Browsing by Subject "Fibrinolisis"

Now showing 1 - 3 of 3
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    Actualización de los cuidados de enfemería en la administración de fibrinolíticos
    (Murcia : Servicio de Publicaciones de la Universidad de Murcia, 2006) Martínez Cornellat, D.; Carmona Simarro, J.V.; Gómez Gil, B.
    El objetivo de nuestro artículo es, por un lado, recordar los principales fibrinolíticos utilizados en el síndrome coronario agudo (SCA), en lo que se refiere a los cuidados específicos de enfermería, y por otro, describir uno de los últimos fibrinolíticos utilizados, la tenecteplasa (Metalyse®); indicaciones, posología, control de efectos adversos e interacciones.
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    Elaboración de un plan de cuidados en el ictus agudo: Trombolisis arterial.
    (Servicio de Publicaciones - Universidad de Murcia, 2003) Alcaraz Escribano, Mª. L.; Ibáñez Nicolás, Mª. J.; Medina Quijada, Mª. I.; Orcajada López, J.; Meseguer Lorca, C.
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    Histological and histochemical evaluation of human oral mucosa constructs developed by tissue engineering
    (Murcia : F. Hernández, 2007) Sánchez-Quevedo, M.C.; Alaminos, M.; Capitan, L.M.; Moreu, G.; Garzon, I.; Crespo, P.V.; Campos, Antonio
    Reconstruction of large oral mucosa defects is often challenging, since the shortage of healthy oral mucosa to replace the excised tissues is very common. In this context, tissue engineering techniques may provide a source of autologous tissues available for transplant in these patients. In this work, we developed a new model of artificial oral mucosa generated by tissue engineering using a fibrin-agarose scaffold. For that purpose, we generated primary cultures of human oral mucosa fibroblasts and keratinocytes from small biopsies of normal oral mucosa using enzymatic treatments. Then we determined the viability of the cultured cells by electron probe quantitative X-ray microanalysis, and we demonstrated that most of the cells in the primary cultures were alive and had high K/Na ratios. Once cell viability was determined, we used the cultured fibroblasts and keratinocytes to develop an artificial oral mucosa construct by using a fibrin-agarose extracellular matrix and a sequential culture technique using porous culture inserts. Histological analysis of the artificial tissues showed high similarities with normal oral mucosa controls. The epithelium of the oral substitutes had several layers, with desmosomes and apical microvilli and microplicae. Both the controls and the expression of cytokeratin 13 and low expression of cytokeratin 10. All these results suggest that our model of oral mucosa using fibrin-agarose scaffolds show several similarities with native human oral mucosa.