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KSR Publishing, Inc.
Copyright © 2012

People, Places, Processes & Products that Influence the Supply Chain

 

INSIDE THE CURRENT ISSUE

November 2011

2011 Endoscope Care Guide

INSIDE THE GUIDE...


Choosing between OEMs and ISOs for repair services


Five primary cost saving tips


Handling reprocessing breakdowns before they happen


Instrument inspections made easier

Quick Reference Tools

·  Flexible GI Endoscopes

·  Small Diameter Flexible

    Endoscopes

·  Rigid Endoscopes


Maintenance and repair secrets that will save you money


Maintenance and repair services


Myths debunked about scope processing


The inherent dangers of reprocessed residue


Understanding manufacturer reprocessing instructions


Warning signs your endoscopes may need service


When the FDA halts the use of your processing technology

 

 
Endoscope Repair
Warning Signs

• Angulation is inadequate and does not meet manufacturer performance standards.

• Air/water functions diminished or not working at all.

• Difficult or impossible to pass brushes or instruments through channels.

• Distal tip (C-cover) damaged and/or chipped.

• Diminished light output.

• Poor image

• Insertion tube peeling.

• Failed leak test

Source:
Jonathan Hart, product manager, Integrated Medical Systems International Inc.

The 411 on manufacturer IFU

One of the more common complaints about reprocessing performance, as well as culprits for reprocessing breakdowns, involves adhering to the manufacturer’s instructions for use (IFU) – be they for the device
being processed or the materials doing the processing.

In fact, sterile processing professionals may not follow the manufacturer’s IFU either out of ignorance or defiance.

Carol Stevens

Here are two of the more prominent misunderstood or overlooked device manufacturer instructions for cleaning, disinfecting and sterilizing and why they make the list, according to Carol K. Stevens, BSN, R.N., CGRN, clinical education consultant, Advanced Sterilization Products.

"Proper reprocessing of endoscopes is a multi-step process and if even one step is not completed or missed, patient care can be compromised," Stevens insisted. "As such, following the manufacturer’s instructions for use (IFU) is critical to ensuring you are delivering the highest standard of care in your facility.
A couple of the most commonly overlooked instructions include:

  • "Leak testing: Leak testing must occur every time an endoscope is reprocessed, as a leak can indicate damage to the endoscope. An advantage of the EVOTECH Endoscope Cleaner and Reprocessor (ECR) from Advanced Sterilization Products is its built-in, automated leak testing for every endoscope during every cycle. If there is a leak, the EVOTECH ECR will automatically cancel the cycle and will not move the endoscope forward in the cleaning and high-level disinfecting process. In fact, the system performs complete monitoring of critical parameters including minimum effective concentration (MEC), block detection, temperature and pressure every second of the cycle.

  • "Enzymatic solution: When it comes to enzymatic solution, some think that more is better. But if the quantity of solution used or the concentration of the solution is too high, it can create a film on the lens of the scope. This could ultimately lead to visual impairment for the physician during a patient procedure. Always follow the IFU for your enzymatic solution, and be wary as the manufacturer could make changes to the concentration or IFU."