Abstract
Transesophageal echocardiography continues to have a central role in the diagnosis of infective endocarditis and its sequelae. Recent technological advances offer the option of 3-dimensional imaging in the evaluation of patients with infective endocarditis. We present an illustrative case and review the literature regarding the potential advantages and limitations of 3-dimensional transesophageal echocardiography in the diagnosis of complicated infective endocarditis.
A 51-year-old man, an intravenous drug user who had undergone bioprosthetic aortic valve replacement 5 months earlier, presented with prosthetic valve endocarditis. Preoperative transesophageal echocardiography with 3D rendition revealed a large abscess involving the mitral aortic intervalvular fibrosa, together with a mycotic aneurysm that had ruptured into the left atrium, resulting in a left ventricle-to-left atrium fistula. Three-dimensional transesophageal echocardiography enabled superior preoperative anatomic delineation and surgical planning. We conclude that 3-dimensional transesophageal echocardiography can be a useful adjunct to traditional 2-dimensional transesophageal echocardiography as a tool in the diagnosis of infective endocarditis.
Keywords: Abscess/ultrasonography; echocardiography, transesophageal; echocardiography, three-dimensional/methods; endocarditis, bacterial/complications/diagnosis/therapy/ultrasonography; image enhancement/methods; imaging, three-dimensional/methods
Transesophageal echocardiography (TEE) plays a key role in diagnosing infective endocarditis (IE), in identifying its sequelae, and in guiding its management. Recent technologic advances offer the option of 3-dimensional (3D) imaging in the evaluation of IE patients. We present an illustrative case wherein 3D TEE provided accurate evaluation of IE sequelae before surgery, and we review the usefulness of 3D TEE in the management of IE.
Case Report
A 51-year-old man presented with fever and dyspnea. He had a history of intravenous drug use and of Corynebacterium endocarditis that had affected his native bicuspid aortic valve (replaced, 5 months earlier, with a bioprosthesis). His vital signs were normal; auscultation revealed a widely radiating grade 3/6 pansystolic apical murmur. The patient's comorbidities included type 1 diabetes mellitus, hepatitis C, dyslipidemia, hypertension, and bipolar disorder. Preoperative TEE with 3D rendition revealed a large abscess involving the mitral aortic intervalvular fibrosa, together with a mycotic aneurysm that had ruptured into the left atrium, resulting in a left ventricle-to-left atrium fistula (Fig. 1 and Figs. 2A–C). Blood cultures grew Haemophilus parainfluenzae. In addition, the patient had sustained multifocal acute and subacute small-vessel cerebral infarcts secondary to septic emboli. He proceeded to surgery, where the TEE findings were confirmed intraoperatively (Figs. 2D and E). He underwent concomitant valve replacement: the mitral valve with a 29-mm Hancock® porcine tissue valve (Medtronic, Inc.; Minneapolis, Minn) and the aortic valve with a 27-mm Carpentier-Edwards Perimount pericardial tissue valve (Edwards Lifesciences Corporation; Irvine, Calif). He also underwent reconstruction of the left ventricular outflow tract and intervalvular fibrosa by means of bovine pericardial patches. A postoperative transthoracic echocardiogram revealed satisfactory prosthetic valve function. The patient was discharged to the referring medical center on postoperative day 9. He received a 6-week course of intravenous antibiotics (ceftriaxone and vancomycin), followed by chronic suppression with oral amoxicillin.
Fig. 1.

Transesophageal echocardiograms show prosthetic aortic valve endocarditis with native mitral valve involvement A) from the surgeon's view (left atrial perspective) of the mitral valve (note prominent mycotic aneurysm of the intervalvular fibrosa), and B) from the opening of the mycotic aneurysm above the mitral valve (arrowheads). ©2015 Mayo Foundation for Medical Education and Research. All rights reserved.
AML = anterior mitral leaflet
Fig. 2.

Transesophageal echocardiograms in our patient reveal prosthetic aortic valve endocarditis: A) a large periprosthetic aortic valve vegetation/abscess, B) the destruction of the aorto-mitral intervalvular fibrosa, abscess of the aortic root, and C) the resultant left ventricle–left atrium (LV–LA) fistula. Intraoperative images depict the D) abscess and E) fistula. ©2015 Mayo Foundation for Medical Education and Research. All rights reserved.
AML = anterior mitral leaflet; Ao = aorta; AV = aortic valve
Discussion
In 1994, Durack and colleagues1 proposed for the diagnosis of infective endocarditis the addition of 1 to 3 major criteria—vegetation, abscess formation, or new prosthetic valve dehiscence—all of which include echocardiographic features as a major component. Currently, the European Association of Echocardiography2 recommends that transthoracic echocardiography be used first, because of its noninvasive nature. However, TEE remains the gold-standard investigative tool and is to be applied in most suspected cases of IE.2 Echocardiography is valuable in identifying patients who are likely to fail medical therapy, and who therefore will need surgical intervention. The echocardiographic features of severe valvular insufficiency—in combination with heart failure, perivalvular infective extension, or large mobile vegetations (increased risk of embolic phenomena)—are the main indications for surgical intervention.3
Since its emergence, 3D echocardiography has gained popularity as a diagnostic tool in cardiac surgery for patients who present with IE. Whereas 2D echocardiography amounts to a single tomographic slice through a region of interest, 3D echocardiography can provide visual information about the entire region. The 3D data set is constructed by simultaneously acquiring multiple 2D sectors to form a pyramidal 3D volume, which can then be adjusted both automatically and manually for easier interpretation. When the entire volume is acquired in a single beat, it is viewed live and is described as “real-time”—although this necessarily gives lower temporal image resolution than do volumes acquired over several heartbeats. Superior guidance during catheter-based procedures has led to the widespread use of live 3D TEE—a technology that can also be applied in diagnosing IE when cases involve either native valves or prosthetic devices, as our clinical case shows.
The sensitivity of 2D TEE for the detection of vegetations is 85% to 90%, with a specificity of approximately 90% to 100%.4 Furthermore, 2D TEE is particularly useful in the evaluation of sequelae, such as abscesses (sensitivity 90% and specificity 90%),5 fistulae, pseudoaneurysms, and perforated leaflets. Given this excellent sensitivity and specificity, what is the added value of 3D TEE? The true strength of 3D echocardiography lies in its role as a complement to 2D echocardiography, in providing additional information that improves diagnostic accuracy. Especially when large vegetations are present, 2D TEE fails to provide sufficient information regarding the relationship between vegetations, prosthesis, and adjacent structures. Furthermore, the investigators in one case series6 noted that only 48% of abscesses detected intraoperatively correlated with preoperative 2D TEE findings. Because abscesses typically are not limited to specific tissue planes, they can extend in directions beyond the planes that routinely are acquired in 2D viewing. Conversely, the improved spatial orientation of 3D TEE enables more precise and complete examination of intracardiac anatomy.7,8 Furthermore, 3D TEE is superior in identifying the sequelae of IE—in particular, in locating and evaluating prosthetic dehiscence, perivalvular abscesses, and valvular perforation.9–13 Hansalia and colleagues10 compared 3D TEE and 2D TEE in 13 patients with valvular vegetations and concluded that 3D TEE was superior in determining, during surgery, the overall presence and exact site of valvular vegetations. These authors further ventured the possibility that 3D TEE can measure the volume of vegetations, and they showed low interobserver variability between measurements performed by means of 3D echocardiography.10 The accuracy and reproducibility of vegetation measurements has become particularly important after a 2012 study showed the effectiveness of early operation in patients with large vegetations.14 Our experience at the Mayo Clinic has shown that 3D TEE can be used to identify abscess-related sequelae and the extent of IE (Figs. 1–3*), which might enable better risk stratification, surgical decision-making, and operative planning. In addition, 3D TEE can be useful when there is right-sided valvular involvement (Fig. 4*).
Fig. 4.*.

Transesophageal echocardiogram shows extensive tricuspid valve endocarditis. This global view of the heart reveals a large vegetation on the tricuspid valve with involvement of the aortic valve (arrowhead). ©2015 Mayo Foundation for Medical Education and Research. All rights reserved.
ATL = anterior tricuspid leaflet
Fig. 3.*.

Transesophageal echocardiograms show A) infective endocarditis involving both atria and the internal crux of the heart and B) the large vegetation (arrows) in both atria (magnified view). The left atrial and right atrial vegetation are in continuity with the internal crux (black arrow). ©2015 Mayo Foundation for Medical Education and Research. All rights reserved.
The acquisition of 3D information enables surgeons to anticipate operative findings and to plan appropriate repair.15 The availability of information on such matters as fistula formation, valvular perforation, concomitant leaflet clefts, and commissural mitral regurgitation is crucial to operative planning. In our patient, the accuracy of the images provided by 3D TEE was confirmed intraoperatively (Fig. 2). This has been similarly described in other case reports.10–16 A particular strength of 3D TEE is its ability to accurately portray the mitral valve from the perspective of the left atrium (the “surgeon's view”). The mitral valve can be seen from a single 3D echocardiographic view, in contrast to the extensive manipulation frequently imposed by 2D imaging. The 3D image improves communication within the operative team by greatly reducing the need for “mental reconstruction.”
Because of the large amount of imaging data acquired, low temporal resolution remains a fundamental limitation of real-time 3D TEE. This can be overcome by multi-beat acquisition, a technique by which the 3D volume of interest is divided into subvolumes and data are acquired for each subvolume at separate time points. The subvolumes are then electronically “stitched together” to form the complete 3D data set.
Another limitation is the presence of dropout artifacts that can mimic a periprosthetic leak or leaflet perforation.17 To establish the diagnosis of a true defect, color-flow Doppler mode is used to document the presence or absence of flow through the defect.
In addition, the use of 3D TEE has focused predominantly on the aortic and mitral valves, because the distance from the transducer limits the role of that technique in examining the tricuspid valve.
Finally, Hansalia and colleagues10 have observed that the posterior mitral valve leaflet is not well viewed in 3D TEE, which results in missed diagnoses when perforation is present. Although this problem might be operator dependent, they emphasized the need, in the evaluation of IE, for combined 2D TEE and 3D TEE.
Conclusion
Three-dimensional TEE is a useful adjunct to traditional 2D TEE as a diagnostic tool in IE. Whereas 2D TEE effectively reveals signs of endocarditis on native and prosthetic valves, the advent of 3D TEE enables superior preoperative anatomic delineation and evaluation for complications of IE, with consequent improvement in surgical planning.
Acknowledgments
We acknowledge the contribution of Dr. Lawrence J. Sinak, Mayo Clinic, Rochester, Minnesota, in his helpful collection of data on our patient.
Footnotes
From: Division of Cardiothoracic Surgery (Dr. Yong), The Alfred Hospital, 3181 Melbourne, Australia; Department of Cardiology (Dr. Coffey), Oxford University Hospitals Trust, Oxford OX3 9DU, United Kingdom; and Division of Cardiovascular Surgery (Drs. Burkhart and Saxena), Department of Internal Medicine (Drs. Killu and Wan), and Division of Cardiovascular Disease (Drs. Killu and Malouf), Mayo Clinic, Rochester, Minnesota 55905
Dr. Saxena is now at the Alfred Hospital, Melbourne, Australia.
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