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Results of the combined U.S. multicenter postapproval study of the Nit‐Occlud PDA device for percutaneous closure of patent ductus arteriosus

OBJECTIVES: To report the results of the Nit‐Occlud PDA prospective postapproval study (PAS) along with a comparison to the results of the pivotal and continued access trials. BACKGROUND: The Nit‐Occlud PDA (PFM Medical, Cologne, Germany), a nitinol coil patent ductus arteriosus (PDA) occluder, was...

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Detalles Bibliográficos
Autores principales:	Kobayashi, Daisuke, Salem, Morris M., Forbes, Thomas J., Gordon, Brent M., Soriano, Brian D., Dimas, Vivian, Goldstein, Bryan H., Owada, Carl, Javois, Alexander, Bass, John, Jones, Thomas K., Berman, Darren P., Gillespie, Matthew J., Moore, John W., Levi, Daniel S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2018
Materias:	PEDIATRIC AND CONGENITAL HEART DISEASE
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587820/ https://www.ncbi.nlm.nih.gov/pubmed/30511498 http://dx.doi.org/10.1002/ccd.27995

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