Editor's Note Boston Scientific announced December 13 that it had received Food & Drug Administration (FDA) 510(k) clearance for the EXALT Model D Single-Use Duodenoscope for use in endoscopic retrograde cholangiopancreatography (ERCP) procedures. The EXALT Model D, which was granted Breakthrough Device Designation from the FDA, eliminates the need for…

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Editor's Note The Food and Drug Administration (FDA) on December 16 announced that Medtronic has recalled its SynchroMed II implantable infusion pump. The pump is being recalled because of the potential presence of foreign particles inside the pump motor assembly that may lead to a pump motor stall. Medtronic has…

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Editor's Note Integrating artificial intelligence (AI) with surgical decision making could transform care by augmenting the decision to perform surgery, informed consent process, identification and mitigation of modifiable risk factors, decisions on postoperative management, and shared decision for resource use, this review finds. Surgical decision making involves hypothetical-deductive reasoning, individual…

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Editor's Note Researchers at UT Southwestern Medical Center in Dallas have developed a new software tool that uses artificial intelligence (AI) to recognize cancer cells from digital pathology images, a December 9 UT Southwestern news release reports. The spatial distribution of different types of cells can reveal a cancer’s growth…

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Editor's Note The Center for Fluorescence-Guided Surgery at UC San Diego Health is the first in the country dedicated to delivering a new caliber of surgical accuracy that allows surgeons to identify cancerous or critical tissues with GPS-like precision by lighting them up, the December 5 UC San Diego Health…

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Editor's Note GE Healthcare introduced the newest advancements in its Edison artificial intelligence (AI) programs and new imaging systems at the Radiological Society of North America’s annual meeting, the December 2 AuntMinnie.com reports. GE designed the Edison Open AI Orchestrator to simplify AI implementation and support of multiple AI applications…

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Editor's Note Two artificial intelligence-based algorithms predicted the probability of a patient dying in the ICU within 30 days of traumatic brain injury with accuracies up to 81% and 84%, in this study from Finland. The first algorithm is based on objective monitor data, and the second one includes data…

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Editor's Note The Food and Drug Administration (FDA) on November 19 updated the device failure associated with Getinge’s Maquet/Datascope Intra-aortic Balloon Pumps (IABPs) in a letter to health care providers. Since 2017, the FDA has received more than 75 reports of the IABPs shutting down while running on battery. Five…

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Editor's Note Artificial intelligence (AI) was able to predict which patients were likely to develop an irregular heart rhythm, even when physicians interpreted results as normal, and identified patients at increased risk of dying of any cause within 1 year, in this study presented November 16 at the American Heart…

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Editor's Note The Food & Drug Administration (FDA) on November 15 announced that it had cleared for marketing in the US the first duodenoscope with a sterile, disposable elevator component. The clearance of the Pentax Medical Video ED34-i10T2 duodenoscope represents a major step toward lowering the risk of infection in…

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