Sterilization & Disinfection
Study: Anesthetic management of patients with suspected COVID-19 during emergency surgical procedures
Editor's Note This retrospective, multicenter study from four hospitals in Wuhan, China, found that Novel Coronavirus 2019 (COVID-19) specific guidelines for emergency surgical procedures in patients with confirmed or suspected COVID-19 infection can effectively prevent cross-infection in the OR. The guidelines include: negative pressure ORs level 3 protective measures for…
Endoscope drying effectiveness, microbial levels in automated drying vs standard storage cabinets
Editor's Note An automated drying and storage cabinet with forced filtered air is advantageous for rapid drying of endoscope internal and external surfaces and reducing the risk of microbial growth after reprocessing, this study finds. Using the automated drying cabinet, internal channels of all bronchoscopes, colonoscopes, and duodenoscopes studied were…
Study: Inadequate precleaning can jeopardize sterilization of surgical tools
Editor's Note This study by William A. Rutala, PhD, MPH, and colleagues at the University of North Carolina at Chapel Hill, which compared three low-temperature sterilization technologies to steam sterilization of simulated inadequately precleaned surgical tools, found steam sterilization to be the most effective and with the largest margin of…
Challenges in achieving high-level endoscope disinfection
Editor's Note In this review article, Cori L. Ofstead, MSPH, and associates highlight the reasons endoscope reprocessing is often ineffective and microbes frequently remain on endoscopes after high-level disinfection. Among the reasons: non-adherence to guidelines use of damaged endoscopes use of insoluble products during endoscopy insufficient cleaning contaminated rinse water…
Latest sterilization packaging guideline backed by evidence
In October 2019, AORN released its updated Guideline for Sterilization Packaging, which is based on evidence from peer-reviewed literature. This article includes recommendations from that guideline and addresses common misconceptions about sterilization packaging. Other resources for proper use of sterilization packaging include the Association for the Advancement of Medical Instrumentation…
Medline’s Illinois ethylene oxide sterilization facility hopes to reopen end of January
Editor's Note Medline Industries has not operated its Waukegan, Illinois, sterilization facility since December 13, 2019, when it was temporarily closed because it couldn’t meet Illinois’ new state standards for ethylene oxide, the January 21 MedTech Dive reports. A Lake County Health Department update on January 17 says Medline began…
Boston Scientific receives FDA clearance for single-use duodenoscope
Editor's Note Boston Scientific announced December 13 that it had received Food & Drug Administration (FDA) 510(k) clearance for the EXALT Model D Single-Use Duodenoscope for use in endoscopic retrograde cholangiopancreatography (ERCP) procedures. The EXALT Model D, which was granted Breakthrough Device Designation from the FDA, eliminates the need for…
Sterilization trumps high-level disinfection for semicritical items
In the never-ending quest to improve patient care, we are always seeking better ways to process medical devices. Many leading experts now recommend transitioning from high-level disinfection (HLD) to sterilization for semicritical items. Semicritical items are instruments or objects that contact mucous membranes or nonintact skin of a patient, but…
ECRI Institute opposes proposed ban of EtO sterilization
Editor's Note ECRI Institute on November 7 announced that it opposes a total ban of commercial ethylene oxide (EtO) sterilization operations because it could result in widespread shortages of sterile medical devices. Hospitals around the country reported device shortages after a large Illinois-based sterilization plant closed because of state environmental…
FDA of device shortages because of sterilization facility closures
Editor's Note The Food and Drug Administration (FDA) on October 25 released a statement warning of possible device shortages because of interruptions in ethylene oxide (EO) sterilization services due to facility closures in Illinois and Georgia. In the statement, the acting FDA Commissioner, Ned Sharpless, noted that “at this time…
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- FDA draft guidance addresses pulse oximeter accuracy, AI devices
- AAMI updates sterilization materials compatibility guidance
- Study: Esophagectomy outcomes worse at private equity hospitals
- Study: Black CABG patients disadvantaged in accessing best hospitals
- Health system to pilot AI-powered OR cameras; leaders acknowledge privacy challenges
- 3D modeling advances cardiovascular surgery at Boston Children's Hospital
- Report: Healthcare ransomware compromises millions of patient records, costs billions in downtime
- First ACS cancer report highlights neoadjuvant therapy expansion, improvements
- Hospitals continue to grapple with IV fluid shortage
- Proposed tariffs, stricter immigration policies threaten healthcare workforce, supply chain