News | Sudden Cardiac Arrest

For patients at risk for sudden cardiac arrest (SCA) who are being evaluated for a permanent implantable cardioverter ...

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News | Cardiovascular Ultrasound

DiA Imaging Analysis has partnered with Konica Minolta Healthcare Americas Inc. to expand analysis capabilities of Konica Minolta's Exa Cardio PACS platform (cardiovascular information system) with DiA's LVivo Toolbox for cardiac analysis.

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This is a view of the virtual reality system Stanford created to train staff and educate patients and parents about congenital heart conditions and procedures. This video reached more than 36,000 people on Facebook and was the highest performing video from the 2019 Cardiology AI-Med Conference in June.
Feature | Dave Fornell, Editor

July 2, 2019 — Here is the list of the most popular content on the Diagnostic and Interventional Cardiology (DAIC) ...

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News | Artificial Intelligence

vRad (Virtual Radiologic), a Mednax company recently made a scientific presentation, “Screening for Aortic Dissection on CT Angiography Using a Convolutional Neural Network,” at the Society for Imaging Informatics in Medicine (SIIM) Annual Meeting, June 26-28 in Aurora, Colo.

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Technology | EP Mapping and Imaging Systems

Catheter Precision Inc. announced that the U.S. Food and Drug Administration (FDA) has cleared its new VIVO (View into Ventricular Onset) system for market release in the United States. VIVO is a pre-procedure planning tool that offers 3-D cardiac mapping to aid in localizing the sites of origin of idiopathic ventricular arrhythmias in patients with structurally normal hearts prior to electrophysiology studies. The novel VIVO system uses magnetic resonance imaging (MRI) or a computed tomography (CT) scan along with a standard 12-lead ΕCG to computer-generate color-coded 3-D mapping images of the heart to indicate the area of earliest activation.

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News | Implantable Cardiac Monitor (ICM)

Biotronik announced the market release of its new injectable cardiac monitor (ICM), Biomonitor III, following approval in the CE region. The novel device is designed to help patients with irregular heart rhythms by documenting suspected arrhythmia or unexplained syncope with increased clarity.

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Videos | Cardiovascular Ultrasound

Federico Asch, M.D., FASE, director of cardiac imaging research and director of the cardiovascular imaging lab, MedStar ...

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Videos | Cardiovascular Ultrasound

Partho Sengupta, M.D., MBBS, chief of cardiology, West Virginia Heart and Vascular Institute, explains how wearable ...

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Videos | Contrast Media

Sharon Mulvagh, M.D., FASE, FACC, FRCPC, professor of medicine, division of cardiology, Dalhousie University, Halifax ...

Home June 28, 2019
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Videos | Artificial Intelligence

This is a quick example of how artificial intelligence (AI) is being integrated on the back end of cardiac ultrasound ...

Home June 28, 2019
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Videos | Cardiovascular Ultrasound

Marielle Scherrer-Crosbie, M.D., Ph.D., director of echocardiography at the Hospital of the University of Pennsylvania ...

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Videos | Heart Failure

Federico Asch, M.D., FASE, director of cardiac imaging research and director of the cardiovascular imaging lab, MedStar ...

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Videos | Cardiovascular Ultrasound

Judy Hung, M.D., director of echocardiography, Division of Cardiology, Massachusetts General Hospital, Boston, explains ...

Home June 27, 2019
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Videos | Virtual and Augmented Reality

Roberto Lang, M.D., director of cardiac imaging at the University of Chicago, has been working with TomTec for the past ...

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News | Cardiovascular Ultrasound

The U.S. Food and Drug Administration (FDA) issued the final guidance: Marketing Clearance of Diagnostic Ultrasound Systems and Transducers. This final guidance provides detailed recommendations for manufacturers seeking marketing clearance of diagnostic ultrasound systems and transducers.

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