A virtual histology intravascular ultrasound analysis of coronary chronic total occlusions

Jun Guo1, Akiko Maehara, Gary S Mintz

  • 1Columbia University Medical Center and the Cardiovascular Research Foundation, New York, NY, USA.

Insights

Virtual histology intravascular ultrasound (VH-IVUS) revealed two chronic total occlusion (CTO) plaque compositions. Most CTOs with VH-fibroatheroma suggest acute coronary syndrome origin, while others indicate atherosclerosis progression.

Area of Science:

  • Cardiovascular Imaging
  • Interventional Cardiology
  • Atherosclerosis Research

Background:

  • Limited in vivo data exists on the plaque composition of chronic total occlusions (CTOs).
  • Understanding CTO composition is crucial for developing effective treatment strategies.

Purpose of the Study:

  • To investigate the plaque composition of chronic total occlusions (CTOs) using virtual histology intravascular ultrasound (VH-IVUS).
  • To differentiate CTO morphologies and infer potential formation mechanisms.

Main Methods:

  • VH-IVUS analysis was performed on 50 CTO lesions in 49 patients.
  • Plaque composition, including necrotic core (NC), was analyzed in CTO segments and reference arteries.
  • VH-IVUS phenotypes, specifically VH-fibroatheroma (defined by >10% confluent NC), were assessed.

Main Results:

  • CTO lesions showed a high percentage of maximum necrotic core (NC), similar to proximal reference segments.
  • 42 out of 50 CTOs exhibited a VH-fibroatheroma phenotype, characterized by more NC and dense calcium.
  • CTOs without VH-fibroatheroma had increased fibrotic and fibrofatty plaque; 60.5% of VH-fibroatheroma CTOs had thin-cap fibroatheroma in the proximal reference.

Conclusions:

  • CTO morphology can be categorized into two patterns: with or without VH-fibroatheroma.
  • The presence of VH-fibroatheroma suggests a majority of CTOs may originate from acute coronary syndrome and thrombosis.
  • The absence of VH-fibroatheroma suggests a minority of CTOs may result from gradual atherosclerosis progression.
Abstract

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