People are living longer today; however, the older a person is, the higher the risk of cardiovascular disease, heart attack or stroke. Despite this fact, prevention guidelines for cardiovascular events are the least aggressive for those 75 years and above due to limited clinical data. Researchers at Baylor College of Medicine and Johns Hopkins University are using data from the long-term study Atherosclerosis Risk in Communities (ARIC) to pinpoint the best recommendations for prediction, treatment and prevention for the aging population.

Western Connecticut Health Network (WCHN) cardiothoracic surgeons Cary Passik, M.D., and Robert Gallagher, M.D., were the first in Connecticut to implant the Edwards Intuity Elite sutureless aortic valve in two patients at Danbury Hospital. This new technology in aortic valve replacement (AVR) surgery presents a safe and effective option for patients with severe aortic valve disease. The valves were implanted using the Edwards Intuity valve system, a rapid deployment device approved by the U.S. Food and Drug Administration (FDA) in August 2016.

Medtronic plc announced the U.S. Food and Drug Administration (FDA) has approved its Freezor Xtra Cryoablation Catheter for treating patients with atrioventricular nodal re-entrant tachycardia (AVNRT), a life- threatening abnormal heart rhythm.

February 15, 2017 — GE Healthcare announced U.S. Food and Drug Administration (FDA) 510(k) clearance of GSI Xtream on Revolution CT (computed tomography). The company also announced the first series of clinical images and first installations at Duke University Medical Center (USA), Robarts Research Institute (Canada) and The First Affiliated Hospital of Dalian Medical University (China).

February 15, 2017 — Deep learning, also known as artificial intelligence, will increasingly be used in the interpretation of medical images to address many long-standing industry challenges. This will lead to a $300 million market by 2021, according to a new report by Signify Research, an independent supplier of market intelligence and consultancy to the global healthcare information technology industry.

Mercator MedSystems announced that the national co-principal investigators of the company’s DANCE trial each presented comprehensive 13-month trial data during Late-Breaking sessions at ISET (International Symposium on Endovascular Therapy) in Hollywood, Fla., and LINC (Leipzig Interventional Course) in Leipzig, Germany.

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.

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