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(Stroke. 2000;31:1661.)
© 2000 American Heart Association, Inc.
Original Contributions |
From the Departments of Neurology (C.P., T.S.) and Cardiology (K.T., H.B.), University of Bonn, Bonn, Germany. The first 2 authors contributed equally to this work.
Correspondence to C. Pohl, MD, Department of Neurology, University of Bonn, Sigmund-Freud-Straße 25, D-53105 Bonn, Germany. E-mail c.pohl{at}uni-bonn.de
Background and PurposeExperimental and clinical data suggest that insonation of echo-contrast agents with high acoustical power produces disintegration of microbubbles, resulting in a pseudo-Doppler phenomenon called stimulated acoustic emission (SAE). The purpose of this study was to investigate whether SAE might be detected by transcranial color Doppler imaging and whether these signals might be used for cerebral tissue perfusion measurements.
MethodsNonmoving microbubbles (SHU 563 A) were insonated in vitro through the temporal parts of a human cadaver skull, and contrast signals were detected by velocity-coded color Doppler and power Doppler recordings. Transcranial color as well as power Doppler investigations were performed in 10 healthy volunteers with the echo-contrast agent Levovist (SHU 508 A).
ResultsColor Doppler signals indicating SAE were observed in
vitro and in transcranial human investigations. These
signals were characterized by a mosaic of color Doppler pixels
ranging over the full color scale. Apparent velocity information and
spatial distribution of SAE signals changed from image frame to image
frame. In the experimental model, the intensity of SAE signals
decreased exponentially over time. With an increase of acoustic power,
there was a significant increase of the maximum signal intensity
(P<0.01) and a significantly shortened signal duration
(P<0.01), consistent with stronger and more
rapid disintegration. In humans, SAE signals were clearly detected in
cerebral tissue regions. The intensity of SAE signals in those regions
(eg, temporal cortex, 3.7±1.2 dB) was
8 times lower than the signal
enhancement in the major cerebral arteries (eg, in the MCA,
29.5±5.6).
ConclusionsEcho-contrast specific color Doppler signals known as SAE are detectable by transcranial color and power Doppler sonography. Signals due to SAE might represent tissue perfusion, thereby providing a method for imaging flow with transcranial ultrasound.
Key Words: stimulated acoustic emission power Doppler imaging transcranial color Doppler echo-contrast agents
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