Because of the potential for serious infections, flash sterilization is not recommended for implantable devices (i.e., devices placed into a surgically or naturally formed cavity of the human body); however, flash sterilization may be unavoidable for some devices (e.g., orthopedic screw, plates). If flash sterilization of an implantable device is unavoidable, recordkeeping (i.e., load identification, patient’s name/hospital identifier, and biological indicator result) is essential for epidemiological tracking (e.g., of surgical site infection, tracing results of biological indicators to patients who received the item to document sterility), and for an assessment of the reliability of the sterilization process (e.g., evaluation of biological monitoring records and sterilization maintenance records noting preventive maintenance and repairs with dates). Low-Temperature Sterilization Technologies Ethylene oxide (ETO) has been widely used as a low-temperature sterilant since the 1950s.
Autoclave Indicator Tape, Bowie & Dick Test Packs, Indicator Labels, Multi-Variable Steam Indicator, Class 4, Steam Indicator, Class 6, Helix Control Test Package, Container Seals, Container Key, sterilization equipments, sterilization products, sterilization control, sterilization monitoring, bowie dick test, infection control, cssd, Steam sterilization
It has been the most commonly used process for sterilizing temperature- and moisture-sensitive medical devices and supplies in healthcare institutions in the United States. Two types of ETO sterilizers are available, mixed gas and 100% ETO. Until 1995, ethylene oxide sterilizers combined ETO with a chloroflourocarbon (CFC) stabilizing agent, most commonly in a ratio of 12% ETO mixed with 88% CFC (referred to as 12/88 ETO). For several reasons, healthcare personnel have been exploring the use of new low-temperature sterilization technologies825, 851. First, CFCs were phased out in December 1995 under provisions of the Clean Air Act 852. CFCs were classified as a Class I substance under the Clean Air Act because of scientific evidence linking them to destruction of the earth’s ozone layer. Second, some states (e.g., California, New York, Michigan) require the use of ETO abatement technology to reduce the amount of ETO being released into ambient air from 90 to 99.9% depending on the state. Third, OSHA regulates the acceptable vapor levels of ETO (i.e., 1 ppm averaged over 8 hours) due to concerns that ETO exposure represents an occupational hazard318. These constraints have led to the development of alternative technologies for low-temperature sterilization in the healthcare setting. Alternative technologies to ETO with chlorofluorocarbon that are currently available and cleared by the FDA for medical equipment include 100% ETO; ETO with a different stabilizing gas, such as carbon dioxide or hydrochlorofluorocarbons (HCFC); immersion in peracetic acid; hydrogen peroxide gas plasma; and ozone. Technologies under development for use in healthcare facilities, but not cleared by the FDA, include vaporized hydrogen peroxide, vapor phase peracetic acid, gaseous chlorine dioxide, ionizing radiation, or pulsed light 400, 758, 853. However, there is no guarantee that these new sterilization technologies will receive FDA clearance for use in healthcare facilities. These new technologies should be compared against the characteristics of an ideal lowtemperature (95%) medical devices and materials tested884, 894, 895. Peracetic Acid Sterilization Overview. Peracetic acid is a highly biocidal oxidizer that maintains its efficacy in the presence of organic soil. Peracetic acid removes surface contaminants (primarily protein) on endoscopic tubing711, 717. An automated machine using peracetic acid to sterilize medical, surgical, and dental instruments chemically (e.g., endoscopes, arthroscopes) was introduced in 1988. This microprocessor-controlled, low-temperature sterilization method is commonly used in the United States107. The sterilant, 35% peracetic acid, and an anticorrosive agent are supplied in a single-dose container. The container is punctured at the time of use, immediately prior to closing the lid and initiating the cycle. The concentrated peracetic acid is diluted to 0.2% with filtered water (0.2 μm) at a temperature of approximately 50o C.