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Effectiveness of endoscope processing: An update
Cori L Ofstead1, Abigail G Smart1, Larry A Lamb1
1Ofstead & Associates, Inc, Minneapolis, MN.
Reusable endoscope reprocessing is often inadequate, leading to patient infections. Routine audits, cleaning verification, and visual inspection are crucial for safety. Sterilization offers a superior safety margin over high-level disinfection.
Area of Science:
- Healthcare-associated infections
- Medical device reprocessing
- Patient safety
Background:
- Endoscopy-associated outbreaks highlight risks from improperly reprocessed reusable endoscopes.
- Pathogen survival and transmission are linked to endoscope cleanliness, integrity, and dryness.
Purpose of the Study:
- To evaluate the effectiveness of current reusable endoscope processing standards.
- To identify common issues and deficiencies in endoscope reprocessing.
Main Methods:
- Systematic review of peer-reviewed articles, governmental agency reports, and adverse event data.
- Analysis of sterile processing breaches, endoscope defects, and microbial contamination.
- Compilation of evidence on endoscope processing effectiveness.
Main Results:
- Widespread nonadherence to endoscope processing standards is evident.
- High-level disinfection is insufficient for reliable microbial elimination.
- Many patient-ready endoscopes exhibit defects, residual soil, or retained fluid.
Conclusions:
- Routine audits and quality assurance measures (cleaning verification, visual inspection) are essential for improving reprocessing outcomes.
- Sterilization provides a greater safety margin than high-level disinfection due to automated systems, quality indicators, and protected packaging.
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