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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 2002 Apr;72(4):467–472. doi: 10.1136/jnnp.72.4.467

Dynamic cerebral autoregulation and beat to beat blood pressure control are impaired in acute ischaemic stroke

P Eames 1, M Blake 1, S Dawson 1, R Panerai 1, J Potter 1
PMCID: PMC1737824  PMID: 11909905

Abstract

Objectives: Hypertension and chronic cerebrovascular disease are known to alter static cerebral autoregulation (CA) but the effects of acute stroke on dynamic CA (dCA) have not been studied in detail. Those studies to date measuring dCA have used sympathetically induced blood pressure (BP) changes, which may themselves directly affect dCA. This study assessed whether dCA is compromised after acute stroke using spontaneous blood pressure (BP) changes as the stimulus for the dCA response.

Methods: 56 patients with ischaemic stroke (aged 70 (SD 9) years), studied within 72 hours of ictus were compared with 56 age, sex, and BP matched normal controls. Cerebral blood flow velocity was measured using transcranial Doppler ultrasound (TCD) with non-invasive beat to beat arterial BP levels, surface ECG, and transcutaneous CO2 levels and a dynamic autoregulatory index (dARI) calculated.

Results: Beat to beat BP, but not pulse interval variability was significantly increased and cardiac baroreceptor sensitivity (BRS) decreased in the patients with stroke. Dynamic CA was significantly reduced in patients with stroke compared with controls (strokes: ARI 3.8 (SD 2.2) and 3.2 (SD 2.0) for pressor and depressor stimuli respectively v controls: ARI 4.7 (SD 2.2) and 4.5 (SD 2.0) respectively (p<0.05 in all cases)). There was no difference between stroke and non-stroke hemispheres in ARI, which was also independent of severity of stroke, BP, BP variability, BRS, sex, and age.

Conclusion: Dynamic cerebral autoregulation, as assessed using spontaneous transient pressor and depressor BP stimuli, is globally impaired after acute ischaemic stroke and may prove to be an important factor in predicting outcome.

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Selected References

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  1. Aaslid R., Lindegaard K. F., Sorteberg W., Nornes H. Cerebral autoregulation dynamics in humans. Stroke. 1989 Jan;20(1):45–52. doi: 10.1161/01.str.20.1.45. [DOI] [PubMed] [Google Scholar]
  2. Bamford J., Sandercock P., Dennis M., Burn J., Warlow C. Classification and natural history of clinically identifiable subtypes of cerebral infarction. Lancet. 1991 Jun 22;337(8756):1521–1526. doi: 10.1016/0140-6736(91)93206-o. [DOI] [PubMed] [Google Scholar]
  3. Britton M., Carlsson A. Very high blood pressure in acute stroke. J Intern Med. 1990 Dec;228(6):611–615. doi: 10.1111/j.1365-2796.1990.tb00287.x. [DOI] [PubMed] [Google Scholar]
  4. Britton M., Carlsson A., de Faire U. Blood pressure course in patients with acute stroke and matched controls. Stroke. 1986 Sep-Oct;17(5):861–864. doi: 10.1161/01.str.17.5.861. [DOI] [PubMed] [Google Scholar]
  5. Carey B. J., Eames P. J., Blake M. J., Panerai R. B., Potter J. F. Dynamic cerebral autoregulation is unaffected by aging. Stroke. 2000 Dec;31(12):2895–2900. doi: 10.1161/01.str.31.12.2895. [DOI] [PubMed] [Google Scholar]
  6. Dawson S. L., Blake M. J., Panerai R. B., Potter J. F. Dynamic but not static cerebral autoregulation is impaired in acute ischaemic stroke. Cerebrovasc Dis. 2000 Mar-Apr;10(2):126–132. doi: 10.1159/000016041. [DOI] [PubMed] [Google Scholar]
  7. Dawson S. L., Manktelow B. N., Robinson T. G., Panerai R. B., Potter J. F. Which parameters of beat-to-beat blood pressure and variability best predict early outcome after acute ischemic stroke? Stroke. 2000 Feb;31(2):463–468. doi: 10.1161/01.str.31.2.463. [DOI] [PubMed] [Google Scholar]
  8. Dawson S. L., Manktelow B. N., Robinson T. G., Panerai R. B., Potter J. F. Which parameters of beat-to-beat blood pressure and variability best predict early outcome after acute ischemic stroke? Stroke. 2000 Feb;31(2):463–468. doi: 10.1161/01.str.31.2.463. [DOI] [PubMed] [Google Scholar]
  9. Harper G., Fotherby M. D., Panayiotou B. J., Castleden C. M., Potter J. F. The changes in blood pressure after acute stroke: abolishing the 'white coat effect' with 24-h ambulatory monitoring. J Intern Med. 1994 Apr;235(4):343–346. doi: 10.1111/j.1365-2796.1994.tb01084.x. [DOI] [PubMed] [Google Scholar]
  10. Iglesias S., Marchal G., Rioux P., Beaudouin V., Hauttement A. J., de la Sayette V., Le Doze F., Derlon J. M., Viader F., Baron J. C. Do changes in oxygen metabolism in the unaffected cerebral hemisphere underlie early neurological recovery after stroke? A positron emission tomography study. Stroke. 1996 Jul;27(7):1192–1199. doi: 10.1161/01.str.27.7.1192. [DOI] [PubMed] [Google Scholar]
  11. Jørgensen H. S., Nakayama H., Raaschou H. O., Olsen T. S. Effect of blood pressure and diabetes on stroke in progression. Lancet. 1994 Jul 16;344(8916):156–159. doi: 10.1016/s0140-6736(94)92757-x. [DOI] [PubMed] [Google Scholar]
  12. Lipsitz L. A., Mukai S., Hamner J., Gagnon M., Babikian V. Dynamic regulation of middle cerebral artery blood flow velocity in aging and hypertension. Stroke. 2000 Aug;31(8):1897–1903. doi: 10.1161/01.str.31.8.1897. [DOI] [PubMed] [Google Scholar]
  13. MAHONEY F. I., BARTHEL D. W. FUNCTIONAL EVALUATION: THE BARTHEL INDEX. Md State Med J. 1965 Feb;14:61–65. [PubMed] [Google Scholar]
  14. Meyer J. S., Shinohara Y., Kanda T., Fukuuchi Y., Ericsson A. D., Kok N. K. Diaschisis resulting from acute unilateral cerebral infarction. Quantitative evidence for man. Arch Neurol. 1970 Sep;23(3):241–247. doi: 10.1001/archneur.1970.00480270051007. [DOI] [PubMed] [Google Scholar]
  15. Newell D. W., Aaslid R., Lam A., Mayberg T. S., Winn H. R. Comparison of flow and velocity during dynamic autoregulation testing in humans. Stroke. 1994 Apr;25(4):793–797. doi: 10.1161/01.str.25.4.793. [DOI] [PubMed] [Google Scholar]
  16. Olesen J. The effect of intracarotid epinephrine, norepinephrine, and angiotensin on the regional cerebral blood flow in man. Neurology. 1972 Sep;22(9):978–987. doi: 10.1212/wnl.22.9.978. [DOI] [PubMed] [Google Scholar]
  17. Panerai R. B., Dawson S. L., Eames P. J., Potter J. F. Cerebral blood flow velocity response to induced and spontaneous sudden changes in arterial blood pressure. Am J Physiol Heart Circ Physiol. 2001 May;280(5):H2162–H2174. doi: 10.1152/ajpheart.2001.280.5.H2162. [DOI] [PubMed] [Google Scholar]
  18. Paulson O. B., Olesen J., Christensen M. S. Restoration of autoregulation of cerebral blood flow by hypocapnia. Neurology. 1972 Mar;22(3):286–293. doi: 10.1212/wnl.22.3.286. [DOI] [PubMed] [Google Scholar]
  19. Robinson T. G., James M., Youde J., Panerai R., Potter J. Cardiac baroreceptor sensitivity is impaired after acute stroke. Stroke. 1997 Sep;28(9):1671–1676. doi: 10.1161/01.str.28.9.1671. [DOI] [PubMed] [Google Scholar]
  20. Robinson T., Potter J. Cardiopulmonary and arterial baroreflex-mediated control of forearm vasomotor tone is impaired after acute stroke. Stroke. 1997 Dec;28(12):2357–2362. doi: 10.1161/01.str.28.12.2357. [DOI] [PubMed] [Google Scholar]
  21. Rubin G., Levy E. I., Scarrow A. M., Firlik A. D., Karakus A., Wechsler L., Jungreis C. A., Yonas H. Remote effects of acute ischemic stroke: A xenon CT cerebral blood flow study. Cerebrovasc Dis. 2000 May-Jun;10(3):221–228. doi: 10.1159/000016060. [DOI] [PubMed] [Google Scholar]
  22. Serrador J. M., Picot P. A., Rutt B. K., Shoemaker J. K., Bondar R. L. MRI measures of middle cerebral artery diameter in conscious humans during simulated orthostasis. Stroke. 2000 Jul;31(7):1672–1678. doi: 10.1161/01.str.31.7.1672. [DOI] [PubMed] [Google Scholar]
  23. Tiecks F. P., Lam A. M., Aaslid R., Newell D. W. Comparison of static and dynamic cerebral autoregulation measurements. Stroke. 1995 Jun;26(6):1014–1019. doi: 10.1161/01.str.26.6.1014. [DOI] [PubMed] [Google Scholar]
  24. Wallace J. D., Levy L. L. Blood pressure after stroke. JAMA. 1981 Nov 13;246(19):2177–2180. [PubMed] [Google Scholar]

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