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In partnership with the American Academy of Orthopaedic Surgeons (AAOS), the AJRR was founded in 2009 with the goal to optimize patient outcomes through collection of data on all primary and revision total joint replacement procedures in the U.S., while enhancing patient safety, improving quality of care, and reducing the cost for patients.
A joint replacement registry is a system of collecting information of arthroplasty outcomes at a population (often national) level, in order to provide an evidence-base for safe and effective treatment options.
American Joint Replacement Registry; J. Joint replacement registry; N. National Hip Fracture Database This page was last edited on 14 September 2014, at 18:20 ...
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The American Joint Replacement Registry (AJRR) launched their Level III patient-reported outcome (PRO) platform in November 2015 [18] and switched to a new version created and hosted by Ortech Systems in 2016. AJRR imports the PRO data into the AJRR's Demand Reporting & Electronic Dashboard system.
Countries like Australia, Britain, Norway, Sweden, [14] and America [15] have a national joint replacement registry to track patients with artificial joints. "The use of joint registries has proven beneficial abroad.
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Nurse registry, a licensed staffing agency that provides hospitals and individuals with nursing personnel; American Joint Replacement Registry, an organization that collects and reports hip and knee replacement data to provide actionable information to guide physicians and patient decision making to improve care