Skip to main content

Home/ ITGS News/ Group items tagged open source

Rss Feed Group items tagged

Madeline Brownstone

DoD Software Tech News - 0 views

  •  
    The Department of Defense and open source.
Madeline Brownstone

Open Ed at Creative Commons - 0 views

  •  
    Open Source Education
Madeline Brownstone

Schools creating new rules for social networking policies - USATODAY.com - 2 views

  •  
    "beginning of the academic year warning them of social networking issues. Source: Individual schools * Share * Yahoo! Buzz * Add to Mixx * Facebook * Twitter * More o Fark o Digg o Reddit o MySpace o StumbleUpon o Propeller o LinkedIn * Subscribe * myYahoo * iGoogle * More o Netvibes o myAOL * By Kyle Oppenhuizen, USA TODAY More college athletic departments are developing or publicizing online social networking policies for student athletes, experts say. USA TODAY researched social networking policies for 27 schools in six major conferences, including the University of Iowa, which will implement a new monitoring policy Friday. Last fall, pictures emerged on Facebook of two 19-year old Hawkeye football players holding cash and liquor bottles. Five of these schools already have specific monitoring policies in effect - Auburn, Iowa State, Ohio State, Miami and North Carolina. Others warn athletes of the potential dangers of sites such as Facebook and MySpace through student-athlete handbook policies, meetings, coach's discussions and even letters. Some schools don't have a specific policy but allow coaches to monitor at their discretion, or take action if inappropriate material online is reported. Iowa's policy puts senior leaders in charge of monitoring profiles of athletes' on their team and bring problems to administrators, who then work with the athlete, associate athletic director Fred Mims said. Administrators will not get involved, Mims said, unless issues are brought to their attention, in which case they will talk to the athlete about addressing the issue and check out the profile, public or private. Ohio State, on the other hand, requires athletes to have a public profile or add coaches and administrators as friends (which gives access to the private profile). Fred Stutzman, a Ph.D. cand
nicholas n

U.S. Tries Open-Source Model for Health Data Systems - NYTimes.com - 1 views

  •  
    This article is about the idea of putting all existing medical records into electronic form. This would cut the costs needed for storage of such information, this would also increase how fast a medical official can access the records of a sick patient. However, as listed in Strand 1, there are many positive and negative social/ethical issues. One such issue is security. By making the records digitized and put into the hospital database, people without the proper authorization would not be able to gain access to the data. This can also coincide with authenticity. The information that relates to the patient should be accessible by the patient. The patient would need to be able to get through the encryption of the data. Another social/ethical issue would be the equality of access, this would allow only certain people the ability to look at the data. Even with these positive social/ethical issues there are some negative issue. One negative issue would be integrity. There are people who can hack the encryption of this data and tamper with it. This would cause the data to be different in other places and a breach in security. This would be a great help to organizing data. Using a paper file system, the doctor would have to go through a lot of papers and cabinets to find the patient's medical history. By using a paper file cabinet documents are more likely to go missing or get mixed up with another patient's records. However, by using a database this data is much more organized. There is a smaller chance of losing the patient's data, by using back-ups the data could be easily restored. There is also a much smaller change or mixing up multiple patient's data. If the wrong data was use for the wrong person, the person may not have the correct medical treatment they need. With databases the information is much more organized. The patient's data can be found very fast, compared to a paper file system (this could take more than an hour depending on the amount of patients).
  •  
    Continued...The hardware involved with creating databases in the health industry would be a DBMS Engine. This is also known as a Database Managing System. This takes the logical request from DBMS subsystems and converts them to physical equivalents. This also requires interactive processing. This replaces batch processing. This allows users to interact with data through terminals and view values online in real time. By having real time the doctors can give the patients what they need at the moment the patient needs it. The stakeholders in this specific case would be the hospitals adapting the database managing system and the patients whose information is stored in this database. If the database is tampered and there are not back-ups the patient would not have his/her medical history. This could cause the patient to be on a delay for an operation that is extremely important to their life. This could also place a lawsuit on the hospital.
Noreen C

U.S. Tries Open-Source Model for Health Data Systems - NYTimes.com - 1 views

  • easily and securely share information
  • A fancy electronic patient record, unconnected, is just an expensive way to capture data.
  • Getting many different health care providers and suppliers of specialized software to agree on how to do that is no simple task.
  • ...2 more annotations...
  • The solution the group agreed to is essentially Internet-based e-mail and public key encryption technology, tailored for health care.
  • For health care technology companies, the data-sharing standards, experts say, should stimulate the market for electronic health records and allow them to focus their efforts on making their individual offerings more affordable and easier to use.
  •  
    This article is primarily about setting standards and protocols so that an electronic health records could world easily and securely for many health care providers and suppliers. The reason the introduction of an EHR hasn't worked before, is that there were no data-sharing standards, which would ensure that the data is transmitted securely across the internet. These standards are also in accordance of many of the interests of all of the health providers and stakeholders involved, which was a major problem previously. Without the issue of connecting the EHR from provider to provider, then the records would be a "fancy...way to capture data," and it's full potential would never be recognized. However, these new standards and protocols, filled with secure transactions based on encryptions, have made the introduction of an electronic health record possible. There are many benefits to the use of an EHR, including productivity and financial improvement for the companies and the employees. For example, doctors/nurses no longer need to spend time pulling a patient's file, or writing the details of the visit afterwards. There are also fewer repetitive tasks, and improved communication between doctor and nurse, or doctor and another doctor. Quality of care may also improve because doctors have quick access to a patient's information, there is better monitoring and discovery of chronic illnesses, and doctors can return phone calls/ provide medication refills immediately. Also, in general, the electronic charts allow for a more efficient office, which leads to a less stressful environment and more attention on the patients' care rather than searching for their charts. This can only be done through the introduction of an EHR, leading to easier queries, instant reorganization, and file management that could be transmitted to both the patient and any other doctors. This minimizes the ambiguity of not having tests results from one doctor, and allows all doctors treating a p
  •  
    patient to see all of the patient's history. This is important in having a correct diagnosis and treatment. However, there are also some drawbacks. Initially, doctors who chose to engage in the implementation of a EHR, see some decreases in productivity. This is because entering information and learning how to use the software takes some time. Some doctors also do not have the money to invest in such software and accompanying hardware to, and others no not want to because they are accustomed to their hand-written charts. There are also some security issues, leading to greater privacy issues. The EHR maintains very personal data about a patient, and if the records are breached, then the privacy of the patient may be put at risk. There is also the issue of interoperability, which was brought up in the article. Many of the companies in different countries wishing to engage in the implementation of EHR have different standards involving the usage. This could harm the usage of an international EHR.
Elisavet M

An Unforeseen Complication of Electronic Medical Records - 0 views

  •  
    This article focuses specifically upon the negative implications that surface with the installation and adaptation of electronic medical records (EMR) for medical professionals targeting specifically the level of doctor/patient relationships. The author, a medical specialist within a facility, talks about his experience with the proven efficiency of the EMR system's effective retrieval of patient medical history and advanced medical database, but further accentuates emphasis on the system's flawed influence upon medical professional and patient relations. One of the primary stakeholders, the medical doctors and physicians complain that the system itself places limitations upon doctors' interactions with patients during the time of consultation (a critical part of constructing medical diagnoses); the author places emphasis upon the way he had to consistently go back and forth from the patient to the computer, in order to type in the retrieved information gained from the conversation. The act of going back and forth between patient and technological system (EMR) discouraged and urged the patient into silence, thus limiting conversation with the doctor, due to the lack of complete face to face, non interrupted evaluation and reflection of medical symptoms, history, prior experiences from the perspective of the patient. Thus, the second primary stakeholder, the patient himself, feels that he or she is not properly or fully being examined; more importantly this places the patient into the position of feeling less significant, as if his/her perspective doesn't truly matter when in reality it is the patient's responsibility to be clear and coherent with the medical professional, to help navigate the doctor into generating the correct diagnosis that will help save patient lives. The IT system involved is the EMR (electronic medical record) system that operated with the help of dozens of computer terminals that were positioned in individual workstations (hardware com
  •  
    (continuation) component) and worked on the same networking service. The software programming that came with the system helped improve the retrieval and sharing of patient medical history, organization of data, efficiency and flexibility of keying in and updating medical information etc. In connection to the scenario of Health, the limiting influence forced upon doctor/patient relationships sourced from the integration of EMR systems targets a flaw in the advantage of having instant connection to patient medical information. Not only are doctors forced to focus on correctly typing in the necessary information, thus avoiding or diminishing patient relations, but the great magnitude of medical information stored and available in EMR systems, "can push some doctors into what one EMR expert refers to as "cognitive overload" while trying to balance patient input with medical history data on the spot. Furthermore, the system's software tool, such as the fee-for-service payment system, which helps tabulate symptoms while simultaneously facilitating the billing process, continues to discourage doctors from executing patient consultation. One major issue that surfaces is reliability; the EMR system itself consists of hardware and software components that transition the doctor's attention from the patient directly onto the transferring of information into the system while in the mode of confrontation. The correspondence of data with the real world comes into significance, as the data may become unreliable due to the fact that it may be entered incorrectly (the doctor may have been focusing more upon data transmission, rather than what the patient actually stated), and additionally the use of EMR systems increase the risk of data becoming outdated, for it is solely up to the doctor's skills and attention that medical history, symptoms, side effects of the patient be kept at a steady consistency once entered into the system. Thus, although physicians and he
Madeline Brownstone

NOVA Online | Cracking the Code of Life | Watch the Program - 7 views

  •  
    Please use this bookmark to post your reflections. Using a Paper 2 style approach, CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. CRITERION D) Evaluate the efficacy of a solution to the problem.
  • ...10 more comments...
  •  
    Criterion A- The IT system (research DNA database) that allows medical researchers to record and track medical histories throughout generations, arise a variety of issues. One of these issues is privacy, where the database holds genetic information that many ethical doctors call a "future diary". These medical databases can be analyzed by a variety of people and those who have access to this information are handling private information. The major stakeholders were those patients who gave up their DNA because their genetic information put into the hands of these medical doctors creates the privacy issue. This information needed to be well stored and doctors take implications such as encoding social security numbers and no names are used. Criterion B- These research DNA databases begin with the obtainment of genetic information. In a relational database, there are several tables containing various information. Each table contains data that all have attributes related to the subject of the table. All of the tables might be interconnected, as well. For example, a retail business using a relational database would likely have one table containing data regarding employees, another with data regarding customers, another table listing inventory and so on. A database user could run a report to find connections between data in different tables, such as the customer table and the inventory table. Criterion C- From the point of view of the major stake holders (patients who given up their genetic information) the IT system (research DNA databases) (Not done)
  •  
    Criterion A) The IT system is a database. This database is a link of DNA records, health records, and family trees. Major stakeholders of this issue are citizens of Iceland who agree to let their information be put on these databases and analyzed. Criterion B) The database works in parts. First, there is already a database of family trees in place. This family tree generator works by inputting an individual's social security number. After this is in place, the name of many generations of ancestors of this individual is shown in a tree. Then, the creator of the database asks for the permission, of family members, to add the DNA code and the health record of each person. This allows for a social security number and a disease to be input at the same time. With this, the scientist can see those who have it, and those who don't. Then, with the use of the DNA codes, they can "hunt down" genes that cause certain diseases. The database is related to an issue of privacy. This is because those who allow their health records and DNA code, are letting the medical team and users of the database know all things about them. With just a social security number, a user that has access to the database may learn more things about you than you may want: such as your family, what diseases you may have, and many other things. Another issue is in reliability. There is the possibility that the medical teams that try to track genetic code differences between those with a disease and those without it, may come to realize that a difference they find is only a coincidence and not helpful. (not completed)
  •  
    The IT system being used is the DNA database that are being kept on the Icelandic people. The DNA database holds a lot of information of the people in the database and even things that they do not know such as their DNA and what it means. The major stakeholder is the people that are sending their DNA information, blood samples, medical histories and family trees. The issue of privacy is then involved because of the personal information that others can go through by accessing the database. The database is run by first getting the blood sample of the patient who willingly gives permission to give their DNA information to the company, deCODE. The information is then entered into the database which organizes the information by each person's social security number. The relational database is used to organize the information. (Cont.) The impacts of the database is both negative and positive. The database can be
  •  
    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. * The IT system described in this video is a medical database. The major stakeholder are the doctors who manage the data of patients in the relational databases. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). * A relational database, there are several tables containing various information. Each table contains data that all have attributes related to the subject of the table. All of the tables might be interconnected, as well. For example, a retail business using a relational database would likely have one table containing data regarding employees, another with data regarding customers, another table listing inventory and so on. A database user could run a report to find connections between data in different tables, such as the customer table and the inventory table. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. * One of the positive impacts of these medical databases are that the family tree is in a database and all health records can be found for each patient and because this is a relational database, all of the patient's information is linked to their families and other people who have similar diseases. This is beneficial because experts can see trends in the people who have a certain disease and once they figure out the "spelling" of the genetic code with the disease, they can work on coming up for cures for that particular disease. A negative impact of the medical databases can be privacy. The doctors have access to every patients information and they can know everything about a certain person or family if he/she wanted to. This would then raise an issue of integrity.
  •  
    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. The IT system is the database and the issue is who has access of the Database which has medical records of individuals. The major stakeholders are the Doctors and Patients. Doctors are trying to find information on specific DNA that create sickness and diseases. Finding the relationship between the family members and there DNA, can possibly improve medicine and also allow doctors figure out what an individual can have(sickness) in future references, making inferences of what might happen. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). A data base function is that it is a computer stored software that contains tables of various information and organizes all the data into categories. One subject/category can be related to another with little difference. This is why the database makes it easier for information to be viewed and interpreted much faster. By entering data on the tables one can interlink topics in order to find specific information needed. The person who enters the data can use software like Openoffice to create a database to view DNA and the relationship with the other individuals. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. The primary issue of the negative impact on Databases, have on the skateholders for DNA purposes is Privacy. Privacy has a big part in the stakeholders because many of the patient give away there Social Security number which is something private to them. With the Social Security Number the doctors can have access to other information not related in there investigation of finding a cure. This can cause reliability with the doctors to decrease. The database would have information of all sort on there medical records which should not be something that would be public for eve
  •  
    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues: The IT system in these videos were medical databases containing records of many patients. Specialists use these databases to help them identify where a certain disease came from and whether or not it could be treated. they do this by viewing the patients ancestors records and seeing who had the disease in that family tree. CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). Specialists (with the permission of the patient) insert a patients social security number into the medical database and let the database generate the patients entire family tree. Using this family tree, doctors were able to "hunt" down the origin of diseases, by looking at the genes of the ancestors. That way, by matching the DNA of the patient affected by a certain disease with the DNA of one of his/her ancestors DNA that suffered the same disease, and looking for similarities or patterns. CRITERION C) Evaluate the impacts on society -- both positive and negative or from differing stakeholder's P.O.V. There were several positive and negative impacts regarding this "hunting down" of diseases. By looking at family trees specialists and doctors would be able to determine what caused the disease and possibly come up with a cure or treatment for it. However, many patients are concerned with doctors going through their records and DNA due to there being a lack of privacy. If patients grant permission, specialists would be able to find out and know absolutely everything about their health history. Specialists argue that it would be of great benefit to detect diseases early so they could be treated by doing this. Chips are being created were thousands of babies genes could be looked at to look for any abnormalities. Some people argue that even if a disease were detected, there's two possibilities, one
  •  
    Criterion A) The IT system at work here is the database run by the company deCODE. This company created a medical database in order to determine human diseases present amongst family. This leaves the stakeholders to be the Iceland citizens who use this system. The relationship between the Iceland citizens who use this system and the issue is that there is a security issue. The company, deCODE, paid a sum of one million dollars to the government for access to the medical history's and information of the Iceland citizens. This could be stolen by others or it could be hacked by an outsider. Criterion B) This system works through a series of steps to figure out what medical diseases are passed on throughout the family tree. In this case it would be a relational database. This database works by first obtaining permission from the Icelandic citizen to use their social security number and their medical history. This is put into the system and the medical records are accessed. Then the family records and past can be seen. This is multiple tables containing different pieces of information. Each table has something that is related to the previous table. Then make sure that the database is easily navigational. When the social security number is entered into the database the company must have it in the record. If the social security number is not properly encoded then the social security card could be stolen by and employee of an outside hacker. This is related to security if the hardware or software is not properly secured it can be obtained by a criminal. This can lead to identity theft and loss of financial security. Another issue would be privacy. The medical records and DNA code is allowed full use to the company. The social security number could be used in ways that the civilian did not agree to and is not known by the civilian. Criterion C) This system can cause many positive and negative impacts. One positive impact would be that this would help the patient know who e
  •  
    Criterion A) The IT system at work here is the database run by the company deCODE. This company created a medical database in order to determine human diseases present amongst family. This leaves the stakeholders to be the Iceland citizens who use this system. The relationship between the Iceland citizens who use this system and the issue is that there is a security issue. The company, deCODE, paid a sum of one million dollars to the government for access to the medical history's and information of the Iceland citizens. This could be stolen by others or it could be hacked by an outsider. Criterion B) This system works through a series of steps to figure out what medical diseases are passed on throughout the family tree. In this case it would be a relational database. This database works by first obtaining permission from the Icelandic citizen to use their social security number and their medical history. This is put into the system and the medical records are accessed. Then the family records and past can be seen. This is multiple tables containing different pieces of information. Each table has something that is related to the previous table. Then make sure that the database is easily navigational. When the social security number is entered into the database the company must have it in the record. If the social security number is not properly encoded then the social security card could be stolen by and employee of an outside hacker. This is related to security if the hardware or software is not properly secured it can be obtained by a criminal. This can lead to identity theft and loss of financial security. Another issue would be privacy. The medical records and DNA code is allowed full use to the company. The social security number could be used in ways that the civilian did not agree to and is not known by the civilian. Criterion C) This system can cause many positive and negative impacts. One positive impact would be that this would help the patient know who e
  •  
    CRITERION A) identify the IT system and describe the issues. Identify the relationship of the major stakeholders to the issues. The IT system involved is the DNA database system, identified as an organized collection of age old family trees, accompanied by state of the art DNA analysis and computer technology. Systematically, genetic information (DNA) is stored in related tables, distinguished by individuals' own security number codes. One centralized ethical and social consideration is privacy, mainly a major concern of the involved DNA suppliers (the public), that place their given personal information (genetic data, reference to family origins, medical history etc) in a national database system, from which the accessing of medical records and history of one's entire family can become manipulated or misused. In addition to the elevated risk of data misuse, once the involved participants (Icelandic citizens) give access to their personal information, there are no limitations placed on the utilization of the data within the national database, as it becomes accessible for the government, medical researchers and operating staff. Thus, the implications are straining to the individual donor, unable to determine when, how and to what extent the information given is shared amongst other groups. Furthermore, the privacy of the participants undesirably opens access to the medical information of related family members, as cross-referencing and data matching give the research staff operating the DNA database, access to retrieve a plethora of other members' data mainly for the purpose of effective data mining (the retrieval of hidden predictive patterns, as a diagnostic tool to decode the occurrence of genetic disorders/diseases). CRITERION B) Describe step-by-step how the system works and describe how the system is related to the issue(s). With the possession of participant's medical data, including blood type, isolated samples of DNA, medical health records e
  •  
    The primary IT system in use is a DNA database, which includes information about patients, illnesses, and virtually one's make up as a human. DNA databases allow researchers to find patterns in a human genome, by looking at the DNA from various family members and determining the difference or similarities between the DNA of family members. This is done through database functions such as data mining, and data matching. Locations such as Iceland, have a database that traces back all of the people within the country to their Viking ancestors. These family trees have been paired with DNA analysis in order to trace diseases back to their start. Some more tests could be conducted in order to determine which of the living relatives of one family with arthritis, for example, have the disease. Then, the DNA can be compared in order to identify the exact gene that is at fault for the disease. This process is very easy to do because the database with all of the ancestral information is accessible with the presence of one of the family member's SSN. A simple data query can then bring together all of the person's information. Moreover, DNA, health records, and the family trees of Iceland were proposed to be linked. This could be very beneficial because new drugs could be made available to suit the specific disease of a patient. It could also be a way for diagnosed patients to take early preventative measures. This could increase the probability for a cure, and in general this would increase the life expectancy of certain areas. However, some doctors in Iceland opposed to this linkage, because the information is representative of each person's medical history, and potentially their future medical history. This information, according to the plans of the linkage of medical records and the family tree, would be available on a central database that would bring together private information about a person and connect it to all of their family members, past, present, and future. T
  •  
    There is another issue along with this involving the ability of researchers to have full access to the information about anyone. Many people want to maintain their right to privacy, but others argue that this could lead to new knowledge about diseases, and the development of new medicines. For those who are afraid of risking their privacy, there are standards developed in order to protect them. Their information, such as SSNs are encoded for security reasons and the DNA part of the project is voluntary, and not imposed. However, ethicists are still afraid of this database. They claim that the future of DNA is a valuable thing because it can predict the probability of diseases, life expectancies, etc. But all copies can be made available to the FBI, schools, etc. at the time of birth. For the Biotech Industry, this is seen as a huge advantage because people an be tested for hundreds of diseases. The awareness of the disease is a great thing, because it could lead to early prevention. However, the system is faulty because it sometimes doesn't provide certainty of a disease and it limits a person's privacy. Other times, there is no cure for the disease, so the patient cannot do anything even if they know. In relation to this, there also will arise severe psychological impacts of a person knowing that they have the possibility for getting a life threatening disease. If this is a disease that will affect them later on in life, it would be detrimental for a person to live their life without the hope of a prosperous future. A solution to this problem could be giving patients the choice of knowing or not.
  •  
    Criterion A - The IT system is the DNA database containing information about the genetic past, present, and future of the patients. The primary issues associated with this database are of privacy and anonymity. These issues arise when patients, who are one of the major stakeholders, feel that that the information in these databases shouldn't be accessible to others, or anyone for that matter. While some believe this is private information, others believe that the information should not be known by anyone because of the ethical issues associated with knowing what will come in the future. Criterion B - The medical database is a relational database meaning that it establishes relationships between different tables in the database. The smallest building blocks of a relational database are items. Items are individual pieces of information in tables. These items are organized into fields and records. Fields are columns in a table that that represent different categories of information. Records are rows that represent all the information for a specific patient. At the cross-section of a particular record and field lies the item associated with a specific piece of information related to the specified patient. These tables are related to each other through links which are established by unique primary keys assigned to each patient. This system is related to the issue of privacy because the information contained within it is considered by many to be privileged and access to it should be very limited or altogether eliminated. Criterion C - The impacts of such a database on society are varied. Some people are very against the entire idea of a genetic database because of its ethical concerns. When people have their blood analyzed for DNA, they are giving up their genetic make-up. The information that can be obtained from such tests is considered by many to be privileged, and by others to be completely unethical in every way. Often people are against very private medical
1 - 7 of 7
Showing 20 items per page