Aortale Bildgebung als Schlüssel zur Therapie genetischer Aortenerkrankungen
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Aortale Bildgebung als Schlüssel zur Therapie genetischer Aortenerkrankungen. / Baumgartner, D.; von Kodolitsch, Y.
In: GEFASSCHIRURGIE, Vol. 21, No. 6, 01.10.2016, p. 411-417.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Aortale Bildgebung als Schlüssel zur Therapie genetischer Aortenerkrankungen
AU - Baumgartner, D.
AU - von Kodolitsch, Y.
N1 - Publisher Copyright: © 2016, The Author(s).
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Background: Imaging is a key factor in the management of individuals with genetic aortic diseases, such as Marfan syndrome, vascular Ehlers-Danlos syndrome and Loeys-Dietz syndrome. Imaging is essential for identifying individuals with genetic aortic syndromes and for diagnostics of acute aortic syndromes in affected individuals. Imaging modalities for elective and emergency diagnostics comprise transthoracic echocardiography, transesophageal echocardiography, computed tomography (CT) with CT angiography and magnetic resonance imaging (MRI) with MR angiography. Objectives: The importance of echocardiographic M‑mode image segmentation method for measurement of changes in stiffness of the aorta. Materials und Methods: Study on measurement of stiffness of the aorta in Marfan syndrome in comparison to healthy subjects. Results: Using the non-invasive semiautomatic echocardiographic M‑mode image segmentation method, reduction in the elastic properties of the aorta can be exactly and objectively measured in young patients with Marfan syndrome. Conclusions: Imaging procedures are essential for identifying genetic aortic diseases, for stratifying aortic risk and for diagnosing acute aortic syndrome. For reasons of radiation protection, echocardiography and MRI should be preferentially used for follow-up in young patients.
AB - Background: Imaging is a key factor in the management of individuals with genetic aortic diseases, such as Marfan syndrome, vascular Ehlers-Danlos syndrome and Loeys-Dietz syndrome. Imaging is essential for identifying individuals with genetic aortic syndromes and for diagnostics of acute aortic syndromes in affected individuals. Imaging modalities for elective and emergency diagnostics comprise transthoracic echocardiography, transesophageal echocardiography, computed tomography (CT) with CT angiography and magnetic resonance imaging (MRI) with MR angiography. Objectives: The importance of echocardiographic M‑mode image segmentation method for measurement of changes in stiffness of the aorta. Materials und Methods: Study on measurement of stiffness of the aorta in Marfan syndrome in comparison to healthy subjects. Results: Using the non-invasive semiautomatic echocardiographic M‑mode image segmentation method, reduction in the elastic properties of the aorta can be exactly and objectively measured in young patients with Marfan syndrome. Conclusions: Imaging procedures are essential for identifying genetic aortic diseases, for stratifying aortic risk and for diagnosing acute aortic syndrome. For reasons of radiation protection, echocardiography and MRI should be preferentially used for follow-up in young patients.
KW - Aortic stiffness
KW - Distensibility
KW - Echocardiography
KW - Magnetic resonance imaging
KW - Marfan syndrome
UR - http://www.scopus.com/inward/record.url?scp=84989182965&partnerID=8YFLogxK
U2 - 10.1007/s00772-016-0189-8
DO - 10.1007/s00772-016-0189-8
M3 - SCORING: Zeitschriftenaufsatz
AN - SCOPUS:84989182965
VL - 21
SP - 411
EP - 417
JO - GEFASSCHIRURGIE
JF - GEFASSCHIRURGIE
SN - 0948-7034
IS - 6
ER -