Identification of Hemodynamic Compromise by Cerebrovascular Reserve and Oxygen Extraction Fraction in Occlusive Vascular Disease

Cerebrovascular reserve (CVR) and oxygen extraction fraction (OEF) are used to identify hemodynamic compromise in symptomatic patients with carotid occlusive vascular disease, but evidence suggests that they are not equivalent. The authors studied the relationship between CVR and OEF to evaluate their equivalence and stages of hemodynamic compromise. Symptomatic patients (N = 12) with carotid occlusion were studied by stable xenon–computed tomography CBF after intravenous acetazolamide administration for CVR, followed within 24 hours by positron emission tomography (PET) for OEF. Middle cerebral artery territories were analyzed by hemisphere and level. Hemispheric subcortical white matter infarctions were graded with magnetic resonance imaging. Both hemispheric and level analysis of CVR and OEF showed a significant (P = 0.001), negative linear relationship [CVR (%) = −1.5 (OEF) + 83.4, (r = −0.57, P = 0.001, n = 24]. However, 37.5% of the hemispheres showed compromised CVR but normal OEF and were associated (P = 0.019) with subcortical white matter infarction. CMRO2 was elevated in stage II hemodynamic compromise (CVR < 10%, OEF > 50%). CVR and OEF showed a significant negative linear relationship in stage II hemodynamic compromise but revealed hemispheres in hemodynamic compromise by CVR but normal OEF that were associated with subcortical white matter infarction.

[1]  KazuoKitagawa,et al.  Detection of Misery Perfusion With Split-Dose 123I-Iodoamphetamine Single-Photon Emission Computed Tomography in Patients With Carotid Occlusive Diseases , 2002 .

[2]  T. Yoshimoto,et al.  Use of Cerebrovascular Reactivity in Patients with Symptomatic Major Cerebral Artery Occlusion to Predict 5-Year Outcome: Comparison of Xenon-133 and Iodine-123-IMP Single-Photon Emission Computed Tomography , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[3]  Takashi Yoshimoto,et al.  Cerebrovascular Reactivity to Acetazolamide and Outcome in Patients With Symptomatic Internal Carotid or Middle Cerebral Artery Occlusion: A Xenon-133 Single-Photon Emission Computed Tomography Study , 2002, Stroke.

[4]  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.

[5]  Kiyohiro Houkin,et al.  Long-Term Prognosis of Medically Treated Patients With Internal Carotid or Middle Cerebral Artery Occlusion: Can Acetazolamide Test Predict It? , 2001, Stroke.

[6]  W J Powers,et al.  Comparison of PET oxygen extraction fraction methods for the prediction of stroke risk. , 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[7]  C Caltagirone,et al.  Impaired cerebral vasoreactivity and risk of stroke in patients with asymptomatic carotid artery stenosis. , 2000, JAMA.

[8]  V. Hachinski,et al.  Internal borderzone infarction: a marker for severe stenosis in patients with symptomatic internal carotid artery disease. For the North American Symptomatic Carotid Endarterectomy (NASCET) Group. , 2000, Stroke.

[9]  H. Fukuyama,et al.  SIGNIFICANCE OF INCREASED OXYGEN EXTRACTION FRACTION IN 5-YEAR PROGNOSIS OF SYMPTOMATIC MAJOR CEREBRAL ARTERIAL OCCLUSIVE DISEASES , 2000 .

[10]  H. Fukuyama,et al.  Significance of increased oxygen extraction fraction in five-year prognosis of major cerebral arterial occlusive diseases. , 1999, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[11]  W J Powers,et al.  Count-based PET method for predicting ischemic stroke in patients with symptomatic carotid arterial occlusion. , 1999, Radiology.

[12]  W J Powers,et al.  Importance of hemodynamic factors in the prognosis of symptomatic carotid occlusion. , 1999, JAMA.

[13]  William J. Powers,et al.  Importance of Hemodynamic Factors in the Prognosis of Symptomatic Carotid Occlusion , 1998 .

[14]  M. Skalej,et al.  Small rosarylike infarctions in the centrum ovale suggest hemodynamic failure. , 1998, AJNR. American journal of neuroradiology.

[15]  H. Batjer Qualitative Versus Quantitative Assessment of Cerebrovascular Reserves , 1998 .

[16]  K. Minematsu,et al.  Effect of Acetazolamide Reactivity and Long-term Outcome in Patients With Major Cerebral Artery Occlusive Diseases , 1998 .

[17]  J. Baron,et al.  Relationships between High Oxygen Extraction Fraction in the Acute Stage and Final Infarction in Reversible Middle Cerebral Artery Occlusion: An Investigation in Anesthetized Baboons with Positron Emission Tomography , 1996, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  H. Yonas,et al.  Physiological diagnosis and surgical treatment of recurrent limb shaking: case report. , 1996, Neurosurgery.

[19]  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.

[20]  D. Newport,et al.  Evaluation of simulation-based scatter correction for 3-D PET cardiac imaging , 1995 .

[21]  T Nariai,et al.  Vascular reserve in chronic cerebral ischemia measured by the acetazolamide challenge test: comparison with positron emission tomography. , 1995, AJNR. American journal of neuroradiology.

[22]  Kazuo Minematsu,et al.  Acetazolamide Reactivity on 123I-IMP Single Photon Emission Computed Tomography in Patients with Major Cerebral Artery Occlusive Disease: Correlation with Positron Emission Tomography Parameters , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[23]  H Yonas,et al.  Correlation of Xenon‐Enhanced Computed Tomography‐Defined Cerebral Blood Flow Reactivity and Collateral Flow Patterns , 1994, Stroke.

[24]  H Yonas,et al.  Increased stroke risk predicted by compromised cerebral blood flow reactivity. , 1993, Journal of neurosurgery.

[25]  G. Marchal,et al.  PET imaging of cerebral perfusion and oxygen consumption in acute ischaemic stroke: relation to outcome , 1993, The Lancet.

[26]  J. Mazziotta,et al.  Rapid Automated Algorithm for Aligning and Reslicing PET Images , 1992, Journal of computer assisted tomography.

[27]  C J Thompson,et al.  Oxygen Consumption of the Living Human Brain Measured after a Single Inhalation of Positron Emitting Oxygen , 1992, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  H. Fukuyama,et al.  High-intensity area in the deep white matter indicating hemodynamic compromise in internal carotid artery occlusive disorders. , 1991, Archives of neurology.

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

[30]  M. Swash,et al.  Small deep cerebral infarcts associated with occlusive internal carotid artery disease. A hemodynamic phenomenon? , 1990, Archives of neurology.

[31]  J. Baron Depression of Energy Metabolism in Distant Brain Structures: Studies with Positron Emission Tomography in Stroke Patients , 1989, Seminars in neurology.

[32]  F. Shishido,et al.  Oxygen Extraction Fraction at Maximally Vasodilated Tissue in the Ischemic Brain Estimated from the Regional CO2 Responsiveness Measured by Positron Emission Tomography , 1988, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[33]  J. Baron,et al.  Effects of thalamic stroke on energy metabolism of the cerebral cortex. A positron tomography study in man. , 1986, Brain : a journal of neurology.

[34]  I. Kanno,et al.  Error Analysis of a Quantitative Cerebral Blood Flow Measurement Using H215O Autoradiography and Positron Emission Tomography, with Respect to the Dispersion of the Input Function , 1986, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[35]  M. Raichle,et al.  Cerebral Blood Flow and Cerebral Metabolic Rate of Oxygen Requirements for Cerebral Function and Viability in Humans , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[36]  M. Mintun,et al.  Brain oxygen utilization measured with O-15 radiotracers and positron emission tomography. , 1984, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[37]  T Jones,et al.  Serial observations on the pathophysiology of acute stroke. The transition from ischaemia to infarction as reflected in regional oxygen extraction. , 1983, Brain : a journal of neurology.

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

[39]  D Comar,et al.  Reversal of Focal "Misery‐Perfusion Syndrome" By Extra‐Intracranial Arterial Bypass in Hemodynamic Cerebral Ischemia: A Case Study with 15O Positron Emission Tomography , 1981, Stroke.

[40]  on Cerebral Blood , 2005 .

[41]  H. Yonas,et al.  Stages and thresholds of hemodynamic failure. , 2003, Stroke.

[42]  H. Kuwabara,et al.  Verbal working memory and solvent exposure: a positron emission tomography study. , 2000, Neuropsychology.

[43]  G. Pontone,et al.  Oxygen consumption. , 1999, Cardiologia.

[44]  M.E. Casey,et al.  Evaluation of simulation-based scatter correction for 3D PET cardiac imaging , 1995, 1995 IEEE Nuclear Science Symposium and Medical Imaging Conference Record.