INSTRUMENT READINESS
INSTRUMENT READINESS
INSTRUMENT READINESS
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Results<br />
Endoscopic evaluation of Arthoscopic instruments<br />
revealed retained tissue in the lumen of the<br />
inflow/outflow cannulae and arthroscopic shaver hand<br />
piece.<br />
Changes in instrument reprocessing protocols were<br />
implemented<br />
Safety alert issued by US FDA about concern of retained<br />
tissue in arthroscopic shavers<br />
Conclusions<br />
SSI related to surgical instrument contamination with<br />
Pseudomonas during instrument reprocessing<br />
Retained tissue in inflow/outlaw cannula and shaver<br />
hand pieces could have allow bacteria to survive<br />
sterilization procedures.