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obrother.bsky.social
Des nouvelles de l'intégration de l'IA en médecine.
Spécifiquement : au bloc opératoire (le YOLO est total)

Spoiler : c'est criminel.

#QuiAuraitPuPrévoir
#LaSurpriseMenTombeDuPikachu
wolvendamien.bsky.social Dr. Damien P. Williams can't think of a fun display name right n @wolvendamien.bsky.social · 2d
*my biggest and most exhausted sigh*

"As AI Enters the Operating Room, Reports Arise of Botched Surgeries and Misidentified Body Parts"
www.reuters.com/investigatio...
Screenshot of text reading At least 10 people were injured between late 2021 and November 2025, according to the reports. Most allegedly involved errors in which the TruDi Navigation System misinformed surgeons about the location of their instruments while they were using them inside patients’ heads during operations. Cerebrospinal fluid reportedly leaked from one patient’s nose. In another reported case, a surgeon mistakenly punctured the base of a patient’s skull. In two other cases, patients each allegedly suffered strokes after a major artery was accidentally injured. Screenshot of text reading In May 2023, Dean was using TruDi in another sinuplasty operation when patient Donna Fernihough’s carotid artery allegedly “blew.” Blood “was spraying all over” – even landing on an Acclarent representative who was observing the surgery, according to a lawsuit Fernihough filed in U.S. District Court in Fort Worth against Acclarent and several manufacturers. One of Fernihough’s carotid arteries was damaged. She suffered a stroke the day of the surgery, according to her suit. Acclarent “knew or should have known that the purported artificial intelligence caused or exacerbated the tendency of the integrated navigation system product to be inconsistent, inaccurate, and unreliable,” the suit alleges. Screenshot of text reading The FDA requires clinical trials for new drugs, but medical devices face different screening. Most AI-enabled devices coming to market aren’t required to be tested on patients, according to FDA rules. Instead, makers satisfy FDA rules by citing previously authorized devices that had no AI-related capabilities, says Dr. Alexander Everhart, an instructor at Washington University’s medical school in St. Louis and an expert on medical device regulation.
February 10, 2026 at 6:24 AM