Article

Innovations in treating aortic diseases: the abdominal aorta.

Department of Anesthesia, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA.
Journal of cardiothoracic and vascular anesthesia (impact factor: 1.06). 01/2011; 26(5):959-65. DOI:10.1053/j.jvca.2010.10.003 pp.959-65
Source: PubMed

ABSTRACT Patients with an abdominal aortic aneurysm (AAA) could benefit from earlier diagnosis to improve long-term outcomes. Candidate serum biomarkers for earlier AAA diagnosis include D-dimer, fibrinogen, low-density lipoprotein, high-density lipoprotein, lipoprotein(a), and the proteolytic enzymes known as matrix metalloproteinases. Furthermore, biomarkers such as brain natriuretic peptide significantly stratify perioperative risk in AAA repair. Statins significantly improve outcomes after AAA repair. They may also significantly slow AAA growth to allow pharmacologic arrest of AAA development. Recent trials have focused attention on fluid management for AAA repair. Although restrictive fluid management may significantly improve clinical outcomes, current evidence does not clearly support crystalloid or colloid for AAA repair. There may be an increased risk of renal dysfunction associated with hetastarch therapy. Endovascular repair has revolutionized the clinical management of AAAs. Recent trials have shown its significant outcome advantages. Furthermore, it is also applicable in high-risk operative cohorts and, in the future, may be suited for earlier AAA repair. This technology continues to advance with the development of branched and fenestrated grafts as well as total percutaneous endovascular AAA repair. Regardless of these advances, the clinical management of endoleaks will remain a major clinical focus. Taken together, these advances in the management of AAAs likely will significantly influence future clinical approaches to this challenging patient cohort.

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Keywords

AAA development
 
AAA diagnosis
 
AAAs
 
AAAs likely
 
abdominal aortic aneurysm
 
Candidate serum biomarkers
 
challenging patient cohort
 
clinical management
 
fenestrated grafts
 
fluid management
 
hetastarch therapy
 
high-density lipoprotein
 
high-risk operative cohorts
 
major clinical focus
 
pharmacologic arrest
 
proteolytic enzymes
 
renal dysfunction
 
restrictive fluid management
 
significant outcome advantages
 
total percutaneous endovascular AAA
 

Balachundar Subramaniam