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2.1 · Pelvic andLeg Arteries
a
b
103
2
. Fig. 2.36 Restenosis after stenting. a Patient with in-stent restenosis of the external iliac artery. Hemodynamic grading based on the peak systolic
velocity (PSV) ratio indicates 50–60% stenosis (PSV ratio>2, calculated from intrastenotic PSV of 341cm/s and prestenotic PSV of 148cm/s). The wave­form was obtained by moving the transducer over the skin, while maintaining a constant Doppler angle, from the prestenotic segment to the site of stenosis (indicated by “> <”). b Stent in supercial femoral artery with excessive neointimal proliferation causing circumferential narrowing of a long portion of the stented arterial segment with high- grade stenosis at the distal stent end (arrow; PSV ratio of approx. 5, calculated from intrastenotic PSV of 249cm/s and prestenotic PSV of 55cm/s). The angiogram obtained before repeat PTA conrms narrowing of the stent lumen with stenosis at the distal stent end (arrow). The example illustrates the problem of stenosis grading. The intrastenotic PSV of 249cm/s is low for the degree of stenosis. Good collateralization (ow divider, see angiogram) results in reduced ow and ow velocity in the femoral artery, as reected by the low prestenotic PSV of 55cm (see . Figs.2.16b and 1.46b, c and . Table 1.10). The PSV ratio of 5, however, is consistent with high-grade stenosis and better reects the hemodynamic situation here. Conversely, use of absolute intrastenotic PSV alone (cutos determined by ROC analysis; see . Figs.2.18 and 2.19) underestimates the severity of stenosis in this case, illustrating the superiority of the PSV ratio over absolute PSV for stenosis grading
A stent is identied by its serrated or mesh-like appear­ance. A focal increase in ow velocity is the most important sign of residual or recurrent stenosis aer PTA, stenting (where special attention must be paid to the stent ends), and bypass graing (primarily at the anastomotic sites) (. Fig.2.36).
In most cases, ow evaluation within a stent requires a higher color gain. Eddy currents and turbulent ow at the proximal and distal ends suggest that the stent does not t snugly to the wall, which can promote restenosis.
e accurate diagnosis of complications such as arteriove­nous (AV) stula, pseudoaneurysm, and hematoma and the timely identication of residual or recurrent stenosis are cru­cial for post-PTA patency. A hemodynamically signicant
residual or recurrent stenosis
is suggested by focal doubling of the ow velocity within the treated segment. e detection of a hemodynamically signicant stenosis by duplex ultra­sound is a predictor of patency. e above- quoted study of Mewissen etal. (1992) reported a 1-year patency rate of 83% in the absence of stenosis as opposed to only 15% when a functional stenosis was diagnosed (Mewissen etal. 1992).
Several studies have shown duplex imaging to be more sensitive than angiography in detecting residual stenosis or residual ow disturbance following PTA.In one study,
20% of residual stenoses >50% based on duplex ultrasound were classied as causing <30% diameter reduction at angiography. e sonographic stenosis criteria were PSV >180cm/s (. Fig.2.37) and an intrastenotic-to-prestenotic PSV ratio>2.5 (Kinney etal. 1991; Mewissen etal. 1992). e presence of residual stenosis classied as causing >50% diameter reduction by duplex scanning was found to pre­dict late failure (15% success rate) while late patency was observed for <50% diameter reduction (84% success rate). Based on these results, it is recommended to perform a
follow-up duplex scan within 1 month of PTA to iden-
tify patients with residual/recurrent stenosis who should undergo reintervention.
Earlier studies in other vascular territories (carotid artery, renal artery) identied 10–20% higher PSV cutos (ROC curve analysis) for in-stent restenosis (due to greater wall rigidity and smaller lumen of the stented segment) compared with native arteries. In contrast, more recent studies in stented peripheral arteries suggest that PSV cutos should rather be lower than for untreated arteries. ese studies report sensitivities and specicities as well as negative predic­tive values (NPV) and positive predictive values (PPV) on the order of 95% for the following absolute PSV and PSV ratio cutos (Baril etal. 2008; Shrikhande etal. 2011):
104
Chapter 2 · Extremity Arteries
2
a b
. Fig. 2.37 a Patient after PTA and stenting of high-grade common iliac artery stenosis. In the gray-scale image (left), the stent is identied by
its serrated appearance. The color duplex image shows aliasing at the proximal stent end and backward and forward ow components within the stent (red and blue) (A = aorta, A.I.C = common iliac artery, V = common iliac vein, VA = vibration artifact, SA = mirror artifact). The Doppler wave­form from the site of aliasing demonstrates very turbulent ow with a PSV of 422cm/s, consistent with high-grade stenosis. b Angiogram fails to adequately show the stenosis or its cause. The patient underwent repeat PTA on the basis of the duplex ultrasound ndings. Following repeat PTA, the patient’s clinical symptoms resolved (patient’s walking distance before reintervention was limited to 180m), color duplex conrmed elimina­tion of the stenosis, and the ABI normalized from 0.8 to 1.1
5 >50% stenosis: PSV >190cm/s and PSV ratio>1.5 5 >70% stenosis: PSV >223cm/s and PSV ratio>2.5 5 >80% stenosis: PSV >275cm/s and PSV ratio>3.5
e PSV ratio is a very reliable parameter for identication of in-stent restenosis. However, according to the continuity equation, one would expect the cuto ratio to be 2 for 50% stenosis and 4 for 75% stenosis. ese theoretically pre­dicted PSV ratios are based on the assumption that stenosis is caused by concentric plaque. Hence, the lower actual ratios suggest that in-stent restenosis tends to be caused by eccentric luminal narrowing. Remember that an eccentric stenosis results in a smaller cross-sectional area reduction than a concentric stenosis with the same diameter reduc­tion. erefore, the hemodynamic eect of an eccentric stenosis is less pronounced and the sonographically mea­sured intrastenotic increase in PSV is smaller (. Fig.2.17d).
2.1.7.3 Bypass Graft Surveillance
e sonographic appearance of a bypass depends on the material used.
e thin wall of an autologous venous bypass graft is very dicult to delineate when occlusion has occurred. Such a bypass is easier to identify, in particular in older occlusion, if the examiner has information on its course (anatomic, extra­anatomic). In patients with a venous bypass gra, the entire length must be scanned because the former valves are common sites of stenosis, especially in an in situ bypass with residual valve cusps. An AV stula developing from a perforating vein that has not been ligated can be identied by the presence of perivascular tissue vibration artifacts in the color duplex mode.
In contrast, the walls of a synthetic bypass graft are always clearly seen. A PTFE (polytetrauoroethylene) prosthesis has a characteristic double-line appearance and a Dacron bypass a sawtooth-like appearance.
In the postoperative evaluation and surveillance of a syn­thetic gra, special attention must be paid to possible anasto­motic stenoses. Narrowing within the bypass is due to neointimal hyperplasia and occurs later. About 20–30% of venous bypass gras develop strictures on the basis of neo­intimal hyperplasia within the rst year of surgery.
Dierent factors can cause occlusion of a bypass at dif­ferent times aer surgery:
5 Immediate postoperative occlusion within the rst days
aer surgery may be due to an inadequate surgical
technique, resulting in anastomotic stenosis, or poor
distal runo. erefore, the examination should include
hemodynamic evaluation of the recipient artery.
5 Early occlusion, within the rst year, chiey results from
neointimal hyperplasia, predominantly causing stenosis
at the proximal or distal anastomosis, or from deteriora-
tion of the outow situation due to progression of
atherosclerosis distal to the bypass. If the occlusion is
due to an impaired inow secondary to atherosclerotic
lesions of the proximal artery with loss of the triphasic
waveform, the examiner must carefully evaluate the
native artery upstream of the bypass to identify the site
of obstruction.
5 Late occlusion is predominantly caused by progression
of atherosclerosis, especially in the segments close to the
bypass ends.
Abnormal uid around a bypass gra should be punctured under ultrasound guidance for microbiologic testing, in par­ticular in patients with clinical signs of infection. Before puncture, a suture aneurysm should be ruled out by color duplex imaging (see
. Fig.2.72 (Atlas)). Hematoma, seroma,
and suture aneurysm appear as pulsatile masses at the site of anastomosis, each having a characteristic color duplex appearance, which allows it to be dierentiated at a glance.
2.1 · Pelvic andLeg Arteries
105
2
2.1.7.3.1 Methodological Considerations
andStenosis Criteria
Duplex ultrasound is a valid imaging modality for identify­ing bypass gra complications (stenosis, occlusion). Published data suggest good agreement with CTA and DSA (Willmann etal. 2004) as well as good interobserver agree­ment with 85% sensitivity, 93% specicity, and 91% diagnos­tic accuracy compared with DSA (Ihlberg etal. 1998).
e criteria for grading stenosis severity in a bypass gra are based on those for the native peripheral arteries. However, the hemodynamic changes in a bypass gra may occasionally lead to a monophasic waveform that does not suggest abnor­mal ow. Eddy currents at the anastomoses cause spectral broadening, which is likewise normal (. Figs. 2.41, 2.74 (Atlas), 2.75 (Atlas), and 2.76 (Atlas)).
Normal peak systolic velocity (PSV) is a function of the relative cross sections of the bypass and the proximal and distal native arteries. e complex relationships make it dif­cult to give a reliable general threshold velocity. Still, one can rule out a hemodynamically signicant stenosis with some condence if PSV at the site of anastomosis is below 2m/s on condition that there is no size mismatch between the gra and the native artery (. Table2.15).
Flow within a gra is inuenced by several factors, which should be borne in mind when interpreting spectral Doppler recordings from within the gra to predict bypass patency. is is especially important in patients with severe athero­sclerosis and in assessing bypass gras onto a calf artery (. Fig.2.43). Pulsatility is physiologically dependent on the demand-oriented widening of the arterioles (monophasic ow). In a bypass, pulsatility is additionally aected by dier­ences in elasticity (depending on the material used for the gra) and an increase in outow resistance if there is stenosis distal to the bypass (more pulsatile ow). ese opposing eects on the ow prole preclude simple monocausal inter-
. Table 2.15 Duplex ultrasound criteria in bypass graft
surveillance. Identication of complications: suture aneurysm,
abscess, imminent occlusion (failing bypass), stenosis
(. Figs.2.38, 2.41, and 2.42)
Method (indirect/direct
criteria)
Single PSV measure-
ment in the bypass graft
(indirect sign of ow
obstruction/stenosis in
the graft)
Analysis of representa-
tive spectral waveform
(indirect criterion)
Mapping of bypass graft
and anastomoses:
increased PSV indicates
stenosis (direct criterion)
Interpretation of criteria
Reduced PSV in the bypass graft: PSV <45 cm/s suggests failing bypass (exceptions) Distal to stenosis: damped waveform, delayed systolic rise
Triphasic: good graft function Monophasic: ow obstruction, peripheral vasodilation
PSV ratio >2: moderate stenosis PSV ratio >4: high-grade stenosis PSV >2–2.5 m/s: moderate stenosis PSV >3–3.5 m/s: high- grade stenosis
pretation of the waveform obtained from a bypass gra. Hence, slow ow should prompt an evaluation of both the distal anastomosis and the recipient artery for the presence of stenosis even if the waveform is triphasic (see
. Fig. 2.73
(Atlas)).
While a synthetic gra should primarily be searched for stenosis at the proximal and distal ends (the preferred sites of stenosis in this type of gra), the entire length of an autologous venous gra must be examined for stenosis at valve sites (see . Fig.2.76 (Atlas)). As with native arteries, the examiner can save time by comparing Doppler wave­forms from representative sites to narrow down possible sites of stenosis. When scanning an autologous in situ venous bypass immediately aer surgery, the examiner must also look for any patent perforating veins, which could give rise to an AV stula and would thus need to be ligated aer having been localized sonographically.
PSV cutos ranging from 2m/s (Passman etal. 1995) to
3m/s (Westerband etal. 1997) have been proposed to iden­tify stenosis that should prompt gra revision. It should be clear, though, that there is no single PSV cuto that applies throughout a gra. For example, a PSV of up to 2.5m/s may be considered normal at the distal anastomosis, especially when there is a transition from a wide bypass lumen to a nar­row recipient vessel as is the case with a crural bypass. A PSV of 2.5m/s is abnormal, however, when it occurs at the proxi­mal anastomosis or within the gra.
Other investigators use the ratio of intrastenotic PSV to PSV in the normal proximal segment to identify hemody­namically relevant bypass gra stenosis. However, the
ratio
(also known as peak velocity ratio/PVR) above which
PSV
>70% stenosis requiring gra revision is assumed ranges from 3 (Calligaro etal. 1996; Dougherty etal. 1998) to 4 (Idu etal. 1999). Overall, cutos proposed for moderate stenosis (50–70%) in a bypass gra range from 2–4 for PSV ratios (Wixon etal. 2000; Mills etal. 2001) and from 2–3.5m/s for absolute PSV (. Table2.16).
When grading the severity of anastomotic stenoses in synthetic gras, the PSV ratio must be used with caution due
. Table 2.16 Stenosis grading in the sonographic surveillance
of bypass grafts and therapeutic consequences (Modied from
Mills etal. 2001 and Wixon etal. 2000)
Stenosis criteria in bypass
graft
Normal PSV<200cm/s
PSV ratio<2
Moder-
ate
stenosis
High-
grade
stenosis
PSV of 200–300cm/s PSV ratio of 2–4
PSV>300cm/s PSV ratio>4
Suggested management
Low risk follow-up
Moderate risk close follow-up, revision in case of progression
High risk (PSV in graft >45cm/s) elective intervention Highest risk (PSV in graft <45cm/s) urgent intervention
106
Chapter 2 · Extremity Arteries
to mismatches in size and elasticity between the bypass gra and the proximal native artery. With these limitations in mind, it may be assumed that a PSV ratio >2.5 indicates
2
>60% stenosis. Size mismatches between the gra and the recipient artery oen result in a ow acceleration down­stream of the distal anastomosis, in particular when the anas­tomosis is located below the knee. Here, an even higher PSV ratio (>3) should be used as a cuto in order to minimize false-positive results (Polak 1992).
Mapping of an entire bypass gra including the proximal and distal anastomes is very time-consuming. erefore, protocols have been proposed to make sonographic gra surveillance more ecient. Such protocols rely on the com­parison of Doppler waveforms from a few representative sites using the same indirect criteria as in native peripheral arter­ies (. Figs.2.14, 2.37, 2.38, 2.39, 2.40, 2.41, and 2.43). e ow prole and PSV are evaluated. If there is triphasic ow with a PSV of 55cm/s or greater in the gra, then higher- grade ste­nosis within the gra or at the anastomoses is unlikely – especially if the bypass was established for critical ischemia of the leg. In this situation, a stenosis would lead to a mono­phasic waveform (resulting from reduced peripheral resis­tance due to demand-adjusted widening of arterioles). If the waveform is not triphasic and ow velocity is slow, the entire bypass must be mapped for the presence of stenosis, with special attention being paid to the anastomoses. However, a monophasic waveform may also be obtained if no stenosis is present in the gra, especially if the bypass was established to improve inow in patients with multilevel obstruction and there is persistent poor perfusion in the periphery due to additional stenoses more distally. In contrast, an initially tri­phasic ow prole in a bypass gra that becomes monopha­sic at later follow-up indicates peripheral vasodilation in response to an
impairment of peripheral perfusion. is
again warrants sonographic evaluation of the entire bypass and the anastomoses. Another possible cause of impaired peripheral perfusion is progressive atherosclerosis with ste­notic narrowing of the segments proximal and distal to the bypass gra.
Based on these considerations, a
graft surveillance strategy
is proposed (. Figs.2.38, 2.41,
time-efficient bypass
and 2.42), which relies on duplex imaging and spectral Doppler interrogation at the following sites (. Figs. 2.39 and 2.43):
5 Femoral artery bifurcation 5 Proximal gra anastomosis with spectral Doppler
interrogation
5 Distal gra anastomosis with spectral Doppler interro-
gation including the receiving artery just distal to the
anastomosis and the gra just upstream of the anasto-
mosis
nation (e.g., the feeding artery). Waveforms are obtained by moving the transducer across the proximal and distal anasto­moses, and interpretation of the waveforms from these repre­sentative sites using the indirect stenosis criteria provides information on inow and outow. Comparison of the spec­tral tracings from the proximal and distal ends of the bypass allows the examiner to suspect or rule out stenosis within the gra (see, however, . Fig.2.43).
Long-term bypass graft patency depends on the devel-
opment of stenosis within the gra (predominantly involving the anastomoses) and ow in the recipient artery. Poor runo aects the blood ow velocity in the gra and, in conjunction with systemic factors such as a hypercoagulable state, can lead to occlusion. Several investigators use PSV as the most important parameter in the surveillance of bypass gras (Bandyk etal. 1985, 1989; Buth et al. 1991; Calligaro etal. 1996; Grigg et al. 1988; Lundell et al. 1995; Passman et al.
1995). Postoperative mean or median PSVs reported in the literature range from 0.68 to 1.12 m/s (Belkin et al. 1994; Nielsen etal. 1995; WölfIe etal. 1994) and decrease thereaer if the gra remains patent (from 1.125 to 1m/s aer 1year according to Wöle etal. and by 30% within the rst 6months according to Nielsen etal. 1993).
A markedly reduced overall PSV in a bypass graft has
been proposed as a supplementary indicator of a poor prognosis (Calligaro etal. 1996; Hoballah etal. 1997). Slow ow in a bypass can point to an outow obstruction caused by stenosis of the distal anastomosis or poor runo (steno­sis of recipient artery, obstructed collateral outow). Hence, various velocity thresholds have been suggested as predictors of imminent bypass occlusion. Most authors assume that a bypass is likely to fail if blood ow velocity drops below 45cm/s (Calligaro etal. 1996; Hoballah etal. 1997; Mohan etal. 1995), while others propose thresholds of 40cm/s (Green etal. 1990) or 55 cm/s (Nielsen et al.
1995). Other data suggest that assuming a single velocity threshold for all types of bypass gras and recipient vessels is not sensitive and specic enough to identify a failing bypass (Chang etal. 1990; Hoballah etal. 1997; Idu etal. 1999; Mohan etal. 1995; Treiman etal. 1999). Since ow velocity in a bypass is determined by its diameter and by the diameter and outow of the recipient vessel, crural bypass gras with far distal anastomoses have slower ow velocities even under normal conditions. Still, slow ow in a bypass is a risk factor for occlusion, especially in patients with other predisposing conditions such as a hypercoagu­lable state, increased blood viscosity, or low systemic blood pressure. Some authors therefore investigated the predic­tive power of a prognostic factor combining an increased focal PSV and a low global PSV in the gra (Calligaro etal.
1996). In a study of 85 PTFE gras, this combined crite-
rion had 81% sensitivity, 93% specicity, a PPV of 63%, Spectral Doppler interrogation of these sites will directly identify most gra complications/stenoses, guiding the examiner to abnormal segments that warrant closer exami-
and an NPV of 93% (similar results were reported by Green
et al. 1990). Other investigators (Hoballah et al. 1997;
Mohan etal. 1995) did not conrm these results. In the
2.1 · Pelvic andLeg Arteries
107
2
a
c
. Fig. 2.38a–c Bypass graft surveillance. Duplex examination of a venous femoropopliteal bypass graft (P3 segment). There is no agreement
about the need for sonographic venous bypass graft surveillance or the extent of the examination. An ecient procedure is to obtain Doppler waveforms from representative sites to identify those patients who should undergo comprehensive mapping. At a minimum, a Doppler waveform is obtained from an arbitrary site in the main body of the graft (a) and interpreted with regard to bypass prognosis and signs of stenosis. A more comprehensive evaluation comprises examination of the proximal and distal anastomoses (where most stenoses occur) and a site within the graft slightly distal to the anastomosis (duplex and spectral Doppler). Signs of abnormal ow should prompt mapping of the entire graft, which may also include evaluation of the inow artery. a The color ow image and waveform from a site within the graft show normal ndings. The waveform is triphasic with a PSV of 129cm/s– there is no sign of bypass graft stenosis and no risk of imminent bypass failure. No further evaluation would be required in this patient. b For illustration, the examination proceeds with evaluation of the proximal anastomosis (to rule out anastomotic stenosis or neointimal hyperplasia with relevant luminal narrowing). This is done by placing the sample volume at the origin of the venous bypass graft (V.BP) from the common femoral artery; triphasic Doppler waveform indicates adequate inow. The profunda femoris artery and supercial femoral artery (A.F.S) arise distally (to the right of the anastomosis). c Examination of the distal anastomosis: Doppler waveform from the bypass target artery distal to the anastomosis shows high PSV (70cm/s), steep systolic upstroke, and pulsatile ow as evidence of good outow, ruling out relevant proximal stenosis. Overall, there is no evidence of imminent bypass failure in this case
b
study of Hoballah et al., 24 of 27 patients with bypass occlusion showed no abnormalities in the preceding duplex examination (low ow manifested by PSV<45cm/s or threefold focal increase in PSV compared with adjacent segment).
A noteworthy nding is that low-ow bypass gras identi­ed by duplex ultrasound (drop in blood ow velocity below 45cm/s) appear to benet from
lation treatment
(warfarin). While continuation of antico-
maintenance of anticoagu-
agulation was found to result in a markedly higher patency rate in low-ow gras (decrease in occlusion rate from 24% to 4%, p<0.0001), no benet was observed for high-ow gras
(Brumberg etal. 2008). Surprisingly, gra PSV in this study of 130 bypass gras was <45cm/s in 47% of cases.
2.1.7.3.2 Controversy About theBenet ofDuplex
Bypass Graft Surveillance Programs
Although studies present conicting evidence (Wixon etal. 2000; Golledge etal. 1996; Davies etal. 2005), many authors advocate duplex ultrasound surveillance aer bypass gra­ing, at least for vein gras and during the rst postoperative
. Table2.15) when the risk of occlusion is highest and
year ( the prognosis of bypass revision is good (Harris etal. 1988; Passman etal. 1995; Taylor etal. 1990).
108
A
P
artery
Common femoral artery
Chapter 2 · Extremity Arteries
2
. Fig. 2.39 Common sites of bypass graft stenosis and corresponding
spectral Doppler changes (A, B) illustrated for femoropopliteal bypass graft bridging occluded supercial femoral artery. I Stenosis of proximal bypass anastomosis (A) with poststenotic waveform (B). II Stenosis within vein graft (at former valve site) with focal doubling of ow velocity (A) compared with prestenotic waveform (C) and postocclusive ow prole distal to the stenosis (B). III Stenosis of distal bypass anastomosis (A) with poststenotic ow prole in the popliteal outow tract (B). IV Stenosis of the native artery proximal to the bypass anastomosis, which is due to progressive atherosclerosis: stenotic waveform (A) in the arterial seg­ment proximal to the stenosis and poststenotic ow prole in the artery distal to the stenosis and in the bypass graft (B). V Stenosis of the artery distal to the lower bypass anastomosis: stenotic waveform (A) at the site of stenosis with poststenotic ow prole distally (B) and prestenotic waveform (C) in the proximal arterial segment and in the bypass graft
. Fig. 2.40 A venous bypass graft is susceptible to a number of spe-
cic complications (I–VI), which must be taken into account in bypass surveillance in addition to the preferred sites of stenosis illustrated in
. Fig.2.39. I A reversed vein graft is prone to stenosis just distal to the
proximal stenosis, the narrowest portion of the graft. II Scar formation with narrowing at valve sites. III Dilatation with elongation and kinking of the graft. IV In situ vein graft with a narrow distal end can result in luminal narrowing just proximal to the distal anastomosis. V Failure to ligate all perforating veins communicating with an in situ vein can give rise to an AV stula (between the bypass graft and the venous system). VI Residual valve in an in situ vein graft giving rise to graft stenosis or occlusion
Common
femoral
artery
opliteal
IV
A
C
II
A
C
Vein
Popliteal artery
B
I
A
B
III
AA
V
VI
Notwithstanding the ongoing controversy, it seems
important to document the baseline ow characteristics dur-
B
ing the rst 3months aer surgery. If there is a decrease in PSV or triphasic ow becomes monophasic over time, this
A
should prompt a search of the gra, the anastomoses, and the inow and outow segments for stenosis using the criteria described above.
In a cost-eectiveness analysis, infrainguinal venous
B
bypass gra surveillance with revision for duplex-detected stenoses resulted in a 1-year patency rate of 93% versus 57% for gras revised aer thrombosis (Wixon etal. 2000). e
C
B
amputation rate was also lower (2% vs. 33%). Especially patients with critical leg ischemia at the time of bypass gra­ing appear to benet from sonographic surveillance and gra revision (Visser et al. 2001). In this study, patients in the
V
duplex surveillance group had a major amputation rate of
1.7% compared with 7.7% in patients undergoing surveil­lance with clinical examination and ABI only. e cost of diagnosis and treatment was only half as high in the duplex group. e subgroup of patients with intermittent claudica­tion at the time of bypass surgery beneted less from sono­graphic surveillance.
Overall, these ndings show a benet of routine duplex surveillance for patients with autologous vein gras, while a benet is less apparent for patients with synthetic gras. Many studies are limited by the fact that they investigated mixed populations of patients with venous and synthetic bypass gras. e poorer predictive value of routine surveil­lance in patients with synthetic gras seems to be attribut­able to the complexity of factors that can cause occlusion of these gras. Oen, a stenotic lesion is not detectable and the mechanism of occlusion remains unclear. It is obvious, then, that duplex surveillance can contribute little to the identica­tion of failing synthetic gras.
A large meta-analysis (Golledge etal. 1996) comparing
I
2680 duplex surveillance and 3369 nonsurveillance vein gras showed that routine duplex surveillance improved bypass patency rates but not the (long-term) limb salvage rate.
II
e Vein Gra Surveillance Randomised Trial (VGST) had great impact regarding the role of routine duplex sur-
III
veillance in patients with venous gras (Davies etal. 2005). In this prospective, randomized multicenter trial of 594 patients, no dierence was found between clinical and duplex surveillance in terms of primary patency, primary
IV
assisted patency, secondary patency, and amputation rates. A limitation of the VGST is that no subgroup analysis was done.
us, while there is no added benet of routine duplex monitoring of leg bypass gras (as shown by Kaplan–Meier analysis), a duplex ultrasound evaluation is warranted when­ever serial clinical examination, pulse status, or the ABI shows deterioration. Moreover, patients with venous bypass gras who have a poorer prognosis from the start also ben­et from being enrolled in a duplex surveillance program. Several gra-related and patient-related factors contribute to a poorer prognosis (. Table2.17):
ab
e
2.1 · Pelvic andLeg Arteries
109
2
c d
f
. Fig. 2.41 Bypass graft surveillance. a Long stenosis in a femorocrural reversed vein bypass graft just distal to the proximal anastomosis (due
to use of a small-caliber vein segment for grafting). Spectral Doppler interrogation of the stenotic segment (indicated by aliasing in the color image) demonstrates monophasic ow with a peak systolic velocity (PSV) of 4.1m/s and an end- diastolic velocity (EDV) of 1m/s. b The Dop­pler waveform from within the graft downstream of the anastomotic stenosis shows a monophasic, poststenotic pattern with slow ow (PSV of 25cm/s). c If no ow obstruction is present above, within, or below a bypass graft, an altered ow velocity within the graft may be due to a size mismatch between the graft (synthetic or venous) and the recipient artery (e.g., a calf artery). Very slow ow in the absence of upstream or downstream stenosis can occur when a synthetic graft with too large a diameter has been used or a vein graft has become dilated over time (as in the example, where PSV is 21cm/s). A triphasic waveform obtained in a bypass graft indicates good graft function with adequate peripheral perfusion. In the example, the vein graft anastomosed onto the tibiobular trunk is dilated to 1.3cm, and the bular artery is the only patent calf artery. d An in situ vein graft must be scrutinized for the presence of an AV stula (arising from a nonligated branch or perforating vein), especially if peripheral pulses are poorer than would be expected after a bypass procedure. There is monophasic ow with a large diastolic com­ponent in the graft segment proximal to and within the AV stula due to direct outow into the venous system (BP=bypass). The site of the AV stula is marked for ligation. e High-grade stenosis at the proximal bypass anastomosis (AN) due to neointimal hyperplasia (hypoechoic). f Ilia­cofemoral bypass graft (BP) with high-grade proximal stenosis in the common iliac artery (A.I.C.) giving rise to a monophasic Doppler waveform with a PSV of 550m/s. A poststenotic waveform is obtained in the bypass graft (as in b). A.I.I. = internal iliac artery; A.I.E. = occluded external iliac artery
110
Chapter 2 · Extremity Arteries
loss. e 65% of patients without stenosis had a cumulative patency rate of 82% (Modi etal. 2009). Tinder etal. (2008) found a similar association between early detection of steno-
2
sis and bypass patency in a study of 353 venous bypasses. In this study, patients with normal duplex ndings had a cumu­lative bypass patency rate of 84% at 54months compared with 62% in patients with stenosis (including mild and mod­erate stenotic lesions). Investigators reporting angiographic ndings for comparison found a surprisingly high percent­age of early postoperative stenoses (25–37%) within the rst
a
3months (neointimal proliferation) despite normal intraop­erative completion angiograms. Over time, the rate of de novo stenosis decreased, and patients with early duplex­identied stenosis had a signicantly higher occlusion rate (Ihnat etal. 1999; Mercer etal. 1999).
decision for bypass revision is based on the severity
e of stenosis and poststenotic ow rates; clinical symptoms alone may be misleading as they vary with the patient’s dis­ease stage at the time of the bypass procedure (
. Fig.2.43).
erefore, demonstration of a higher-grade stenosis by duplex ultrasound should prompt an intervention (typically PTA) to maintain gra patency, even in asymptomatic patients. In estimating the degree of gra stenosis, the pro­posed threshold velocities must be applied exibly, taking into account the diameters of the gra and recipient artery.
b
Future studies should establish rened threshold velocities for dierent types of gras (autologous vein versus pros-
. Fig. 2.42 a High-grade venous bypass graft stenosis. Stenosis in
a vein graft is typically due to scar formatiom at retained valve cusps and is graded most reliably using the peak systolic velocity (PSV) ratio. In the example, the waveform shows the prestenotic situation on the left (PSV<50cm/s) and the intrastenotic situation on the right (PSV>3.5m/s). b Neointima (hypoechoic area around patent lumen) in a synthetic femoropopliteal bypass graft (7mm in diameter), reducing the patent lumen to 2.6mm (calipers). Unlike a focal stenosis, a very long segment of luminal narrowing is associated with ow reduction (due to friction) instead of a circumscribed increase in PSV.However, downstream of the narrowed graft, a postenotic ow prole is obtained
thetic gras, bypass diameter), level of bypass (target vessel above or below the knee), and other factors (status of runo vessels).
2.1.7.4 Ultrasound Vein Mapping Prior
toPeripheral Bypass Surgery
Autologous vein gras are superior to other materials in peripheral bypass surgery in terms of short-term and long­term patency rates. However, vein preparation may be time­consuming in patients with anatomic variants, such as an
5 Low-ow bypass and small-caliber vein gra 5 Non-great-saphenous vein gras and composite gras 5 Abnormal intra/postoperative ndings 5 Bypass graing in chronic critical limb ischemia (no
alternative options for restoring blood ow)
5 Distal-origin bypass in patients with severe inow
atherosclerosis.
aberrant course or duplication, and in obese patients. When the great or small saphenous vein is considered, the super­cial course can be identied with a high-resolution trans­ducer (6.5–10MHz) and marked on the skin before surgery. Moreover, duplicated veins can be localized and the most suitable branch selected for graing. When an in situ bypass is planned, perforating veins can also be marked for intraop­erative ligation to prevent development of an AV stula. e
Other investigators explored the benet of a single duplex
follow-up examination
3–6months aer surgery to estimate bypass prognosis and identify patients requiring revision or continuing duplex surveillance (Modi etal. 2007; Tinder etal. 2008). In a study of 365 patients, a single postoperative duplex examination performed 6 months aer vein gra bypass surgery to identify gras at risk (PSV ratio, PSV<45cm/s) demonstrated that critical stenosis was asso­ciated with much poorer gra patency and that most inter­mediate lesions identied by early duplex surveillance showed progression (>75%), resulting in gra dysfunction or
vein diameter is measured in transverse orientation with the great saphenous vein normally having a diameter of 3–4mm below the knee; very thin veins (<2mm) are unsuitable for graing. If two branches are present, the one with the larger caliber is selected. Finally, preoperative ultrasound avoids unnecessary dissection by identifying unsuitable varicose or postthrombophlebitic veins with thickened walls and sclero­sis. Overall,
selection of a suitable graft
preoperative sonographic vein mapping for
shortens the length of surgery and can prevent unnecessary incisions and extensive expo­sure (. Figs. 3.81 and 2.67 (Atlas)).
bc
2.1 · Pelvic andLeg Arteries
a
111
2
. Fig. 2.43 a In a crural bypass, a stenosis just below the distal anastomosis has the same signicance as an anastomotic stenosis. The color duplex
examination reveals high-grade stenosis of the anterior tibial artery (ATA), resulting in slow ow in the bypass (<30cm/s). These ndings suggest a failing bypass and are an indication for graft revision to maintain patency, even in an asymptomatic patient (rightmost image: angiogram obtained during PTA). b, c Femorocrural bypass (BP) onto the anterior tibial artery (A.TIB.ANT) with high-grade stenosis (b) just distal to the anastomosis (PSV of 440cm/s). In this case, a single measurement within the graft would have failed as an indirect stenosis criterion because the PSV of 71cm/s measured in the graft (c) in this patient is above the cuto of 45cm/s. While the waveform shows adequate, pulsatile ow in the graft and runo through the proximal anterior tibial artery, this case also underlines that reliance on a single midgraft PSV measurement is an inadequate criterion. PSV in a bypass crucially depends on graft conguration and outow hemodynamics rather than bypass complications alone
. Table 2.17 Dierentiated approach to the use of duplex ultrasound in the surveillance of patients with lower extemity bypass grafts.
The strategy recommended here has been derived from the conicting scientic evidencea and is based on a single postoperative duplex follow-up examination (after 3–6months) in all patients, with further ultrasound examinations necessary depending on the type of bypass graft and clinical ndings (regular clinical follow-up with ABI at 6-month intervals, duplex ultrasound only in case of bypass deterioration)
Expected benet of routine duplex surveillance at 6-month intervals
No benet, except for a single examination 3– 6 months after surgery
Probably no benet, except for a single examination 3– 6 months after surgery
Benet likely Venous bypass graft:
Bypass graft material and perioperative ndings
Infrainguinal synthetic bypass graft Exception: clinical deterioration (decrease in ABI) Search for underlying cause using duplex ultrasound
Venous bypass graft (in situ, reversed) in patients who meet the following conditions: – Large-caliber bypass graft vein (>5 mm), normal graft vein – Normal intra-/postoperative completion study – Bypass grafting performed in patients with stage II PAOD (intermittent claudication) – Good patient compliance
Thin bypass vein – Non-great-saphenous-vein grafts and composite grafts – Abnormal intra-/postoperative ndings (increased outow resistance, low ow, poor runo vessel) – Bypass grafting performed in patients with chronic critical limb ischemia (stage III or IV PAOD) – Poor patient compliance – All distal-origin bypasses with upstream atherosclerosis
a
Study of Davies etal. (2005) not taken into account because it does not present a subgroup analysis for a dierentiated approach
112
Chapter 2 · Extremity Arteries
2.1.8 Role of(Color) Duplex Ultrasound
Compared withOther Modalities: Problems andPitfalls
2
In the stepwise diagnostic workup of peripheral arterial occlusive disease (PAOD), the patient’s history, clinical examination with evaluation of pulses, and determination of the ankle-brachial index (ABI) should be followed by nonin­vasive duplex imaging before invasive angiography is con­templated (. Fig. 2.7). e clinical stage of PAOD and the sonographic ndings are the basis for further patient man­agement, either initiation of treatment or additional diagnos­tic tests (. Tables 2.18 and 2.19).
For example, patients with sonographically diagnosed iliac or femoropopliteal stenosis can undergo diagnostic angiography with PTA standby. In contrast, patients with
longer occlusions of the pelvic or thigh arteries and sono­graphically adequate peripheral runo with patency of the popliteal artery can be scheduled for bypass surgery without prior angiography if indicated on clinical grounds. Ultrasound alone is also sucient in patients with a popliteal artery aneurysm.
Patients in whom ultrasound reveals external compres­sion (popliteal entrapment syndrome, adventitial cystic disease) can also be operated on without prior angiogra­phy, which provides no additional information and merely serves to document the vascular status. Depicting only the vessel lumen, angiography is inferior to ultrasound in evaluating perivascular structures. A further drawback of angiography is the reduction of the three-dimensional ves­sel lumen to the two-dimensional plane of the lm (see
. Fig. 5.27).
With this limitation, the diameter reduction randomly depicted in the imaging plane does not necessarily repre­sent the true cross-sectional area reduction, as the wall
. Table 2.18 Advantages and disadvantages of duplex
imaging
Advantages Disadvantages
changes may vary along the length of the stenosis (concen­tric– eccentric; regular– irregular). Angiographic stenosis severity may thus dier from the degree determined by spectral Doppler, which reects the hemodynamic eects of
Noninvasiveness Evaluation in dierent planes Evaluation of – Wall morphology – Surrounding structures – Intraluminal structures – Plaque Stenosis grading based on – Morphology – Hemodynamics Low cost
Documentation of ndings Evaluation of collateral pathways Long training period Poor visualization of terminal vascular bed Specic methodological limitations (calcication, air, obesity, edema)
the stenosis. Even dierent ultrasound modes may yield dis­crepant results regarding the degree of luminal narrowing caused by atherosclerotic plaque because they process dif­ferent types of information: conventional B-mode imaging relies on the morphologic gray-scale appearance of the arte­rial lumen in the longitudinal plane, color duplex on the absence of ow signals in the lumen, and spectral Doppler on the hemodynamic eects of the stenotic lesion in terms of ow acceleration. For accurate and reproducible mor­phologic quantication by both B-mode ultrasound and angiography, it is thus necessary to always evaluate a steno­sis in dierent planes (
. Table 2.17). is is especially
important when assessing the pelvic arteries and femoral
. Table 2.19 Advantages and disadvantages of angiography
trifurcation, where eccentric plaques of the posterior wall are common. e mere morphologic assessment of an
Advantages Disadvantages
Documentation of ndings Visualization and evaluation of collateral pathways Adequate evaluation of terminal vascular bed Fairly short training period
Invasiveness and complications (pseudoaneurysm, embolism, bleeding, local thrombosis, AV stula) Visualization of patent lumen only Projection-related problems: – Stenosis grading – Evaluation of bifurcations Some vascular territorities cannot be consistently evaluated in 2 (or 3) planes (iliac artery, femoral bifurca­tion) No information on hemodynamic relevance of dierent plaque congurations Nonvisualization: – Vessel wall – Surrounding structures High cost Radiation exposure and contrast medium administration
eccentric plaque aorded by angiography may overestimate the resulting stenosis compared with its hemodynamic eects, even when evaluated in dierent planes. Moreover, stenosis caused by eccentric plaque may be overlooked or underestimated if only an anteroposterior angiogram is available.
An aspect that tends to be overlooked in the scientic dis­cussion is that
plaque conguration (concentric versus
eccentric) determines the hemodynamic severity of the resulting stenosis in terms of peripheral perfusion impair­ment and the patient’s clinical symptoms. e hemodynamic severity in turn depends on the cross-sectional area reduc­tion, which is the basis for calculating the sonographic degree of stenosis from intrastenotic ow acceleration (see . Fig.
5.27
). Recall that a concentric stenosis that reduces the vessel diameter by 50% reduces the cross-sectional area by 75% as opposed to 50% or less when an eccentric stenosis with the same diameter reduction is present. Sonographically, the for­mer is classied as higher-grade stenosis (PSV ratio of 4