Tag: medical devices

Flexible sticker device detects postoperative gastrointestinal leaks

Editor's Note A medical device developed by researchers at Northwestern University and Washington University School of Medicine could enable clinicians to monitor the health of a patient’s organs following surgery. The findings appeared in the journal Science on March 7.  Patients who undergo gastrointestinal surgeries—including pancreatic surgery—can develop anastomotic leaks…

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By: Brita Belli
March 8, 2024
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Negative pressure wound therapy reduces SSI across surgical specialties

Editor's Note Compared with standard wound dressings, single-use negative pressure wound therapy (NPWT) devices can reduce the incidence of surgical site infection (SSI) in at-risk patients with closed surgical incisions across a range of surgical specialties, according to a data review highlighted in the February issue of the American Journal…

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By: Matt Danford
March 6, 2024
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Study: Dedicated smoke evacuators reduce exposure to particles, VOCs

Editor's Note Dedicated smoke evacuators reduce the number of particles and levels of acetaldehyde and formaldehyde in surgical smoke during laparotomy, according to a study published online October 25, 2023 and in the March 2024 issue of the Journal of the American College of Surgeons The randomized, double-blind clinical trial…

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By: Matt Danford
February 29, 2024
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Bedside portable device offers real-time monitoring for pancreatic fistulas, other conditions

Editor's Note Researchers at the Helmholtz-Zentrum Dresden-Rossendorf (HZDR) and the University Hospital Dresden (UKD) have developed a portable, droplet-based millifluidic device that can monitor patients for postoperative pancreatic fistula in the critical first days after surgery. The same technology might also be expanded to analyze other body fluids and diseases.…

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By: Matt Danford
February 27, 2024
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Unveiling ECRI’s 2024 top 10 health technology hazards list

What is the purpose of the top 10 health technology hazards list, released every year by ECRI? “Our number one goal at ECRI is to reduce preventable harm,” stresses Jason Launders, MSC, former director of operations, device evaluation, at ECRI. “We know that every healthcare provider has a lot they…

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By: Tarsilla Moura
February 27, 2024
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Why OR leaders should revisit sterile processing basics

Sterile Processing Department (SPD) managers and technicians know a thing or two about pressure. In a recent webinar covering sterile processing basics, Cori L. Ofstead, MSPH, president and CEO of Ofstead & Associates, Inc, and Abby Smart, MPH, research associate, cited the example of a 480-bed hospital that performed 13,650…

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By: Uyen Vo, BSN, MBA
February 27, 2024
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Virtual-reality brain measurements illuminate real-world health conditions

Editor's Note Two researchers from South China University of Technology have developed an affordable electroencephalogram (EEG) measurement system that can be incorporated into virtual reality (VR) headsets. In the future, the researchers hope to use the device to explore people's brain activity while navigating specific virtual environments and to study…

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By: Brita Belli
February 26, 2024
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FDA issues warning on fraudulent, unreliable medical device testing data

Editor's Note The FDA has issued a warning regarding fraudulent, duplicated and otherwise unreliable data coming from third party test labs that produce data for medical device companies, including many based in India and China. Issued February 20, the alert warns medical device manufacturers that they are responsible for confirming the…

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By: Brita Belli
February 21, 2024
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Transcatheter therapy system becomes first to earn FDA approval for treating tricuspid regurgitation

Editor's Note Patients with severe cases of tricuspid regurgitation (in which a critical heart valve fails to close properly) now have a new treatment option thanks to the recent US Food and Drug Administration (FDA) approval of the ENVOQUE tricuspid valve replacement system, according to a February 2 press release…

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By: Matt Danford
February 14, 2024
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FDA announces urgent chest drain recall

Editor's Note The FDA has announced a recall of the Atrium Express Dry Suction Dry Seal Chest Drain, a disposable device used to remove air and/or fluid from the chest cavity or mediastinum and to aid in lung expansion and breathing. The drain is being recalled by maker Maquet Cardiovascular,…

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By: Brita Belli
February 9, 2024
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