Many of the following links will provide you with the most up to
date information for recommended practices for your Dental
practice. Some states have their regulations posted below
hyperlinked to the corresponding law.
The CDC
(Center for Disease
Control and Prevention)
www.cdc.gov
Recommended Infection-Control Practices for Dentistry, 1993.
“Proper functioning of sterilization cycles should be verified by
the periodic use (at least weekly) of biological indicators (i.e.
spore tests). Heat sensitive chemical indicators (e.g. those that
change color after exposure to heat) alone do not ensure adequacy of
a sterilization cycle but may be used on the outside of each pack to
identify packs that have been processed through the heating cycle.
A simple and inexpensive method to confirm heat penetration to all
instruments during each cycle is the use of a chemical indicator
inside and in the center of either a load of unwrapped instruments
or in each multiple instrument pack; this procedure is recommended
for use in all dental practices. Instructions provided by the
manufacturers of medical/dental instruments and sterilization
devices should be followed closely.”
Morbidity and Mortality Weekly Report (MMWR)
41(RR-8), May 28, 1993
“This report is based on the recommendations of the Centers for
Disease Control and Prevention (see the CDC recommendations above)
and other publications in the medical and dental literature. The
recommendations in this document have been accepted by the Council
on Scientific Affairs and the Council on Dental Practice. The
Councils strongly urge practitioners and dental laboratories to
comply with these infection control practices…Since this document is
not intended to cover every aspect of infection control compliance,
the dentist, his or her staff and that of dental laboratories should
refer to the referenced publications.” Infection Control
Recommendations for the Dental Office and the Dental Laboratory
ANSI / AAMI
(American National Standards Institute Inc. /
Association for the Advancement of Medical Instrumentation)
www.aami.org
“Biological indicators should be used within PCDs for routine
sterilizer efficacy monitoring at least weekly, but preferably every
day that the sterilizer is in use.” ANSI/AAMI ST79:2006,
Section 10.5.3.2
To view a
State’s law regarding spore testing, click directly onto the State.
* this State has
adopted infection control standards as recommended by the CDC or ADA
DISCLAIMER:
This information has been disclosed to ATS visitors as a courtesy and is
intended as a general information resource only. ATS takes no
responsibility regarding the accuracy of the information provided.
Although every effort has been made to make the information provided
herein accurate and timely, users should understand that State laws are
constantly being revised and updated. Please rely on the official State
versions of their rules, laws, statutes, and policy. (If you do discover
inaccuracies, we would appreciate being notified as soon as possible so
that we can correct it for others. Thank you).
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.