NEW ADDITION: Developing Objective Performance Criteria (OPC) for Outcomes after Hip and Knee Replacement

Title: Developing Objective Performance Criteria (OPC) for Outcomes after Hip and Knee Replacement

Technology of Interest: Knee and Hip Implants

Disease Area: Orthopedics

Duration: 12 months

Network Collaborator(s): MDEpiNet

The objective of this Test-Case is to develop objective performance criteria (OPC) or goals (OPG) for major outcomes following (Class II or III) implantable device use in primary hip and knee replacements.

Hip and knee joint replacements are the most common procedures in the US, and there has been a continuous increase in the use of these two procedures over time.  The major outcome measures following hip and knee replacements are revisions, and quality of life (QoL) changes. However, specific objective measures for outcomes after treatment have not been developed by the healthcare community.  An OPC is a target performance that was derived from historical data from clinical studies and/or registries which may be used for comparison of safety or effectiveness endpoints for medical devices.

This Test-Case aims to develop OPC measures for all-cause and cause-specific revisions and reoperations at two years following primary hip and knee replacements, by utilizing real-world evidence (RWE) in registries and claims data within the OrthoCRN Network—Kaiser Permanente joint implant registries, FORCE-TJR, etc.).  Further, data from literature review will be used concurrently to understand incidences when registry data is missing or considered incomplete.  The study will explore the feasibility to use number of real-world data (RWD) sources to scientifically develop OPC that could be utilized generally in pre-market device regulation of new devices, pre-market investigational device exemption (IDE) clinical studies, and to support label change decisions of existing devices.  This project will help the U.S. Food and Drug Administration (FDA), device innovators, and manufacturers to adopt a least burdensome approach for evidence generation and reduce the costs of clinical trials.

Working collaboratively with NESTcc will enable engagement between partners from different areas and obtain expert knowledge during the study.  Collaboration with NESTcc also allows for discussion with the community with respect to project methodologies and dissemination, helping demonstrate the impact of real-world evidence (RWE) on device total product life-cycle (TPLC).