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Doppler evaluation of femoral arteries in children after aortic balloon valvuloplasty or coarctation balloon angioplasty

dc.contributor.authorBengur, A. Resaien_US
dc.contributor.authorVermilion, Roger P.en_US
dc.contributor.authorSnider, A. Rebeccaen_US
dc.contributor.authorBeekman III, Robert H.en_US
dc.date.accessioned2006-09-11T19:46:08Z
dc.date.available2006-09-11T19:46:08Z
dc.date.issued1993-01en_US
dc.identifier.citationVermilion, Roger P.; Snider, A. Rebecca; Bengur, A. Resai; Beekman, Robert H.; (1993). "Doppler evaluation of femoral arteries in children after aortic balloon valvuloplasty or coarctation balloon angioplasty." Pediatric Cardiology 14(1): 13-18. <http://hdl.handle.net/2027.42/48099>en_US
dc.identifier.issn1432-1971en_US
dc.identifier.issn0172-0643en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48099
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8456015&dopt=citationen_US
dc.description.abstractTo assess long-term femoral artery complications after aortic balloon valvuloplasty or coarctation balloon angioplasty, we examined 19 children who were 3 weeks to 21 years old (mean 7.6 years) at the time of catheterization. Two-dimensional and Doppler echocardiographic examinations of the common, superficial, and deep femoral arteries were performed at an average of 2.0 years after balloon dilatation. Pulsatility index (PI) was calculated as the maximum velocity minus the minimum velocity divided by the mean velocity. No patient was suspected clinically of having peripheral arterial disease prior to the echocardiographic examination. Fourteen patients had normal femoral arteries. Of these, 10 had normal two-dimensional and Doppler echocardiographic examinations of both femoral arteries. These patients had triphasic flow patterns (forward in systole, reverse in early diastole, forward in middiastole) and Pls of 3.7–41.6 (mean 9.5). Four of the 14 normal patients had abnormal pulsed Doppler examinations showing continuous forward flow and low Pls (1.7–3.5) reflecting residual coarctation (10–30 mmHg gradients). Five patients had abnormal femoral arteries. Of these, two had no visible obstruction by two-dimensional echocardiography and color-flow imaging but had abnormal pulsed Doppler patterns (continuous forward flow and low Pls of 2.5 and 2.9) only on the side of the balloon catheter insertion. Three of the five abnormal patients had visible obstructions by two-dimensional echocardiography and color-flow imaging and had abnormal pulsed Doppler patterns (continuous forward flow and low Pls from 1.1–3.6). One of these three had bilateral occlusions of the common femoral arteries with multiple collateral vessels; the second had occlusion of the right common femoral artery; and the third had 1–2-cm long severely narrowed segments in both common femoral arteries. All three children were <1 year old at the time of catheterization and had balloon catheter insertions in the affected arteries.en_US
dc.format.extent1882368 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag New York Inc.en_US
dc.subject.otherFemoral Arteriesen_US
dc.subject.otherCardiologyen_US
dc.subject.otherDoppler Echocardiographyen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherVascular Surgeryen_US
dc.subject.otherCardiac Surgeryen_US
dc.subject.otherBalloon Dilatationen_US
dc.titleDoppler evaluation of femoral arteries in children after aortic balloon valvuloplasty or coarctation balloon angioplastyen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics, C.S. Mott Children's Hospital, University of Michigan Medical Center, 48109-0204, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics, C.S. Mott Children's Hospital, University of Michigan Medical Center, 48109-0204, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics, C.S. Mott Children's Hospital, University of Michigan Medical Center, 48109-0204, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics, C.S. Mott Children's Hospital, University of Michigan Medical Center, 48109-0204, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid8456015en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48099/1/246_2004_Article_BF00794838.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00794838en_US
dc.identifier.sourcePediatric Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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