Identification of ultrasound contrast agent dilution systems for ejection fraction measurements

IEEE Trans Ultrason Ferroelectr Freq Control. 2005 Mar;52(3):410-20. doi: 10.1109/tuffc.2005.1417263.

Abstract

Left ventricular ejection fraction is an important cardiac-efficiency measure. Standard estimations are based on geometric analysis and modeling; they require time and experienced cardiologists. Alternative methods make use of indicator dilutions, but they are invasive due to the need for catheterization. This study presents a new minimally invasive indicator dilution technique for ejection fraction quantification. It is based on a peripheral injection of an ultrasound contrast agent bolus. Left atrium and left ventricle acoustic intensities are recorded versus time by transthoracic echocardiography. The measured curves are corrected for attenuation distortion and processed by an adaptive Wiener deconvolution algorithm for the estimation of the left ventricle impulse response, which is interpolated by a monocompartment exponential model for the ejection fraction assessment. This technique measures forward ejection fraction, which excludes regurgitant volumes. The feasibility of the method was tested on a group of 20 patients with left ventricular ejection fractions going from 10% to 70%. The results are promising and show a 0.93 correlation coefficient with echographic bi-plane ejection fraction measurements. A more extensive validation as well as an investigation on the method applicability for valve insufficiency and right ventricular ejection fraction quantification will be an object of future study.

Publication types

  • Clinical Trial
  • Validation Study

MeSH terms

  • Algorithms*
  • Echocardiography / methods*
  • Feasibility Studies
  • Heart Ventricles / diagnostic imaging*
  • Humans
  • Image Enhancement / methods*
  • Image Interpretation, Computer-Assisted / methods*
  • Imaging, Three-Dimensional / methods
  • Indicator Dilution Techniques
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Stroke Volume / physiology*
  • Ventricular Function*