Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience database for adverse events involving Amplatzer septal occluder devices and comparison with the Society of Thoracic Surgery congenital cardiac surgery database-Reference-Cited by-同舟云学术

Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience database for adverse events involving Amplatzer septal occluder devices and comparison with the Society of Thoracic Surgery congenital cardiac surgery database

Published:2009-06 Issue:6 Volume:137 Page:1334-1341
ISSN:0022-5223
Container-title:The Journal of Thoracic and Cardiovascular Surgery
language:en
Short-container-title:The Journal of Thoracic and Cardiovascular Surgery

Author:

DiBardino Daniel J.,McElhinney Doff B.,Kaza Aditya K.,Mayer John E.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,Surgery

Reference22 articles.

1. U.S. Food and Drug Administration Web site. Available at: http://www.fda.gov/default.htm.

2. GraphPad Software Web site. Available at: www.graphpad.com.

3. Major complications associated with transcatheter atrial septal occluder implantation: a review of the medical literature and the MAUDE database;Delaney;Congenit Heart Dis,2007

4. Erosion of Amplatzer septal occluder device after closure of secundum atrial septal defects: review of registry of complications and recommendations to minimize future risk;Amin;Catheter Cardiovasc Interv,2004

5. Embolization and retrieval of the Amplatzer septal occluder;Levi;Catheter Cardiovasc Interv,2004

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