Better hospital supply chain management leads to better quality of care and supports patient safety, according to a new Cardinal Health survey of hospital staff and decision makers. Despite respondents rating their supply chain processes as “good,” one in four hospital staff have seen or heard of expired product being used on a patient, and 18 percent have seen or heard of a patient being harmed due to a lack of necessary supplies.

Doctors at the University of Alabama at Birmingham have implemented the first U.S. Food and Drug Administration (FDA)-approved patent foramen ovale occluder in Alabama.

The PRO-Kinetic Energy Cobalt Chromium (CoCr) Coronary Stent System from Biotronik has gained U.S. Food and Drug Administration (FDA) approval utilizing results from the BIOHELIX-I clinical study. This stent, which has already been used to treat more than 650,000 patients worldwide, is now available in the United States.


In the current era of healthcare reform and the push toward evidence-based medicine to both lower costs and improve patient outcomes, the heart team approach to cardiac care has gained momentum. This is especially true in the area of structural heart intervention, where the concept was pioneered during the CoreValve and Sapien transcatheter aortic valve replacement (TAVR) trials.


Biotronik has developed an online tool that streamlines the workflow for physicians selecting the right magnetic resonance (MR)-conditional heart monitor or pacing or implantable cardioverter defibrillator (ICD) system for their patients.

The National Institute for Health and Care Excellence (NICE) in the United Kingdom recently issued guidance for use of the HeartFlow FFRct (fractional flow reserve computed tomography) Analysis to help determine the cause of stable chest pain in patients. Developed by HeartFlow Inc., the HeartFlow FFRct Analysis is the first non-invasive technology to provide insight into both the extent of coronary artery disease and the impact that disease has on blood flow to the heart, enabling clinicians to select an appropriate treatment.

Stents were the key focus of interventional cardiology for more than 20 years, but the focus has changed in recent years in favor of novel, more sexy technologies in areas of structural heart repair, transcatheter valves, and new interventional therapies for hypertension, heart failure and stroke.

Vascular Dynamics Inc. (VDI) announced that the U.S. Food and Drug Administration (FDA) has approved the company’s application to participate in the Expedited Access Pathway (EAP) program for its MobiusHD device for the treatment of resistant hypertension.

February 13, 2017 — Vital Images Inc. announced that it will be demonstrating new image sharing capabilities for current Vital customers at the 2017 annual meeting of the Healthcare Information and Management Systems Society (HIMSS), Feb. 19-23 in Orlando, Fla. The solution allows users to share images from different types of media between providers, hospitals and patients.

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