Abstract
The aim of this study was to assess the results of bone ingrowth into the glenoid component of one design of Total Shoulder Arthroplasty (TSA) in which hydroxyapatite (HA) coating of the glenoid baseplate was introduced since 1997.
Glenoid loosening is one of the most important complications of both cemented and uncemented TSA. Between May 1993 and April 1997 over 140 uncemented, porous coated, metal backed glenoid component were used in our Unit. By 1997 it had become clear that a significant number of these glenoid components had developed mechanical loosening and some required revision. We therefore started using an HA coated glenoid component for our TSAs from April 1997.
One hundred and seventy-four shoulder arthroplasty procedures were performed between April 1997 and October 1999 of which 37 were TSAs using the HA coated uncemented glenoid. The indications included osteoarthritis (22), rheumatoid arthritis (nine), revision TSA (three), avascular necrosis (two) and cuff arthropathy with cuff reconstruction (one). The minimum follow-up was 18 months. The X rays were evaluated using the MLS (Migration, Lucent lines, Screw problems) system, which had been developed and reported previously. This system of evaluation has been shown to be reproducible for assessment of glenoid fixation.
There was one case in which the glenoid liner became displaced and had to be replaced. Our early results at a mean FU of approximately 2 years show an improved radiological fixation compared with those glenoids inserted without HA.
The abstracts were prepared by Mr Roger Emery. Correspondence should be addressed to him at the British Orthopaedic Association, Royal College of Surgeons, 35-43 Lincoln’s Inn Fields, London WC2A 3PN
