The featured products reflect the company’s continued commitment to developing comprehensive, high-performance solutions which advance the practice of interventional cardiology by improving efficiencies and giving physicians more control.
The company’s latest products and technologies for access, intervention, hemostasis management, cardiac rhythm management, and valve replacement will be demonstrated and on display on Sept. 23 and Sept. 24 from 9 a.m. to 5 p.m. and Sept. 25 from 9 a.m. to 2 p.m. at the St. Jude Medical booth (#1704) including:
St. Jude Medical access products are designed to provide simple, consistent and repeatable methods that help physicians gain and maintain arterial access during diagnostic and interventional procedures. High-quality vascular access is a critical component of any procedure’s success, and St. Jude Medical is dedicated to providing products that make the entire procedure more effective and efficient from access to closure.
St. Jude Medical now offers PressureWire(TM) technology, adding an interventional product to its portfolio of leading cardiovascular technologies. The landmark FAME study, published in the New England Journal of Medicine in January 2009, demonstrated superior clinical outcomes for FFR-guided (fractional flow reserve) therapy using St. Jude Medical PressureWire products compared to those whose treatment was guided only by angiography. Notably, there was a statistically significant difference of 28% in Major Adverse Cardiac Events (MACE) such as death, myocardial infarction and repeat revascularization; in addition to better patient outcomes, material costs of the procedure were also reduced by about 11%.
The two-year results from the FAME study will be presented at TCT on Wednesday, Sept. 23 at 12:15 p.m. during the late-breaking session: “Two-Year Follow-up from a Prospective Randomized Trial of FFR-Guided vs. Angiography-Guided PCI in Patients with Multi-vessel Coronary Artery Disease.”
From active vascular closure to compression-assist devices, St. Jude Medical has the most complete portfolio of products to aid physicians in achieving hemostasis following cardiovascular interventions. St. Jude Medical presents the eighth generation of the successful Angio-Seal product family with the most advanced design yet – the Angio-Seal(TM) Evolution(TM). With the addition of two compression-assist devices following the acquisition of Radi Medical Systems, RadiStop(TM) Compression-Assist Device and FemoStop(TM) Gold Compression-Assist Device, the company can now offer physicians a full spectrum of closure technology to aid hemostasis.
Cardiac Rhythm Management (CRM) and Valves:
St. Jude Medical is committed to developing smarter, more active products which reduce patient risk and improve physician control during procedures. The company’s comprehensive portfolio of wireless CRM technologies is changing the way that physicians view connectivity and more efficiently manage their patients. Additionally, St. Jude Medical is continuing its efforts to develop additional products and technologies for patients suffering from debilitating cardiac diseases with durable tissue and mechanical valves.
For additional information about the products displayed in the St. Jude Medical booth, please visit SJMprofessional.com.
In addition, the results from the two-year follow-up of the landmark FAME study is being presented as a late-breaking trial at TCT on Wednesday, Sept. 23 at 12:15 p.m. Results from the study, which was sponsored by St. Jude Medical, will reveal updated information about MACE, procedural time and material costs, among other topics. For additional information about the FAME study visit FAMEstudy.com.
St. Jude Medical will also host a breakfast symposium titled “Implementing Evolving Tools for Percutaneous Coronary Interventions: Access, Lesion Assessment, Closure” on Thursday, Sept. 24 from 6:30 a.m. to 8:00 a.m. Dr. Robert J. Applegate, Medical Director of the Cardiac Catheterization Laboratory at Wake Forest University Baptist Medical Center, will be speaking on Integrating Access and Vascular Closure and Dr. Augusto Pichard, Director of the Catheterization Laboratory at Washington Hospital Center, will be speaking on implementing an FFR program at a high-volume PCI center.
Transcatheter Cardiovascular Therapeutics (TCT) is the annual scientific symposium of the Cardiovascular Research Foundation. The 2009 Conference takes place September 21-25 at The Moscone Center in San Francisco, CA. TCT is the world’s largest educational meeting specializing in interventional cardiovascular medicine. For more than 20 years, TCT has been the center of cutting-edge educational content. This year’s program will reflect the advances and changes in the field while maintaining a long-standing commitment to TCT’s core values: focus on therapy innovation, trust in evidence-based medicine and dedication to putting patients first.
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. Headquartered in St. Paul, Minn., St. Jude Medical employs more than 15,000 people worldwide and has four major focus areas that include: cardiac rhythm management, atrial fibrillation, cardiovascular and neuromodulation. For more information, please visit sjm.com.
About Transcatheter Cardiovascular Therapeutics (TCT)
Transcatheter Cardiovascular Therapeutics (TCT) is the annual scientific symposium of the Cardiovascular Research Foundation. Attended by over 10,000 participants each year, TCT gathers leading medical researchers and clinicians from around the world to present and discuss the latest developments in the field of interventional cardiovascular medicine.
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 Quarterly Report on Form 10-Q for the fiscal quarter ended April 4, 2009 and July 4, 2009. 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
St. Jude Medical
Sara Spafford Freeman, 651-756-6702
Investor and Media Relations