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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More

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…

Read More