echoes of the original sound beam initially created by placing the ultrasound transducer in contact with
the tissue. The B-mode component of the duplex machine analyzes the strength (intensity) and origin of
the reflected echo. The Doppler component analyzes shifts in frequency of the original sound wave
produced by the transducer that result when the ultrasonic wave encounters moving reflectors.
B-Mode Ultrasound
As a sound wave passes through tissue, its strength moving away from the transducer depends upon the
degree to which the beam is attenuated, scattered, and reflected. The strength of the reflected echo
depends in part, upon relative differences in acoustic impedance between two different media. Major
differences in acoustic impedance result in reflection of a large proportion of the sound beam back to
the transducer, whereas small differences result in comparatively little reflection and continued
propagation of the beam through the tissue.
In B-mode ultrasound, the strength of the returning echo is reflected in the brightness of the
individual pixels comprising the ultrasound image. This is the ultrasound grayscale and the resulting
image is termed a grayscale image. (As we will see below, the primary purpose of the grayscale image in
duplex ultrasonography is to aid in properly positioning the Doppler sample volume.)
Very bright pixels represent sites of large differences in acoustic impedance between media, whereas
less dramatic differences are represented by proportionally less bright pixels on the B-mode image. Thus
gallstones, which differ dramatically in acoustic properties from soft tissue, result in strong echoes and
proportionally brighter pixels on an ultrasound image, whereas blood, which differs little from soft
tissue in acoustic characteristics, frequently cannot be distinguished from soft tissue in a grayscale
image.
The strength of the reflected echo will also be dependent upon the strength of the sound beam at the
point of its reflection. Grayscale images do not show the percentage of the beam reflected, but rather
represent the absolute strength of the reflected echo arriving back at the transducer. Thus if the sound
beam is very weak at the site of its reflection, even areas of significant differences in acoustic
impedance will not result in a bright pixel on the ultrasound image.
The strength of the ultrasound beam at any point also depends on the degree to which the beam has
been attenuated as it passes through the tissue. Attenuation of a sound wave as it traverses tissue
weakens the wave and depends upon the tissue traversed and the frequency of the wave. The frequency
of the wave depends upon the frequency of the transducer used to generate the wave (see discussion
above and Equation 87-1). Sound waves resulting from higher-frequency transducers are attenuated
more rapidly than those produced with lower-frequency transducers. Higher-frequency transducers
therefore provide relatively weak echoes to be reflected from a deep structure and thus a comparatively
poor B-mode image compared to a lower frequency transducer.
The linear resolution of an ultrasound image depends upon the ability to focus the beam. Sound
beams emanating from high-frequency transducers can be more precisely focused than those from lowfrequency transducers and thus provide clearer B-mode images of more superficial structures. Because
the carotid artery is superficial, higher-frequency transducers can be used to provide much clearer Bmode images than is possible with deeper vessels such as the aorta, renal, or iliac arteries.
Doppler Ultrasound
In a continuous wave Doppler, a transducer continually emits vibrations into the tissue. Echoes are
therefore continually reflected back to the transducer. A transducer cannot, however, simultaneously
generate and receive an echo. Continuous wave Doppler therefore must have separate transmitters and
receivers to both generate and receive echoes.
1 Duplex devices utilize pulse Doppler. A pulse Doppler uses the same transducer to generate and
receive echoes. Because the speed of sound is relatively constant in tissue, with a pulse Doppler it can
be determined when an echo is generated and when it is received and therefore it is possible to
calculate the depth in the tissue where a reflected echo originated. The sample volume of the duplex
device is thus determined by specifying from what depth one wishes the pulse Doppler to receive
reflected echoes.
The transducer is gated, based on the total time from original sound-wave generation to arrival of the
reflected echo back at the transducer, to only receive echoes from the specified depth of the sample
volume. The desired “position” of the sample volume is determined by the operator of the duplex device
from the B-mode image, and in duplex examination of arterial and venous flow corresponds to
particular points within the lumen of the vessel examined. Because B-mode images and Doppler
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waveforms cannot be generated simultaneously, the technologist must continually update the B-mode
image during the course of the examination to insure proper placement of the sample volume.
2 When a sound wave encounters moving reflectors, such as red blood cells, so-called Rayleigh
scatters, within the lumen of an artery or vein, the frequency of the reflected wave changes from that of
the original wave generated by the transducer. Velocity is a vector with both speed and direction
therefore, the magnitude of the frequency shift depends upon the velocity of the moving reflectors and
their angle with the incident sound beam. Because the frequency of the original sound wave is known,
and the frequency of the received echo can be determined by the software of the duplex machine, the
velocity of the moving reflectors (red blood cells) can be calculated provided the angle of the incident
sound beam with the moving reflectors is also known. This relationship is reflected in the Doppler
equation:
Where fr is the received frequency, fo
is the originating frequency, v is the velocity of the reflector, c
is the speed of sound in tissue, and θ is the angle of the incident sound beam with the moving reflectors,
the so-called Doppler angle.
A Doppler angle of 0 degrees is ideal for velocity calculations as the cosign of 0 is 1 and measured
reflected velocity changes are therefore 100% of what actually occurred. However 0-degree Doppler
angles are difficult to obtain as it is not generally possible to look directly down the lumen of a vessel
from a percutaneous approach. Therefore to solve the Doppler equation for the velocity of the moving
reflectors, the Doppler angle must be known. To standardize the results of duplex scanning, it has been
traditionally recommended that examinations be conducted as close as possible to a Doppler angle of 60
degrees. The cosign of 60 is 0.5, therefore at this angle the measured reflected velocity is half the actual
reflected velocity. Errors in velocity calculations secondary to misreading of the Doppler angle are small
as a percentage of the true velocity at ≤60 degrees as cosigns vary comparatively little with
incremental changes in angle below 60 degrees. When the Doppler angle approaches 70 degrees,
changes in the cosign of the angle become more pronounced with incremental increases in angle, and
errors in velocity calculations secondary to improper angle measurement become much more
significant. Small errors in determining the Doppler angle when the angle of insonation is <60 degrees
have little overall impact on the calculation of the velocity of the moving red cells. Indeed, Doppler
angles from 45 to 60 degrees are acceptable for most clinical studies. Most often an angle of 60 degrees
can be easily obtained in carotid artery and extremity artery duplex examinations and, in line with
traditional teaching, 60 degrees is chosen whenever possible as the Doppler angle in such studies. In
examination of intra-abdominal vessels it may be much more difficult to adhere to a 60-degree angle.
As noted above, pulse Doppler both transmits and receives echoes with the same transducer. This dual
function places limits on the frequencies that can be displayed in the spectral waveform. The maximum
frequency that can be displayed is half the pulse-transmitting frequency or pulse-repetition frequency
(PRF), and is known as the Nyquist limit. If frequencies are encountered that exceed the Nyquist limit,
they are flipped and appear on the reverse-flow side of the spectrum. This is termed aliasing. If aliasing
is encountered, the PRF should be increased to increase the Nyquist limit. The PRF can be adjusted by
changing the scale displayed on the right side of the spectral waveform or by adjusting the baseline. If
aliasing still occurs, the operator should consider switching to a lower frequency transducer or to the
use of a continuous-wave Doppler. A continuous-wave Doppler is not affected by aliasing.
Color Flow
A color flow image is produced by assigning color to Doppler shifts. Returning echoes that are not
Doppler shifted are shown in grayscale. The net result is what appears to be color pasted or
superimposed on a grayscale image. This pasting process can in effect obscure the edges of the grayscale
image resulting in obfuscation of the true lumen of the grayscale image limiting somewhat the accuracy
of color images to define stenosis. The hue and intensity of the color are determined by the direction
and magnitude of the Doppler shifts. The technologist can adjust the color settings as desired. Varying
shades of red and blue are generally used to distinguish flow toward or away from the transducer. By
convention, red is most often assigned to arterial flow and blue to venous flow.
When the Doppler angle is 90 degrees, there is no Doppler shift. When this occurs, the assigned color
is black and corresponds to the horizontal black bar serving as the baseline on the color scale that
appears on the right side of a color flow image (Fig. 87-1). Aliasing can be readily recognized on a color
flow image as a mosaic pattern or as a transition from red-to-blue or blue-to-red without an intervening
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black line. In areas of actual reverse flow, the blue and red colors are separated by a black border. Just
as with pulsed Doppler, color aliasing can be reduced by increasing the PRF. This is often quite
important, as an extensive mosaic pattern can obscure clear visualization of a stenotic site.
Power Doppler is a variant of color Doppler. Power Doppler, however, assigns no direction of flow to
the color image and velocity information is not calculated. Any detected Doppler shift is colorized
without consideration of the direction of the Doppler shift or the magnitude of the Doppler shift. It is
therefore not subject to aliasing or affected by Doppler angle. Its principle utility lies in the ability to
detect blood moving at very low velocity and in outlining the course of tortuous vessels. It can be quite
useful in detecting flow in small distal veins and flow in arteries distal to a very high-grade stenosis.
It is tempting to try a direct estimate of the severity of a stenosis from the color flow image.
However as discussed above such estimates are probably less accurate than measurements of stenosis
derived from spectral analysis. Color serves primarily as a guide in locating the vessels and selecting
specific sites for examination with the pulse Doppler. The absence of color can indicate extensive mural
calcification and difficulty in obtaining a pulse Doppler waveform.
Figure 87-1. Flow separation with reverse flow along the wall of the carotid bulb as indicated by direct transition from blue to red
with an intervening black line is a normal finding and indicates an artery without significant plaque.
Carotid and Vertebral Arteries
The vascular laboratory began with assessing internal carotid artery (ICA) stenosis. Doppler diagnosis of
ICA stenosis, and arterial stenosis in general is based on duplex ultrasound and focuses on three areas,
the prestenotic region, the stenosis itself and the poststenotic region. Detecting carotid stenosis involves
a combination of spectral analysis, color and grayscale imaging and, in selected cases, power Doppler.
The primary interest is in the detection of increased flow velocities within the area of suspected stenosis
and therefore in most cases spectral analysis dominates in the detection of carotid stenosis. The
exception is in distinguishing ICA occlusion from a very high-grade stenosis where color flow or power
Doppler flow can identify very low flow in the area of the stenosis or distal to the stenosis that may not
be detected by pulse Doppler.
In all cases, the pulsed Doppler and color flow findings should be crosschecked for concordance. If
there is disagreement between the impression obtained with color and pulsed Doppler examinations
(i.e., color Doppler suggests high-grade stenosis but velocities are only moderately elevated), the
findings of both should be reviewed to resolve the discrepancy.
Common Carotid Artery (CCA) Waveforms
3 In the majority of cases, carotid stenosis or occlusion occurs in the proximal ICA at or just beyond the
carotid bifurcation. A normal ICA waveform reflects the low resistance of the cerebral circulation with
high flow at the end of the diastolic component of the waveform. In the presence of a distal ICA
occlusion resistance to flow increases and there is decreased flow in diastole (Fig. 87-2A,B). The
external carotid artery (ECA) supplies the relatively higher-resistance circulation of the scalp and face
and therefore has a low-end diastolic flow component (Fig. 87-2C). The common carotid artery
waveform reflects the fact that normally 80% of CCA flow is directed to the ICA. CCA end-diastolic flow
is therefore generally well above baseline and exceeds ECA diastolic flow (Fig. 87-2D). In the presence
of a very high-grade ICA stenosis or ICA occlusion, outflow is primarily through the higher-resistance
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external carotid circulation. The CCA waveform then takes on the high-flow resistance characteristics of
an ECA, with flow to zero, or nearly zero, in end diastole (Fig. 87-3).1 In addition, the PSV and the
overall flow velocity may be substantially lower than normal because of reduced carotid artery flow. By
observing these changes in the CCA, one can reliably predict the presence of high-grade stenosis or
occlusion of the ICA.
Figure 87-2. A: A normal internal carotid artery (ICA) waveform with high diastolic flow (white arrow) reflecting the low
resistance of the cerebral circulation. B: Absence of ICA diastolic flow (red arrow) indicates more distal occlusion or severe stenosis
of the extracranial or intracranial ICA. C: Normal external carotid artery waveform. The external carotid artery has low diastolic
flow reflecting the high resistance circulation of the scalp and face. D: Normal common carotid artery waveform. The common
carotid artery waveform has diastolic flow well above the baseline as the majority of flow is directed to the low resistance internal
carotid artery circulation.
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Figure 87-3. In a patient with internal carotid occlusion common carotid artery (CCA) diastolic flow approaches 0 (arrows) as CCA
flow is now routed to the high resistance external carotid circulation.
The CCA contralateral to an ICA stenosis or occlusion may demonstrate an increased flow velocity
with particular elevation of the velocity at the end of diastole; the so-called end-diastolic velocity
(EDV). These changes represent a compensatory increase in blood flow volume in the nonobstructed
ICA in response to reduced contribution to cerebral perfusion from the opposite high-grade stenotic or
occluded ICA. This compensatory hemodynamic change can be substantial and flow velocities may be
artificially elevated on the side with compensatory high-volume flow giving a false impression of the
presence of a stenosis or a higher degree of stenosis than is actually present.2
In the presence of a significant stenosis at the origin of a CCA or the inominate artery, the ipsilateral
CCA waveform may be dampened, with low overall peak systolic velocities (PSVs) and EDVs and a
slower rise to peak systole when compared with the contralateral CCA waveform and potentially
reverse flow in the ICA (Fig. 87-4A,B). The CCA flow changes seen with proximal stenosis are also
important in the diagnosis of ICA stenosis because the overall reduction in flow velocity may artificially
lower velocities in an ipsilateral ICA stenosis, leading to underestimation of the severity of ICA stenosis.
In some cases of proximal CCA or innominate artery stenosis, the stenotic lesion may not be accessible
to direct insonation by the duplex scanner. In such cases, a stenotic lesion can be suspected as the
ipsilateral CCA waveform will often exhibit poststenotic turbulence low in the neck, reflecting disturbed
flow distal to the more proximal stenosis.
ICA Waveforms
As noted above, the normal ICA spectral waveform is indicative of high flow in a low-resistant
circulation. The systolic upstroke is rapid, PSV is <125 cm/s, and flow is maintained throughout
diastole (Fig. 87-2A).3 In the absence of plaque there is generally a clear spectral window under the
outline of the spectral waveform as there is little turbulent flow. The presence of color shifts, indicating
high-velocity flow, and color mosaics, indicating poststenotic turbulence, aids in selecting potential
areas for examination with the pulsed Doppler.
Hemodynamic quantification of the severity of ICA stenosis is primarily achieved by analysis of
Doppler spectral waveforms and measurements of peak systolic and EDV or comparison of PSVs in the
ICA to those in the CCA just proximal to the carotid bifurcation, ICA/CCA ratio. As a stenosis develops,
the PSV first becomes elevated. PSV is the primary measure of stenosis severity. EDV lags behind,
relatively speaking, as stenosis severity progresses but rises rapidly as the stenosis becomes severe
(diameter reductions of ≥60%). Thus, elevation of EDV is a good marker for high-grade stenosis (Fig.
87-5).4 The ICA/CCA ratio is also a very important measure of stenosis severity.5 Because it is a ratio, it
compensates for abnormally high- and low-flow states that may skew the PSV and EDV upward or
downward.
To accurately measure flow velocity, the sample volume must be placed within the area of greatest
stenosis. Color flow imaging has demonstrated that the orientation of the stenotic jet within a stenosis is
frequently not along the longitudinal axis of the vessel. This finding has resulted in controversy with
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