Surgery/Specialties

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February 2025
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Joint replacement manufacturer recalls products after FDA packaging warning

Editor's Note A January complaint about inefficient packaging for joint replacement products has prompted the manufacturer to recall certain knee and shoulder system devices after initially declining to take the products off the market, according to an April 23 report in Health Exec. The manufacturer, Exactech, is now recalling a…

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By: Matt Danford
April 25, 2024
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Gene-edited pig kidney, heart pump combined in transplant surgery milestone

Editor's Note The second-ever living recipient of a gene-edited pig kidney was the first to have the new organ paired with a mechanical heart pump, according to an April 24 CNN report. The subject, 54-year-old Lisa Pisano, underwent the milestone surgery at NYU Langone Health. She had heart failure and…

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By: Matt Danford
April 25, 2024
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Catheter sterility concerns prompt Class 1 FDA recall for surgery trays

Editor's Note The US Food and Drug Administration has designated DeRoyal Industries’ recall of GeoMed custom tracecarts a class 1, the most serious type of recall indicating a risk of serious injury or death. According to the April 24 FDA notice, the recall is due to sterility concerns with the…

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By: Matt Danford
April 24, 2024
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One patient’s recovery highlights benefits of outpatient endoscopic spine surgery

Editor's Note A 64-year-old patient sought a second opinion with Kern Singh, MD, an orthopedic surgeon, when told he needed a second spine surgery to address complications from a previous procedure. Dr Singh, director of spine surgery at Midwest Orthopaedics at RUSH in Chicago, performs endoscopic spine surgery in the…

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By: Tarsilla Moura
April 24, 2024
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FDA approves imaging drug for detecting cancer after lumpectomy

Editor's Note The US Food and Drug Administration (FDA) approved Lumisight (pegulicianine), a fluorescent imaging drug used to detect cancerous tissue during lumpectomy, on April 17. Administered intravenously prior to surgery, Lumisight is designed for use with the Lumicell Direct Visualization System (DVS) or another imaging device that is FDA-approved…

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By: Matt Danford
April 22, 2024
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Penn Medicine anesthesia, waste initiatives boost OR sustainability

Editor's Note Penn Medicine has made significant strides in reducing the environmental footprint of the OR through department- and team-level initiatives, according to a March 29 report in Penn Medicine news. Driven by CIRCE: Medicine, a faculty group consisting of providers from Penn Medicine and Children’s Hospital of Philadelphia, examples…

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By: Matt Danford
April 22, 2024
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Unveiling ECRI’s 2024 Top 10 Patient Safety Concerns list

From integrating new technology to navigating shifts in care delivery and mitigating burnout, the most pressing challenges for healthcare organizations tend to be multifaceted problems that demand multifaceted solutions. For evidence of that, look no further than the Top 10 Patient Safety Concerns 2024 list from ECRI. For every risk…

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By: Heather David, MSN, CRNP, AGACNP-BC, CSSYB
April 19, 2024
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Neurosurgery trial: Early evacuation improves long-term hemorrhage outcomes

Editor's Note Medical management care with evacuation surgery could yield better 180-day outcomes than without in patents treated within 24 hours for acute intracerebral hemorrhage, according to study results covered in an April 10 MedPage Today report. The ENRICH (Early MiNimally-invasive Removal of IntraCerebral Hemorrhage (ICH)) trial is a multicenter,…

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By: Matt Danford
April 18, 2024
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Propofol anesthesia for colonoscopy could help find polyps, prevent cancer

Editor's Note By putting the patient into deeper sedation during colonoscopy, propofol could help doctors find difficult-to-spot, potentially cancerous “serrated” polyps, according to a study published April 17 in Anesthesiology. As an alternative to moderate, “conscious” sedation, propofol facilitates a more thorough exam that is more likely to identify serrated…

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By: Matt Danford
April 17, 2024
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FDA Class 1 recall renews concern about historically problematic heart pumps

The US Food & Drug Administration (FDA) announced a Class 1 recall on Monday for Abbott/Thoratec Corp.’s HeartMate II and HeartMate 3 Left Ventricular Assist System (LVAS) due due to biological material buildup obstructing the devices. According to an April 16 CBS News report, surgeons first noticed problems with the…

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By: Matt Danford
April 17, 2024
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