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?
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.
Mighty Mesh: Extracellular Matrix Identified as Source of Spreading in Biofilms
January 23rd 2012New research at Harvard explains how bacterial biofilms expand to form slimy mats on teeth, pipes, surgical instruments and crops. Through experiment and mathematical analysis, researchers have shown that the extracellular matrix (ECM), a mesh of proteins and sugars that can form outside bacterial cells, creates osmotic pressure that forces biofilms to swell and spread. The ECM mechanism is so powerful that it can increase the radius of some biofilms five-fold within 24 hours. The results have been published in the Proceedings of the National Academy of Science.
IAHCSMM, States Making Headway on CSSD Certification Efforts
January 13th 2012The central sterile supply (CSS) discipline is ever-evolving and routinely faces new technology, instrumentation and standards. Staying abreast of these changes is a pervasive challenge, yet is essential for ensuring quality in the central sterile supply department (CSSD), providing exemplary service to the Operating Room and other hospital customers, and, above all, promoting the delivery of safe, high-quality patient care.
FDA, AAMI Examine Medical Device Reprocessing Issues
January 6th 2012Reprocessing medical devices is an intricate, complicated task, and lapses in infection prevention practices can lead to poor patient outcomes and infections. Cognizant of these implications and the role that medical device preprocessing plays in the larger healthcare arena, last summer the Food and Drug Administration (FDA) launched a coordinated effort focusing on improvements in device design, reprocessing procedures and validation methodologies, and healthcare facility quality assurance practices.