Littérature scientifique sur le sujet « PATIENT'S INFORMATION »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Sommaire
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « PATIENT'S INFORMATION ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "PATIENT'S INFORMATION"
Rangkuti, A. Haris. « Deteksi 4 Tanda Vital Pasien Rumah Sakit Berbasis Fuzzy Database ». ComTech : Computer, Mathematics and Engineering Applications 4, no 1 (30 juin 2013) : 529. http://dx.doi.org/10.21512/comtech.v4i1.2799.
Texte intégralLytle, James H. « A Patient's Perspective on Health Information Management ». HLRP : Health Literacy Research and Practice 1, no 1 (1 mars 2017) : e11-e13. http://dx.doi.org/10.3928/24748307-20170307-03.
Texte intégralKumar, Jatinder, et Gagandeep Sharma. « Accessing Patient's Information Using Cloud Computing Solution ». INROADS- An International Journal of Jaipur National University 7, si (2018) : 34. http://dx.doi.org/10.5958/2277-4912.2018.00007.3.
Texte intégralKeizer, Mary. « Book Review : The Cancer Patient's Information Binder ». Journal of Palliative Care 7, no 4 (décembre 1991) : 58–59. http://dx.doi.org/10.1177/082585979100700416.
Texte intégralMauser-Bunschoten, E. P., M. J. Hamers, D. De Roode, G. Terlingen-Van Baaren, P. De Kleijn, R. Bos et H. M. Van Den Berg. « Improvement of patient education and information : development of a patient's information dossier ». Haemophilia 7, no 4 (12 juillet 2001) : 397–400. http://dx.doi.org/10.1046/j.1365-2516.2001.00517.x.
Texte intégralStevens, Stella. « Information sharing in health care : a patient's perspective ». Australian Health Review 29, no 4 (2005) : 398. http://dx.doi.org/10.1071/ah050398.
Texte intégralWarren, Emily, Katharine Footman, Michela Tinelli, Martin McKee et Cécile Knai. « Do cancer-specific websites meet patient's information needs ? » Patient Education and Counseling 95, no 1 (avril 2014) : 126–36. http://dx.doi.org/10.1016/j.pec.2013.12.013.
Texte intégralEstey, Angela, Alison Musseau et Linda Keehn. « Patient's understanding of health information : a multihospital comparison ». Patient Education and Counseling 24, no 1 (août 1994) : 73–78. http://dx.doi.org/10.1016/0738-3991(94)90027-2.
Texte intégralTiwari, Basant, et Vivek Tiwari. « An Intelligent Multi-Objective Framework of Pervasive Information Computing ». International Journal of Healthcare Information Systems and Informatics 13, no 4 (octobre 2018) : 15–27. http://dx.doi.org/10.4018/ijhisi.2018100102.
Texte intégralChien, Jen-Chien, Jeng-Pang Wang, Chien-Lung Cho et Fok-Ching Chong. « SECURITY BIOSIGNAL TRANSMISSION BASED ON FACE RECOGNITION FOR TELEMEDICINE ». Biomedical Engineering : Applications, Basis and Communications 19, no 01 (février 2007) : 63–69. http://dx.doi.org/10.4015/s1016237207000069.
Texte intégralThèses sur le sujet "PATIENT'S INFORMATION"
Engström, Birgitta. « Information to the patient : an attempt to satisfy the patient's need for information ». Doctoral thesis, Umeå universitet, Neurologi, 1986. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-100591.
Texte intégralS. 1-56: sammanfattning, s. 57-137: 4 uppsatser
digitalisering@umu
Isetta, Valentina. « Advances in the application of information and communication technologies in healthcare at the patient's home ». Doctoral thesis, Universitat de Barcelona, 2013. http://hdl.handle.net/10803/121468.
Texte intégralAndersson, Boman Oskar, et Andreas Eriksson. « Upplevelser av information på akutmottagningar ur ett patientperspektiv : En litteraturöversikt ». Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-384650.
Texte intégralBackground: Previous research has shown the importance of information for the patients care experience and safety. Still there is clear evidence that information is lacking at emergency departments [ED]. It is therefore important to gather patient experiences on the subject. Purpose: To investigate patient experiences of information in emergency departments. Method: Descriptive design with a literature review as method where 16 scientific qualitative original articles was analyzed. Results: Five themes was created: Initial care at the ED; following waiting time; condition and treatment; understanding and ability to remember; and final care at the ED. Both positive and negative experiences emerged. Most prominently was negative experiences regarding lack of information about subjects such as waiting times, condition and treatment. Conclusion: Information is a crucial part of the care at the ED and this study highlights its importance from the patient perspective. A lot of different experiences emerged in the result that displays the relevance of the problem area. The need of further research regarding patient experiences of information is considered needed. Flaws and opportunities for improvement has also been revealed by highlighting patient experiences, which may be of use for nurses in their profession.
Jacobsson, Annie, et Andreas Åkervall. « Informationsbehov : Hur tillfredställs patienters informationsbehov ? Är fokusgrupper användbar som metod ? » Thesis, Växjö University, School of Mathematics and Systems Engineering, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-95.
Texte intégralFör att få fram rätt information krävs en metod som belyser patienters behov och på så sätt kan hjälpa sjukvården att på bättre sätt ta hjälp av patienters åsikt. Syftet med uppsatsen är därför att få fram hur patienter upplever att deras informationsbehov av hälsoinformation tillfredställs. Vi vill även ta reda på hur detta behov ser ut idag och på vilka sätt det kan tillfredställas bättre.
Vi vill även testa om fokusgrupper är lämplig som metod för att besvara vårt syfte.
För att uppfylla syftet har vi samlat in data genom två fokusgrupper. En grupp bestod av personer med mer kontakt med sjukvården medan den andra bestod av personer med mindre kontakt med sjukvården. Med hjälp av resultatet från fokusgrupperna genomfördes en analys där vi fann områden som var särskilt viktiga. Vi har även utvärderat fokusgrupper som metod genom att jämföra med tidigare forskning inom området. Utifrån det insamlade materialet har vi utarbetat en modell som visar hur patienters informationsbehov kan tillfredställas. Denna modell är indelad i fyra delar utifrån hur stort behov patienten har av egen samt allmän information.
Wessman, Anja, et Sofie Börjesson. « Patienters upplevelser av kommunikation och information på akutmottagningen : en litteraturöversikt ». Thesis, Sophiahemmet Högskola, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:shh:diva-3675.
Texte intégralBackground: Patients are spending more time at the emergency department in 2018 compared to the previous year. They are often left alone for many hours while waiting for treatment or care. A lack of communication and information between healthcare professionals and patients might affect the patient's experience of the stay at the emergency department. The aim of the study was to describe patients’ experience of communication and information during a visit at the emergency department. The method used was a general literature review of both quantitative and qualitative articles. Sixteen articles were included. A content analysis was performed, including identifying meaning units, coding and synthesizing the content into categories. Results: Three main categories emerged: Experience of the organization, experience of the care environment and experience of the care relationship. Patients were in need of clearer information about the expected course of events and management. Also lack of communication such as updating of waiting times, examinations and test results were identified. The patients wanted more frequently interactions with the healthcare staff and could endure the waiting times if only they were given information about the delays. Conclusion: Patients might feel abandoned and forgotten at the emergency department. To use a person-centered care at an emergency department is a challenge, even if the need exists. An improved communication between nursing staff and patients might affect the patient's experience of emergency care in an already vulnerable situation.
Wong, Sau-Yee, et 黃秀怡. « Determinants of patient satisfaction towards medication information inSOPD patients : DISMIS study ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31972330.
Texte intégralWong, Sau-Yee. « Determinants of patient satisfaction towards medication information in SOPD patients DISMIS study / ». Click to view the E-thesis via HKUTO, 2004. http://sunzi.lib.hku.hk/hkuto/record/B31972330.
Texte intégralÅdahl, Kerstin. « Transparency of critical information for patient empowerment in eHealth / ». Karlskrona : Department of Interaction and System Design, Blekinge Institute of Technology, 2007. http://www.bth.se/fou/forskinfo.nsf/allfirst2/60e6233bfe16bde0c125739100510ccb?OpenDocument.
Texte intégralFram, Fawaz. « Patient information provision and involvement of patients by stroke professionals : implications for the patient-provider relationship ». Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/31381.
Texte intégralHerrera, De Leon Morayma, et Metin Bircan. « Individanpassad information till patienter med typ 2 diabetes : En litteraturstudie om patienters erfarenheter av information från sjukvården ». Thesis, Ersta Sköndal högskola, Institutionen för vårdvetenskap, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:esh:diva-2201.
Texte intégralBackground: Diabetes type 2 is one of the largest forms of lifestyle disease in the developed countries, but in later years, also in development countries. Patients are in need of accurate information to learn how to manage and live with the disease. Therefore it is important that nurses have knowledge of how patients perceive information from health care. Aim: The aim of the present study was to investigate what experiences patients with diabetes type two has regarding information from health care. Method: A literature study based on previous research regarding diabetes type two and information to patients. Twelve scientific articles with qualitative approach was analysed with text analysis. Result: The results show that the patients call for information that is tailored to them as unique individuals and that is easy to understand and adapt to, as they need tools for their self-care. Four themes emerged: Difficulties to accept and adapt to information, Information adapted to cope with daily life, Differences in information from the physician and the nurse and Accessible information. Discussion: The results are discussed in relation to Orem theory of self-care. Since patients often have difficulty adjusting to their disease, they need support in terms of information to be able to live as normal a life as possible. This becomes increasingly important, as diabetes type two is a disease that younger and younger ages, and it is therefore something they have to live a long time with.
Livres sur le sujet "PATIENT'S INFORMATION"
Kiley, Robert. The patient's internet handbook. London : Royal Society of Medicine, 2002.
Trouver le texte intégralFreed, Melvyn N. The patient's desk reference : Where to find answers to medical questions. New York : Macmillan Pub. Co., 1994.
Trouver le texte intégralA patient's right to know : Information disclosure, the doctor and the law. Aldershot, Hants, England : Dartmouth, 1989.
Trouver le texte intégralMcLean, Sheila A. M. A patient's right to know : Information disclosure, the doctor and the law. Aldershot : Dartmouth, 1989.
Trouver le texte intégralAssociation of British Pharmaceutical Industry. et Long-Term Medical Conditions Alliance, dir. Medicines & patients : Patient information. London : Association of the British Pharmaceutical Industry, 1997.
Trouver le texte intégralHarvey, L. Pre-operative visits in preparation for surgery : The effect of pre-operative information on the patient's satisfaction withcare. [Larne] : [Moyle Hospital], 1990.
Trouver le texte intégralGreat Britain. Department of Health. et Great Britain. Central Office of Information., dir. The Patient's charter and family doctor services : [prepared by the Department of Health and Central Office of Information]. [London] : HMSO, 1993.
Trouver le texte intégralCorbett, Margo. The savvy patient's toolkit : A comprehensive guide to better health care through the right information, in the right way, at the right time. West Conshohocken, PA : Infinity Publishing.com, 2008.
Trouver le texte intégralHarvey, Lindsay. Pre-operative visits in preparation for surgery : The effect of pre-operative information on the patient's satisfaction with care. [Whiteabbey] : Loughside Unit of Management, NHSSB, 1990.
Trouver le texte intégralAl-Amer, Khalifa Ahmed. Development of a hospital information system to improve patient's admission, transfer and discharge activitieswithin the Ministry of Health in Bahrain. Salford : University of Salford, 1992.
Trouver le texte intégralChapitres de livres sur le sujet "PATIENT'S INFORMATION"
Cremerius, Jonas, Maximilian König, Christian Warmuth et Mathias Weske. « Patient Discharge Classification Based on the Hospital Treatment Process ». Dans Lecture Notes in Business Information Processing, 314–26. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-98581-3_23.
Texte intégral« Right To Information ». Dans Patient's Interest First, 53–59. WORLD SCIENTIFIC / S'PORE UNIV PRESS (PTE) LTD, 1998. http://dx.doi.org/10.1142/9789812816030_0005.
Texte intégralFoa, Edna B., Kelly R. Chrestman et Eva Gilboa-Schechtman. « Gathering Information Module ». Dans Prolonged Exposure Therapy for Adolescents with PTSD Therapist Guide, 75–80. Oxford University Press, 2008. http://dx.doi.org/10.1093/med:psych/9780195331745.003.0006.
Texte intégralTiwari, Basant, et Vivek Tiwari. « An Intelligent Multi-Objective Framework of Pervasive Information Computing ». Dans Data Analytics in Medicine, 456–69. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-1204-3.ch025.
Texte intégralSultana, H. Parveen, et Nalini Nagendran. « Mobile Patient Surveillance ». Dans Advances in Healthcare Information Systems and Administration, 58–84. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-5036-5.ch005.
Texte intégralVaz, Nafisa Fatima Maria. « Patient Satisfaction ». Dans Advances in Healthcare Information Systems and Administration, 186–200. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-3946-9.ch010.
Texte intégralElgujja, Abba Amsami. « Impact of Information Technology on Patient Confidentiality Rights ». Dans Research Anthology on Securing Medical Systems and Records, 788–810. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-6684-6311-6.ch037.
Texte intégralElgujja, Abba Amsami. « Impact of Information Technology on Patient Confidentiality Rights ». Dans Advances in Medical Technologies and Clinical Practice, 365–87. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-0047-7.ch018.
Texte intégralShah, Mohd Asif, et Ramesh Sekaran. « The AI-Based COVID-19 Personal Protective Equipment Is Smarty and Secure ». Dans Advances in Healthcare Information Systems and Administration, 125–36. IGI Global, 2023. http://dx.doi.org/10.4018/978-1-6684-6894-4.ch007.
Texte intégralAlsalamah, Shada, Hessah Alsalamah, Alex W. Gray et Jeremy Hilton. « Information Security Threats in Patient-Centred Healthcare ». Dans Advances in Healthcare Information Systems and Administration, 298–318. IGI Global, 2016. http://dx.doi.org/10.4018/978-1-4666-9861-1.ch015.
Texte intégralActes de conférences sur le sujet "PATIENT'S INFORMATION"
Otani, Kagari, et Yasunobu Ito. « Acquisition and sharing of knowledge and skills of visiting nurses in Japan ». Dans 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002554.
Texte intégralNwosu, Kingsley C., et Okey Igbonagwam. « None invasive biometrie for patient information satisfying patient's security concerns ». Dans 2016 IEEE Symposium on Technologies for Homeland Security (HST). IEEE, 2016. http://dx.doi.org/10.1109/ths.2016.7568900.
Texte intégralSivaranjani, B., et N. Radha. « Securing patient's confidiential information using ECG steganography ». Dans 2017 2nd International Conference on Communication and Electronics Systems (ICCES). IEEE, 2017. http://dx.doi.org/10.1109/cesys.2017.8321135.
Texte intégralBarinov, Evgeny, Nadezhda Dobrovolskaya, Anastasia Ivanova, Ruslan Kalinin, Alexander Manin, Natalya Mikheeva et Pavel Romodanovsky. « Patient dissatisfaction with medical dental care ». Dans Issues of determining the severity of harm caused to human health as a result of the impact of a biological factor. ru : Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/conferencearticle_5fdcb03a353ad3.76128786.
Texte intégralKim, Jonghyeok, Hosung Kwon, Jonghyeon Kim, Jinsoo Park, Soong-Un Choi et Sookyung Kim. « PillGood : Automated and Interactive Pill Dispenser Using Facial Recognition for Safe and Personalized Medication ». Dans Thirty-First International Joint Conference on Artificial Intelligence {IJCAI-22}. California : International Joint Conferences on Artificial Intelligence Organization, 2022. http://dx.doi.org/10.24963/ijcai.2022/854.
Texte intégralAhmed, Ejaz, Nik Bessis et Yong Yue. « Customizing interactive patient's diagnosis user interface ». Dans 2010 Fifth International Conference on Digital Information Management (ICDIM). IEEE, 2010. http://dx.doi.org/10.1109/icdim.2010.5664654.
Texte intégralKrey, Mike, et Ruben Ramirez Garcia. « Voice Assistants in Healthcare : The Patient's Perception ». Dans 2022 8th International Conference on Information Management (ICIM). IEEE, 2022. http://dx.doi.org/10.1109/icim56520.2022.00029.
Texte intégralGuiling, Li, Zhang Chundi, Ming Yue, Yang Liqun et Zhang Lihua. « Modeling of Hypertensive Patient's Behavior Based on the Health Information ». Dans 2015 Seventh International Conference on Measuring Technology and Mechatronics Automation (ICMTMA). IEEE, 2015. http://dx.doi.org/10.1109/icmtma.2015.165.
Texte intégralMo, Zhiwei. « On the Product Service System Design of Diabetes Management for Patients ». Dans Human Interaction and Emerging Technologies (IHIET-AI 2022) Artificial Intelligence and Future Applications. AHFE International, 2022. http://dx.doi.org/10.54941/ahfe100922.
Texte intégralEls, Floyd, et Liezel Cilliers. « Improving the information security of personal electronic health records to protect a patient's health information ». Dans 2017 Conference on Information Communication Technology and Society (ICTAS). IEEE, 2017. http://dx.doi.org/10.1109/ictas.2017.7920658.
Texte intégralRapports d'organisations sur le sujet "PATIENT'S INFORMATION"
Haut, Elliott, Brandyn Lau, Deborah Hobson, Dauryne Shaffer, Peggy Kraus, Jonathan Aboagye, Norma Farrow et al. Preventing Venous Thromboembolism : Empowering Patients and Enabling Patient-Centered Care via Health Information Technology. Patient-Centered Outcomes Research Institute (PCORI), novembre 2018. http://dx.doi.org/10.25302/11.2018.ce.12114489.
Texte intégralMcCullough, Jeffrey, Stephen Parente et Robert Town. Health Information Technology and Patient Outcomes : The Role of Organizational and Informational Complementarities. Cambridge, MA : National Bureau of Economic Research, janvier 2013. http://dx.doi.org/10.3386/w18684.
Texte intégralYuan, Bo, Wei Cao, Xieyu Zhang, Yue Yang et Jiahe Zhao. Telemedicine effect on rheumatoid arthritis : A protocol for a systematic review and meta-analysis of randomized controlled trials. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, janvier 2022. http://dx.doi.org/10.37766/inplasy2022.1.0109.
Texte intégralFrakes, Michael, Jonathan Gruber et Anupam Jena. Is Great Information Good Enough ? Evidence from Physicians as Patients. Cambridge, MA : National Bureau of Economic Research, juillet 2019. http://dx.doi.org/10.3386/w26038.
Texte intégralFang, Mingxing, Yan Li, Qi Zhang, Na LIu, XIaoyan Tan et Hai Yue. The effect of driving pressure-guided ventilation strategy on the patients with mechanical ventilation : A Meta-Analysis of Randomized Controlled Trial. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, avril 2022. http://dx.doi.org/10.37766/inplasy2022.4.0113.
Texte intégralSadeghsalehi, Hamidreza, Parinaz Onikzeh, Afshin Heidari, Aida Kazemi, Parisa Najjariasl, Kamran Dalvandi et Hadi Zamanian. Application of smartphone apps in assessment after spine surgeries : a systematic review protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, octobre 2021. http://dx.doi.org/10.37766/inplasy2021.10.0054.
Texte intégralAlves-Nogueira, Ana Cláudia, Ana Carolina Góis, Maria Cristina Canavarro, Cláudia Melo et Carlos Carona. Examining the associations between physician-patient communication and adjustment outcomes of patients and physicians : A systematic review protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, juin 2022. http://dx.doi.org/10.37766/inplasy2022.6.0062.
Texte intégralGallegos, J., V. Hamilton, T. Gaylor, K. McCurley et T. Meeks. Information integrity and privacy for computerized medical patient records. Office of Scientific and Technical Information (OSTI), septembre 1996. http://dx.doi.org/10.2172/392809.
Texte intégralRogalska, Marta, Lukasz Antkowiak, Anna Kasperczuk, Wojciech Scierski et Maciej Misiolek. Transoral robotic surgery in the management of submandibular gland sialoliths : a systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, mars 2023. http://dx.doi.org/10.37766/inplasy2023.3.0068.
Texte intégralBerkman, Nancy D., Eva Chang, Julie Seibert, Rania Ali, Deborah Porterfield, Linda Jiang, Roberta Wines, Caroline Rains et Meera Viswanathan. Management of High-Need, High-Cost Patients : A “Best Fit” Framework Synthesis, Realist Review, and Systematic Review. Agency for Healthcare Research and Quality (AHRQ), octobre 2021. http://dx.doi.org/10.23970/ahrqepccer246.
Texte intégral