In this study, the transmit power was kept at 0 dB to produce the maximum power output, and the preprocessing was kept at zero to avoid introducing high values
from edges. Log compression: at 40 to 50 dB or middle range; persistence: at 2 or 3, to obtain some noise reduction by frame averaging; postprocessing: 0, 2, or
6 to assess the effect of the compression; gain at -5, 0, and +5 dB, at single transmit zone and multiple transmit zones.
*For convenience, preprocessing, persistence, and postprocessing values are written for example, as 0/2/0, where the numbers represent respective settings.
†For the in vitro work, attenuation is effectively zero, because the interest was the plaque morphology and a flat depth gain compensation curve is required.
Statistics
The ideal machine setting at which the MPV has the greatest ability
to discriminate between various tissues was determined as follows:
all tissue types on each of the 9 subjects were scanned at 72 machine
settings. The MPV for each setting was obtained, as well as their
variances. The variance of these means was calculated (A) and the
means of the variance at each setting was calculated (B) with the
StatView Statistics computer program.
The HID was calculated for each setting by the equation HID5A/B.
The HID represents the ability to discriminate between the various types
of tissues. The optimum setting of the machine is that which has the
greatest HID to discriminate between blood and fatty tissue as soft
materials and fibrocalcific structures. Statistical analysis of the results
was performed with the StatView Statistics computer program (version
4.5 for Apple Macintosh, Abacus Concepts, Inc). This study was performed at the vascular laboratory at the Middlesex Hospital, London,
UK. The approval of the University College London Hospitals Ethics
Committee was obtained, and patients included in the study gave
informed consent.
Results
In part 1 of this series of investigations, 3240 ultrasound images
were recorded of 9 controls (7 men, 2 women). Their MPV was
calculated in each selected setup. For each of the ultrasound
machine settings, the HID value was detected and plotted on the
vertical axis. A fairly small range of settings resulted in favorable
levels of discrimination.
Optimum machine settings were at log compression 40 dB,
preprocessing 0, persistence 2, and postprocessing 0, with gain
of 25 dB. These values gave an HID of 82%. Increasing the
machine gain to 0 dB from 25 dB but leaving other parameters
unchanged resulted in an HID of 64% whether the persistence
setting was 2 or 3. The remaining settings resulted in an HID that
ranged between 6% and 42%.
Computer-assisted image analysis for the image recorded at
the optimum setup showed that the MPV of the soft tissues
(blood, fat, and muscle) was < 50 (blood MPV range 1 to 4, fat
2 to 16, and muscle 1 to 43), whereas that of the fibrocalcific
tissues was < 150 (MPV 135 to 200).
In part 2 of this investigation, 17 carotid plaque scans were
performed (transient ischemic attacks were reported by 15
patients, whereas 2 were asymptomatic with 99% carotid artery
stenosis; these patients were part of the Asymptomatic Carotid
Surgery Trial [ACST]). One plaque was found to be grade 1, 5
plaques were grade 2, 8 plaques were grade 3, 3 plaques were
grade 4, and none were grade 5.
The MPV was compared with the Gray-Weale classification.
The MPV for grade 1 varies from 30 to 90, whereas grade 2
varies between 135 and 171, grade 3 between 140 and 180, and
grade 4 between 170 and 223.
Figure 2. Spearman correlation between MPV of the gray scale
ultrasound image and histological structures of the carotid
plaques. The figure demonstrates that as the fibrocalcific contents
of the plaque reach 90% of the plaque, the MPV reading
is > 150 (x2 = 9.7, P=0.0025), and as the soft content reaches
40% of the plaque, the MPV reading is < 50.
With Spearman rank correlation (Figure 2), the MPV of
whole plaque was significantly correlated with its histological
structure (r=0.8, P=0.002; 95% confidence interval for r was
0.91 to 0.5). If the fibrocalcific contents of the plaque reach 90%
of the plaque, the MPV reading is found to be > 150 (x2=9.7,
P=0.0025), and if the soft content is 40% or more, the MPV
reading is < 50. The present study has shown that the MPV of
fibrocalcific plaques was > 150 compared with soft plaques, for
which it was < 50 (P=0.002).
Figure 3. Bland and Altman statistics used to assess interobserver and intraobserver variation. With this graphical method, the difference
between the 2 techniques are plotted against the mean. The horizontal lines are drawn at the mean difference, as well as at the
mean difference plus or minus 1.96 times the SD.
With regard to the histological part of this study, Figure 3
demonstrates the interobserver and intraobserver variation, in
which there was insignificant difference between observers to
identify the plaque structures. The difference between the 2
techniques is plotted against the mean. The horizontal lines are
drawn at the mean difference, as well as at the mean difference
plus or minus 1.96 times the standard deviation.
Discussion
The North American Symptomatic Carotid Endarterectomy
Trial (NASCET)15 and the European Carotid Surgery Trial
(ECST)16 have clearly demonstrated that patients with symptomatic 70% to 90% carotid artery stenosis have a substantial
risk of ipsilateral ischemic stroke over the next few years. They
also highlighted the benefit of surgery in the symptomatic group.
Identification of other factors may be of value in predicting the
development of embolic events in the cerebral circulation.
Duplex ultrasound scanning has the ability to determine the
degree of carotid artery stenosis and also plaque structure, which
has the potential to identify high-risk patients.
Gray-Weale et al[3] classified carotid plaques on the basis of
their ultrasound images into 4 types based on echogenicity, and
Geroulakos et al,17 in their modification, added a fifth type
(calcified plaque). This fifth type is identified on ultrasound
imaging by the presence of “shadows” cast by plaques, attributable
to strong absorption of ultrasound energy by this plaque.
This type has been excluded in the present study. Gray-Weale et
al3 also stated that intraplaque hemorrhage and ulceration were
frequently found in type 1 and 2 plaques, whereas type 3 and 4
plaques were more calcified and largely fibrous; this classification
was also used by Langsfeld et al.[18,19].
In a histological study, el-Barghouty et al4 scanned patients
before surgery and selected the center part of the atherosclerotic
plaque (after carotid endarterectomy) for analysis (whole plaque
was not assessed). These authors correlated the median of
gray-scale image intensity (the ultrasound image was scanned
but was not recorded electronically, which caused a loss of
resolution of the image) to their histological structure and found
that the gray-scale median (GSM) of the ultrasound image
decreased as the mean percentage of the fat and hemorrhage
increased, whereas it increased as the fibrocalcific material
increased. They also reported that in the symptomatic group,
GSM decreased as the fat and hemorrhage content increased,
whereas in the asymptomatic group, both GSM and fibrocalcific
content increased. However, the effect of the surgical manipulation
during carotid endarterectomy on plaque architecture may
have led to a discrepancy between the center of the plaque in the
ultrasound image and that of the carotid specimen.
In the present study, ultrasound images were recorded electronically
by the QV 200 image-processing computer. Tissues of
known type in a human volunteer were examined (blood, fat,
muscle, and fibrous and calcified tissues) with a range of
different machine settings. This allowed identification of those
settings at which images were obtained in which the computer
was best able to differentiate between tissues. All images were
analyzed and the image statistics obtained objectively. The MPV
of the pixels in the tissue of interest in the image was used as the
parameter to identify the echogenicity of the structure. The
histological study was designed to test whether the findings in
the previous study could be extended to the assessment of the
morphology of atheromatous plaques. The findings of computerassisted
gray-scale image analysis of these specimens have been
verified by the histological findings, and a good correlation has
been shown. This study has shown that as the soft (fat and blood)
content of the plaque increased, the MPV decreased, and as the
fibrocalcific tissue content of the plaque increased, the MPV
increased. This relation between the MPV and plaque histology
has been found to be significant (P,0.002).
In the future, this work may be extended to involve online
image analysis of atherosclerotic plaque characterization (in vivo
as well as in vitro) and possibly the investigation of second-order statistics. Also, if future study demonstrates a good correlation
between MPV and the Gray-Weale classification, better objective
assessment of atherosclerotic plaque will be achieved.
Computer-assisted image analysis system is an objective that
may be of value in identifying unstable atherosclerotic plaques
in the carotid territory. This has the potential to revolutionize the
treatment of asymptomatic carotid artery disease.
Acknowledgments
We acknowledge Prof Blackwell, professor of medical physics at
University College London, for his support, and Prof Senn, professor
of medical physics at University College London, for his support and
designing HID statistics.
References
1. Olinger CP. Ultrasonic carotid echoarteriography. Am J Roentgenol
Radium Ther Nucl Med. 1969;106:282–295.
2. Lusby R. Plaque characterisation: does it identify high risk group? In:
Bernstein E, Callow A, Nicolaides A, Shifrin E, eds. Cerebral
Re-vascularisation. London, UK: Med-Orion Publishing Co; 1993:93–107.
3. Gray-Weale AC, Graham JC, Burnett JR, Byrne K, Lusby RJ. Carotid artery
atheroma: comparison of preoperative B-mode ultrasound appearance with
carotid endarterectomy specimen pathology. J Cardiovasc Surg (Torino).
1988;29:676–681.
4. el-Barghouty N, Nicolaides A, Bahal V, Geroulakos G, Androulakis A. The
identification of the high risk carotid plaque. Eur J Vasc Endovasc Surg.
1996;11:470–478.
5. Wegener O. Mathematical principles of the image. In: Whole-Body
Computed Tomography. 2nd ed. Boston, Mass: Blackwell Scientific Publications;
1992:3–4.
6. Wegener O. Image reconstruction. In: Whole-Body Computed Tomography.
2nd ed. Boston, Mass: Blackwell Scientific Publications; 1992:5–8.
7. Winters K, Busch D. Image resolution. In: Teach Yourself Photoshop 3.0.
New York, NY: MIS Press; 1995:259–281.
8. Strandness DE Jr, Slagsvold E, Morken B, Alker H, Bjordal J. Three dimensional
visualisation of peripheral arterial disease. In: Greenhalgh R, ed.
Vascular Imaging for Surgeons. London, UK: WB Saunders Co Ltd; 1995:
71–80.
9. Einenkel D, Bauch KH, Benker G. Treatment of juvenile goitre with levothyroxine,
iodide, or a combination of both: the value of ultrasound grey scale
analysis. Acta Endocrinol Copenh. 1992;127:301–306.
10. Becker W, Frank R, Borner W. The importance of quantitative grey scale
analysis of the sonogram in diffuse thyroid disease. Rofo Fortschr Geb
Rontgenstr Nuklearmed. 1989;150:66–71.
11. Huber S, Delorme S, Knopp MV, Junkermann H, Zuna I, von Fournier D,
van Kaick G. Breast tumours: computer-assisted quantitative assessment with
color Doppler US. Radiology. 1994;192:797–801.
12. Zendel W, Wakat P, Fischer G, Treisch J, Langer R. A comparison of the
quantified determination of the echogeneity of the liver by ultrasound and the
density of the liver by CT [in German]. Rontgenblatter. 1989;42:114–117.
13. Hess CF, Wolf A, Kolbel G, Kurtz B. Subjective evaluation and quantitative
gray-scale analysis in the sonographic diagnosis of diffuse changes in the
liver parenchyma [in German]. Rofo Fortschr Geb Rontgenstr Nuklearmed.
1986;145:140–144.
14. Bland M, Altman D. Statistical methods for assessing agreement between
two methods of clinical measurement. Lancet. 1986;1:307–310.
15. North American Symptomatic Carotid Endarterectomy Trial Collaborators.
Beneficial effect of carotid endarterectomy in symptomatic patients with
high-grade carotid stenosis. N Engl J Med. 1991;325:445–453.
16. European Carotid Surgery Trialists’ Collaborative Group. MRC European
Carotid Surgery Trial: interim results for symptomatic patients with severe
(70–99%) or with mild (0–29%) carotid stenosis. Lancet. 1991;337:
1235–1243.
17. Geroulakos G, Sonecha T, Nicolaides A, Fernandes J. The management of
patients with asymptomatic carotid stenosis. In: Bernstein E, Callow A,Nicolaides
A, Shifrin E, eds. Cerebral Re-vascularisation. London, UK:
Med-Orion Publishing Co; 1993:565(b).
18. Langsfeld M, Lusby RJ. The spectrum of carotid artery disease in asymptomatic
patients. J Cardiovasc Surg (Torino). 1988;29:687–691.
19. 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 Surg. 1989;9:548–557.