The use of porous titanium acetabular augments in primary total hip arthroplasty for hip dysplasia or rapidly destructive coxopathy.

AIMS

This study aimed to evaluate the efficacy of porous titanium acetabular augments in primary total hip arthroplasty (THA) for reconstruction of superolateral acetabular bone defects in patients with Crowe II or higher classes of developmental dysplasia of the hip (DDH) or rapidly destructive coxopathy (RDC).

METHODS

We conducted a retrospective evaluation of 27 patients (30 hips) who underwent primary THA using cementless cups and porous titanium acetabular augments. The follow-up periods ranged from two to 11 years, with a mean of 5.0 years. The cohort included 22 females (24 hips) and five males (six hips), with a mean age of 67 years (45 to 83) at the time of surgery.

RESULTS

At the final follow-up, there was no radiological evidence of loosening or radiolucency around the cups and augments, indicating successful biological fixation in all cases. Clinically, there was a significant improvement in the Western Ontario and McMaster Universities Osteoarthritis Index score, which improved from a mean of 39.1 (SD 14.7) preoperatively to 5.1 (SD 6.4) postoperatively.

CONCLUSION

The use of cementless cups and porous acetabular titanium augments in primary THA for patients with DDH and RDC can lead to considerable clinical improvements and reliable biological fixation, suggesting their potential as a viable solution for managing challenging acetabular defects in these conditions.