Basics of Healthcare Data access rights in USA

You must access, view, and transfer medical information.

Seeing ways you can log in to some web portals and see the data.

It’s not very useful, but everyone should be able to. It is very useful if you want to see the data the doctor is talking about, but if the doctor talks with you, the information is too much. You want to see him later at home, where you can spend time with him. The idea is also that you have the opportunity to think about questions at the next meeting with your doctor. These “views” of data are often not the highest quality or easy to understand.

The download means you can download a copy of the data through the same web portal.

“Should” be higher quality and should be in “standard” format. So my job came. Most items are available in a brief report. It can be called a “blue button,” a meaningless marketing term, but it’s something to mobilize the health community around them. This summary report may be a plain text file, something not available, or a PDF file. I expect the format of the CDA format is more complete (often referred to as CCD, C32, CCDA, C-CDA, etc.). Images like MRI use standard DICOM.

If you download these CDA or DICOM criteria, you can send it to another doctor or secondary view, or solve the problem in the future. You can also find online applications that you can use to investigate these things yourself. You can also find online services that you can study to get a second opinion about the computer (dangerous in my opinion). You can send this data to clinical research projects that you want to use your data for better future treatment of your problems.

The goal is that your data is your data. You can do whatever you want. You can also be stupid and leave it in a place where it is not supposed to.

Transport means data will be sent to other locations. This is the best thing I can define in my work …

1) Exchange: You’re in California, where a strong health exit is taking place. Changing health is related to other countries through national exchange. You can enable data flow through this network, and maybe you can say you do not want to transfer data. The benefit of this type of health exchange is that data is often where you do not need when the patient is passing away. For example, in an emergency, when you are away from home. Or during a natural disaster, when you are forced to leave the house. This network, which I’m explaining to the CA, is used to help those who have lost fire in the forest. The change is what most patients think is logical. This change helped Granny Gloria’s journey between Wisconsin and Texas. You do not need anything unless you agree.

2) Direct: There is an agreed protocol to send health data to the healthcare provider you choose. It is another network and concept. In that case, you’ll need to enter something like an email address (that’s really, but in a secure way). You choose the data you want to send. And send it this moment. It works well if you want to get a second opinion or move to a new home. However, it is necessary for you to request a transfer that will be performed once.

3) Applications: The latest hot technology (ie not widely available) is a third way to enable applications. This is what Apple adds to their phones. If you own an Apple phone, you have an Apple app that can get your data. That is, if your healthcare provider provides data through “This API,” especially the API that complies with the FHIR standard. This standard is very standard and is not ready for use. Not only does Apple have a health care application. There is a lot The struggle is so happy that there are many problems that need to be resolved. For those interested, that’s fun. For others, it will only be frustrating for the next two or three years.

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