Pulmonary artery size as an indication for thoracoscopic repair of congenital diaphragmatic hernia i...
Pulmonary artery size as an indication for thoracoscopic repair of congenital diaphragmatic hernia in neonates
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Purpose
We reviewed 24 consecutive cases of prenatally or immediately postnatally diagnosed left-sided congenital diaphragmatic hernia (CDH) to evaluate pulmonary artery (PA) size as an indication for thoracoscopic repair (TR).
Methods
CDH repair is planned once echocardiography confirms improvement in pulmonary hypertension. TR is chosen...
Alternative Titles
Full title
Pulmonary artery size as an indication for thoracoscopic repair of congenital diaphragmatic hernia in neonates
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1038227629
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1038227629
Other Identifiers
ISSN
0179-0358
E-ISSN
1437-9813
DOI
10.1007/s00383-012-3148-9
