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294
Ophthalmic artery
Circle of Willis
Right common carotid ar
ab
EF
Chapter 5 · Extracranial Cerebral Arteries
Supraorbital artery
Supratrochlear artery
Superficial temporal artery
5
Facial artery
Right vertebral artery
Right subclavian artery
tery
Aorta
Internal carotid artery External carotid artery Left common carotid
artery Left vertebral artery
Left subclavian artery
AB CD
c
. Fig. 5.1 a Diagram of the arteries supplying the brain (marked are the sites for taking representative measurements and documenting
results). b Variants resulting from elongation of the internal carotid artery (ICA) (shown for the left artery): A C-shaped course, B S-shaped course, C coiling, D double coiling, E kinking, F double kinking. c Color ow image showing severe kinking of the ICA (corresponding to E in b), indicated by a change in blood ow direction relative to the transducer (change from blue to red color coding). d Color ow image showing coiling of the ICA (corresponding to C in b), indicated by a change in color coding due to a change in ow direction relative to the transducer (blue– away from transducer/toward the heart; red– toward transducer)
e normal brachiocephalic trunk on the right has a length of 4–5 cm. It crosses under the brachiocephalic vein and, behind the right sternoclavicular joint, divides into the right subclavian artery and the right CCA.
e two CCAs course cranially accompanied by the vagus nerve and the internal jugular vein, which runs anterolateral to the carotids. e carotid bifurcation is usually located at the C4–C5 level, which roughly corresponds to the level of the thyroid cartilage, but there is wide interindividual variation (. Fig.5.2). Typically, the larger ICA arises from the postero­lateral aspect. It has a widened portion at its origin, called the carotid bulb. Unlike the external carotid artery (ECA), the ICA does not give o branches along its extracranial course.
d
Elongation of the ICA is associated with kinking (90°
angle between adjacent segments) or coiling (360° loop) (. Fig.5.1b–d). Carotid elongation develops with age. Arte­rial hypertension is considered a predisposing factor. Kink­ing or coiling results from the limited space available between the two points of xation, the bifurcation and the base of skull, but even severe kinking rarely causes hemodynami­cally signicant stenosis (see . Fig.5.51 (Atlas)).
e ECA arises from the anteromedial aspect of the ICA; in approx. 10% of individuals its point of origin is lateral or posterolateral. On its course, it rst gives o the superior thy­roid artery (STA) and then branches to supply the skin and extracranial organs (facial and temporal arteries).
trunk
5.1 · Normal Vascular Anatomy andImportant Variants
a
Carotid
ICA
295
5
V3
V2
b
c
. Fig. 5.2 Transducer positions for examination of the extracranial
carotid artery and vertebral artery (courses indicted by thick black lines). a Anterolateral transducer position (in front of sternocleidomas­toid muscle) for scanning the carotid artery. b Posterolateral position (behind sternocleidomastoid muscle) for scanning the carotid artery. c Transducer position for scanning the origin of the vertebral artery

5.1.2 Vertebral Arteries

e two vertebral arteries originate from the ipsilateral sub­clavian arteries at the C6 level and then pass through the transverse foramina of the corresponding vertebrae, thus
Superior
thyroid artery
CCA
Vertebral artery
Subclavian artery
. Fig. 5.3 Vascular anatomy of the extracranial cerebral arteries.
Transducer positions for imaging the carotid bifurcation and the extra­cranial vertebral artery segments (V0/1, V2, and V3)
V0/1
Thyrocervical
taking a partially intraosseous course on their way to the skull base. ey oen dier in caliber and may exhibit unilat­eral hypoplasia or aplasia, which is compensated for by con­tralateral hypertrophy. e le vertebral artery typically has a larger caliber and, in up to 4% of the population, arises directly from the aortic arch.
Somewhat distal to the vertebral artery, the thyrocervical trunk arises from the subclavian artery. e dierentiation is signicant in the duplex ultrasound examination. For a pre­cise description of the site of lesions, the vertebral artery is divided into ve segments (
. Fig.5.3):
5 e V0 segment, which is the origin of the vertebral
artery from the subclavian artery
5 e V1 segment, which extends from the origin to the
C6 transverse process
5 e V2 segment, which is the part coursing through the
cervical vertebral foramina
5 e V3 segment, which takes an arched course around
the atlas and is therefore also referred to as the atlas loop
5 e V4 segment, which is the intracranial part of the
vertebral artery.
e V2 segment of the vertebral artery communicates with branches of the thyrocervical trunk and the V3 segment with the occipital artery (ECA branch).
Anatomic variants of the vertebral artery render the diag­nosis more dicult. ese include unilateral hypoplasia, an origin directly from the aortic arch (5% for the le vertebral artery, no risk of subclavian steal syndrome), and an abnor­mal course (entry into the cervical spine below or sometimes above the C6 level in 10% of individuals).
296
Chapter 5 · Extracranial Cerebral Arteries
5.2 Examination Technique andProtocol
Sonomorphologically, the normal arterial wall is com-
posed of three layers: an inner layer depicted as a hyperechoic
Given their supercial location, the cerebral arteries can be examined with a high-frequency transducer (5–7.5MHz or even 10MHz), yielding B-mode images with high spatial resolution. e ultrasound examination is performed with the patient in the supine position and the head slightly hyperextended. While some examiners prefer to sit to the right of the patient, it is recommended that the examiner sit at the patient’s head, from were all transducer positions
5
(anterolateral, posterolateral) can be reached with little movement and without exerting undue pressure because his or her elbow can rest on the edge of the couch (. Fig.5.2). is is important for continuously evaluating the course of the carotid artery and for performing the temporal artery tap maneuver to identify the ECA and dierentiate it from the ICA (. Fig. 5.6). e course of the arteries and the carotid bifurcation are identied in the transverse plane, while the Doppler waveform is sampled longitudinally. As in the ultrasound examination of other body regions, the le of the screen is superior and the right is inferior.
line next to the lumen; a middle zone seen as a somewhat broader, hypoechoic layer; and an outer layer of slightly higher echogenicity, which is poorly demarcated from the perivascular fatty tissue. Since ultrasound does not visualize tissues or tissue layers directly but rather the echoes reected by interfaces between zones of dierent acoustic impedance, the three layers seen do not exactly match the three anatomic wall layers– the intima, media, and adventitia. e intima and media are sonographically indistinguishable, which is why it is not possible to evaluate the intima alone. It is there­fore common practice to measure the thickness of the intima–media complex instead.
e sonographic
thickness of the intima–media complex
is used as an early indicator of subclinical atherosclerosis and a measure of therapeutic outcome in interventional studies (e.g., to monitor statin therapy). It is therefore desirable that a standardized method for measuring carotid intima–media thickness (IMT) be used to minimize interobserver variability. A perpendicular angle of incidence ensures optimal evalua­tion of the vessel wall, which is the case if the target vessel courses parallel to the skin surface. If the angle is smaller, the examiner should move the transducer back and forth or rotate

5.2.1 Carotid Arteries

it slightly to ensure that the wall is evaluated in a plane show-
ing the maximum vessel diameter. IMT is measured in the far e examination begins by obtaining a survey of the carotid bifurcation in transverse orientation to determine the loca­tion and course of the internal carotid artery (ICA) and external carotid artery (ECA) in relation to each other. e following variants may be encountered:
5 In approx. 90% of the population, the ICA courses
posterolateral to the ECA.
5 In approx. 10% of individuals, the ICA is seen at the
same level and medial to the ECA.
5 In rare cases, the ICA is located anterior to the ECA.
wall of the CCA to exploit the blood-lled lumen as an acous-
tic window for optimal visualization of the two echogenic lines
demarcating the intimal and medial layers. e leading-edge
method (see
7 Sect. 1.1.2.4 and . Fig.5.5) is recommended to
minimize blooming artifacts (which appear at boundaries
with a large mismatch in acoustic impedance). Serial IMT
measurements should always be performed at the same site;
most investigators prefer the far wall 2–3cm proximal to the
carotid bifurcation. Use of a high-frequency transducer (>
10MHz) is recommended for evaluation of the wall as axial
resolution and measurement accuracy increase with trans­For Doppler angle correction and precise identication of stenosis or plaque, the examiner must move the transducer around to obtain a view depicting the carotid bifurcation as a tuning fork. ere are three standardized approaches for lon­gitudinal imaging:
5 Positioning of the transducer between the larynx and
sternocleidomastoid muscle for sagittal anteroposterior sections (. Fig.5.2a)
5 Lateral approach through the sternocleidomastoid
muscle
5 Posterolateral approach with the transducer posterior to
the sternocleidomastoid muscle (. Fig.5.2b)
ducer frequency (see . Table 1.2). Note, however, that
although it is technically feasible, dierentiation of structures
smaller than 0.01mm is beyond the resolution capacity of the
human eye (and may introduce measurement errors, bloom-
ing, etc.). Finally, it is recommended that the measurement of
IMT be performed at end diastole to minimize variations
through the cardiac cycle (Meyer and Strobel 2008).
No agreement exists regarding the need for detailed sonomorphologic characterization of plaque in routine clini­cal examination. While most patients with over 70% stenosis (according to ECST criteria, which corresponds to 50% ste­nosis according to NASCET criteria) are candidates for sur­gery based on this degree of stenosis alone, plaque
e posterolateral transducer position will enable good visu­alization of the bifurcation in most patients whose ICA fol­lows a normal course. In this position the ICA is depicted near the transducer.
B-mode ultrasound is used for preliminary exploration of carotid artery anatomy and for obtaining initial information on the vessel wall in transverse orientation and in the longi­tudinal views presented above (. Fig.5.4).
morphology becomes relevant for therapeutic decisions in patients with 60–70% stenosis and in patients with asymp­tomatic high-grade stenosis.
e morphologic evaluation of the vessel wall and plaque is followed by spectral Doppler measurement in the longitu­dinal plane. Color duplex imaging can provide clues regard­ing steno-occlusive lesions: stenosis is suggested by aliasing and an occlusion by the absence of color lling in the lumen.
ICA
a
5.2 · Examination Technique andProtocol
297
5
ICA
ECA
CCA
ECA
ICA
ECA
ICA
STA
STA
CCA
ICA
ICA
CCA
AS
AS
1
b
2
c
. Fig. 5.4 a Diagrams illustrating the ultrasound examination of the carotid bifurcation. The leftmost drawing illustrates the sites of transverse
examination for an overview and identication of the carotid arteries. The second drawing illustrates the posterolateral transducer position, which usually depicts the carotid bifurcation as a tuning fork with the internal carotid artery (ICA), which runs posteriorly, appearing closer to the transducer and the external carotid artery (ECA) appearing farther away from it. Often, this transducer position allows sonoanatomic identi­cation of the ICA by demonstrating its wider bulb and also of the ECA by visualizing the superior thyroid artery (STA) arising from it; this position also enables evaluation of plaque morphology. The third drawing illustrates the anterior transducer position, which is used for plaque evaluation or spectral Doppler interrogation in cases where acoustic shadowing due to calcied plaque impairs imaging in the posterolateral position. b Diagram illustrating how posterior acoustic shadowing (AS) obscuring the lumen can be circumvented by rotating the transducer from posi­tion 1 (e.g., posterolateral position) to position 2 (e.g., anterior position) to enable evaluation of plaque morphology/surface and assessment of stenosis in the presence of calcied plaque. Position 2, unlike position 1, will also allow spectral Doppler imaging. The drawings illustrate how even a small, calcied plaque can impair evaluation of the vascular lumen if the vessel is examined in only one plane. c The left image (obtained with the transducer in a posterolateral position) illustrates how acoustic shadowing from calcied plaque in the carotid bulb completely eliminates ow signals from the ICA and ECA and obscures vascular structures in the B-mode. The second image, obtained after changing the transducer position to circumvent the sickle-shaped calcied plaque, allows evaluation of both the bulb and the ICA.There are no signs of hemodynamically relevant luminal narrowing. No ow acceleration is demonstrated by color duplex or spectral Doppler, ruling out relevant stenosis caused by the plaque
Moreover, the color duplex mode can facilitate identication of the course of a kinked or coiled ICA.
While color duplex imaging is optional for initial orienta­tion, angle-corrected Doppler waveforms in the longitudinal plane must be obtained for quantication of blood ow veloc­ity in the CCA, ICA, and ECA (. Table5.2). Spectral Doppler sampling should be performed in the ICA at short intervals. Use of a larger sample volume will oen enable continuous examination of the CCA and ICA in the duplex mode, espe­cially from the posterolateral approach. In this way, a continu­ous spectrum can be obtained and analyzed throughout the CCA and ICA, similar as with CW Doppler ultrasound. e
ECA is scanned only at its origin for dierentiation from the ICA and for the identication of possible stenosis.
e posterolateral transducer position is usually superior to the anterior position for spectral Doppler interrogation. From this transducer position, the bifurcation appears as a tuning fork with the ICA close to the transducer, and the CCA, the bulb, and long segments of the ICA and ECA can be evaluated in a single view. is facilitates angle correction, and the intervening so tissue improves visualization. How­ever, when the ICA is kinked or coiled, dierent scanning planes are necessary to identify a long enough straight seg­ment of the artery for angle correction.
298
ternal bright line
method
Chapter 5 · Extracranial Cerebral Arteries
To minimize errors in flow velocity measurement in
the ICA angle of < 60°
, the examiner should try to achieve a Doppler
(see . Fig. 1.23 and 7 Sect. 1.1.4.6). is requires selection of an adequate transducer. When a linear transducer with beam steering is used, even maximum cra­nial deection (technically limited to 20°) gives an angle of insonation no smaller than 70° for an artery coursing paral­lel to the skin surface (90°20°=70°). While a linear trans­ducer provides the best resolution for morphologic assessment of the vessel wall in the B-mode, a curved-array
5
transducer with a small footprint aords greater exibility in achieving an adequate angle for spectral Doppler inter­rogation along the tortuous course of the ICA. Curved-
array transducers are also superior to linear transducers in patients with short necks and in interrogating vessel seg­ments near the base of the skull. e view is optimal when the artery is depicted with parallel walls along the entire width of the monitor. In the 10% of individuals with a medial origin of the ICA, the tuning fork view of the bifur­cation is occasionally obtained when an anterior approach is used. If this is not possible, the transducer is rst tilted for selective visualization of the origin of the ECA and then tilted laterally for visualization of the origin of the ICA.
Longitudinally, the ICA is continuously followed to the
base of the skull, for which the posterolateral transducer
position
works best in most patients. Dierent approaches may be required to follow a coiled or kinked ICA and to iden­tify concomitant stenosis. Whenever the duplex ndings are inconclusive, a Doppler waveform should be obtained.
A lower-frequency (5 MHz) curved-array transducer
Ex
Internal bright line
(with a small footprint) should be used in patients with poor insonation conditions or for evaluation of the deeper por­tions of the extracranial ICA near the base of the skull.
When
IMT using leading-edge
and pulse repetition frequency (PRF) must be chosen so as to ensure good color lling of the vessel lumen without aliasing (color reversal from red to blue or vice versa). Transverse
color-coded duplex ultrasound is used, the gain
views are obtained with the transducer slightly tilted to achieve
. Fig. 5.5 Measurement of intima–media thickness (IMT). The intima
and media cannot be distinguished sonographically. The rst bright echo is the interface between the blood and the intima (interface between tissues of dierent acoustic impedance) with the second bright echo representing the border between the adventitia and the perivascular connective tissue. The wall layer between these two reec­tions is the intima–media complex. Its thickness is measured using the leading-edge method (see . Figs. 1.28 and 5.52 (Atlas))
an adequate Doppler angle. With adequate instrument set­tings, changes in the color ow pattern suggest pathology, which must then be conrmed by spectral Doppler analysis.
Calcied plaques completely reect the ultrasound
pulse and thus cast acoustic shadows, impairing both color duplex and conventional duplex as well as B-mode imaging. Color coding is most severely aected by acoustic shadow-
. Table 5.2 Ultrasound examination of the carotid arteries (sequence of steps)
Ultrasound method Purpose
B-mode: transverse plane Course, possibly dierentiation of ICA/ECA (STA origin,
vessel diameter)
B-mode: longitudinal plane (anterior and posterolateral transducer positions)
Color duplex (optional): posterolateral transducer position, anterior approach as needed
Spectral Doppler (PW Doppler): in longitudinal orientation (never transverse plane); posterolateral or anterior transducer position (angle <60°). Adequate Doppler angle may be easier to achieve using a curved array transducer with a small radius (can be tilted)
Additional B-mode examination with high-resolution transducer (linear array) for evaluation of plaque morphology: patients with 60–70% ICA stenosis by ECST criteria/local degree (equivalent to 40–50% NASCET stenosis)/stage II or 60–80% stenosis/stage I
Power mode, B-ow mode, or CEUS in selected patients Plaque ulcer, detailed evaluation of plaque surface
CEA carotid endarterectomy, CEUS contrast-enhanced ultrasound, ECA external carotid artery, ECST European Carotid Surgery Trial, GSM gray-scale median, ICA internal carotid artery, NASCET North American Symptomatic Carotid Endarterectomy Trial, STA superior thyroid artery, PW pulsed wave
Search for plaque, plaque characterization, dierentiation of nonatherosclerotic vascular disease
Course (kinking, coiling), initial clues regarding the presence of stenosis (aliasing). Supplementary information when ICA/ ECA dierentiation is dicult (STA origin)
Conrmation of stenosis, stenosis grading Dierentiation of ICA and ECA (temporal artery tap) Indication for surgery (CEA)
Plaque morphology: echolucent/echogenic, homogeneous/ inhomogeneous, smooth/irregular surface; standardized analysis of echogenicity, e.g., GSM, may be used (indication for repair and type of repair)
5.2 · Examination Technique andProtocol
. Table 5.3 Criteria for dierentiating the ICA and ECA
Criterion Reliability
ICA posterolateral to ECA This is the case in only 90% of individuals, while 10% have a medial
ICA origin
Less pulsatile ow (large diastolic ow component) in ICA compared to ECA
Larger lumen of ICA, especially of bulb Fairly reliable under normal conditions but not valid in the presence
Doppler waveform from ECA shows pulsation transmitted upon intermittent tapping of temporal artery
ECA gives o arterial branches (1st branch: STA) and ICA does not Reliable if origins can be identied but often impaired by multiple
ECA external carotid artery, ICA internal carotid artery, STA superior thyroid artery
Reliable under normal conditions; patients with ECA stenosis will also have a large diastolic ow component in the ECA waveform
of multiple (calcied) plaques
Reliable
plaques with acoustic scattering and shadowing
299
5
ing. In such situations, the pulsed Doppler, enabling focused application of a higher beam intensity with a high gain, will usually provide a Doppler waveform with a weak amplitude that still allows assessment of blood ow. If the calcication does not involve the entire inner circumference, the exam­iner can try and improve ow evaluation in the residual lumen by insonating the vessel from a dierent direction to obtain a view that depicts the calcied plaque on the wall away from the transducer (. Fig.5.4).
Under normal conditions, the ICA and ECA are easily dif-
ferentiated
on the basis of their sonoanatomic relationship, the demonstration of branches arising from the external but not from the internal carotid artery, and the widened bulb at the origin of the ICA.Compared with the ICA, the ECA has more pulsatile ow with a smaller diastolic component in the Doppler waveform. However, in patients with high-grade ste­nosis of the carotid bifurcation, acoustic scattering and shad­owing may impair B-mode evaluation, and the stenosis-related hemodynamic changes also aect the ow prole in the ECA in that diastolic ow increases and the waveform becomes less distinct from the ICA waveform. Internalization is also observed when the ECA is recruited as a collateral for an occluded ICA.In such cases, the examiner can use the tempo­ral tap sign to identify the ECA.e temporal tap maneuver involves rhythmical tapping of the temporal artery (anterior to the ear). e oscillations will be transmitted to the ECA and appear in the Doppler waveform from the ECA origin, especially in diastole (. Table5.3), regardless of whether the artery is normal or whether stenosis is present (. Fig.5.6). Weaker transmission will still be noted in the CCA, while the tap maneuver has no eect on the ICA waveform.

5.2.2 Vertebral Arteries

e vertebral artery can be examined by ultrasound from its origin to just before the atlas loop in the longitudinal plane from a lateral approach in the supine patient. It is not possible to scan the entire length of the vertebral artery because seg-
ments of it are obscured by the transverse processes of the cervical vertebrae. e origin from the subclavian artery is best appreciated using a curved-array transducer with a small radius, while the remainder can also be scanned with a linear probe, ideally with a frequency of 5–7.5MHz. e
ment
with its accompanying vein is easiest to identify
V2 seg-
between the acoustic shadows from the transverse processes. Because the paired vertebral arteries are linked via several pathways, steno-occlusive disease in one branch has dierent hemodynamic eects than an obstruction in an unpaired, organ-supplying artery. In terms of ow physiology, the ver­tebral circulation constitutes a parallel circuit of vascular resistances. Kirchho’s second law states that, in a parallel circuit, current is inversely proportional to resistance. According to the Hagen-Poiseuille law, a small change in vas­cular diameter (hyperplastic vertebral artery, atherosclerotic stenosis, or luminal narrowing caused by dissection) will markedly reduce ow in the artery because the eect that vascular diameter has on ow in the equation is raised to the fourth power. Because the vertebral arteries are paired, 60–70% stenosis will reduce blood ow by 90–95%, and the contralateral artery largely maintains blood supply to the posterior circulation, spontaneous thrombosis of the verte­bral artery is quite common when higher-grade stenosis is present.
Stenosis at the origin of the vertebral artery may be di­cult to identify and evaluate, especially in obese patients with a short neck. In addition, marked tortuosity of the vertebral artery at its origin from the subclavian artery can impair Doppler angle correction. Tortuosity may further contribute to poor ow, but this is not uncommon at the origin of the vertebral artery and does not necessarily mean that stenosis is present. Identication of vertebral stenosis by color duplex imaging is easier and more reliable in the V2 segment, but higher-grade stenosis of the V2 segment is rare, and luminal narrowing of this segment is more commonly caused by dis­section. e technically less challenging examination of the V2 segment is sucient in patients with suspected subclavian steal syndrome. In general, however, the V0/V1 segment
300
bc
de
Chapter 5 · Extracranial Cerebral Arteries
. Fig. 5.6 Duplex ultrasound
examination of the carotid bifurcation and dierentiation of the internal carotid artery (ICA) and external carotid artery (ECA). Flow in the ECA is more pulsatile and is modulated by the signal transmitted upon rhythmical tap­ping of the temporal artery (a I and b), especially during diastole (X). The oscillations resulting from the temporal tap do not aect
5
the waveform from the ICA (a I and c). When stenosis is present, dierentiation between the ICA and ECA on the basis of pulsatility is dicult, and plaque may impair identication of the superior thyroid artery (A.T.S) arising from the ECA or of the wider bulb of the ICA.The temporal artery tap, however, still provides a clearcut dierentiation, as the oscillation is not transmitted into a stenotic ICA (a II and d). The Doppler waveform from a stenotic ECA (a III and e) shows similar pulsatil­ity of ow as the waveform from a stenotic ICA, and transmission of the oscillations produced by temporal tapping (X) into the ECA allows dierentiation of the two arteries in this situation
a
III III
should be examined because it is the preferred site of verte­bral artery pathology (curved-array transducers are more suitable than linear transducers).
To evaluate the vertebral arteries, the examiner can pro-
ceed in one of two ways: in slender patients with good
insonation conditions, the vertebral artery is its origin from the subclavian artery
(. Figs.5.2c and 5.3),
identied at
where stenosis can be ruled out by obtaining a Doppler wave­form in longitudinal orientation. In patients with a poor acoustic window or complex sonoanatomy, the examiner rst locates the CCA longitudinally to then identify the ver­tebral artery between the transverse processes of the cervical vertebrae; this is accomplished by slight posterolateral move­ment and medial angulation of the transducer (see . Fig.5.87 (Atlas)). Acoustic shadowing from the transverse processes at regular intervals precludes complete evaluation of the V2 segment (. Fig.5.7). From the V2 segment, the examiner can then follow the artery downward to identify its origin. e atlas loop will come into view when the transducer is moved cranially and angled (. Fig.5.87 (Atlas)).
In the color duplex mode, the examiner follows the
length of the vertebral artery to its origin, looking for luminal narrowing or aliasing. Any luminal narrowing should be quantied by obtaining a Doppler waveform.
A full evaluation includes measurement of the vertebral artery diameter and comparison with its counterpart in order to dierentiate a pathology. Arterial diameters are determined in the V2 seg­ment (B-mode).
When a patient with trauma and suspected vertebral
artery dissection
examination should be on the segment running through the cervical vertebral foramina (V2 segment). When looking for
atherosclerotic vertebral artery stenosis, on the other hand, it
is the origin from the subclavian artery which requires close attention. To locate the origin, it may be necessary to rst iden­tify the subclavian artery in the cervical triangle and then use the color mode to identify the vertebral origin (V0/V1) at the cra­nial edge of the subclavian artery. Because of its tortuous course at the origin, the vertebral artery may easily move out of the scan plane. e vertebral artery origin must not be confused with the thyrocervical trunk, which arises more distally and is easier to visualize. e two can be distinguished from one another by rhythmically tapping the vertebral artery below the mastoid (atlas loop); this signal is transmitted to the vertebral artery and modulates the Doppler waveform from the vertebral artery ori­gin (see procedure described for identication of the ECA using the temporal tap at the end of 7 Sect. 5.2.1 and . Fig.5.7b).
hypoplastic artery from other vascular
is examined, the focus of the ultrasound
5.4 · Normal Findings
a
301

5.3 Documentation

Normal ndings should be documented in longitudinal views (B-mode) of both CCAs, ICAs, and ECAs, vertebral arteries (V1 or V2 segment), and subclavian arteries with the corresponding Doppler waveforms (including angle­corrected ow velocity measurements) (see sites for taking representative measurements in . Fig.5.1a). Abnormal nd­ings are documented in additional B-mode images and the corresponding Doppler waveforms obtained from the sites of pathology in longitudinal orientation. Systolic and end­diastolic ow velocities obtained with angle correction must reect the degree of stenosis. Finally, the report should con­tain information on the localization of stenotic and nonste­notic plaques (B-mode images for documentation) and a description of plaque morphology.

5.4 Normal Findings

5.4.1 Carotid Arteries

5
b
. Fig. 5.7 a Image showing the V2 segment of the vertebral artery
(A) between the vertebral processes (WK, acoustic shadowing). A segment of the vertebral vein (blue) is also seen (SA=mirror arti­fact). b Vertebral artery (A.VERT) at its origin (V0/V1 segment) from the subclavian artery (A.S.) with a monophasic waveform typical of low-resistance flow. The peak systolic velocity (PSV) is 72cm/s, and the end-diastolic velocity (EDV) is 18cm/s. Oscillations generated by tapping the vertebral artery below the mastoid are transmitted to the vertebral artery and appear in the waveform (left portion)
In the vertebral artery, spectral Doppler evaluation is also important to determine the direction of blood ow. In patients with normal vertebral artery ow at rest and sus­pected exercise-induced subclavian steal syndrome due to subclavian artery stenosis or occlusion, the increased demand during muscle activity can be reproduced during the exami­nation. With continuous spectral Doppler recording in the vertebral artery, a blood pressure cu around the upper arm is inated to over 250mmHg and then released aer 3–5min to induce reactive hyperemia in the arm. If high-grade steno­sis or occlusion of the proximal subclavian artery with sub­clavian steal and vertebrovertebral crossover is present, this maneuver will induce ow reversal in the ipsilateral vertebral artery and an increase in ow velocity in the contralateral vertebral artery.
e common carotid artery (CCA) has a constant luminal diameter of approx. 7mm. Flow is pulsatile with a large dia­stolic component. e internal carotid artery (ICA) has a peak systolic velocity (PSV) ranging from 60 to 100cm/s (. Table5.4). At its origin, the wider lumen (bulb) and vessel branching lead to eddy currents even under normal condi­tions. PSV is lower in the bulb, and ow separation may lead to retrograde ow on the side opposite the external carotid artery (ECA), seen as color reversal in color duplex images (see . Figs.5.49 (Atlas) and . 1.45b).
e normal thickness of the intima–media complex measured in the B-mode (from the lumen–intima interface, the rst bright line, to the media-adventitia interface, the sec­ond bright line) is 0.5–0.6mm and increases somewhat with age.
Supplying the brain, the ICA has low-resistance ow with a
Doppler waveform that is characterized by a steep systolic
upslope followed by monophasic ow with a fairly large dia-
. Table 5.4 Average blood ow velocities and diameters of
the extracranial cerebral arteries (meta-analysis)
Artery PSV (cm/s) EDV (cm/s) D (mm)
CCA 50–80 15–30 6.0–7.5
ICA 60–90 20–40 4–6
ECA 60–100 10–20 3.5–4.5
Vertebral artery 20–70 5–35 3–5
CCA common carotid artery, D diameter, ECA external carotid
artery, EDV end-diastolic velocity, ICA internal carotid artery, PSV
peak systolic velocity
302
Chapter 5 · Extracranial Cerebral Arteries
. Table 5.5 Causes of abnormal pulsatility (Doppler
waveform) in the extracranial cerebral arteries
Change Cause
Reduced pulsatility High-grade proximal ow obstruction
AV stula or angioma in distal segment Hyperperfusion (e.g., in hyperthyroidism) Aortic stenosis
Increased pulsatility High-grade distal ow obstruction
Increased intracranial pressure
5
AV arteriovenous
Severe cerebral microangiopathy Aortic insuciency Low heart rate
5.5 Clinical Role ofDuplex Ultrasound

5.5.1 Carotid Arteries

e carotid bifurcation is the preferred site of carotid artery stenosis. An important underlying mechanism is turbulent ow with increased wall tension resulting from the abrupt change in diameter in the bulb and ow division in the bifur­cation. is mechanism and shear forces cause higher inti­mal stress in the carotid bulb. As a result, carotid plaque tends to develop along the outer wall opposite the ow divider (. Fig. 5.10). is stressful hemodynamic situation with ow division is also visible on color duplex ultrasound (. Figs. 1.44b and 5.49 (Atlas)).
e aim of sonographic assessment of the extracranial cerebral arteries is to prevent cerebral infarction with its harmful sequelae and permanent decits (. Fig.5.8).
stolic component. Conversely, ow in the ECA is more pulsatile with a smaller diastolic component. e common carotid artery, supplying both territories, has a mixed waveform. As in all other vascular territories, pulsatility in the carotid system is determined by peripheral resistance and vessel elasticity and therefore increases with age (
. Table5.5).
Several duplex ultrasound parameters can contribute to estimating a patient’s cardiovascular risk. Besides intima­media thickness (IMT) measured in the common carotid artery (CCA), the resistive index (Pourcelot index) deter­mined in the internal carotid artery (ICA) is gaining signi­cance in the assessment of early stages of atherosclerosis and as a predictor of cardiovascular morbidity and mortality. A study investigating RI progression from a baseline RI of

5.4.2 Vertebral Arteries

0.66 ±0.08 found a continuous increase in cardiovascular events as the RI increased (Utho etal. 2008).
Published data on blood ow velocities in the vertebral arter­ies vary widely from 19 to 98cm/s for peak systolic velocity (PSV) and from 6 to 30 cm/s for end-diastolic velocity (EDV). e resistance index (RI) ranges from 0.62 to 0.75 (Tratting et al. 1992). Assessment of the vertebral artery, especially at its origin, is impaired by caliber variation and the occurrence of congenital hypoplasia. At the same time, evaluation of the origin is important because it is the most common site of stenosis.
e normal diameter of the vertebral artery is 3–5mm but it is common for one vertebral artery to be larger than the other, resulting in right–le diameter dierences of over 2mm.
In case of lateral dierences in ow velocity and poor visualization of the origin, the examiner must dierentiate a proximal stenosis from hypoplasia.
e following criteria suggest hypoplasia:
5 Unilateral caliber reduction (luminal diameter typically
<2cm)
5 Contralateral hyperplasia (luminal diameter typically
>3.5) and side dierence typically >2mm
5 Flow velocity (PSV) lower than on the contralateral side 5 Unchanged waveform; however, ow is oen more
pulsatile with a reduced diastolic ow component (see
. Figs.5.87 (Atlas), 5.39, and 5.40).
While diagnostic ultrasound and treatment of peripheral vessels are symptom-oriented, the purpose of carotid artery evaluation is prognosis-oriented in that it aims at identifying patients at risk for stroke and initiating adequate preventive measures in these high-risk patients (. Tables 5.6 and 5.7). Duplex ultrasound examinations of the extracranial cerebral arteries are performed for the following reasons:
5 Identication of the underlying cause in patients with a
transient ischemic attack (TIA), prolonged reversible
ischemic neurologic decit (PRIND), or stroke (addi-
tional CT and echocardiography)
5 Workup of asymptomatic carotid artery stenosis
suspected on clinical grounds (auscultation, risk factors,
atherosclerosis with coronary heart disease or pelvic
artery stenosis)
5 Indication for operative treatment of carotid stenosis:
plaque morphology, hemodynamic stenosis grading
5 Workup of a pulsatile neck mass (aneurysm, transmis-
sion of pulsation through extravascular tumor)
5 Workup of traumatic intimal dissection 5 Diagnostic evaluation for inammatory disease (Takaya-
su’s arteritis, temporal arteritis)
5 Workup of disturbed perfusion in the posterior circula-
tion (vertebral artery stenosis, subclavian steal syndrome
due to subclavian artery occlusion)
5 Diagnosis of brain death
In contrast, stenosis is indicated by less pulsatile ow, a smaller systolic component, and more pronounced diastolic ow in the waveform obtained downstream of the lesion.
5 Follow-up aer surgical repair (carotid endarterectomy)
or PTA with stenting (immediately aer intervention,
then at 6-month intervals).
5.5 · Clinical Role ofDuplex Ultrasound
StageClinical presentation/symptoms
303
5
Stage I
Asymptomatic carotid artery stenosis
IA Asymptomatic stenosis without high-grade contralateral carotid
stenosis or contralateral occlusion
IB Asymptomatic stenosis with high-grade contralateral carotid
stenosis or contralateral occlusion
Stage II
Symptomatic carotid stenosis: ipsilateral transient deficit within the preceding 6 months
IIA Amaurosis fugax
IIB
Hemispheric symptoms reversible within 24 h (TIA)
Stage III Indications for emergency carotid TEA
IIIA Crescendo TIA
IIIB Acute/Progressive stroke
Stage IV
Symptomatic carotid stenosis: ipsilateral stroke within the preceding 6 months
Rankin 0Stroke with fully reversible neurologic deficits (duration > 24h,
PRIND)
Rankin 1Stroke without significant disability
Rankin 2Mild stroke with slight disability and/or slight aphasia
Rankin 3Moderate stroke with moderate disability with preserved ability to
walk and/or moderately severe aphasia
Rankin 4Severe stroke, unable to walk without assistance, and/or complete
aphasia
Rankin 5Stroke with severe disability: patient bedridden or requiring
wheelchair (exceptional indication)
Severity
III A
Duration
III B
. Fig. 5.8 Classication of extracranial carotid artery stenosis. Higher-grade carotid stenosis 50% (by NASCET criteria) or 70% (by ECST criteria)
based on angiography or ultrasound. Graphic representation of the duration (horizontal axis) and severity (vertical axis) of the respective neurologic de­cits. PRIND prolonged reversible ischemic neurologic decit, TEA thromboendarterectomy, TIA transient ischemic attack
. Table 5.6 Risk of stroke in surgically versus medically managed patients with carotid artery stenosis. Perioperative risk (stroke/death)
and absolute risk reduction (ARR) of ipsilateral stroke over a 5-year period in patients with symptomatic carotid artery stenosis
Degree of carotid stenosis (%)
< 30 6.7 12 10.0 2.2 0.05
30–49 8.4 15 18.2 3.2 0.6 31
50–69 8.4 14 18.6 4.6 0.04 22
70–99 6.2 10 26.0 15.9 < 0.001 6
ECST European Carotid Surgery Trial, NASCET North American Symptomatic Carotid Endarterectomy Trial, NNT number needed to treat
a
Summary of results obtained in 6029 randomized patients from the ECST (n=3018), the VA (Veterans Aairs) trial 309 (n=189), and the
NASCET (n=2885)
b
All strokes/deaths occurring within 30days; a total of 3248 patients were operated on
c
Including perioperative stroke/death
Operative riskb (%) Risk of stroke ARRc (%) P NNT
Surgical (%) Medical (%)
a