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ORIGINAL RESEARCH<br />

<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Identifying</strong><br />

<strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

<strong>of</strong> 50% or More<br />

Mehmet Yurdakul, MD, Muharrem Tola, MD<br />

Objectives—The proximal segment <strong>of</strong> the vertebral artery is a frequent site <strong>of</strong> obstructive<br />

atherosclerosis. The purpose <strong>of</strong> this study was to determine <strong>Doppler</strong> criteria <strong>for</strong><br />

identifying proximal vertebral artery stenosis <strong>of</strong> 50% or more by comparison with digital<br />

subtraction angiography.<br />

Methods—Forty-eight patients with vertebral artery stenosis were examined prospectively<br />

with color <strong>Doppler</strong> sonography and digital subtraction angiography. The peak<br />

systolic velocity (PSV), end-diastolic velocity (EDV), peak systolic velocity ratio<br />

(PSVr), and end-diastolic velocity ratio (EDVr) were evaluated by receiver operating<br />

characteristic curve analysis <strong>for</strong> their ability to detect vertebral artery stenosis <strong>of</strong> 50% or<br />

more. The optimal criteria <strong>for</strong> identifying proximal vertebral artery stenosis <strong>of</strong> 50% or<br />

more were determined.<br />

Results—For identifying vertebral artery stenosis, the parameter with the highest accuracy<br />

was the PSVr (area under the receiver operating characteristic curve, 0.967 [95%<br />

confidence interval, 0.899–0.994]). A PSVr <strong>of</strong> greater than 2.2 was found to be the optimal<br />

criterion <strong>for</strong> identifying proximal vertebral artery stenosis <strong>of</strong> 50% or more, with<br />

sensitivity and specificity <strong>of</strong> 96% and 89%, respectively. The optimal thresholds <strong>for</strong> the<br />

other <strong>Doppler</strong> parameters in identifying proximal vertebral artery stenosis <strong>of</strong> 50% or<br />

more were as follows: PSV, greater than 108 cm/s; EDV, greater than 36 cm/s; and<br />

EDVr, greater than 1.7.<br />

Conclusions—Color <strong>Doppler</strong> sonography is an accurate method <strong>for</strong> identifying proximal<br />

vertebral artery stenosis. The PSVr is superior to other <strong>Doppler</strong> parameters <strong>for</strong> detecting<br />

vertebral artery stenosis.<br />

Key Words—color <strong>Doppler</strong> sonography; stenosis; vertebral artery<br />

Received July 8, 2010, from the Department <strong>of</strong> Radiology<br />

Turkiye Yüksek Ihtisas Hospital, Ankara, Turkey.<br />

Revision requested August 7, 2010. Revised manuscript<br />

accepted <strong>for</strong> publication August 28, 2010.<br />

Address correspondence to Mehmet Yurdakul,<br />

MD, Department <strong>of</strong> Radiology, Türkiye Yüksek Ihtisas<br />

Hospital, Kizilay Sokak 4, 06100 Sihhiye, Ankara,<br />

Turkey.<br />

E-mail: myurdakul@tyih.gov.tr<br />

Abbreviations<br />

AUC, area under the curve; EDV, end- diastolic<br />

velocity; EDVr, end-diastolic velocity ratio; PSV,<br />

peak systolic velocity; PSVr, peak systolic velocity<br />

ratio; ROC, receiver operating characteristic<br />

<strong>Vertebral</strong> artery stenosis decreases posterior brain perfusion,<br />

causing vertebrobasilar insufficiency, and is source <strong>of</strong><br />

emboli to the posterior circulation. 1,2 The origin and V1<br />

segment (the portion extending from the origin to the entry into<br />

the transverse <strong>for</strong>amen <strong>of</strong> C6) <strong>of</strong> the vertebral artery are common<br />

sites <strong>for</strong> atherosclerotic occlusive disease. 3 About 20% <strong>of</strong> patients<br />

with posterior ischemia have occlusive disease in the proximal vertebral<br />

artery. 1,4 The mortality associated with vertebrobasilar circulation<br />

stroke is 20% to 30%, which is substantially greater than that<br />

<strong>of</strong> carotid circulation stroke. 5<br />

Recently, percutaneous angioplasty with stenting has become<br />

an accepted method <strong>for</strong> treatment <strong>of</strong> vertebral artery stenosis. 6–20<br />

Unlike carotid artery stenosis, there is no well-established indication<br />

<strong>for</strong> treatment <strong>of</strong> vertebral artery stenosis.<br />

©2011 by the American Institute <strong>of</strong> Ultrasound in Medicine | J Ultrasound Med 2011; 30:163–168 | 0278-4297/11/$3.50 | www.aium.org


Yurdakul and Tola—<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

Color <strong>Doppler</strong> sonography, which is a noninvasive<br />

and cost-effective method, is a suitable screening test <strong>for</strong><br />

proximal vertebral artery stenosis. However, very few studies<br />

have been per<strong>for</strong>med to determine <strong>Doppler</strong> criteria <strong>for</strong><br />

identifying proximal vertebral artery stenosis. 21,22 The purpose<br />

<strong>of</strong> this study was to determine <strong>Doppler</strong> criteria <strong>for</strong><br />

identifying proximal vertebral artery stenosis <strong>of</strong> 50% or<br />

more by comparison with digital subtraction angiography.<br />

Materials and Methods<br />

From June 2008 to December 2009, 48 consecutive patients<br />

(28 men and 20 women; age range, 43–88 years;<br />

mean age, 64.7 years) were referred by the cardiovascular<br />

surgery clinic <strong>for</strong> digital subtraction angiography, which<br />

showed vertebral artery stenosis <strong>of</strong> 50% or more. These<br />

patients were examined by color <strong>Doppler</strong> sonography after<br />

digital subtraction angiography. Patients were excluded<br />

from this study if they had any <strong>of</strong> the following: (1) previous<br />

surgery or stenting, (2) calcification extensive enough<br />

to obscure the ultrasound signal intensity in the stenotic<br />

area, (3) an aortic origin <strong>of</strong> the vertebral artery, (4) a hypoplastic<br />

(diameter 50%). All patients gave their oral in<strong>for</strong>med consent,<br />

and the Institutional Review Board approved the<br />

study.<br />

Digital subtraction angiography was per<strong>for</strong>med with<br />

an Integris Allura system (Philips Healthcare, Best, the<br />

Netherlands). All catheterizations were per<strong>for</strong>med by a<br />

transfemoral approach with standard diagnostic catheters.<br />

After aortic arch injection, selective supra-aortic (carotid<br />

and subclavian) artery injections were per<strong>for</strong>med. Nonionic<br />

contrast media were used. <strong>Vertebral</strong> artery stenosis<br />

was calculated by comparison with the nearest normal distal<br />

segment.<br />

For color <strong>Doppler</strong> sonography, a LOGIQ 7 system<br />

(GE Healthcare, Tokyo, Japan) was used. All examinations<br />

were per<strong>for</strong>med while the patient was in a supine position<br />

with the head slightly turned to opposite side. First, the<br />

common carotid artery was located in the longitudinal<br />

plane with a 2.5- to 7-MHz linear transducer. The vertebral<br />

artery was then shown between the transverse<br />

processes by posterolateral movement <strong>of</strong> the transducer.<br />

The presence and direction <strong>of</strong> flow were determined, and<br />

a velocity wave<strong>for</strong>m was obtained. The peak systolic velocity<br />

(PSV) and end-diastolic velocity (EDV) <strong>of</strong> blood<br />

flow in the V2 segment <strong>of</strong> the vertebral artery (the portion<br />

extending from the transverse <strong>for</strong>amen <strong>of</strong> C6–C1)<br />

were recorded. The measurements in this segment were<br />

used only as reference measurements <strong>for</strong> velocity ratio<br />

calculations. The vertebral artery was followed downward<br />

to image the origin and V1 segment the vertebral<br />

artery with a 2.5- to 7-MHz linear or 1.5- to 4.5-MHz<br />

convex transducer. A velocity wave<strong>for</strong>m was obtained<br />

routinely from the origin <strong>of</strong> the vertebral artery. The V1<br />

segment was sampled proximally to distally, where color<br />

flow imaging showed areas <strong>of</strong> abnormal flow such as<br />

color aliasing and color bruits. The highest PSV and EDV<br />

<strong>of</strong> blood flow in the V1 segment were recorded. The peak<br />

systolic velocity ratio (PSVr) and end-diastolic velocity<br />

ratio (EDVr) were calculated as the maximum PSV and<br />

EDV <strong>of</strong> the V1 segment divided by the corresponding velocities<br />

<strong>of</strong> the V2 segment. The color <strong>Doppler</strong> sonographic<br />

examinations were per<strong>for</strong>med by the same<br />

experienced radiologist (M.T.), who was unaware <strong>of</strong> clinical<br />

data (digital subtraction angiographic results, any<br />

other imaging data, physical examination results, laboratory<br />

results, and patient history). The insonation angle<br />

was kept at 60° or less.<br />

For statistical analyses, the right and left sides <strong>of</strong> each<br />

patient were accepted as separate cases. The highest PSV<br />

and EDV at the V1 segment and the PSVr and EDVr<br />

were evaluated by receiver operating characteristic<br />

(ROC) curve analysis <strong>for</strong> their ability to detect vertebral<br />

artery stenosis <strong>of</strong> 50% or more. The ROC curves based on<br />

these <strong>Doppler</strong> data were compared by measuring the areas<br />

under the curves (AUCs). The AUCs were compared by<br />

a z test, as described by Hanley and McNeil. 23 For each<br />

<strong>Doppler</strong> parameter, the threshold at which sensitivity and<br />

specificity were optimum was determined. P < .05 was considered<br />

statistically significant.<br />

Results<br />

In our study, 19 vertebral arteries were excluded (1 with<br />

extensive calcification, 1 with an aortic origin, 4 hypoplastic<br />

arteries, 12 with occlusion, and 1 with subclavian artery<br />

occlusion). One right vertebral artery with extensive calcification<br />

and 1 left vertebral artery originating from the aorta<br />

could not be completely visualized by color <strong>Doppler</strong><br />

sonography. In no patient were both vertebral arteries excluded.<br />

All <strong>of</strong> the occlusions were correctly diagnosed by<br />

color <strong>Doppler</strong> sonography. The remaining 77 vertebral arteries<br />

(36 right and 41 left) were included in the statistical<br />

evaluation. Thirty-two patients had single-sided and 16<br />

had double-sided stenosis <strong>of</strong> 50% or more or occlusion.<br />

The overall distribution <strong>of</strong> vertebral arteries with respect<br />

to the degree <strong>of</strong> stenosis is shown in Figure 1. Images from<br />

a patient are shown in Figure 2.<br />

164<br />

J Ultrasound Med 2011; 30:163–168


Yurdakul and Tola—<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

An ROC analysis was per<strong>for</strong>med <strong>for</strong> proximal vertebral<br />

artery stenosis <strong>of</strong> 50% or more based on the <strong>Doppler</strong><br />

velocity parameters, and AUCs <strong>for</strong> the parameters were<br />

calculated and compared (Figure 3 and Tables 1 and 2).<br />

The PSVr was found to be the most accurate parameter<br />

(AUC, 0.967 [95% confidence interval, 0.889–0.994]).<br />

For each parameter, the optimal threshold was determined<br />

by ROC curve analysis (Table 1). The optimal thresholds<br />

<strong>for</strong> identifying stenosis <strong>of</strong> 50% or more were as follows:<br />

PSV, greater than 108 cm/s; EDV, greater than 36 cm/s;<br />

PSVr, greater than 2.2; and EDVr, greater than 1.7. Accuracy<br />

ratios <strong>for</strong> these threshold values are shown in Table 1.<br />

Figure 2. Severe right vertebral artery stenosis in a 70-year-old woman.<br />

A, Angiogram showing 60% stenosis at the origin <strong>of</strong> the right vertebral<br />

artery. B, Color <strong>Doppler</strong> sonogram showing high-velocity flow at the origin<br />

<strong>of</strong> the right vertebral artery with a peak systolic velocity <strong>of</strong> 203 cm/s<br />

and an end-diastolic velocity <strong>of</strong> 60 cm/s. C, Color <strong>Doppler</strong> sonogram<br />

showing a peak systolic velocity <strong>of</strong> 56 cm/s and an end-diastolic velocity<br />

<strong>of</strong> 26 cm/s in the V2 segment <strong>of</strong> the right vertebral artery.<br />

A<br />

Discussion<br />

The vertebral arteries typically arise from the superoposterior<br />

aspect <strong>of</strong> the first part <strong>of</strong> the subclavian artery and are<br />

usually the first branches <strong>of</strong> this vessel. In 6% <strong>of</strong> patients,<br />

they arise directly from the aortic arch between the origin <strong>of</strong><br />

the left common carotid and left subclavian arteries. 24 The<br />

vertebral arteries supply a low-resistance system to the<br />

brainstem and posterior cerebral circulation vessels. They<br />

also make an important contribution to the anterior circulation<br />

in certain circumstances. Both vertebral arteries deliver<br />

approximately 20% <strong>of</strong> the total cerebral blood flow. 25<br />

Atherosclerosis is the dominant nontraumatic condition<br />

seen in the vertebral artery. 26 The most frequent site<br />

<strong>of</strong> involvement is the vertebral artery origin from the subclavian<br />

artery. 3,27 The reference standard <strong>for</strong> detection <strong>of</strong><br />

stenosis <strong>of</strong> craniocervical vessels is still conventional<br />

catheter angiography; however, it is an invasive procedure<br />

associated with a low but definite incidence <strong>of</strong> complications.<br />

28–30 Noninvasive tests, such as color <strong>Doppler</strong><br />

sonography, magnetic resonance angiography, and, most<br />

B<br />

Figure 1. Distribution <strong>of</strong> vertebral artery stenosis according to angiographic<br />

measurements.<br />

C<br />

J Ultrasound Med 2011; 30:163–168<br />

165


Yurdakul and Tola—<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

Figure 3. Receiver operating characteristic curves <strong>for</strong> detection vertebral<br />

artery stenosis <strong>of</strong> 50% or more based on <strong>Doppler</strong> velocity parameters.<br />

EDV indicates end-diastolic velocity; EDVr, end-diastolic velocity<br />

ratio; PSV, peak systolic velocity; and PSVr, peak systolic velocity ratio.<br />

recently, computed tomographic angiography, have been<br />

used without digital subtraction angiography in screening<br />

<strong>for</strong> craniocervical vessel disease. Although magnetic resonance<br />

angiography and computed tomographic angiography<br />

are valuable imaging methods, these techniques are<br />

expensive and need additional contrast medium administration.<br />

Color <strong>Doppler</strong> sonography is a noninvasive and<br />

inexpensive method used to evaluate craniocervical vessels<br />

that provides anatomic and hemodynamic in<strong>for</strong>mation<br />

about those vessels.<br />

Color <strong>Doppler</strong> sonography is the most appropriate<br />

method <strong>for</strong> diagnosis <strong>of</strong> carotid artery stenosis, but it is not<br />

as appropriate <strong>for</strong> vertebral artery stenosis. It is difficult to<br />

show the proximal vertebral artery because <strong>of</strong> its many<br />

anatomic characteristics, such as a small diameter, a deep<br />

location, tortuosity, and a perpendicular origin from the<br />

subclavian artery. There<strong>for</strong>e, most vascular laboratories<br />

simply determine the presence and direction <strong>of</strong> blood flow<br />

in the midcervical vertebral artery without extensive exploration<br />

<strong>of</strong> the origin and proximal portion. For identifying<br />

proximal vertebral artery stenosis, indirect criteria are<br />

used, such as turbulent flow and spectral broadening at the<br />

origin or markedly reduced pulsatility beyond the area <strong>of</strong><br />

stenosis compared to the contralateral vessel.<br />

The origin and proximal segment <strong>of</strong> the vertebral artery<br />

can be easily identified by using the color mode. 31 In<br />

this study, the V2 segment <strong>of</strong> the vertebral artery was followed<br />

downward with the help <strong>of</strong> the color mode to identify<br />

the V1 segment and origin <strong>of</strong> the vertebral artery.<br />

Our study showed that the PSVr and EDVr had better<br />

diagnostic accuracy than the PSV and EDV, respectively.<br />

The PSV was found to be superior to the EDV, but<br />

the PSVr was the most accurate. The optimal PSVr threshold<br />

<strong>for</strong> identifying vertebral artery stenosis was 2.2, and its<br />

sensitivity and specificity were 96% and 89%, respectively.<br />

Two recently published retrospective studies aimed<br />

to develop <strong>Doppler</strong> criteria <strong>for</strong> identifying vertebral artery<br />

stenosis 21,22 ; however, the absolute velocity criteria obtained<br />

in those studies were different from those <strong>of</strong> our<br />

study. Although the PSVr values were similar, the PSV was<br />

the most accurate parameter in those studies, whereas the<br />

PSVr was the most accurate in our study. The reason <strong>for</strong><br />

this discrepancy may have been that the patient populations<br />

were different: whereas patients with carotid and contralateral<br />

vertebral artery disease were excluded in 1 <strong>of</strong><br />

those studies, our patient population included patients<br />

with occlusive carotid artery disease, and patients with<br />

contralateral vertebral artery disease were not excluded<br />

from our study. As is known, in occlusive carotid artery<br />

and contralateral vertebral artery disease, the collateral<br />

flow that develops from the ipsilateral vertebral artery<br />

by way <strong>of</strong> the circle <strong>of</strong> Willis may cause an increase in<br />

absolute flow velocities.<br />

In addition to occlusive disease <strong>of</strong> the carotid artery<br />

and contralateral vertebral artery, other conditions also<br />

cause vertebral artery flow variation. Asymmetry is the rule<br />

in the vertebral arteries, unlike the carotid arteries. In a<br />

dominant vertebral artery, the flow velocity is relatively<br />

high. In a vertebral artery ending at a posteroinferior cerebellar<br />

artery, flow is low. Tandem lesions in vertebral or<br />

Table 1. Diagnostic Accuracy <strong>of</strong> Color <strong>Doppler</strong> Sonography <strong>for</strong> <strong>Identifying</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong> <strong>of</strong> 50% or More<br />

Parameter AUC (95% CI) <strong>Criteria</strong> Sensitivity, % Specificity, % PPV, % NPV, %<br />

PSV 0.884 (0.790–0.945) >108 cm/s 88 71 84 77<br />

EDV 0.774 (0.664–0.862) >36 cm/s 61 86 88 56<br />

PSVr 0.967 (0.899–0.994) >2.2 96 89 94 93<br />

EDVr 0.871 (0.775–0.936) >1.7 80 86 91 71<br />

AUC indicates area under the curve; CI, confidence interval; EDV, end-diastolic velocity; EDVr, end-diastolic velocity ratio; NPV, negative predictive<br />

value; PPV, positive predictive value; PSV peak systolic velocity; and PSVr, peak systolic velocity ratio.<br />

166 J Ultrasound Med 2011; 30:163–168


Yurdakul and Tola—<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

Table 2. Comparison <strong>of</strong> Areas Under the Curves <strong>of</strong> <strong>Doppler</strong> Velocity<br />

Parameters <strong>for</strong> <strong>Identifying</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

Parameters Difference Between AUCs (95% CI) P<br />

PSV and EDV 0.110 (0.034–0.185) .005<br />

PSV and PSVr 0.083 (0.022–0.145) .007<br />

PSV and EDVr 0.013 (–0.060–0.086) .724<br />

EDV and PSVr 0.193 (0.095–0.291) .001<br />

EDV and EDVr 0.097 (0.006–0.187) .037<br />

PSVr and EDVr 0.097 (0.035–0.158) .002<br />

AUC indicates area under the curve; CI, confidence interval; EDV, enddiastolic<br />

velocity; EDVr, end-diastolic velocity ratio; PSV peak systolic<br />

velocity; and PSVr, peak systolic velocity ratio.<br />

basilar arteries also cause low flow. For these reasons, use<br />

<strong>of</strong> the PSVr seems to be appropriate <strong>for</strong> identifying vertebral<br />

artery stenosis.<br />

A limitation <strong>of</strong> our study was that the patients were<br />

not selected from a general population. All patients in our<br />

study had occlusive carotid artery disease. Because <strong>of</strong> this,<br />

the results obtained from this study do not represent the<br />

general population. The use <strong>of</strong> a single view on digital subtraction<br />

angiography, which is the reference standard <strong>for</strong><br />

identifying stenosis, was another limitation.<br />

In conclusion, color <strong>Doppler</strong> sonography is an accurate<br />

method <strong>for</strong> identifying proximal vertebral artery stenosis.<br />

The PSVr is superior to other <strong>Doppler</strong> parameters <strong>for</strong><br />

detecting vertebral artery stenosis.<br />

References<br />

1. Wityk RJ, Chang HM, Rosengart A, et al. <strong>Proximal</strong> extracranial vertebral<br />

artery disease in the New England Medical Center Posterior Circulation<br />

Registry. Arch Neurol 1998; 55:470–478.<br />

2. Caplan LR, Amarenco P, Rosengart A, et al. Embolism from vertebral artery<br />

origin occlusive disease. Neurology 1992; 42:1505–1512.<br />

3. Castaigne P, Lhermitte F, Gautier JC, et al. Arterial occlusions in the<br />

vertebro-basilar system: a study <strong>of</strong> 44 patients with post-mortem data.<br />

Brain 1973; 96:133–154.<br />

4. Caplan LR, Wityk RJ, Glass TA, et al. New England Medical Center Posterior<br />

Circulation Registry. Ann Neurol 2004; 56:389–398.<br />

5. Moufarrij NA, Little JR, Furlan AJ, Williams G, Marzewski DJ. <strong>Vertebral</strong><br />

artery stenosis: long-term follow-up. Stroke 1984; 15:260–263.<br />

6. Storey GS, Marks MP, Dake M, Norbash AM, Steinberg GK. <strong>Vertebral</strong><br />

artery stenting following percutaneous transluminal angioplasty. J Neurosurg<br />

1996; 84:883–887.<br />

7. Malek AM, Higashida RT, Phatouros CC, et al. Treatment <strong>of</strong> posterior<br />

circulation ischemia with extracranial percutaneous balloon angioplasty<br />

and stent placement. Stroke 1999; 30:2073–2085.<br />

8. Jenkins JS, White CJ, Ramee SR, et al. <strong>Vertebral</strong> artery stenting. Cathet<br />

Cardiovasc Interv 2001; 54:1–5.<br />

9. Mukherjee D, R<strong>of</strong>fi M, Kapadia SR, et al. Percutaneous intervention <strong>for</strong><br />

symptomatic vertebral artery stenosis using coronary stents. J Invasive Cardiol<br />

2001; 13:363–366.<br />

10. Piotin M, Spelle L, Martin JB, et al. Percutaneous transluminal angioplasty<br />

and stenting <strong>of</strong> the proximal vertebral artery <strong>for</strong> symptomatic stenosis.<br />

AJNR Am J Neuroradiol 2000; 21:727–731.<br />

11. Albuquerque FC, Fiorella D, Han P, Spetzler RF, McDougall CG. A reappraisal<br />

<strong>of</strong> angioplasty and stenting <strong>for</strong> the treatment <strong>of</strong> vertebral origin<br />

stenosis. Neurosurgery 2003; 53:607–616.<br />

12. SSYLVIA Study Investigators. Stenting <strong>of</strong> Symptomatic Atherosclerotic<br />

Lesions in the <strong>Vertebral</strong> or Intracranial Arteries (SSYLVIA): study results.<br />

Stroke 2004; 35:1388–1392.<br />

13. Lin YH, Juang JM, Jeng JS, Yip PK, Kao HL. Symptomatic ostial vertebral<br />

artery stenosis treated with tubular coronary stents: clinical results<br />

and restenosis analysis. J Endovasc Ther 2004; 11:719–726.<br />

14. Wehman JC, Hanel RA, Guidot CA, Guterman LR, Hopkins LN. Atherosclerotic<br />

occlusive extracranial vertebral artery disease: indications <strong>for</strong><br />

intervention, endovascular techniques, short-term and long-term results.<br />

J Interv Cardiol 2004; 17:219–232.<br />

15. Coward LJ, McCabe DJ, Ederle J, Featherstone RL, Clifton A, Brown<br />

MM. Long-term outcome after angioplasty and stenting <strong>for</strong> symptomatic<br />

vertebral artery stenosis compared with medical treatment in the Carotid<br />

and <strong>Vertebral</strong> <strong>Artery</strong> Transluminal Angioplasty Study (CAVATAS):<br />

a randomized trial. Stroke 2007; 38:1526–1530.<br />

16. Qureshi AI, Kirmani JF, Harris-Lane P, et al. <strong>Vertebral</strong> artery origin stent<br />

placement with distal protection: technical and clinical results. AJNR Am<br />

J Neuroradiol 2006; 27:1140–1145.<br />

17. Vajda Z, Miloslavski E, Güthe T, et al. Treatment <strong>of</strong> stenoses <strong>of</strong> vertebral<br />

artery origin using short drug-eluting coronary stents: improved followup<br />

results. AJNR Am J Neuroradiol 2009; 30:1653–1656.<br />

18. Taylor RA, Siddiq F, Memon MZ, et al. <strong>Vertebral</strong> artery ostial stent placement<br />

<strong>for</strong> atherosclerotic stenosis in 72 consecutive patients: clinical outcomes<br />

and follow-up results. Neuroradiology 2009; 51:531–539.<br />

19. Yu SC, Leung TW, Lam JS, Lam WW, Wong LK. Symptomatic ostial<br />

vertebral artery stenosis: treatment with drug-eluting stents—clinical and<br />

angiographic results at 1-year follow-up. Radiology 2009; 251:224–232.<br />

20. Jenkins JS, Patel SN, White CJ, et al. Endovascular stenting <strong>for</strong> vertebral artery<br />

stenosis. J Am Coll Cardiol 2010; 55:538–542.<br />

21. Koch S, Romano JG, Park H, Amir M, Forteza AM. Ultrasound velocity<br />

criteria <strong>for</strong> vertebral origin stenosis. J Neuroimaging 2009; 19:242–245.<br />

22. Hua Y, Meng XF, Jia LY, et al. Color <strong>Doppler</strong> imaging evaluation <strong>of</strong> proximal<br />

vertebral artery stenosis. AJR Am J Roentgenol2009; 193:1434–1438.<br />

23. Hanley JA, McNeil BJ. A method <strong>of</strong> comparing the areas under receiver<br />

operating characteristic curves derived from the same cases. Radiology<br />

1983; 148:839–843.<br />

24. Kadir S. Regional anatomy <strong>of</strong> the thoracic aorta. In: Kadir S (ed). Atlas <strong>of</strong><br />

Normal and Variant Angiographic Anatomy. Philadelphia, PA: WB Saunders<br />

Co; 1991:19–54.<br />

J Ultrasound Med 2011; 30:163–168<br />

167


Yurdakul and Tola—<strong>Doppler</strong> <strong>Criteria</strong> <strong>for</strong> <strong>Proximal</strong> <strong>Vertebral</strong> <strong>Artery</strong> <strong>Stenosis</strong><br />

25. Savitz SI, Caplan LR. Vertebrobasilar disease. N Engl J Med 2005;<br />

352:2618–2626.<br />

26. Hutchison E, Yates P. Carotico-vertebral stenosis. Lancet 1957; 2:2–11.<br />

27. Schwartz CJ, Mitchell JR. Atheroma <strong>of</strong> the carotid and vertebral arterial<br />

systems. Br Med J 1961; 2:1057–1063.<br />

28. Berteloot D, Leclerc X, Leys D, Krivosic R, Pruvo JP. Cerebral angiography:<br />

a study <strong>of</strong> complications in 450 consecutive procedures [in French].<br />

J Radiol 1999; 80:843–848.<br />

29. Hankey GJ, Warlow CP, Molyneux AJ. Complications <strong>of</strong> cerebral angiography<br />

<strong>for</strong> patients with mild carotid territory ischaemia being considered<br />

<strong>for</strong> carotid endarterectomy. J Neurol Neurosurg Psychiatry 1990;<br />

53:542–548.<br />

30. Hankey GJ, Warlow CP, Sellar RJ. Cerebral angiographic risk in mild cerebrovascular<br />

disease. Stroke 1990; 21:209–222.<br />

31. Kuhl V, Tettenborn B, Eicke BM, Visbeck A, Meckes S. Color-coded duplex<br />

ultrasonography <strong>of</strong> the origin <strong>of</strong> the vertebral artery: normal values <strong>of</strong><br />

flow velocities. J Neuroimaging 2000; 10:17–21.<br />

168<br />

J Ultrasound Med 2011; 30:163–168

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