Publication BriefsThe authors discuss the need for a current study to test the integrity of commonly utilized ultrasound probe barriers used in clinical practice for transvaginal ultrasound examinations.
View DetailsPublication BriefsMicrobes can remain on endoscopes following reprocessing with high-level disinfectants (HLDs). Factors that can contribute to ineffective endoscope reprocessing include: non-compliance to reprocessing guidelines or facility processes; inadequate device cleaning; using contaminated water for rinsing; remains of insoluble products on devices; insufficient endoscope drying techniques; or HLD chemistry or monitoring issues.
View DetailsPublication BriefsIn this systematic review, the authors examine 14 studies pertaining to outbreaks of Burkholderia cepacian complex in healthcare facilities, all of which were determined to have directly resulted from contaminated ultrasound gel.
View DetailsPublication BriefsIn this publication, the authors examine the outcomes of a clinical study analyzing the effectiveness of longer clean storage hanging times (the time frame in which a medical device can be stored in a contained, controlled environment that limits damage and exposure to moisture, while also protecting the device from harmful human pathogens) in reducing the presence of harmful pathogens on transesophageal (TEE) probes.
View DetailsPublication BriefsIn this review, the authors set out to establish if the use of glow powder to simulate contamination within a sonography environment would serve as an effective teaching technique for sonography students learning proper infection protection and control (IPC).
View DetailsPublication BriefsIn this review, the authors examine an assortment of previously published guidelines regarding the proper methodology for preventing central line-associated bloodstream infections (CLABSIs).
View DetailsPublication BriefsIn this systematic review, the authors evaluate seven individual studies, each of which focused on outbreaks of infection that were traced back to failures in the decontamination process of ultrasound devices.
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