Pulmonary Hypertension in Congenital Heart Diseases View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

1994

AUTHORS

D. Journois , M. Levy

ABSTRACT

Several congenital heart diseases (CHD) are associated with pulmonary artery hypertension (PAH). Despite adequate surgical repair of the underlying congenital heart lesion, this complication is largely responsible for the high morbidity and mortality (50%) observed in the early postoperative period [1]. This is particularly unfortunate considering that a satisfactory surgical treatment for most of these CHD can be achieved and that the risk of PAH decreases rapidly within a few days. Several recent developments on the knowledge of endothelial metabolism have widely modified both physiological and therapeutic approaches of these diseases. More... »

PAGES

364-373

Book

TITLE

Yearbook of Intensive Care and Emergency Medicine 1994

ISBN

978-3-540-57613-6
978-3-642-85068-4

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-642-85068-4_33

DOI

http://dx.doi.org/10.1007/978-3-642-85068-4_33

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028009795


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