News | Hypertension

Vascular Dynamics Inc. announced interim results of the company’s first-in-human trial of its MobiusHD implant presented in a podium presentation at the European Society of Cardiology (ESC) in Barcelona. The data showed an average reduction of ambulatory systolic blood pressure of 20 mmHg from baseline in the first 40 patients (of an anticipated 50) to reach the six-month endpoint in studies conducted in the U.S. and E.U.

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Videos | Heart Valve Technology

Azeem Latib, M.D., MBBCh, FCP, interventional cardiologist at Columbus Hospital in Milan, Italy, discusses the latest ...

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News | Radiopharmaceuticals and Tracers

ARTMS Products Inc. signed a strategic partnership with GE Healthcare around ARTMS’ proprietary QUANTM99 Irradiation System (QIS) for radioisotope production. The goal of the partnership is to supply equipment, technologies and research that supports the production and processing of radioisotopes on GE’s PETtrace 800 platform of medical cyclotrons. The QIS integrates on to the GE PETtrace 800 series cyclotron to enable an alternative, non-reactor supply of valuable medical isotopes including technetium-99m, copper-64, gallium-68 and zirconium-89.

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Technology | Ventricular Assist Devices (VAD)

Abbott announced it has received U.S. Food and Drug Administration (FDA) approval for its Full MagLev HeartMate 3 Left Ventricular Assist System. The HeartMate 3 system provides a new option for physicians managing advanced heart failure patients in need of short-term hemodynamic support (bridge-to-transplant or bridge to myocardial recovery). The system also provides patients living with their device new benefits that embody the evolution of left ventricular assist device (LVAD) therapy, such as improved blood flow in a pump that uses full magnetic levitation to reduce trauma to blood passing through the system.

Home August 29, 2017
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Abbott. St. Jude Medical has updated its firmware to address cybersecurity issues with its Allure Quadra MP and other EP devices
Feature | EP Lab | Dave Fornell

August 29, 2017 — The U.S. Food and Drug Administration (FDA) approved a firmware update that is now available to reduce ...

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News | Contrast Media

August 29, 2017 — The European Medicines Agency (EMA) issued a final opinion that recommended restricting the use of ...

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Technology | Drug-Eluting Balloons

C.R. Bard Inc. announced the Lutonix 035 Drug Coated Balloon PTA Catheter (DCB) has been granted premarket approval (PMA) by the U.S. Food and Drug Administration (FDA) for a new indication. With this approval, the device becomes the first and only drug-coated balloon that is FDA-approved as safe and effective in end-stage renal disease (ESRD) patients with stenotic lesions in dialysis arteriovenous (AV) fistulae.

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Videos | Cardiovascular Ultrasound

This video educational session, provided in partnership with the American Society of Echocardiography (ASE), is titled ...

Home August 28, 2017
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Videos | Cardiovascular Ultrasound

This video educational session, provided in partnership with the American Society of Echocardiography (ASE), is titled ...

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News | Antiplatelet and Anticoagulation Therapies

August 28, 2017 — Bristol-Myers Squibb Company and Pfizer Inc. announced results from an analysis of real-world data ...

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News | FFR Technologies

August 28, 2017 — Philips Healthcare and HeartFlow Inc. announced they entered into a collaboration agreement to improve ...

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Videos | Nuclear Imaging

Prem Soman, M.D., director of nuclear cardiology at the Heart and Vascular Institute, University of Pittsburgh, and ...

Home August 24, 2017
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Videos | Nuclear Imaging

Randy Thompson, M.D., attending cardiologist, St. Luke’s Mid-America Heart Institute, Kansas City, explains protocols ...

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News | Radial Access

Merit Medical Systems Inc. will partner with internationally renowned interventional cardiologist Ferdinand Kiemeneij, M.D., Ph.D., to deliver the next generation in educational opportunities for interventional cardiologists and interventional radiologists.

Home August 23, 2017
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News | Embolic Protection Devices

PinnacleHealth is the first hospital in Pennsylvania and one of the first 10 in the country to introduce new technology shown to help protect patients from the risk of stroke during transcatheter aortic valve replacement (TAVR).

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