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Acute Aortic Disease.. - Index of

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320 Hackmann et al.<br />

Patients with Chronic <strong>Aortic</strong> Dissection<br />

Similar to patients with small asymptomatic aneurysms, patients with chronic<br />

descending aortic dissection receive nonoperative management (i.e., anti-impulse<br />

therapy and imaging surveillance) until symptoms or significant aortic expansion<br />

occur. Unfortunately, the current pharmacologic approach has limited efficacy.<br />

Aneurysm expansion occurs in 43% to 81% <strong>of</strong> patients receiving nonoperative<br />

management <strong>of</strong> chronic descending aortic dissection, and fatal rupture occurs in<br />

up to 23% (87,129–132). Patients who ultimately require surgical treatment<br />

undergo extensive aortic replacement, an operation that carries substantial morbidity<br />

and mortality. Enhancements in pharmacologic treatment could improve<br />

the prognosis <strong>of</strong> chronic dissection.<br />

Patients with Predisposing Conditions<br />

Many patients are born with disorders that predispose them to aortic dilatation and<br />

aortic dissection. Patients with these conditions, including MFS, Ehlers–Danlos<br />

syndrome type IV, Loeys-Dietz syndrome, and congenital bicuspid aortic valve,<br />

<strong>of</strong>ten develop aortic complications at an early age (4,70,133). In addition, the<br />

rates <strong>of</strong> rupture are higher in patients with these syndromes. Suppressive medical<br />

therapy before aneurysm formation might dramatically alter the course for patients<br />

with known matrix defects.<br />

Similarly, the risk for developing aortic aneurysms and dissections is high<br />

in some families. About 15% <strong>of</strong> patients diagnosed with AAAs have a first-degree<br />

relative who had an AAA (134). Mutations causing familial predisposition to<br />

TAAs and dissection have been described in several families (69,135,136). Young<br />

patients with a known family history <strong>of</strong> aortic aneurysms or dissection are screened<br />

aggressively so that aneurysms can be detected and treated before rupture. Longterm<br />

suppressive therapy may reduce the incidence <strong>of</strong> aneurysms and decrease the<br />

risk <strong>of</strong> dissection or rupture in these families.<br />

Patients Undergoing Nonaortic Operations<br />

Patients with aortic aneurysms who undergo nonaortic operations, such as cardiac,<br />

abdominal, and orthopedic procedures, are at risk <strong>of</strong> postoperative aneurysm<br />

rupture (137). Several retrospective or autopsy studies have suggested a 2% to 3%<br />

risk <strong>of</strong> aneurysm rupture in the months after any major surgery. Postoperative<br />

suppressive therapy may decrease this risk.<br />

Patients Who Have Had Open or Endovascular <strong>Aortic</strong> Repair<br />

Both open and endovascular repairs have limited durability. During open repair,<br />

the prosthetic graft is sutured to aorta that is prone to continued deterioration,<br />

resulting in new adjacent aneurysms or anastomotic pseudoaneurysms. The durability<br />

<strong>of</strong> endovascular repair relies on the ability <strong>of</strong> the stent graft to maintain an

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