0SWV3JZ
Revision Knee Joint, Tibial Surface, Right to No Qualifier with Synthetic Substitute, Percutaneous Approach
Procedural Specifications
| Clinical Axis | Detail Definition |
|---|---|
| Section | 0 Medical and Surgical |
| Body System | S Lower Joints |
| Operation | W Revision |
| Body Part | V Knee Joint, Tibial Surface, Right |
| Approach | 3 Percutaneous |
| Device | J Synthetic Substitute |
| Qualifier | Z No Qualifier |
Operation Definition
Correcting, to the extent possible, a portion of a malfunctioning device or the position of a displaced device
Procedure Overview
Revision procedures correct a malfunctioning device already implanted in a lower joint, or reposition a device that has shifted out of place, without necessarily removing and replacing the whole implant. Examples include tightening a loosened hip component, adjusting a worn knee liner, or repositioning a dislocated joint implant back into alignment. The reason for surgery is a problem with hardware from an earlier operation rather than new injury to native tissue.
These procedures are often needed years after an initial joint replacement, as components can loosen, wear, or shift with normal use. Surgeons aim to fix the specific mechanical problem while preserving as much of the existing implant and surrounding bone as possible, since more extensive revisions carry greater surgical risk and longer recovery.
Anatomy & Axis Detail
Knee Joint, Tibial Surface, Right
Revision of the right knee joint at the tibial surface addresses failure of the tibial component of a prior total knee arthroplasty, including subsidence of the tibial baseplate into the proximal tibia, loosening at the bone-cement or bone-implant interface, or wear and delamination of the polyethylene insert seated on the tray. Because the tibial component bears substantial compressive and rotational forces during weight-bearing and must remain level and well-fixed to prevent progressive bone loss, revision often involves exchanging the polyethylene liner, replacing the entire tibial tray, or correcting its position, sometimes requiring bone grafting for defects created by loosening. Documentation should clearly indicate that the corrective procedure addressed the tibial component specifically, as opposed to the femoral side of the same knee replacement.
Approach: Percutaneous
Percutaneous describes entry by needle or instrument puncture through the skin or mucous membrane to reach the site of the procedure, without cutting the tissue open or using a visualizing scope. It differs from Open in that the site itself is never exposed, and from Percutaneous Endoscopic in that no endoscope is used to see internal structures. Common examples include needle biopsies and injections.
Device: Synthetic Substitute
Synthetic Substitute designates a device made from manufactured, non-biologic material, such as mesh or prosthetic components, used to replace or augment a body part. It is distinguished from the two tissue substitute categories by its artificial composition, which carries different considerations for integration and long-term durability than biologic grafts.
Coding & Documentation
Documentation needs to identify that an existing device was the target of correction, whether through repositioning, adjustment, or partial component exchange, and that the fix did not amount to a full swap of the entire prosthesis. Notes describing loosening, malposition, or component wear typically support Revision. A common error arises when a full component exchange occurs during a documented revision surgery; if the entire device is replaced, the correct root operation is Replacement, even though the surgeon may call it revision arthroplasty.