Anesthesiologists
FDA: Class I recall of Cardiosave Hybrid, Rescue IABPs
Editor's Note The Food and Drug Administration (FDA), on August 31, identified the recall by Getinge/Maquet/Datasocpe of its Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) as Class I, the most serious. The FDA posted four recalls for four separate reasons: Because they may overheat when the device’s internal temperature…
Study: Introducing propofol to ambulatory anesthesia may improve endoscopy quality metrics
Editor's Note A study presented at the 2023 annual meeting of the Society for Ambulatory Anesthesia suggests that implementing ambulatory anesthesia services with propofol can significantly enhance various quality metrics in outpatient endoscopy procedures, Anesthesiology News August 28 reports. The study, led by Justin Routman, MD, director of non-OR anesthesia…
Nature-themed recharge room lowers HCW stress, anxiety
Editor's Note This study by nurse researchers at Hackensack Meridian Jersey Shore University Medical Center, Neptune, and Hackensack Meridian Health, Edison, New Jersey, finds that a nature-themed recharge room helped reduce healthcare worker (HCW) stress and anxiety. A total of 160 HCWs who used the recharge room and 131 who…
Report: Physician starting salary surging, medical specialties in high demand
Editor's Note According to this annual report from the AMN Healthcare’s Physician Solutions division (formerly known as Merritt Hawkins), titled "2023 Review of Physician and Advanced Practitioner Recruiting Incentives" and published on July 24, the average "starting salaries for physicians have rebounded from the COVID-19 pandemic," an AMN Healthcare August…
FDA: Class I recall of Draeger Carina Sub-Acute Care Ventilators
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…
FDA: Class I recall of certain Philips Respironics ventilators
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…
Association of intraop opioid administration with postop pain, opioid use
Editor's Note This study led by researchers at the Massachusetts General Hospital and Harvard Medical School, Boston, examines the association between intraoperative opioid administration and postoperative pain and opioid use. A total of 61, 249 surgical patients were included in the analysis. The researchers found that increased intraoperative: fentanyl and…
FDA: Class I recall of Baxter SIGMA Spectrum, Spectrum IQ infusion pumps
Editor's Note The Food and Drug Administration (FDA), on August 1, identified the recall by Baxter Healthcare Corporation of its SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) and Spectrum IQ Infusion System with Dose IQ Safety Software (Version 9) as Class I, the most serious. The recall…
FDA: Class I recall of GE HealthCare’s TruSignal SpO2 sensors
Editor's Note The Food and Drug Administration (FDA), on July 28, identified the recall by GE HealthCare of its TruSignal SpO2 [arterial oxygen saturation] sensors as Class I, the most serious. The recall was initiated because of issues that may reduce the amount of energy sent to the heart during…
Medical confidentiality breaches on Twitter by anesthesiology, intensive care HCWs
Editor's Note This French study examines the rate of medical confidentiality breaches in tweets by anesthesiology and intensive care healthcare workers (HCWs). Data from 431 tweets with photographs and 9,000 text-only tweets from 1,831 accounts were included in the analysis. Among the findings: There were 44 (10.2%) breaches of medical…
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