Anesthesiologists

Latest Issue of OR Manager
October 2024
Home Anesthesia > Anesthesiologists

FDA: Class I recall of Walnut Wearable Smart Thermometers

Editor's Note The Food and Drug Administration, on June 12, identified the recall of the rechargeable Walnut Wearable Smart Thermometer as Class I, the most serious. BearCare, Inc, is recalling the thermometers after receiving reports of skin burns and irritation resulting from use of the device. The company reports five…

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By: Judy Mathias
June 14, 2023
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FDA letter on supply shortage of nonsterile, single-use pneumatic tourniquet cuffs

Editor's Note In a June 5 letter to healthcare providers, the Food and Drug Administration (FDA) says it is aware of US healthcare facilities and providers experiencing supply constraints of nonsterile, single-use pneumatic tourniquet cuffs. The cuffs are used in elective limb surgeries and in emergency and trauma settings. During…

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By: Judy Mathias
June 12, 2023
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The Joint Commission revises CAH requirements to align with CMS

Editor's Note The Joint Commission, on May 31, announced that it has added several new and revised elements of performance (EPs) for critical access hospitals (CAHs) that address restraint and seclusion, the complaint process, and unified and integrated structures for CAHs that are part of a multihospital system, effective June…

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By: Judy Mathias
June 1, 2023
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FDA: Class I recall of Draeger Medical’s Seattle PAP Plus, breathing circuit/anesthesia kits

Editor's Note The Food and Drug Administration (FDA), on May 24, identified the recall by Draeger Medical of the Seattle PAP Plus as well as VentStar and other breathing circuit/anesthesia kits as Class I, the most serious. The recall was initiated after finding that glued connections may loosen before or…

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By: Judy Mathias
May 26, 2023
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Projected growth of nursing, OR-related occupations 2021-2031

Editor's Note According to the Bureau of Labor Statistics, the percent of employment growth from 2021 and projected to 2031 for nursing and operating room-related occupations include: Nurse practitioners—45.7% Physician assistants—27.6% Nurse anesthetists—11.8% Nurse midwives—7.5% Licensed practical and licensed vocational nurses—6.3% Registered nurses—6.2% Surgical technologists—5.9% Nursing assistants—4.7 Surgeons—3.4% Anesthesiologists—1.1%.

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By: Judy Mathias
May 24, 2023
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Effect of COVID-19 on emergency CABG outcomes

Editor's Note Though the processes of care for emergency coronary artery bypass graft (CABG) surgery were altered by the COVID-19 pandemic, patient mortality did not change for COVID-19-negative patients; however, COVID-19 positive patients did have significantly higher mortality as well as infectious complications, finds this study presented May 6 at…

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By: Judy Mathias
May 9, 2023
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SHEA: New SSI guidance recommends antibiotics be discontinued after incision is closed

Editor's Note This update to the 2014 "Strategies to Prevent Surgical Site Infections in Acute Care Hospitals" recommends that antibiotics be discontinued after a patient’s incision has been closed in the OR, even if drains are present. The expert panel members writing the update add that continuing antibiotics after closure…

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By: Judy Mathias
May 4, 2023
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Physician vs AI chatbot responses to patient questions

Editor's Note This study, led by researchers at the University of California San Diego, La Jolla, finds that an artificial intelligence (AI) chatbot assistant can provide responses to patient questions that are of comparable quality and empathy to those of physicians. A total of 195 randomly drawn patients’ medical questions…

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By: Judy Mathias
May 1, 2023
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FDA updates Safety Communication on Halyard surgical N95 respirators

Editor's Note In response to questions, on April 21, the Food and Drug Administration (FDA) provided an update to its Safety Communication that enables the use of existing inventory of the O&M Halyard FLUIDSHIELD Surgical N95 Respirator Masks, Orange (Regular), Level 3, (Model 46727). The FDA recommends that, if necessary,…

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By: Judy Mathias
April 25, 2023
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FDA: Class I recall of Ivenix Infusion System

Editor's Note The Food and Drug Administration (FDA), on April 19, identified the recall by Fresenius Kabi USA of its Ivenix Infusion System as Class I, the most serious. The recall was initiated because of a leak in the system that allows fluid to enter the administration set loading area…

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By: Judy Mathias
April 19, 2023
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