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Baxter lanza el hemostático sellador HEMOPATCH, una almohadilla de colágeno para hemostasia y sellado
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Baxter International Inc.

News provided by

Baxter International Inc.

May 20, 2025, 02:00 ET

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-Baxter lanza el hemostático sellador HEMOPATCH, una almohadilla de colágeno a temperatura ambiente aprobada para hemostasia y sellado, adecuada para cirugía abierta y procedimientos quirúrgicos mínimamente invasivos (MIS).

DEERFIELD, Ill., 20 de mayo de 2025 /PRNewswire/ -- "El hemostático sellador Hemopatch representa un avance significativo de Baxter, y la introducción de la versión a temperatura ambiente pone de relieve nuestra dedicación continua a la innovación en el manejo de tejidos", afirmó Steve Wallace, presidente de Cirugía Avanzada de Baxter.

Tras una década de éxito en el mercado, Baxter se complace en presentar el hemostático sellador Hemopatch, que ahora ofrece la comodidad de almacenamiento a temperatura ambiente y una vida útil prolongada de 3 años.

See Indications and Important Risk Information at the end of this video. Baxter and Hemopatch are trademarks of Baxter International Inc. or its subsidiaries.
See Indications and Important Risk Information at the end of this video. Baxter and Hemopatch are trademarks of Baxter International Inc. or its subsidiaries.

El funcionamiento del hemostático sellador Hemopatch implica la interacción de dos componentes que pueden crear una hemostasia rápida y duradera sellando la superficie sangrante. La cara blanca del hemostático sellador Hemopatch, orientada hacia el tejido, está recubierta con una fina capa de NHS-PEG. Al entrar en contacto con la sangre u otros fluidos corporales, el NHS-PEG forma un hidrogel que mejora sus propiedades adherentes y sella la superficie del tejido. En contacto con la sangre, el colágeno induce la agregación plaquetaria. Las plaquetas se depositan en grandes cantidades en la estructura del colágeno, se degranulan y liberan factores de coagulación que, junto con los factores plasmáticos, permiten la formación de fibrina. La estructura del hemostático sellador Hemopatch proporciona una matriz tridimensional que absorbe fácilmente los fluidos y proporciona un refuerzo mecánico adicional al coágulo. Estudios preclínicos sugieren que la reabsorción y la reposición con el tejido huésped se producen en aproximadamente 6 a 8 semanas con escasa reacción tisular.

La tasa de reabsorción y reemplazo por el tejido huésped puede ser mayor, ya que depende de varios factores, como la cantidad de producto remanente y el lugar de aplicación.

El hemostático sellador Hemopatch ofrece múltiples beneficios clínicos, como sellar el tejido, detener y prevenir fugas, lograr una hemostasia rápida y eficaz en 2 minutos, y ser absorbido y reemplazado por el tejido huésped.

Para obtener información sobre las indicaciones del hemostático sellador Hemopatch y riesgos importante, vea el video en la parte superior de este artículo o visite https://advancedsurgery.baxter.eu/hemopatch#isi

Para obtener información sobre el hemostático sellador Hemopatch, visite: https://advancedsurgery.baxter.eu/hemopatch

Fabricante:

Baxter Healthcare SA
Thurgauerstrasse 130 Glattbrugg,
ZÜRICH, 8152 Suiza

Clase de dispositivo: III

CE 0123

Este contenido está dirigido exclusivamente a profesionales de la salud y no debe interpretarse como consejo médico. Consulte con un profesional de la salud cualificado si tiene alguna duda sobre su salud.

El hemostático sellador Hemopatch está aprobado para su uso únicamente en países seleccionados. Para obtener información específica sobre la disponibilidad y la normativa del hemostático sellador Hemopatch RT en su país, le recomendamos que se ponga en contacto con su representante de ventas local de Baxter Healthcare.

Video - https://mma.prnewswire.com/media/2687592/EMA_HemopatchCustomer.mp4 
Logo - https://mma.prnewswire.com/media/2687591/Baxter_International_Inc_Logo.jpg 

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