Echocardiography

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CHAPTER 6 Echocardiography

DESCRIPTION OF TECHNICAL REQUIREMENTS

Because the quality of an ultrasound study is operator dependent, it is highly recommended that the operator have a solid knowledge of ultrasound physics and the various options available on the ultrasound equipment used.

Moreover, information such as patient identification, blood pressure measurements, any other specific clinical condition during which the study is recorded (e.g., the use of a specific drug, electrocardiogram tracing) are all necessary for a clear understanding of the problem to be studied. Specific details regarding each of the echocardiography techniques are discussed below.

Techniques

M Mode

The M (for motion) mode consists of a graphic in which it is possible to analyze the motion of cardiac structures over time. It is necessary for the correct position of a cursor line along the anatomic cardiac structure to be studied and this cursor line has its origin point at the ultrasound transducer itself. Errors in measurements with M mode are possible because some planes might be in an oblique orientation. This can be corrected with the anatomic M mode, an adjustable cursor line (angle up to 180 degrees), available in actual echocardiograph machines. The M mode is used for cardiac dimensions, subtle cardiac motion abnormalities, and assessment other time-related parameters (Fig. 6-1).

Doppler Echocardiography and Color Flow Imaging

Doppler echocardiography uses ultrasound waves to calculate blood flow velocities based on the way the flowing blood reflects the ultrasound waves. The reflected ultrasound frequency is higher when the blood flows toward the transducer, and the opposite effect is true when it flows away from the transducer. One important aspect of the way Doppler works is the angle of interrogation. The more parallel the reflected waves to the transducer, the higher the reflected sound waves (called Doppler shift) and the peak velocities. Pulsed wave Doppler uses only one crystal to transmit and receive the reflected frequency. This kind of Doppler is used to study lower blood flow velocities such as mitral and tricuspid diastolic flows. The continuous wave Doppler uses one crystal to send and another one to receive the sound frequency from the blood and it can measure highest velocities along the way of its beam, such as the flow through a stenotic aortic valve. The color flow Doppler uses the same principle as the pulsed wave Doppler, with the difference being for the several sampling sites along multiple ultrasound beams, so it can analyze the blood flow in different velocities, directions, and extent of turbulence. The flow is coded in multiple colors: blue for the flow going away from the transducer and red if it is coming toward the transducer. Properly configured, the green color can also show turbulence and its extent.

Important hemodynamic information can be obtained by using 2D and Doppler techniques but none of them, not even the invasive approach, is perfect, being influenced by several other hemodynamic factors. Flow velocities can be converted to pressure gradients by using the modified Bernoulli equation1:

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where v is peak velocity. It is modified because several other elements can be ignored such as the velocity proximal to a fixed orifice and also flow acceleration and viscous friction. The pressure gradient obtained by this equation represents the instantaneous gradient, which is different from the peak-to-peak pressure measurement in the catheterization (cath) lab because those two peaks are not simultaneous. Several pressure measurements can be made using this equation such as: aortic stenosis gradient, right ventricle systolic pressure, pulmonary end-diastolic and mean arterial pressure, left atrial systolic pressure, and left ventricular end-diastolic pressure.

With the use of Doppler, it is also possible to obtain the stroke volume and cardiac output based on the equation that uses the hydraulic orifice formula, which is1:

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The flow velocity is given by the sum of all instantaneous velocities of the curve by Doppler tracings, after tracing the area enclosed by the baseline and the Doppler spectrum. The CSA is given by the assumption that the orifice is a perfect circle so the diameter is measured and applied in the equation:

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in which “D” means diameter. To calculate the systolic volume, the left ventricular outflow tract (LVOT) area is used in the first equation. And then, to get the cardiac output, the systolic volume is multiplied by the heart rate. Any flow across an orifice in the heart can be calculated using this method. Hence, it is possible to get the right ventricular outflow tract (RVOT) flow and, together with the LVOT flow, to get the ratio between pulmonary and systemic flows—important in some quantification of severity in congenital abnormalities. This method is also useful to obtain the regurgitant volume across a heart valve, such as mitral or aortic regurgitation (Fig. 6-3).

Transesophageal Echocardiography (TEE)

Since its first use, TEE has been considered not only an accessory imaging technique but in some circumstances, it is the main imaging modality for cardiac diagnoses, such as mitral valve disease, aortic dissection, endocarditis and its complications, atrial septum defects, cardiac tumors, and electrophysiology studies monitoring. In patients with atrial fibrillation, TEE information can be decisive in the choice of treatment.

The TEE uses a gastroesophageal endoscopy probe modified with a 7 to 10 MHz transducer on the tip. The study technique consists of inserting the probe through the esophagus, making it possible to get high resolution images of the heart. The study is performed in a special room, with emergency-trained personnel, suction and oxygen devices, and all necessary resuscitation equipment. The probe then can be anteflexed and retroflexed, moved from side to side, rotated clockwise and counterclockwise manually and the planes can be moved from 0 to 180 degrees wide with the touch of one button (Fig. 6-4).

Intracardiac Echocardiogaphy (ICE)

By using small diameter probes, it is possible to get intracardiac images. These probes are inserted until they reach the right atrium, from which all the image planes are made, and because those probes are multifrequency they have capabilities of complete 2D and Doppler study. The great advantage of ICE is for interventional studies such as transcatheter closure device placement for atrial septum defects, including a more detailed study of the defect, its size, and associated congenital defects such as pulmonary vein anatomy, and the margins of the defect—all this information being useful to predict the success of the closure. Ablation procedures, such as pulmonary vein isolation for atrial flutter, with better visualization of the tissue for radiofrequency energy application, avoids complications such as pulmonary valve stenosis owing to inadvertent ablation.

Indications

In the following sections, the most important clinical situations for the use of echocardiography will be discussed, including transthoracic and transesophageal echocardiography, as well as other techniques.

Systolic Function and Quantification of Cardiac Chambers

The 2D echocardiography is the main tool for the evaluation of systolic function and chamber quantification, even considering the newer techniques such as 3D echocardiography, tissue Doppler, strain and strain rate imaging. With 2D images of the LV it is possible to analyze the thickening of ventricular walls and provide not only a subjective evaluation of LV function but also the quantitative assessment, which can be done by calculating changes in size and volume of the chamber. The systolic function is crucial for guiding the patient’s treatment and prognosis; the evaluation of regional contractility is important for patients with suspected or diagnosed coronary heart disease.

Left ventricle. The LV size can be obtained by the 2D image of parasternal short axis view and the M mode for that plane at the level of the papillary muscles or from the long axis view. This method can be used for normal hearts or with no regional wall motion abnormalities and the mass also can be calculated from the measurements of the interventricular septum and posterior wall thickness. LV function is calculated from the diastolic and systolic diameters and also by the Simpson method. From the diameter values, it is possible to calculate the fractional shortening, the percentage change in LV dimensions, by the following formula:

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in which LVEDD means left ventricular end-diastolic diameter and LVESD means left ventricular end-systolic diameter. The Simpson method can be used to obtain LV volumes and then the calculated ejection fraction (EF) by the following formula2:

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Regional wall motion analysis is the most important tool for the evaluation and diagnosis of patients with suspected or confirmed coronary heart disease. For this purpose, the LV is divided into 16 segments. First into three levels: basal, mid, and apical. The basal and mid levels have six segments: antero-septum, anterior, lateral, posterior, inferior, infero-septum; and the apex is then divided into four segments being the anterior, lateral, inferior, and septum. There was only 1 change for an additional “apical cap” segment by the Association Writing Group on Myocardial Segmentation for Cardiac Imaging with the total of 17 segments.3 Each segment is scored according to its contractility: 1-normal; 2-hypokinesis; 3-akinesis, 4-dyskinesis, and 5-aneurysmal. Each value of each segment is summed and the total is divided by the number of segments analyzed for the wall motion score index (WMSI), being normal if equal to 1.

Right ventricle (RV). The RV size is best measured from the apical four-chamber view and its thickness from the subcostal view at the peak R on the ECG. RV size is useful to detect volume and/or pressure overload and can be accompanied by RV wall thickness higher than 5 mm, the abnormal value.2

Left atrium (LA). The left atrium size is measured from the parasternal long axis view (PLAX) at end systole. This view can provide some underestimation on the chamber size because the LA can enlarge longitudinally. Because of this aspect of LA diameter, the best method is to calculate its volume from two orthogonal apical views using one of the four methods available (Fig. 6-5).2

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image FIGURE 6-5 Ejection fraction (EF) calculation based on the modified Simpson rule, showing left ventricle volumes in diastolic and systolic phases (white arrows). A and B, four-chamber views. C and D, two-chamber views. The EF for the four-chamber views is EF = end diastolic volume − end systolic volume/end diastolic volume = 106 − 37/106 = 65%. Using the same formula, the EF for the two-chamber view is 73%, and the final EF is then 69%. ESV(Mod), end systolic volume by modified Simpson rule; EDV(Mod), end diastolic volume by modified Simpson rule. E, Images of LV segmentation for wall motion analysis. On the top panel, the three apical views are shown: four-chamber, two-chamber and three-chamber view or long axis; the bottom panel shows three short axis views: basal, mid, and apical levels. These levels are displayed in the heart drawing on the left side of this picture. All wall regions are identified in each view. The apical cap can be used for wall motion analysis but is especially considered for studies such as myocardial perfusion or contrast studies. F, same arrangement for images is shown: top panels for three apical views and bottom panels showing three levels of short axis views. In this image, the coronary supply is shown for each wall and region. LV, left ventricle; CX, circumflex artery; LAD, left anterior descending artery; RCA, right coronary artery. G, H, left atrial (LA) volume calculations. The LA is shown in two apical views, four-chamber (G) and two-chamber (H), with measurements displayed on the top left corner (white arrows). Considering the area-length method: Left atrial volume = 8/3π[(A1)(A2)/(L)], in which A1 and A2 correspond to the two area numbers (Ad) and L corresponds to the length (Ld) and the highest number is included in the formula; then, LA = 0.85[(13.9)(19.9)]/(4.9) = 48 mL. Another method of LA volume calculation is using the modified Simpson rule, the same rule used for left ventricle ejection fraction measurement. The final volume is obtained tracing the endocardial border of the left atrial chamber in the final systole and the final volume is the average of the two orthogonal volumes in the two apical views, which in this case is 49.5 mL, the number comparable with the area-length method (48 mL). LA, left atrium; Ld, length; LV, left ventricle; RA, right atrium; RV, right ventricle.

(F, Modified from Lang RM, et al. Recommendations for Chamber Quantification: A Report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, Developed in Conjunction with the European Association of Echocardiography, a Branch of the European Society of Cardiology. J Am Soc Echocardiogr 2005; 18:1440-1463.)

Diastolic Function

With the increase in aging population and the options of treatment of several cardiac diseases, especially hypertension and coronary heart disease, diastolic heart failure is becoming more prevalent and it is important to correctly evaluate those patients. The majority of those patients have symptoms of heart failure but not necessarily systolic dysfunction and this is the reason myocardial relaxation abnormalities must be completely studied with available Doppler techniques. Not only the study of flow velocities through the mitral and tricuspid valves and central veins, but also the additional information on how myocardial tissue changes, by using tissue Doppler tracings, makes the use of echocardiography a powerful option in this setting. Increment value can be included if 2D findings are associated, such as the increase in LA diameter, LV thickness (e.g., hypertension, hypertrophic cardiomyopathy [HCM], obesity).

Mitral inflow velocities. With mitral inflow tracings obtained by the use of pulsed wave Doppler, it is possible to measure peak velocities of early (E wave) and late (A wave) diastolic filling, the time from peak E wave to baseline (deceleration time—DT) and also the isovolumic relaxation time (IVRT), between the aortic valve closure and before mitral valve opening. Usually the DT and IVRT are prolonged in relaxation abnormalities because it takes a longer time for the LV filling pressure, in those cases, to equilibrate the LA pressure. And both are shortened in normal individuals or in situations of a higher filling pressure in the LV (with higher LA pressure).1

Mitral annulus velocities. Typical tracings of mitral annulus velocities obtained by tissue Doppler include three waves: one systolic (S′) and two diastolic: an early diastolic wave (E′) and a late diastolic wave (A′). For the purpose of evaluating diastolic function, the most important among those three waves is the E′. It is lower in patients with abnormal relaxation and does not increase with exercise, which is an opposite effect in normal subjects. In general E′ velocity remains lower and E wave velocity increases with higher filling pressures. It has been used as a ratio between those waves to estimate diastolic dysfunction.1

Pulmonary vein flow velocities. There are four different waves in tracings of pulmonary vein flow: two systolic, one diastolic velocity and one atrial flow reversal. Among those, the atrial flow reversal component is the most important, especially its size and morphology.1

Left atrium. The importance of LA dimension is that with progressing LV diastolic stiffness, the LA volume increases being considered one of the best parameters of chronic diastolic dysfunction and is related to further cardiac events such as atrial fibrillation, heart failure, stroke, and death (Figs. 6-5GH and 6-6).4

Pulmonary Hypertension

It is part of the routine echocardiography to measure the pulmonary artery systolic pressure (PASP) using the tricuspid regurgitation velocity. Pulmonary hypertension is when the PASP is greater than 25 mm Hg at rest. Not only can the PASP be obtained by the Doppler techniques, but also the mean and the diastolic pulmonary artery pressure, associating the tracings of pulmonary regurgitation, as discussed earlier.

It is important to distinguish between acute and chronic pulmonary hypertension. Usually acute pulmonary hypertension is due to pulmonary embolism. Chronic pulmonary hypertension causes are related to cor pulmonale. Important findings in both cases are enlargement of right chambers with the LV being “compressed” by the pressure overloaded RV, and also the RV decreased systolic function. It is possible to find images compatible with thrombi, more related to pulmonary embolism. In some cases, it can be difficult to differentiate the acute and chronic pulmonary hypertension. The presence of increased RV thickness may be found in patients with chronic pulmonary hypertension (Fig. 6-7).

Coronary Artery Disease (CAD)

Echocardiography is one of the best noninvasive tools to evaluate patients with suspected CAD or patients submitted to risk stratification because of CAD. It is already known that quantification of global and regional contractility by echocardiography has a close relation to the patient’s short- and long-term prognosis. Evaluation of global LV function by 2D echo was discussed previously. Regional contractility analysis was also addressed previously and what is important to point out in this section is that the higher the wall motion score index, the bigger the infarcted area, which in turn might correlate with a poor prognosis.5 Another important aspect of the regional contractility analysis is that wall motion changes may occur before any ST-T segment elevation in the electrocardiography (ECG) or even before symptoms. Doppler is useful to analyze diastolic function and the initial abnormality is altered myocardial relaxation with prolonged IVRT, DT, lower E, and higher A waves. The restrictive pattern is associated with severe LV systolic dysfunction. Using tissue Doppler parameters is also useful and the E/E′ ratio can be a predictor of survival after acute myocardial infarction (AMI).6

Also important about echocardiography in CAD especially in AMI setting, is that not all patients show ECG changes because of low sensitivity of this technique. In patients with prolonged chest pain and no ECG typical findings, echocardiography is used to exclude any other cause of chest pain such as aortic dissection, cardiac tamponade, and pulmonary embolism. In the follow-up of an unstable post-AMI patient, echocardiography is used to evaluate the presence of any complications such as: LV failure, RV infarct, free wall rupture and pseudoaneurysm, ventricular septal rupture, papillary muscle rupture, ischemic mitral regurgitation, true LV aneurysm, and thrombus.

Tako-tsubo cardiomyopathy. This specific kind of myocardial infarction is characterized by usually apical akinesia not associated with coronary obstruction. There is a relation with psychologic and physical stress situations. It is possible to find typical ECG and cardiac marker abnormalities. This group of patients can show unstable hemodynamics, but almost all of them recover fully.7

Stress echocardiography. Usually after an AMI episode, patients need to be evaluated regarding risk assessment and myocardial viability. Echocardiography is considered the best imaging technique for that purpose by the stress testing. There are two types of stress testing: exercise and pharmacologic. The exercise test includes the use of treadmill or bicycle—the latter is done in the supine position. In the treadmill exercise stress test, the images are acquired in baseline and right after the peak exercise. In the bicycle exercise test, the images can be acquired even during peak exercise.

For the patients who cannot exercise for any number of reasons, the pharmacologic stress test is used and the drugs used are dobutamine, dipyridamole, and adenosine. Stress echocardiography is capable to detect any of the following findings: worsening of wall motion abnormalities (WMA) and/or development of new ones, which are related to stress-induced ischemia. Specifically for pharmacologic test, myocardial viability can be evaluated if there is an improvement in contractility with low-dose dobutamine and worsening with higher doses of the drug, the so called biphasic response. Other findings include: LV dilation and/or decrease in systolic function, which might be related to severe CAD. More detailed information on pharmacologic stress agents can be found in Chapter 26.

Contrast echocardiography. There are two types of contrast agent that can be used to increase the accuracy of echocardiography in diagnosis and quantification of cardiac diseases: gas-filled microbubbles and agitated saline.

The first type of contrast uses artificially made microbubbles small enough to pass through the pulmonary circulation without being destroyed and to make possible LV opacification. This is useful for better definition of endocardial border and thus for LV function measurements using the Simpson method. It is also is better for the WMA and in HCM to distinguish between apical dyskinesia and cases of mid LV or apical hypertrophy.

The microbubbles injected have the capability to reflect the ultrasound signals with twice the frequency transmitted, called the harmonic signal, the reason for the enhancement of picture definition in the LV. But at the same time after some specific adjustments on probe used in these studies, the ultrasound signals can be strong enough to destroy the microbubbles and then it is possible to see myocardial perfusion image, after the myocardial tissue is replenished with those bubbles. That is the reason for the great usefulness of this type of contrast in diagnosis and follow-up of patients with CAD.

The other type of contrast agent, agitated saline, consists of 10 mL of saline which is agitated with a three-way stopcock and two syringes five times before the injection in the venous circulation. The bubbles appear first in the right chamber and then in the left side. The main indication for this technique (also known as a “bubble study”) is to study right-to-left shunts such as through a patent foramen ovale (PFO). If there is flow through the PFO, the contrast appears immediately in the left atrium right after the right one (see Fig. 6-4). Another indication for this technique is to study intrapulmonary shunts, in which the contrast can also be seen in the left atrium immediately after the injection. Normally it is not possible for the bubbles to be seen before at least three consecutive beats. Another useful situation for this saline contrast is to increase the tricuspid regurgitation signal to measure right ventricular systolic pressure because one third of patients may not show a good tricuspid regurgitation Doppler signal (Fig. 6-8).

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image FIGURE 6-8 Myocardial infarction. In A and B, apical four-chamber views of an anteroapical akinetic area (white arrows) in end systole (red lines in electrocardiography tracings). C and D, apical three-chamber views of the same patient showing the akinetic apical region in end systole. LV, left ventricle. Myocardial infarction complications. In E and F, apical four-chamber views showing a thrombus in an akinetic apical region (white arrow) with bright round contour. G and H, apical four-chamber views showing a left ventricle pseudoaneurysm in apical region (asterisk), with a discontinuity of the apical region, due to a tear or rupture of the myocardial wall and thus held the epicardial layer of the pericardium. Stress echocardiography. Each picture shows four still frames: (clockwise) apical four-chamber; apical two-chamber; parasternal long axis and short axis views. I, baseline images in a normal stress study. J, peak stress images with hypercontractility of the walls. K, baseline of positive stress echocardiography study. L, peak stress phase of a positive study showing hypokinesia of apical, anterior, and anteroseptum (white arrows). Note that the left ventricle cavity is enlarged compared to the baseline images and to the normal peak stress images at the top panel. M, left ventricle contrast image with opacification of the cavity in a hypertrophic cardiomyopathy patient. The interventricular septum thickness is best delineated and the measurement is shown. IVS, interventricular septum; LA, left atrium; LV, left ventricle; PW, posterior wall; RA, right atrium; RV, right ventricle.

Mitral Stenosis (MS)

The most common cause of MS is rheumatic heart disease. Infrequent causes of MS include degenerative calcification, hypereosinophilia, medication toxicity, and vegetation. 2D echocardiography is extremely useful in MS because it can provide information used to select patients for mitral balloon valvuloplasty in the cath lab. Each morphologic item is given a grade from 0 to 4 and the total sum must be equal or less than 8, which is related to a good result after valvuloplasty procedure (Wilkins-Block score). Doppler echocardiography can reliably measure the pressure gradient across the mitral valve but can sometimes be variable because of its volume relationship. The mitral valve area calculation is a more reliable method for MS evaluation and can be done with one of the three methods: pressure half time (PHT) (Fig. 6-9), the continuity equation, and the proximal iso-velocity surface area (PISA).

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image FIGURE 6-9 Heart valve disease—aortic stenosis (AS). A, parasternal long axis view of an AS patient showing a calcified aortic valve and left ventricle hypertrophy (thickened septum and posterior wall). B, comparison of a calcified aortic valve in short axis view image with a normal aortic valve (small square image on the bottom right). C, continuous wave Doppler curve with peak transaortic gradient of 102 mm Hg and 99.2 mm Hg (peak velocity of 5.05 m/s and 4.98 m/s, respectively) and a mean gradient value of 65.6 mm Hg (severe if peak velocity ≥ 4 m/s and mean gradient ≥ 40 mm Hg (red arrows); time-velocity integral (TVI) of 124 cm (yellow arrow); and an aortic valve area (AVA) of 0.6 cm2 (severe if ≤ 1.0 cm2) (green arrow). D, left ventricle outflow tract (LVOT) pulsed wave Doppler curve showing VTI values of 24.1 cm and 21.8 cm (yellow arrows). The LVOT/aortic VTI ratio in this case is: 22.95/124 (the first number being the average of 24.1 and 21.8) = 0.18 (severe AS is considered if it is ≤0.25). Mitral stenosis (MS). E, parasternal long axis view of an MS case showing an enlarged LA and the “hockey-stick” appearance of the anterior mitral leaflet during the diastolic phase (white arrowheads). F, apical four-chamber view with the color Doppler showing the turbulence in the diastolic filling from the mitral valve (predominant yellow and red color toward the left ventricle) together with an enlarged left atrium. G, continuous wave Doppler curve of diastolic flow in a stenotic mitral valve with the calculations for mitral valve area by the pressure half time (PHT) method (green arrow). H, same curve used for calculations of peak and mean transvalvular gradients (green arrow) being 26 mm Hg and 17.5 mm Hg, respectively. Aortic regurgitation. I, parasternal long axis view with color Doppler showing a blue jet in left ventricle outflow tract (LVOT) directed toward the left ventricle (LV) cavity in diastolic phase. J, apical four-chamber view with color Doppler with the regurgitant jet in red and yellow in the LV cavity during diastolic phase. K, pulsed wave Doppler curve for AR with the regurgitant jet being demonstrated during diastolic phase (white arrows). Because the regurgitant jet has a higher velocity, it is shown as an aliasing effect, or as a “distortion,” if compared with the systolic flow (negative directed curves), due to a low pulsed repetition frequency (PRF), typical feature of pulsed wave Doppler mode. L, same patient being studied with the continuous wave Doppler to measure the pressure half time (PHT) (= 295 ms), which is consistent with moderate AR. Ao, aorta; LA, left atrium; RA, right atrium; RV, right ventricle. Mitral regurgitation (MR). M, parasternal long axis view showing a protrusion of the posterior leaflet in the left atrial chamber due to mitral valve prolapse (white arrows in the zoomed image in N). O, parasternal long axis view with color Doppler showing the blue and yellow regurgitant jet (high velocity turbulent flow) in the left atrial chamber during systole. P, apical four-chamber view showing blue and yellow regurgitant jet in the left atrial chamber during systole, reaching the right superior pulmonary vein (white arrow). Ao, aorta; Aov, aortic valve; LA, left atrium; LV, left ventricle; MV, mitral valve; PA, pulmonary artery; PW, posterior wall; RA, right atrium; RV, right ventricle; RVOT, right ventricular outflow tract.

ENDOCARDITIS

Echocardiography is the best imaging tool for analyzing patients with suspected or diagnosed endocarditis with a sensitivity ranging from 60% to 80%. Vegetation found on an echocardiography study is one of two major criteria for the diagnosis of endocarditis. Vegetations are usually highly mobile, linear, or round and are found on the atrial side of atrioventricular valves or ventricular face of semilunar valves. Echocardiography is also important for the detection of endocarditis complications, especially for vegetations greater than 10 mm. TEE has the best accuracy for diagnosis of endocarditis with 95% sensitivity and is usually performed in patients with a nondiagnostic TTE and also to detect complications, especially if aortic valve is involved such as: mitral-aortic intervalvular fibrosa aneurysm and/or perforation with communication into the LA, aortic annular abscess, or perforation of the mitral leaflet (Fig. 6-10).

CARDIOMYOPATHIES

There are five major forms of cardiomyopathies, according to pathophysiologic mechanism or etiologic/pathogenic factor: (1) dilated cardiomyopathy; (2) hypertrophic cardiomyopathy; (3) restrictive cardiomyopathy; (4) arrhythmogenic right ventricular dysplasia or cardiomyopathy; and (5) noncompaction cardiomyopathy.

Noncompaction Cardiomyopathy (Isolated Ventricular Noncompaction)

Because of an embryonic defect in the compaction mechanism, the LV wall in this cardiomyopathy can show marked trabeculations and intratrabecular recesses with blood flow mapped by color flow Doppler. Patients with this condition may present during the follow-up with heart failure, thromboembolic events, ventricular tachycardia, and sudden death (Fig. 6-11).

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image FIGURE 6-11 Dilated cardiomyopathy. A, parasternal long axis view showing enlargement of left atrial and ventricle chambers, with diastolic diameter of 87 mm. B, apical four-chamber view with color Doppler showing mitral regurgitation (MR) jet in the left atrial chamber in blue and yellow in systolic phase, together with the more spherical geometry of the left ventricle. C and D, apical four-chamber views with measurements of diastolic (308 mL), systolic volumes (265 mL) and ejection fraction (0.14 or 14%) by Simpson modified rule (white arrows). Hypertrophic cardiomyopathy (HCM). E, parasternal long axis view showing thickened interventricular septum and posterior wall, together with enlargement of the left atrial chamber. Typical feature of HCM is the systolic anterior mitral leaflet motion toward the basal region of interventricular septum during systole and thus contributing to left ventricle outflow tract obstruction (white arrows) seen as a predominant red and yellow jet flow directed toward the ascending aorta in F. G, apical four-chamber view with color Doppler showing a mitral regurgitation jet as in blue flow inside the left atrial chamber. H, because of the interventricular septum hypertrophy and the systolic anterior motion of mitral leaflet, left ventricle outflow tract gradient can be obtained by continuous wave Doppler shown in this image with the 64 mm Hg peak value. Restrictive cardiomyopathy. I, parasternal long axis view showing a normal end diastolic diameter of the left ventricle (49 mm), which can be frequently seen in this kind of cardiomyopathy, and an enlargement of the left atrial chamber. J, apical four-chamber view showing enlargement of both atrial chambers, a typical finding in restrictive cardiomyopathy. K, mitral inflow pulsed wave Doppler curves on a typical restrictive pattern with an E/A ratio ≥1.5 and tissue Doppler curve with a restrictive pattern with low diastolic velocities (L). Tissue Doppler curves: S′, systolic velocity; E′, early diastolic velocity; A′, late diastolic velocity. Arrhythmogenic right ventricular dysplasia/cardiomyopathy. M, parasternal long axis view showing a right ventricle enlargement (compare with a normal parasternal image in the small box on the top right). N, apical four-chamber view showing the right ventricle end diastolic diameter at the mid region (40 mm) which can be compatible with a moderately abnormal enlargement. Ao, aorta; IVS, interventricular septum; LA, left atrium; LV, left ventricle; PW, posterior wall; RA, right atrium; RV, right ventricle.

PERICARDIAL DISEASES

Two important pericardial diseases are promptly recognized by echocardiography: pericardial effusion and constrictive pericarditis. In pericardial effusion, if the echo-free space image is seen throughout the cardiac cycle, the amount of effusion is about 25 mL; smaller amounts can be seen only in systole and in posterior localization.

TUMORS AND MASSES

DISEASES OF THE AORTA

Echocardiography is extremely valuable for the diagnosis of aortic abnormalities. The finding of atherosclerosis or debris in the aortic images has been related to cerebrovascular events, and they appear as mobile and irregularly shaped images. Aneurysms, frequently found in patients with history of hypertension, atherosclerosis, and Marfan syndrome must be promptly measured, using TTE or TEE because of the risk of rupture with diameters equal to or greater than 5 cm. The risk of rupture is also found in aneurysms of the sinus of Valsalva because of the absence of media layer. This type of aneurysm must be distinguished from aneurysm of membranous ventricular septum and other complications can be present such as embolic events, endocarditis, fistulous communications, and left-to-right shunts.

Other types of aortic disease can also be completely studied by echocardiography. Aortitis, caused by Takayasu disease, giant cell arteritis, ankylosing spondylitis, rheumatoid arthritis, and infection such as syphilis, appears as narrowing or even obstruction of thoracic or abdominal aorta or just thickened aortic wall, which sometimes is hard to distinguish from intramural hematoma. Coarctation of aorta is a narrowing of the descending thoracic portion, after the subclavian artery. Because it is a cause of hypertension in young patients, the study of the descending thoracic section must be done extensively in this group of patients with the use of continuous wave Doppler.

Aortic Dissection

There are several publications that studied the feasibility and accuracy of echocardiography in the diagnosis of aortic dissection. TTE is usually the option for screening and TEE is the imaging technique for a complete study. It is possible to visualize the thoracic aorta and the proximal portion of its abdominal section. The TEE must be detailed enough to find the point of intimal tear, or even an intramural hematoma, which can be the precursor lesion of dissection. Intramural hematoma is an echodense image between the intima and adventitia and it is different from atherosclerotic plaque because the latter has an irregular surface. Also important in aortic dissection is the identification of the true and false lumen, as well as complications such as coronary involvement, hemopericardium, aortic regurgitation, and LV dysfunction (Fig. 6-15).

Congenital Heart Disease

Complex Congenital Cardiac Malformations

TISSUE DOPPLER AND STRAIN IMAGING

Conventional Doppler uses the sound reflection capabilities of blood cells to record flow velocities. For tissue velocities, some special adjustments are necessary in Doppler settings. Those adjustments are usually automatically set in commercially available machines, and they include the exclusion of high velocities and low intensity reflectors, such as the blood cells. Tissue velocities are much lower than blood flow (<30 cm/sec) and it is possible to use color flow mapping to translate different velocities patterns in the same image. The main limitation of tissue Doppler tracings is the fact that in some circumstances the accuracy is low due to the complex movement of the heart (translational movement) and tethering.

Two other contractility parameters can be derived from tissue velocities, used to correct those limitations. Strain (e) is the amount of shortening of a myocardial fiber and is expressed in percentage (%) and strain rate (ε) is the rate of change in length and is calculated as the difference between two velocities normalized to the distance between them, expressed as seconds−1 or s−1. Both parameters are expressed as negative numbers for the normal systolic shortening and positive for diastolic or stretching.

The last parameter obtained by tissue Doppler imaging is displacement, which is the distance a region of interest moves relative to its original location. It is calculated as an integration of tissue velocity in a given time.

Another method of obtaining strain and strain rate and even tissue velocities is to use 2D images, which has the advantage of angle independence, compared to Doppler-derived parameters. The 2D method uses the speckles to track the complex movements of the heart. Speckles are acoustic points or markers in the myocardial tissue produced by the ultrasound and they are used to track movement in a frame-by-frame manner to calculate shortening, stretching, and the complex heart motion such as twisting and rotation.

All these parameters have been used extensively to study global and regional contractility as well as diastolic function; rest and stress studies in coronary heart disease, and left ventricular dyssynchrony (Fig. 6-17).1013

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image FIGURE 6-17 Tissue velocities. A, isolated anterior wall with colored tissue Doppler image and a sample volume placed in the basal region of a normal patient showing a normal tissue velocity curve with systolic velocity (S′) of 5.9 cm/s and an early diastolic velocity (E′) of −8.6 cm/s. B, same image in an anterior myocardial infarction patient showing low values for S′ and E′ of 1.8 cm/s and 3.4 cm/s, respectively. Strain rate curves. C, isolated anterior wall image of a normal patient showing a normal strain rate curve with systolic strain rate (sSR) of 1.3 cm/s. D, same image of an anterior myocardial infarction patient with a sSR of −0.8 cm/s. Strain curve. E, strain image and curve of a normal patient showing a systolic strain (sS) of −27%. F, same image of an anterior myocardial infarction patient showing an sS of −4.1%. Tissue velocities in dyssynchrony analysis. G, apical four-chamber view with color tissue velocity image. The curves are used to measure the time from the onset of QRS in the electrocardiogram to the peak systolic velocity (time-to-peak) (dashed white vertical lines and white arrows) with the comparison between the interventricular septum and the lateral walls. The comparison is based on the difference between the two time-to-peak intervals in the two walls. In this case, the difference is 30 ms in a normal patient. H, same image in a heart failure patient, using the same parameters in the same wall regions with a difference in time-to-peak intervals of 60 ms. Bidimensional (2D) strain and strain rate. Apical four-chamber view used for strain (I) and strain rate curves (J) based on 2D method or speckle tracking. Note the difference in the point for the peak systolic strain curves for each wall (white arrows). A′, late diastolic velocity; E′, early diastolic velocity; S′, systolic velocity; sS, systolic strain; sSR, systolic strain rate; eSR, early diastolic strain rate; aSR, late diastolic strain rate; LV, left ventricle.

Pitfalls and Solutions

Pitfalls can be considered when the examiner is not experienced and not familiar with the correct technique, not only for the TTE but for the TEE as well. When a good acoustic quality window is possible, one of the major sources of pitfalls in both TTE and TEE is the blood flow study using Doppler. Taking aortic and mitral stenosis as examples, care must be taken with the source of the high velocity jet as being aortic or mitral regurgitation in origin and the angle between ultrasound beam and the jet. In the evaluation of mitral stenosis, a coexisting aortic regurgitation can lead to erroneous measurements of valve area and gradients based on Doppler interrogation.

All measurements made by 2D echocardiography and especially by Doppler can have some variability due to changes in stroke volume related to changes in blood pressure and heart rate, respiratory variation and, considering the examiner’s learning curve, an intra- and interobserver expected difference.

Transesophageal echocardiography has several pitfalls that must be considered during the analysis. Many anatomical structures that are not well seen in transthoracic echocardiography can be confused with masses, thrombus (such as pectinate muscles in atria and atrial appendages or surgical sutures of prosthetic valves, or other patch material); the thickened atrial septum in lipomatous hypertrophy can be misinterpreted as a mass such as myxoma; the eustachian valve, in the right atrium at the orifice of the inferior vena cava can appear as a mobile membrane or mass.14

The quality of studies of aortic dissection can be compromised due to the existence of artifacts produced by the lungs in the mid-descending aorta and linear artifacts can be confused with dissection flaps. Caution must always be taken when suspected images such as these are found and when the final quality of the images is compromised by air.14

All the pitfalls discussed here can be minimized by the use of several planes of view in the transthoracic echocardiography and the use of multiplane probes for the transesophageal echocardiography, and most importantly by the experience of the examiner.14

REFERENCES

1 Quiñones MA, Otto CM, Stoddard M, et al. Recommendations for quantification of Doppler echocardiography: A report from the Doppler quantification task force of the nomenclature and standards committee of the American Society of Echocardiography. J Am Soc Echocardiogr. 2002;15:167-184.

2 Lang RM, Bierig M, Devereux RB, et al. Recommendations for Chamber Quantification: A Report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, Developed in Conjunction with the European Association of Echocardiography, a Branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005;18:1440-1463.

3 Cerqueira MD, Weissman NJ, Dilsizian V, et al. Standardized Myocardial Segmentation and Nomenclature for Tomographic Imaging of the Heart: A Statement for Healthcare Professionals From the Cardiac Imaging Committee of the Council on Clinical Cardiology of the American Heart Association. Circulation. 2002;105:539-542.

4 Abhayaratna WP, Seward JB, Appleton CP, et al. Left Atrial Size: Physiologic Determinants and Clinical Applications. J Am Coll Cardiol. 2006;47:2357-2363.

5 Møller JE, Hillis GS, Oh JK, et al. Wall motion score index and ejection fraction for risk stratification after acute myocardial infarction. Am Heart J. 2006;151:419-425.

6 Møller JE, Søndergaard E, Poulsen SH, et al. Color M-mode and pulsed wave tissue Doppler echocardiography: powerful predictors of cardiac events after first myocardial infarction. J Am Soc Echocardiogr. 2001;14:757-763.

7 Tsuchihashi K, Ueshima K, Uchida T, et al. Transient left ventricular apical ballooning without coronary artery stenosis: a novel heart syndrome mimicking acute myocardial infarction. J Am Coll Cardiol. 2001;38:11-18.

8 Otto CM. Valvular Aortic Stenosis: Disease Severity and Timing of Intervention. J American Coll Cardiol. 2006;47:2141-2151.

9 Zoghbi WA, Enriquez-Sarano M, Foster E, et al. Recommendations for evaluation of the severity of native valvular regurgitation with two-dimensional and Doppler echocardiography. J Am Soc Echocardiogr. 2003;16:777-802.

10 Abraham TP, Belohlavek M, Thomson HL, et al. Time to onset of regional relaxation: feasibility, variability and utility of a novel index of regional myocardial function by strain rate imaging. J Am Coll Cardiol. 2002;39:1531-1537.

11 Yip G, Abraham T, Belohlavek M, Khandheria BK. Clinical applications of strain rate imaging. J Am Soc Echocardiogr. 2003;16:1334-1342.

12 Sutherland GR, Di Salvo G, Claus P, et al. Strain and strain rate imaging: a new clinical approach to quantifying regional myocardial function. J Am Soc Echocardiogr. 2004;17:788-802.

13 Yu CM, Zhang Q, Fung JW, et al. A novel tool to assess systolic asynchrony and identify responders of cardiac resynchronization therapy by tissue synchronization imaging. J Am Coll Cardiol. 2005;45:677-684.

14 Khandheria BK, Seward JB, Tajik AJ. Critical appraisal of transesophageal echocardiography: limitations and pitfalls. Crit Care Clin. 1996;12:235-251.

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