O1154 MOLECULAR BIOLOGY DIAGNOSIS OF INFECTED TOTAL HIP REPLACEMENT

Abstract

Aims: Identifying low-grade infection in failed total hip replacements (THR) is an important but often difficult task. Recently, there has been interest in the use of molecular biology techniques as potential sensitive tests for low-grade infection by identifying fragments of bacterial DNA within human tissue. Methods: We investigated the ability of a molecular biology technique known as the polymerase chain reaction (PCR) to identify low-grade infection during revision of THR considered to have failed from aseptic causes. We analysed 113 specimens of tissue and synovial fluid from 31 THR revised for aseptic loosening and compared them to 105 control specimens taken during 28 primary THR. All cases were performed in laminar flow theatres. No primary or revision specimen had positive microbiological cultures. No revision specimen had histological evidence suggestive of infection. Results: Using PCR, we identified bacterial DNA in 39 of 85 revision THR tissue specimens (46%) compared to 18 of 84 primary THR specimens (21.4%, p=0.001). Bacterial DNA was identified within the synovial fluid in three specimens taken from 28 revision THR (10.7%) and in two specimens taken from 21 primary THR (9.5%, p=0.36). As multiple specimens were sent per case, 16 of 31 revision THR (52%) and eight of 28 primary THR (29%) were considered to be infected (p=0.072). Conclusions: Our results suggest that many aseptically loose revision THR actually contain bacterial DNA within the peri-prosthetic tissue, but infrequently within the synovial fluid. With an overall specimen contamination rate of 19%, however, PCR has poor specificity for routine diagnostic use in revision THR.