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International experience with secundum atrial septal defect occlusion by the buttoned device

dc.contributor.authorRao, P. Syamasundaren_US
dc.contributor.authorSideris, Eleftherios B.en_US
dc.contributor.authorHausdort, Gerden_US
dc.contributor.authorRey, Christianen_US
dc.contributor.authorLloyd, Thomas R.en_US
dc.contributor.authorBeekman III, Robert H.en_US
dc.contributor.authorWorms, Ann Marieen_US
dc.contributor.authorBourlon, Francoisen_US
dc.contributor.authorOnorato, Eustaquioen_US
dc.contributor.authorKhalilullah, Mohameden_US
dc.contributor.authorHaddad, Jorgeen_US
dc.date.accessioned2006-04-10T17:48:15Z
dc.date.available2006-04-10T17:48:15Z
dc.date.issued1994-11en_US
dc.identifier.citationRao, P. Syamasundar, Sideris, Eleftherios B., Hausdort, Gerd, Rey, Christian, Lloyd, Thomas R., Beekman, Robert H., Worms, Ann Marie, Bourlon, Francois, Onorato, Eustaquio, Khalilullah, Mohamed, Haddad, Jorge (1994/11)."International experience with secundum atrial septal defect occlusion by the buttoned device." American Heart Journal 128(5): 1022-1035. <http://hdl.handle.net/2027.42/31234>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6W9H-4BM5GN0-CR/2/2b78d0f28a89390b2a4d85c8faa3b7ecen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31234
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7942465&dopt=citationen_US
dc.description.abstractSeveral devices are available for transcatheter occlusion of atrial septal defect. This report describes the international experience with the buttoned device. During a 4.5-year period ending in February 1993, 180 transcatheter atrial septal defect occlusions were performed with the buttoned device. Patient age varied between 0.6 and 76 years and stretched atrial defect diameter between 5 and 25 mm. The defects were closed with 25 to 50 mm devices delivered through 8F (148 patients) or 9F (32 patients) sheaths. Twelve patients were adults whose defects were closed to prevent recurrence of cerebrovascular accidents caused by presumed paradoxic embolism. In the remaining patients the atrial defect was closed to treat the left-to-right shunt. The atrial septal defects were effectively occluded as demonstrated by (1) decrease in pulmonary-to-systemic flow ratio from 2.1 +/- 0.6 (mean +/- SD) to 1.05 +/- 0.1 (p 2 and disappearance of the diastolic murmur by auscultation; and (3) improvement in right ventricular volume overloading by echocardiogram. However, trivial to small shunts could be detected by color Doppler studies in 76 (45%) of 168 patients in whom such data are available. Complications included unbuttoning in 13 and whole-device embolization in 1. All patients remained stable, and retrieval of the device and surgical closure of the atrial septal defect were accomplished in 10 patients. Transcatheter retrieval was used in the remaining 4 patients. The incidence of unbuttoning, a major complication of the procedure, appeared to decrease with the increasing experience of the investigators and with device modification (third-generation). The follow-up duration varied between 1 month and 4 years. Six patients required surgery during the follow-up period. In the remaining patients (n = 160), clinical examination did not reveal signs of atrial shunts. Color Doppler studies revealed either complete disappearance of the previously demonstrated shunts or further diminution of their size. The results indicate that transcatheter occlusion of the atrial septal defects with buttoned devices is feasible, relatively safe, and effective, and it appears to be a viable alternative to surgery for some patients with secundum atrial septal defect. Complications are infrequent and should improve with experience.en_US
dc.format.extent6729843 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleInternational experience with secundum atrial septal defect occlusion by the buttoned deviceen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Mich., USA; University of Arizona, Tucson, Ariz., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Mich., USAen_US
dc.contributor.affiliationotherUniversity of Wisconsin Medical School, Madison, Wis., USAen_US
dc.contributor.affiliationotherCustom Medical Devices, Amarillo, Texas, USA; Athenian Institute of Pediatric Cardiology, Athens, Greece.en_US
dc.contributor.affiliationotherGerman Heart Center, Berlin, Germanyen_US
dc.contributor.affiliationotherHospital Cardiologique, Lille, Franceen_US
dc.contributor.affiliationotherUniversity of Nancy, Nancy, Franceen_US
dc.contributor.affiliationotherCardiothoracic Center, Monacoen_US
dc.contributor.affiliationotherSan Donato Milaneze, Milan, Italyen_US
dc.contributor.affiliationotherG. B. Pant Hospital, New Delhi, Indiaen_US
dc.contributor.affiliationotherHospital do Coracao de Ribeirão-Preto, Ribeirão Preto, Brazilen_US
dc.identifier.pmid7942465en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31234/1/0000139.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-8703(94)90602-5en_US
dc.identifier.sourceAmerican Heart Journalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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