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 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 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…
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…
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…
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…
Editor's Note On July 14 and 15, the American Society of Anesthesiologists (ASA) hosted a virtual event, the Anesthesia Quality and Patient Safety Meeting, which brought to light new research on when to administer epidural anesthesia in the OR, an anesthesiologist-led infection prevention program reducing rates of surgical site infections…
Editor's Note The Food and Drug Administration (FDA), on July 13, identified the recall by Draeger Medical of its Oxylog 3000 Plus Emergency and Transport Ventilators as Class I, the most serious. The recall was initiated because of reports that the ventilator may not automatically switch back to using AC…
Editor's Note This multi-center study led by Humana Inc, Louisville, Kentucky, finds that a bundled payment program offered by a Medicare Advantage insurer for lower extremity joint replacements was associated with reduced spending without changes in quality. A total of 23,034 lower extremity joint replacement surgical episodes (6,355 bundled, 16,679…
Editor's Note Because of recent studies, the evolving nature of COVID-19, and widespread vaccination, the American Society of Anesthesiologists (ASA) and Anesthesia Patient Safety Foundation (APSF) on June 20 released a joint statement providing updated recommendations for the timing of elective surgery and anesthesia after COVID-19 infection. The recommendations include:…