Author/Authors :
ERSCHBAMER, Matthias Department of Orthopaedics and Traumatology, Kantonsspital St. Gallen, Switzerland , ZDRAVKOVIC, Vilijam Department of Orthopaedics and Traumatology, Kantonsspital St. Gallen, Switzerland , ERHARDT, Johannes Department of Orthopaedics and Traumatology, Kantonsspital St. Gallen, Switzerland , ÖHLSCHLEGEL, Christian Department of Pathology, Kantonsspital St. Gallen, Switzerland , GROB, Karl Department of Orthopaedics and Traumatology, Kantonsspital St. Gallen, Switzerland
Abstract :
Background and purpose — Biodegradable cement restrictors
are widely used in hip arthroplasty. Like others, we observed
osteolytic reactions associated with a specifi c cement restrictor
(SynPlug; made of PolyActive) and reviewed our patients.
Patients and methods — We identifi ed 703 patients with suit-
able radiographs from our database (2007 to 2012) who under-
went cemented hip arthroplasty and received a SynPlug biode-
gradable cement restrictor. We reviewed all available radiographs
to determine the incidence, severity, and progression of osteolysis.
Mean postoperative follow-up was 1.8 (1–7) years
Results — 1 year after implantation, the femoral cortex showed
thinning by 12% in the anterior-posterior view and by 8% in
the axial view. This had increased to 14% and 12%, respectively,
at the latest available follow-up postoperatively (at a mean of 4
years). Cortical thinning of less than 10% was found in 37% of
patients, but cortical thinning of 10–30% was found in 56% of
patients. In the remaining 7%, a reduction of more than 30% of
the original cortical thickness was observed.
Interpretation — Osteolytic changes associated with the Syn-
Plug biodegradable bone restrictors are inconsistent and highly
variable. While some patients showed increased weakening of the
femoral cortex with the potential risk of periprosthetic fracture,
in others the degree of osteolysis only increased slightly or sta-
bilized after 2 or more years. Any cortical bone loss after total
hip replacement should be avoided, so the use of PolyActive bio-
degradable cement restrictors should be discontinued. Patients
with a PolyActive cement restrictor in place should be followed
up closely after surgery.