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Gotowa bibliografia na temat „PATIENT'S INFORMATION”

Autor: Grafiati

Data publikacji: 11 września 2023

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Artykuły w czasopismach na temat "PATIENT'S INFORMATION"

Rangkuti, A. Haris. "Deteksi 4 Tanda Vital Pasien Rumah Sakit Berbasis Fuzzy Database". ComTech: Computer, Mathematics and Engineering Applications 4, nr 1 (30.06.2013): 529. http://dx.doi.org/10.21512/comtech.v4i1.2799.

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To assist the performance of medical technicians in nursing patients effectively and efficiently, information technology appears as a dominant support. Utilizing information technology, patient’s diagnoses can be reported to a doctor as soon as possible, as well as the patient's condition which needs to be monitored regularly. It is necessary to build a monitoring information system of hospital that is able to present timely information regarding the patient's condition characterized by four vital signs which are temperature, blood pressure, pulse, and respiration. For the four vital signs monitoring, fuzzy logic concept is implemented. If vital signs approach 1, the patient is close to recovery. Conversely, if the signs are 0, the patient still needs medical treatment. This system also helps nurses in order to provide answers to the families of patients who want to know the development of the patient's condition, as well as the recovery based on the average percentage of Fuzzy max of four vital signs. By Fuzzy-based monitoring system, monitoring the patient's condition becomes simpler and easier.

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Lytle, James H. "A Patient's Perspective on Health Information Management". HLRP: Health Literacy Research and Practice 1, nr 1 (1.03.2017): e11-e13. http://dx.doi.org/10.3928/24748307-20170307-03.

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Kumar, Jatinder, i 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.

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Keizer, Mary. "Book Review: The Cancer Patient's Information Binder". Journal of Palliative Care 7, nr 4 (grudzień 1991): 58–59. http://dx.doi.org/10.1177/082585979100700416.

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Mauser-Bunschoten, E. P., M. J. Hamers, D. De Roode, G. Terlingen-Van Baaren, P. De Kleijn, R. Bos i H. M. Van Den Berg. "Improvement of patient education and information: development of a patient's information dossier". Haemophilia 7, nr 4 (12.07.2001): 397–400. http://dx.doi.org/10.1046/j.1365-2516.2001.00517.x.

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Stevens, Stella. "Information sharing in health care: a patient's perspective". Australian Health Review 29, nr 4 (2005): 398. http://dx.doi.org/10.1071/ah050398.

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When it comes to getting ideas for improvement, no vantage point in health care is better than the horizontal position.1 THERE ARE FEW INDUSTRY SECTORS more in need of better solutions to information sharing and knowledge management than health care. The issues surrounding information management in the health care sector are pressing and complex. This paper explores my subjective experience of information sharing as a patient within a medium-sized Australian public hospital and illustrates the potential impact on safety and quality. I am a health services researcher. My case was not urgent or complex, I am not disadvantaged or seriously ill, and the hospital?s waiting list for the procedure was short. The outcome of the surgery was good and my satisfaction high. The case is, however, extremely pertinent to the current debate around information sharing in health care.

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Warren, Emily, Katharine Footman, Michela Tinelli, Martin McKee i Cécile Knai. "Do cancer-specific websites meet patient's information needs?" Patient Education and Counseling 95, nr 1 (kwiecień 2014): 126–36. http://dx.doi.org/10.1016/j.pec.2013.12.013.

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Estey, Angela, Alison Musseau i Linda Keehn. "Patient's understanding of health information: a multihospital comparison". Patient Education and Counseling 24, nr 1 (sierpień 1994): 73–78. http://dx.doi.org/10.1016/0738-3991(94)90027-2.

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Tiwari, Basant, i Vivek Tiwari. "An Intelligent Multi-Objective Framework of Pervasive Information Computing". International Journal of Healthcare Information Systems and Informatics 13, nr 4 (październik 2018): 15–27. http://dx.doi.org/10.4018/ijhisi.2018100102.

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This article describes how electronic healthcare has been the key application of pervasive computing innovations to enhance healthcare quality and protect human lives. Specific patients of constant sicknesses and elderly individuals, by and large, may oblige continuous observing of their wellbeing status wherever they are. In this regard, remote patient monitoring technology plays the various important role through wearable devices to monitor patient's physiological figures. But, this must ensure some broad issues like, wearability, adaptability, interoperability, integration, security, and network efficiency. This article proposes a data-driven multi-layer architecture for pervasively remote patient monitoring that incorporates aforesaid issues. It enables the patient's care at the real time and supports anywhere and anytime requirement with using network infrastructure efficiently.

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Chien, Jen-Chien, Jeng-Pang Wang, Chien-Lung Cho i Fok-Ching Chong. "SECURITY BIOSIGNAL TRANSMISSION BASED ON FACE RECOGNITION FOR TELEMEDICINE". Biomedical Engineering: Applications, Basis and Communications 19, nr 01 (luty 2007): 63–69. http://dx.doi.org/10.4015/s1016237207000069.

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In telemedicine, an insecure and vulnerability medicine information system is important for nursing staff and patients. Relatively private information stolen by others still can be corrected. However, if attacked by hackers, mistakes in diagnosis can threaten the patient's life. In order to simplify the procedures in the authentication of telemedicine and to emphasize security in the patient's data, this paper proposes utilizing the symmetric key cryptography and the biometric authentication. We use a face eigenvector to insert the patient's physiological signals and to combine symmetric key cryptography thus protecting the integrity of the patient's data and improving the mode of operations.

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Rozprawy doktorskie na temat "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.

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Dissatisfaction with medical information is a common problem among patients. There is also evidence that patients lack information that physicians believe they have given to the patient. The aims of this study were to 1) survey patients' subjective need for, and satisfaction with, the information that they received during their hospital stay 2) develop and evaluate systematic routines for giving information to the patients and also communication and collaboration between the medical and nursing staff concerning the satisfaction of the patients' need for information. The study was an intervention project and the research perspective was organizational psychology. Survey study. The patients experienced a considerable need for medical information, especially about the examination results and prognosis. The patients' need for information regarding prognosis was the least satisfied. Intervention 1. A general improvement of the information to the patients occurred when the systematic routines were established. The patients' subjective need for information was unchanged throughout two years. Their satisfaction with information, after an initial improvement, did not increase throughout these two years. There was low correlation between the patients' and their physicians' estimations concerning the patients' need for information on diagnosis, prognosis and examination results. Likewise, concerning the adequacy of that information. Intervention 2. Communication and collaboration between the medical and nursing staff included a system for assessment and solution of the patients' information problems. Problem-solving took place at a multidisciplinary team conference (MTC). Medical problems were better elucidated than the patients' psychological problems. After training of registered nurses (RN) as conference chairpersons, the patients need for information was better understood. The staff reported 42 information problems after training compared to two before. For half of the information problems decisions were discussed on steps to be taken in order to satisfy the patients' need for information. A year after the system for assessment and solution of information problems was established, the patients were more satisfied with information about examinations and their results and on information about medication (p< 0.05). Further, new norms for the patients' need for information were established and a change was initiated. The results are discussed with regard to how and why patients' shall have information, by whom and to whom information shall be given, when and where information shall be given and which content it shall have.

S. 1-56: sammanfattning, s. 57-137: 4 uppsatser

digitalisering@umu

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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.

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INTRODUCTION The pressure to contain health costs, particularly by avoiding hospitalizations and promoting the early discharge of patients, is generating a greater demand for home healthcare at a time when this resource is rapidly becoming less available. Telemedicine has been defined as the use of information and communications technologies (ICT), to deliver health services and transmit health information at distance for the purpose of improving patient’s care and education and to facilitate communication between patients and healthcare professionals. Most of the studies on telemedicine showed a lot of potentialities and possibilities, but did not develop further in the clinical routine because of problems and difficulties involving the use of this technology. Therefore, it seems clear the need of simple and straightforward applications, which can provide useful and widely applicable services to healthcare and as well as reliable data to assess the actual impact of telemedicine on homecare. 2) GENERAL AIM To design, develop, validate and assess the benefit of new Information and Communication Technology (ICT) applications in healthcare at patient’s home. 3) HYPOTHESES 1. An Internet-based support system for monitoring newborn patients after discharge from nursery would improve care, be well accepted by parents and reduce unplanned healthcare, particularly visits to the emergency department; 2. The development of a specific web-based tool could introduce a new strategy for the continuous positive airway pressure (CPAP) therapy follow-up of patients with obstructive sleep apnea syndrome (OSAS), which could improve the CPAP compliance, reduce face-to-face clinical visits, and be more cost-effective; 3. A new telemedicine system for remote CPAP therapy monitoring could provide valuable and useful data about treatment compliance and efficacy for the follow-up of OSAS patients. 4) STUDY 1 - A new Internet-based monitoring tool for the neonatal home care after discharge was successfully developed; - This new monitoring approach resulted in a high level of parental satisfaction with the service; - Using a societal perspective, the cost of the Internet-based follow-up resulted much lower than that of the conventional hospital-based follow-up. Additionally, ED visits in the first month of patients’ life decreased with the use of the Internet-based monitoring system. This telemedicine follow-up strategy proved absolute dominance (both more clinically effective and less costly) over the standard follow-up based on hospital visits; - This Internet-based tool has been effectively transferred to the health system since it is in routine clinical use at the Hospital de Sant Pau in Barcelona (www.petitsacasa.santpau.cat). 5) STUDY 2 - The opinion of the interviewed patients and medical staff about the helpfulness and satisfaction of the telemedicine monitoring approach indicated that the web-based support tool together with the televisit are potentially useful to support the home follow-up of CPAP treatment in OSAS patients; - The high patients’ compliance to the remote monitoring through the online questionnaire suggested this strategy to be helpful and practical for the long-period CPAP therapy control; - The multicenter support system we developed represents a new telemedicine approach to CPAP therapy follow-up for OSAS patients, which seeks enforcing patients’ confidence and improving therapy adherence; - The developed telemedicine support system has been effectively transferred to the health system since it is in use in a multinational clinical trial currently involving 18 hospitals (www.mi-cpap.com). 6) STUDY 3 - The geometry of the telemonitoring device (NOWAPI) does not influence the CPAP treatment; - NOWAPI showed good compatibility with the CPAP machines and an excellent performance in estimating the duration of the CPAP treatment and in detecting residual respiratory events in simulated OSAS patients. The results of this study demonstrated that NOWAPI system could be a valuable tool for telemonitoring the treatment of obstructive sleep apnea;

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Andersson, Boman Oskar, i 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.

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Bakgrund: Tidigare forskning har visat på vikten av information för patienters vårdupplevelse och säkerhet. Ändå finns tydliga belägg för att informationen brister på akutmottagningar. Det är därför viktigt att sammanställa patienters upplevelser inom området. Syfte: Att undersöka patienters upplevelser av information på akutmottagningar. Metod: Deskriptiv design med litteraturöversikt som metod där 16 vetenskapliga kvalitativa originalartiklar analyserades. Resultat: Fem teman skapades: Initial vård på akutmottagningen; efterföljande väntetid; tillstånd och behandling; förståelse och minnesförmåga; samt avslutande vård på akutmottagningen. Både positiva och negativa upplevelser framkom. Mest framträdande var negativa upplevelser angående bristande information om saker som väntetider, tillstånd och behandling. Slutsats: Information är en viktig del av vården på en akutmottagning och denna studie belyser dess betydelse ur ett patientperspektiv. I resultatet framkom en mängd olika upplevelser som visar på problemområdets relevans. Behov av mer forskning specifikt gällande patienters upplevelser av information anses behövas. Genom att belysa patienters upplevelser har brister och även möjligheter till förbättringar synliggjorts, vilket kan vara av nytta för sjuksköterskor i sin profession.
Background: 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.

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Jacobsson, Annie, i 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.

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För 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.

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Wessman, Anja, i 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.

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Bakgrund: Patienter tillbringar längre tid på akutmottagningen under 2018 jämfört med året innan. De lämnas ofta ensamma under många timmar i väntan på handläggning eller vårdplats. Kommunikationen och informationen mellan vårdpersonal och patienter är stundtals bristfällig vilket kan påverka patientens upplevelse av vistelsen på akutmottagningen. Syftet med studien var att beskriva patienters upplevelse av kommunikation och information vid ett besök på akutmottagningen. Metoden som användes var en allmän litteraturöversikt av både kvantitativa och kvalitativa artiklar. Sexton artiklar inkluderades. En innehållsanalys gjordes på artiklarnas resultat inklusive identifiering av meningsbärande enheter, kodning och syntetisering av innehållet till kategorier. Resultatet bildade tre huvudkategorier: Upplevelse av organisationen, upplevelse av vårdmiljön och upplevelse av vårdrelationen. Patienterna var i behov av en tydligare information gällande verksamhet och handläggning. Även brister i kommunikationen gällande exempelvis uppdatering av väntetider, undersökningar och provresultat framkom. Patienterna önskade en mer frekvent interaktion med sjukvårdspersonalen och kunde stå ut med väntetiderna bara de fick kontinuerlig information om förseningarna. Slutsats: Patienter kan känna sig övergivna och bortglömda på akutmottagningen. Att arbeta med personcentrerad vård på en akutmottagning är en utmaning även om behovet finns. En förbättrad kommunikation mellan vårdpersonal och patient kan påverka patientens upplevelse av akutsjukvård i en redan sårbar situation.
Background: 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.

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Wong, Sau-Yee, i 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.

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Wong, 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.

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Ådahl, 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.

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Fram, 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.

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Despite significant moves to inform and involve patients in their care, implementation of this vision has only been achieved with limited success. Part of the problem appears to stem from an insufficient consideration of the processes underpinning patient participation in the first instance. To help resolve this, we ask what factors drive the patient information provision and participation processes and how these factors have their impact. A significant barrier to the improvement of patient information and empowerment is the incomplete understanding of the interaction between patients and health professionals - commonly termed the patient-provider relationship (PPR). We argue that the PPR has not been fully developed in the context of stroke care specifically and we therefore propose a revised framework for understanding the nature of the patient-provider interaction, specific to stroke care. The new framework more realistically conveys the context for stroke care services in the UK today. The work first evaluates the research literature on the PPR in general, before focusing on the PPR in the acute phase of stroke care. We therefore place stroke care in the context of what is already theorised about the PPR. Based on the results from 50 semi-structured telephone interviews with stroke professionals, we then propose that a revision of our understanding of stroke PPR is needed to more fully take into account the dynamic external influences acting upon it. The general analytical approach is an inductively driven constant comparative method of qualitative analysis, conducted in line with grounded theory. Significant findings include: (i) the provider may no longer be the most important source of information for the patient within a revised stroke PPR model; (ii) stroke physicians reported cases involving lucid patients refusing thrombolytic treatment. Studies reporting stroke patients playing active, participatory roles in acute decision making do not appear in the literature and policymakers have tended to assume that the involvement of patients should only begin after the hyper-acute stages of care have passed. The findings here challenge this position and suggest that participation in decision-making during the hyper-acute phase is feasible and should be considered in clinical practice and policy making. Further, stroke care policy and practice recommendations arising from the study include: (i) greater consideration needs to be given to the allocation of resources designed to psychologically support stroke patients, (ii) audits must be designed to assess better the quality of stroke patient information provision, (iii) more information should be provided to patients and their families about what they can reasonably expect from the service they are using, (iv) priority should be given to the production of high-quality online material to complement the existing offline offering, (v) longer-term strategies should be developed for sustaining the sense of empowerment stroke patients have outside the hospital, when they generally ask more questions and demand more say in their care.

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Herrera, De Leon Morayma, i 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.

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Bakgrund: Diabetes typ 2 är en av de stora folksjukdomarna i västvärlden och numer även i utvecklingsländerna. Då patienterna är i behov av korrekt information för att lära sig att hantera och leva med sjukdomen är det viktigt att sjuksköterskor har kunskap om hur patienterna upplever information från vården. Syfte: Syftet var att utforska vad för erfarenheter patienter med diabetes typ två har av information från vården. Metod: En litteraturstudie som är baserad på tidigare forskning om diabetes typ två och information. Tolv vetenskapliga artiklar med kvalitativ ansats har analyserats med textanalys. Resultat: Resultatet i denna uppsats visar att patienterna efterlyser information som är anpassad till dem som unika individer och som är lätt att förstå och hantera, då de behöver verktyg för sin egenvård. Fyra teman som framkom: Svårigheter att ta emot och anpassa sig efter information, Information anpassad till att klara av dagligt liv, Skillnader på information från läkaren och sjuksköterskan och Anpassad information. Diskussion: Resultatet diskuteras bl a i förhållande till Orems teori kring egenvård. Då patienterna ofta har svårt att anpassa till sin sjukdom behöver de stöd i form av information för att klara av att leva ett så normalt liv som möjligt. Detta blir allt viktigare då diabetes typ två är en sjukdom som kryper allt lägre ner i åldrarna och det därmed är något man ska leva länge med.
Background: 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.

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Książki na temat "PATIENT'S INFORMATION"

Kiley, Robert. The patient's internet handbook. London: Royal Society of Medicine, 2002.

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Freed, Melvyn N. The patient's desk reference: Where to find answers to medical questions. New York: Macmillan Pub. Co., 1994.

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A patient's right to know: Information disclosure, the doctor and the law. Aldershot, Hants, England: Dartmouth, 1989.

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McLean, Sheila A. M. A patient's right to know: Information disclosure, the doctor and the law. Aldershot: Dartmouth, 1989.

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Association of British Pharmaceutical Industry. i Long-Term Medical Conditions Alliance, red. Medicines & patients: Patient information. London: Association of the British Pharmaceutical Industry, 1997.

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Harvey, L. Pre-operative visits in preparation for surgery: The effect of pre-operative information on the patient's satisfaction withcare. [Larne]: [Moyle Hospital], 1990.

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Great Britain. Department of Health. i Great Britain. Central Office of Information., red. The Patient's charter and family doctor services: [prepared by the Department of Health and Central Office of Information]. [London]: HMSO, 1993.

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Corbett, 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.

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Harvey, 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.

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Al-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.

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Części książek na temat "PATIENT'S INFORMATION"

Cremerius, Jonas, Maximilian König, Christian Warmuth i Mathias Weske. "Patient Discharge Classification Based on the Hospital Treatment Process". W 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.

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AbstractHeart failure is one of the leading causes of hospitalization and rehospitalization in American hospitals, leading to high expenditures and increased medical risk for patients. The discharge location has a strong association with the risk of rehospitalization and mortality, which makes determining the most suitable discharge location for a patient a crucial task. So far, work regarding patient discharge classification is limited to the state of the patients at the end of the treatment, including statistical analysis and machine learning. However, the treatment process has not been considered yet. In this contribution, the methods of process outcome prediction are utilized to predict the discharge location for patients with heart failure by incorporating the patient’s department visits and measurements during the treatment process. This paper shows that, with the help of convolutional neural networks, an accuracy of 77% can be achieved for the hospital discharge classification of heart failure patients. The model has been trained and evaluated on the MIMIC-IV real-world dataset on hospitalizations in the US.

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"Right To Information". W Patient's Interest First, 53–59. WORLD SCIENTIFIC / S'PORE UNIV PRESS (PTE) LTD, 1998. http://dx.doi.org/10.1142/9789812816030_0005.

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Foa, Edna B., Kelly R. Chrestman i Eva Gilboa-Schechtman. "Gathering Information Module". W 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.

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This module gathers information about the trauma, identifies unhelpful thoughts that may interfere with the patient's recovery, and, if necessary, motivates the patient by assessing her strengths and resources. The information gathered here will help you understand the patient's view of the trauma and how her cognitions may be playing a role in maintaining PTSD symptoms.

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Tiwari, Basant, i Vivek Tiwari. "An Intelligent Multi-Objective Framework of Pervasive Information Computing". W Data Analytics in Medicine, 456–69. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-1204-3.ch025.

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Sultana, H. Parveen, i Nalini Nagendran. "Mobile Patient Surveillance". W Advances in Healthcare Information Systems and Administration, 58–84. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-5036-5.ch005.

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Surveillance is defined as providing security in critical situations or monitoring certain places where safety and security are important. Surveillance takes the lead in healthcare departments or sections. Surveillance is also helpful in diagnosing the errors that occur in the automated systems and happening of adverse events in patient care. The main objective of patient surveillance is to observe the changes that occur in any patient's health to provide appropriate medication through automation process. Initially, the comparison is made between surveillance and monitoring. Later the chapter discusses the wireless technologies and mobile applications used for patient surveillance. Using mobile healthcare systems surveillance data that includes not only patient's clinical information but also analyses clinical scenario periodically, the clinical information gathered is disseminated among various teams of specialists for decision making. The advancement in wireless devices not only monitors the patient's conditions but also provides required information or data. This is possible only when sensed data is communicated at an appropriate time to avoid unexpected events in critical care units. This wireless technology helps the nursing staff in improving the surveillance and guaranteeing patient's safety. This chapter explores mobile patient surveillance.

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Vaz, Nafisa Fatima Maria. "Patient Satisfaction". W Advances in Healthcare Information Systems and Administration, 186–200. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-3946-9.ch010.

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This chapter describes how there are three major stakeholders in a patient's hospitalization: the patient, the healthcare providers, and the hospital. Satisfaction with the care and hospital experience is important to the patient because evidence suggests satisfied patients are more likely to adhere to self-care instructions and have better clinical outcomes. Hospitals have aimed to provide care and service that is highly satisfying to patients because it is the right thing to do and because reputation affects volume and revenues which in turn impacts the fiscal bottom line. Unfortunately, not all patients enjoy equal levels of satisfaction in the health care system. To succeed amongst today's competition; healthcare organizations must be patient-centered and win the loyalty of their patients by providing an outstanding patient experience, then retaining these patients, increasing the number of patients through positive word of mouth and continually delivering greater value.

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Elgujja, Abba Amsami. "Impact of Information Technology on Patient Confidentiality Rights". W 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.

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Advances in information technology, be it by way of social media or use of the electronic medical information systems, has changed the way we deal with patient confidential information. The hitherto clear professional relationship with the patient has been blurred using social media, just like the unprecedented rate at which electronic health information is used to access and share patient's confidential information among healthcare professionals. However, given the special professional relationship of confidence which traditionally bonds the healthcare practitioner with the patient, use of these technologies by the healthcare professionals portends the risk of breach of that duty of confidentiality. Although the patient's right to demand confidentiality of his information is not absolute, an unlawful breach could result in a crime, actionable tort, or become a subject of disciplinary action. This chapter undertakes a general review of the benefits and dangers of embracing these new information technologies and their impact on the confidentiality of sensitive health data.

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Elgujja, Abba Amsami. "Impact of Information Technology on Patient Confidentiality Rights". W Advances in Medical Technologies and Clinical Practice, 365–87. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-0047-7.ch018.

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Shah, Mohd Asif, i Ramesh Sekaran. "The AI-Based COVID-19 Personal Protective Equipment Is Smarty and Secure". W Advances in Healthcare Information Systems and Administration, 125–36. IGI Global, 2023. http://dx.doi.org/10.4018/978-1-6684-6894-4.ch007.

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Detecting SARs-COV'19 at early stages is essential for both providing suitable medical facility to the patients and also to safeguard the unaffected people. The dangerous part of COVID-19 infection occurs in patients with lower levels of immunity, say older people, patients with cardiovascular diseases, diabetes, chronic respiratory diseases, or cancer, in which case a serious illness develops and at last leads to the death of the patient. The chatper aims at monitoring the SpO2, heartbeat, and temperature of the COVID-19-infected patients in critical care units and takes immediate action by supplying oxygen or medicated aerosol to the needy patients. A supervised machine learning technique is used for effective prediction of the patient's condition based on the monitored parameters. Experimental results show that this model can predict the abnormal condition of the patient with an efficiency of 94% and revert back to normal conditions with an efficiency of 95%.

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Alsalamah, Shada, Hessah Alsalamah, Alex W. Gray i Jeremy Hilton. "Information Security Threats in Patient-Centred Healthcare". W Advances in Healthcare Information Systems and Administration, 298–318. IGI Global, 2016. http://dx.doi.org/10.4018/978-1-4666-9861-1.ch015.

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Healthcare is taking an evolutionary approach towards the adoption of Patient-Centred (PC) delivery approach, which requires the flow of information between different healthcare providers to support a patient's treatment plan, so the Care Team (CT) can seamlessly and securely access relevant information held in the different discrete Legacy Information Systems (LIS). Each of these LIS deploys an organisational-driven information security policy that meets its local information sharing context needs. Nevertheless, incorporating these LIS in collaborative PC care brings multiple inconsistent policies together, which raises a number of information security threats that can block the CT access to critical information across a patient's treatment journey. Using an empirical study, this chapter identifies information security threats that can cause the issue, and defines a common collaboration-driven information security design. Finally, it identifies requirements in LIS to address the inconsistent policies in modern PC collaborative environments that would help improve the quality of care.

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Streszczenia konferencji na temat "PATIENT'S INFORMATION"

Otani, Kagari, i Yasunobu Ito. "Acquisition and sharing of knowledge and skills of visiting nurses in Japan". W 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002554.

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The purpose of this study is to clarify, through ethnographic research, how nurses acquire and share their knowledge and skills of home nursing in clinical settings. The field research took place at a visiting nurse station in Nagoya, Japan between 2013 and November 2021. Research method used were participant observations and interviews at visiting nurse station and patients’ homes. One of the authors is an assistant professor of nursing at a university’s Nurse and Health department who also leads students in the clinical training at the visiting nurse station. The research data were acquired from periodical nurse station visits and from accompanying nurses in their activities.visiting nurses considered patients and family as partners, and they explored the preferred care together with the patient to create tailored care. We showed the following in a paper at AHFE-HSSE conference in 2021: the visiting nurses read into the patient’s societal background, life and beliefs, and visiting nurses analyzed the living style patients wish for, in order to propose the method which materialize this kind of living. The value co-created by the nurses and patient formulated the “normal living style” wished to be sustained by the patient (Otani and Ito 2021).Incidentally, in nursing education in Japan, universities nursing faculties and nursing schools educate students in basic knowledge and skills of nursing in wards to home nursing in Japan. The co-creative practices and techniques of visiting nursing care need to be learned while working in a clinical setting after the nurse is licensed. The paper revealed the following: The visiting nurse "co-created" with the patient to produce a nursing technique that fit the patient's needs based on the "sticky information" (von Hippel 1994) obtained in the patient's home. At the visiting nurse station, the nurses reported new information obtained at the patient's home or communicated to the patient during daily conferences. The nurse illustrated and demonstrated the nursing techniques that fit the patient to colleague nurses.In addition, the nurses had a joint conference with physical, occupational, and speech therapists working in the same station. The participants reported to each other the new information the patient during their stay at the patient's home, and described the techniques of each specialist that fit the patients. The information revealed in the conference was recorded into the patient's medical chart each time. The nursing skills created in the patient's home through co-creation with the patient are sticky information that is difficult to transfer, but they are shared and accumulated through gestural demonstrations at conferences by the health professionals.

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Nwosu, Kingsley C., i Okey Igbonagwam. "None invasive biometrie for patient information satisfying patient's security concerns". W 2016 IEEE Symposium on Technologies for Homeland Security (HST). IEEE, 2016. http://dx.doi.org/10.1109/ths.2016.7568900.

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Sivaranjani, B., i N. Radha. "Securing patient's confidiential information using ECG steganography". W 2017 2nd International Conference on Communication and Electronics Systems (ICCES). IEEE, 2017. http://dx.doi.org/10.1109/cesys.2017.8321135.

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Barinov, Evgeny, Nadezhda Dobrovolskaya, Anastasia Ivanova, Ruslan Kalinin, Alexander Manin, Natalya Mikheeva i Pavel Romodanovsky. "Patient dissatisfaction with medical dental care". W 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.

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The article provides information on the results of studying the materials of 150 commission of forensic medical examinations on the facts of patient dissatisfaction with the provision of medical care. The relevance of the problem of the legal relationship between a doctor and a patient is revealed and shown. The lack of information on these issues leads to a high probability of disputed situations in the providing dental care, so there is an urgent need for an integrated approach to the implementation of legally defined rights of patients. Media coverage of the above-mentioned problems plays an important role in improving the level of legal competence of patients. At the same time, the direct relationship between the doctor and the patient is the most important mechanism for implementing the patient's rights at the dental appointment and preventing conflicts. Behavior of doctors in such cases should be strictly regulated by normative legal acts. The process of information sharing with patients and transfer of information to the patient's relatives should receive in medical preventive institution specific legal basis under sections 30, 31, 48, 61 “Principles of legislation of the Russian Federation about health protection of citizens”, to be fixed in job descriptions with the designation of responsibility.

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Kim, Jonghyeok, Hosung Kwon, Jonghyeon Kim, Jinsoo Park, Soong-Un Choi i Sookyung Kim. "PillGood: Automated and Interactive Pill Dispenser Using Facial Recognition for Safe and Personalized Medication". W 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.

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Safety of taking medicine prescribed differently to each patient in hospital relies on the discernment of medical professionals who deals with measuring pill quantity, packaging, and distributing. It is difficult and time consuming to keep track of medication record of each patient. Also, medication safety is prone to be in risk due to the human error. To help patients get accurate medication following their prescription plan with minimizing human labors and mistakes, we developed PillGood, an automated smart pill dispenser system using facial recognition technique. PillGood provides real-time and personalized guidance to take the correct medicine by alarming patients and distributing exact quantity of pills at specific time following each patient's prescription table. The system notify patients through mobile app and speaker when they need to take the medicine, and detect who the patient is through the machine learning based face recognition. Then, based on each patient's prescribing information, the controller distributes pills to each patient. Results show that PillGood enable highly accurate personalized pill dispensation followed by precise face recognition, benefiting both patients and medical professionals. Videos for demonstrating the system can be found on https://youtu.be/Wx7bXxRGjXA

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Ahmed, Ejaz, Nik Bessis i Yong Yue. "Customizing interactive patient's diagnosis user interface". W 2010 Fifth International Conference on Digital Information Management (ICDIM). IEEE, 2010. http://dx.doi.org/10.1109/icdim.2010.5664654.

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Krey, Mike, i Ruben Ramirez Garcia. "Voice Assistants in Healthcare: The Patient's Perception". W 2022 8th International Conference on Information Management (ICIM). IEEE, 2022. http://dx.doi.org/10.1109/icim56520.2022.00029.

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Guiling, Li, Zhang Chundi, Ming Yue, Yang Liqun i Zhang Lihua. "Modeling of Hypertensive Patient's Behavior Based on the Health Information". W 2015 Seventh International Conference on Measuring Technology and Mechatronics Automation (ICMTMA). IEEE, 2015. http://dx.doi.org/10.1109/icmtma.2015.165.

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Mo, Zhiwei. "On the Product Service System Design of Diabetes Management for Patients". W Human Interaction and Emerging Technologies (IHIET-AI 2022) Artificial Intelligence and Future Applications. AHFE International, 2022. http://dx.doi.org/10.54941/ahfe100922.

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The increasing number of chronic patients is still a problem for the Italian medical system. In the age of digitalization, digital technology offers many opportunities for helping these patients solve problems, through advanced technologies such as the Internet of Things, big data, and cloud computing, smart devices can be used to collect and analyze the health information of diabetic patients, and transmit it to medical institutions in a form of visual models for obtaining reasonable treatment recommendations timely. This smart product can analyze the patient's health data in real time, meet the needs of the patient, and facilitate the connection between the patient and various medical institutions. This paper studies the product service system centered on diabetic patients, designs a smart device with blood sugar testing, and provides an Italian localized solution.

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Els, Floyd, i Liezel Cilliers. "Improving the information security of personal electronic health records to protect a patient's health information". W 2017 Conference on Information Communication Technology and Society (ICTAS). IEEE, 2017. http://dx.doi.org/10.1109/ictas.2017.7920658.

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Raporty organizacyjne na temat "PATIENT'S INFORMATION"

Haut, Elliott, Brandyn Lau, Deborah Hobson, Dauryne Shaffer, Peggy Kraus, Jonathan Aboagye, Norma Farrow i in. Preventing Venous Thromboembolism: Empowering Patients and Enabling Patient-Centered Care via Health Information Technology. Patient-Centered Outcomes Research Institute (PCORI), listopad 2018. http://dx.doi.org/10.25302/11.2018.ce.12114489.

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McCullough, Jeffrey, Stephen Parente i Robert Town. Health Information Technology and Patient Outcomes: The Role of Organizational and Informational Complementarities. Cambridge, MA: National Bureau of Economic Research, styczeń 2013. http://dx.doi.org/10.3386/w18684.

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Yuan, Bo, Wei Cao, Xieyu Zhang, Yue Yang i 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, styczeń 2022. http://dx.doi.org/10.37766/inplasy2022.1.0109.

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Review question / Objective: The role of telemedicine has been highlighted by researchers in many fields as a potential advantage for improving quality of life, increasing patient adherence, and alleviating patient concerns. Telemedicine is patient-acceptable with high satisfaction rates in patients with rheumatoid arthritis (RA). However, there is a lack of consistent results among important indicators regarding RA, such as patient pain assessment and health-related quality of life. Thus, we plan to perform a systematic review and meta-analysis to assess the effect of telemedicine on patients with RA. Information sources: PubMed, Embase, and Cochrane Library databases.

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Frakes, Michael, Jonathan Gruber i Anupam Jena. Is Great Information Good Enough? Evidence from Physicians as Patients. Cambridge, MA: National Bureau of Economic Research, lipiec 2019. http://dx.doi.org/10.3386/w26038.

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Fang, Mingxing, Yan Li, Qi Zhang, Na LIu, XIaoyan Tan i 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, kwiecień 2022. http://dx.doi.org/10.37766/inplasy2022.4.0113.

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Review question / Objective: The aim of this study was to evaluate the effect of driving pressure (DP)guided ventilation strategy on the patients with mechanical ventilation in the hospital. RCTs were included to study. Eligibility criteria: Studies were included based on the following criteria: 1. Study type: Randomized controlled trials (RCTs); 2. Patient population: Patients with MV aged ≥ 18 years; 3. Intervention group: driving pressure guided ventilation strategy; 4. Control group: lung protective ventilation (LPV) strategy. Information sources: The articles published in PubMed, the Cochrane Library, the China National Knowledge Information (CNKI), Wei Pu, Wan fang database and Web of science from inception to September 2021 were retrieved.

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Sadeghsalehi, Hamidreza, Parinaz Onikzeh, Afshin Heidari, Aida Kazemi, Parisa Najjariasl, Kamran Dalvandi i 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, październik 2021. http://dx.doi.org/10.37766/inplasy2021.10.0054.

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Review question / Objective: The aim of this systematic review is to investigate applications of smartphone apps in assessment and monitoring of postoperative symptoms and patient functions after spine surgeries. Condition being studied: Some patients with spinal problems, such as Discopathy, need surgery. These patients need frequent follow-up and assessment of symptoms and function after surgery. Currently, the use of mobile applications is a new way to monitor and evaluate patients after spinal surgeries. Information sources: Following databases were searched until 2021-03-16: Pubmed, Scopus, Embase via Embase, Web of Science Core Collection, CINAHL via EBSCO, Cochrane Central Register of Controlled Trials Via Ovid, ACM, Psycinfo.

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Alves-Nogueira, Ana Cláudia, Ana Carolina Góis, Maria Cristina Canavarro, Cláudia Melo i 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, czerwiec 2022. http://dx.doi.org/10.37766/inplasy2022.6.0062.

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Review question / Objective: The aims of this systematic review are: first, to critically synthesize current evidence for the associations between physician-patient communication (PPC) and patients’ adjustment outcomes; second, to analyse and describe the associations reported to date between PPC and physicians' adjustment outcomes; and third, to identify needs for future research on the outcomes and correlates of PPC. To this end, the proposed systematic review will address the following question: How is PPC related to patients' and physicians' adjustment outcomes? Information sources: Literature systematic search will be conducted on the following electronic databases: PubMed/Medline, PsycINFO (host: OVID), Embase (host: OVID), SocIndex (host: EBSCO) and Communication Source (host: EBSCO). References cited in articles and in previous systematic reviews will also be further reviewed to locate any additional relevant articles that may have not been retrieved within the primary search.

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Gallegos, J., V. Hamilton, T. Gaylor, K. McCurley i T. Meeks. Information integrity and privacy for computerized medical patient records. Office of Scientific and Technical Information (OSTI), wrzesień 1996. http://dx.doi.org/10.2172/392809.

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Rogalska, Marta, Lukasz Antkowiak, Anna Kasperczuk, Wojciech Scierski i 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, marzec 2023. http://dx.doi.org/10.37766/inplasy2023.3.0068.

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Review question / Objective: The purpose of the present study was to systematically review the literature to determine the efficacy and safety of transoral robotic surgery (TORS) in the management of SMG sialolithiasis. Patient, Participant, or population: Patients with submandibular gland sialolithiasis who underwent robot-assisted sialolithotomy. Information sources: The PubMed, Embase, and Cochrane databases. Additionally, the reference lists in all preselected articles were screened for further relevant papers.

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Berkman, Nancy D., Eva Chang, Julie Seibert, Rania Ali, Deborah Porterfield, Linda Jiang, Roberta Wines, Caroline Rains i 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), październik 2021. http://dx.doi.org/10.23970/ahrqepccer246.

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Background. In the United States, patients referred to as high-need, high-cost (HNHC) constitute a very small percentage of the patient population but account for a disproportionally high level of healthcare use and cost. Payers, health systems, and providers would like to improve the quality of care and health outcomes for HNHC patients and reduce their costly use of potentially preventable or modifiable healthcare services, including emergency department (ED) and hospital visits. Methods. We assessed evidence of criteria that identify HNHC patients (best fit framework synthesis); developed program theories on the relationship among contexts, mechanisms, and outcomes of interventions intended to change HNHC patient behaviors (realist review); and assessed the effectiveness of interventions (systematic review). We searched databases, gray literature, and other sources for evidence available from January 1, 2000, to March 4, 2021. We included quantitative and qualitative studies of HNHC patients (high healthcare use or cost) age 18 and over who received intervention services in a variety of settings. Results. We included 110 studies (117 articles). Consistent with our best fit framework, characteristics associated with HNHC include patient chronic clinical conditions, behavioral health factors including depression and substance use disorder, and social risk factors including homelessness and poverty. We also identified prior healthcare use and race as important predictors. We found limited evidence of approaches for distinguishing potentially preventable or modifiable high use from all high use. To understand how and why interventions work, we developed three program theories in our realist review that explain (1) targeting HNHC patients, (2) engaging HNHC patients, and (3) engaging care providers in these interventions. Theories identify the need for individualizing and tailoring services for HNHC patients and the importance of building trusting relationships. For our systematic review, we categorized evidence based on primary setting. We found that ED-, primary care–, and home-based care models result in reduced use of healthcare services (moderate to low strength of evidence [SOE]); ED, ambulatory intensive caring unit, and primary care-based models result in reduced costs (low SOE); and system-level transformation and telephonic/mail models do not result in changes in use or costs (low SOE). Conclusions. Patient characteristics can be used to identify patients who are potentially HNHC. Evidence focusing specifically on potentially preventable or modifiable high use was limited. Based on our program theories, we conclude that individualized and tailored patient engagement and resources to support care providers are critical to the success of interventions. Although we found evidence of intervention effectiveness in relation to cost and use, the studies identified in this review reported little information for determining why individual programs work, for whom, and when.

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