Automated quantification of the spatial extent of perfusion defects and viability on myocardial contrast

Antonio Micari1, Jiri Sklenar, Todd A Belcik

  • 1Cardiovascular Division, University of Virginia, Charlottesville, USA.

Insights

Pixel intensity threshold analysis (PITA) automates myocardial contrast echocardiography (MCE) to assess perfusion defect size. This method accurately quantifies infarct size, aiding in coronary artery disease patient treatment and clinical trials.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Computational Pathology

Background:

  • Assessing myocardial perfusion and viability is crucial for managing coronary artery disease.
  • Current methods for quantifying perfusion defects can be time-consuming and subjective.
  • Automated analysis offers potential for more efficient and objective assessment.

Purpose of the Study:

  • To evaluate the efficacy of computerized pixel intensity threshold analysis (PITA) for automated assessment of perfusion defect size in myocardial contrast echocardiography (MCE).
  • To validate PITA's accuracy in determining infarct size compared to established methods.

Main Methods:

  • MCE was performed in dogs for calibration, with infarct size determined by PITA using a 10% threshold.
  • Clinical validation involved MCE in 30 acute myocardial infarction patients before and after percutaneous coronary intervention (PCI).
  • PITA's defect size measurements were compared with expert reader planimetry on background-subtracted images.

Main Results:

  • A 10% threshold in PITA demonstrated strong correlation with histologic staining for infarct size in canine models.
  • In patients, PITA-derived defect size strongly correlated with expert planimetry (r = 0.95, P < .001).
  • The PITA method proved effective in measuring both risk area and infarct size sequentially post-PCI.

Conclusions:

  • Automated analysis of perfusion defect size using PITA on MCE is feasible and accurate.
  • PITA offers a rapid, objective tool for analyzing ischemia and viability extent.
  • This technique is valuable for clinical research requiring precise, sequential perfusion defect assessment.