“This FDA clearance confirms RAPID as the de facto standard in neuroimaging, not only for the automated analysis of brain images derived from CT and MRI, but now for the diagnosis and treatment of stroke,” said Don Listwin, CEO of iSchemaView. “The new clearance will particularly benefit smaller community hospitals and the patients they serve. Because RAPID enables stroke treatment decisions that are based on intuitive and easily interpretable real-time views of brain perfusion, physicians will quickly and easily be able to determine which patients can be treated locally and which require urgent transfer to thrombectomy centers—bolstering the capabilities of smaller hospitals and therefore improving patient care.”
In addition to having the broadest FDA clearance of any cerebrovascular imaging software, RAPID is the only platform that is clinically validated in more than 10 major trials—including use for patient selection in landmark stroke studies such as SWIFT PRIME, EXTEND IA, and most recently, EXTEND. The RAPID platform was also the exclusive imaging system used for patient selection for two landmark stroke trials published in The New England Journal of Medicine, DAWN and DEFUSE 3, that successfully treated patients up to twenty-four hours after onset. The results of these studies changed the American Heart Association and American Stroke Association’s 2018 stroke guidelines to expand the stroke treatment window from six hours to 24 hours for eligible patients.
Developed by leading stroke experts, RAPID’s artificial intelligence framework combines unmatched expert feature extraction and proprietary algorithms to deliver the best-in-class platform, which includes tools for CT perfusion, MR diffusion and perfusion, CT angiography and CT ASPECT scoring. RAPID modules feature custom notifications, custom thresholding, hypoperfusion, and cerebral blood volume indexes and golden hour thresholds.