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Projection flow imaging by bolus tracking using stimulated echoes
Author(s) -
Foo Thomas K. F.,
Perman William H.,
Poon Colin S. O.,
Cusma Jack T.,
Sandstrom John C.
Publication year - 1989
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.1910090206
Subject(s) - projection (relational algebra) , computer science , bolus (digestion) , magnetic resonance imaging , computer vision , nuclear medicine , nuclear magnetic resonance , artificial intelligence , radiology , medicine , physics , algorithm , anatomy
Previous investigators have employed the concept of bolus tracking using either spin echoes or gradient echoes. In this paper we introduce two methods of bolus tracking using planar‐and volume‐selective stimulated echoes. The planar method employs a selective 90° rf pulse which tags all spins in a particular plane. At a time τ 1 , later, a nonselective 90° rf pulse is employed, followed after a time r 2 , by another nonselective rf pulse. Only spins which experience all three rf pulses form a stimulated echo at time τ 1 after the third rf pulse. A balanced pair of flow‐compensated dephasing (crusher) gradients further ensures that the stimulated echo is due only to the effect of all three rf pulses while minimizing flow dephasing. The first part of this gradient pair is applied after the initial rf pulse in the first τ 1 period to dephase the tagged spins. The second part of this gradient pair is applied after the third rf pulse to rephase the spins. Since the plane of the excited slice is orthogonal to the readout direction, flowing spins are imaged in an angiographic manner as they inove away from the excited slice. A modification to this basic sequence excites only a small volume. In this manner, the suppression of stationary spins is effected by volume‐selective excitation. In both the planar‐and the volume‐selective techniques, the excited spins undergo T 1 and T 2 relaxation during the τ 1 period but only T 1 relaxation in the τ 2 period. In blood, where T 1 is much greater than T 2 , keeping τ as short as possible minimizes signal loss due to T 2 dephasing. These methods demonstrate increased sensitivity compared to similar bolus tracking methods using either spin echoes or gradient echoes. © 1989 Academic Press, Inc.