This review summarizes the risk factors, genetic underpinnings, medical therapies, and surgical management strategies for thoracic aortic aneurysm and dissection.
Patients with or at risk for thoracic aortic aneurysm and dissection
Medical therapies (beta-blockers, angiotensin receptor blockers, angiotensin-converting enzyme inhibitors), prophylactic surgery, and endovascular management
This review provides a comprehensive overview of thoracic aortic aneurysm and dissection, covering risk factors, genetics, medical therapies, and surgical management.
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.
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Judith Z. Goldfinger
Jonathan L. Halperin
Michael L. Marin
Journal of the American College of Cardiology
Icahn School of Medicine at Mount Sinai
Michigan Medicine
Cardiovascular Institute of the South
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Goldfinger et al. (Wed,) conducted a review in Thoracic Aortic Aneurysm and Dissection. This review summarizes the risk factors, genetic underpinnings, medical therapies, and surgical management strategies for thoracic aortic aneurysm and dissection.
www.synapsesocial.com/papers/69ebde446651671f0a73fab4 — DOI: https://doi.org/10.1016/j.jacc.2014.08.025
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