This is a multicentre, retrospective study investigating short-term outcomes in 153 consecutive patients receiving REDAPT™ Revision Femoral System.
The READAPT™ Femoral Revision System demonstrates favourable early clinical, radiological and patient-reported outcomes in revision total hip arthroplasty (rTHA).
This retrospective, observational study compares rates of subsidence >5mm in modular versus non-modular tapered, fluted, titanium (TFT) stems.
The technique description herein is made available to the healthcare professional to illustrate the suggested treatment for the uncomplicated procedure. In the final analysis, the preferred treatment is that which addresses the needs of the patient.
This document highlights the surgical technique when using the Redapt™ Revision Acetabular Shell.
The REDAPT™ Acetabular Augments are developed for use in revision total hip arthroplasty cases where bone voids exist that may not be able to be addressed solely through placement of an acetabular shell.
Buttress-type augments have successfully been used as part of acetabular revision surgery to prevent shell migration in severe acetabular defects (Paprosky Type IIIA/IIIB) with good short to mid-term outcomes.
The REDAPT™ Fully Porous Shell is fabricated through additive manufacturing, which permits greater design flexibility compared to standard, subtractive manufacturing (i.e., machining).
Computer-guided THA is associated with reduced risk of revision and increased patient satisfaction compared to conventional THA in the National Joint Registry (NJR) of England, Wales and Northern Ireland
R3™ Poly XLPE Liner Offering Chart
R3™ Optimized XLPE Liners
This dual mobility (DM) acetabular component is designed to deliver increased range of motion with good stability to address dislocation whilst reducing wear.