A New Proxy Server of CHIS Based on Caché

2011 ◽  
Vol 65 ◽  
pp. 427-430
Author(s):  
Guang Ming Li ◽  
Gai Hong Lian ◽  
Zhen Qi He

The data accessing technology is the core and foundation technology of the community health information systems. In the process of designing the system, the relational database compared with the Caché database from the data model, extensibility, scalability, etc. Study the associated technology about the heterogeneous data sharing with the Caché database. After analyzed the common solution of heterogeneous data sharing then the paper proposed a new data sharing solution, which design a middle proxy server. With the middle proxy, the implementation class completed the uploading and sharing of data access and other functions.

Author(s):  
Mario Sicuranza ◽  
Mario Ciampi ◽  
Giuseppe De Pietro ◽  
Christian Esposito

2020 ◽  
Vol 30 (Supplement_5) ◽  
Author(s):  
D Zenner

Abstract Despite significant efforts, for example within the EU/ EEA, there are currently only few Health information systems (HIS) which are standardized across international borders, and even within countries there can be significant variations. Modalities, technologies and terminologies differ. In the field of migration health, challenges and variations can be more significant. This talk will explore the specific challenges in migration health related HIS, provide an overview of the current HIS landscape pertaining to migration health and sketch out some potential solution to achieve greater harmonization and data sharing across countries.


Author(s):  
Soumya Purohit ◽  
Prasad Calyam ◽  
Mauro Lemus Alarcon ◽  
Naga Ramya Bhamidipati ◽  
Abu Mosa ◽  
...  

2008 ◽  
Vol 47 (05) ◽  
pp. 435-442 ◽  
Author(s):  
S. Nerur ◽  
W. Raghupathi

Summary Objectives: The health information systems (HIS) field is characterized as being associated with health care and information systems. Drawing on several disciplines, a body of knowledge has come together that help define the core internal structure of the field. This study attempts to identify the emerging sub-fields using the bibliometric technique of author-cocitation analysis. Methods: Co-citation data for members of editorial boards of several health information systems journals for the period of 1998-2006 was collected and analyzed (N = 166). We performed numerous multivariate analyses, including cluster analysis, factor analysis and multidimensional scaling to extract the sub-fields. Results: Our findings indicate the presence of several strong sub-fields, including HIS evaluation, communication and e-health, and clinical DSS. In addition, we identified other sub-fields that are distinct but still emerging, such as adoption, outcome and policy, and use and impact of HIS. The study also confirms the existence of several historical sub-fields and contrasts technology-oriented sub-fields with managementoriented sub-fields. Topics on the periphery of HIS provide links to other disciplines as well. Conclusions: The study provides a unique perspective on the field of HIS, and the results indicate opportunities for further research that explores collaborations and social networks among the sub-fields.


Author(s):  
Naveen John ◽  
Shatheesh Sam

Personal health record (PHR) system has become the most important platform to exchange health information, in which the patients can share and manage personal health information more effectively in cloud storage. However, the cloud server is unreliable, and the secure data of users may be disclosed. Therefore, a secure data sharing mechanism is developed in this research using the proposed session password, data access key, and circular interpolation (SKC)-based data-sharing approach for the secure sharing of PHR in the cloud. The proposed SKC-based data sharing approach provides high efficiency and high-security guarantee. It effectively satisfies various security properties, such as tamper resistance, openness, and decentralization. The proposed SKC-based data sharing approach is the reliable mechanism created for the doctors to share the PHR and to access the patient historical data while meeting the privacy preservation.


2018 ◽  
Vol 27 (01) ◽  
pp. 163-169 ◽  
Author(s):  
Pascal Staccini ◽  
Annie Lau ◽  

Objective: To summarize the state of the art during the year 2017 in consumer health informatics and education, with a special emphasis on sharing health data and accessing personal health information (PHI) from patients' and consumers' perspective. Methods: We conducted a systematic search of articles published in PubMed using a predefined set of queries which identified 228 potential articles for review. The section editors then screened these articles according to topic relevance and selected 15 candidate best papers for full review and scoring by a panel of international experts. Based on the scores and the reviews, four papers received the highest score and were selected in a consensus meeting as the best papers on health data access and sharing from consumers' and patients' perspective. Results: These four papers were categorised into the following topics: 1) data sharing for research and governance in privacy protection; 2) use of personal health information and individual privacy concerns; and 3) consumers' views and demographic characteristics regarding health data sharing and the use of digital health portals. Overall, it was surprising to see only a small number of papers reporting original research in this area. Conclusions: Patients understand the need for sharing information to facilitate best care and to enrich biomedical knowledge. When confronted with the reality of accessing information systems for their own information, patients are concerned about usability as well as privacy. Overall, there is a need for more emphasis on: 1) considering privacy as a feature defined by design; 2) using specific consent approaches and data sharing mechanisms for recruiting clinical trial participants; 3) taking into account socio-demographic characteristics when promoting consumer access to personal health information; and 4) defining indicators of high-quality care to incorporate healthcare professionals' level of caution when accessing patients' medical information and fostering patient trust in data exchange. Ultimately, privacy mechanisms should be part of the design process and not only be implemented when security has been breached and violated.


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