Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database

PURPOSE: The purpose of this study is to identify adverse events (device- and patient-related) associated with thoracic aortic stent graft systems and their timing post-procedure. MATERIALS AND METHODS: The Food and Drug Administration’s Manufacturer and User Facility Device Experience (FDA-MAUDE) v...

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Detalles Bibliográficos
Autores principales: Mansukhani, Neel A, Haleem, Meraaj S, Eskandari, Mark K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861529/
https://www.ncbi.nlm.nih.gov/pubmed/31814779
http://dx.doi.org/10.2147/MDER.S206269

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861529/
https://www.ncbi.nlm.nih.gov/pubmed/31814779
http://dx.doi.org/10.2147/MDER.S206269

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