Detection of coronary artery disease with myocardial contrast echocardiography: comparison with 99mTc-sestamibi

S Kaul1, R Senior, H Dittrich

  • 1Cardiovascular Division, University of Virginia School of Medicine, Charlottesville 22908, USA. sk@virginia.edu

Circulation
|August 5, 1997
PubMed

Insights

Myocardial contrast echocardiography (MCE) effectively detects coronary artery disease (CAD) at rest and during stress. This noninvasive method shows promise for assessing human myocardial perfusion, mirroring results from SPECT imaging.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Diagnostic Techniques

Background:

  • Coronary artery disease (CAD) diagnosis relies on accurate myocardial perfusion assessment.
  • Current diagnostic methods may have limitations in detecting CAD during rest and stress.

Purpose of the Study:

  • To evaluate the efficacy of myocardial contrast echocardiography (MCE) in detecting CAD.
  • To compare MCE with single-photon emission computed tomography (SPECT) for myocardial perfusion imaging.

Main Methods:

  • Thirty patients with suspected CAD underwent MCE and SPECT at rest and after dipyridamole infusion.
  • Myocardial perfusion was assessed in ten segments per patient using a scoring system (1=normal, 0.5=mildly reduced, 0=severely reduced).
  • Perfusion abnormalities were classified as reversible or irreversible based on changes between rest and stress imaging.

Main Results:

  • MCE demonstrated high concordance with SPECT in segmental scoring (92%) and overall CAD detection (86%).
  • Agreement between MCE and SPECT for identifying normal perfusion versus defects was 90%.
  • MCE accurately identified the location and physiologic relevance (reversible/irreversible) of perfusion abnormalities.

Conclusions:

  • Myocardial contrast echocardiography (MCE) is a viable tool for detecting CAD during rest and pharmacological stress.
  • MCE provides similar information on perfusion abnormalities and their significance as SPECT.
  • MCE shows significant potential for noninvasive myocardial perfusion assessment in humans.
Abstract

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