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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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Dettagli Bibliografici
Pubblicato in:Catheter Cardiovasc Interv
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley & Sons, Inc. 2018
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6587820/
https://ncbi.nlm.nih.gov/pubmed/30511498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccd.27995
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