December 6, 2010 – The U.S. Food and Drug Administration (FDA) has given conditional approval for a trial that will investigate the role of a device in reducing infarct size in patients with ST-elevation myocardial infarction (STEMI). The MINI-AMI trial will use the Impella 2.5, from Abiomed, for 24 hours following primary percutaneous intervention (PCI).
December 6, 2010 - A blood vessel dysfunction that is linked to cardiovascular illness also appears to play a role in the development of Alzheimer's disease. Supporting data from the study was published in Circulation Research: Journal of the American Heart Association.
December 6, 2010 – A new stent shows favorable outcomes compared to bare metal stents (BMS) for treating coronary artery bifurcation lesions. Data for the Genous Stent, from OrbusNeich, was published online in the journal, Atherosclerosis.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
December 6, 2010 – The American College of Cardiology (ACC) has partnered with Philips Healthcare on a new Hospital to Home (H2H) Learning Destination that will show how to improve the continuum of care. It will be featured at the ACC’s 60th Annual Expo in New Orleans.
December 6, 2010 – A panel of medical imaging experts discussed medical imaging appropriateness, ionizing radiation and efforts to curb overutilization, decrease radiation dose and educate patients.
December 3, 2010 – The initial patients have been enrolled in a trial for treating atrial fibrillation (AF). The DEEP AF trial will evaluate the safety and efficacy of a dual epicardial/endocardial procedure, or hybrid procedure, using AtriCure’s minimally invasive surgical ablation platform. In addition, it will use Thermocool catheter ablation products from Biosense Webster.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
December 3, 2010 – The U.S. Food and Drug Administration (FDA) has given conditional approval for an Investigational Device Exception (IDE) application for a system for treating coronary artery disease. The pivotal trial will look at the Tryton Side Branch Stent.
December 3, 2010 – For the first time, data has shown that cardiac resynchronization therapy (CRT) is cost-effective in mildly symptomatic heart failure (HF) patients. Data from an economic sub-study of the REVERSE trial was published in the European Heart Journal.
November 30, 2010 – The U.S. Food and Drug Administration (FDA) has given 510(k) clearance for a suite of clinical applications that is directly integrated into PACS and cardiovascular systems. FujiFilm Medical’s Synapse 3D is vendor neutral, multi-modality capable, and can be used with virtually any advanced imaging system.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
November 30, 2010 – New clinical and reporting capabilities have been added to a cardiovascular image and information system (CVIS). Version 4.0.5 of Synapse Cardiovascular, by FujiFilm Medical Systems, now features 3-D and intelligent structured reporting (ISR), enabling faster creation of consistent, high-quality echocardiography reports. Synapse 3D
November 29, 2010 – Independent research firm Frost and Sullivan has given TeraRecon the North American Growth Leadership of the Year award in Advanced Visualization and Clinical Applications. This is the sixth time in the past 10 years that Frost and Sullivan has given the company an award. The company also received the European Company of the Year award for medical imaging.
November 24, 2010 – A new advanced visualization and analysis software suite has passed a detailed evaluation and testing process and is now available for sale. The Vitrea Enterprise Suite version 6.0, from Vital Images, has achieved VMware Ready status and is now listed on the VMware Partner Product Catalog.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
November 24, 2010 – Data from the PICTURE trial showed that an insertable cardiac monitor led to diagnosis and treatment for 78 percent of patients who experienced a recurrent syncopal (fainting) event during the study. The Reveal family of insertable cardiac monitors, by Medtronic, also showed that 75 percent of those diagnosed were shown to have a cardiac cause of their syncopal event.
November 24, 2010 – Results for a trial comparing a drug-eluting stent to balloon angioplasty and bare metal stenting in treating restenosis after angioplasty were announced at the VEITHsymposium. The Zilver PTX drug-eluting stent met the trial's 12-month primary endpoints. The stent has CE mark approval in Europe for the superficial femoral artery.
November 24, 2010 – Researchers at Northwestern are utilizing a patient’s own stem cells to regenerate heart and vascular tissue, offering a potential new treatment for cardiovascular disease. Northwestern Medicine is the lead site for a study examining stem cell transplantation as treatment for critical limb ischemia.