Prognostic Value of T2-FLAIR Hyperintense Vessel Sign for Cerebral Hyperperfusion Syndrome and Feasibility of

Dongdong Wan1, Chao Wang2, Hua Liu1

  • 1Department of Neurosurgery, The Second People's Hospital of Shizuishan, Ningxia, China.

World Neurosurgery
|July 8, 2026
PubMed

Insights

Preoperative T2-FLAIR hyperintense vessel sign (HVS) grading reliably predicts cerebral hyperperfusion syndrome (CHS) risk after carotid artery stenting (CAS). An HVS-guided management strategy is feasible and safe, showing promising clinical application.

Area of Science:

  • Neurology
  • Radiology
  • Vascular Surgery

Background:

  • Cerebral hyperperfusion syndrome (CHS) is a risk after carotid artery stenting (CAS).
  • Predictive markers for CHS are crucial for patient management.
  • T2-FLAIR hyperintense vessel sign (HVS) is a potential imaging marker.

Purpose of the Study:

  • To evaluate the prognostic performance of preoperative T2-FLAIR HVS grading for CHS after CAS.
  • To assess the clinical feasibility and safety of an HVS-guided risk-stratified perioperative management strategy.

Main Methods:

  • A single-center prospective cohort study of 128 patients undergoing elective CAS.
  • Patients were stratified into low-risk (HVS 0-1), intermediate-risk (HVS 2), and high-risk (HVS 3) groups.
  • Tailored interventions included staged angioplasty and tiered blood pressure control.

Main Results:

  • The 30-day symptomatic CHS incidence was 6.3%, with stepwise increases across HVS risk groups (0% to 24%, P<0.001).
  • HVS grade ≥2 (OR=6.87) and incomplete circle of Willis (OR=3.72) correlated with higher CHS odds.
  • No intergroup differences in procedural complications; CHS incidence was lower than historical controls.

Conclusions:

  • Preoperative T2-FLAIR HVS grading is a reliable prognostic marker for CHS risk stratification in CAS patients.
  • The HVS-guided risk-stratified perioperative management is clinically feasible and safe.
  • HVS is a promising, accessible imaging indicator for routine clinical practice, warranting further multicenter validation.
Abstract

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