Healthcare Industry News: Trifecta
News Release - March 16, 2011
St. Jude Medical Celebrates Two Millionth Mechanical Heart Valve ImplantMilestone highlights the reliability and durability of the St. Jude Medical heart valve technology
ST. PAUL, Minn.--(Healthcare Sales & Marketing Network)-- St. Jude Medical, Inc. (NYSE:STJ ), a global medical device company, today announced that the company will celebrate the treatment of more than 2 million patients with its mechanical heart valve technology. This milestone, a landmark achievement for prosthetic heart valves, demonstrates the company’s commitment to cardiac surgery and improving patient outcomes.
For more than 30 years, St. Jude Medical has offered patients the gold standard in mechanical heart valve performance and durability. Today, with more than 2 million patients benefiting from its proven valve technology, St. Jude Medical commemorates this important milestone with leading physicians and institutions around the world that have contributed to the success of its mechanical heart valve products.
“I’m very confident using the St. Jude Medical mechanical heart valve in almost all circumstances where a valve replacement is indicated,” said Dr. Denton A. Cooley, M.D., Cardiologist at St. Luke’s Episcopal Hospital, Houston, Texas. “Its record over the past three decades has proven to be one of the most reliable of all cardiac valve prostheses.”
As a pioneer in heart valve technology, St. Jude Medical continues to innovate replacement technologies for patients with diseased, damaged or malfunctioning heart valves. Using the same market-leading expertise as was used for its mechanical heart valve technology, St. Jude Medical has developed the Trifecta™ heart valve, a next-generation tissue valve that has a tri-leaflet stented pericardial design for excellent hemodynamic performance. Designed to be implanted in the supra-annular aortic position, the valve features leaflets manufactured from pericardial tissue attached to the exterior of the valve stent. This design allows the leaflets to open more fully and efficiently, mimicking the performance of a healthy aortic heart valve, while also minimizing tissue abrasion through tissue-to-tissue (stent-to-leaflet) contact.
“For years, St. Jude Medical has worked closely with physicians and institutions around the world to develop our exceptional valve technology,” said Frank J. Callaghan, president of the St. Jude Medical Cardiovascular Division. “This significant milestone is more than just a number, it signifies the trust and confidence physicians have in St. Jude Medical valves. As we move forward with new technologies like our Trifecta valve, we are not only continuing the legacy that was instilled by our mechanical valves, but innovating advanced, best-in-class life-saving technologies.”
The St. Jude Medical valve product portfolio includes market-leading mechanical heart valves, valve annuloplasty rings, porcine tissue valves with superior durability for both the aortic and mitral positions and Trifecta, the newest stented bovine pericardial tissue valve designed for superior hemodynamics.
The Trifecta valve received European CE Mark approval and was fully launched in Europe in 2010. The Trifecta valve is not approved for use in the United States.
About St. Jude Medical
St. Jude Medical develops medical technology and services that focus on putting more control into the hands of those who treat cardiac, neurological and chronic pain patients worldwide. The company is dedicated to advancing the practice of medicine by reducing risk wherever possible and contributing to successful outcomes for every patient. St. Jude Medical is headquartered in St. Paul, Minn. and has four major focus areas that include: cardiac rhythm management, atrial fibrillation, cardiovascular and neuromodulation. For more information, please visit sjm.com.
This news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that involve risks and uncertainties. Such forward-looking statements include the expectations, plans and prospects for the Company, including potential clinical successes, anticipated regulatory approvals and future product launches, and projected revenues, margins, earnings and market shares. The statements made by the Company are based upon management’s current expectations and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. These risks and uncertainties include market conditions and other factors beyond the Company’s control and the risk factors and other cautionary statements described in the Company’s filings with the SEC, including those described in the Risk Factors and Cautionary Statements sections of the Company’s Annual Report on Form 10-K for the fiscal year ended January 1, 2011. The Company does not intend to update these statements and undertakes no duty to any person to provide any such update under any circumstance.
Source: St. Jude Medical
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