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Long-Term Follow Up of Secundum Atrial Septal Defect Closure with the Amplatzer Septal Occluder

dc.contributor.authorKnepp, Marc D.en_US
dc.contributor.authorRocchini, Albert P.en_US
dc.contributor.authorLloyd, Thomas R.en_US
dc.contributor.authorAiyagari, Ranjit M.en_US
dc.date.accessioned2011-01-13T19:40:06Z
dc.date.available2011-01-13T19:40:06Z
dc.date.issued2010-01en_US
dc.identifier.citationKnepp, Marc D.; Rocchini, Albert P.; Lloyd, Thomas R.; Aiyagari, Ranjit M.; (2010). "Long-Term Follow Up of Secundum Atrial Septal Defect Closure with the Amplatzer Septal Occluder." Congenital Heart Disease 5(1): 32-37. <http://hdl.handle.net/2027.42/78631>en_US
dc.identifier.issn1747-079Xen_US
dc.identifier.issn1747-0803en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78631
dc.description.abstractDuring the past 15 years, closure of a secundum atrial septal defect (ASD) has moved from a surgical to a percutaneous transcatheter approach. Few long-term studies of the efficacy and safety of closure of an ASD by an Amplatzer septal occluder (ASO) exist.To examine the long-term results of secundum ASD closure using the ASO, data on 94 patients who underwent secundum ASD closure with the ASO between 1998 and 2002 were available and reviewed. Data regarding residual shunt, chest pain, palpitations, arrhythmias, headaches, transient ischemic attacks, cerebrovascular accidents, and mortality were collected.Seven (7.4%) subjects had residual shunts immediately following ASO placement. During follow-up, 4 residual shunts closed for a complete closure rate of 97%. Eighteen (19%) patients reported chest pain during the follow-up period. Twenty-three patients (24%) reported palpitations during the follow up period, 7 were documented arrhythmias, including supraventricular tachycardia, atrial fibrillation, and premature ventricular beats. Migraine headaches were new-onset in 4 patients. Migraine cessation occurred in 2 patients after secundum ASD closure. One child died from a cerebral vascular event 18 months following device placement. Only 1 patient developed mild aortic insufficiency.These data indicate that for up to 120 months of patient follow-up, the ASO continues to be a safe device. Residual shunts and arrhythmias have low incidence post-ASO placement. Given the mortality in one high-risk patient, further investigation into anti-platelet therapy after device placement is warranted.en_US
dc.format.extent168827 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.subject.otherPalpitationsen_US
dc.subject.otherAmplatzer Septal Occluderen_US
dc.subject.otherAtrial Septal Defecten_US
dc.titleLong-Term Follow Up of Secundum Atrial Septal Defect Closure with the Amplatzer Septal Occluderen_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.identifier.pmid20136855en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78631/1/j.1747-0803.2009.00358.x.pdf
dc.identifier.doi10.1111/j.1747-0803.2009.00358.xen_US
dc.identifier.sourceCongenital Heart Diseaseen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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