Assessing collateral cerebral perfusion with Technetium-99m-HMPAO SPECT during temporary internal carotid artery occlusion Academic Article uri icon


MeSH Major

  • Arterial Occlusive Diseases
  • Brain
  • Carotid Artery Diseases
  • Cerebrovascular Circulation
  • Collateral Circulation
  • Organotechnetium Compounds
  • Oximes
  • Tomography, Emission-Computed, Single-Photon


  • Cerebral infarction following internal carotid artery occlusion results from either embolism or inadequate collateral blood flow. Although risk of embolism can be minimized, detecting compromised collateral circulation is more difficult. Cerebral angiography, carotid stump pressures and clinical evaluation during internal carotid artery occlusion are of limited utility. Xenon-133 radionuclide studies and stable xenon computed tomography are not readily available. We evaluated 99mTc-HMPAO SPECT, during temporary carotid artery occlusion, in 20 patients considered for internal carotid artery occlusion. Fourteen demonstrated symmetric cerebral perfusion during occlusion; eleven underwent transient and three had permanent carotid artery occlusion without complications. Five patients had ipsilateral globally decreased perfusion during temporary occlusion. One patient underwent transient occlusion of this vessel and one underwent carotid sacrifice without bypass grafting; both recovered without sequelae. The three remaining patients underwent carotid artery bypass grafting prior to sacrifice of this vessel. One patient with a small focal perfusion defect underwent carotid artery sacrifice without bypass grafting and developed acute neurologic deficits postoperatively. These initial results suggest that symmetric cerebral perfusion during temporary occlusion indicates that internal carotid artery occlusion will be tolerated. Although its implications are not yet well defined, the abnormal study identifies patients potentially at risk for postocclusion complications, thus providing a basis for neurosurgical management.

publication date

  • January 1993



  • Academic Article



  • eng

PubMed ID

  • 8326377

Additional Document Info

start page

  • 1235

end page

  • 8


  • 34


  • 8