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Usefulness of the bidirectional Glenn procedure as staged reconstruction for the functional single ventricle

dc.contributor.authorPridjian, Ara K.en_US
dc.contributor.authorMendelsohn, Alan M.en_US
dc.contributor.authorLupinetti, Flavian M.en_US
dc.contributor.authorBeekman, III, Robert H.en_US
dc.contributor.authorDick, Macdonald IIen_US
dc.contributor.authorSerwer, Gerald A.en_US
dc.contributor.authorBove, Edward L.en_US
dc.date.accessioned2006-04-10T15:47:33Z
dc.date.available2006-04-10T15:47:33Z
dc.date.issued1993-04-15en_US
dc.identifier.citationPridjian, Ara K., Mendelsohn, Alan M., Lupinetti, Flavian M., Beekman, III, Robert H., Dick, II, Macdonald, Serwer, Gerald, Bove, Edward L. (1993/04/15)."Usefulness of the bidirectional Glenn procedure as staged reconstruction for the functional single ventricle." The American Journal of Cardiology 71(11): 959-962. <http://hdl.handle.net/2027.42/30841>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4C7VHS4-PH/2/a29ae160e0147bf39e6d8915e110de03en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30841
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8465789&dopt=citationen_US
dc.description.abstractThe bidirectional Glenn operation may be particularly useful as an intermediate procedure before Fontan correction in high-risk patients. From October 1989 through February 1992, 50 patients 1 to 60 months old (median 12) have undergone a bidirectional Glenn operation. Diagnoses included hypoplastic left heart syndrome in 21 patients, pulmonary atresia with intact ventricular septum in 10, tricuspid valve atresia in 9, other complex univentricular heart defects in 9, and Ebstein's anomaly in 1. Mean pulmonary vascular resistance was 2.2 +/- 0.2 Wood U (range 0.5 to 7.3) and mean pulmonary artery area Nakata index was 318 +/- mm2/m2 (range 80 to 821). Additional procedures were performed in 17 patients, including pulmonary artery reconstruction in 15 (29%) and bilateral caval anastomoses in 5 (10%). There were 4 hospital deaths (8%). Two deaths resulted from myocardial infarction in patients with pulmonary atresia with intact ventricular septum and sinusoids and 1 from severe pulmonary vascular disease in a patient with hypoplastic left heart syndrome. There was 1 late death from pneumonia. Actuarial survival is 92 +/- 4% at 1 month and beyond, with a mean follow-up of 13.4 +/- 1 months. Risk factor analysis showed that pulmonary vascular resistance &gt;3 Wood U and pulmonary artery distortion were associated with increased mortality. Twelve patients have undergone a Fontan procedure at a mean duration after bidirectional Glenn of 18 months with 1 death (8%). The bidirectional Glenn procedure provides excellent palliation in high-risk patients and appears useful as a staging procedure before Fontan correction.en_US
dc.format.extent529844 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleUsefulness of the bidirectional Glenn procedure as staged reconstruction for the functional single ventricleen_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.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationumDepartment of Surgery, Section of Thoracic Surgery and Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan School of Medicine, Ann Arbor, Michigan, U.S.A.en_US
dc.identifier.pmid8465789en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30841/1/0000503.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(93)90914-Xen_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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