Technology

December 13, 2011 โ€“ Boston Scientific announced the U.S. launch of its Charger PTA Balloon Catheter, a 0.035-inch percutaneous transluminal angioplasty (PTA) balloon catheter designed for a wide range of peripheral angioplasty procedures. The Charger PTA Balloon Catheter is Boston Scientific's third new peripheral balloon catheter introduced in 2011.

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Boston Scientific recently announced U.S. Food and Drug Administration (FDA) approval for the Promus Element Plus everolimus-eluting platinum chromium coronary stent system, the company's next-generation drug-eluting stent (DES) technology. The Promus Element, designed to provide physicians improved DES performance in treating patients with coronary artery disease, is built on a platinum chromium (PtCr) platform with the DES market-leading everolimus drug. The company plans to begin marketing the product in the United States immediately.

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December 12, 2011 โ€“ Hansen Medical UK Ltd., a subsidiary of Hansen Medical Inc., a developer of robotic technology for accurate 3-D control of catheter movement, announced a new multi-center worldwide survey evaluating the safety and efficacy of atrial fibrillation (AF) ablation by robotic navigation with the Sensei robotic catheter system. The abstract was presented by Luigi Di Biase, M.D., Ph.D., in a poster session at the American Heart Association Scientific Sessions 2011 at the Orange County Convention Center in Orlando, Florida on November 14th, 2011.

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December 12, 2011 - CardioMEMS announced that the U.S. Food and Drug Administration's (FDA) Circulatory Systems Devices advisory panel voted against the Champion heart failure monitoring system. It is the first wireless, permanently implantable device that allows cardiologists to monitor heart failure (HF) patients from their homes. While the panel agreed with a 9-1 vote that the CardioMEMS technology is safe, the majority did not vote positively that the system is effective and that reasonable assurance of the risks associated with the device outweigh the potential clinical benefits of the technology.

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December 9, 2011 โ€” Maquet announced Thursday it has restructured its U.S. Sales and Services Unit to meet the broader needs of customers across all areas of clinical care. As part of this restructuring, the company now offers a comprehensive disease therapy team dedicated to servicing customers who are building a hybrid operating room (OR).

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December 9, 2011 โ€” Abbott announced Thursday the initiation of ABSORB II, the first randomized, controlled, multi-center clinical trial evaluating the safety, efficacy and performance of the Absorb bioresorbable vascular scaffold (BVS). The Absorb BVS will be compared to the company's Xience Prime everolimus-eluting coronary stent system.

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December 9, 2011 โ€” The American Society of Echocardiography (ASE) and the Society of Cardiovascular Anesthesiologists (SCA) have released a new performance guideline for heightening the use of ultrasound in guided vascular cannulation. The process involves the insertion of a catheter, or tube, into a major vein or artery. The guideline also contains recommendations on training for these life-saving procedures.

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December 8, 2011 โ€” Two new studies report that echocardiography has a central role to play in identifying patients at risk of suffering heart damage from cancer therapies. They also report the procedure can be used in evaluating potential cardio protective treatments. Both studies were presented at EUROECHO 2011, held Dec. 7-10 in Budapest, Hungary.

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December 8, 2011 โ€” Speckle training echocardiography (STE) is the subject of two studies being presented at EUROECHO 2011, Dec. 7-10 in Budapest, Hungary. They compare STE, a recent echocardiography technique, with magnetic resonance imaging (MRI) in quantifying infarct size (IS) after ST-elevation myocardial infarction (STEMI). MRI is the current gold standard for IS quantification.

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December 8, 2011 โ€” A new survey released by the Siemens Radiation Reduction Alliance (SIERRA) reveals awareness and familiarity with medical imaging tests lead to clearer decisions for United States adults about their healthcare. The survey โ€” released at RSNA 2011 โ€” was conducted in response to increased scrutiny over medical imaging scans and the use of radiation.

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December 7, 2011 โ€” At RSNA 2011, Siemens Healthcare is unveiling the Somatom Perspective. It is the first computed tomography (CT) scanner to offer the eMode software solution, which helps determine the best correlation between dose, efficiency and image quality; it can also adjust the required scan parameters automatically.

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Videos | Cath Lab

The Miracor Picso Impulse system is supposed to prevent reperfusion injury and the no-flow phenomenon following ...

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Feature | Dave Fornell

After spending a week walking the show floor and meeting with scores of vendors at the Radiological Society of North America (RSNA) 2011 annual meeting, the following are my choices for the most innovative new technologies presented.

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December 6, 2011 โ€“ Heart Imaging Technologies (Heart IT), which pioneered the first U.S. Food and Drug Administration (FDA)-approved zero-footprint medical imaging workstation, and Johns Hopkins Medicine, announced the award of a National Institutes of Health (NIH) grant to enable the inclusion of medical images in the Nationwide Health Information Network (NHIN). The NHIN is a federal initiative of the National Office of the Coordinator for Health Information Technology.

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December 6, 2011 โ€“ Findings on coronary CT angiography (CTA), a noninvasive test to assess the coronary arteries for blockages, show different risk scenarios for men and women, according to a study presented today at the Radiological Society of North America (RSNA).

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