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Right-Heart Thrombus
Right-heart thrombi (RHT) can develop within the right heart (RH) or in the deep venous circulation and be seen in the RH
as thrombi in transit to the pulmonary vasculature. Risk factors for the development of an RHT can be divided into (1)
patient factors including age >65 years, male gender, obesity, smoking, trauma, recent surgery, immobility, pregnancy,
and hypercoagulable states; (2) disease-driven factors including cardiomyopathies, right-ventricular infarction, rightventricular contusion, AF, chronic obstructive lung disease, end-stage renal disease on hemodialysis, and inflammatory
bowel disease; (3) device-related factors including central venous catheter and pacemakers, among others; and (4) certain
drugs like oral contraceptives, amphotericin, and total parenteral nutrition [72].
TTE is the initial modality of choice for the evaluation of suspected RHT because of its widespread availability,
portability, low cost, and noninvasive nature (Fig. 7.9). However, TTE may yield false-negative results, particularly in
patients with congenital heart disease, previous cardiac surgery, and intracardiac devices. Inexperienced operators may also
incorrectly identify the crista terminalis, Eustachian valve, or Chiari network as right-atrial thrombi and the rightventricular moderator band as a right-ventricular thrombus [73]. TEE is more sensitive for the diagnosis of RHT, offering a sensitivity of approximately 97%, compared with 50%e60% for TTE [74] . The use of contrast provides a more
detailed assessment of a suspected RHT, further enhancing the sensitivity of both TTE and TEE. Currently available
echocardiographic contrast agents in the United States are Optison (General Electric Healthcare, Princeton, NJ, USA) and
Definity (Lantheus Imaging, North Billerica, MA, USA).
Other imaging modalities, including CCTA and CMRI, have also been used for the evaluation of suspected RHT.
These modalities provide higher sensitivity than TTE while avoiding the need for an invasive procedure like TEE. The use
of CCTA or CMRI has become particularly helpful in patients with suspicious lesions identified on TTE (Fig. 7.10). In
addition, CCTA offers the advantage of visualizing the pulmonary artery circulation during the same study. As such, it can
identify thrombi that have embolized to the pulmonary circulation.
Heart Valve Thrombus
Anatomical and functional abnormalities of the native heart valves can result in abnormal flow and subsequent risk of
thrombosis. The risk is further increased when a native heart valve has been replaced by a prosthetic valve. Heart valve
thrombosis may result in increased transvalvular gradients that can be nonobstructive (subclinical) or obstructive (clinical).
(A)
(C)
FIGURE 7.9 (A) Transthoracic echocardiogram revealing a central venous catheter projecting into the right atrium (black arrow) with an associated
pedunculated echodensity with acoustic properties similar to those of the myocardium (white arrow). (B) Contrast injection presents the pedunculated
mass as a filling defect separated from the myocardium (black arrow) confirming a catheter-associated right atrial thrombus. (C) Transthoracic echocardiogram demonstrating a right-heart thrombus in transit moving in and out of the tricuspid valve (arrows).
(B)

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(A)
(B)
(C) (D) (E) (F)
FIGURE 7.10 Still-frame images of a cardiac/coronary computed tomography angiography (CCTA) and cardiac magnetic resonance imaging (CMRI)
demonstrating a right-ventricular thrombus. (A) CCTA shows a mixed low-density and calcified thrombus (white arrow). (BeF) CMRI shows a lowsignal-intensity right-ventricular thrombus on cine images (white arrow on axial B, black arrow on coronal C, black arrow on short axis D), no
perfusion (black arrow on E), and no contrast enhancement (black arrow on F), all characteristic of thrombus. CCTA has an advantage over CMRI in
identifying calcification.
In addition, heart valve thrombosis carries the risk of systemic or pulmonary embolism depending on the valve affected.
The risk of heart valve thrombosis is closely related to the valve affected and the status of the valve (i.e., native, bioprosthetic, or metallic), with metallic prosthetic valves carrying the highest risk. While the number of prosthetic heart valve
replacements continues to increase worldwide and is expected to reach 850,000 per year by the year 2050, the use of
metallic prosthetic valves has decreased, comprising only 21% of the total prostheses used in 2006 according to one
registry [75,76]. In addit ion, the recent surge in transcatheter heart valve interventions, mainly transcatheter aortic valve
replacement (TAVR), has uncovered a new complication related to valve thrombosis known as hypoattenuated leaflet
thickening (HALT) [77]. HALT refers to a subclinical finding of aortic valve leaflet thickening frequently associated with
reduced leaflet motion noted on computed tomography and is thought to be an early marker for prosthetic valve thrombosis
[78e80].
The evaluation of a suspected heart valve thrombus begins with echocardiography. TTE offers the advantage of
informing about the anatomical and functional characteristics of the heart valves. However, small thrombi can be difficult
to assess or missed entirely. TEE offers a more precise assessment of the heart valve leaflets and can be used to further
assess valve compromise when clinical conditions allow. Nevertheless, evaluation with TEE can be hindered by prosthesisrelated shadowing [81,82]. Advanced imaging modalities, including CCTA and CMRI, can be used when TTE is negative
or equivocal, clinical suspicion remains high, there is need for further evaluation of the thrombus characteristics, or an
invasive test like TEE is contraindicated (Fig. 7.11). The modality used is dictated by the type of valve being studied and
other patient characteristics. CCTA has the relative advantage of higher spatial resolution, while CMRI has higher temporal
resolution, although still lower than for echocardiography. Computed tomography has been studied for the routine evaluation to detect subclinical thrombosis in patients following TAVR [77e79].

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(A) (B)
FIGURE 7.11 Still-frame images of a cardiac/coronary computed tomography angiography (CCTA) performed in a patient with a mechanical mitral
valve and suspected valve thrombosis after a transthoracic echocardiogram revealed abnormally elevated gradients across the prosthetic mitral valve.
(A) CCTA performed in systole reveals a 1-cm hypodensity (black arrow) abutting the atrial side of the fixed posterior mitral valve leaflet, confirming a
prosthetic valve thrombus. (B) CCTA performed in diastole demonstrates the prosthetic valve thrombus (black arrow) leading to fixation of the posterior
leaflet in the closed position (white arrow).
In conclusion, while echocardiography remains the cornerstone in the initial evaluation, advances in technology and
increased availability have made multidetector computed tomography and magnetic resonance integral modalities in the
evaluation of a suspected intracardiac thrombus. CCTA and CMRI should be used as complementary technologies to assist
the clinician in the evaluation of a patient with a suspected intracardiac thrombus.
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Chapter 8
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Utilization of Magnetic Resonance
Imaging and Magnetic Resonance
Angiography for Cardiac Thrombus
Rhoda B. Brosnan
University of North Carolina Asheville School of Medicine, Asheville, NC, United States
INTRODUCTION
Accurate detection of cardiac thrombi is clinically important because of their association with stroke and systemic embolism. Approximately 14%e30% of ischemic strokes are cardioembolic in origin [1]. Hospital mortality, persistent
disability in survivors, and recurrence are high. Early recognition of conditions that predispose to cardiac thrombi or
visualization of the thrombus provides the rationale for treatment with anticoagulation. The most frequent cardioembolic
conditions are atrial fibrillation and cardiomyopathy. Cardiac magnetic resonance imaging (CMRI) is now the preferred
imaging modality for assessment of ventricular thrombus presence, size, and location [2]. CMRI with magnetic resonance
angiography (MRA) is being investigated for its utility in assessing left atrial and left atrial appendage thrombus in the
setting of atrial fibrillation.
TECHNIQUE AND IMAGE ACQUISITION
CMRI is a noninvasive imaging modality capable of providing high-resolution anatomic and functional cardiac images in
multiple traditional and unique planes. Unlike other cardiac imaging modalities, CMRI provides information on tissue
characterization. To simplify, MRI exposes the heart to a strong magnetic field, in most cases 1.5 T [3]. The heart, like all
human tissues, contains water. The hydrogen protons in the nuclei of water become polarized in the direction of the
magnetic field. Smaller spatially selected gradients are applied for localization. Within the slice, a selective radio-frequency
pulse is applied that tips the magnetization of the hydrogen nuclei, which then slowly “relax” back to equilibrium in the
field. As the protons relax they admit a radio-frequency pulse, which when captured produces an image. Depending on the
gradients and radio-frequency pulses applied, different types of images can be produced. These may be static or moving
with a black blood pool (signal from blood in the image is suppressed and appears dark) or a white blood pool (signal from
blood in the image is enhanced and appears bright). Tissue characteristics are determined by their variable hydrogen
content and relaxation times [3].
A standard study begins with a stack of static axial, coronal, and sagittal images to assess anatomy and morphology.
Cine images follow in traditional two-chamber, three-chamber, and four-chamber long-axis views to qualitatively assess
ventricular and valvular function. A stack of short-axis cine views is obtained t o quantify right- and left-ventricular
function. Gado liniu m contrast is given to assess first-pass perfusion and to obtain delayed enhancement imaging.
Gadolinium is a paramagnetic agent that shortens the relaxation times of blood and tissue and creates increased signal.
As it is injected, images are acquired as it passes through the cardiac c hamb ers and then quic kly perfuses the
myocardium. After approximately 10 min a scout image is obtained to assess the myocardium at various relaxation times
to determine the inversion time (TI) at which the normal myocardial si gnal is “nulled” or black. Delayed enhancement
imaging is then performed. Myocardial delayed enhancement sequences are perhaps the most important images routinely
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FIGURE 8.1 Mechanism of action for contrast uptake
after myocardial injury [4].
obtained and put MRI at the forefront for assessing the changes characteristic of distinct diseases that cause
cardiomyopathy.
Gadolinium chelates are extracellular contrast agents that cannot cross healthy myocyte membranes. In normally
perfused myocardium there is very little extracellular space and gadolinium simply passes through that space. In the setting
of myocardial damage from infarction, extracellular space is increased in proportion to the amount of scar produced and
gadolinium will enhance the scarred area [4]. Gadolinium also highlights areas of scar secondary to inflammation in
characteristic patterns that help distinguish causes of nonischemic cardiomyopathy, such as myocarditis or sarcoidosis. In
the setting of an infiltrative cardiomyopathy such as amyloid, extracellular space is globally expanded and gadolinium
enhancement is diffuse. In the case of infarct specifically it is well accepted that the distribution and transmural extent of
abnormal delayed enhancement predict viability [5] (Fig. 8.1).
CARDIOMYOPATHY AND LEFT-VENTRICULAR THROMBUS
Cardiomyopathy is a prerequisite for left-ventricular thrombus formation. It provides a milieu, including endothelial injury,
blood stasis, and hypercoagulability, that fulfills Virchow’s triad. As the use of CMRI has increased for evaluation of
cardiomyopathy, its utility in identifying associated left-ventricular thrombus is now well recognized. Left-ventricular
thrombus can be small or large, protuberant or mural. Transthoracic echocardiography with or without contrast identifies thrombus based on its anatomic appearance and therefore is best at detecting larger protuberant thrombi (Picture 1).
PICTURE 1 Large apical thrombus on transthoracic
echo.

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During the course of a conventional CMRI study many thrombi are identified on cine imaging, but like echo, these
images can miss small, mural thrombi. Delayed enhancement CMRI adds the component of tissue characterization that is
necessary to detect small and, particularly, mural thrombi. Weinsaft et al. reported an echo sensitivity of 33% in routine
studies not necessarily performed specifically to evaluate for thrombus. Sensitivity was as high as 60% in their study when
the echo was specifically ordered to assess for thrombus, particularly when contrast was used [6]. Cine MRI sensitivity was
similar at 58%. In that study delayed enhancement CMRI was able to visualize thrombi not detected by echo or cine
images and show that some suspected thrombi were not present. Delayed enhancement CMRI was pathologically validated
by Sirachi et al. in 160 patients undergoing left-ventricular reconstruction surgery. They reported that CMRI yielded a
greater than threefold higher diagnostic accuracy compared with transthoracic echo (87% vs. 27%) [7]. Improved accuracy
was predominantly due to increased sensitivity for CMRI versus echo (88% vs. 23%). These sensitivities are summarized
in Fig. 8.2 by Delewi et al. [2] (Fig. 8.2).
The increased detection of ventricular thrombus by delayed enhancement CMRI is clinically relevant. In an earlier
study by Weinsaft et al. 709 patients who underwent CMRI were followed for 6 months [8]. Patients with thrombus on
delayed enhancement CMRI had a sevenfold difference in study end points, including transient ischemic attack (TIA),
cerebral vascular accident (CVA), or pathologically verified thrombus, compared with those without identified thrombus
(15.1% vs. 2.1%).
The type and nature of the cardiomyopathy identified at the time of the CMRI are important because it provides the
basis for an underlying substrate that predisposes to clot formation. In the setting of coronary artery disease, left-ventricular
thrombi adhere to the zone of infarcted myocardium. In autopsy studies of p atients with fatal myocardial infarction prior to
the advent of aggressive anticoagulation and revascularization, 10% of patients had evidence of thrombus on day 1, 60%
by day 7, and 90% by 1 month [9]. The incidence of cardiac thrombus reported from autopsy studies in dilated cardiomyopathy was 49%, most of which occurred in the left ventricle. The overall incidence of cardiac thrombus in the modern
era of treatment for infarct and cardiomyop athy is clearly much lower. However, the observation that thrombi are more
likely to occur in ischemic cardiomyopathy than in nonischemic cardiomyopathy holds true. In a study by Weinsaft et al.,
784 consecutive patients with systolic dysfunction undergoing CMRI for evaluation of viability, in the case of ischemic
cardiomyopathy, and characteristic scar patterns to identify type of nonischemic cardiomyopathy were reviewed [8].
Thrombus was identified in 7% of patients with delayed enhancement CMRI. Of those, 80% were in the apex. In the study,
patients with thrombus were more likely to have an underlying ischemic cardiomyopathy (9.2% vs. 1.7%, P ¼ .0002)
despite a similar mean ejection fraction consistent with historical data. The likelihood of thrombus increased with an
ejection fraction less than or equal to 30%, and was as high as 14% in ischemic cardiomyopathy with a left-ventricular
ejection fraction less than or equal to 30%, and 3% in nonischemic cardiomyopathy with a left-ventricular ejection
fraction less than or equal to 30%. Scar size and prevalence were markedly higher in those with thrombus versus those
FIGURE 8.2 Sensitivities and specificities of various diagnostic modalities for the detection of left-ventricular thrombus formation. CMRI, cardiac
magnetic resonance imaging; CT, computed tomography; DE, delayed enhancement; LV, left ventricular; TOE, transesophageal echocardiography; TTE,
transthoracic echocardiography.
Sensitivity Specificity
%09%53EOT
Routine clinical TTE 35–40% 90%
TTE (indication suspect LV thrombus) 60% 90%
ETThtiwelbarapmoCTC
%09%06CMRIeniC
%99%88CMRI-ED

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without. In patients specifically with acute myocardial infarction, the presence of left-ventricular thrombus on CMRI was
independently associated with infarct size and anterior location [10].
CARDIAC MAGNETIC RESONANCE CHARACTERISTICS OF THROMBUS
Thrombus has a unique appearance on CMRI. In addition to identifying throm bi with a high sensitivity, CMRI helps
distinguish thrombi from other masses. This is generally more important in the rare circumstance when the thrombus in
question is in an unusual location, such as the right atrium or right ventricle. In the left ventricle, as described previously,
thrombus is typically located in areas of wall motion abnormality and adjace nt to scar. Unlike some tumors, thrombi are
noninvasive. In general, thrombi exhibit a homogeneous appearance and are relatively small 1.6e2.9 cm
thrombus is avascular, it does not enhance on first-pass perfusion and does not take up gadolinium. On delayed
enhancement imaging thrombus characteristically appears isointense or hyperintense at TIs less than 250 ms. Thrombi are
commonly dark gray with a black border at TIs of 250e350 ms (when the myocardium is nulled), giving them an “Etch-aSketch” appearance [6]. This is speculated to be due to different layers within the thrombus, with fresher thrombi in the
periphery. Thrombus is characteristically hypointense, or black, at long TIs of 500e600 ms, whereas myocardium appears
gray. This typical TI pattern was present in 94% of thrombi imaged in a study by Pazos Lopez et al. and had an accuracy
for differentiating thrombus from tumor of 95% [11]. On serial studies thrombus, unlike tumor, will shrink or resolve with
chronic anticoagulation. These characteristics are demonstrated in the following cases (Cases AeD).
All tissues have an inherent T1 longitudinal relaxation time based on their water, protein, fat, and iron contents. T2
relaxation time specifically reflects the water content of tissue. T1 and T2 mapping sequences are now available that can
accurately quantify T1 and T2 times for myocardial tissue. T1 and T2 times pre- and postcontrast for myocardium are
characteristically affected by disease processes that increase edema and fibrosis [12]. Investigators are looking into
comparisons of the T1 and T2 times of myocardium with those of tumors and thrombus to see if differences can be used to
help distinguish them. Because thrombi are avascular, TI times are long and similar to those of unperfused myocardium
(1000 ms). T2 is longer for thrombus than myocardium (74 ms vs. 51 ms, P < .0001). Most masses have higher T1 and T2
times compared with thrombus or myocardium [13].
In addition, thrombus in the setting of acute myocardial infarction has to be distinguished from microvascular
obstruction or no reflow. On delayed enhancement imaging microvascular obstructi on in acutely infarcted myocardium
appears white with a central black, necrotic or avascular, core. When this occurs the rim of hyperenhanced tissue is thin and
it can be hard to distinguish from a small mural thrombus (Picture 2). Typically, additional delayed enhancement images
over time can show the gradual enhancement of a new reflow zone as contrast seeps into the necrotic core. Thrombus size
remains unchanged [8].
2
[11]. Because
CASE A Ischemic cardiomyopathy
in a patient with an out-of-hospital
anterior myocardial infarction and a
large associated apical thrombus,
with typical appearance of the
myocardium and thrombus with
variable TI. TI, inversion time.
Four-chamber view with TI 300 ms
Four-chamber view TI 600 ms
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