Sterile Processing
The Infection Control Today® sterile processing page provides an inside look into the sterile processing (or central supply) department in the hospital where surgical instruments are cleaned, sterilized, and reprocessed in order to disinfect, remove bioburden, and prep for upcoming procedures. Sterile processing applies to not only the knives, scalpels, scissors, forceps, and clamps used in surgery, but also instruments such as endoscopes and duodenoscopes. ICT® reports on the latest technology but also on the means to disinfect that technology. Also, the trend toward making more disposable surgical equipment. What does that mean for the sterile processing team?
Latest News
November 19th 2024
Learn how Germitec’s Chronos uses patented UV-C technology for high-level disinfection of ultrasound probes in 90 seconds, enhancing infection control, patient safety, and environmental sustainability.
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ChannelCheck Verification Test as a Tool to Assess Endoscope Cleanliness
January 24th 2011The purpose of this study was to determine the real-world effectiveness of healthcare facilities flexible endoscope cleaning procedures by utilizing the ChannelCheck residual soil test, a product of Healthmark Industries Co, Inc. The ChannelCheck test detects the presence of organic contaminants and can serve as a quality control tool to identify potential deficiencies in endoscope reprocessing effectiveness, typically failure results from not following reprocessing standards and guidelines or the use of damaged or defective equipment.
Addressing Fast Turnovers of Surgical Instrumentation
January 24th 2011Turning surgical instrumentation over quickly for the operating room (OR) has always been, and may remain, a constant hot topic. It is a critical issue for several reasons. Flashing is not a viable option for non-emergencies. Capital funds for inventory are not as robust as in years past. Sterile processing departments are often not located within or adjacent to many OR suites at most facilities. Surgical instrumentation and other medical devices are more complex and require unique and extensive processing more then ever. Furthermore, organisms are just as complex as the instruments we are trying to process, so, room for error is much less.
Exploring the Science Behind Antimicrobial Products and Technologies
December 27th 2010Manufacturers make claims about their products' efficacy in killing disease-causing pathogens, but what do infection preventionists really know about the validity of these claims? In a series of articles, we'll take a look at what practitioners in infection prevention should understand about the science behind label claims and marketing hype, including the FDA clearance and EPA registration processes, as well as testing protocols that preceded a product's appearance in the marketplace. In this first article, we talk to Wallace Puckett, PhD, vice president of science and technology for STERIS Corporation, about the knowledge gaps that currently exist relating to research and development of disinfectants, antibacterials, antimicrobials, microbicides and sporicides.
