The bicuspid aortic valve View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2010

AUTHORS

J. F. Matthias Bechtel , M. Misfeld , C. Schmidtke , Hans-H. Sievers

ABSTRACT

The bicuspid aortic valve (BAV) is the most common congenital cardiac malformation. Despite being a seemingly simple and harmless anatomic variation, BAV is said to cause more morbidity than any other congenital cardiac defect [52]. BAV may lead to aortic valve stenosis (AS) or regurgitation (AR), endocarditis, an ascending aortic aneurysm, and/or devastating dissection or rupture. Although these potential consequences of BAV were first described long ago [19, 35, 36], only recently have clinicians become fully aware that the presence of a BAV poses a serious health risk. However, the so-called bicuspid aortic valve syndrome [14] is extremely heterogeneous with some patients having rapidly progressive valve and/or aortic disease, while some individuals with BAV remain free of complications throughout their lifetime. In this article, we review current concepts regarding etiology, pathomechanisms, diagnosis, and treatment of BAV with special emphasis on topics relevant for cardiac surgeons. More... »

PAGES

89-101

Book

TITLE

Aortic Root Surgery

ISBN

978-3-7985-1868-1
978-3-7985-1869-8

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-7985-1869-8_9

DOI

http://dx.doi.org/10.1007/978-3-7985-1869-8_9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037005825


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