Editor's Note Recent research delved into the connection between the transmission of antibiotic-resistant bacteria in the anesthesia work area and the occurrence of surgical site infections (SSIs), Anesthesiology News July 19 reports. While it was previously recognized that reducing microbial transmission through the anesthesia work area is crucial for preventing…
Editor's Note The Food and Drug Administration (FDA), on August 30, identified the recall by Hamilton Medical of its HAMILTON-C1, C2, C3, and T1 ventilators as Class I, the most serious. The recall was initiated because of software issues that may cause the ventilators to stop without notice. There have…
Editor's Note This Canadian study examines whether surgeon gender is associated with long-term postoperative patient outcomes. A total of 1,165,711 patients (151,054 treated by female surgeons and 1,014,657 treated by male surgeons) were included in the analysis. Multivariate adjusted rates of adverse postoperative events (ie, death, readmission, or complication) showed…
Editor's Note The Food and Drug Administration (FDA), on August 23, identified the recall by Draeger Medical of its Carina Sub-Acute Care Ventilators as Class I, the most serious. The recall was initiated because of the presence of contaminants in the device’s airpath. The contaminants exceed acceptable levels if the…
Editor's Note The Food and Drug Administration (FDA), on August 17, identified the recall by Abiomed of the labeling for its Impella RP Flex with Smart Assist System Catheter as Class I, the most serious. The recall was initiated because the catheters’ instructions for use did not appropriately address precautions…
Editor's Note This study from the University of Miami examines the effect of a preoperative walkthrough of a patient’s day of surgery using augmented reality (AR) on perioperative anxiety levels. A total of 95 patients undergoing elective orthopedic surgery at an outpatient surgery center were randomized to an AR intervention…
Editor's Note The Food and Drug Administration (FDA), on August 14, identified the recall by Philips Respironics of its Trilogy Evo, Evo 02, EV300, and Evo Universal Ventilators as Class I, the most serious. The recall was initiated after detecting dust and dirt from the environment in the air path…
Editor's Note The Food and Drug Administration (FDA), on August 10, identified the recall by Datascope/Maquet/Getinge of its Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) as Class I, the most serious. The recall was initiated because the pumps may shut down unexpectedly due to electrical failures in the Power…
Editor's Note The COVID-19 Omicron subvariant EG.5 is now the dominant variant in the US, replacing Arcturus XBB.1.16, according to the August 4 US News & World Report. EG.5 accounts for more than 17% of new COVID-19 cases in the US in the past 2 weeks, and it is increasing…
Editor's Note This study from researchers at Carolina Neurosurgery and Spine Associates and SpineFirst, Atrium Health, Charlotte, North Carolina, examines the cost-utility of anterior cervical discectomy and fusion (ACDF) performed in an ASC vs an inpatient hospital setting at 1-year follow-up. A total of 6,504 patients having 1-to 2-level ACDF…