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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.

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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.

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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.

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Technology

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.

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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

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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.

Home November 28, 2010
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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.

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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.

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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.

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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.

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November 24, 2010 – Cardiologists and primary care physicians now perceive AstraZeneca's Crestor as comparable to Pfizer’s Lipitor in treating and reducing mortality in dyslipidemia patients, according to a survey by Decision Resources. This finding has changed from Decision Resources' 2009 analysis in which surveyed cardiologists viewed Lipitor as significantly better.

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November 24, 2010 - Rotational computed tomography angiography (CTA), a new noninvasive imaging modality, has the ability to display angiography in 3-D formats. This allows for considerable simplification of orientation of complex fenestrated/branched stent grafts in 3-D views, as well as catheterization of target vessels.

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November 23, 2010 - The preliminary findings of the CREST study have so far failed to squelch the debate between proponents of the two different interventions for preventing stroke in patients with carotid stenosis. And at least one prominent vascular surgeon sees a most-unscientific phenomenon - “presenter bias” - as one reason the controversy is likely to continue.

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November 23, 2010 – Boston Scientific will acquire Sadra Medical, a development-stage company in Los Gatos, Calif. Boston Scientific will pay $193 million up front, plus potential payments of up to $193 million upon achievement of specified regulatory and revenue-based milestones through 2016. The transaction is expected to be completed in the fourth quarter 2010 or early 2011.

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November 23, 2010 – A device for peripheral transluminal angioplasty (PTA) and for capturing and containing embolic material during angioplasty in the lower extremities has been approved by the U.S. Food and Drug Administration (FDA). The Proteus device, by Angioslide, can be used in the femoral, iliac, iliofemoral, popliteal, tibial, peroneal and profunda arteries.

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