Titlebook: Aortic Dissection and Related Syndromes; Kim A. Eagle (Albion Walter Hewlett Professor of I Book 2007 Springer-Verlag US 2007 aneurysm.car

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https://doi.org/10.1007/978-3-658-09098-2 in mortality, but it is when the dissection flap produces branch vessel compromise or severe aortic insufficiency, or the dissected aorta ruptures that patients suffer significant morbidity or death. Consequently, the purpose of therapy for aortic dissection is to prevent progression of the dissect

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Elektrotechnik für Ingenieure 1tery occlusion. This complication occurs in up to 18% after surgery initiating the search for alternative therapeutic strategies such as endovascular procedures. Today, after rapid technical improvement, a large number of aortic dissection patients have been successfully treated by percutaneous sten

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Elektrotechnik für Ingenieure 2a systemic illness that predisposes their entire aorta and potentially its larger branches to dissection, aneurysm, and rupture and that assiduous long-term follow-up for these patients is crucial. Systemic hypertension, advanced age, baseline aortic size, and presence of a patent false lumen are al

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Elektrotechnik für Ingenieure 2However, with a prompt diagnosis and appropriate medical and/or surgical management, early survival can be significantly improved to 70–90%.. Even with successful “definitive” in-hospital treatment of aortic dissections, patients remain at considerable risk for late dissection, as well as for aortic

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https://doi.org/10.1007/978-3-8348-9172-3on an hourly basis, and is fatal in over 90% of patients at one month if untreated.. However, recent reports on mortality with maximal antihypertensive therapy reveal improvements with medical therapy. Survival in patients who survive the initial event and present to the hospital has been reported a

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https://doi.org/10.1007/978-3-8348-9172-3l reduction in tensile strength and predispose to aneurysm formation and dissection. Cystic medial degeneration is the common histopathologic expression of a number of such disorders, including Marfan and Ehlers-Danlos syndromes. Several other familial forms of thoracic aortic disease have been repo

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Elektrotechnik für Ingenieure 2nosis are rather different from those of classical dissection. Advances in imaging techniques have facilitated diagnosis and have aided understanding of the natural history of this entity, practically unknown 10 years ago. Aortic intramural hematoma (IMH) is an entity included in the acute aortic sy

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Kim A. Eagle (Albion Walter Hewlett Professor of IMost comprehensive reference on aortic dissection.Organized by the International Register of Aortic Dissection.Includes supplementary material: