspects juridiques et éthiques du recueil des données médicales aux fins d'analyses épidémiologiques". Bordeaux 4, 2000. http://www.theses.fr/2000BOR40001.
Pełny tekst źródłaFayard, Jean-Dominique. "Données électrocardiographiques d'une population de 950 marathoniens et de 61 coureurs de 100 km". Bordeaux 2, 2000. http://www.theses.fr/2000BOR2M109.
Pełny tekst źródłaNgo, Thanh Nghi. "Une approche PLM pour supporter les collaborations et le partage des connaissances dans le secteur médical : Application aux processus de soins par implantation de prothèses". Thesis, Ecole centrale de Nantes, 2018. http://www.theses.fr/2018ECDN0013/document.
Pełny tekst źródłaMedical sector is a dynamic domain that requires continuous improvement of its business processes and assistance to the actors involved. This research focuses on the medical treatment process requiring prosthesis implantation. The specificity of such a process is that it makes in connection two lifecyclesbelonging to medical and engineering domains respectively. This implies several collaborative actions between stake holders from heterogeneous disciplines. However, several problems of communication and knowledge sharing may occur because of the variety of semantic used and the specific business practices in each domain. In this context, this PhD work is interested in the potential of knowledge engineering and product lifecycle management approaches to cope with the above problems. To do so, a conceptual framework is proposed for the analysis of links between the disease (medicaldomain) and the prosthesis (engineering domain) lifecycles. Based on this analysis, a semantic ontology model for medical domain is defined as part of a global knowledge-based PLM approach proposition. The application of the proposition is demonstrated through an implementation of useful function in the AUDROS PLM software
Bernard, Françoise. "Un système d’information collaboratif en appui à la gouvernance des territoires d’action agro-environnementale à enjeu eau-pesticides". Thesis, Paris, Institut agronomique, vétérinaire et forestier de France, 2017. http://www.theses.fr/2017IAVF0022.
Pełny tekst źródłaDiffuse pollution generated by pesticides is a major problem both for aquatic ecosystems and human health. Despite years of efforts by policy-makers to limit their use and impact, the volumes of chemicals used by farmers have remained the same, and even increased in some areas, with no reduction in their presence in water. To address this situation, public policy is aiming to become more effective by using more localised, participative solutions. Local stakeholders in charge of action plans are looking for decision tools to help them assess the potential impact of agro-environmental measures, as well as applying them to the best areas. The aim of this thesis is to develop a tool suitable for this purpose, namely a multi-scale collaborative information system. The first main contribution made by this thesis is the creation of "SIGPA" (Information System for Action Plan Governance), which models assisted governance in pesticide action programs in various contexts. The second contribution is a method for modelling exchanges of information within a network of institutional stakeholders, based on a "Grenelle" action plan in the Charente river basin. The "Stakeholder" model represents exchanges between stakeholders, as well as the production of the information available within their networks. The third contribution is the "Scenario" model, which organises information in order to aid decision making based on possible developments in agriculture in the area studied. The fourth contribution is the design of a method by which to identify agricultural systems and practices and assess future developments in agriculture. The fifth and final contribution of this thesis is the creation of a spatial data warehouse and the use of a number of multidimensional cubes to represent stakeholders’ needs at various scales. The conceptual models presented provide an interactive way to discuss the most effective and least expensive ways of limiting pesticide pollution within the stakeholder network. A prototype of the spatial data warehouse has been implemented using field data collected within the BAC Coulonge action plan and the outputs discussed with stakeholders. By allowing for data and knowledge from stakeholder networks in multiple action plans to be pooled, the SIGPA approach is in keeping with the OSAGE model (Loireau et al, 2017), which provides the making process of an agro-environmental and multifunctional observatory
Schieber, Anne-Cécile. "Étude de la relation patient-médecin généraliste : quel éclairage sur les inégalités sociales de santé ? : analyse des données épidémiologiques et des productions interdisciplinaires issues du projet INTERMEDE". Toulouse 3, 2014. http://thesesups.ups-tlse.fr/2418/.
Pełny tekst źródłaThe work produced in this dissertation aims to understand mechanisms' communication at play during the interaction between a patient and his - or her - general practitioner (GP) which could contribute to social inequalities in health. It uses the qualitative and quantitative data of the project INTERMEDE. The epidemiological analysis reveal the influence of the gender concordance/discordance between patients and GPs on their disagreement on the advice given during the consultation, and the role played by a social distance perceived by the physician on their disagreement on patients' perceived health status. The interdisciplinary analysis have been conducted within an innovate methodology inspired from the Delphi technique. It led to a core of shared knowledge, revealing the convergence of different disciplinary approaches
Kudjawu, Yao Cyril. "Délais d’accès au traitement des patients atteints de cancers en France et impact des inégalités sociales de santé : étude à partir des bases de données médico-administratives". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS023/document.
Pełny tekst źródłaBackground: timeliness of cancer treatment is an important aspect of health quality. Care centers are expected to treat a growing number of patients with cancer. Our objectives were to examine treatment times from diagnosis to first-course therapy for patients with colon (CC), rectum-anus (RC), and lung (LC) cancers and assess factors associated with time to-treatment and the impact of deprivation index.Methods: using the international classification of diseases and medical procedures codes, from national hospital discharge database which has been crossed with long term illness data and French deprivation Index information, we selected patients newly diagnosed for CC, RC or LC in 2009-2010 who had undergone treatment.Results: We included 15,694, 6,623 and 14,596 patients diagnosed and treated for CC, RC and LC respectively. Median times from endoscopy to: 1) surgery in patients with a surgical treatment pathway for CC, RC, and LC were 22 (Q25 = 14; Q75 = 34), 97 (Q25 = 34; Q75 = 141), and 44 (Q25 = 26; Q75 = 82) days, respectively; 2) to chemotherapy for patients with a non-surgical treatment pathway, for CC, RC, and LC were 36 (Q25 = 21; Q75 = 59), 40 (Q25 = 27; Q75 = 59), and 33 (Q25 = 22; Q75 = 49) days respectively; 3) to radiotherapy in RC and LC patients were 53 (Q25 = 39; Q75 = 78) and 88 (Q25 = 46; Q75 = 162) days respectively; 4) to first treatment, irrespective of pathway and treatment combination for CC, RC and LC were 23 (Q25 = 14; Q75 = 35), 43 (Q25 = 27; Q75 = 74), and 34 (Q25 = 22; Q75 = 50) days respectively.Time to first treatment vary across regions. It was longer in most northern regions and in overseas districts and shorter in Île-de-France, southern, eastern and sometimes in western regions for the three cancers. In multilevel analysis, Age and status of the first care center were significantly associated to time to first treatment in CC patients. Similar factors, including Deprivation index, were significantly associated to time to first treatment in RC and LC patients. The time to first treatment increased with age. It was higher in public hospitals compared to private hospitals and low in patients with low deprivation index compared to patients with high deprivation index. Conclusion: To our knowledge, this is the first study based on medico-administrative database describing time to first treatment after endoscopy in patients suffering from cancers in France. The results, which will complement those from cancer registry data and regional networks of cancerology, could inform decision-making policies on the implementation of guidelines on timeframes for cancer treatment access
Lourdais, Chloé. "Optimisation d'une interface numérique de santé à distance pour une meilleure expérience-patient". Electronic Thesis or Diss., Ecole centrale de Nantes, 2022. http://www.theses.fr/2022ECDN0054.
Pełny tekst źródłaRemote health services, in a medical or well-being context, are currently growing rapidly, raising new challenges. Through the use of digital health interfaces (apps, connected devices or websites), these services are increa-singly integrated into the daily lives of patients, at home and without medical support, changing the way they consult their health data. This research work investigates the emotional impact of the consultation of sensitive personal data and aims at improving the patient expe-rience in the use of health interfaces. A first experiment assessed emotional res-ponses to the consultation of health data. The results showed the impacts on the perceived stress, the duration of the data consultation and the cardiac activity of the participants, sug-gesting the need to consider emotions in the design of remote health tools. A patient-centered design method of a health interface is then proposed. It includes: a cul-tural comparison of existing tools, a survey on patients' expériences and preferences, and an experiment based on an Interactive Genetic Algorithm optimizing the interface design to im-prove patient satisfaction. The representation of blood sugar data on a diabetes app is used as an application case. The results show the interest of optimizing health interface to im-prove patient experience and encourage heal-thy behaviors. Customization of these interfa-ces to meet individual needs is also suggested
Książki na temat "Gouvernance des données – Aspect médical"
Commission du droit du Canada. Gouvernance de la recherche en santé avec des sujets humains (RSSH). Ottawa, Ont: Commission du droit du Canada, 2000.
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