Treatment of Periprosthetic Joint Infections Guided by Minimum Biofilm Eradication Concentration (MBEC) in Addition to Minimum Inhibitory Concentration (MIC); a Prospective Randomized Clinical Trial

In the infectious process, biofilms may form early on biomaterials. There is ample evidence to the several-fold increase in antimicrobial concentrations required to eradicate even immature biofilms. In clinical practice the choice of antimicrobials is guided by susceptibility testing based on minimum inhibitory concentrations (MIC), which poorly reflect the increased antimicrobial resistance in biofilms. Minimum biofilm eradicating concentrations (MBEC) might better correspond to in vivo efficacy in the treatment of PJI, and other biofilm-centred infections. There is a need to develop methods, which are reproducible, low-cost, and time-efficient, for in vitro susceptibility testing of clinical biofilm bacteria.

This prospective randomized study aim to compare antibiotic treatment regimens for PJI guided by MIC or MBEC combined with MIC, and how it affects infection resolution, drug tolerability and relapse strain resistance patterns.

The investigors hypothesize that a standardised surgical debridement, antibiotics and implant retention (DAIR) for PJI followed by antibiotic guiding MBEC-diagnostics on deep tissue specimens will increase treatment efficacy and decrease the incidence of infection relapses compared to standard of care.

Following standardised debridement and 14 days of parenteral antibiotics; cloxacillin for methicillin sensitive staphylococci or vancomycin for methicillin resistant staphylococci, patients will be randomized to receive oral antibiotic combinations with either cell wall active standard of care antibiotic combination (MIC-guided) for 6 weeks or non cell wall active antibiotic combination according to a MIC- and MBEC-guided decision algorithm for 6 weeks.

Patients will be included at the Orthopaedic Infection Centre (OIC), Sahlgrenska University Hospital/Mölndal, which is a unit dedicated to optimizing management of orthopaedic infections. Patient consent acquisitions and randomisations (20 patients in each group) will be performed during post-operative hospitalisation. MIC determination and disk diffusion will be performed at the SWEDAC (Swedish Accreditation Body) certified clinical bacteriological laboratory. At the department of Biomaterials (University of Gothenburg), a previously developed clinical diagnostic tool will be employed for the MBEC determination. It consists of the combination of the Calgary Biofilm Device (MBECTM P&G Assay, Innovotech) and a custom-made susceptibility plate (Substrata department, Sahlgrenska Hospital) with 6 antimicrobial agents commonly used to treat orthopaedic infections.