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      NICE emite la aprobación para la ablación mecanoquímica endovenosa para venas varicosas en el Reino Unido

      Vascular Insights Logo

      News provided by

      Vascular Insights, LLC

      Jul 14, 2016, 07:22 ET

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      - National Institute for Health and Care Excellence (NICE) emite la aprobación mediante la Interventional Procedure Guidance IPG557 para la ablación mecanoquímica endovenosa para venas varicosas en el Reino Unido

      QUINCY, Massachusetts, 14 de julio de 2016 /PRNewswire/ -- El National Institute for Health and Care Excellence (NICE) ha emitido recientemente la aprobación mediante la Interventional Procedure Guidance IPG557 para ablación mecanoquímica endovenosa para el tratamiento de las venas varicosas en el Reino Unido. Las directrices NICE ofrecen guía basada en evidencia y asesoramiento en un rango de temas y condiciones de salud. Este movimiento coloca la ablación mecanoquímica endovenosa en disposiciones estándares para el tratamiento de las venas varicosas.

      Logo - http://photos.prnewswire.com/prnh/20160713/389341LOGO

      En su guía actualizada, publicada en mayo de 2016, NICE Guidance reportó:
      La actual evidencia en la seguridad y eficacia de la ablación mecanoquímica endovenosa para las venas varicosas parece adecuada para apoyar el uso de este procedimiento, dado que las disposiciones estándares están en marcha para el consentimiento, auditoría y gobernancia clínica.

      Una directriz NICE describe las recomendaciones para el diagnóstico y tratamiento de las venas varicosas. Muchas personas tienen venas varicosas que no causan ningún síntoma o necesitan tratamiento en instalaciones médicas. Sin embargo, algunas personas necesitarán tratamiento para el alivio de los síntomas o si hay evidencia de descoloración de la piel, inflamación o ulceración. Las opciones de tratamiento incluyen ablación endotermal, escleroterapia de espuma guiada por ultrasonido y cirugía (normalmente stripping y ligadura de las venas safenas magna y menor, y flebectomías).  

      "Las directrices recientemente publicadas permitirán más opciones de tratamiento para los que padecen insuficiencia venosa", comentó el cirujano vascular Peter Holt, PhD, FRCS del St. George's Vascular Institute, Londres, Inglaterra. "El catéter ClariVein® OC es una tecnología única que se ha utilizado ampliamente en los mercados europeos desde 2010, en procedimientos mecanoquímicos con excelentes resultados".

      El ClariVein® OC es un catéter de inyección especializado para la inyección de agentes médicos específicos en la vasculatura periférica, incluyendo la oclusión endovascular de venas incompetentes en pacientes con reflujo venoso superficial.  El ClariVein® OC se utiliza comúnmente con procedimiento mecanoquímicos endovenosos. El ClariVein® OC no está disponible en Estados Unidos.  

      Acerca de la Compañía
      Vascular Insights®, LLC se implica en el diseño, desarrollo, fabricación y marketing de dispositivos médicos para el tratamiento mínimamente invasivo de la enfermedad vascular periférica. Tenga en cuenta que la disponibilidad de producto depende de cada país.  

      Sitio web:
      www.vascularinsights.com

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