Cerebral Hemodynamics in Asymptomatic and Symptomatic Patients With High-Grade Carotid Stenosis Undergoing Carotid Endarterectomy

Background and Purpose— Asymptomatic patients with carotid stenosis benefit less from carotid endarterectomy (CEA) than symptomatic patients because the risk of embolic events is lower, but it is not known whether the hemodynamic effect of CEA is different between the groups. We evaluated hemodynamics of symptomatic and asymptomatic patient groups before and after CEA. Methods— Forty-six independent patients with a unilateral high-grade carotid stenosis, 23 asymptomatic and 23 symptomatic, underwent dynamic susceptibility contrast MRI (DSC-MRI) and transcranial Doppler ultrasound (TCD) evaluation before CEA and 3 and 100 days afterward. Quantitative perfusion parameters were calculated separately in selected regions of white and gray matter and watershed regions in each hemisphere, and mean transit time (MTT) maps were assessed visually by 2 independent observers. Vasomotor reactivity was determined with breath-holding index and flow impedance with pulsatility index ipsilaterally. Results— In contrast to the asymptomatic carotid stenosis group, symptomatic carotid stenosis patients had preoperatively increased MTT and lower cerebral blood flow values in the ipsilateral hemisphere, more in white matter and watershed regions than in gray matter. Visually detected perfusion deficits were associated with symptomatic status. The interhemispheric asymmetries were abolished by CEA. The improving trend over time was greater in the symptomatic carotid stenosis group and was best seen in MTT. On TCD, pulsatility index was lower in symptomatic carotid stenosis patients preoperatively, with no postoperative difference, whereas the breath-holding index improved only in the symptomatic carotid stenosis group after CEA. Conclusions— Patients with asymptomatic and symptomatic carotid stenosis differ significantly by means of DSC-MRI and TCD before and in response to CEA.

[1]  D G Gadian,et al.  Quantification of Perfusion Using Bolus Tracking Magnetic Resonance Imaging in Stroke: Assumptions, Limitations, and Potential Implications for Clinical Use , 2002, Stroke.

[2]  William J Powers,et al.  Variability of cerebral blood volume and oxygen extraction: stages of cerebral haemodynamic impairment revisited. , 2002, Brain : a journal of neurology.

[3]  W. Lin,et al.  Quantitative measurements of cerebral blood flow in patients with unilateral carotid artery occlusion: A PET and MR study , 2001, Journal of magnetic resonance imaging : JMRI.

[4]  V. Kiselev On the theoretical basis of perfusion measurements by dynamic susceptibility contrast MRI , 2001, Magnetic resonance in medicine.

[5]  P. Pasqualetti,et al.  Effect of Collateral Blood Flow and Cerebral Vasomotor Reactivity on the Outcome of Carotid Artery Occlusion , 2001, Stroke.

[6]  H. Markus,et al.  Severely impaired cerebrovascular reactivity predicts stroke and TIA risk in patients with carotid artery stenosis and occlusion. , 2001, Brain : a journal of neurology.

[7]  L. Kappelle,et al.  Sustained Bilateral Hemodynamic Benefit of Contralateral Carotid Endarterectomy in Patients With Symptomatic Internal Carotid Artery Occlusion , 2001, Stroke.

[8]  M. Mato,et al.  Antiproliferative Effect and Cell Cycle Modulation by Melatonin on GH3 Cells , 2000, Hormone Research in Paediatrics.

[9]  D. Gadian,et al.  Delay and dispersion effects in dynamic susceptibility contrast MRI: Simulations using singular value decomposition , 2000, Magnetic resonance in medicine.

[10]  NorbertNighoghossian,et al.  Vasodilatory Response of Border Zones to Acetazolamide Before and After Endarterectomy , 2000 .

[11]  J C Froment,et al.  Vasodilatory response of border zones to acetazolamide before and after endarterectomy : an echo planar imaging-dynamic susceptibility contrast-enhanced MRI study in patients with high-grade unilateral internal carotid artery stenosis. , 2000, Stroke.

[12]  R J Seitz,et al.  Diffusion- and perfusion-weighted MRI: influence of severe carotid artery stenosis on the DWI/PWI mismatch in acute stroke. , 2000, Stroke.

[13]  M E Moseley,et al.  Quantification of cerebral blood flow by bolus tracking and artery spin tagging methods. , 2000, Magnetic resonance imaging.

[14]  Y. Sohn,et al.  Arterial pulsatility as an index of cerebral microangiopathy in diabetes. , 2000, Stroke.

[15]  G. Schlaug,et al.  The ischemic penumbra: operationally defined by diffusion and perfusion MRI. , 1999, Neurology.

[16]  W J Powers,et al.  Cerebral hemodynamic impairment , 1999, Neurology.

[17]  G. Brix,et al.  Cerebral Blood Flow and Cerebrovascular Reserve Capacity: Estimation by Dynamic Magnetic Resonance Imaging , 1998, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  P. Johannsen,et al.  Cerebral Blood Flow Measurements by Magnetic Resonance Imaging Bolus Tracking: Comparison with [15O]H2O Positron Emission Tomography in Humans , 1998, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[19]  M A Viergever,et al.  Long-term hemodynamic effects of carotid endarterectomy. , 1998, Stroke.

[20]  E Michel,et al.  Gosling's Doppler pulsatility index revisited. , 1998, Ultrasound in medicine & biology.

[21]  C. Tulleken,et al.  Symptomatic carotid artery occlusion. A reappraisal of hemodynamic factors. , 1997, Stroke.

[22]  B. Rosen,et al.  High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part I: Mathematical approach and statistical analysis , 1996, Magnetic resonance in medicine.

[23]  C. Caltagirone,et al.  Transcranial Doppler assessment of cerebrovascular reactivity in symptomatic and asymptomatic severe carotid stenosis. , 1996, Stroke.

[24]  B. Rosen,et al.  High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part II: Experimental comparison and preliminary results , 1996, Magnetic resonance in medicine.

[25]  Y Yonekura,et al.  Evidence of misery perfusion and risk for recurrent stroke in major cerebral arterial occlusive diseases from PET. , 1996, Journal of neurology, neurosurgery, and psychiatry.

[26]  P. Adeleine,et al.  Hemodynamic parameter assessment with dynamic susceptibility contrast magnetic resonance imaging in unilateral symptomatic internal carotid artery occlusion. , 1996, Stroke.

[27]  W. Hartl,et al.  Effect of Carotid Endarterectomy on Patterns of Cerebrovascular Reactivity in Patients With Unilateral Carotid Artery Stenosis , 1994, Stroke.

[28]  P. Adeleine,et al.  Cerebral Blood Flow Reserve Assessment in Symptomatic Versus Asymptomatic High‐Grade Internal Carotid Artery Stenosis , 1994, Stroke.

[29]  D. Sackett,et al.  Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. , 1991, The New England journal of medicine.

[30]  W. Powers Cerebral hemodynamics in ischemic cerebrovascular disease , 1991, Annals of neurology.

[31]  R. Hobson,et al.  Carotid endarterectomy for asymptomatic carotid stenosis. , 1989, Stroke.

[32]  E. Ringelstein,et al.  Effect of internal carotid artery occlusion on intracranial hemodynamics. Transcranial Doppler evaluation and clinical correlation. , 1988, Stroke.

[33]  B. Rosen,et al.  Dynamic imaging with lanthanide chelates in normal brain: Contrast due to magnetic susceptibility effects , 1988, Magnetic resonance in medicine.

[34]  H. Damasio,et al.  A computed tomographic guide to the identification of cerebral vascular territories. , 1983, Archives of neurology.

[35]  M Buxton-Thomas,et al.  Quantitative perfusion imaging in carotid artery stenosis using dynamic susceptibility contrast-enhanced magnetic resonance imaging. , 2000, Magnetic resonance imaging.

[36]  K. Weinfurt,et al.  Repeated measures analyses : ANOVA MANOVA, and HLM , 2000 .

[37]  Paul R. Yarnold,et al.  Reading and understanding MORE multivariate statistics. , 2000 .

[38]  W. Yuh,et al.  Severe occlusive carotid artery disease: hemodynamic assessment by MR perfusion imaging in symptomatic patients. , 1999, AJNR. American journal of neuroradiology.

[39]  V. Zbornikova,et al.  Early haemodynamic changes in the ophthalmic artery, siphon and intracranial arteries after carotid endarterectomy estimated by transcranial Doppler and duplex scanning. , 1998, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

[40]  R. Vanninen,et al.  Hemodynamic effects of carotid endarterectomy by magnetic resonance flow quantification. , 1995, Stroke.

[41]  RitvaVanninen,et al.  Hemodynamic Effects of Carotid Endarterectomy by Magnetic Resonance Flow Quantification , 1995 .

[42]  M. Raichle,et al.  The effect of hemodynamically significant carotid artery disease on the hemodynamic status of the cerebral circulation. , 1987, Annals of internal medicine.