Title of article
Thoracic Aortic Aneurysm and Dissection
Author/Authors
Goldfinger، نويسنده , , Judith Z. and Halperin، نويسنده , , Jonathan L. and Marin، نويسنده , , Michael L. and Stewart، نويسنده , , Allan S. and Eagle، نويسنده , , Kim A. and Fuster، نويسنده , , Valentin، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2014
Pages
15
From page
1725
To page
1739
Abstract
Aortic dissection is the most devastating complication of thoracic aortic disease. In the more than 250 years since thoracic aortic dissection was first described, much has been learned about diseases of the thoracic aorta. In this review, we describe normal thoracic aortic size; risk factors for dissection, including genetic and inflammatory conditions; the underpinnings of genetic diseases associated with aneurysm and dissection, including Marfan syndrome and the role of transforming growth factor beta signaling; data on the role for medical therapies in aneurysmal disease, including beta-blockers, angiotensin receptor blockers, and angiotensin-converting enzyme inhibitors; prophylactic surgery for aneurysm; surgical techniques for the aortic root; and surgical and endovascular management of aneurysm and dissection for different aortic segments.
Keywords
Aortic aneurysm , Cardiac surgical procedures , endovascular procedures , risk factors , Marfan syndrome , Transforming growth factor beta
Journal title
JACC (Journal of the American College of Cardiology)
Serial Year
2014
Journal title
JACC (Journal of the American College of Cardiology)
Record number
1759512
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