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(Stroke. 1998;29:673-676.)
© 1998 American Heart Association, Inc.


Original Contributions

A New Noninvasive Technique for Imaging Atherosclerotic Plaque in the Aortic Arch of Stroke Patients by Transcutaneous Real-Time B-Mode Ultrasonography

An Initial Report

Jesse Weinberger, MD; Salman Azhar, MD; Fabio Danisi, MD; Richard Hayes, MD; Martin Goldman, MD

From the Department of Neurology (J.W., S.A., F.D.), and the Division of Cardiology, Department of Medicine (R.H., M.G.), The Mount Sinai School of Medicine, New York, NY.

Correspondence to Jesse Weinberger, MD, Department of Neurology, Box 1052, The Mount Sinai School of Medicine, 1 Gustav Levy Place, New York, NY 10029. E-mail JesseWeinberger{at}mstplink.mssm.edu


*    Abstract
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*Abstract
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Background and Purpose—Aortic arch atherosclerotic plaque is a probable source of atheroembolic stroke. Transesophageal echocardiography (TEE) has been used to image the aorta of patients with stroke to identify atherosclerotic plaque. TEE is moderately invasive and does not always visualize plaques present in the distal ascending aorta and proximal aortic arch.

Methods—In the current study, transcutaneous B-mode ultrasonography was performed to image the aortic arch through a lateral supraclavicular window, and the results were compared with those of TEE in 20 patients. The aorta was subdivided into the proximal ascending (PAsc), distal ascending (DAsc), proximal aortic arch (PAA), and distal aortic arch (DAA) to be certain the plaques identified by each technique were the same. Plaques were characterized as simple (<4 mm thick) or complex (>4 mm thick).

Results—In the PAsc, 8 simple plaques were identified with TEE but not with B-mode. In the DAsc, 1 complex plaque was identified with both techniques, and B-mode identified 1 additional complex and 1 simple plaque. In the PAA, 6 simple and 5 complex plaques were identified by both techniques, and TEE identified 1 additional complex plaque. In the DAA, TEE identified 2 simple and 2 complex plaques; B-mode identified 3 complex plaques.

Conclusions—B-mode imaging compared favorably with TEE in identification of plaques in the aortic arch and distal ascending aorta, although it could not identify simple plaques in the proximal ascending. B-mode could visualize plaques not seen by TEE in the distal ascending aorta. B-mode ultrasonography is complementary to TEE in performance of a comprehensive assessment of plaque in the aortic arch and provides a noninvasive method for sequential studies of plaques that can be visualized.


Key Words: aortic arch • atherosclerosis • echocardiography, transesophageal • ultrasonography


*    Introduction
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Morphological studies of postmortem specimens and clinical studies with transesophageal echocardiography (TEE) have established an association between atherosclerotic plaque in the aortic arch and ischemic stroke for which no other coexisting etiology could be identified.1 2 3 4 5 6 7 8 9 10 TEE is now performed on a routine basis in stroke patients to identify plaques in the aortic arch that could be a potential source of atheroembolic stroke. TEE is moderately invasive and cannot be tolerated by all patients. In addition, the distal ascending aorta as it curves into the aortic arch often cannot be visualized well because of obstruction by the bronchi.11

In the current study, noninvasive percutaneous real-time B-mode ultrasonography was used to visualize the aortic arch and identify atherosclerotic plaque. B-mode ultrasonography is an established technique for defining atheroma in the carotid artery bifurcation and has provided the basis for many studies of the relationship between plaque morphology and atheroembolic stroke from the carotid.12 13 14 15 16 17 18 19 Correlation with TEE was made in 20 consecutive stroke patients to determine whether B-mode was able to visualize aortic plaque and to compare the morphological characteristics revealed by B-mode with those shown by TEE.


*    Subjects and Methods
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Patients
B-mode ultrasonography of the aortic arch was performed on 20 consecutive stroke patients. TEE was performed on 20 of these patients within 3 days of the B-mode study. The TEE was performed without knowledge of the B-mode results, and the B-mode was performed without knowledge of the TEE results. The results of both studies were compared at the end of the collection of 20 sequential cases. The location of the plaque and the morphology of the plaque were determined in each study before comparison of the results.

The B-mode studies were performed by one of the investigators (J.W.), who was aware of the clinical findings of the patient. The TEE studies were performed without knowledge of the clinical findings in the patient.

B-Mode Ultrasonography
B-mode ultrasonography of the aortic arch was performed with an Acuson XP 128 color-flow duplex Doppler instrument, with use of an L7 phased-array linear probe at 7.5 MHz. Doppler examination was performed at 5.0 MHz. A lateral supraclavicular approach was used to visualize the ascending aorta, aortic arch, and proximal descending aorta. The angle of insonation required to visualize the arch produces an image that is inverse to the true direction of the arch, with the ascending aorta to the right and the arch curving to the left toward the descending aorta. A schematic diagram of the technique for imaging the aortic arch is shown in Fig 1Down.



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Figure 1. Schematic diagram of the technique of performing real-time B-mode ultrasonography of the aortic arch. The patient is examined in a sitting or lying position, but the sitting position provides better visualization. The probe is placed in the supraclavicular fossa, imaging from the right to the left. The position of the aortic arch in the sonographic beam is shown as it traverses from right to left and posteriorly over the heart. The B-mode image is seen in reverse, with the ascending on the left and the descending on the right, because it is taken in a lateral view as the arch courses posteriorly over the heart.

For purposes of comparing TEE and B-mode ultrasonography, the arch was subdivided into segments: the proximal ascending aorta, distal ascending aorta, proximal aortic arch, and distal aortic arch. This ensured that the same plaque was being imaged by each technique. The origin of the innominate artery was taken as the border between the proximal and distal arch, as seen in the schematic diagram of the arch (Fig 2Down).



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Figure 2. Schematic diagram of the results of B-mode and TEE examination of the aortic arch is shown. The location of plaques in the aortic arch was divided into subdivisions: proximal ascending aorta, distal ascending aorta, proximal aortic arch, and distal aortic arch. The locations of complex and simple plaques seen with B-mode imaging and TEE in the subdivisions of the aortic arch are identified. Complex plaques are denoted as large, irregular shapes and simple plaques as small, regular shapes.

TEE was performed with the patient in the lateral decubitus position. A multiplane probe (ATL HDI 300 or Hewlett Packard HP-2500), with frequencies ranging from 5 to 7 Mhz, was used. Topical anesthesia was accomplished with Cetacaine (Cetylite Industries) and lidocaine, and intravenous sedation when needed was titrated with Demerol (Sanofi Winthrop) and Versed (Roche Laboratories). Twenty sections of the arch were visualized and aortic plaque was identified. The aorta was subdivided into the same segments as the B-mode scans for comparison. Calculations of sensitivity and specificity comparing B-mode and TEE were not made, because it is known that TEE does not visualize all aortic plaques that can be seen with open aortography, particularly in the distal ascending aorta.11

Plaques were characterized as simple if they were <4 mm thick and complex if they were >4 mm thick.7 9 They were also described as sessile, crescentic, pedunculated, or flat.


*    Results
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*Results
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TEE identified 8 simple plaques on the wall of the proximal segment of the ascending aorta. This segment could not be visualized well with B-mode ultrasonography, although the wall of the proximal ascending aorta could be seen in 12 of the 20 cases with B-mode. In the distal ascending aorta, B-mode identified 2 complex and 1 simple plaque, whereas TEE identified only 1 complex plaque (Fig 2Up). In the proximal aortic arch, TEE identified 6 simple and 4 complex plaques, and B-mode identified 6 simple and 3 complex plaques. In the distal aortic arch, TEE identified 2 simple and 2 complex plaques; B-mode identified 3 complex plaques. The additional complex plaque seen in the distal aortic arch on B-mode was the same as the additional plaque seen as being in the proximal aortic arch on TEE, but it was localized to different segments by the two techniques. The results are summarized in the TableDown and in a schematic diagram (Fig 2Up).


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Table 1. Localization of Simple and Complex Plaques in the Proximal Ascending Aorta, Distal Ascending Aorta, Proximal Aortic Arch, and Distal Aortic Arch Visualized With B-Mode Ultrasonography and TEE

All complex plaques visualized with TEE were also identified with B-mode sonography. The morphological conformation of the plaques were also similar, indicating that the same plaques were being seen. Both techniques showed the plaques as pedunculated (Fig 3Down) and proliferative (Fig 4Down). Mobility of plaque could be seen as well with both techniques. TEE was able to detect simple plaques not seen with B-mode imaging, particularly in the proximal ascending aorta.



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Figure 3. A pedunculated plaque in the proximal aortic arch visualized with B-mode ultrasonography (A) and TEE (B). The shape of the plaque is the same, though linear scanning with B-mode appears to delineate layers of density and lucency not visualized by sector scanning with TEE.



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Figure 4. A large proliferative plaque is seen with B-mode (A) and TEE (B) at the curvature of the distal arch into the descending aorta. The plaque is of intermediate echodensity, but no underlying lucencies are seen.


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
*Discussion
down arrowReferences
 
An association has been established between aortic plaque identified by TEE and atheroembolic cerebrovascular disease. Tunick et al1 first described the identification of protruding masses with mobile components with TEE in patients who had systemic embolic events during cardiac catheterization. These observations were further extended to patients with embolic stroke, and it was confirmed through pathological examination that these masses were atherosclerotic.2 Amarenco et al3 performed pathological examinations of 500 consecutive patients with cerebrovascular and other neurological diseases and found a prevalence of aortic plaque of 57.8% in patients with no known cause of cerebral infarction and 22% in patients with other possible etiologies of cerebral infarction.

Toyoda et al5 reported a 42% prevalence of aortic atheroma identified by TEE in 62 patients with clinical criteria of embolic stroke. Amarenco et al4 found complex aortic plaques in 50% of 12 patients with embolic stroke for which no other etiology had been determined. Horowitz et al6 reported mobile aortic plaques in 4% of 183 patients with cerebral infarction.

Amarenco et al7 demonstrated that the prevalence of complex aortic plaques >4 mm thick on TEE was significantly higher in stroke patients compared with control patients, a finding confirmed by Jones et al.8 The French Study of Aortic Plaques in Stroke Study Group9 documented an incidence of recurrent brain infarction of 11.9 per 100 person-years in stroke patients with aortic wall thickness of >4 mm and 3.5 per 100 person-years in stroke patients with aortic wall thickness of <4 mm, indicating that complex atherosclerotic plaque in the aortic arch is a significant predictor of recurrent brain infarction. The increased frequency of recurrent brain infarction in patients with complex aortic plaques was confirmed by Mitusch et al.10 In these studies the population was small, and treatment modalities and concomitant risk factors were not accounted for.20 21 22 Repeat TEE to document changes in aortic plaque morphology consistent with an embolic event was not performed, so it is uncertain whether embolization of aortic plaque was the etiology or whether aortic arch atherosclerosis was a marker for more severe cerebrovascular disease.20 21 22

Correlation of the plaque morphology of ultrasound images of aortic plaque on TEE and pathological specimens has been limited because most aortic plaques are not removed surgically. Tunick et al2 reported morphological correlation of one complex symptomatic plaque removed surgically with the presence of thrombus. Amarenco et al3 identified ulceration on pathological specimens of aortic plaque described at autopsy but did not correlate these findings with ultrasound images.

The correlation of ultrasonographic carotid plaque morphology and histology has been described in several studies. Heterogeneous lucencies have been associated with intraplaque and intraluminal thrombus and acute hemorrhage into plaque.12 13 18 These findings are significantly more frequent in symptomatic plaques12 13 and have predictive value for future symptoms.14 15 19 Plaque configuration also appears to play a role, with crescentic plaques with scalloped borders having a greater frequency of ipsilateral ischemic events.17 19 Recurrent symptoms are associated with plaque growth in a crescentic configuration.19 Imaging aortic plaque with the same linear real-time B-mode ultrasonographic technique used to image carotid plaque may allow for extrapolation of plaque characteristics from the carotid to the aortic arch.

Noninvasive B-mode imaging can visualize atherosclerotic plaque in the distal ascending aorta and aortic arch. Plaques in the proximal ascending aorta that are seen with TEE cannot be visualized, but almost all of these are simple plaques. Complex plaques visualized with epiaortography during cardiac surgery are located primarily in the curvature of the arch from the distal ascending aorta to the proximal descending aorta,11 which can all be seen with B-mode ultrasonography in most patients. B-mode may be more sensitive than TEE in identifying plaques at the junction of the ascending aorta and the arch, which can be obscured by the bronchi.11

Real-time B-mode ultrasonography of the aortic arch is a noninvasive method that can be incorporated into the neurovascular evaluation of patients with stroke and transient ischemic attack at the time duplex examination of the carotid bifurcation is performed. Patients who would not normally undergo TEE can be screened for aortic plaque, and if plaque is identified a TEE can be performed to corroborate the findings. In patients for whom visualization of the aortic arch is not definitive with B-mode, TEE can be performed if there is a clinical indication that the stroke was embolic. TEE is often performed in patients suspected of having a cardioembolic stroke. In these patients, B-mode can supplement the TEE to visualize the portions of the arch that may be difficult to visualize with TEE. A combination of transthoracic echocardiography and B-mode ultrasonography of the aortic arch may be sufficient in some patients to rule out an embolic source. B-mode imaging of the aortic arch should also be useful for sequential studies of plaques identified with TEE that can be visualized with B-mode without subjecting the patient to the discomfort of repetitive TEE examinations. This may be of value in therapeutic trials of agents to prevent stroke from aortic arch plaque, so that morphologic changes in plaque can be correlated with method of treatment and cerebrovascular events.

The current study was performed to establish the technique of percutaneous B-mode imaging of the aortic arch and determine whether the plaques identified were similar to those seen with TEE. The number of patients was small, and correlation with methods of treatment and risk factors was not obtained. Further studies will be required to establish the interobserver and intraobserver reliability of the technique, and the sensitivity and specificity must be documented in large numbers of patients before the technique can achieve general applicability.

The technique has the potential for become a standard method of visualizing atherosclerotic plaque in the arch of the aorta.

Received October 2, 1997; revision received January 5, 1998; accepted January 5, 1998.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowSubjects and Methods
up arrowResults
up arrowDiscussion
*References
 
1. Tunick PA, Kronzon I. Protruding atherosclerotic plaque in the aortic arch of patients with systemic embolization: a new finding seen by transesophageal echocardiography. Am Heart J. 1990;120:658–660.[Medline] [Order article via Infotrieve]

2. Tunick PA, Culliford AT, Lamparello PJ, Kronzon I. Atheromatosis of the aortic arch as an occult source of multiple systemic emboli. Ann Int Med. 1991;114:391–392.

3. Amarenco P, Duyckaerts C, Tzourio C, Henin D, Bousser M-G, Hauw J-J. The prevalence of ulcerated plaques in the aortic arch in patients with stroke. N Engl J Med. 1992;326:221–225.[Abstract]

4. Amarenco P, Cohen A, Baudrimont M, Bousser M-G. Transesophageal echocardiographic detection of aortic arch disease in patients with cerebral infarction. Stroke. 1992;23:1005–1009.[Abstract/Free Full Text]

5. Toyoda K, Yasaka M, Nagata S, Yamaguchi T. Aortogenic embolic stroke: a transesophageal echocardiographic approach. Stroke. 1992;23:1056–1061.[Abstract/Free Full Text]

6. Horowitz DR, Tuhrim S, Budd J, Goldman ME. Aortic plaque in patients with brain ischemia: diagnosis by transesophageal echocardiography. Neurology. 1992;42:1602–1604.[Abstract/Free Full Text]

7. Amarenco P, Cohen A, Tzourio C, Bertrand B, Hommel M, Besson G, Chauvel C, Touboul P-J, Bousser M-G. Atherosclerotic disease of the aortic arch and the risk of ischemic stroke. N Engl J Med. 1994;331:1474–1479.[Abstract/Free Full Text]

8. Jones EF, Kalman JM, Calafiore P, Tonkin AM, Donnan GA. Proximal aortic atheroma: an independent risk factor for cerebral ischemia. Stroke. 1995;26:218–224.

9. The French Study of Aortic Plaques in Stroke Group. Atherosclerotic disease of the aortic arch as a risk factor for recurrent ischemic stroke. N Engl J Med. 1996;334:1216–1221.[Abstract/Free Full Text]

10. Mitusch R, Doherty C, Wucherpfennig H., Memmesheimer C, Tepe C, Stierle U, Kessler C, Sheikhzadeh A. Vascular events during follow-up in patients with aortic arch atherosclerosis. Stroke. 1997;28:36–39.[Abstract/Free Full Text]

11. Konstadt SN, Reich DL, Quintana C, Levy M. The ascending aorta: how much does transesophageal echocardiography see? Anesth Analg. 1994;78:240–244.[Medline] [Order article via Infotrieve]

12. Reilly LM, Lusby RJ, Hughes I Ferrel LD, Stoney RJ, Ehrenfeld WK. Carotid plaque histology using real-time ultrasonography: clinical and therapeutic implications. Am J Surg. 1983;146:188–193.[Medline] [Order article via Infotrieve]

13. Steffen CM, Gray-Weale AC, Byrne KE, Lusby RJ. Carotid artery atheroma: ultrasound appearance in symptomatic and asymptomatic vessels. Aust N Z J Surg. 1989;59:529–534.[Medline] [Order article via Infotrieve]

14. Langsfeld M, Gray-Weale AC, Lusby RJ. The role of plaque morphology and diameter reduction in the development of new symptoms in asymptomatic carotid arteries. J Vasc Surg. 1989;9:548–557.[Medline] [Order article via Infotrieve]

15. Johnson JM, Kennelly MM, Decesare D, Morgan S, Sparrow A. Natural history of asymptomatic carotid plaque. Arch Surg. 1985;120:1010–1012.[Abstract/Free Full Text]

16. Mercuri M, Bond MG. B-mode ultrasound characterization of atherosclerosis. J Cardiovasc Technol. 1992;10:277–291.

17. Weinberger J, Robbins A. Neurologic symptoms associated with nonobstructive plaque at carotid bifurcation: analysis by real-time B-mode ultrasonography. Arch Neurol. 1983;40:489–492.[Abstract/Free Full Text]

18. Weinberger J, Marks SJ, Gaul JJ, Goldman B, Schanzer J, Jacobson J, Dikman S. Atherosclerotic plaque at the carotid artery bifurcations: correlation of ultrasonographic imaging with morphology. J Ultrasound Med. 1987;6:363–366.[Abstract]

19. Weinberger J, Ramos L, Ambrose JA, Fuster V. Morphologic and dynamic changes of atherosclerotic plaque at the carotid artery bifurcation: sequential imaging by real time B-mode ultrasonography. J Am Coll Cardiol. 1988;12:1515–1521.[Abstract]

20. Davila-Roman VG, Barzilai B, Wareing TH, Murphy SF, Schectman KB, Kouchoukos NT. Atherosclerosis of the ascending aorta: prevalence and role as an independent predictor of cerebrovascular events in cardiac patients. Stroke. 1994;25:2010–2016.[Abstract]

21. DiTullio MR, Sacco RL, Gersony D, Nayak H, Weslow RG, Kargman DE, Homma S. Aortic atheromas and acute ischemic stroke: a transesophageal echocardiographic study in an ethnically mixed population. Neurology. 1996;46:1560–1566.[Abstract/Free Full Text]

22. Di Tullio MR, Sacco RL, Homma S. Atherosclerotic disease of the aortic arch as a risk factor for recurrent ischemic stroke. N Engl J Med. 1996;335:1464. Letter.[Free Full Text]




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