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MiStent SES demuestra ser único en el entorno clínico
Date:10/28/2013

da con pruebas de la función endotelial realizadas en dos ensayos demostraron la cicatrización de tipo de stent de metal desnudo con mantenimiento de la función endotelial normal.

El doctor Ormiston comentó: "MiStent es el único producto en su clase en optimizar las propiedades de suministro de fármaco local ofreciendo hasta nueve meses de presencia de farmaco con solo tres meses de absorción de polímero. Dado que el fármaco persiste tres veces más que el polímero, MiStent elimina el efecto inflamatorio del polímero rápidamente y retiene el fármaco antiinflamatorio y antirrestenótico seis meses más allá de la presencia del polímero".

Dennis Donohoe, M.D., asesor médico de Micell, añadió: "Estamos encantados con los hallazgos clínicos de dos años en DESSOLVE I y II y específicamente con respecto al hallazgo único de una falta de progresión de pérdida de lumen tardía en un período de 18 meses, en combinación con una excelente cicatrización de tejido como se muestra mediante la imagen clínica detallada".

Los datos incluidos en el TCT se incluyeron recientemente en un documento revisado por homólogos publicado por JACC Cardiovascular Interventions: "First-in-Human Evaluation of a Bioabsorbable Polymer–Coated Sirolimus–Eluting Stent: Imaging and Clinical Results of the DESSOLVE I Trial (DES With Sirolimus and a Bioabsorbable Polymer for the Treatment of Patients With De Novo Lesion in the Native Coronary Arteries)". Los autores de este documento incluyeron los investigadores jefe del ensayo DESSOLVE I, William Wijns, M.D., Ph.D., del Cardiovascular Center, Aalst, Bélgica, y John Ormiston, M.B.Ch.B., de la Mercy Angiography Unit, Auckland, Nueva Zelanda.

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SOURCE Micell Technologies
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