Patterns of perfusion-weighted imaging in patients with carotid artery occlusive disease

Claudia J Chaves1, Irina Staroselskaya, Italo Linfante

  • 1Department of Neurology, Lahey Clinic, Burlington, Mass 01805, USA. claudia.j.chaves@lahey.org

Archives of Neurology
|February 13, 2003
PubMed

Insights

Perfusion-weighted imaging (PWI) identified distinct patterns of brain perfusion related to stroke symptoms in patients with internal carotid artery (ICA) disease. These findings support hypoperfusion as a key factor in carotid artery occlusive disease pathophysiology.

Area of Science:

  • Neurology
  • Radiology
  • Vascular Medicine

Background:

  • Hemodynamic factors in internal carotid artery (ICA) stenosis or occlusion and their role in stroke pathophysiology are debated.
  • Perfusion-weighted imaging (PWI) may offer insights into these hemodynamic changes.

Purpose of the Study:

  • To determine if PWI can categorize patients with symptomatic and asymptomatic ICA occlusive disease based on pathophysiological patterns.
  • To correlate PWI findings with clinical presentation and degree of ICA stenosis/occlusion.

Main Methods:

  • Thirty-eight patients with ICA occlusion or severe stenosis underwent PWI.
  • PWI patterns were analyzed in relation to clinical presentation (stroke, transient ischemic attack, asymptomatic) and degree of ICA disease.

Main Results:

  • Three PWI patterns emerged: extensive hypoperfusion (25 patients), localized border zone deficits (8 patients), and normal perfusion (5 patients).
  • Extensive deficits correlated with acute stroke, while border zone deficits were more common in transient ischemic attacks.
  • Asymptomatic patients showed normal perfusion; patterns were independent of occlusion vs. severe stenosis.

Conclusions:

  • PWI patterns correlate with clinical presentation in ICA occlusive disease, not the degree of stenosis.
  • These findings support the hypothesis that hypoperfusion significantly contributes to the pathophysiology of carotid artery occlusive disease.
Abstract