Editor's Note The Food and Drug Administration (FDA) sent warning letters August 12 to three manufacturers of duodenoscopes involved in transmitting deadly bacteria earlier this year, the Boston Globe reports. The FDA says the companies (Olympus, Pentax, and Fujifilm) failed to: report problems with the scopes as required by law…
The Association for the Advancement of Medical Instrumentation (AAMI) has published its first standard on flexible endoscope reprocessing. ANSI/AAMI ST91: 2015 Flexible and Semi-rigid Endoscope Processing in Health Care Facilities was developed from research and input from manufacturers of flexible endoscopes, users, consultants, and regulatory bodies. The new standard, which…
Editor's Note The Food and Drug Administration on August 4 released a Safety Communication that contains supplemental measures to enhance duodenoscope reprocessing. The measures emerged from an expert panel meeting earlier this year. In addition to following manufacturer reprocessing instructions, the FDA says facilities can use one or more of…
Editor's Note Surgical teams at Northwesterm Memorial Hospital in Chicago are decreasing the rate of urinary tract infections by focusing on the use of catheters before and immediately after surgical procedures. A process improvement program reduced the number of UTIs associated with catheters placed in patients in the OR from…
Editor's Note The Society for Healthcare Epidemiology of America and the Infectious Diseases Society of America have updated the 2008 Strategies to Prevent Surgical Site Infections in Acute care Hospitals. The evidence-based recommendations include 15 strategies for SSI prevention and a special section on implementation that emphasizes a team-based approach…
Editor's Note A diagnostic tool developed by researchers at McMaster University, Hamilton, Ontario, can detect the smallest traces of compounds that signal the presence of an infectious disease, such as C difficile, MRSA, hepatitis C, and other superbugs. The test has the best sensitivity ever reported for a detection system.…
Relations between the OR and the sterile processing department (SPD) are not always smooth. OR staff need timely, accurate instrument trays that meet the highest standards of safety. Anything short of 100% performance leads to complaints about the SPD. But many OR staff members do not appreciate the challenges faced…
Instruments that are still damp or wet after being sterilized cannot be placed in storage. The moisture that remains on or inside of a package can create a pathway for microorganisms to travel from the outside to the inside of the package. Moisture may be in the form of visible…
Disinfection robots are first on the ECRI Institute’s 2015 Top 10 Hospital C-Suite Watch List, which includes new and emerging technologies healthcare providers should know about. Hospital-acquired infections (HAIs) are a persistent problem, and a recent study supports the efficacy of disinfection robots. However, the technology is expensive, and experts…
The Food and Drug Administration (FDA) on March 17 published a final guidance on reprocessing reusable medical devices. This guidance, which provides manufacturers with recommendations to validate their reprocessing instructions, comes on the heels of a host of “superbug” bacteria outbreaks related to reprocessing of endoscopic retrograde cholangiopancreatography (ERCP) duodenoscopes.…