• 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