Editor's Note Authors of a recent study evaluating the effectiveness of a forced-air drying system for endoscopes argue that the results reinforce the need to re-evaluate standard drying practices. Findings were published February 24 in the American Journal of Infection Control. Wet environments resulting from inadequate drying practices can result…
Editor's Note New standards from The Environmental Protection Agency promise to cut nationwide emissions of ethylene oxide—employed to sterilize more than half of US medical devices—by more than 90 percent. According to a March 15 MedPage Today report, the aim is to reduce cancer risk among the 13 to 14…
Sterile Processing Department (SPD) managers and technicians know a thing or two about pressure. In a recent webinar covering sterile processing basics, Cori L. Ofstead, MSPH, president and CEO of Ofstead & Associates, Inc, and Abby Smart, MPH, research associate, cited the example of a 480-bed hospital that performed 13,650…
Editor's Note A recent study shows show skin antisepsis with iodine povacrylex in alcohol could result in fewer surgical-site infections among patients with closed extremity fractures than antisepsis with chlorhexidine gluconate in alcohol. Published February 1 in the New England Journal of Medicine, the study shows similar results between the…
Immediate use steam sterilization (IUSS, a standard steam sterilization cycle with little to no dry time) is considered safe for patient care when the processes recommended in Association for the Advancement of Medical Instrumentation (AAMI) standards and AORN guidelines are followed. IUSS is a valuable option in an emergency. Lack…
Editor's Note: Adherence to routine disinfection procedures may not be enough to prevent potentially harmful bacterial contamination of high-touch hospital surfaces, according to findings published January 10 in the American Journal of Infection Control. Manikins, bed rails, and workstations-on-wheels were the most contaminated surfaces. The study involved sampling and culturing…
Editor's Note Recent announcements from The US Food and Drug Administration (FDA) validate vaporized hydrogen peroxide (VHP) as an established device sterilization method and warn against the use of the Synovo Total Hip Replacement system. Issued January 8, the announcement about VHP is part of the agency’s multi-pronged approach to…
Takeaways • Failure to understand the complexity of the work performed in the sterile processing department (SPD) can lead to staff shortages, errors, and significant financial loss. • Strategies for addressing SPD staffing include effective orientation, certification, competency assessment, analyzing staffing needs, and leader visibility. • SPD schedules should reflect…
Editor's Note Researchers for a long time have expressed concern about how time and temperature might contribute to changes that affect the cleaning and sterilization of instruments. However, there have been few studies examining these claims. A September 2023 study in Biomedical Instrumentation and Technology from the Association for the…
Editor's Note In a June 27 letter, the American Hospital Association (AHA) urged the Environmental Protection Agency (EPA) “to avoid disrupting healthcare delivery through the unintentional fracturing” of the medical device supply chain with its proposed ethylene oxide (EtO) standards. The EPA proposes: reducing EtO emissions by 80% adding new…