Endovascular treatment of genetically linked aortic diseases

Endovascular treatment of genetically linked aortic diseases Leitthema 1 1 1 2 1 Gefässchirurgie 2017 · 22 (Suppl 1):S1–S7 D. Böckler ·K.Meisenbacher ·A. S.Peters · C. Grond-Ginsbach ·M.S.Bischoff DOI 10.1007/s00772-016-0221-z Klinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinikum Heidelberg, Heidelberg, Published online: 9 January 2017 Germany © The Author(s) 2016. This article is available at Klinik für Neurologie, Universitätsklinikum Heidelberg, Heidelberg, Germany SpringerLink with Open Access. Endovascular treatment of genetically linked aortic diseases (TAA) and PAU and, in the case of as well as postoperatively. The Cleveland Introduction complex type B dissections or IMH, on working group led by Ourielund and Over the past 10 years endovascular symptoms, the presence of organ com- Greenberg was able to show the effect treatment has become the method of plications or imaging predictors of rapid of gender on the outcome of EVAR in first choice for both infrarenal aortic progression [15]. their own patient population (n = 704, aneurysms (AAA) and thoracic aortic Technical and clinical success is based 606 males, 86.1%) [17]. Although fe- disease, e.g. aneurysms, Stanford B dis- inthelongandtheshorttermonadequate maleshadsomewhatsmallerAAA(5.2vs. section, intramural hematoma (IMH), and “healthy” landing zones, both proxi- 5.4 cm), both groups were comparable in penetrating aortic ulcer (PAU) and mal and distal to the http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Gefässchirurgie Springer Journals

Endovascular treatment of genetically linked aortic diseases

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Publisher
Springer Medizin
Copyright
Copyright © 2016 by The Author(s)
Subject
Medicine & Public Health; Vascular Surgery
ISSN
0948-7034
eISSN
1434-3932
D.O.I.
10.1007/s00772-016-0221-z
Publisher site
See Article on Publisher Site

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