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October 17, 2011 β€” Maquet Cardiovascular announced it has signed a three-year, dual-source contract with Premier Healthcare Alliance to provide intra-aortic balloon pumps (IABP) to the Premier membership.

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October 17, 2011 β€” New research adds to the mounting evidence that consuming chocolate seems to lower the risk of stroke; and now it appears to be more protective against certain types of stroke. Moreover, women who ate the most chocolate β€” 66.5 grams each week, which amounts to roughly two chocolate bars β€” had a 20 percent lower risk of having a stroke. The conclusions are according to a research correspondence report in the Oct. 18 issue of the Journal of the American College of Cardiology (JACC).

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October 17, 2011 β€” The U.S. Food and Drug Administration (FDA) and the Centers for Medicare and Medicaid Services (CMS) have established a pilot program for concurrent review of medical devices. Under the process, certain FDA premarket review submissions and CMS national coverage determinations will be simultaneously reviewed.

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Technology

October 17, 2011 β€” The Detroit Medical Center (DMC) Cardiovascular Institute (CVI) has become the first cardiac care facility in Michigan to successfully open a patient's blocked artery with a breakthrough technology similar to an electrically powered "corkscrew drill." The technique painlessly removes the plaque buildup which causes peripheral artery disease (PAD).

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October 17, 2011 β€” The Joint Commission and the American Heart Association/American Stroke Association (AHA/ASA) are helping organizations provide more comprehensive care for patients at certified primary stroke centers and heart failure programs nationwide.

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October 17, 2011 β€” The U.S. Food and Drug Administration (FDA) has approved LeGoo, a gel allowing surgeons to temporarily stop blood flow during surgery. This makes it possible to join blood vessels without clamps or elastic loops.

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October 17, 2011 – The number of Americans who report they have coronary heart disease – which includes heart attack and angina (chest pain) – continues to decline but rates vary widely from state to state and by race and ethnicity, according to a new report published today in the Morbidity and Mortality Weekly Report of the Centers for Disease Control and Prevention (CDC).

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Feature | Dave Fornell

A U.S. Food and Drug Administration (FDA) review panel has given its unanimous recommendation for the market approval of the Zilver PTX stent. It is the first device of its kind on several fronts to go before FDA review. It is the first drug-eluting stent (DES) for peripheral leg vessels, the first self-expanding DES and the first DES that does not use a polymer to load and elute its drug.

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October 14, 2011 β€” GE Healthcare received U.S. Food and Drug Administration (FDA) clearance of the Discovery MR750w wide bore 3.0T system with GEM (Geometry Embracing Method) suite of coils.

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October 14, 2011 – CardioFocus Inc., developer of the HeartLight endoscopic ablation system (EAS) for the treatment of atrial fibrillation (AF), announced that its HeartLight EAS was used to achieve successful acute pulmonary vein (PV) isolation and restore sinus rhythm in a persistent AF patient during a live case at the Venice Arrhythmias 2011 conference, Oct. 9-12 in Venice, Italy.

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October 14, 2011 β€” The American Society of Echocardiography (ASE) is preparing a guideline document on using strain echocardiography to evaluate cancer patients for early signs of cardiac toxicity due to their medical treatments. The group has also funded a research study to enhance identification of patients who are at risk.

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Technology

October 12, 2011 – The Logiq S8 portable ultrasound system from GE Healthcare fits easily into small exam rooms, can be rolled to where it is needed and provides images across a variety of clinical areas including abdominal, musculoskeletal, breast, vascular and cardiology.

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Feature | Dave Fornell

The Holy Grail sought for more than two decades by interventional cardiology has been proof that minimally invasive, percutaneous coronary interventions (PCI) procedures can perform as well or better than the gold-standard of coronary artery bypass graft surgery (CABG). Abbott Vascular is now pitting its Xience V stent against CABG in a new trial.

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October 5, 2009 – In a breakthrough development that could dramatically reduce the number of leg amputations and painful bypass graft surgeries performed annually on European patients, a first-of-its kind drug-eluting stent for a widespread form of peripheral arterial disease (PAD) is now available to physicians throughout the European Union.

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January 20, 2011 – Drug-coated stents hold promise as a safe and lasting solution for the treatment of clogged leg arteries, suggest two-year results of the Zilver PTX Trial being presented at the 23rd annual International Symposium on Endovascular Therapy (ISET). Blocked leg arteries are a symptom of peripheral arterial disease (PAD), which affects 8 to 12 million Americans.

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