Unicompartmental knee arthroplasty

Unicompartmental knee arthroplasty (UKA) is a surgical procedure used to relieve arthritis in one of the knee compartments in which the damaged parts of the knee are replaced. UKA surgery may reduce post-operative pain and have a shorter recovery period than a total knee replacement procedure, particularly in people over 75 years of age. Moreover, UKAs may require a smaller incision, less tissue damage, and faster recovery times. In the United States, the procedure constitutes approximately 8% of knee arthroplasties. In comparisons with a more extensive surgical procedure called high tibial osteotomy, UKA has equal or better outcomes. In the early 1950s, Duncan C. McKeever theorized that osteoarthritis could be isolated to only one compartment of the knee joint, and that replacement of the entire knee might not be necessary if only one knee compartment were affected. The UKA concept was designed to cause less trauma or damage than traditional total knee replacement by removing less bone and trying to maintain most of the person’s bone and anatomy. The concept was also designed to use smaller implants and thereby keep most of the person’s bone, helping them return to normal function faster. Initially, UKAs were not always successful, because the implants were poorly designed, people needing the surgery were not thoroughly screened for suitability, and optimal surgical techniques were not developed. Advancements have been made to improve the design of the implants. Also, choosing the best-suited people was emphasized to ensure that surgeons followed the indications and contraindications for partial replacement. Proper selection, following the indications/contraindications, and performing the surgery well are key factors for the success of UKA. UKA may be suitable for people with moderate joint disease caused by painful osteoarthritis or traumatic injury, a history of unsuccessful surgical procedures or poor bone density that precludes other types of knee surgery. People who may not be eligible for a UKA include those with an active or suspected infection in or about the knee joint, may have a known sensitivity to device materials, have bone infections or disease that result in an inability to support or fixate the new implant to the bone, have inflammatory arthritis, have major deformities that can affect the knee mechanical axis, have neuromuscular disorders that may compromise motor control and/or stability, have any mental neuromuscular disorder, are obese, have lost a severe amount of bone from the shin (tibia) or have severe tibial deformities, have recurring subluxation of the knee joint, have untreated damage to the knee cap and thigh bone joint (patellofemoral joint), have untreated damage to the opposite compartment or the same side of the knee not being replaced by a device, and/or have instability of the knee ligaments such that the postoperative stability the UKA would be compromised. The anterior cruciate ligament (ACL) should be intact, although this is debated by clinicians for people who need a medial compartment replacement. For people needing a lateral compartment replacement, the ACL should be intact and is contraindicated for people with ACL-deficient knees because the lateral component has more motion than the medial compartment. A physical examination and getting the subject’s history is performed before getting surgery. A person with pain in one area of the knee may be a candidate for UKA. However, a person with pain in multiple areas of the knee may not be a good candidate for UKA. The doctor may take some radiographs (e.g., x-rays) to check for degeneration of the other knee compartments and evaluate the knee. The physical exam may also include special tests designed to test the ligaments of the knee and other anatomical structures. Most likely, the surgeon will decide to do a UKA during surgery where he/she can directly see the status of the other compartments. The surgeon may choose which type of incision and implant to use for the subject’s knee. During the surgery, the surgeon may align the instruments to determine the amount of bone to remove. The surgeon removes bone from the (tibia) and thigh bone (femur). The surgeon may decide to check if the appropriate amount of bone was removed during the surgery. In order to make sure that the proper size implant is used, a surgeon may choose to use a temporary trial. After making sure the proper size implant is selected, the surgeon will put the implant on the ends of the bone and secure it with pegs. Finally, the surgeon will close the wound with sutures.