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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5760_Библиотеки_им_академика_М_И_Перельмана.pdf
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Common iliac artery stenosis
)
2.1 · Pelvic andLeg Arteries
63
2
(PTA and stent) Internal iliac artery stenosis
External iliac artery stenosis (PTA) Common femoral artery stenosis (TEA
Stenosis at profunda femoris origin (TEA for stages II, III/no preop. angiography necessary)
Profunda femoris artery
Superficial femoral artery stenosis (conservative/( PTA))
Superficial femoral artery occlusion (bypass for stages (llb), Ill, IV)
Entry site stenosis
Popliteal artery stenosis/occlusion (PTA, bypass)
Lower leg artery occlusion (cons.)
. Fig. 2.8 Diagram of atherosclerotic stenotic lesions that can be
diagnosed by duplex imaging and initial treatment based on duplex ndings (dierent therapeutic management may be required based on the clinical stage or in patients with multilevel involvement)
arteries is not necessary in these cases as the primary surgical approach is not aected by occlusions distal to the popliteal artery or trifurcation. Outow to the foot may be evaluated along with intraoperative completion angiography if this information is deemed necessary for patients who are likely to require additional surgical or interventional measures.
In the following two settings, the decision to perform
thromboendarterectomy (TEA)
can also be made without additional imaging tests: (1) if duplex ultrasound demon­strates stenosis of the common femoral artery or profunda femoris origin – with occlusion of the supercial femoral artery– and if the examination also rules out occlusion in the pelvic territory, or (2) if, in case of occlusion of the supercial femoral artery, the duplex examination conrms resupply of the P1 popliteal segment without major popliteal artery nar­rowing. In these cases, TEA at the inguinal level is the rst therapeutic step, with further measures depending on the clinical outcome. is therapeutic approach is independent of the status of the arteries below the knee, and the benet of using preoperative anteroposterior angiography to evaluate collateral circulation in the thigh in cases of supercial femo­ral artery occlusion is disputed.
Only the main branch of the profunda femoris artery pro­vides relevant collateral ow in patients with an occluded super­cial femoral artery. is branch runs almost parallel to the latter and is the only artery that needs to be evaluated with sonography as it is only here that a stenosis compromising collateral function would require surgical repair (see . Fig.2.60 (Atlas)).
e author’s experience in 180 patients conrms that duplex sonography is a reliable preoperative imaging modality both for identifying patients with stenosis of the femoral bifur­cation or arterial occlusion above the knee who require sur­gery and for planning the surgical procedure. In this patient population, the sonographic examination allowed adequate evaluation of the pelvic arteries in 95% of the patients; in these cases, ultrasound correctly diagnosed 96% of all pelvic artery stenoses and occlusions, and the therapeutic approach was modied accordingly (e.g., pelvic artery PTA). Overall, the sonographic ndings led to a correct therapeutic decision in 94% of the patients with clinically indicated vascular recon­struction of the iliacofemoropopliteal segment (PTA, TEA, bypass with preoperative planning) (see
. Table2.19).
A duplex ultrasound examination of the infrapopliteal arter­ies is time-consuming. Acoustic shadowing produced by calci­ed plaques or edema can impair detection and grading of stenosis in small arteries. is is especially problematic if indirect stenosis criteria (ow prole) do not apply because the patient has multilevel occlusive disease with proximal obstruction.
Several studies (Grassbaugh et al. 2003; Karacagil et al. 1996; Boström etal. 2002; Mazzariol etal. 2000) show duplex ultrasound to be highly accurate in localizing and grading steno-occlusive disease of the calf arteries and to enable reli­able planning of the surgical approach and
potential bypass target below the knee
identication of a
, with bypass patency rates similar to those in patients examined by preoperative angiography. e choice of the preoperative imaging modal­ity in patients with popliteal occlusion and involvement of the calf arteries in stage III and IV PAOD depends not only on the expected diagnostic information but also, and importantly, on the examiner’s skills and experience with duplex ultra­sound, the time available (see 7 Sect. 2.1.8), and the organiza­tion and workow in the department (in Germany, most duplex ultrasound examinations are performed by clinicians, in particular angiologists and vascular surgeons).
An exception to the restrictive use of diagnostic angiog­raphy is the examination of patients with long-standing dia­betes mellitus and secondary macro- and microangiopathy. Medial sclerosis in diabetics may preclude complete sonog­raphic evaluation of the calf arteries, and serial stenoses may thus be overlooked. Nevertheless, the identication of all macro- and microangiopathic lesions is still necessary for initiation of appropriate therapeutic measures.
hemodynamic eect of arterial stenosis is evaluated
e using hemodynamic parameters. Flow models and in vivo studies indicate that a reduction in arterial diameter of 50% or more becomes hemodynamically signicant and will cause an increase in peak systolic velocity (PSV). In higher­grade stenosis, peak end-diastolic velocity (EDV) is increased as well. e increase in PSV correlates with the degree of ste­nosis (see . Fig. 5.20).
In contrast to the carotid artery territory, B-mode evalua­tion of plaque morphology for estimating the risk of embo­lism has no role in the examination of the leg arteries. is is obvious given the diculties one faces in assessing the risk of embolism associated with carotid artery stenoses in B-mode sonography and the rare occurrence of interdigital artery
64
Chapter 2 · Extremity Arteries
embolism (blue toe). Nevertheless, one must be aware that, as in the carotid territory, the risk of embolism increases with the degree of stenosis and plaque thickness.
2
Determining the degree of stenosis from the vessel diame­ter and the residual perfused lumen using transverse color ow images is less reliable than hemodynamic grading based on spectral Doppler velocity measurement. e former is done only for preliminary orientation and is susceptible to artifacts caused by calcied plaques. Moreover, physical and technical limitations necessitate the wider spacing of color scan lines, and the interpolation which then becomes necessary oen overesti­mates the patent lumen and underestimates the stenosis.
e hemodynamic degree of stenosis determined by duplex ultrasound correlates better with its ischemic eects and with the patient’s clinical symptoms than the morphologic degree determined by imaging modalities such as angiogra­phy or MRI.Morphologic methods have inherent limitations resulting from the fact that the apparent luminal narrowing caused by an eccentric plaque changes with the imaging plane. ese limitations can only be minimized by evaluating all nor-
. Table 2.4 Duplex ultrasound criteria for arterial evaluation
Technique Criteria
B-mode Assessability
Anatomy (course, variants)
Vessel contour (aneurysm, stenosis)
Vessel wall changes (calcication, plaque, cysts)
Pulsation (axial, longitudinal)
Perivascular structures (hematoma, abscess, tumor, other compressing structures)
Doppler Demonstration of ow
Flow direction
Flow pattern (laminar, turbulent)
Flow prole (monophasic/triphasic)
Flow velocity
mal and diseased arterial segments in two or three planes. Another drawback of morphologic stenosis grading is the fail­ure to adequately account for plaque conguration and how it aects the hemodynamic relevance of a stenosis. A concentric plaque causing the same diameter reduction as an eccentric
2.1.5 Normal Duplex Ultrasound ofPelvic
andLeg Arteries
plaque has more marked hemodynamic eects because the decrease in cross-sectional area is greater (see
. Fig.2.17d).
Flow in the limb arteries is pulsatile and nearly laminar, due to the high peripheral resistance, which is reected in the Doppler waveform by a narrow bandwidth with a clear sys-
2.1.4 Interpretation andDocumentation
tolic window. e typical triphasic waveform is characterized
by a steep systolic upslope and rapid return to baseline, fol­Minimum documentation of a duplex ultrasound examina­tion of the legs consists of longitudinal B-mode images and angle-corrected spectral Doppler waveforms from the repre­sentative sites, which are the common femoral artery, the origins of the deep and supercial femoral arteries, and the popliteal artery (P1 and P3 segments). In patients in whom the arterial status below the knee is clinically relevant, the documentation is supplemented by B-mode images and Doppler waveforms from the anterior and posterior tibial arteries proximally and at the level of the ankle. If the nd­ings at these sites are inconclusive or if a specic clinical question has to be answered, additional images and Doppler waveforms from the common and external iliac arteries, pos­sibly the below-knee arteries as well, are documented. In addition, steno-occlusive lesions are documented with longi­tudinal images and waveforms. Intra- and peristenotic spec­tral Doppler waveforms are analyzed (
. Table2.9) to estimate
the degree of stenosis based on pre- and intrastenotic peak systolic velocity (PSV) and the poststenotic ow pattern (from preserved triphasic prole to monophasic waveform). An aneurysm must be documented in two planes and its diameter measured in the transverse plane. Partial thrombo­sis, if present, should be reported as well. Documentation of additional color ow images (transverse view of aneurysm, longitudinal view of stenosis) may be helpful but is optional.
e report should describe the morphologic changes and
Doppler results on which the diagnosis is based (. Table2.4).
lowed by a short early diastolic reversal of ow and subse-
quent diastolic forward ow varying in magnitude and
duration with the body region supplied (. Fig. 1.43). e
brief diastolic ow reversal is due to high peripheral resis-
tance (7 Sect. 1.2.2).
e character of the Doppler waveform varies with the elasticity of the vessel wall and peripheral resistance and is inuenced by systemic and local hypercirculatory eects (fever, hyperthyroidism, phlegmon). e amount of ow per­sisting during diastole is subject to physiologic factors and pathologic changes including sympathetic tone, wall elastic­ity, compliance of the aorta, and heart rate. In addition, the waveform shape is inuenced by the ratio of skin to muscle supply, which is why diastolic ow is higher in the profunda femoris than in the supercial femoral artery (. Fig.2.9).
e main factors inuencing the ow prole (Doppler waveform) can be summarized as follows:
5 Wall elasticity (atherosclerosis, medial sclerosis) 5 Peripheral resistance:
5 Physiologic:
Ȥ Muscle activity
5 Abnormal:
Ȥ Inammation, phlegmon (stage IV PAOD)
(. Fig.2.9c) Ȥ Hypercirculation Ȥ Medications Ȥ Postocclusive vasodilatation
abc
2.1 · Pelvic andLeg Arteries
65
. Fig. 2.9 a Peak systolic velocity (PSV) in the leg arteries decreases toward the periphery, but the triphasic ow pattern persists. The example
shows normal blood ow in the bular artery with the corresponding triphasic waveform. The artery has a diameter of 2.7mm. b Sonoanatomy of the anterior tibial artery origin. The popliteal artery gives o the anterior tibial artery, which courses anteriorly to pierce the interosseous mem­brane, in front of which it descends, initially taking a course close to the bula. The image shows the anterior tibial artery scanned from a posterior approach (transducer in popliteal fossa), with ow displayed in blue (ow away from transducer), below its origin from the popliteal artery (A.POP) as it pierces the interosseous membrane (hyperechoic structure between tibia and bula). With the transducer slightly tilted, the anterior tibial vein comes into view (blue, ow toward transducer) along its course parallel to the artery and as it enters the popliteal vein. c Hyperemia. Peripheral inammation is another factor that can alter the Doppler waveform besides an increased ow resulting from exercise-induced hyperemia or when an artery is recruited as a collateral. In the example, a phlegmon of the foot results in a monophasic waveform with reduced pulsatility and a rather high end-diastolic velocity (EDV) of 22cm/s. An upstream stenosis is ruled out here as the steep systolic upslope is preserved and a PSV of 130cm/s is measured (which is relatively high for an artery below the knee, see a). The variation in PSV in this patient is attributable to absolute arrhythmia. A mirror artifact is present (<SA)
2
. Table 2.5 Normal diameters (D) and peak systolic velocities
(PSV) with standard deviations determined in the lower extremity arteries of 30 healthy subjects
Artery D (cm) PSV (cm/s)
External iliac artery 0.85±0.11 116±29.7
Common femoral artery 0.81±0.17 112.2±22.7
Proximal supercial femoral artery
Profunda femoris artery 0.55±0.14 95.1±21.5
Popliteal artery 0.58±0.12 71.6±12.4
0.65±0.14 93.95±15.9
Arterial diameters and PSV are subject to wide interindivid­ual variation and decrease toward the periphery (. Table2.5), while the triphasic ow prole is preserved.
Investigations of
leg arteries
(Jäger etal. 1985; Kohler 1990; Karasch et al.
normal ow velocity in the pelvic and
1990; Polak etal. 1992) have revealed wide variations between dierent study populations and individual subjects within a study population. It is therefore somewhat more dicult to dene an absolute systolic velocity threshold above which a hemodynamically eective stenosis should be assumed, as is the case for the diagnosis of carotid and renal artery stenosis. Given the wide variation in blood ow velocities in the peripheral arteries, the normal velocities measured by our group (. Table2.5) are comparable to those reported by oth- ers (Jäger etal. 1985; Kohler 1990).
In addition to PSV and changes in the normal triphasic ow prole, the acceleration index has become an estab- lished parameter for describing occlusive and postocclusive changes in blood ow. Higher-grade stenosis or occlusion is associated with a postocclusive decrease in PSV and delayed systolic upstroke (see . Figs. 6.8 and 1.49). e acceleration
index is the quotient of PSV and the pulse rise time from the onset of systole to the rst peak.
e pulsatility index (PI) can be used to describe the pul­satility of ow (see formula in . Fig. 1.29). As the postste­notic decrease in PSV (. Fig. 2.10) and increase in EDV become more pronounced through dilatation of the arteri­oles and the resulting decrease in peripheral resistance, tri­phasic ow becomes monophasic, and the magnitude of this change correlates with the decrease in PI (see . Figs. 1.29,
2.9, and 2.52 (Atlas)).

2.1.6 Abnormal Findings

e following subsections describe the therapy-oriented sonographic workup of vascular conditions aecting the leg arteries, including relevant sonographic ndings and param­eters, and discuss the role of ultrasound in the diagnostic management of the respective disease entities.
2.1.6.1 Atherosclerotic Occlusive Disease
Most atherosclerotic lesions occur in the thigh vessels (approx. 40%), followed by the pelvic and calf vessels, each accounting for approx. 20–30% (Schoop 1988). More than 20% of patients already have occlusive lesions of more than one level at the time of diagnosis. Since vascular sclerosis is a generalized process, it typically involves both legs, but oen, one side will be aected more severely.
Vascular duplex ultrasound of the leg arteries is pre-
dominantly used for the stepwise diagnostic workup of patients presenting with typical symptoms of peripheral arte­rial occlusive disease (PAOD) (. Fig.2.7), treatment plan­ning, and dierentiation of atherosclerosis from other vascular conditions (. Table2.6).
e duplex ultrasound ndings, in conjunction with the clinical disease stage, guide the further diagnostic and thera-
66
ab c
Chapter 2 · Extremity Arteries
2
. Fig. 2.10a–c Segmental duplex ultrasound of the lower extremity arterial tree based on spectral Doppler analysis and identication of postocclu-
sive waveform changes to localize occlusive disease. a Normal triphasic Doppler waveforms (no hemodynamically relevant stenosis or occlusion) from the common femoral artery, popliteal artery, and anterior and posterior tibial arteries. b Pelvic artery occlusion is indicated by postocclusive monopha­sic waveforms from the common femoral, popliteal, and anterior and posterior tibial arteries. The postocclusive ow pattern is seen in all arteries distal to the occlusion. c In isolated occlusion of the proximal anterior tibial artery, ow is triphasic in the common femoral, popliteal, and posterior tibial arteries, while a postocclusive waveform is obtained from the anterior tibial/dorsalis pedis artery
. Table 2.6 Indications for (color) duplex ultrasound of the leg arteries
Indication Diagnostic tasks
Stepwise diagnostic workup of PAO D
Diagnostic evaluation of aneurysm Localization
Arterial compression Entrapment syndrome
AV stula Localization
Follow-up of surgical or interven­tional procedures
Localization of ow obstruction (above the knee, below the knee, pelvic level, vessel origin) Identication of type of ow obstruction (stenosis, occlusion) Length of ow obstruction (length of occlusion, sequential stenoses) Stenosis grading (high-grade versus low-grade) Cause of occlusion (embolism, atherosclerosis, trauma, compression, dissection) Evaluation of postocclusive outow tract Therapeutic decision making: medical treatment, radiologic intervention, surgery
Characterization (saccular, spindle- shaped, false) Extent (infrarenal, aortoiliac, popliteal) Thrombosis (partial, complete) Treatment: compression therapy of pseudoaneurysm, thrombin injection
Adventitial cystic disease Thoracic outlet syndrome Compression by tumor
Flow volume in stula
Bypass grafting (anastomotic stenosis, suture aneurysm, infection, occlusion, ow velocity inside bypass graft: prognosis) PTA (residual stenosis, restenosis, puncture aneurysm, hematoma) Endovascular stenting (patency, stenosis)
def
2.1 · Pelvic andLeg Arteries
67
abc
. Fig. 2.11a–f Collateral circulation in pelvic artery occlusion. a Occlusion of the external iliac artery (A.I.E) after PTA and stent (S) implantation.
The common iliac artery (A.I.C) is displayed in red. The internal iliac artery (A.I.I) is also patent with ow coded in blue. Flow in the external iliac vein (V.I.E) posterior to the artery is toward the center (blue); ow in the internal iliac vein (V.I.I) as it ascends from the true pelvis and enters the com­mon iliac vein is displayed in red (toward transducer). b The common femoral artery (A.F.C) with ow toward the periphery (blue, postocclusive ow signal) is lled via the epigastric artery (EPIGASTR A), where ow is retrograde (blue). The stented external iliac artery (A.I.E) is occluded. c The femoral circumex artery (A.C.F) with retrograde ow displayed in red lls the proximal profunda femoris artery (A.P.F), resulting in retrograde ow (red, toward transducer) in a short segment of the profunda femoris directly at the site of entry of the femoral circumex. d In the supercial femo­ral artery (A.F.S), ow is orthograde with a postocclusive Doppler waveform (monophasic, delayed systolic rise). e Distal to the site of entry of the femoral circumex artery (A.C.F), there is orthograde ow in the profunda femoris artery as well (A.P.F, blue, ow toward the periphery). f Doppler waveforms (ow volume, ow direction) reect the changing intravascular pressure at the site of sampling (compare waveforms obtained at the sampling sites in d and e). While the color duplex image shows retrograde systolic ow toward the center (toward transducer) in the profunda femo­ris artery (A.P.F>) close to its origin from the common femoral artery (A.F.C), Doppler interrogation demonstrates to-and-fro ow in this segment. In contrast, the waveform in c shows high retrograde ow because part of the blood ows toward the periphery through the profunda femoris down­stream of the sampling site (seen in c to the right of the A.C.F). The to-and-fro ow at the profunda femoris origin is due to the fact that this artery contributes to relling of the common femoral artery, which receives only insucient collateral ow from epigastric arteries. The Doppler waveform very accurately reects the hemodynamic situation as a function of local pressure and pressure variation through the cardiac cycle (see . Fig.2.58 (Atlas)). In the absence of collateral ow through the femoral circumex artery, the waveform sampled here would be the same as in c
2
peutic strategy (. Fig.2.7). e overall motto is: No further (invasive) diagnostic test without therapeutic consequences. is means that additional diagnostic tests, especially inva­sive ones, should not be ordered unless they are expected to provide relevant supplementary information for adequate treatment planning.
distal aortic anaeurysm), dissection (see and stenosis due to bromuscular dysplasia.
In patients with occlusion at the pelvic level, collateral ow mainly occurs through the internal iliac artery systems. Additional collateral pathways include the inferior mesen­teric artery and internal iliac artery in common iliac artery occlusion and the epigastric arteries (entering just above the
2.1.6.1.1 Pelvic Arteries
Lower extremity steno-occlusive disease aects the pelvic arteries in 11% of cases. Isolated occlusions at this level occur in the common iliac artery in approx. 54% of cases, in the external iliac in 21%, and in the internal iliac in 13% (Schoop
1988). e clinical presentation of pelvic artery occlusion varies with the presence of collateral pathways and concomi­tant involvement of distal arteries (40–50% incidence of combined femoropopliteal obstruction). Reconstruction of the occluded pelvic artery to improve inow of blood is par­ticularly important in patients with additional supercial femoral artery occlusion. Moreover, pelvic artery repair has a good long-term prognosis and patency rate. Important non­atherosclerotic conditions aecting the arteries at the pelvic level include aneurysmal disease (especially in patients with
groin) in external iliac artery occlusion ( addition to the typical claudication symptoms of the lower leg, occlusion in this territory is associated with specic clau­dication pain of the gluteal, hip, and thigh muscles.
When the external iliac artery is occluded and the lateral circumex artery provides collateral ow, backward ow occurs in the proximal profunda femoris and common femo­ral arteries. is is seen in the Doppler examination as reversed ow with a monophasic character. Additionally, col­lateral ow through the lateral circumex artery lls the supercial femoral artery, while the common femoral artery oen receives collateral ow from epigastric arteries entering just above the inguinal ligament (see . Fig.2.53i (Atlas)).
If direct evidence in the form of increased blood ow velocity in the stenotic segment cannot be obtained, especially
7 Sect. 2.1.6.4.7),
. Fig. 2.11a–f). In
68
Chapter 2 · Extremity Arteries
when evaluation is impaired due to overlying bowel gas or obesity, spectral Doppler imaging of the proximal common femoral or distal external iliac artery can provide indirect evi-
2
dence of upstream obstruction.
A stenosis of less than 50–60% has no relevant eect on the poststenotic Doppler waveform. Only higher-grade ste­noses produce ow changes including a decrease in PSV, a less steep systolic rise, and a delayed diastolic drop with per­sistent ow toward the periphery in the poststenotic segment (see . Fig.2.52 (Atlas)). e lower PSV and the delayed sys­tolic rise are primarily due to the upstream ow obstruction while monophasicity indicates peripheral vasodilatation in response to a mismatch of blood supply and demand. is peripheral situation in turn also inuences the prestenotic waveform via the collaterals.
e ankle-brachial index (ABI) decreases aer exercise, and ow becomes less pulsatile, which may result in a mono­phasic waveform. In the absence of vascular disease, the ABI and Doppler waveform will return to normal aer a short rest. is is why a short
waiting period following positioning
of the patient on the couch (>3min) is necessary to obtain accurate quantitative measurements and spectral Doppler information. On the other hand, an additional spectral Doppler measurement during the recovery phase can help in dierentiating absence of stenosis from high-grade proximal stenosis with good collateralization. e latter is character­ized by a relatively normal Doppler waveform at rest (. Fig.2.53 (Atlas)) but a markedly delayed return to normal aer activity (. Fig.2.12).
. Figs.2.52 and 2.53 (both Atlas)), giving rise to false-
index ( negative results. A pulsatility index with a cuto of 4 was found to have 94% sensitivity and 82% specicity for identi­fying isolated aortoiliac obstruction (iele et al. 1983). Indirect stenosis criteria can be used when the insonation conditions in the true pelvis are poor. Whenever abnormal ndings are encountered, however, an attempt should also be made to identify the stenosis directly. Under normal scan­ning conditions, state-of-the-art (color) duplex ultrasound equipment oen allows faster direct localization of stenosis or occlusion than is possible with use of indirect criteria.
While waveform analysis alone is used in many studies with a standardized design, one should be aware of potential pitfalls. Another important parameter, which is especially relevant in order not to miss moderate stenosis or steno­occlusive disease with very good collateralization, is mea­surement of peak systolic velocity (PSV) in comparison with the opposite side (>30% dierence). Audible analysis of the Doppler signal is another option. Upstream stenosis is sug­gested when the systolic whipping sound is weaker compared with the contralateral side. However, to use this criterion, it is pivotal to perform the Doppler interrogation with a small (<50°) and identical angle on both sides (Schäberle et al.
2013). For an experienced examiner, the acoustic signal is the best criterion for ruling out pelvic artery stenosis. While this acoustic criterion does not lend itself to standardization, the change in the acoustic signal in the presence of upstream ste­nosis at the pelvic level is visually reected in the waveform (damping and less steep systolic rise).
e potential pitfalls discussed above show that wave-
2.1.6.1.2 Time-Ecient Examination Based
onWaveform Analysis
erapeutically relevant stenosis in the pelvis and thigh can be reliably and eciently ruled out by segmental spectral Doppler evaluation of blood ow in the common femoral and popliteal arteries and comparison with the contralateral leg. Relevant stenosis is unlikely proximally if the waveform shows normal, triphasic ow. Compared with angiography, this method has 88–95% sensitivity and 81–98% specicity in identifying hemodynamically relevant stenosis at the pel­vic level (Eiberg et al. 2001; De Morais Filho et al. 2004; Fontcuberta etal. 2005; Sensier et al. 2000; Cossman etal. 1989; Skaalan etal. 2003). Spronk etal. (2005) report poor sensitivity of only 56% but good specicity using the crite­rion of a sharp monophasic waveform for diagnosing aor­toiliac obstructive disease. However, this study is limited by the use of MR angiography as the standard of reference.
Another parameter used to rule out hemodynamically signicant, higher-grade stenosis is the (. Fig. 1.28c). A signicant stenosis of the aortoiliac segment is unlikely if the pulsatility index is greater than 5.5 (Johnson etal. 1983; Neuerburg etal. 1991). e following pulsatility indices have been determined: 8.5±3.5in a normal popula­tion, 2.8 ± 1.6 in isolated stenosis at the pelvic level,
2.3 ± 1.0 in concomitant pelvic and thigh occlusion, and
6.3±2.6in isolated femoral artery occlusion. Note, though, that eective collateralization results in a higher pulsatility
pulsatility index
form phasicity alone is not a reliable criterion (e.g., stenosis of femoral artery bifurcation,
. Fig.2.12f) and this may also
explain the discrepancy of results reported by investigators using this parameter. To be on the safe side, the examiner should combine evaluation of waveform phasicity, PSV, and
acceleration time
on the aected side in comparison to the contralateral side to make allowance for the fact that the pel­vis is rich in arteries that can be recruited as collaterals. is is how the author’s group achieved 95% sensitivity and 98% specicity in the detection of >60% stenoses in 85 patients with suspected pelvic artery stenosis (intermittent claudica­tion, pulses, ABI) (Schäberle etal. 1998). Stenosis was con­rmed by angiography in 32 of the patients.
As noted, a triphasic waveform merely indictes that there is adequate peripheral perfusion at rest. To avoid misinterpreta­tion, it is helpful to compare spectral Doppler ndings obtained aer activity (i.e., immediately aer positioning of the patient on the couch) with the ndings aer the usual rest of approx. 3–4 min. Muscle activity induces physiological peripheral vasodilation, reected in the waveform as a larger diastolic ow component (
. Fig.2.9). In individuals without vascular
pathology, blood ow quickly returns to normal (within 1min), and identical triphasic Doppler waveforms are obtained from both sides. In patients with moderate stenosis, well col­lateralized high-grade stenosis (. Figs.2.12 and 2.53 (Atlas)), or with very well collateralized occlusion, the waveform will also return to normal but it takes longer. erefore, spectral
ab
cd
ef
2.1 · Pelvic andLeg Arteries
69
2
. Fig. 2.12a–e Pitfalls in grading common iliac artery stenosis. a The Doppler waveform obtained in the left groin (common femoral artery)
shows monophasic ow, consistent with upstream stenosis. The waveform was obtained immediately after positioning of the patient, who had walked from the waiting room to the examination room. b After 5min of rest, the waveform shows normal triphasic ow with a slightly delayed systolic upstroke (acceleration time of 182ms, peak systolic velocity (PSV) of 96cm/s). However, the PSV here is markedly dierent from the PSV measured on the contralateral side (PSV of 170cm/s), which should prompt continuous duplex imaging of the pelvic segment despite the tri­phasic waveform. c The Doppler spectrum from the contralateral common femoral artery is triphasic with a PSV of 170cm/s. d Monophasic ow with delayed return to normal and reduced PSV in this patient was found to be caused by a stenosis of the common iliac artery at its origin from the aorta. The waveform recorded immediately after positioning of the patient for the examination shows criteria of high-grade stenosis (>90%; PSV>6m/s and end-diastolic velocity (EDV)>1m/s, monophasic ow). e The correct degree of stenosis can be estimated from the Doppler wave­form obtained in the stenotic segment after 5min of rest and is approx. 70% (PSV of 380cm/s, triphasic ow). This example illustrates the impor­tance of performing spectral Doppler analysis at rest to ensure accurate stenosis grading by spectral analysis (PSV, indirect criteria). fAnother pitfall that must be borne in mind is that high-grade obstruction downstream of the spectral Doppler sampling site can mimic steno-occlusive disease at the pelvic level because it presents with the same changes in the waveform (monophasic ow, reduced PSV). In the example shown, the waveform from the external iliac artery/common femoral artery (AFC) junction is consistent with upstream obstruction (PSV of 30cm/s, monopha­sic ow). However, this patient has no iliac artery stenosis and the abnormal waveform is due to high grade-stenosis at the origins of the supercial and profunda femoris arteries (PSV>300cm/s, not shown), as indicated by aliasing in the color ow image
70
Chapter 2 · Extremity Arteries
Doppler analysis 1min aer activity allows dierentiation of transient physiologic changes from vascular pathology.
In conclusion, segmental spectral Doppler analysis
2
requires combined bilateral determination of PSV and eval-
uation of waveform phasicity
in order not to overlook hemodynamically relevant stenosis. Any abnormality should prompt continuous mapping of the proximal terri­tory to search for steno-occlusive lesions. A triphasic Doppler waveform alone is not sucient to rule out upstream stenosis.
Another pitfall to be aware of is that high-grade obstruc­tion downstream of the spectral Doppler sampling site can mimic iliac steno-occlusive disease, because it causes similar changes in the waveform (reduced pulsatility and lower PSV) (. Fig.2.12f). For instance, a patient with profunda femoris stenosis and supercial femoral artery occlusion or high­grade stenosis at the supercial femoral artery origin will have a similar waveform as a patient with iliac artery obstruc­tion (except that the steep systolic rise is preserved). In this situation, the examiner must rule out iliac artery stenosis by direct evaluation (see direct and indirect criteria in
2.1.6.1.4
).
7 Sect.
velocity in the normal arterial segment upstream of the stenosis. e intrastenotic PSV increase is typically calcu­lated as the ratio of intrastenotic PSV to prestenotic PSV, or PSV ratio for short. In general, a PSV ratio>2 is inter­preted to indicate >50% stenosis and a ratio>4 to indicate >75% stenosis. PSV ratios cannot be used when a stenosis is located in a bifurcation or at the origin of an artery (iliac artery or profunda femoris origin). At these sites, thresh­old velocities determined by ROC analysis with angiog­raphy as the gold standard can be used instead. Several studies investigated a PSV cuto of 180cm/s, which was originally proposed for identication of hemodynamically relevant profunda femoris artery stenosis (Strauss et al.
1991), and found 71–96% sensitivities and 92–95% speci­cities (Moneta etal. 1992; Aly et al. 1998; Katsamouris etal. 2001). A drawback is that absolute PSV is inuenced by systemic factors, as underlined by the results of a study using a PSV threshold of 200cm/s, for which the authors found a high sensitivity of 95%, while specicity was only 55% (de Smet etal. 1996).
e increase in blood ow velocity in a stenotic segment is associated with a pressure drop. e pressure gradient across a hemodynamically relevant stenosis results in a
2.1.6.1.3 Stenosis Grading
An intrastenotic peak systolic velocity (PSV) of over 180– 200cm/s and focal doubling of PSV have emerged as criteria for hemodynamically relevant stenosis in ow models and invivo. Using these thresholds, investigators reported sensi­tivities of 71–100% with specicities of 92–100% (Whyman etal. 1993; Moneta etal. 1992; Aly etal. 1998; Katsamouris etal. 2001). On the other hand, receiver operating character­istic (ROC) curve analysis identied markedly lower velocity thresholds of 120cm/s for 50% stenosis and 160 cm/s for 70% stenosis (Sacks etal. 1990), but these turned out to be unsuitable in the routine clinical setting. e threshold velocities identied by ROC analysis vary greatly, depending on the study population investigated (e.g., proportion of patients with hypertension or diabetes mellitus).
Conventional angiography is limited in the grading of
stenosis at the pelvic level, especially in patients with stenosis at the common iliac artery origin caused by eccentric poste­rior wall plaque. Strict lateral views are required for reliable
decrease in peripheral systolic blood pressure and can be measured by determining the ankle-brachial index (ABI). A decrease in ABI suggests arterial disease. Strauss etal. (1995) used the PSV measured by duplex ultrasound in stenotic seg­ments at the pelvic level to calculate the pressure gradient across the stenosis using the simplied Bernoulli equation and compared the results with direct intra-arterial pressure measurement. In this study, the following correlations were found between angiographic parameters and duplex ultra­sound:
5 Cross-sectional area reduction determined densito-
metrically and the hemodynamic degree of stenosis
based on the PSV ratio: R=0.64
5 PSV and densitometrically determined cross-sectional
area reduction: R=0.56
5 Pressure gradient calculated from the ow velocity
determined by color duplex ultrasound using the
Bernoulli equation (
. Fig.2.13) and the pressure
gradient measured by intra-arterial catheter: R=0.86
grading of this type of stenosis. For more distally located pel­vic artery stenoses, the standard anteroposterior projection (oen the only projection available) should ideally be supple­mented by le and right anterior oblique views (which are perpendicular to each other). Lateral projections are required for exact grading because most stenoses in this territory, especially in the external iliac artery, are caused by eccentric plaque on the posterior wall. CT angiography using thin slices (1mm) is an alternative option, while MR angiography tends to overestimate stenosis severity.
Hemodynamic stenosis grading by
imaging
is based on the identication of a focal increase
spectral Doppler
in peak systolic velocity (PSV) compared to the blood ow
While this study found the best agreement between invasive angiography and noninvasive duplex ultrasound for the pres­sure gradient across the stenosis (. Fig. 2.13), the author’s experience suggests that the pressure gradient calculated from PSV using the simplied Bernoulli equation can be misleading, especially when higher-grade stenosis is present. e pressure drop expressed in the ABI reects the degree of stenosis but ignores the eects of collateralization. For a given degree of stenosis, the ABI is lower in the absence of collateralization and increases with the magnitude of collat­eralization. Better collateralization also results in less damp­ing of the poststenotic waveform.
mmHg
Mean Doppler gradient
Mean catheter gradient
2.1 · Pelvic andLeg Arteries
40
30
20
10
0
010203040
. Fig. 2.13 Correlation (R=0.86) of the mean pressure gradient
across a pelvic artery stenosis calculated from color duplex ultrasound using the simplied Bernoulli equation (p=4×PSV2) and the pressure gradient measured by intra-arterial catheter (Strauss etal. 1995)
eoretically, one would expect the magnitude of the pressure gradient across an iliac artery stenosis to also reect collateralization, meaning that good collateralization should result in a smaller increase in PSV across the stenotic seg­ment and hence a less steep pressure gradient compared with a stenosis of the same degree but poorer collateralization (comparable to the situation in supercial femoral artery ste­nosis; . Fig.2.16b). In steno-occlusive disease of more cen­tral arteries, however, the intrastenotic increase in PSV is less dependent on collateralization.
Another issue to be borne in mind is that eccentric
plaque
, which is frequent in the iliac and common femoral arteries, causes less severe stenosis in terms of hemodynamic relevance than circumferential plaque with the same degree of angiographic diameter reduction. is is due to the fact that a 50% diameter reduction reduces the vascular cross­sectional area by 75% when caused by circumferential steno­sis as opposed to only 50% when caused by eccentric stenosis (. Fig. 2.17d). Circumferential stenosis thus has more marked hemodynamic eects, resulting in a greater increase in intrastenotic PSV and more severe peripheral ischemia. is explains the discrepancies between morphologic and hemodynamic methods of stenosis grading and why a hemo­dynamic method such as duplex ultrasound is oen a better indicator of the patient’s clinical situation than radiologic methods based on morphology alone.
2.1.6.1.4 Leg Arteries
Preferred sites of atherosclerotic femoral artery stenosis are the bifurcation (supercial and profunda femoris origins) and the adductor canal.
mmHg
71
Isolated stenosis or occlusion of the common femoral artery is rare (approx. 4%); most patients with common femoral artery stenosis have concomitant obstructions of the supercial femoral and below-knee arteries. Occlusion of the common femoral artery or femoral bifurcation is of considerable clinical signicance and, whenever possible, should be treated by surgical repair (TEA); collateralization here is poor, as all collateral pathways (via the iliac and pro­funda femoris arteries) comprise the femoral bifurcation, and auxiliary collaterals have a low capacity. e
femoris artery
supplies the thigh muscles and is the most
profunda
important collateral in all arterial obstructions distal to the femoral bifurcation. As a phylogenetically old vessel, the profunda femoris artery is rarely aected by sclerotic changes distal to its origin. All isolated obstructions of the profunda femoris are due to embolism or occur in patients with diabetes mellitus. Stenosis at the origin of the profunda femoris artery is more common in patients with atheroscle­rosis of the femoral bifurcation and is clinically relevant due to the key role of the profunda femoris as a collateral in obstruction of the femoropopliteal circulation. Surgical repair of the profunda femoris artery is the treatment of choice.
e
supercial femoral artery is the preferred site of ath-
erosclerotic lesions and is the most common site of isolated occlusions, which have an incidence of 27%. Occlusion of both the femoral and popliteal arteries occurs in 40–45% of cases. In all cases of isolated popliteal artery occlusion, thrombosed popliteal aneurysm and nonatherosclerotic vas­cular disorders (which preferably aect the popliteal artery) must be ruled out in the dierential diagnosis.
e treatment of femoropopliteal artery occlusion depends on the clinical presentation, cause, site, and length of the occluded segments. ese frequently aected and hence clinically signicant vessels are easily accessible to duplex scanning as they lie close to the surface and there are no intervening scatterers. Many studies have conrmed the diagnostic accuracy of duplex ultrasound in evaluating fem­oropopliteal occlusive disease (. Table 2.7). e precise information on the site and length of an occlusion provided by duplex ultrasound is necessary for therapeutic decision making; however, treatment is ultimately dictated by what is required clinically (
B-mode imaging will show atherosclerotic wall lesions as
. Fig.2.8).
irregularities of the wall contour, intimal thickening, or plaques (. Table2.8). In larger arteries, the B-mode image already allows a rough estimate of the degree of luminal nar­rowing when caused by echogenic, noncalcied plaques; however, the hemodynamic degree of luminal narrowing is always derived from the Doppler waveform.
An atherosclerotic occlusion is suggested if extensive intraluminal plaques are depicted and the arterial wall is no longer visible. e B-mode examination thus allows dieren­tiation of stenotic lesions caused by atherosclerosis from luminal narrowing caused by external structures.
2
72
Chapter 2 · Extremity Arteries
. Table 2.7 Sensitivity, specicity, and diagnostic accuracy of duplex ultrasonography compared with angiography in the diagnosis of
hemodynamically relevant stenosis (>50%), occlusion, and aneurysm of the pelvic and leg arteries (see . Table2.20)
2
Author Vascular territory Duplex technique Reference method Sensitivity (%) Specicity (%) Accuracy (%)
Kohler etal. (1987)
Legemate etal. (1991)
Allard etal. (1994)
Cossman etal. (1989)
Mulligan etal. (1991)
Moneta etal. (1992)
Strauss (2001) Iliac
Schäberle (1998)
Polak etal. (1990)
Landwehr etal. (1990)
Koennecke etal. (1989)
Legemate etal. (1991)
Ranke etal. (1992)
Katsamouris etal. (2001)
Aly etal. (1998) Aortoiliac
Khan etal. (2011)
Femoropopliteal Conventional Conventional angio 82 92
Aortoiliac Conventional IA DSA 89 92 91
Aortoiliac Femoropopliteal
Iliac Common femoral Supercial femoral Profunda femoris Popliteal
Femoropopliteal Color Conventional angio 89 91
Iliac Common femoral Supercial femoral Profunda femoris Popliteal
Common femoral Supercial femoral Profunda femoris Popliteal
Femoropopliteal, iliac, proximal segments of crural arteries
Femoropopliteal Color Angiography or
Femoropopliteal Color Angiography or
Femoropopliteal Color Angiography or
Aortoiliac Femoropopliteal Tibial
Femoropopliteal Crural
Femoropopliteal Color Angiography 94.5 99
Conventional Conventional angio 83
87
Color Conventional angio 81
70 87 71 85
Color Conventional angio
or IA DSA
Color Conventional angio
or IA DSA
Color Conventional angio
or IA DSA; intraop­erative
IA DSA
IA DSA
IA DSA
Color Angiography 84 96
Color Angiography 87 94
Color Angiography 86
Color Angiography 89
89 76 87 83 67
87 75 94 79 94
97 98 97
88 95 93
92 99 96
97 97 97
99 80
100
82
96 93
98 97 85 95 97
99 99 98 97 99
73 91 72 96 92
90 94 91
99 99 99
92 90
92 93 87 93 93
83 86 88 86 93
88 96 83
IA DSA intra-arterial digital subtraction angiography