S32.4
Conditions
Interventions
Group 1: Acetabulum treatment with total endoprosthesis (TEP)
Group 2: Acetabulum treatment with open reduction and plate osteosynthesis (ORIF)
Sponsors
Klinik für Orthopädie, Unfall- und Wiederherstellungschirurgie (Uniklinik RWTH Aachen)
Eligibility
Sex/Gender
All
Age
55 Years to No maximum
Inclusion criteria
Inclusion criteria: Age of 55 years or older, surgical treatment performed by the same pelvic surgeon, and a follow-up period of at least six months.
Exclusion criteria
Exclusion criteria: Patients under 55 years old who received treatment by other pelvic surgeons for periprosthetic acetabular fractures, excluding cases with accompanying injuries that directly affect weight-bearing ability, and excluding those with a follow-up period of less than six months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Function (measured using the Harris Hip Score at 1 week, 6 weeks, and 6 months after the surgery) | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative general and implant-associated complications (e.g., pneumonia, urinary tract infection, secondary fracture dislocation, peri-implantary infections, delirium) Radiological results: positioning and stability of the acetabulum for the total endoprosthesis (TEP) cohort, postoperative step-offs/gaps, as well as progression of osteoarthritis and periarticular ossifications for the ORIF cohort. | — |
Countries
Germany
Contacts
Public ContactEftychios Bolierakis
Klinik für Orthopädie, Unfall- und Wiederherstellungschirurgie (Uniklinik RWTH Aachen)
Outcome results
None listed