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August 5, 2011 – New software aimed at making computed tomography (CT) safer for patients estimates the radiation risk based on age, gender and size rather than using the current “one size fits all” approach. The software program, tested on more than 6,500 scans, was introduced at the 2011 Joint Meeting of the American Association of Physicists in Medicine (AAPM) and Canadian Organization of Medical Physicists (COMP).

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August 5, 2011 — Heart failure circulatory support system maker Thoratec Corp. announced it acquired the medical business of ventricular assist device (VAD) maker Levitronix Medical. The company developed a pediatric VAD, which is currently pending U.S. Food and Drug Administration (FDA) clearance. Levitronix was purchased in a cash payment of $110 million, as well as potential future cash earnout payments of up to $40 million.

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August 5, 2011 — BridgePoint Medical Inc., a Minnesota-based medical device company, has enrolled its first patient in the Peripheral Facilitated Antegrade Steering Technique in Chronic Total Occlusions (PFAST-CTOs) study.

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August 5, 2011 — Vessix Vascular Inc. (formerly known as Minnow Medical Inc.), developer of novel percutaneous radiofrequency (RF) balloon catheter technology for peripheral leg vessels, announced it has completed a $23 million Series B preferred stock financing.

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August 5, 2011 — Christiana Care Health System's William S. Weintraub, M.D., the John H. Ammon chair of cardiology and director of Christiana Care Center for Outcomes Research, is now serving as president-elect of the American Heart Association Great Rivers Affiliate board of directors.

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August 5, 2011 – Children’s Memorial Hospital in Chicago will install Merge Healthcare’s iConnect software suite (vendor-neutral archive [VNA], access and share) at its 270-bed facility.

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August 5, 2011 — BG Medicine Inc., a company specializing in novel, biomarker-based diagnostics, will present results from several studies utilizing its galectin-3 test at the upcoming European Society of Cardiology (ESC) Congress 2011. The conference will be held Aug. 27-31, in Paris, France.

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Feature

August 3, 2011 — Texas Children's Hospital (TCH) is the nation's first pediatric hospital to both surgically implant and later explant a mechanical ventricular assist device (VAD) inside the chest of a teen with chronic heart failure. The procedure acted as a bridge to recovery, avoiding heart transplantation.

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August 3, 2011 — Siemens Healthcare announced that its syngo.via advanced visualization software will be exclusively used by researchers from the National Center for Image Guided Therapy (NCIGT) at Brigham and Women’s Hospital (BWH) in Boston.

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August 3, 2011 — AmbiCom Holdings Inc., developer of wireless products for medical equipment suppliers, announced that it has signed an agreement with a major medical device manufacturer to jointly develop a Wi-Fi card application for its cardiac defibrillator product.

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August 3, 2011 — Merge Healthcare, provider of enterprise imaging and interoperability solutions, announced that Mon General Hospital, located in Morgantown, West Virginia, is installing its full suite of enterprise-level cardiology solutions. Mon General is one of West Virginia’s leading acute care community hospitals

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Technology

August 2, 2011 – The U.S. Food and Drug Administration recently cleared Abbott Vascular’s RX Herculink Elite Renal Stent System. The balloon-expandable, cobalt chromium, laser-cut stent is used to re-open narrowed regions of the renal arteries that supply blood to the kidneys. The device comes in 12, 15 and 18 mm lengths and in diameters from 4 to 7 mm.This device is indicated for use in patients with atherosclerotic disease of the renal arteries following sub-optimal percutaneous transluminal renal angioplasty of a de novo or restenotic atherosclerotic lesion located within 10 mm of the renal ostium.

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August 2, 2011 — The American College of Cardiology’s (ACC) 61st annual scientific session will highlight the organization’s focus on lifelong learning and practice improvement. The event will be held March 24 – 27, 2012 in Chicago.

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August 2, 2011 — Results from a large, United States-based cohort study show that current smokers double their risk of developing atrial fibrillation (AF) compared to people who have never smoked, after more than 13 years of follow-up. The study, published in the August edition of HeartRhythm, the official journal of the Heart Rhythm Society (HRS), indicates a trend towards significantly lower risk of developing AF for those who quit smoking cigarettes versus those who continue to smoke.

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August 2, 2011 — St. Jude Medical Inc. today announced the first patient was enrolled in the EAST (Early comprehensive Atrial fibrillation Stroke prevention Trial) clinical trial.

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