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Public health systems around the world
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In this paper, we provide some basics about open data and how this concept applies within the public health sector. Open data as a concept is widely applicable in several sectors and its importance have been articulated in a few commissioned documents as will be identified within this paper. Governments around the world are already creating policies to enhance data openness that is, providing detailed descriptions of how data relating to public welfare are managed. There are more emphases on making these data available to the public for free and also in the formats that can enhance reusability. Generally, open data can be said to be an umbrella term that is used to describe all forms of data that should be made open to the public, and public …show more content…
It can help researchers working on health related topics in accessing the details they need and by extension enhance a healthier city, state, nation and the world at large. As mentioned in the preceding paragraph, the drive for data openness is gaining significant support in various quarters. For example, the concept of openness has gained significant strength within the technology environment with focus on open source application development and code sharing, the scientific community has also been pushing for open access to scholarly work and a number of initiatives have been launched in the past few years to support this. In addition, government agencies around the world are creating policies to enhance access and use of government data by …show more content…
What are the factors that may enhance or inhibit openly available public health data and how do we position ourselves to solve these problems. Problems can range from policy to technical capability depending on which of this is dominant and some of these have been identified in the research literature. For example, research conducted by Vest and Issel (2014) which was a cross-sectional analysis of organizational factors associated with gaps in data sharing between state health agencies and local health departments in the areas of childhood immunizations, vital records, and reportable conditions reported that the proportion of local health departments experiencing a data sharing gap was 34.0 percent for immunizations, 69.8 percent for vital records, and 81.8 percent for reportable conditions. They further reported that increased state health agencies technological capacity and size reduced the odds of gaps. This is a problem relating technical capability. To provide an example relating to policy, Gasner, Fuld, Ann, and Jay (2014) conducted a study in New York that examined public health laws and agency policies for data sharing across HIV, sexually transmitted disease, tuberculosis, and viral hepatitis surveillance programs. They reported that recent changes to state laws provide greater opportunities for data sharing but that agency policies must be updated because they limit
Friedman, D. J., Parrish, G., & Ross, D. A. (2013). Electronic Health Records and US Public Health: Current Realities and Future Promise. American Journal of Public Health, 103(9), 1560-1567
Introduction “Health informatics is the science that underlies the academic investigation and practical application of computing and communications technology to healthcare, health education and biomedical research” (UofV, 2012). This broad area of inquiry incorporates the design and optimization of information systems that support clinical practice, public health and research; understanding and optimizing the way in which biomedical data and information systems are used for decision-making; and using communications and computing technology to better educate healthcare providers, researchers and consumers. Although there are many benefits of bringing in electronic health systems there are glaring issues that associate with these systems. The
With continuous use of the networks, more and more institutions will be able to follow their example. Each of these have become a positive impact to the way health information technology is being used. The patients that are being helped are tremendous. Sooner than later both the CHIN and RHINO records will be able to be made better and be transformed into a NHIN that will be widespread nationwide and not just to a certain area. The HITECH Act will also continue to be helpful in increase use of health information technology and resolve the problems associated with the privacy and security of the vital information contained in the system. As years go by more and more new systems will be created and health information exchange will become advanced, in a way that it will change the way people view health care
Population Health Data Population health data is an important component of the Meaningful Use Program. The program requires healthcare providers to collect and report data on a variety of measures related to population health, such as
Health informatics is best described as the point where information science, medicine, and healthcare all meet. It encompasses the resources, devices, and methods required to optimize the acquisition, storage, retrieval, and the use of information in health and biomedicine. Health informatics incorporates tools such as: computers (hardware and softwar...
The use of electronic medical records has both positive and negative impacts on our struggling healthcare system. The positive effects are improved communication among healthcare providers, decrease cost to patient and insurance companies by eliminating repeat diagnostic tests and unnecessary procedures, and improve the health conditions throughout the country by collecting data information. Immunization registries, bio surveillance, and public health can be monitored to improve the “fiscal an...
State and local public health departments throughout the country have the responsibility for improving health in workplaces, schools, and communities through identifying top health problems within society and developing a plan to improve. Barriers the public health system has encountered over the years include: changes in the overall health system that support cost containment and improved health, and an increase in the number of individuals with insurance coverage for direct preventive services; reduction of qualified public health professional and funding at all levels of government; increasing focus on accountability, with higher expectations for demonstrating a return on investment in terms of cost and health improvement (Trust, 2013). In the near future, health departments ...
The objectives of meaningful use will take form in three stages, to be rolled out over a five year period. Stage one took place between 2011 and 2012 which involved data capture and sharing. Within this stage the criteria focused on electronically obtaining health data in a standardized format, using health information to track clinical conditions, instigating the reporting of public health information and clinical quality measures, and finally using these materials to involve patients and their families in their healthcare.
"The Need Is Real: Data." Organdonor.gov | Welcome to Organdonor.gov. U.S. Department of Health and Human Services, n.d. Web. 15 Dec. 2013.
Privacy challenges. Privacy is a circumstance of restricted right of entry to an information regarding an individual (Knoppers, 2015). Brothers and Rothstein (2015) noted numerous other kinds of privacy, comprising physical, decisional, proprietary and relational or associational privacy. This study emphasizes on informational health privacy. When it comes to privacy issues the crucial question to explore is; how can leadership balance the right of privacy with the advantageous requirement for clinical data-access in EHR? The Privacy Act of 1974 is the US law that represents national standards to protect the private health information of individuals by mandating appropriate safeguards and limitations on the right to use and release of (PHI)
The debate is still going on today about what can and cannot be done legitimately with patients health information. There are worries about who should be able to access the patient’s information and for what reasons do they have to be accessing the patient’s health information. While on the other side there is an increasing need for performance assessments, efficient health guard, and a proficient administration for more and better information. Health care services are now starting to realize that they have a lot of work to do to be in compliance with the current health laws on the state and federal level guidelines when it comes to dealing with protecting patient data.
Health information opponents has question the delivery and handling of patients electronic health records by health care organization and workers. The laws and regulations that set the framework protecting a user’s health information has become a major factor in how information is used and disclosed. The ability to share a patient document using Electronic Health Records (EHRs) is a critical component in the United States effort to show transparency and quality of healthcare records while protecting patient privacy. In 1996, under President Clinton administration, the US “Department of Health and Human Services (DHHS)” established national standards for the safeguard of certain health information. As a result, the Health Insurance Portability and Accountability Act of 1996 or (HIPAA) was established. HIPAA security standards required healthcare providers to ensure confidentiality and integrity of individual health information. This also included insurance administration and insurance portability. According to Health Information Portability and Accountability Act (HIPAA), an organization must guarantee the integrity, confidentiality, and security of sensitive patient data (Heckle & Lutters, 2011).
Because state and local public health programs are often funded at least in part with Federal dollars, accountability is often a key issue (“Ten Essential Public Health Services.” 2015). Public health programs therefore document progress towards positive change in health behavior or health status indicators (“Ten Essential Public Health Services.” 2015). Data such as these can be presented to policymakers to document the value or effectiveness of a program (“Ten Essential Public Health Services.” 2015). Those data can also be used for continued program planning and modification (“Ten Essential Public Health Services.” 2015). Policies have positive or negative influences on health. Examples of health policies include safety standards, which influence the incidence of injuries; tobacco regulations affect personal health; and safe city parks can affect the ability for people are active (California Department of Public Health “Strategic Plan”, 2013). It is a systematic process to utilize appropriate data, develop and track measurable health objectives, establish strategies and actions to guide the targeted improvements (California Department of Public Health “Strategic Plan”, 2013). The targeted strategies may be laws, codes, regulations and/or
...s in the health industry. It is set to change the way doctors and patient’s access information as it will make information more available in a clear and efficient way.
Health care and research are no longer two different paths, but instead because the emphasis on reducing cost and increasing quality outcomes they are converging to make a LHCS. With the introduction of LHCS’s, research and treatment will converge into a new way of managing patient data. Expansion of technology and increased patient involvement in their health care will continue to create the need to reassess what privacy and confidentiality look like to the patient, researcher, practitioner, health plan and other business