The older literature (1960–1982) partially supports this assumption and iodine contrast agents have been modernized considerately. Is the effect the modern contrast agents have on the micro-organisms the cause of the fault negative culture results?
Staphylococcus aureus Staphylococcus epidermidis Enterococcus faecalis Streptococcus pyogenes Bacillus cereus Escherichia coli (E. coli) Pseudomonas aeruginosa Candida albicans Corynebacterium jeikeium Propionibacterium acnes Three different techniques were used: a disk diffusion test (classical resistance determination) and time-killing curves tests with a high inoculum (1,5*108 cfe/ml) and a low inoculum (10*3 cfe/ml) at 0, 2 and 24 hours.
The high and low inoculum tests: only the combinations Telebrix with both P. aeruginosa and E. coli showed any growth inhibition but a non-significant (p = 0.07) growth inhibition of log-1. This however, did not impede the detection of these bacteria. And with all other combinations there was no significant inhibition compared to the saline control and in every combination the percentage surviving number of bacteria was always higher than 30%.
Aspiration arthrography using an iodinated contrast medium is a useful tool for the investigation of septic or aseptic loosening of arthroplasties and of septic arthritis. Previously, the contrast media have been thought to cause false negative results in cultures when present in aspirated samples of synovial fluid, probably because free iodine is bactericidal, but reports have been inconclusive. We examined the influence of the older, high osmolar contrast agents and the low osmolar media used currently on the growth of ten different micro-organisms capable of causing deep infection around a prosthesis. Five media were tested, using a disc diffusion technique and a time-killing curve method in which high and low inocula of micro-organisms were incubated in undiluted media. The only bactericidal effects were found with low inocula of The low and iso-osmolar iodinated contrast media used currently do not impede culture. Future study must assess other causes of false negative cultures of synovial fluid and new developments in enhancing microbial recovery from aspirated samples.