The
number and types of viable microorganisms with which an
item is
contaminated; this is also called
bioload or microbial load. Bioburden is microorganisms
existing on a product, instrument, device and/or
package.
The most
important step to
decontaminating
all reusable medical devices is thorough cleaning and
rinsing. This doesn’t kill microorganisms, but removes
the bioburden masses, which is then followed by a
disinfection or
sterilization process. Prior to
cleaning, instruments should be presoaked in enzymatic
solution and thoroughly rinsed afterwards. This loosens
the bioburden to allow for thorough cleaning of the
device.
As there
are many different types of medical devices which
include trays, containers, instruments, etc., it is
therefore critical that users follow manufacturer’s
recommendations for proper cleaning, prior to
disinfection or sterilization.
DID YOU KNOW?
§
Autoclave Testing Service, Inc. is one of the first
companies nationwide to offer a
Mail-In
sterilizer monitoring service using biological
indicators. Serving the healthcare industry throughout
the United States and Canada since 1986, we have
thousands of satisfied customers.
§
We
have on-line test
results allowing you to access your results at
your convenience! Your Sterilizer Test Report (STR) is
posted
on-line upon completion
of culturing, offering minimum turn-around time.
§
We
have 24-hour test results for Steam sterilizers!
§
We
have a comprehensive Glossary of Terms related to the
sterile processing area (scroll below to view the
Glossary). This is invaluable information, assisting
you with this important area of your facility.
ATS,
Inc. now stocks sterilization pouches, sterilizer
cleaners, chemical indicator products, sterilizers (new
and used), ultrasonic cleaners, water distillers, and
more! (see
Supplies).
In-Office and Mail-To-Lab Testing!
Verify the sterilization process of all steam
sterilizers which include Statim, Midmark,
Tuttnauer, Lisa, Mocom and Pelton & Crane
sterilizers.
Bowie-Dick Test
Packs should be used daily to evaluate the
performance of air-removal (vacuum) system of
dynamic pre-vacuum type sterilizers. Available
as test cards or preassembled test packs.
Internal CI’s should be used within
each pouch or package, tray, or container. Class 5
Integrators should be used in conjunction with
physical monitoring and biological indicator
testing for verifying the efficacy of a
sterilization system. (See AAMI ST79:2006)
Recordkeeping is a must for all
sterile processing departments. This ensures
accountability and allows operators to trace
errors to their source. Tips on sterilizer
maintenance and technical advice are included with
each book.