Quantification of Retrograde Blood Flow in the Descending Aorta Using Transesophageal Echocardiography in Comparison

Thomas Wehrum1, Miriam Kams, Felix Günther

  • 1Department of Neurology, University Medical Center Freiburg, Freiburg, Germany.

Insights

Routine 2D transesophageal echocardiography (TEE) can estimate retrograde flow length in the descending aorta (DAo), a potential source of brain embolism. While TEE offers a cost-effective screening method, 4D flow MRI remains essential for precise embolization pathway assessment.

Area of Science:

  • Cardiovascular Imaging
  • Neurology
  • Medical Technology

Background:

  • Retrograde diastolic blood flow in the proximal descending aorta (DAo) is a potential source of brain embolism.
  • Plaques ≥4 mm thick in the DAo can connect with brain-supplying arteries.
  • Currently, only 4D flow MRI can visualize and quantify these embolization pathways in vivo.

Purpose of the Study:

  • To determine if routine 2D transesophageal echocardiography (TEE) can estimate the extent of retrograde flow in the DAo.
  • To correlate TEE-derived velocity-time-integral ratio (VTIratio) with retrograde pathline length visualized by 4D flow MRI.

Main Methods:

  • Prospective study of 48 acute stroke patients undergoing routine TEE.
  • Doppler examinations at the aortic arch-DAo transition zone using a 20 mm sample volume.
  • Calculation of VTIratio and correlation with 4D flow MRI-derived retrograde pathline length.

Main Results:

  • Mean VTIratio was 0.53 ± 0.16, with a mean retrograde pathline length of 3.1 ± 1.4 cm.
  • VTIratio independently predicted retrograde pathline length (r = 0.44; p = 0.002).
  • A VTIratio threshold of 0.6012 differentiated large (≥3 cm) from small (<3 cm) retrograde flow with 92% specificity.

Conclusions:

  • TEE can predict retrograde pathline length in the DAo.
  • TEE may serve as a cost-effective tool for large-scale studies on DAo flow reversal predictors.
  • TEE has limited value as a screening tool; 4D flow MRI is indispensable for precise individual embolization pathway assessment.
Abstract