Structural Heart Disease

Structural heart diseases include any issues preventing normal cardiovascular function due to damage or alteration to the anatomical components of the heart. This is caused by aging, advanced atherosclerosis, calcification, tissue degeneration, congenital heart defects and heart failure. The most commonly treated areas are the heart valves, in particular the mitral and aortic valves. These can be replaced through open heart surgery or using cath lab-based transcatheter valves or repairs to eliminate regurgitation due to faulty valve leaflets. This includes transcatheter aortic valve replacement (TAVR). Other common procedures include left atrial appendage (LAA) occlusion and closing congenital holes in the heart, such as PFO and ASD. A growing area includes transcatheter mitral repair or replacement and transcatheter tricuspid valve repair and replacement.

ATS under investigation by shareholders for Medtronic takeover

ATS Medical of Minneapolis is under investigation after reports that the company breached fiduciary duty to its shareholders by agreeing to sell the company to Medtronic in a cash deal valued at almost $370 million.

Edwards defeats Cook in German heart valve patent case

The Federal Patent Court in Munich has ruled in Edwards Lifesciences favor, finding Cook's German transcatheter heart valve patent invalid.

NCHS: 45% of adult Americans suffer from cardiac-related diseases

Nearly 45 percent of the population suffers from hypertension, hypercholesterolemia or diabetes and a majority go undiagnosed. Additionally, incidence rates of these chronic conditions differ among racial and ethnic groups, according to data published by the National Center for Health Statistics (NCHS).

Medtronic seeks to buy ATS Medical for $370M

Medtronic has signed a definitive agreement to acquire ATS Medical for the approximate price of $370 million, which includes the purchase of ATS' stock and assumption of net debt.

FDA expands external defib recall to 280K devices

The FDA has expanded an external defibrillator Class 1 recall, suggesting that about 280,000 devices could malfunction due to faulty components of 14 models made by Cardiac Science when used on patients experiencing sudden cardiac arrest.

Forest drops out of $340M diabetes drug deal with Phenomix

After Phenomix released reportedly optimistic results from its phase 3 clinical trial studying the effectiveness of dutogliptin to treat type 2 diabetes on April 20, Forest Laboratories said that it is bailing out on the almost $340 million deal, in which the companies entered Oct. 23, 2009, to co-develop and commercialize dutogliptin, Phenomixs home-grown dipeptidyl peptidase-4 (DPP-4) inhibitor.

Edwards enrolls patients into trial to evaluate trancatheter heart valve

Edwards Lifesciences has begun enrolling patients into the PREVAIL Japan clinical trial to study the safety and efficacy of transcatheter aortic heart valves, specifically its Sapien XT.

FDA issues Class I recall for Physio's Lifepak devices

The FDA has issued a class I recall for Physio-Control's Lifepak 15 monitors/defibrillators after the company found that the devices have the potential to malfunction and power on and off unexpectedly.

Around the web

Ron Blankstein, MD, professor of radiology, Harvard Medical School, explains the use of artificial intelligence to detect heart disease in non-cardiac CT exams.

Eleven medical societies have signed on to a consensus statement aimed at standardizing imaging for suspected cardiovascular infections.

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