Medium-term Results of the LPS™ System for Segmental Resection of the Distal Femur, a Multicenter Retrospective Study (RESIF)

Regional University Hospital Center (CHRU)

Status: Invitation-only

Conditions: Prosthesis Failure

Treatments: Procedure: Femur replacement

Study type: Observational

Funder types: Other

Identifiers

NCT06928948

29BRC24.0294 - RESIF

Details and patient eligibility

About

The reconstruction of the distal femur using modular systems has become increasingly popular over the years, surpassing primary arthrodesis or amputation. Despite the significant advantages of using megaprostheses, complications are not uncommon. Although the Limb Preservation System™ (LPS™, DePuy Synthes; Warsaw, USA) is one of the most widely used megaprostheses in the French market, there is currently no national evaluation of this system, and only two studies have been conducted worldwide.

The aim of our study is to present the mid-term survival rates of the LPS™ implant in order to answer three main questions:

1. What are the overall outcomes of the LPS™ system in distal femur replacement?
2. What factors are associated with a reduced survival rate of the implant?
3. What is the cumulative risk of complications according to Henderson's classification?

The secondary objective is to analyze the occurrence of specific failures, providing insights for potential improvements in the design and use of the LPS™ implant.

Enrollment: 77 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients who underwent distal femoral reconstruction using the LPS system.

Exclusion criteria

• Lost to follow-up before 3 months.
• Associated tibial reconstruction using the LPS system.
• Total femoral reconstruction using the LPS system.