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The best care starts with the best information
Beyond serving as a unique tool to help improve patient care, the RISE Registry is a valuable source of information for those interested in discovering ways to better care for rheumatology patients.
The ACR will begin accepting requests to use RISE data in 2017. In the meantime, please contact us at RISE@rheumatology.org with any questions.
Because RISE automatically extracts data from electronic health records (EHR), research using RISE data can advance our understanding of the natural history, outcomes and treatment of rheumatic disease.
Demonstrate Value of Rheumatology
Data from the RISE Registry will enable the development, testing and rapid implementation of novel measures to define “value” in rheumatology. This is critically important as payers, particularly Medicare, increasingly tie payments to value assessments.
The RISE Registry offers unique benefits as a source of patient data for research:
The ACR has a process through which researchers interested in using RISE data for their work can request use of the data. See details >