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* From the Department of Cardiology, Ochsner Clinic Foundation, New Orleans, LA.
Correspondence to: Richard V. Milani, MD, Vice Chairman, Director, Echocardiography Laboratories, Department of Cardiology, Ochsner Clinic Foundation, 1514 Jefferson Hwy, New Orleans, LA 70121; e-mail: rmilani{at}ochsner.org
| Abstract |
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Key Words: infective endocarditis patent foramen ovale prosthetic heart valves transesophageal echocardiography
| Introduction |
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| Indications for TEE |
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Endocarditis
Several studies have demonstrated the role of TEE in the detection of native and prosthetic valve vegetation due to IE. The sensitivity of TEE for vegetation on native valves in patients with IE is 90 to 100%, compared to 60% for TTE.2
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In patients with prosthetic valve IE, TEE has become an essential diagnostic tool in situations in which the sensitivity of TTE is a mere 36% compared to 85% for TEE.5
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As a result, it appears justified to begin with TEE rather than TTE in the workup of patients with suspected prosthetic valve IE. TTE can be a useful screening tool for native valve IE but should be followed by TEE if the findings are nondiagnostic.
The specificity of echocardiography for the presence of native valve IE may be lowered by erroneous diagnosis attributable to lesions that resemble vegetation such as Lambl excrescences, valvular fibrin strands, ruptured or redundant chordae, nonspecific valvular thickening, or calcification. Distinguishing a vegetation from other types of masses seen by echocardiography requires knowledge of its most and least likely echocardiographic characteristics, which are influenced by echogenicity, shape, location, and mobility.4 7
Factors that influence the sensitivity and specificity of echocardiography for detecting native valve IE also impact prosthetic valve IE. Moreover, acoustic shadowing from prosthetic material, which can obscure lesions distal to the prosthesis, can lower the sensitivity of echocardiography in the diagnosis of IE. Thus, the sensitivities for detecting prosthetic valve IE vs native valve IE are lower with TTE (35% vs 60%, respectively) compared to TEE (85% vs 95%, respectively).2 5 6 8 The specificities, however, of echocardiography for prosthetic valve IE and native valve IE are similar. False-positive findings, however, may occur from the erroneous interpretation of artifactual phantoms, sewing ring suture, surgically severed or retained chordae tendinae, fibrin strands, or periprosthetic material.9
TEE is a crucial diagnostic aide in the detection of structural complications from IE such as myocardial abscesses, fistulas, mycotic aneurysms, valvular aneurysms or perforations, flail leaflets, or prosthetic valve dehiscences. These serious complications are harbingers of significant morbidity and mortality, and may warrant urgent surgical intervention.10 11 12 Several of the following echocardiographic findings demand that surgical intervention be strongly considered: ring abscess or fistula; severe valvular regurgitation, particularly if the mitral valve is involved and can be repaired; and mechanical prosthetic valve IE (eradication of infection with antibiotic therapy alone is difficult).
Perivalvular abscess occurs more commonly with prosthetic valve IE compared to native valve IE. Myocardial abscess are found more frequently in the periaortic valvular region compared to other perivalvular areas, and they appear on echocardiograms as an echolucent region within the myocardium or fibrosa.10 11 12 TEE in combination with clinical variables can be utilized to predict adverse outcomes in patients with IE.10
Prosthetic Valves
TEE is used routinely to evaluate prosthetic valves, both at the time of implantation as well as for the later development of complications. Prosthetic valves are classified either as biological (ie, tissue) or mechanical. Biological valves are subsequently subdivided into homografts (ie, allografts) or heterografts (ie, xenografts). Mechanical heart valves are subdivided into ball-in-cage, single-tilting disk, or double-tilting disk types. Annular rings are classified as mechanical valves, although, technically, they are not prosthetic heart valves.
Homograft valves are aortic and pulmonary valves that are harvested from human cadavers. Valves are either stented or free sewn (ie, unstented). When implanted into the aortic position, the valve may not be stented. These unstented homografts in the aortic position may be difficult to distinguish from native aortic valves. The only evidence of an unstented homograft may be an increase in the echodensity and thickness of the aortic annulus as a result of the sutures. Stented homografts have echo appearances and flow characteristics similar to those of a porcine xenograft bioprosthesis.
Heterografts generally are made up of three leaflets, and, typically, they are porcine valves or made of bovine pericardium. A stent usually arises from each of the three commissures of the valve.
Ball-in-cage valves, when in the open position, have blood flow across the sewing ring and around the ball occluder on all sides. When the valve is closed, a small amount of regurgitation occurs around the ball.
A single-tilting disk valve generally will have two orifices, one larger than the other, within a symmetric flow profile. The bileaflet tilting disk valve, when open, will have two large valve orifices with a small narrow central orifice. Flow through the central orifice will result in relatively high velocities with localized gradients often higher than the overall gradient across the entire valve (vena contracta). Common complications resulting from the use of a mechanical prosthesis are listed in Table 1 .
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A complete TEE should examine the myocardium in all three coronary distributions. In this setting, the transgastric short-axis images are particularly valuable since they tend to avoid the foreshortening of the apex that is inherent in images obtained from the esophageal window.
Hypovolemia is not an uncommon cause of hypotension in the early postoperative setting, in which the pulmonary capillary wedge pressure may provide misleading data due to changes in LV compliance resulting from cardiopulmonary bypass. In this setting, TEE images reveal reduced cavity size and hyperdynamic systolic function, thereby requiring fluid resuscitation.15
As a compensatory mechanism, patients with aortic stenosis develop concentric LV hypertrophy in order to normalize wall stress. Marked concentric LV hypertrophy in this setting can present difficulties for the surgeon during AVR. The sudden reduction in afterload, coupled with anemia, hypovolemia, and high catecholamine tone, leads to enhanced systolic function and an extremely small end-systolic volume. Moreover, tachycardia resulting from the high catecholamine state and the use of positive chronotropic agents may prevent adequate LV filling. These changes can result in severe hypotension, either in the operating room or in the early postoperative period (ie, days 1 to 3).16 This is more likely to occur in elderly patients (> 15%) undergoing AVR and is associated with as much as a threefold increase in mortality.17 Doppler gradients often vary with loading conditions and correlate well with invasively determined gradients. Therapy is best guided by TEE, and includes fluid administration, withdrawal of therapy with inotropic agents, and therapy with beta-blockers to slow the heart rate.16 17 18
TEE has become an integral part in the evaluation of patients for mitral valve repair. Data have increased the enthusiasm for earlier valve repair for mitral regurgitation (MR) caused by myxomatous degeneration of the mitral valve.19 20 A quality echocardiographic examination of the mitral valve apparatus is necessary to determine the anatomic pathology of the mitral apparatus as well as the abnormal flow characteristics across it. Knowledge of the anatomic structure aids the surgeon in deciding which of the following surgical procedures to perform: chordal shortening; chordal transfer; placement of artificial (Gore-Tex; WL Gore; Sunnyvale, CA) chords; posterior leaflet quadrangular resection; posterior leaflet-sliding technique; posterior leaflet and chordal transposition to the anterior leaflet; anterior leaflet resection; and placement of an annular ring.
A thorough anatomic examination of the mitral apparatus via multiplane TEE, delineating where the pathology is and what type of pathology is being detected, becomes a necessity. During the TEE examination, the relationship of chordal attachments between the papillary muscle and the leaflet should be noted and used to define the anatomic location of the leaflets visualized.21 The mitral leaflet section can be defined by visualizing a papillary/chordal attachment to a leaflet. Using multiplane views, the leaflet surface anatomy can be defined.22 Based on data from Grewal et al,23 67% of myxomatous pathology of the posterior leaflet involved the middle scallop (P2). The frequency of successful repair when the pathology involves the middle scallop is approximately 70%. Therefore, it is important that the echocardiographer be familiar with this subset of myxomatous mitral valve pathologies.
The mitral annulus is the transition area where the LA, mitral valve leaflets, and LV come together. The mitral leaflets form a membranous curtain attaching to the mitral annulus. The anterior circumferential portion of the mitral annulus that is associated with the left trigone, intertrigonal space, and the right trigone remains constant during the cardiac cycle and is not prone to dilatation because of its rigid structure.15 22 23 This area is the attachment point of the anterior leaflet of the mitral valve. Its margins are defined surgically by two dimples that are raised at the border of the right and left trigone when lifting the anterior leaflet.
The annulus fibrosus of the mitral annulus becomes thinner and more poorly defined as it extends posteriorly from the left and right trigones. This portion of the annulus is poorly supported and is prone to dilatation in pathologic states.20 21 22 23 The posterior leaflet of the mitral valve attaches to this portion of the annulus, explaining why the posterior leaflet accounts for 70% of native mitral regurgitant defects, with P2 accounting for 32% of all native defects. Dilatation of the annular attachment of the posterior leaflet creates increased tension on the middle scallop of the posterior leaflet, explaining the 60% occurrence of chordal tears at P2. Table 3 lists intraoperative complications during mitral valve repair, which can be detected by intraoperative TEE, and their appropriate management.
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Several TEE features have been associated with thromboembolism in patients with nonvalvular AF, including LA/LAA thrombus, LA/LAA spontaneous echo contrast (or "echo smoke"), reduced LAA flow velocity by pulsed-Doppler evaluation, and aortic atheromatous abnormalities.29 30 The Assessment of Cardioversion Using Transesophageal Echocardiography trial demonstrated that a TEE-guided cardioversion strategy produces a similar rate of stroke (ie, < 1%) as that for the more traditional method of anticoagulation therapy for 3 weeks prior to the performance of elective direct current cardioversion.31 As such, a negative TEE can replace moderate-term anticoagulation in patients with recent onset AF prior to direct current cardioversion.
A common part of the evaluation for cryptogenic stroke is the elucidation of a possible PFO, for which TEE is currently considered to be the reference standard for its detection. To this end, a femoral injection of agitated saline solution contrast medium combined with a Valsalva maneuver has been shown to be the most sensitive method for identifying a PFO, as the inferior vena cava flow is directed preferentially toward the interatrial septum (IAS) and foramen ovale.32 Conversely, the crista interveniens directs the superior vena cava flow away from the IAS, significantly reducing the sensitivity of an arm injection of contrast medium. A reduced degree of sedation may be necessary for this type of patient as cooperation is fundamental for the performance of a Valsalva maneuver.
Several studies have further quantitated the PFO diameter by the degree of TEE contrast intensity seen in the LA, specifically, the maximum number of microbubbles visualized in the LA within three cardiac cycles after contrast filling of the right atrium was determined. Grade 1 was defined as 1 to 5 bubbles, grade 2 was defined as 6 to 25 bubbles, and grade 3 was defined as > 25 bubbles. This grading system provided an excellent correlation of contrast intensity to PFO diameter.33
Shunt size has been found to correlate with the incidence of future ischemic neurologic events. Large shunts (ie, > 20 microbubbles) have been found to correlate with a high rate (31%) of subsequent embolic events, including transient ischemic attack and stroke, despite the use of antiplatelet or anticoagulant therapy.32
In contrast, small shunts (ie,
3 but < 20 microbubbles) respond well to medical therapy, with a reported 0% rate of subsequent neurologic events.
During the TEE examination for PFO, it is necessary to evaluate for the presence of ASA as well as a Chiari network because these conditions are associated with a significant number of PFOs. M-mode TEE of the IAS helps to facilitate the measurement of the septal excursion, where an excursion of
15 mm yields the diagnosis of ASA.34
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Aorta
Another value of TEE in the evaluation of cryptogenic stroke is the assessment of atheromatous disease of the aorta. Several studies have evaluated the role of various imaging techniques in the diagnosis of atheromatous aortic disease. Aortography provides only an inexact view of the aortic lumen, without clear identification of the endothelial surface. CT scanning and MRI can provide an enhanced evaluation; however, the imaging is not performed in real time. TEE is ideally suited to providing high-resolution real-time imaging, which also provides atherosclerotic plaque morphology and mobility, as well as the dynamic effect of flow. Various authors36
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have reported significant aortic atheroma in up to 50 to 60% of patients with unexplained stroke. Stroke risk is highest, however, with the identification of large (ie, > 4 to 5 mm), mobile, and ulcerated plaques.36
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Investigators have used various grading systems for aortic atheroma, and, to date, no single unified system has been widely accepted. All systems agree, however, that the highest risk patients are those with mobile plaques, ulcerated plaques, and plaques that protrude into the aorta by > 4 to 5 mm. As such, these plaque characteristics should be specifically reported in any patient undergoing TEE. We have chosen the following system to grade atheromatous disease of the aorta identified by TEE: grade 1, minimal intimal thickening; grade 2, extensive intimal thickening; grade 3, sessile atheroma of < 4 mm; grade 4, protruding atheroma of
4 mm; and grade 5, mobile or ulcerated atheroma.
Lesions of grade 4 and 5 lesions carry a risk of peripheral embolization that is almost fourfold more than that with grade 1 lesions. Moreover, in patients undergoing coronary artery bypass grafting, these high-grade lesions have been associated with an incidence of stroke approaching 25% and an early mortality rate of 15%,38
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where grade 3 suggested a PFO diameter of
10 mm and grade 1 suggested a PFO diameter of
2 mm.
Aortic dissection is another condition in which the improved image resolution and Doppler sensitivity of TEE are particularly suited to rapid diagnosis. In addition to the previous "gold standard" of aortography for the diagnosis of dissection, TTE, TEE, CT scanning, and MRI have defined roles in the diagnosis of dissection. Although each of these modalities has certain advantages and limitations, the accuracy, speed, relatively low cost, portability, and capability to comprehensively evaluate the heart, aorta, and its branches for complications of dissection have made TEE an attractive first choice for the evaluation of suspected aortic dissection in both the emergency department and in critical care settings.38 44
Aortic dissection is a catastrophic condition with a high mortality rate resulting from an accumulation of blood that dissects the media from the intima and adventitia. Approximately 96% of dissections are associated with an intimal flap.38 44 Approximately 70% of intimal tears occur in the ascending aorta, usually 1 to 3 cm above the right or left aortic sinus. In the remaining 30%, the tear is distal to the origin of the left subclavian artery, at the ligamentum arteriosum. The pathognomonic echocardiographic appearance of dissection is an undulating linear density (ie, an intimal flap) within the aortic lumen separating a true and false channel, which has different Doppler color flow patterns. Aortic dissection should be suspected whenever the normal appearance of the aortic wall consisting of a single dominant echo is replaced by two separate echoes, with one echo presumably representing the intima plus the inner media, and the second echo representing the outer media and adventitia.
Most classifications systems of aortic dissection are based on the location of the intimal tear. The most widely used DeBakey classification recognizes the following three types: types I and II originate in the ascending aorta, with type I extending beyond the aortic arch and type II confined to the ascending aorta; and type III originates in the descending thoracic aorta and extends distally.38 44
The Daily classification delineates two types of dissection. Type A involves the ascending aorta, regardless of the location of the intimal tear, and requires emergency surgery. Type B occurs distal to the origin of the subclavian artery, sparing the ascending aorta, and can be treated medically. Prompt diagnosis and accurate anatomic assessment are critical in guiding therapy.38 45
Penetrating aortic ulcers (PAUs) occur when an ulceration of an atherosclerotic plaque erodes through the internal elastic lamina into the aortic wall media. This process may progress to life-threatening clinical sequelae such as transmural aortic rupture, intramural hematoma, saccular, fusiform, or false aneurysms of the thoracic aorta, or typical dissection.38 44 PAUs are predominantly located in the descending aorta, where atherosclerosis tends to be more severe. Patients are often elderly, have hypertension and diffuse systemic atherosclerosis, and present with a sudden onset of chest or back pain. The echocardiographic features of PAUs are a crater-like out-pouching of the aorta with jagged edges associated with complex atheromatous plaque.
Aortic intramural hematoma (AIH) is a localized separation of the layers of the aortic wall by partially or totally clotted blood in the absence of an intimal tear, presumably caused by rupture of the vaso vasorum in the media.38
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An AIH is generally identified on TEE as an homogeneous mottled thickening of the aortic wall and an inward displacement of intimal calcification. The more formal echocardiographic criteria for the diagnosis of AIH are a
7 mm crescent or circular thickening of the aortic wall extending 1 to 20 cm longitudinally along the thoracic aorta, with no evidence of Doppler flow in the thickened aortic wall, and the absence of an intimal laceration or flap.
Balloon Mitral Valvuloplasty
Another less common indication for TEE is the evaluation of the patient prior to possible balloon mitral valvuloplasty (BMV). The TEE must include a thorough assessment of the LA and LAA for evidence of clots, as well as the quantification of MR, since the presence of either a clot or > 2+ MR is a relative contraindication for BMV. The mitral valve itself should be carefully evaluated for mobility, thickening, and calcification. Together with a characterization of the subvalvular apparatus, the mitral valve-echo scoring system is used to determine a patients suitability for BMV.46
An echo score of < 8 suggests a stenotic mitral valve that is ideally suited for BMV, with a high margin of success. A higher score, however, does not completely preclude a BMV, and valvuloplasty would then depend on the presence and degree of commissural fusion.
| Patient Preparation |
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It is also important to obtain a history of the usage of alcohol, sedative and hypnotic agents, and tranquilizers, and of recreational drug use, as this may affect the dosing of medications during conscious sedation.
Informed consent should be obtained from the patient, or when incapacitated, from their next of kin. IV access to the patient is established, and drug allergies and patient medications are recorded. If an evaluation for possible PFO is intended (ie, to rule out a cardiac source for emboli), then a femoral venous catheter is placed immediately before the procedure.
| Esophageal Intubation |
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The TEE transducer should be inspected for defects and cracks in the waterproof covering before insertion. The mouth should be examined for preexisting injuries and loose teeth. The TEE probe is introduced with the patient in the left lateral decubitus position with gentle flexion of the neck to facilitate entry into the esophagus. The endoscope is always inserted with the transducer facing anteriorly, guided by the index finger of the left hand. With the tip of the probe at the esophageal inlet, the patient is requested to swallow, which assists in directing the probe into the upper esophagus. The probe can be advanced unless one meets resistance, which would require readjustment of the probe centrally or removal. Once in the esophagus, the transducer should never be forced through a resistance. The tip of the transducer should be allowed to return to the neutral position before advancing or withdrawing the probe, and excessive force should never be applied when moving the transducer in the esophagus or flexing the tip with the control wheels.
Many patients will gag until the probe is advanced beyond the carina of the trachea or > 25 cm from the incisors. Thus, a smooth and rapid initial advancement to this point is essential. Once the probe is in the esophagus, most patients become more comfortable and will accept the remainder of the examination.
| Standard Transesophageal Views and Technique |
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| Conclusion |
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| Footnotes |
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Received for publication September 30, 2002. Accepted for publication January 22, 2003.
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