Skip to main content Accessibility help

We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.

Close cookie message
×
Hostname: page-component-76fb5796d-vvkck Total loading time: 0 Render date: 2024-04-27T01:56:50.045Z Has data issue: false hasContentIssue false

18 - Vasomotor reactivity

Published online by Cambridge University Press:  05 May 2016

By
Alexander Gur ,
Attila Csányi  and
Natan M. Bornstein
Edited by
László Csiba  and
Claudio Baracchini
László Csiba
Affiliation:
Department of Neurology, Debreceni Egyetem, Hungary
Claudio Baracchini
Affiliation:
Department of Neuroscience, Università degli Studi di Padova, Italy
Get access

Summary

A summary is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Manual of Neurosonology , pp. 228 - 238
Publisher: Cambridge University Press
Print publication year: 2016

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Dahl, A, Russell, D, Rootwelt, K, et al. Cerebral vasoreactivity assessed with transcranial Doppler and regional cerebral blood flow measurements: dose, serum concentration, and time of the response to acetazolamide. Stroke. 1995;26:2302–2306.CrossRefGoogle ScholarPubMed
Mahon, PJ, Panerai, RB, Deverson, ST, Hayes, PD, Evans, DE. Assessment of the thigh cuff technique for measurement of dynamic cerebral autoregulation. Stroke. 2000;31:476–480.Google Scholar
Aaslid, R, Lindegaard, K-F, Sorteberg, W, et al. Cerebral autoregulation dynamics in humans. Stroke. 1989;20:45–52.CrossRefGoogle ScholarPubMed
Giller, CA, Bowman, G, Dyer, H, et al. Cerebral arterial diameters during changes in blood pressure and carbon dioxide during craniotomy. Neurosurgery. 1993;32:737–741.CrossRefGoogle ScholarPubMed
Reutern, GM, Büdingen, HJ. Ultrasound Diagnosis of Cerebrovascular Disease. Stuttgart: Georg Thieme; 1993, 167–174.Google Scholar
Markus, HS, Harrison, MJG. Estimation of cerebrovascular reactivity using transcranial Doppler, including the use of breath-holding as the vasodilatory stimulus. Stroke. 1992;23:668–673.Google Scholar
Zavoreo, I, Demarin, V. Breath holding index in the evaluation of cerebral vasoreactivity. Acta Clin Croat. 2004;43:15–19.Google Scholar
Aaslid, R. Cerebral autoregulation and vasomotor reactivity. In: Handbook of Neurovascular Ultrasound. Front. Neurol. Neurosci. Vol. 21. Basel: Karger; 2006, 216–238.Google Scholar
Settakis, G, Molnár, C, Kerényi, L, et al. Acetazolamide as a vasodilatory stimulus in cerebrovascular diseases and in conditions affecting the cerebral vasculature. Eur J Neurol. 2003;10:609–620.CrossRefGoogle ScholarPubMed
Karnik, R, Valentin, A, Winkler, WB, et al. Sex-related differences in acetazolamide-induced cerebral vasomotor reactivity. Stroke. 1996;27:56–58.Google Scholar
Dahl, A, Lindegaard, K-F, Russel, D, et al. A comparison of transcranial Doppler and cerebral blood flow studies to assess cerebral vasoreactivity. Stroke. 1992;23:15–19.CrossRefGoogle ScholarPubMed
Rosenkranz, K, Hierholzer, J, Langer, R, et al. Acetazolamide stimulation test in patients with unilateral internal carotid artery obstructions using transcranial Doppler and 99mTc-HMPAO-SPECT. Neurol Res. 1992;14:135–138.Google Scholar
Ringelstein, EB, Van-Eyck, S, Mertens, I. Evaluation of cerebral vasomotor reactivity by various vasodilating stimuli: comparison of CO2 to acetazolamide. J Cereb Blood Flow Metab. 1992;12:162–168.Google Scholar
Settakis, G, Molnar, C, Kerenyi, L, et al. Acetazolamide as a vasodilatory stimulus in cerebrovascular diseases and in conditions affecting the cerebral vasculature. Eur J Neurol. 2003;10:609–620.CrossRefGoogle ScholarPubMed
Sorteberg, W, Lindegaard, KF, Rootwelt, K, et al. Effect of acetazolamide on cerebral artery blood velocity and regional cerebral blood flow in normal subjects. Acta Neurochir (Wien). 1989;97:139–145.Google Scholar
Ringelstein, EB. CO2 – reactivity: dependence from collateral circulation and significance in symptomatic and asymptomatic patients. In Caplan, LR, Shifrin, EG, Nicolaides, AN, Moore, WS, eds. Cerebrovascular Ischemia. Investigation and Management. Nicosia: Med-Orion Publishing Company; 1996, 149–154.Google Scholar
Markus, H, Cullinane, M. Severely impaired cerebrovascular reactivity predicts stroke and TIA risk in patients with carotid artery stenosis and occlusion. Brain. 2001;124:457–467.CrossRefGoogle ScholarPubMed
Silvestrini, M, Vernieri, F, Pasqualetti, P, et al. Impaired cerebral vasoreactivity and risk of stroke in patients with asymptomatic carotid artery stenosis. JAMA. 2000;283:2122–2127.Google Scholar
Valikovics, A, Oláh, L, Fülesdi, B, Munkácsy, CS, Csiba, L. Vasoreactivity changes of healthy volunteers investigated by transcranial Doppler. Clin Neurosci (Hungarian). 1996;49:30–35.Google Scholar
Derdeyn, CP, Grubb, RL, Powers, WJ. Cerebral hemodynamic impairment. Methods of measurement and association with stroke risk. Neurology. 1999;53:251–259.Google Scholar
Provinciali, L, Ceravolo, MG, Minciotti, P. A transcranial Doppler study of vasomotor reactivity in symptomatic carotid occlusion. Cerebrovasc Dis. 1993;3:27–32.CrossRefGoogle Scholar
Reinhard, M, Schwarzer, G, Briel, M, et al. Cerebrovascular reactivity predicts stroke in high-grade carotid artery disease. Neurology. 2014;83:1–8.Google Scholar
Gur, AY, Bova, I, Bornstein, NM. Is impaired cerebral vasomotor reactivity a predictive factor of stroke in asymptomatic patients. Stroke. 1996;22: 2188–2190.Google Scholar
Gur, A, Bornstein, N. Cerebral vasomotor reactivity of the posterior circulation in patients with carotid occlusive disease. Eur J Neurol. 2003;10:75–78.CrossRefGoogle ScholarPubMed
Bornstein, NM, Gur, AY, Geyer, O, Almog, Y. Vasomotor reactivity in the ophthalmic artery: different from or similar to intracerebral vessels? Eur J Ultrasound. 2000;11;1–6.Google Scholar
Gur, AY, Bornstein, NM. Cerebral vasomotor reactivity of bilateral severe carotid stenosis: is stroke unavoidable? Eur J Neurol. 2005;13:183–186.CrossRefGoogle Scholar
Vernieri, F, Pasqualetti, P, Diomedi, M, et al. Cerebral hemodynamics in patients with carotid artery occlusion and contralateral moderate or severe internal carotid artery stenosis. J Neurosurg. 2001;94:559–564.Google Scholar
Matteis, M, Vernieri, F, Caltagirone, C, et al. Patterns of cerebrovascular reactivity in patients with carotid artery occlusion and severe contralateral stenosis. J Neurol Sci. 1999;168:47–51.Google Scholar
Klijn, CJ, Kappelle, LJ, Tulleken, CA, et al. Symptomatic carotid artery occlusion. A reappraisal of hemodynamic factors. Stroke. 1997;28 2084–2093.Google Scholar
Vernieri, F, Pasqualetti, P, Passareli, F, et al. Outcome of carotid artery occlusion is predicted by cerebrovascular reactivity. Stroke. 1999;30:593–598.CrossRefGoogle ScholarPubMed
The EC-IC Bypass Study Group. Failure of extracranial–intracranial bypass to reduce the risk of ischemic stroke. N Engl J Med. 1985;313:1191–1200.CrossRefGoogle Scholar
Karnik, R, Valentin, A, Ammerer, H-P, et al. Elevation of vasomotor reactivity by transcranial Doppler and acetazolamide test before and after extracranial-intracranial bypass in patients with internal carotid artery occlusion. Stroke. 1992;23: 812–817.CrossRefGoogle Scholar
Neff, KW, Horn, P, Dinter, D, et al. Extracranial- intracranial arterial bypass surgery improves total brain blood supply in selected symptomatic patients with unilateral internal carotid artery occlusion and insufficient collateralization. Neuroradiology. 2004;46:730–737.CrossRefGoogle ScholarPubMed
Herzig, R, Hlustik, P, Urbanek, K, et al. Can we identify patients with carotid occlusion who would benefit from EC/IC bypass? Review. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2004;148:119–122.CrossRefGoogle ScholarPubMed
Cao, B, Haseqawa, Y, Yokota, C, et al. Spontaneous improvement in reduced vasodilator capacity in major cerebral arterial occlusive disease. Neuroradiology. 2000;43;19–25.Google Scholar
Zbornikova, V. Long term follow-up of unlateral occlusion of the internal carotid artery including repeated tests of vasomotor reactivity by transcranial Doppler. Neurol Res. 2006;28;220–224.Google Scholar
Demarin, V, Rundek, T, Despot, I, et al. Importance of the evaluation of cerebral vasoreactive capacity in the indication for carotid endarterectomy. Angiologia. 1993;45:10–15.Google Scholar
Hartl, WH, Janssen, I, Fürst, H. Effect of carotid endarterectomy on patterns of cerebrovascular reactivity in patients with unilateral carotid artery stenosis. Stroke. 1994;25:1952–1957.Google Scholar
Bornstein, N, Gur, A, Shifrin, E, Morag, B. Does carotid endarterectomy modify cerebral vasomotor reactivity? Cerebrovasc Dis. 1997;7:201–204.Google Scholar
Russel, D, Dybevold, S, Kjartansson, O, et al. Cerebral vasoreactivity and blood flow before and 3 months after carotid endarterectomy, Stroke. 1990;21:1029–1032.CrossRefGoogle Scholar
Barzό, P, Vörös, E, Bodosi, M. Use of transcranial Doppler sonography and acetazolamide test to demonstrate changes in cerebrovascular reserve capacity following carotid endarterectomy. Eur J Vasc Endovasc Surg. 1996;11:83–89.CrossRefGoogle Scholar
Soinne, L, Helenius, J, Tatlisumak, T, et al. Cerebral hemodynamics in asymptomatic and symptomatic patients with high-grade carotid stenosis undergoing carotid endarterectomy. Stroke. 2003;34:1655–1661.CrossRefGoogle ScholarPubMed
Lucertini, G, Cariati, P, Ermirio, D, et al. Can cerebral vasoreactivity predict cerebral tolerance to carotid clamping during carotid endarterectomy? Cardiovasc Surg. 2002;10:123–127.Google Scholar
Lam, JM, Smielewski, P, al-Rawi, P, et al. Prediction of cerebral ischaemia during carotid endarterectomy with preoperative CO2-reactivity studies and angiography. Br J Neurosurg. 2000;14:441–448.Google Scholar
Molina, C, Sabín, JA, Montaner, J, et al. Impaired cerebrovascular reactivity as a risk marker for first-ever lacunar infarction: a case-control study. Stroke. 1999;30:2296–2301.Google Scholar
Gur, AY, Gücüyener, D, Uzüner, N, et al. Cerebral vasomotor reactivity of patients with acute ischemic stroke: Cortical versus subcortical infarcts: an Israeli-Turkish collaborative study. J Neurol Sci. 2007;257:121–125.CrossRefGoogle ScholarPubMed
Cupini, LM, Diomedi, M, Placidi, F, Silvestrini, M, Giacomini, P. Cerebrovascular reactivity and subcortical infarcts. Arch Neurol. 2001;58:557–581.CrossRefGoogle Scholar
De Reuck, J, Decoo, D, Hasenbroekx, MC, et al. Acetazolamide vasoreactivity in vascular dementia: a positron emission tomographic study. Eur Neurol. 1999;41:31–36.CrossRefGoogle ScholarPubMed
Pfefferkorn, T, Von Stuckrad-Barre, S, Herzog, J, et al. Reduced cerebrovascular CO(2) reactivity in CADASIL: a transcranial Doppler sonography study. Stroke. 2001;32:17–21.Google Scholar
Stoppe, G, Schutze, R, Kogler, A, et al. Cerebrovascular reactivity to acetazolamide in (senile) dementia of Alzheimer’s type: relationship to disease severity. Dementia. 1995;6:73–82.Google ScholarPubMed
Gur, AY, Gücüyener, D, Korczyn, AD, et al. Cerebral vasomotor reactivity and dementia after ischemic stroke. Acta Neurol Scand. 2010;122:383–388.Google Scholar
Gurevich, T, Gur, AY, Bornstein, NM, Giladi, N, Korczyn, AD. Cerebral vasomotor reactivity in Parkinson’s disease, multiple system atrophy and pure autonomic failure.J Neurol Sci. 2006;243:57–60.Google Scholar
Gur, AY, Auriel, E, Korczyn, AD, et al. Vasomotor reactivity as a predictor for syncope in patients with orthostatism. Acta Neurol Scand. 2012;126:32–36.Google Scholar
Kastrup, A, Thomas, C, Hartmann, C, Schabet, M. Cerebral blood flow and CO2 reactivity in interictal migraineurs: a transcranial Doppler study. Headache. 1998;38:608–613.CrossRefGoogle ScholarPubMed
Fülesdi, B, Szatmári, S, Antek, C, et al. Cerebral vasoreactivity to acetazolamide is not impaired in patients with severe sepsis. J Crit Care. 2012;27:337–343.Google Scholar
Sterzer, P, Meintzschel, F, Rösler, A, et al. Pravastatin improves cerebral vasomotor reactivity in patients with subcortical small-vessel disease. Stroke. 2001;32:2817–2820.CrossRefGoogle ScholarPubMed
Bär, KJ, Boettger, MK, Seidler, N, et al. Influence of galantamine on vasomotor reactivity in Alzheimer’s disease and vascular dementia due to cerebral microangiopathy. Stroke. 2007;38:3186–3192.CrossRefGoogle ScholarPubMed
Portegies, ML, de Bruijn, RF, Hofman, A, Koudstaal, PJ, Ikram, MA. Cerebral vasomotor reactivity and risk of mortality: The Rotterdam Study. Stroke. 2014;45:1–7.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×