Philips Spotlights Latest AI-powered, Software-defined Mr Smart Systems At ECR 2022

Royal Philips, a global leader in health technology, announced its SmartSpeed artificial intelligence (AI) powered MR acceleration software has received U.S. Food and Drug Administration (FDA) 510(k) clearance. Adding advanced AI data collection algorithms to Philips' existing Compressed SENSE MR acceleration engine, Philips SmartSpeed delivers higher image resolution with 3 times faster scan times [1] and virtually no loss in image quality, representing a major step forward in diagnostic confidence and MR department productivity. With personalized treatment for complex diseases such as cancer increasing the need for high-confidence precision diagnoses, coupled with soaring caseloads due to aging populations and high levels of clinician burnout, radiology departments are under increasing pressure to improve performance, productivity, and profitability. "Philips' AI-based SmartSpeed reconstruction is the new benchmark among acceleration techniques for us. It improves on the company's existing Compressed SENSE in all aspects and allows a reduction in scan times with excellent image quality and diagnostic confidence," said Dr. Grischa Bratke, radiologist and expert in musculoskeletal imaging at the University Hospital of Cologne, Cologne, Germany.