Published in:
01-01-2011 | Clinical Research
Effect of Prior Salter or Chiari Osteotomy on THA with Developmental Hip Dysplasia
Authors:
Kenji Tokunaga, MD, Nadim Aslam, MD, FRCSC, Rad Zdero, PhD, Emil H. Schemitsch, MD, FRCSC, James P. Waddell, MD, FRCSC
Published in:
Clinical Orthopaedics and Related Research®
|
Issue 1/2011
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Abstract
Background
Controversy exists regarding the outcome of THA after prior pelvic osteotomy.
Questions/purposes
We conducted a retrospective chart and radiographic review to obtain outcome measures for perioperative complications, acetabular and femoral component revisions, Harris hip score, and survivorship and compared these outcomes for patients presenting with developmental dysplasia of the hip treated surgically using THA with and without prior pelvic osteotomy.
Patients and Methods
We performed 103 primary THAs in 87 patients with osteoarthritis secondary to developmental dysplasia of the hip with a minimum 3-year followup. Previous pelvic osteotomy was performed in 52 hips (Salter, 40; Chiari, nine; Salter and Chiari, three), and 51 hips had no previous surgery (control group).
Results
The pelvic osteotomy group did not have higher rates of femoral or acetabular intraoperative fracture or dislocation compared with the control group. The overall revision rate was 28.8% in the pelvic osteotomy group compared with 19.6% in the control group. The revision rate for aseptic loosening was 23.1% in the pelvic osteotomy group compared with 17.6% in the control group. Harris hip scores (range, 20–87) were not compromised, and overall survivorship rates 8 years postoperatively were not different at any time between the pelvic osteotomy (83.3%) and control (88.4%) groups.
Conclusions
Prior pelvic osteotomy did not lead to a higher perioperative complication rate, higher revision rate, compromised Harris hip score, or shortened survivorship in eventual THA in developmental dysplasia of the hip.
Level of Evidence
Level III, therapeutic study. See the Guidelines for Authors for a complete description of levels of evidence.