1994
AUTHORSD. Journois , M. Levy
ABSTRACTSeveral 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... »
PAGES364-373
Yearbook of Intensive Care and Emergency Medicine 1994
ISBN
978-3-540-57613-6
978-3-642-85068-4
http://scigraph.springernature.com/pub.10.1007/978-3-642-85068-4_33
DOIhttp://dx.doi.org/10.1007/978-3-642-85068-4_33
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