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CS
Questions ● CS Answers

Cleaning scopes with brushes;
humidity control; EO monitoring badges
with Ray Taurasi
Questions can be e-mailed to
jakridge@hpnonline.com, called in to Jeannie Akridge at HPN,
(941)927-9345 ext.202, or mailed to: HPN CS Questions, 7650 So. Tamiami,
Ste 10, Sarasota, FL 34231. Names and hospital identification will be
withheld upon request.
CS
Question:
I recently took a second job at an out patient clinic that does a lot of
endoscopic procedures. At the hospital I work at, we were trained that
it was necessary to use a brush when cleaning the scopes .However ,at
this clinic brushes are not used for cleaning. I asked the charge nurse
about this and she said that as long as we flushed all the channels
fully until there was no sign of visible soil and wiped the external
areas with a cloth, that brushes were not necessary. Do you think it is
necessary to use a brush or is she right?
CS Answer: It is important to
remember that the goal of cleaning is to remove all soil from any
object, which is going to be sterilized or disinfected. Any soil visible
or invisible that is not removed may present a barrier to the required
contact of the sterilant or disinfecting agent and thus sterilization or
disinfection may not occur. Remaining soil increases the bioburden/
microbial load and can inactivate the efficacy of the chemical agent and
may also present too high of a microbial count to achieve sterilization
utilizing conventional exposure times. In addition to the infection
risks, residual soil remaining on processed instruments, scopes and
lumen devices can become dislodged during subsequent use being left in a
patient as a foreign body presenting a threat to a patient’s safety and
welfare.
Therefore it is absolutely essential to
use a brush when cleaning all endoscopes. All surfaces and channels of
an endoscope, which can be accessed, must be subjected to vigorous
cleaning action utilizing a soft bristled brush designed for this
purpose. Failing to clean with a brush, the suction and instrument
channel, as well as the suction and air/water valves, is a breach of
technique and increases the liability and the risk of disease
transmission from patient-to-patient.
The design of some endoscopes and
instrumentation poses a real challenge to the cleaning process. The
water jet channel on many scopes is too small to clean with a brush.
Generally these lumens are copiously flushed with an enzymatic
detergent, rinsed, chemically disinfected, rinsed again, flushed with
alcohol and air dried. To date there have been no reports of nosocomial
infections linked to a water jet channel cleaned in the aforementioned
manner.
Advancements in technology and
instrument design are dynamic. This coupled with user demands for more
appropriate cleaning instructions is bringing about improvements in
reprocessing this critical patient care equipment ensuring patient
safety and welfare.
It remains the responsibility of users
to demand, obtain and follow manufacturers’ recommendation for the care,
handling and use of all medical devices.
CS Question: Could you please
provide information on the proper humidity to be maintained in the
sterile processing area? What is the best way to control and monitor
this?
CS Answer: The humidity within
the Sterile Processing Department should be controlled between 30 – 70%
in all work areas. The ideal would be 50% in the preparation and
packaging area and no less than 35% relative humidity (RH). It is
critical that the humidity level never exceed 70% in the sterile storage
area. Excessive humidity levels could result in moisture and the
formation of condensate, which could pose a real threat to the sterile
integrity of wrapped sterile goods. There are all sorts of equipment
available for monitoring humidity levels ranging from hand held probes,
traditional, and digital gauges to more sophisticated computerized
devices. Some of these devices have built in alarming mechanisms,
continuous and intermittent recording systems. Most SPD departments I
have visited are utilizing basic humidity monitoring gauges that are
digital or traditional, which must be viewed and visually read. In
situations like this where there is no automatic recording system a log
should be maintained adjacent to the monitoring device and the humidity
conditions should be documented at specified times throughout the day.
Depending on the size, design and layout of the department it might be
necessary to have monitors strategically positioned in the various work
areas. It might be wise to consult with the HVAC specialist in your
engineering /facilities management department to determine the most
appropriate device and locations for monitoring in your department.
CS Question: We are still
utilizing EO for sterilization and run approximately 3 – 4 cycles a
week. Our previous head nurse used to require us to wear monitor badges
once a month to be sure we were not being exposed to any dangerous
chemicals. We got a new boss about a year ago. When he first arrived he
made us wear the monitors a few times but he has not done any personal
monitoring for at least the past eight months. I am concerned that he
isn’t following the regulations and that we might be in danger. What
should we do?
CS Answer: OSHA (Occupational
Health Safety and Health Administration) is a governmental regulatory
agency and has strict regulations regarding employee monitoring for
potential EO exposures in the work environment. OSHA has established
that the Permissible Exposure Limit (PEL) not exceed 1 ppm over an eight
hour TWA (Time Weighted Average) or 5 ppm over a 15 minute Short Term
Exposure Limit (STEL). Employers are held responsible to conduct
personal exposure tests for both the PEL and STEL for all representative
work areas and personnel where EO is utilized. OSHA has also established
an action level of (0.5 ppm for 8 hr. TWA) which determines requirements
for repeated monitoring. If the STEL is at or below 5 ppm and if the 8
hr TWA is at or below the action level of 0.5 ppm no further monitoring
is required (unless specified changes and circumstance arise).
Circumstances that would require additional monitoring include changes
in production process, personnel changes, sterilizer repairs, or any
suspect events. Taking this all into account the monitoring your manager
conducted may have yielded results, which indicated no additional
monitoring was required. Employers are required to notify employees of
monitoring results within 15 days of receipt. I would urge you to voice
your concerns to your manager and request that he provide you with the
monitoring documents. The use of continuous environmental monitoring
systems sensitive to EO greatly guards employees from over exposures.
HPN
Ray Taurasi is director of professional
services for Case Medical Inc., Ridgefield, NJ.

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