Unicompartmental knee arthroplasty revision
Conditions
Interventions
Robot-assisted revision unicompartmental knee arthoplasty:Robot-assisted revision of unicompartmental knee arthroplasty was adopted.
Traditional revision unicompartmental knee arthoplasty:The traditional manual revision unicompartmental knee arthoplasty was adopted.
Sponsors
The First Affiliated Hospital of Chongqing Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Age and gender: Over 18 years old, no gender restrictions. 2.Surgical history or plan: Patients who have undergone unicompartmental knee arthroplasty, those who have developed complications such as infection, loosening, or failure after the operation and need unicompartmental knee arthroplasty, and those who plan to undergo unicompartmental knee arthroplasty (revision to TKA). 3.The clinical manifestations such as pain after unicompartmental knee arthroplasty are severe. The diagnosis is clear as pain after unicompartmental knee arthroplasty, progression of osteoarthritis in the contralateral ventricle, aseptic loosening, infection, dislocation of the mobile pad, etc. Conservative treatment is ineffective, and there are clear surgical indications. 4.The surgical method adopts robot-assisted revision of the unicompartmental knee joint or traditional manual revision of the unicompartmental knee joint. 5.The general preoperative and postoperative data, imaging data, and follow-up data were complete, and the follow-up period was more than 3 months. 6.Completeness of medical record data: Possessing comprehensive medical record data, including surgical records, postoperative follow-up records, blood tests, nutritional status, and mental health assessment, etc. 7.Consent to personal medical information: Agree to provide personal medical information and follow the research process.
Exclusion criteria
Exclusion criteria: 1.Incomplete or unreliable final data: Patients lacking key clinical data or surgical information, or whose data quality does not meet the research requirements. 2.Hemophilia arthritis and other diseases that seriously affect the postoperative recovery level; 3.History of fractures around the femur, tibia and fibula, and knee joint; 4.Preoperative anemia, abnormal coagulation function and other primary or secondary hematological diseases; 5.Current or previous injuries to the medial and lateral collateral ligaments and cruciate ligaments of the knee joint; 6.Poor compliance.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reoperation rate;WOMAC score;SF-36 score;FJS score;Operation time;Hospital stay;Range of motion of the knee joint;Blood loss; | — |
Secondary
| Measure | Time frame |
|---|---|
| Readmission rate;Overall patient satisfaction;VAS score;HSS score; | — |
Countries
China
Contacts
Public ContactKe Li
The First Affiliated Hospital of Chongqing Medical University
Outcome results
None listed