Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7783
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLipsett, J.-
dc.contributor.authorCool, J.-
dc.contributor.authorRunciman, S.-
dc.contributor.authorKennedy, J.-
dc.contributor.authorMartin, A.-
dc.contributor.authorByard, R.-
dc.contributor.authorFord, W.-
dc.date.issued1997-
dc.identifier.citationPediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association, 1997; 17(5):789-807-
dc.identifier.issn1077-1042-
dc.identifier.urihttp://hdl.handle.net/2440/7783-
dc.description.abstractCongenital diaphragmatic hernia (CDH) in humans is relatively common and associated with high mortality attributed mainly to pulmonary hypoplasia. Previous animal models have induced CDH late in gestation, in contrast to the human situation, and only limited morphometric analyses have been reported. We undertook early surgical creation of CDH in fetal lambs, days 72–74 of gestation (n = 8), with unoperated lambs (n = 8) as controls. At 143 days (term = 145–149) a cesarean section was performed and the lungs were obtained, inflation fixed, divided into lobes, and processed for morphometry. In the CDH group the total lung volumes (51.3 mL compared to 223.8 mL) and gas exchange surface areas (5.85 m2 versus 26.43 m2) were less than one quarter of control values. Capillary loading was reduced from 0.3 mL/m2 in controls to 0.12 mL/m2 in CDH and parenchymal volume reduced from 77% in controls to 57% in CDH. Within parenchyma, gas exchange tissue volume was increased in CDH (66%) compared with controls (50%). CDH lungs had primitive air sacs/alveoli that were smaller (perimeter 83 μm) and more numerous (1321 per mm2) than in controls (perimeter 132 μm, 504 per mm2). The left lung and left upper lobe were affected most. Induction of CDH in the lamb at this early age results in quantifiable, reproducible pulmonary hypoplasia from which comparisons can be made with the human condition.-
dc.description.statementofresponsibilityJ. Lipsett, J. C. Cool, S. C.Runciman, J. D.Kennedy, A. J.Martin, R. W.Byard and W. D. A. Ford-
dc.language.isoen-
dc.publisherTaylor & Francis-
dc.rights© 1997 Taylor & Francis-
dc.source.urihttp://dx.doi.org/10.1080/15513819709168601-
dc.subjectcongenital diaphragmatic hernia-
dc.subjectlung morphometry-
dc.subjectpulmonary hypoplasia-
dc.titleMorphometric analysis of pulmonary development in the sheep following creation of fetal diaphragmatic hernia-
dc.typeJournal article-
dc.identifier.doi10.1080/15513819709168601-
pubs.publication-statusPublished-
dc.identifier.orcidKennedy, J. [0000-0003-2308-1870]-
dc.identifier.orcidMartin, A. [0000-0002-1606-5461]-
dc.identifier.orcidByard, R. [0000-0002-0524-5942]-
Appears in Collections:Aurora harvest
Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.