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MiStent SES erweist sich im klinischen Umfeld als einzigartig
Date:10/28/2013

DURHAM, North Carolina, 28. Oktober 2013 /PRNewswire/ -- Micell Technologies, Inc. gab heute bekannt, dass die Bildaufnahmen und klinischen Ergebnisse der Studien DESSOLVE I und DESSOLVE II bezüglich des MiStent Sirolimus Eluting Absorbable Polymer Coronary Stent System (MiStent SES®) des Unternehmens im Zuge der 25. jährlichen TCT-Konferenz (Transcatheter Cardiovascular Therapeutics) präsentiert wurden, welche vom 27. Oktober bis 1. November 2013 in San Francisco stattfindet. Das MiStent SES ist ein Medikamente freisetzender Stent mit dünner Stützstrebe, der sich durch eine schnell absorbierbare Beschichtung zur gezielten Steuerung der Wirkstofffreisetzung auszeichnet und zur Optimierung der Gefäßheilung bei Patienten mit koronarer Herzkrankheit konzipiert wurde.

Die Datenpräsentation „MiStent: 2-year Randomized Trial Results from a Sirolimus-eluting Stent with a Bioabsorbable Coating" fand am Sonntag, den 27. Oktober im Rahmen des wissenschaftlichen Symposiums „Next Generation DES and Bioabsorbable Scaffolds" statt. John Ormiston, M.B.Ch.B., ein interventioneller Kardiologe der Mercy Angiography Unit in Auckland (Neuseeland), stellte die Daten vor. Dr. Ormiston ist ein Forschungsleiter der DESSOLVE-Studien.

Präsentiert wurden die Daten einer zweijährigen Nachbeobachtung der Studien DESSOLVE I und II. Bei der Studie DESSOLVE I ist im Zuge der Nachbeobachtung eine minimale Progression des späten Lumenverlustes zwischen acht und 18 Monaten festgestellt worden, wobei keine der beobachteten Läsionen über einen Zeitraum von zwei Jahren MACE-Ereignisse aufwies. Bei der randomisierten Studie DESSOLVE II lag die MACE-Rate nach zwei Jahren in der MiStent-Gruppe bei 6,7 % und in der Endeavor DES-Kontrollgruppe bei 13,3 %. In Verbindung mit dem
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SOURCE Micell Technologies
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