Hyperintense Acute Reperfusion Marker on FLAIR in Posterior Circulation Infarction

Alex Förster1, Holger Wenz1, Johannes Böhme1

  • 1Department of Neuroradiology, Universitätsmedizin Mannheim, University of Heidelberg, Mannheim, Germany.

Plos One
|June 22, 2016
PubMed
Abstract

Insights

Hyperintense acute reperfusion marker (HARM) is frequently observed in posterior circulation infarction patients. This blood brain barrier injury finding on FLAIR MRI is linked to vessel recanalization and smaller infarct growth.

Area of Science:

  • Neuroradiology
  • Neuroimaging
  • Vascular Neurology

Background:

  • Posterior circulation infarction (PCI) can lead to significant neurological deficits.
  • Assessing blood-brain barrier (BBB) integrity is crucial for understanding infarct evolution.
  • Hyperintense acute reperfusion marker (HARM) on FLAIR MRI may indicate BBB injury.

Purpose of the Study:

  • To determine the frequency of BBB injury, identified as HARM on FLAIR MRI, in patients with PCI.
  • To explore the association between HARM and reperfusion markers and infarct progression.

Main Methods:

  • Retrospective analysis of MRI scans (DWI, PWI, FLAIR, MRA) from patients with PCI within 12 hours of onset.
  • Follow-up MRI was performed within 24 hours.
  • HARM was identified on FLAIR images using pre-specified criteria for subarachnoid space and/or ventricular enhancement.

Main Results:

  • 16 patients with PCI were included; 81.3% had PCA occlusion, 18.7% had BA occlusion.
  • HARM was observed in 50% of patients on follow-up FLAIR images, always remote from the acute ischemic lesion.
  • HARM was significantly associated with vessel recanalization (p=0.04), minor infarction growth (p=0.01), and smaller infarcts on follow-up DWI (p=0.05).

Conclusions:

  • HARM is a common finding in PCI and correlates with favorable outcomes like vessel recanalization and limited infarct expansion.
  • Neuroradiologists should recognize HARM on short-term follow-up FLAIR MRI in PCI patients who received contrast agents.

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