The transfer of pathogens to a patient from a contaminated device, potentially leading to infection, is a risk of all endoscopic procedures.1 Flexible endoscopes have been associated with more outbreaks of infection than any other reusable medical or surgical device.1
Compliance with reprocessing guidelines is crucial to lower the risk of contamination.1 However, multiple studies have reported that endoscopes can be contaminated with potentially pathogenic microbes even when cleaning and reprocessing guidelines are strictly followed2-4
Over 200 journal articles were published in the last decade involving contamination, cleaning failure, or infections associated with flexible endoscopes.
Incidents of contamination have been reported for all major endoscope types.
Endoscope reprocessing is a highly complicated process that can include dozens of individual steps.
Of these steps, the manual brushing and flushing of endoscope channels is recognized as the most critical for successful reprocessing.6
Manual cleaning is today’s gold standard, but has key problems that need to be addressed. Failure of reprocessing just due to inadequate manual cleaning is well documented.3
In a prospective observational study, 92% of endoscopes had protein or ATP levels that exceeded benchmarks after manual cleaning, indicating contamination. This was despite adherence to the site’s cleaning protocols and reprocessing guidelines.7