Thanks to our triage tools, we enable fast detection of disease and thus a more efficient management.
By addressing radiologist data overload, stress, and fatigue, we help reduce medical errors and misinterpreted cases.
Facilitate decision making, ensure a prompt therapeutic response and ultimately improve patient outcome.
The incidence of Aortic dissection is reported to be rare, but remains a highly morbid diagnosis. There is a high miss rate in patients with aortic dissection due to different factors, the most common of which is an alternative interpretation of clinical symptoms. Every minute counts for a patient with aortic dissection, that is why it is extremely important to accelerate diagnosis.
CINA-AD was designed and developed to identify acute aortic dissection that requires urgent intervention. This solution meets clinicians’ needs to flag and triage urgent aortic dissection cases by providing accurate and fast real-time alerts on Thoraco-abdominal angiography. Through this innovation the patient will have an immediate access to treatment and intervention. Nowadays, CINA-AD is an unique solution for aortic dissection management that shows impressive results in the patient pathway for healthcare systems under pressure.
Pulmonary embolism is one of the major causes of death and hospitalization worldwide. It is difficult to diagnose a pulmonary embolism since it can manifest itself in diverse ways and several clinical signs non-specific to the disease and can be mimicked by a range of other conditions.
Providing rapid automatic pulmonary embolism detection on chest CT Scan, CINA-PE leverages deep learning algorithms to accelerate clinical workflow, providing clinicians with accurate and rapid real-time alerts on the disease and allowing an immediate treatment and intervention to improve patient management and outcome.
CINA, medical images analysis software, is a medical device manufactured Avicenna.AI. This medical device is reserved for health professionals. This software has been designed and manufactured according to the EN ISO 13485 Quality management system. Read the instructions in the notice carefully before any use.
Instructions for Use are available on https://avicenna.ai/
Manufacturer: Avicenna.AI (France).
Medical devices Class I following European Medical Device Directive 93/42/CEE.
Medical devices Class II following the Code of Federal Regulations of the United States of America 21CFR on Medical Devices.
Avicenna.AI has built technologies that change how AI is used.
Partner with us to improve radiologists’ capabilities together.
