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Baxter lance l'hémostat d'étanchéité HEMOPATCH, un tampon de collagène à température ambiante approuvé pour l'hémostase et l'étanchéité, adapté à la chirurgie ouverte et aux procédures chirurgicales mini-invasives
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Baxter International Inc.

News provided by

Baxter International Inc.

May 20, 2025, 02:00 ET

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DEERFIELD, Illinois, 20 mai, 2025 /PRNewswire/ -- « L'hémostat d'étanchéité Hemopatch représente un développement significatif de Baxter, et l'introduction de la variante à température ambiante souligne notre dévouement continu envers l'innovation dans la gestion tissulaire », a déclaré Steve Wallace, président de la chirurgie avancée chez Baxter.

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.

S'appuyant sur une décennie de succès commercial, Baxter est heureuse de dévoiler l'hémostat d'étanchéité Hemopatch (Hemopatch Sealing Hemostat) qui offre désormais la commodité d'un stockage à température ambiante et une durée de conservation prolongée de 3 ans.

La performance de l'hémostat d'étanchéité Hemopatch implique l'interaction de deux composants qui peuvent créer une hémostase rapide et durable en scellant la surface de saignement. La face blanche, orientée vers les tissus, de l'hémostat d'étanchéité Hemopatch est recouverte d'une fine couche de NHS-PEG. Au contact du sang ou d'autres fluides corporels, le NHS-PEG forme un hydrogel qui renforce ses propriétés d'adhésion et scelle la surface du tissu. Au contact du sang, le collagène induit l'agrégation des plaquettes. Les plaquettes se déposent en grand nombre sur la structure du collagène, dégranulent et libèrent des facteurs de coagulation qui, avec les facteurs plasmatiques, permettent la formation de fibrine. La structure de l'hémostat d'étanchéité Hemopatch apporte une matrice tridimensionnelle qui absorbe facilement les fluides et fournit un renforcement mécanique supplémentaire du caillot. Les études précliniques suggèrent que la résorption et le remplacement par le tissu hôte se produisent en 6 à 8 semaines environ, avec une faible réaction tissulaire.

La vitesse de résorption et de remplacement par le tissu hôte peut être plus longue car elle dépend de plusieurs facteurs, notamment la quantité de produit laissée in situ et le site d'utilisation.

L'hémostat d'étanchéité Hemopatch présente de multiples avantages cliniques, tels que l'étanchéité des tissus, l'arrêt et la prévention des fuites, une hémostase rapide et efficace en 2 minutes, ainsi que l'absorption et le remplacement par les tissus de l'hôte.

Pour les indications et informations importantes sur les risques relatives à l'hémostat d'étanchéité Hemopatch, regardez la vidéo en haut de cet article ou visitez https://advancedsurgery.baxter.eu/hemopatch#isi

Pour plus d'informations sur l'hémostat d'étanchéité Hemopatch, visitez le site : https://advancedsurgery.baxter.eu/hemopatch

Fabricant :

Baxter Healthcare SA
Thurgauerstrasse 130 Glattbrugg,
ZÜRICH, 8152 Suisse

Classe d'appareil : III

CE 0123

Ce contenu est destiné uniquement aux professionnels de la santé et ne doit pas être interprété comme un avis médical. Veuillez consulter un prestataire de soins de santé qualifié pour tout problème de santé.

L'hémostat d'étanchéité Hemopatch n'est autorisé que dans certains pays. Pour obtenir des informations spécifiques sur la disponibilité et le statut réglementaire de l'hémostat d'étanchéité Hemopatch RT dans votre pays, veuillez contacter votre représentant local de Baxter Healthcare.

Vidéo - 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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