TCT 2016, TCT.16, main arena, late breaking trials
Feature | Cath Lab

September 28, 2016 — The Cardiovascular Research Foundation (CRF) included 11 late-breaking trials and 16 first report ...

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News | Optical Coherence Tomography (OCT)

Avinger Inc. recently announced the company has received an FSS Contract Award from the U.S. Department of Veterans Affairs (VA). The award establishes terms under which VA hospitals across the country may acquire Avinger’s Lumivascular portfolio of optical coherence tomography (OCT) image-guided catheters for their veterans hospitals.

Home September 27, 2016
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News | EP Lab

In August, the European Heart Rhythm Association (EHRA) and EP Europace journal announced the release of the supplement to its ninth annual EHRA White Book, developed in partnership with Biotronik. The supplement was released just ahead of the 2016 European Society of Cardiology (ESC) Congress, Aug. 27-31 in Rome.

Home September 27, 2016
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News | Holter Monitoring Systems

BioTelemetry Inc. announced in late August that the company has received CE mark approval of its Holter analysis software. The software can be used either on a stand-alone basis or in combination with the company’s family of digital Holter recorders.

Home September 27, 2016
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News | Pharmaceuticals

Nearly 2 out of 5 people with diabetes who could benefit from statin therapy to lower their risk of future heart attack, stroke and related death were not prescribed one, according to a research letter published in the Journal of the American College of Cardiology. The analysis also showed wide variation in statin use across cardiology practices included in the study.

Home September 26, 2016
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Technology | Drug-Eluting Balloons

C. R. Bard Inc. announced the U.S. Food and Drug Administration (FDA) approved an Investigational Device Exemption (IDE) supplemental application to modify the primary endpoint to a six-month time point for the Lutonix 014 Drug Coated Balloon PTA Catheter (DCB). The Lutonix 014 device is currently the only DCB in an IDE clinical trial in the United States for treatment of arteries below the knee (BTK).

Home September 26, 2016
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News | Mobile Devices

Smartphone communication among medical teams at different hospitals can significantly reduce the time it takes for heart attack patients to get lifesaving treatment after a hospital transfer, according to a research letter published in the Journal of the American College of Cardiology.

Home September 23, 2016
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News | Information Technology

A Google search for heart conditions will now prominently display important questions patients should ask their doctor based on clinical guidelines developed by the American College of Cardiology.

Home September 23, 2016
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News | Cardiovascular Business

Technology advances coupled with increased use of social media and personal devices could offer new possibilities for treating patients and improving outcomes, but new approaches must be rigorously evaluated, according to U.S. Food and Drug Administration Commissioner Robert M. Califf, M.D., MACC. Califf’s comments appeared in a column published in the Journal of the American College of Cardiology.

Home September 23, 2016
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News | Drug-Eluting Balloons

New data presented at the Vascular Interventional Advances (VIVA) conference demonstrated the durability, consistency and safety of Medtronic’s IN.PACT Admiral drug-coated balloon. The presentation included three-year results from the pivotal IN.PACT SFA Trial and one-year, real-world results from the full clinical cohort of the IN.PACT Global Study.

Home September 22, 2016
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News | Heart Valve Technology

4Tech Inc. announced that its TriCinch device has been used in the world’s first-ever successful transcatheter tricuspid valve repair without the use of transesophageal echocardiography (TEE) or general anesthesia to successfully treat tricuspid regurgitation (TR). The TriCinch implant took less than one hour and allowed substantial reduction of TR.

Home September 22, 2016
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Technology | Cardiovascular Ultrasound

September 22, 2016 — GE Healthcare announced the global commercial launch of its new generation of high-end portable ...

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Transesophageal Echo, TEE. Interventional echocardiography, interventional echo, Philips, CX50
Feature | Cath Lab Navigation Aids | Dave Fornell

The rapid growth of transcatheter structural heart procedures and the need for increased use of echocardiography as an ...

Home September 21, 2016
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Sponsored Content | Videos | Inventory Management

With bundled payments putting increased pressure on hospitals to manage supply costs while providing quality patient ...

Home September 21, 2016
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News | Embolic Protection Devices

Claret Medical announced its filing of a marketing application with the U.S. Food and Drug Administration (FDA) for clearance of the Sentinel Cerebral Protection System (CPS). The Sentinel CPS is designed to protect the brain by capturing and removing debris dislodged during transcatheter aortic valve replacement (TAVR) that enters cerebral circulation and carries the potential for stroke. There are currently no cerebral embolic protection technologies available in the United States to protect TAVR patients from cerebral embolic events, according to Claret Medical.

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