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Perioperative RBC transfusions linked to postop VTE

Editor's Note In this study, perioperative red blood cell (RBC) transfusions were significantly associated with development of new or progressive postoperative venous thromboembolism (VTE) within 30 days of a surgical procedure. Of 750,937 patients included in the analysis, 47,410 (6.3%) received at lest one perioperative RBC transfusion. Of these, 6,309…

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By: Judy Mathias
June 18, 2018
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FDA issues Safety Alert for compounded drugs containing triamcinolone, moxifloxacin

Editor's Note The Food & Drug Administration (FDA) on June 14 issued a Safety Alert for compounded drugs containing triamcinolone and moxifloxacin by Guardian Pharmacy Services (Dallas, Texas). At least 43 patients have reported adverse events after receiving eye injections of the compounded triamcinolone and moxifloxacin drug during cataract surgery.…

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By: Judy Mathias
June 18, 2018
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American Heart Association, Joint Commission collaborating on cardiovascular certification programs

Editor's Note The American Heart Association (AHA) and Joint Commission are partnering to enhance cardiovascular patient care through a range of disease-specific hospital certification programs, the AHA announced on June 11. Both organizations are expanding their 15-year relationship in stroke certification to in-hospital cardiovascular patient care. The expansion will consolidate…

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By: Judy Mathias
June 14, 2018
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Effect of neuraxial anesthesia for total joints on outcomes

Editor's Note Increased use of neuraxial anesthesia for total hip and knee patients was linked to lower hospitalization costs in this study. National data on 808,237 total knee and 371,607 total hip replacements were used in the analysis. Multivariable associations were measured between hospital neuraxial anesthesia volume (quartiles) and outcomes…

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By: Judy Mathias
June 12, 2018
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Machine-learning algorithm predicts hypotension during surgery

Editor's Note In this study, researchers at UCLA Medical Center in Los Angeles applied machine learning to arterial pressure waveforms to develop an algorithm that predicted intraoperative hypotension 15 minutes before it occurred in 84% of cases. Two sets of data were used to build the algorithm. One set consisted…

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By: Judy Mathias
June 12, 2018
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Researchers identify biomarkers for total hip patients likely to develop osteolysis

Editor's Note Researchers at Rush University Medical Center, Chicago, have identified two protein biomarkers that indicate which total hip patients are likely to develop osteolysis. Osteolysis is the destruction of bone tissue around the hip joint that causes the implant to loosen and results in a revision surgery. The researchers…

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By: Judy Mathias
June 8, 2018
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FDA updates recommendations to reduce surgical fires

Editor's Note The Food & Drug Administration (FDA) on June 5 updated its Safety Communication: “Recommendations to Reduce Surgical Fires and Related Patient Injury.” Among the recommendations: Perform a fire risk assessment before each surgical procedure. Encourage communication among anesthesia personnel, surgeons, and OR staff. Practice safe use and administration…

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By: Judy Mathias
June 8, 2018
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FDA issues Class I Recall of CARDIOSAVE Hybrid Intra-aortic Balloon Pump by Maquet Datascope

Editor's Note The Food & Drug Administration on June 6 identified the recall by Maquet Datascope Corp of its CARDIOSAVE Hybrid Intra-aortic Balloon Pump as Class I, the most serious. The recall was initiated because of a design issue that allows fluid to seep into the device, which can lead…

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By: Judy Mathias
June 7, 2018
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Radial-artery vs saphenous-vein grafts in CABG surgery

Editor's Note In this study, the use of radial-artery grafts for coronary artery bypass grafting (CABG) resulted in a lower rate of cardiac adverse events and a higher rate of patency at 5 years than saphenous-vein grafts. A total of 1,036 patients (534 radial artery, 502 saphenous vein) from six…

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By: Judy Mathias
June 5, 2018
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FDA: Class I recall of HeartWare HVAD system by Medtronic

Editor's Note The Food & Drug Administration on June 1 identified the recall by Medtronic of its HeartWare Ventricular Assist Device (HVAD) system as Class I, the most serious. The recall was initiated because of the possibility for an interruption to occur in the electrical connection between the system’s power…

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By: Judy Mathias
June 4, 2018
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