A new study determined that the Watchman left atrial appendage closure device is more cost-effective than warfarin and non-warfarin oral anticoagulants (NOACs) for stroke reductions in non-valvular atrial fibrillation patients.

The Medicines Company announced Dec. 18 it has entered into a purchase agreement pursuant to which certain subsidiaries of Mallinckrodt plc will acquire The Medicines Company’s global portfolio of hemostasis products.

A new study from the Healthcare Information and Management Systems Society (HIMSS) offers insight from nearly 200 healthcare executives (C-Suite, administrators, directors and vice presidents) on their population health initiatives, and their current and future approach to population health IT solutions and consultants.

Johns Hopkins has demonstrated in animals that applying a pacemaker’s mild electrical shocks to push the heart in and out of normal synchronized contraction for part of each day may be an effective way to slow down the progression of heart failure.

Booz Allen Hamilton  and Kaggle announced that the second annual Data Science Bowl will call on the global data science community to create a set of steps, or algorithms, to help transform diagnosis of heart disease. Through a partnership with the National Institutes of Health (NIH), participants in the 90-day competition will be given magnetic resonance imaging (MRI) images and asked to develop an algorithm to automate the measurements that are key indicators of heart disease.

January 4, 2016 — In a comparison of bleeding complications and mortality between transradial and transfemoral stent placement following a heart attack, researchers from the Perelman School of Medicine at the University of Pennsylvania found those at risk for more bleeding were often treated with the riskier transfemoral approach. – a demonstration of the so-called risk-treatment paradox. The findings, from the largest study of its kind, were detailed in the Dec.

January 4, 2016 — Living with pulmonary arterial hypertension (PH) is challenging, but the chore of treating the rare heart disease may change following promising clinical trial data published in the Dec. 24 issue of the New England Journal of Medicine.

December 31, 2015 — The U.S. Food and Drug Administration (FDA) Circulatory System Devices Panel of the Medical Devices Advisory Committee will meet in February to discuss and gather public recommendations on clinical trial, post-approval study design and physician training requirements for leadless cardiac pacemaker device technology.  The meeting will take place Thursday, Feb. 18, 2016, from 8 a.m. to 6 p.m. at the Hilton Washington DC North/Gaithersburg, Salons A, B, C, and D, 620 Perry Pkwy., Gaithersburg, MD,  20877.

December 31, 2015 - The U.S. Food and Drug Administration (FDA) has cleared Biotronik's Astron Peripheral Self-Expanding Nitinol Stent System. The device is indicated for improving luminal diameter in patients with iliac atherosclerotic lesions in vessel reference diameters between 4.3 and 9.5 mm and lesion lengths up to 105 mm. 

Hitachi Aloka Medical America is proud to partner with AccreditCoach to provide customers assistance with accreditation and add value to their ultrasound purchase. 

Subscribe Now