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      Functional assessment of thoracic aortic aneurysms – the future of risk prediction?

      1 , 2 , 1 , 2 , 3 , 1
      British Medical Bulletin
      Oxford University Press (OUP)

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          Abstract

          <div class="section"> <a class="named-anchor" id="ldw049s1"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e184">Introduction</h5> <p id="d16483643e186">Treatment guidelines for the thoracic aorta concentrate on size, yet acute aortic dissection or rupture can occur when aortic size is below intervention criteria. Functional imaging and computational techniques are a means of assessing haemodynamic parameters involved in aortic pathology. </p> </div><div class="section"> <a class="named-anchor" id="ldw049s2"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e189">Sources of data</h5> <p id="d16483643e191">Original articles, reviews, international guidelines.</p> </div><div class="section"> <a class="named-anchor" id="ldw049s3"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e194">Areas of agreement</h5> <p id="d16483643e196">Computational fluid dynamics and 4D flow MRI allow non-invasive assessment of blood flow parameters and aortic wall biomechanics. </p> </div><div class="section"> <a class="named-anchor" id="ldw049s4"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e199">Areas of controversy</h5> <p id="d16483643e201">Aortic valve morphology (particularly bicuspid aortic valve) is associated with aneurysm of the ascending aorta, although the exact mechanism of aneurysm formation is not yet established. </p> </div><div class="section"> <a class="named-anchor" id="ldw049s5"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e204">Growing points</h5> <p id="d16483643e206">Haemodynamic assessment of the thoracic aorta has highlighted parameters which are linked with both clinical outcome and protein changes in the aortic wall. Wall shear stress, flow displacement and helicity are elevated in patients with bicuspid aortic valve, particularly at locations of aneurysm formation. </p> </div><div class="section"> <a class="named-anchor" id="ldw049s6"> <!-- named anchor --> </a> <h5 class="section-title" id="d16483643e209">Areas timely for developing research</h5> <p id="d16483643e211">With further validation, functional assessment of the aorta may help identify patients at risk of aortic complications, and introduce new haemodynamic indices into management guidelines. </p> </div>

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          Most cited references68

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          2014 ESC Guidelines on the diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the adult. The Task Force for the Diagnosis and Treatment of Aortic Diseases of the European Society of Cardiology (ESC).

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            Hemodynamic shear stress and its role in atherosclerosis.

            Adel Malek (1999)
            Atherosclerosis, the leading cause of death in the developed world and nearly the leading cause in the developing world, is associated with systemic risk factors including hypertension, smoking, hyperlipidemia, and diabetes mellitus, among others. Nonetheless, atherosclerosis remains a geometrically focal disease, preferentially affecting the outer edges of vessel bifurcations. In these predisposed areas, hemodynamic shear stress, the frictional force acting on the endothelial cell surface as a result of blood flow, is weaker than in protected regions. Studies have identified hemodynamic shear stress as an important determinant of endothelial function and phenotype. Arterial-level shear stress (>15 dyne/cm2) induces endothelial quiescence and an atheroprotective gene expression profile, while low shear stress (<4 dyne/cm2), which is prevalent at atherosclerosis-prone sites, stimulates an atherogenic phenotype. The functional regulation of the endothelium by local hemodynamic shear stress provides a model for understanding the focal propensity of atherosclerosis in the setting of systemic factors and may help guide future therapeutic strategies.
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              Aortic diameter >or = 5.5 cm is not a good predictor of type A aortic dissection: observations from the International Registry of Acute Aortic Dissection (IRAD).

              Studies of aortic aneurysm patients have shown that the risk of rupture increases with aortic size. However, few studies of acute aortic dissection patients and aortic size exist. We used data from our registry of acute aortic dissection patients to better understand the relationship between aortic diameter and type A dissection. We examined 591 type A dissection patients enrolled in the International Registry of Acute Aortic Dissection between 1996 and 2005 (mean age, 60.8 years). Maximum aortic diameters averaged 5.3 cm; 349 (59%) patients had aortic diameters <5.5 cm and 229 (40%) patients had aortic diameters <5.0 cm. Independent predictors of dissection at smaller diameters (<5.5 cm) included a history of hypertension (odds ratio, 2.17; 95% confidence interval, 1.03 to 4.57; P=0.04), radiating pain (odds ratio, 2.08; 95% confidence interval, 1.08 to 4.0; P=0.03), and increasing age (odds ratio, 1.03; 95% confidence interval, 1.00 to 1.05; P=0.03). Marfan syndrome patients were more likely to dissect at larger diameters (odds ratio, 14.3; 95% confidence interval, 2.7 to 100; P=0.002). Mortality (27% of patients) was not related to aortic size. The majority of patients with acute type A acute aortic dissection present with aortic diameters <5.5 cm and thus do not fall within current guidelines for elective aneurysm surgery. Methods other than size measurement of the ascending aorta are needed to identify patients at risk for dissection.
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                Author and article information

                Journal
                British Medical Bulletin
                Oxford University Press (OUP)
                0007-1420
                1471-8391
                March 2017
                January 01 2017
                December 18 2016
                March 2017
                January 01 2017
                December 18 2016
                : 121
                : 1
                : 61-71
                Affiliations
                [1 ] Department of Cardiothoracic Surgery & Cardiology, St. George's Hospital, St. George's University of London, Blackshaw Road, London, SW17 0QT, United Kingdom
                [2 ] Department of Biomedical Engineering, Rayne Institute, St. Thomas’ Hospital, King's College London, London SE1 7EH , United Kingdom
                [3 ] Departments of Surgery and Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109 USA
                Article
                10.1093/bmb/ldw049
                5862296
                27989994
                bfe20252-c053-46af-a4f5-d4ad44d9c761
                © 2016
                History

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