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Stent redilation in canine models of congenital heart disease: Pulmonary artery stenosis and coarctation of the aorta

dc.contributor.authorMendelsohn, Alan M.en_US
dc.contributor.authorDorostkar, Parvin C.en_US
dc.contributor.authorMoorehead, Catherine P.en_US
dc.contributor.authorLupinetti, Flavian M.en_US
dc.contributor.authorReynolds, Paul I.en_US
dc.contributor.authorLudomirsky, Achien_US
dc.contributor.authorLloyd, Thomas R.en_US
dc.contributor.authorHeidelberger, Kathleen P.en_US
dc.contributor.authorBeekman III, Robert H.en_US
dc.date.accessioned2006-04-28T16:44:05Z
dc.date.available2006-04-28T16:44:05Z
dc.date.issued1996-08en_US
dc.identifier.citationMendelsohn, Alan M.; Dorostkar, Parvin C.; Moorehead, Catherine P.; Lupinetti, Flavian M.; Reynolds, Paul I.; Ludomirsky, Achi; Lloyd, Thomas R.; Heidelberger, Kathleen; Beekman, Robert H. (1996)."Stent redilation in canine models of congenital heart disease: Pulmonary artery stenosis and coarctation of the aorta." Catheterization and Cardiovascular Diagnosis 38(4): 430-440. <http://hdl.handle.net/2027.42/38176>en_US
dc.identifier.issn0098-6569en_US
dc.identifier.issn1097-0304en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38176
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8853159&dopt=citationen_US
dc.description.abstractIn a canine puppy model, pulmonary artery stenosis was created by banding the left pulmonary artery to 30–40% of its original diameter. Animals underwent right heart catheterization and angiography 1–2 mo later, and Palmaz P308 stents were implanted. Stent redilation was performed 3–5 mo later. One mo postredilation, the animals were restudied and sacrificed. Coarctations of the aorta were created by transverse aortic incision and longitudinal repair. P308 stent implantation was performed 2–3 mo later. Stent redilation was performed after 6–10 mo, and the animals were restudied and sacrificed 1–2 mo later. Stent implantation was performed in 6 puppies with pulmonary artery stenosis, as 2 animals developed postoperative pulmonary arterial hypoplasia, precluding stenting. The stenosis diameter increased from 4.8 ± 0.5 mm to 7.4 ± 0.6 mm (mean ± SE) following stenting ( P = 0.005), and increased further to 9.2 ± 0.7 mm following redilation ( P < 0.001). There were no significant vessel tears or ruptures. Coarctation stenting was performed in 8 animals. The coarctation was dilated from 5.8 ± 0.9 mm to 9.8 ± 0.6 mm ( P < 0.001), and to 13.5 ± 0.5 mm at redilation ( P = 0.002). Redilation could not be performed in 1 animal. Aortic rupture and death occurred in 2 of 7 animals at redilation. Stent implantation and redilation in experimental pulmonary artery stenosis appears safe and effective. Though stent implantation for coarctation of the aorta appears safe, there was a 28% aortic rupture rate at stent redilation in this model. © 1996 Wiley-Liss, Inc.en_US
dc.format.extent1186736 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCardiovascular Medicineen_US
dc.titleStent redilation in canine models of congenital heart disease: Pulmonary artery stenosis and coarctation of the aortaen_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.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michigan ; Children's Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229en_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivisions of Pediatric Cardiology, Cardiovascular Surgery, Anesthesia, and Pathology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.identifier.pmid8853159en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38176/1/24_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-0304(199608)38:4<430::AID-CCD24>3.0.CO;2-Hen_US
dc.identifier.sourceCatheterization and Cardiovascular Diagnosisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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