Interventional Cardiologists Treat Complex Lesions Within 10 Minutes, With Superb Angiographic Results
NEWTON, Mass.–(BUSINESS WIRE)–Tryton Medical, Inc. has marked new milestones in stent technology by
      demonstrating on a global scale how the firm’s Side-Branch Stent offers
      unparalleled ease-of-use and the best option to safely and definitively
      treat bifurcation lesions. Tryton transmitted a live satellite feed of a
      successful clinical case to an audience of interventional cardiologists
      at TCT Asia 2007 in Seoul, Korea, performed by Robert van Geuns, M.D.
      Ph.D., Cardiologist, Thoraxcenter, Erasmus Medical Center. Professor
      Serruys, Head of the Department of Interventional Cardiology,
      Thoraxcenter, Erasmus Medical Center, moderated the event. Tryton’s
      Side-Branch Stent was also featured at the American College of
      Cardiology’s i2 Summit, where a live satellite feed of a clinical case,
      performed by Dr. George Sianos, Senior Interventionalist, Thoraxcenter,
      Erasmus Medical Center, was transmitted to demonstrate the ease-of-use
      and superb angiographic results that can be predictably achieved by
      using Tryton’s stent. The news follows a previous announcement that
      revealed the safety of Tryton’s stent during a live case that was
      performed in front of 1,000 interventional cardiologists at the Joint
      Interventional Meeting (JIM 2007) in Rome.
    
      “Unlike other stents and techniques used to treat bifurcation lesions,
      Tryton’s stent is easy to deliver as it uses standard equipment and
      techniques compatible with 5 and 6 French guiding catheters,” said Dr.
      George Sianos, Senior Interventionalist, Thoraxcenter, Erasmus Medical
      Center. “This device has greatly facilitated the treatment of these
      patients. The Tryton strategy allows the Interventionist to secure the
      side branch and then treat the main vessel with his stent of choice,”
      said Dr. Sianos.
    
      “Tryton continues to demonstrate impressive results and growth as it
      becomes clear that our stent will eventually provide a new standard of
      care, thereby enabling any interventional cardiologists to treat the
      entire spectrum of bifurcation lesions they encounter every day,” said
      H. Richard Davis, CTO, Tryton Medical, Inc. “The benefits of our
      Side-Branch Stent have been witnessed by thousands of interventional
      cardiologists in Asia, Europe and America. While others pursue the
      elusive goal of treating bifurcation lesions, we are already
      definitively treating these lesions. Interventional cardiologists can
      quickly grasp how to use our stent to treat complex lesions. Tryton’s
      dedicated save-the-side branch approach, allows for securing the
      side-branch first, after which the main vessel is stented in a
      predictable manner. These benefits simply are not offered with
      provisional senting,” Davis added.
    
      Every year, over half a million bifurcation coronary lesions are
      sub-optimally treated as no commercially available optimized solution
      exists for treating bifurcation lesions. As a result, cardiologists are
      forced to use a provisional strategy which avoids the deployment of a
      second stent– leaving the side branch vulnerable to thrombosis and
      restenosis. “This technology has the capacity to redefine the treatment
      of bifurcation lesions and resolve a frequent dilemma of the
      interventional cardiologist,” said Professor Patrick W. J. C. Serruys,
      M.D., Head of the Department of Interventional Cardiology, Thoraxcenter,
      Erasmus Medical Center, Rotterdam, Netherlands.
    
About Tryton Medical, Inc.
      Tryton Medical, Inc. is the leading developer of stents that are
      designed to definitively treat bifurcation lesions. 540,000 bifurcation
      coronary lesions are sub-optimally treated every year with a variety of
      time consuming and technically challenging procedures. No optimized
      solution is commercially available for treating bifurcation lesions. As
      a result, cardiologists are forced to use a provisional strategy which
      avoids the deployment of a second stent– leaving the un-stented side
      branch vulnerable to thrombosis and restenosis. The ability to
      definitively treat bifurcation lesions will enable PCI-stenting to
      become the new standard of care for the treatment of left main coronary
      artery disease rather than bypass surgery.
    
      Tryton Medical’s Side-Branch Stent™ has all the characteristics of a
      state-of the art workhorse stent, providing proven stent coverage to
      bifurcation lesions while eliminating the need for provisional stenting.
      For more information on Tryton Medical, Inc., contact Joe Romano,
      Partner, HighGround, Inc. at +1 781-279-1320 x 208, jromano@highgroundinc.com
      or visit trytonmedical.com.
    
