Abstract
Duplex ultrasonography is usually the initial study used to evaluate carotid artery disease. It provides an accurate noninvasive tool to determine the degree of carotid stenosis and plaque morphology. Although this study has a high sensitivity and specificity, it is an operator-dependent study.
Computed tomography angiography (CTA) has been widely used to evaluate carotid artery stenosis. It has a high sensitivity, specificity, and accuracy and provides additional information about the conformation and composition of the plaque. It is less susceptible than magnetic resonance angiography (MRA) in overestimating the severity of carotid stenosis. It is extremely fast and offers submillimeter spatial resolution, is less expensive than contrast-enhanced MRA, and has the ability to visualize soft tissue, bone, and blood vessels at the same time. CTA can interrogate the arterial tree from the aortic arch to the circle of Willis. It cannot be used to evaluate flow dynamics or for the diagnosis of subclavian steal or other flow-based lesions. It carries a risk for ionizing radiation and contrast-induced nephropathy. Currently, CTA is not used in patients with acute renal failure unless other modalities are not available.
MRA has the advantage of being noninvasive, does not require iodinated contrast or ionizing radiation, and provides an unlimited number of projections of the carotid lumen from a single acquisition. MRA can assess intrathoracic and intracranial lesions that are not amenable to duplex interrogation. Using dedicated protocols, MRA can demonstrate specific plaque components, e.g., calcium, lipid, fibrocellular element, or thrombus within the plaques. Unfortunately, however, the use of MRA as a diagnostic tool for carotid stenosis is often dependent on local expertise and familiarity with the test.
Digital subtraction angiography (DSA) is the gold standard for the diagnosis of carotid artery disease, and it offers the highest resolution available for visualizing the carotid artery. It has multiple disadvantages, however, including risks associated with conscious sedation, ionizing radiation, and nephrotoxic contrast agents. It is associated with access-related complications, including atheroembolic disease, thrombosis, dissection, and bleeding. In addition, information regarding the cerebral circulation can be obtained simultaneously, including patency of the carotid siphon and middle cerebral artery. This chapter will summarize the role of each imaging modality in the diagnosis of carotid artery disease.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Sabeti S, Schlager O, Exner M, Mlekusch W, Amighi J, Dick P, Maurer G, Huber K, Koppensteiner R, Wagner O, Minar E, Schillinger M. Progression of carotid stenosis detected by duplex ultrasonography predicts adverse outcomes in cardiovascular high-risk patients. Stroke. 2007;38(11):2887–94.
Bertges DJ, Muluk V, Whittle J, Kelley M, MacPherson DS, Muluk SC. Relevance of carotid stenosis progression as a predictor of ischemic neurological outcomes. Arch Intern Med. 2003;163:2285–9.
North American Symptomatic Carotid Endarterectomy Trial Collaborators (NASCET). Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. N Engl J Med. 1991;325:445.
Barnett HJ, Taylor DW, et al. Benefit of carotid endarterectomy in patients with symptomatic moderate or severe stenosis. North American Symptomatic Carotid Endarterectomy Trial Collaborators. N Engl J Med. 1998;339(20):1415–25.
ECST. Randomized trial of endarterectomy for recently symptomatic carotid stenosis: final results of the MRC European Carotid Surgery Trial (ECST). Lancet. 1998;351(9113):1379–87.
Executive Committee for the Asymptomatic Carotid Atherosclerosis Study. Endarterectomy for asymptomatic carotid artery stenosis. JAMA. 1995;273:1421–8.
European Carotid Surgery Trialists’ Collaborative Group. Risk of stroke in the distribution of an asymptomatic carotid artery. Lancet. 1995;345:209.
Ricotta JJ, Schenck EA, Hassett JM, Deweese JA. Lesion width as a discriminator of plaque characteristics. J Cardiovasc Surg. 1996;4(2):124–9.
Grant EG, Benson CB, Moneta GL, Alexandrov AV, Baker JD, Bluth EI, Carroll BA, Eliasziw M, Gocke J, Hertzberg BS, Katarick S, Needleman L, Pellerito J, Polak JF, Rholl KS, Wooster DL, Zierler E. Carotid artery stenosis: grayscale and Doppler ultrasound diagnosis—Society of Radiologists in ultrasound consensus conference. Ultrasound Q. 2003;19:190–8.
AbuRahma AF, Srivastava M, Stone PA, Mousa AY, Jain A, Dean LS, Keiffer T, Emmett M. Critical appraisal of the carotid duplex consensus criteria in the diagnosis of carotid artery stenosis. J Vasc Surg. 2011;53:53–60.
Busuttil SJ, Franklin DP, Youkey JR, Elmore JR. Carotid duplex overestimation of stenosis due to severe contralateral disease. Am J Surg. 1996;172:144–7.
Comerota AJ, Sales-Cunha SX, Daoud Y, Jones L, Beebe HG. Gender differences in blood velocities across carotid stenoses. J Vasc Surg. 2004;40:939–44.
Lal BK, Hobson RW, Tofghi B, Kapadia I, Cuadra S, Jamil Z. Duplex ultrasound velocity criteria for the stented carotid artery. J Vasc Surg. 2008;47:63–73.
Sitzer M, Rose G, Furst G, Siebler M, Steinmetz H. Characteristics and clinical value of an intravenous echo-enhancement agent in evaluation of high-grade internal carotid stenosis. J Neuroimaging. 1997;7:S22–5.
Ferrer JM, Samso JJ, Serrando JR, Valenzuela VF, Montoya SB, Docampo MM. Use of ultrasound contrast in the diagnosis of carotid artery occlusion. J Vasc Surg. 2000;31:736–41.
Bude RO, Rubin JM, Adler RS. Power vs. conventional color Doppler sonography: comparison in the depiction of normal intrarenal vasculature. Radiology. 1994;192:777–80.
Phillips CD, Bubash LA. CT angiography and MR angiography in the evaluation of extracranial carotid vascular disease. Radiol Clin North Am. 2002;40:783–98.
Cinat M, Lane C, Pham H, Lee A, Wilson S, Gordon I. Helical CT angiography in the preoperative evaluation of carotid artery stenosis. J Vasc Surg. 1998;28:290–300.
Bartlet ES, Walters TD, Symons SP. Quantification of carotid stenosis on CT angiography. AJNR Am J Neuroradiol. 2006;27:13.
Koelemay MJ, Nederkoom PJ, Reitsma JB, Majoie CB. Systematic review of computed tomographic angiography for assessment of carotid artery disease. Stroke. 2004;35:2306–12.
Gronholdt ML. B-mode ultrasound and spiral CT for the assessment of carotid atherosclerosis. Neuroimaging Clin N Am. 2002;12:421–35.
Nederkoorn PJ, Elgersma OE, Mali WP, Eikelboom BC, Kappelle LJ, van der Graaf Y. Overestimation of carotid artery stenosis with magnetic resonance angiography compared with digital subtraction angiography. J Vasc Surg. 2002;36:806–13.
Yuan C, Lin E, Millard J, Hwang J. Closed contour edge detection of blood vessel lumen and outer wall boundaries in black-blood MR images. Magn Reson Imaging. 1999;17:257–66.
Zhang S, Hatsukami T, Polissar N, Han C, Yuan C. Comparison of carotid vessel wall area measurements using three different contrast-weighted black blood MR imaging techniques. Magn Reson Imaging. 2001;19:795–802.
Nederkoom PJ, van der Graaf Y, Hunink MG. Duplex ultrasound and magnetic resonance angiography compared with digital subtraction angiography in carotid artery stenosis: a systematic review. Stroke. 2003;34:1324–32.
Remonda L, Senn P, Barth A, Arnold M, Lovblad KO, Schroth G. Contrast-enhanced 3D MR angiography of the carotid artery: comparison with conventional digital subtraction angiography. Am J Neuroradiol. 2002;23:213–9.
Yuan C, Mitsumori LM, Ferguson MS, et al. In vivo accuracy of multispectral magnetic resonance imaging for identifying lipid-rick necrotic cores and intraplaque hemorrhage in advanced human carotid plaques. Circulation. 2001;104:2051–6.
Hatsukami TS, Ross R, Polissar NL, Yuan C. Visualization of fibrous cap thickness and rupture in human atherosclerotic carotid plaque in vivo with high-resolution magnetic resonance imaging. Circulation. 2000;102:959–64.
Prince MR, Zhang H, Morris M, et al. Incidence of nephrogenic systemic fibrosis at two large medical centers. Radiology. 2008;248:807–16.
Othersen JB, Maize JC, Woolson RF, et al. Nephrogenic systemic fibrosis after exposure to gadolinium in patients with renal failure. Nephrol Dial Transplant. 2007;22:3179–85.
Panda S, Bandyopadhyay D, Tarafder A. Nephrogenic fibrosing dermopathy: a series in a non-western population. J Am Acad Dermatol. 2006;54:155–9.
Hankey GJ, Warlow CP, Molyneux AJ. Complications of cerebral angiography for patients with mild carotid territory ischaemia being considered for carotid endarterectomy. J Neurol Neurosurg Psychiatry. 1990;53:542–8.
Davies KN, Humphrey PR. Complications of cerebral angiography in patients with symptomatic carotid territory ischaemia screened by carotid ultrasound. J Neurol Neurosurg Psychiatry. 1993;56:967–72.
Leonardi M, Cenni P, Simonetti L, Raffi L, Battaglia S. Retrospective study of complications arising during cerebral and spinal diagnostic angiography from 1998 to 2003. Interv Neuroradiol. 2005;11:213–21.
Johnston DC, Chapman KM, Goldstein LB. Low rate of complications of cerebral angiography in routine clinical practice. Neurology. 2001;57(11):2012–4.
Lilly MP, Reichman W, Sarazen AA, Carney WI. Anatomic and clinical factors associated with complications of transfemoral arteriography. Ann Vasc Surg. 1990;4:264–9.
Wardlaw JM, Chappell FM, Stevenson M, et al. Accurate, practical and cost-effective assessment of carotid stenosis in the UK. Health Technol Assess. 2006;10:iii–iv, ix–x, 1–182.
Sabeti M, Tegos T, Nicolaides A, El-Atrozy T, Dhanjil S, Griffin M, Belcaro G, Geroulakos G. Hemispheric symptoms and carotid plaque echomorphology. J Vasc Surg. 2000;31:39–49.
Van den Berg R, Wasser MN, van Gils AP, van der Mey AG, Hermans J, van Buchem MA. Vascularization of head and neck paragangliomas: comparison of three MR angiographic techniques with digital subtraction angiography. Am J Neuroradiol. 21(1):162–70.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Review Questions
Review Questions
-
1.
All of these factors may affect carotid duplex ultrasound velocity except:
-
a.
Contralateral carotid occlusion
-
b.
Gender
-
c.
Obesity
-
d.
Tortuosity
-
e.
All of the above
-
a.
-
2.
Which imaging modality is best for detecting total carotid occlusion:
-
a.
Duplex ultrasound
-
b.
MRA
-
c.
CTA
-
d.
None of the above
-
a.
-
3.
Risk factors associated with nephrogenic systemic fibrosis:
-
a.
Type of gadolinium administered
-
b.
Previous renal disease
-
c.
Acute inflammatory state
-
d.
Elevated phosphate levels
-
e.
All of the above
-
a.
-
4.
Which of the following are complications of DSA:
-
a.
Risk of stroke
-
b.
Risk of hematoma
-
c.
Risk of renal failure
-
d.
Risk of radiation exposure
-
e.
All of the above
-
a.
-
5.
DSA may be the preferred imaging modality:
-
a.
When there is discordance between two different imagings
-
b.
When intervention is possibly needed based on clinical exam
-
c.
In evaluation to definitively define flow lesions such as subclavian steal
-
d.
All of the above are true
-
a.
Answer Key
-
1.
e
-
2.
c
-
3.
e
-
4.
e
-
5.
d
Rights and permissions
Copyright information
© 2017 Springer International Publishing AG
About this chapter
Cite this chapter
Yacoub, M., AbuRahma, Z.T. (2017). Computed Tomography Angiography and Magnetic Resonance Angiography of the Carotids. In: AbuRahma, A. (eds) Noninvasive Vascular Diagnosis. Springer, Cham. https://doi.org/10.1007/978-3-319-54760-2_18
Download citation
DOI: https://doi.org/10.1007/978-3-319-54760-2_18
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-54758-9
Online ISBN: 978-3-319-54760-2
eBook Packages: MedicineMedicine (R0)