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June 22, 2010 – St. Jude Medical Inc. last week announced the first enrollment in its LAPTOP-HF (Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy) study. The goal of the LAPTOP-HF study is to demonstrate that the new investigational left atrial pressure (LAP) management system safely and effectively improves outcomes in patients with heart failure (HF).

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Feature | Keyur B. Shah, M.D.; Daniel P. Tang, M.D.; Michael Hess, M.D; and Vigneshwar Kasirajan, M.D. Virginia Commonwealth University, Richmond, Va., Advanced Heart Failure and Mechanical Circulatory Support Program

The practicality and expense of maintaining patients on total artificial hearts (TAH) may be significantly impacted with the introduction of a new, investigational portable driver unit. The 13-pound unit driver is intended to replace the previous 418-pound driver, which will allow eligible patients to be discharged to wait for a transplant heart at home, rather than in a hospital.

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June 21, 2010 – Seven out of 10 men admitted to hospital for a heart attack, or acute ST segment elevation myocardial infarction (STEMI), had erectile dysfunction (ED) in the six months prior to their admission, according to new data presented last week at the World Congress of Cardiology Scientific Sessions in Beijing, China.

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Technology

June 21, 2010 – This week, 22 new balloon sizes have been added to the PolarCath Peripheral Dilatation System, including balloon lengths of 120 and 150 mm. The Boston Scientific Corp. PolarCath System is used to restore blood flow in patients with critical limb ischemia (severe blockages in the arteries below the knee) and blockages in the femoral and popliteal (behind the knee) arteries.

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June 21, 2010 – Long-term data presented today from Ardian’s Symplicity HTN-1 study demonstrate that the significant reductions in blood pressure achieved using renal denervation (RDN) treatment are sustained through 24 months. The data were presented at the late-breaking trials session of the European Society of Hypertension (ESH) Annual Scientific meeting in Oslo, Norway.

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June 21, 2010 – MADIT-CRT trial data shows women receive greater clinical benefit from cardiac resynchronization therapy defibrillators (CRT-Ds) than men, Boston Scientific Corp. announced last week. The results were presented during the 17th Cardiostim World Congress by Jonathan Steinberg, M.D., chief of cardiology and director of the Al-Sabah Arrythmia Institute, St.

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June 17, 2010 – AGA Medical Holdings Inc. this week announced first patient enrollment in the feasibility phase of the prospective, multicenter, randomized Amplatzer Cardiac Plug clinical trial. William Nicholson, M.D., an interventional cardiologist and structural heart specialist at York Hospital in Pennsylvania, enrolled the first patient in this multicenter, randomized trial.

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June 17, 2010 – The EnSite Contact Technology platform has received European CE Mark approval, St. Jude Medical Inc. announced today at the 17th World Congress in Cardiac Electrophysiology and Cardiac Techniques (CardioStim).

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June 17, 2010 – The Protecta portfolio of defibrillators will soon be available in Europe. Medtronic Inc. today announced the European launch of the Protecta portfolio of implantable cardioverter-defibrillators (ICDs) and cardiac resynchronization therapy-defibrillators (CRT-Ds).

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Technology

June 16, 2010 – A new therapeutic hypothermia system promises faster cooling and warming rates as well as precise temperature control. Royal Philips Electronics recently announced the launch of the Philips InnerCool RTx Endovascular System for cooling and warming, which provides advanced whole body temperature modulation therapy in a closed-loop system from the inside out.

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June 16, 2010 – An updated ultrasound system announced this week will feature automated measurements, enhanced image quality and improved volumetric imaging. Siemens Healthcare announced the 1.5 release of its Acuson SC2000 volume imaging ultrasound system this week at the 21st Annual Scientific Session of the American Society of Echocardiography (ASE).

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June 16, 2010 – A ventricular assist system has received conditional approval from the U.S. Food and Drug Administration (FDA) to begin a new clinical trial. HeartWare International Inc.

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Technology

June 16, 2010 – A new surgical device for excluding the left atrial appendage has received clearance from the U.S. Food and Drug Administration (FDA). AtriCure Inc. announced this week that it received clearance from the FDA for its AtriClip Gillinov-Cosgrove Left Atrial Appendage Exclusion system.

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June 15, 2010 – A new study evaluating the safety of an echocardiography contrast agent found that the agent did not have a significant effect on patients’ pulmonary pressures.

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June 15, 2010 – Patients with smaller abdominal aortic aneurysms (AAAs) (less than 5.5 cm) have no significant differences in clinical outcomes after endovascular repair (EVAR) than those with larger AAAs according to data from a five-year prospective clinical trial setting. The researchers maintain their recommendation that small aneurysms should not be treated surgically.

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