Aortic Valve, Aorta, and Aortic Branches



Aortic Valve, Aorta, and Aortic Branches





Transesophageal echocardiography (TEE) can substantially augment the transthoracic echocardiogram in the workup of the aortic valve and the aorta.


Aortic Valve


Views

The mid-esophageal short- and long-axis views are the most commonly used views. To obtain an optimal short-axis view, the TEE image is rotated from 0° to between 30° and 60°, with flexion of the probe as necessary. The optimal short-axis view is the one in which the valve appears most circular and the three thin leaflets are seen clearly, surrounded by the noncoronary cusp in the upper left and the left and right cusps as one looks clockwise from the noncoronary cusp. This view is particularly useful for determining the number of aortic valve leaflets and assessing their thickening and fusion, as well as for determining the area of the aortic valve and diagnosing and assessing the severity of aortic insufficiency. The approach to positioning for aortic valve planimetry to obtain valve area is discussed in the subsequent text.

The long-axis view of the aortic valve is generated by further rotation of the probe to an angle usually between 90° and 160°, again with flexion as necessary, to optimize the image. This view demonstrates the aortic outflow tract (AOT), aortic valve and sinuses of Valsalva, and the proximal aorta. The normal valve leaflets appear as thin, pliable, widely opening structures. It is important not to misdiagnose the normal mild thickenings at the coaptation point of the aortic valve leaflets (nodules of Arantius) as pathologic. This view is particularly useful for determining the level of aortic outflow obstruction: subvalvular, valvular, or supravalvular. Leaflet structure and separation are well seen in this view. The presence of valve redundancy can be assessed and can be generally distinguished from the presence of vegetation. Eversion of the leaflets (“rolling up” of the edges) is also well demonstrated.

A less commonly used view is the deep transgastric view, the central utility of which is to try to align the ultrasound beam with the aortic jet in order to determine the pressure gradient across the aortic valve. These views are obtained by advancing the scope into the transgastric position and then flexing it to obtain a view that places the aorta and aortic valve in line with the ultrasound beam. This facilitates the measurement of gradients but does not allow sufficient maneuver to ensure that the probe is aligned so as to provide the highest velocity aortic jet.


Aortic Outflow Obstruction

Using TEE, it is possible to diagnose aortic outflow obstruction, determine the level (subvalvular, valvular, or supravalvular), and quantify the severity. Aortic stenosis (AS) is the only valvular lesion commonly associated with sudden cardiac death. It becomes more common with advancing age, so a progressively aging population results in an increase in the prevalence of the lesion. Subvalvular and supravalvular outflow obstruction are less common.

When an adequate study is performed, transthoracic echocardiography (TTE) can be effective for the workup of AS. On TTE, the diagnosis of AS is made by demonstrating a thickened aortic valve and either a high (>approximately 50 mm Hg) transvalvular gradient or a diminished aortic valve area (AVA) (using the continuity equation). In order to estimate the gradient, the beam is aligned with the axis of the highest velocity aortic jet and the velocity recorded. This may require interrogating in multiple views, including the apical five-chamber, suprasternal notch, and right parasternal views. Using a simplified conservation of energy (Bernoulli) equation, the peak gradient is

Δ Pmax = 4 (Vmax – VOT)2

where Vmax is the peak aortic velocity and VOT is the outflow tract velocity. The mean aortic gradient can also be estimated using the time velocity integral.

An indirect calculation of the AVA can be obtained from the continuity equation, which is a statement of the
conservation of mass. Assuming the AOT to be circular, its area (AOT) can be estimated from the measured diameter on the parasternal long-axis view and the outflow tract velocity (VOT), obtained from pulsed-Doppler examination in the parasternal five-chamber view. The peak velocity across the aortic valve is known, and with a variety of simplifying assumptions, the AVA is calculated as

AVA = VOTAOT/Vmax

This equation is valid even in the presence of aortic insufficiency.

In patients with a markedly reduced stroke volume, valve opening can be reduced. Therefore, the low stroke volume results in both a reduced pressure gradient and a smaller valve area. In patients with a low gradient due to low stroke volume, a dobutamine infusion can be used to clarify the picture. With inotropic stimulation, the computed valve area of a normal valve (or one that is not rigid or severely stenosed) will increase with a minimal rise in gradient. A more rigid, severely stenosed valve, on the other hand, will demonstrate an increase in the transvalvular gradient without an increase in the computed valve area.

These same calculations can be performed on the basis of data derived from the TEE transgastric views. However, in practice, this approach is rarely used. The appropriate deep transgastric view is hard to obtain and it is not possible to maneuver the view sufficiently to be certain that the maximum jet is found.

TEE has assumed a prominent role in the echocardiographic examination of the aortic valve because of the superior imaging detail that it provides compared to TTE. Because the multiplane probe permits great flexibility in the selection of the imaging plane, it is far more effective than single and biplane probes in providing a complete study of a variety of lesions. TEE should be considered a complement to, but not a replacement for, TTE.

A number of findings suggest or are consistent with AS. Thickening of the aortic valve is clearly seen on TEE; when limitation of motion is also present, this is consistent with AS. Color Doppler detection of a narrow (7 mm or less at its origin) systolic jet indicates severe stenosis.

Planimetry of the minimum orifice area in the short-axis view (usually best imaged at 30° to 60°) has been shown to correlate well with catheterization-derived AVA. The stenotic valve often has the geometry of a truncated cone. It is important that the topmost part of this cone be studied, because it is the flow-limiting orifice. To ensure that the minimum orifice is imaged, the probe is first moved up the esophagus in the short-axis view until the aortic valve disappears. The probe is then advanced until the full perimeter of the valve just comes into view, which should demonstrate the minimum cross-sectional area (flow-limiting orifice). Gain must be carefully adjusted to minimize the “blooming” effect of the extensive calcium that is usually present in adults, and the probe must be manipulated to avoid acoustic shadowing by the calcium. In the presence of severe calcification it may be difficult to identify the orifice. When this difficulty arises, color Doppler is often helpful because the first signals appear in the orifice at the beginning of systole.

An attempt can be made to position the TEE image so that a pressure gradient can be measured between the left ventricle and the aorta using the transgastric view. If a high gradient is obtained, AS can be diagnosed. However, it is difficult to be certain that the maximum gradient has been measured because TEE has limited capacity for looking for the maximum jet at multiple angles.

Left ventricular hypertrophy is well imaged by TEE and commonly accompanies AS. It is particularly important to exclude the presence of coexisting hypertrophic cardiomyopathy (HCM) because the hypertrophied muscle can be resected at the time of aortic valve replacement. A narrow left ventricular outflow tract (LVOT) (<20 mm) and hypertrophy that is out of proportion to what would be expected from the degree of AS present alert the echocardiographer to the possibility of coexisting HCM. Systolic anterior motion of the mitral valve may be absent in HCM patients with severe AS.

An interesting lesion that can be identified by TEE is the supravalvular AS. This lesion may be congenital, or it may be present in patients with atherosclerosis and very high cholesterol levels.

The morphologic data available from TEE allow detailed examination of the aortic valve. The multiplane probe is substantially more effective than are single or biplane probes. The mild thickening normally present at the points of leaflet coaptation (nodules of Arantius) also may be identified. TEE effectively defines the number of leaflets and the degree of commissural fusion present. The median raphe of a bicuspid valve can be clearly seen. The distinction between tricuspid and bicuspid aortic valve is important because of the difference in prognosis and the implications for valve repair versus valve replacement. The presence of valve redundancy, which may be confused with a vegetation on transthoracic echo, can be delineated. Eversion of the leaflets is also well demonstrated.


Aortic Regurgitation

The causes of aortic regurgitation (AR), including thickening, eversion of the leaflets, infection, dilatation of the proximal aorta with loss of leaflet coaptation, and redundancy, can be delineated. Intermittent AR, caused by varying coaptation points resulting from valve redundancy (especially in a bicuspid valve), can also be detected. Small fenestrations as well as large holes and their exact location and size can be imaged.

TEE is of particular importance in the workup for endocarditis. TEE is far more sensitive for the assessment of vegetations than is TTE. For this reason, in the
appropriate clinical setting, the absence of a vegetation on TTE should prompt the performance of TEE. Abscesses are also far more likely to be seen on TEE than TTE. Their anatomic location and extent are readily imaged, and their communication with other structures is diagnosed using color-flow Doppler.

Assessment of the severity of AR is based on semiquantitation using the fraction of the LVOT at the origin of the diastolic jet on the ventricular aspect of the aortic valve that is covered by the jet. The percent ratio of proximal jet width to LVOT diameter (taken at the same location) of <25% represents mild regurgitation, 25% to 65% represents moderate severity, and >65% is a demonstration of severe regurgitation. Two technical points are important. First, the assessment must be made at the origin of the jet (vena contracta level). Second, the Nyquist limit is important. If it is set higher than 40 to 50 cm/sec, changes in the color filter result in the loss of imaging of lower velocities and therefore changes the size of the proximal jet.


Aorta

Defining aortic anatomy is another important application of TEE. The location and extent of aortic aneurysms are more effectively visualized using TEE than TTE. The ability of TEE to image the entire aorta is an important advantage over TTE. Evidence of rupture can be sought and the extent of associated AR can be assessed using color-flow Doppler. In many centers, TEE is the modality of choice for diagnosing aortic dissection because of its ability to rapidly and accurately make the diagnosis. This is important because these patients may die suddenly if surgery is not performed immediately.

The diagnosis of dissection is based on the demonstration of a flap that separates the true lumen (TL) and the false lumen (FL). It is necessary to examine the aorta in multiple planes because the flap is not well seen in all views. The flap is usually, but not always, mobile, which aids in making the diagnosis. Flow in opposite directions on the different sides of the flap, if present, helps to confirm the diagnosis. A number of features aid in differentiating the TL from the FL and may help confirm the diagnosis of aortic dissection. Flow in the TL usually has higher velocity than flow in the FL; as a result, the signals are generally brighter. In addition, the TL expands in systole and the FL expands in diastole. When a clot is present it is usually in the FL. Communications between the TL and FL seen on color Doppler are helpful in confirming the diagnosis. Because the entire thoracic and proximal abdominal aorta can be imaged using the multiplane probe, the exact location and full extent of dissection can be delineated.

Dissections that involve the ascending aorta, arch, or both, and the descending aorta are DeBakey type I. Dissections that involve the ascending aorta, arch, or both (but not the descending aorta) are DeBakey type II, and those that involve only the descending aorta are Type III. In the Stanford classification, any dissection involving the ascending aorta, the arch, or both is type A, whereas dissection involving only the descending aorta is type B.

TEE is useful in assessing prognosis and making management decisions. A clotted FL has a better prognosis than a flow-filled FL because it acts as a buttress for the TL, thereby diminishing the chance of rupture. Assessment of the cause and severity of AR in patients who had dissection helps in making a decision regarding the necessity of resuspension or replacement of the aortic valve. Involvement of the coronary arteries in the dissection can also be diagnosed. Dissections that involve only the descending aorta do not require surgery unless there is evidence of impending rupture or compromise of organ flow, which occurs rarely.

Atherosclerotic plaques in the aorta are readily identified by TEE. The presentation varies from uniform intimal thickening to large mobile plaques protruding into the lumen. Atherosclerosis in the aorta is a risk factor for stroke and emboli to other parts of the body. The greater the mobility, the higher the risk of embolization. Fixed plaques protruding >5 mm into the lumen are also at high risk for embolization.






FIGURE 3.1. Aortic stenosis. A,B. The valve is mildly thickened and doming but opens well, consistent with mild aortic stenosis (AS). AO, aorta; LA, left atrium, LV, left ventricle; MV, mitral valve; PA, pulmonary artery; RA, right atrium; RV, right ventricle. C–E. Patient with severe calcific AS. The valve is markedly thickened and calcified (arrows), and the opening of the valve is severely restricted. Flow acceleration (arrowheads) and turbulence in the aortic root (E) are indicative of significant AS. This patient underwent aortic valve (AV) replacement. F. The wide aortic jet (arrowheads) in another patient suggests an absence of significant AS. G. The jet (arrowhead) shown in this illustration, on the other hand, is narrow (<7 mm) at its origin, indicative of severe AS. Marked poststenotic dilatation of the aorta is present. It is important to assess the jet width at its exit point from the aortic valve. At surgery, this patient was found to have a heavily calcified, severely stenotic aortic valve. He underwent CarboMedics aortic valve replacement.






FIGURE 3.2. Aortic stenosis. A,B. A thickened aortic valve with markedly restricted opening (arrow). The inset in B shows the valve orifice imaged in short axis. AO, aorta; AV, aortic valve; LA, left atrium; LV, left ventricle; RV, right ventricle; RVO, right ventricular outflow tract. C. Planimetry of the orifice of a thickened valve in the short-axis view is shown in another patient. An area of 0.74 cm2 is found in this patient. The bottom inset in C demonstrates that color Doppler can help to identify the orifice; the top inset shows a narrow jet (arrowheads) consistent with severe stenosis. The probe must be moved carefully up and down the esophagus until the minimum cross-sectional area is found. This yields the flow-limiting orifice area. This point is emphasized in D, which shows that planimetry of the minimum area yields a valve area of 0.68 cm2, whereas planimetry more proximally gives an area of 1.43 cm2. PA, pulmonary artery. E–G. Gross specimens of thickened tri-leaflet aortic valves show calcium in the cusps that restricts opening. (C reproduced with permission from
Kim KS, Maxted W, Nanda NC, et al. Comparison of multiplane and biplane transesophageal echocardiography in the assessment of AS. Am J Cardiol 1997;79:436–441.


)






FIGURE 3.3. Aortic stenosis. A. Planimetry reveals severe bicuspid aortic stenosis (AS) with a valve area of 0.52 cm2. Upper inset panel: A very narrow jet consistent with severe AS. Lower inset panel: Acoustic shadowing that results in the dropout of part of the image so that color does not fill the entire orifice. Careful positioning of the probe is necessary if the valve is to be accurately planimetered. B. Severe bicuspid aortic valve stenosis is seen in another patient. C. Gross specimen shows a thickened and calcified bicuspid aortic valve. AV, aortic valve; LA, left atrium; RVO, right ventricular outflow tract; SVC, superior vena cava. (A reproduced with permission from
Kim KS, Maxted W, Nanda NC, et al. Comparison of multiplane and biplane transesophageal echocardiography in the assessment of AS. Am J Cardiol 1997;79:436–441.


)






FIGURE 3.4. Aortic stenosis. A,B. A bicuspid valve mimicking a tricuspid aortic valve. Although the valve appears to have three leaflets, it was found to be tricuspid at surgery. AO, aorta; AV, atrial valve; LA, left atrium; LAA, left atrial appendage; PA, pulmonary artery; RA, right atrium; RV, right ventricle; RVOT, right ventricular outflow tract; TV, tricuspid valve. C,D. This valve (arrowheads) appeared to be bicuspid but was surgically shown to be tricuspid. E. The narrow jet (arrow) confirms the presence of severe stenosis in this patient. F. In another patient, color Doppler examination was helpful in identifying the eccentric severely stenotic orifice. This patient underwent aortic valve replacement. G. The surgically resected specimen from the patient in F shows a heavily calcified, severely stenotic bicuspid valve.






FIGURE 3.5. Aortic stenosis. Two patients with fixed stenotic orifices are shown. A. Size of the orifice (arrow), which measures 0.36 cm2, does not change from diastole to systole. Color Doppler examination (inset) was helpful in delineating the orifice. AV, atrial valve; LA, left atrium; PA, pulmonary artery; RA, right atrium. B–D. Another patient with a fixed stenotic orifice (arrowheads), which does not change in size from diastole (B) to systole (C). In such cases, color Doppler examination is useful in identifying the orifice (D). (A reproduced with permission from
Kim KS, Maxted W, Nanda NC, et al. Comparison of multiplane and biplane transesophageal echocardiography in the assessment of AS. Am J Cardiol 1997;79:436–441.


)






FIGURE 3.6. Aortic stenosis. Associated LV hypertrophy is shown in the transgastric view. A. The wall thickness measures >20 mm. B,C. Fibroelastosis developing in another patient with aortic stenosis (AS). Note the thickened, hyper-refractile endocardium (arrowheads)






FIGURE 3.7. Aortic stenosis. A. Aortic stenosis (AS) coexisting with hypertrophic cardiomyopathy. A markedly thickened ventricular septum, narrow left ventricular outflow tract, systolic anterior motion (SAM) of the mitral valve, and aortic valve with restricted opening are seen. B,C. Another patient with SAM of the anterior mitral leaflet, hypertrophied ventricular septum, and a thickened aortic valve with marked restriction of the opening. This patient underwent aortic valve replacement for severe stenosis and left ventricular septal myomectomy. LV, left ventricle; RV, right ventricle.






FIGURE 3.8. Aortic valve thickening. A,B. Localized thickenings (arrowheads) called nodules of Arantius are often seen in healthy patients on the aortic valve at the points of leaflet coaptation. AO, aorta; AV, aortic valve; LA, left atrium; LV, left ventricle; RA, right atrium; RV, right ventricle; SAM, systolic anterior motion; VS, ventricular septum. C,D. Another patient with prominent localized thickening (arrow) of the right coronary cusp causing aortic regurgitation (arrow in D). E. Calcification results in mild narrowing of the aorta at the level of the sinotubular junction (arrows). Severe acquired supravalvular aortic stenosis can occur in patients with familial, homozygous hypercholesterolemia. F. Fibrotic thickening (arrowheads) is shown at the base of the aortic leaflets.










FIGURE 3.10. Redundant aortic valve. A,B. Redundant (arrowhead) right coronary cusp is shown with and without color Doppler. The other cusps do not appear to be redundant. LA, left atrium; RA, right atrium; RVOT, right ventricular outflow tract. C,D. In another patient, the linear echo prolapsing into the left ventricular outflow tract (LVOT)(arrowhead) represents cusp redundancy. AO, aorta; LV, left ventricle; RV, right ventricle. E. An M-mode study shows systolic fluttering of the aortic valve (AV), which is a normal finding and is not necessarily related to the redundancy.






FIGURE 3.11. Redundant aortic valve. A. Redundant aortic valve (AV) (arrow) prolapsing into the left ventricular outflow tract. AO, aorta; LA, left atrium; RA, right atrium; LV, left ventricle; PA, pulmonary artery; RV, right ventricle. B,C. Eccentric jets of aortic regurgitation (AR) (arrows). In both patients the AR jet is directed posteriorly and abuts the mitral valve.






FIGURE 3.12. Redundant aortic valve. The arrows show various components of a redundant, noninfected bicuspid aortic valve prolapsing into the left ventricular outflow tract (A–D) with a posteriorly directed regurgitant jet AO, aorta; LA, left atrium; LV, left ventricle; MV, mitral valve; RA, right atrium; RVOT, right ventricular outflow tract. (E,F). The flow acceleration (FA) is large, indicating significant regurgitation although the proximal jet width appears narrow. This is related to the eccentric geometry of the jet and to the high Nyquist limit of 49 cm/sec. G. The systolic frame in the same patient clearly shows a bicuspid aortic valve with a raphe (lower arrow). H. The diastolic frame mimics a tricuspid aortic valve, emphasizing the importance of examining the valve throughout the cardiac cycle. This patient underwent aortic valve annuloplasty.






FIGURE 3.13. Redundant aortic valve. A–C. The diastolic frames show central noncoaptation (NC) of the aortic valve (AV) leaflets that results in aortic regurgitation (arrow in C). LA, left atrium; PA, pulmonary artery; RA, right atrium; RVO, right ventricular outflow tract. D. Cusp separation in diastole is also well seen in the M-mode study.






FIGURE 3.14. Redundant aortic valve with hole in right coronary cusp. A,B. A hole (arrows) in the right coronary cusp of the aortic valve, which prolapses into the left ventricular outflow tract. AO, aorta; LA, left atrium; LV, left ventricle; RVOT, right ventricular outflow tract. C. An area of noncoaptation (arrow) between the left coronary cusps (LCC) and noncoronary cusps (NCC). D. Severe aortic regurgitation with a large flow acceleration (arrow). MV, mitral valve.






FIGURE 3.15. Flail aortic valve. A–C. A flail right coronary cusp (arrows) prolapsing into the left ventricular outflow tract (LVOT) in diastole, resulting in prominent diastolic noncoaptation seen in the long-axis views. AO, aorta; AV, aortic valve; LA, left atrium; LV, left ventricle; RV, right ventricle. D. High-frequency diastolic fluttering (arrow) indicative of a flail aortic valve (AV). There was no evidence of infection. E. Severe eccentric aortic regurgitation (AR) with a large flow acceleration. F,G. Systolic turbulence in LVOT was also seen in this patient and was due to associated hypertrophic cardiomyopathy (IHSS). At surgery, the right coronary leaflet was found torn from its attachment at the commissure between the right and left sinuses. A portion of the autologous pericardium was used to reconstruct the right coronary cusp, and the annulus size was reduced from 24 mm to 18 mm in diameter by performing a triple annuloplasty. MR, mitral regurgitation.






FIGURE 3.16. Eversion of the aortic valve. The distal portion of the left coronary cusp in this patient shows eversion causing noncoaptation with the right coronary cusp, which is only minimally everted. AO, aorta; AV, aortic valve; LA, left atrium; LV, left ventricle; RV, right ventricle.






FIGURE 3.17. Flail aortic valve in systemic lupus erythematosus. A. Prominent prolapse of the right coronary cusp (arrow) into the left ventricular outflow tract during diastole and noncoaptation of the valve leaflets. B. The long-axis view of the aortic valve demonstrates an eccentric jet of severe aortic regurgitation (AR) directed toward the mitral valve. Note the prominent flow acceleration (FA), which also suggests severe regurgitation. C. Excised aortic valve. There is destruction of the right coronary cusp near the commissure (bottom left). No vegetations are seen. D. Gross specimen from another patient shows lupus valvulitis of both mitral and aortic valves. AO, aorta; LA, left atrium; LV, left ventricle; RV, right ventricle. (AC reproduced with permission from
Mehta R, Agrawal G, Nanda NC, et al. Flail aortic valve in systemic lupus erythematosus. Echocardiography 1996;13:431–434.


)






FIGURE 3.18. Aortic valve vegetation. A–C. A large vegetation (arrow) moving into the left ventricular outflow tract in diastole and back into the aortic root in systole. AO, aorta; LA, left atrium; LV, left ventricle; MV, mitral valve; RPA, right pulmonary artery; RV, right ventricle.






FIGURE 3.19. Aortic valve vegetation. A–C. A large vegetation (V) is shown prolapsing into the outflow tract with severe aortic regurgitation (AR). D. Pulsed-Doppler of the distal ascending aorta demonstrates prominent pandiastolic backflow resulting from significant AR. AO, aorta; AV, aortic valve; LA, left atrium; LV, left ventricle; MV, mitral valve; RV, right ventricle.

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Jun 15, 2016 | Posted by in CARDIOLOGY | Comments Off on Aortic Valve, Aorta, and Aortic Branches

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