The Joint Commission issues new Quick Safety on managing packaged sterile supplies, devices
Editor's Note The Joint Commission, on June 28, announced a new Quick Safety advisory on “Managing packaged sterile supplies and devices.” The advisory provides guidance to keep patients safe from infection and harm from expired or compromised supplies and devices and urges healthcare workers (HCWs) to pay close attention to…
Machine learning models predict ambulatory surgery end time, PACU discharge
Editor's Note In this study from the University of California, San Diego, La Jolla, researchers developed a machine learning model that improved the ability to predict surgery end times and PACU discharge at a range of start times in an ambulatory surgery center (ASC). Of 13,447 surgical procedures analyzed, the…
FDA: Class I recall of GE Healthcare’s CARESCAPE R860 Ventilator
Editor's Note The Food and Drug Administration (FDA) on June 28 identified the recall by GE Healthcare of its CARESCAPE R860 Ventilator as Class I, the most serious. The recall was initiated because the ventilator backup batteries, including replacement backup batteries, may run out before they are expected to do…
HHS will not name hospitals where patients contracted COVID-19
Editor's Note According to Politico June 25, the Biden Administration via the Department of Health and Human Services (HHS) decided not to disclose the names of individual hospitals where patients contracted COVID-19, citing “privacy concerns,” Becker’s Hospital Review June 27 reports. This stance is supported by the American Hospital Association…
Impact of COVID-19 on HAIs in Arizona
Editor's Note This study by researchers from the Arizona Department of Health finds that healthcare associated infections (HAIs) significantly increased during the COVID-19 pandemic, especially central line-associated bloodstream infections (CLABSIs). From 2016 through 2019, before the COVID-19 pandemic, Arizona acute care hospitals reported that HAIs decreased significantly: CLABSIs decreased 32%.…
FDA: Class I recall of Baxter’s Volara system with in-line ventilator adaptor
Editor's Note The Food and Drug Administration (FDA) on June 23 identified the recall by Baxter Healthcare Corporation of its Volara system with in-line ventilator adaptor as Class I, the most serious. The Volara system is used to clear mucus out of airways, expand lungs, and treat or prevent pulmonary…
Most hospitals not providing price information for TJAs as required by CMS
Editor's Note This study from the Cleveland Clinic finds that less than one-third of US hospitals were fully compliant in 2021 with the transparency in pricing for total joint arthroplasty (TJA) rule mandated by the Centers for Medicare and Medicaid Services (CMS). Of 400 hospitals analyzed between December 1 and…
CDC: US COVID-19 cases, deaths declining
Editor's Note According to the June 24 Becker’s Hospital Review, the Centers for Disease Control and Prevention’s (CDC’s) latest US COVID-19 statistics include the following: As of June 23, the 7-day average for newly reported COVID-19 cases dropped 5.6% to 97,430. The weekly average for COVID-19 related deaths dropped by…
FDA: Class I recall of Medtronic’s HVAD batteries
Editor's Note The Food and Drug Administration (FDA), on June 23, identified the recall by Medtronic of its HeartWare Ventricular Assist Device (HVAD) batteries as Class I, the most serious. The recall for a single lot (Model Number:1650DE) of HVAD batteries was initiated because of welding defects that allow separation…
Newer COVID-19 subvariants show substantial escape from vaccination, previous infection immunity
Editor's Note In a letter published in the New England Journal of Medicine, researchers at Beth Israel Deaconess Medical Center, Boston, report that the three Omicron subvariants (BA.2.12.1, BA.4, and BA.5) currently dominant in the US substantially escape neutralizing antibodies induced by both vaccination and previous COVID-19 infection. The researchers…
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