Case Report of an Endovascular Repair of a Residual Type A Dissection Using a Not CE Not FDA-Approved Najuta Thoracic Stent Graft System

This report describes an endovascular repair of a residual type A dissection using a medical device that is not marked by european conformity (CE) or Food and Drug Administration (FDA). The patient underwent ascending aortic surgery for acute type A dissection. The 2-year angio–computed tomography d...

Descripción completa

Detalles Bibliográficos
Autores principales: Mangialardi, N., Ronchey, S., Malaj, A., Lachat, M., Serrao, E., Alberti, V., Fazzini, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602650/
https://www.ncbi.nlm.nih.gov/pubmed/25621698
http://dx.doi.org/10.1097/MD.0000000000000436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602650/
https://www.ncbi.nlm.nih.gov/pubmed/25621698
http://dx.doi.org/10.1097/MD.0000000000000436

Ejemplares similares