Evaluation of Safety of Disposable Saliva Ejectors after Autoclaving Sterilisation.

PURPOSE: To identify the bacteria and proteins that remain after cleaning and sterilisation of SEs used in dental practices, and to investigate potential problems when reusing SEs.

MATERIALS AND

METHODS

In total, 105 SEs used on study participants were collected. The collected SEs were immediately immersed in the disinfectant solution and then washed with tap water and a cleaning brush. The SEs were dried, placed in sterile pouches, and sterilised in an autoclave before being used in the experiment. To detect residual bacteria, SE samples were cultured in brain heart infusion (BHI) broth for 10 days, followed by re-culturing on blood agar and BHI agar. Bacterial identification was performed using bacterial colonies. To identify residual proteins, SE samples were stained with phloxine B, and the stained sites and area were analysed.

RESULTS

Residual bacteria were found in one (1.64%) of 61 sterilised SEs. The cultured colonies were identified as Staphylococcus warneri. Residual proteins were observed on the tips of 36 (81.8%) of the 44 SE samples, and on the bodies of all samples (100%). The average stained area of the residual proteins on the SE bodies was 1.78% (standard deviation, 3.1%).

CONCLUSION

The presence of bacteria and proteins in sterilised SEs indicates that their reuse can cause cross-contamination. This study is the first attempt to provide experimental evidence of the problems with reuse of SEs.