Methinks, a digital health Company that specializes in early detection and management of Acute Stroke (AS), using artificial intelligence (AI), has announced that it has received CE mark for its medical imaging software, Methinks Stroke Suite. This followed a milestone year of development progress, enabling commercialization in Europe and to assist in emergency settings for the benefit of AS patients.
Methinks Stroke Suite is the first CE marked medical device that assists in finding large vessel occlusions (LVO) both hyperdense and not. Large Vessel Occlusion (LVO) is the obstruction of large, proximal cerebral arteries which accounts for approximately 30% of Acute Ischaemic Stroke (AIS) patients.
Acute stroke is a serious life-threatening medical condition that affects approximately 17 million people globally each year. Early detection is vitally important to improve the chance of recovery, reduce permanent disability and reduce the need for extensive rehabilitation.
Methinks Stroke Suite, an AI-based software, is a radiological computer-aided triage and notification system which uses AI algorithms to identify suspected LVO on non-contrast computed tomography (NCCT) images and computed tomography angiography (CTA). In addition, the software also has the ability to detect Intracerebral haemorrhages (ICH) on NCCT images. The software works in parallel to the clinical workflow using the simplest CT scan which is available in all hospitals providing AS care globally and will provide early, rapid and precise triaging of AS patients.
Methinks Stroke Suite has the potential to be a valuable tool which will assist trained physicians to support crucial treatment, and triaging in emergency cases by providing notifications of suspected ICH and LVO cases. The device has been validated with 3800 cases from three different stroke reference hospitals.
Pau Rodriguez, CEO of Methinks, said: "We are delighted with the CE mark approval for our medical imaging software, Methinks Stroke Suite, which paves the way to enhance stroke patient outcomes by decreasing detection time and reducing disabilities. Our software has the potential to be used in every hospital globally to improve the standard of care of patients. The approval comes at a pivotal time ahead of US FDA submission and launching a series A financing to accelerate our growth plans by leveraging and personalizing imaging-software."