Editor's Note Without proper nail care, proper handwashing might not be enough to prevent infection and death among infants in the neonatal intensive care unit (NICU). That’s according to a February 8 report from nurse.org, which drove home the importance of following hygiene protocols by highlighting real-world evidence confirming the…
Editor's Note The FDA has issued a Class I recall of Philips’ BrightView, BrightView X and BrightView XCT Single Photon Emission Computed Tomography (SPECT) scanners due to a component failure that could result in the system’s detector falling on patients. Philips sent all affected customers an Urgent Medical Device Correction…
Editor's Note New survey data indicate most nurses have experienced workplace violence within the past year, and the problem appears to be getting worse. Conducted by National Nurses United (NNU), the nation’s largest union and professional association of registered nurses, the nationwide survey gathered data from nearly 1,000 nurses working…
Editor's Note ECRI, an independent, nonprofit organization that aims to improve the safety, quality, and cost-effectiveness of care across all healthcare settings, every year compiles and unveils a list of the top 10 technology hazards affecting patient care. The motivation for producing this list, according to Jason Launders, director of…
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: General Electric (GE) EVair and EVair 03 (Jun-air) air compressors can release dangerous levels of formaldehyde when paired with Carescape R860 and Engström Carestation/Pro ventilators, the U.S. Food and Drug Administration (FDA) warned January 9. Designed to supply the respective ventilators when wall air is not available, the…
Editor's Note Published December 21, a year-long investigation by KFF Health News into medical device malfunctions found that the FDA allows the sale of most medical devices, including many implants, without requiring tests for safety or effectiveness. Instead, manufacturers need to show only that they have “substantial equivalence” to an…
Editor's Note Reports of burn injuries have prompted two medical device recalls: one for Megadyne patient return electrodes and one for Olympus bronchofiberscopes and bronchovideoscopes. According to a December 21 notice from AORN, the former recall is a voluntary correction on the part of Megadyne Medical Products, Inc. Following reports…
Takeaways • The Joint Commission eliminated 56 redundant or outdated Elements of Performance, revised four others, and is using more checklists. • The Joint Commission is emphasizing healthcare equity and identifies it as a priority to address healthcare quality and safety, calling organizations to integrate health equity into their QAPI…
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…