The Limb Loss and Preservation Registry (LLPR) is a national effort in the U.S. aimed at gathering and standardizing data on patients with limb loss or limb differences.
Developed in collaboration with various stakeholders, it collects patient information from hospitals, providers, and patients across all 50 states.
The registry has successfully documented data from over 435,000 patients, enabling improved healthcare practices and guiding national policies through comprehensive data analysis.