Circulation. 1995;91:1894-1895
(Circulation. 1995;91:1894-1895.)
© 1995 American Heart Association, Inc.
Different Roads to the Assessment of Myocardial Viability
Lessons From PET for SPECT
Heinrich R. Schelbert, MD
From the Division of Nuclear Medicine, Department of Molecular and
Medical Pharmacology, UCLA School of Medicine, Los Angeles, Calif.
Correspondence to Heinrich R. Schelbert, MD, Department of Molecular and
Medical Pharmacology, UCLA School of Medicine, Los Angeles, CA 90095-1735.
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Introduction
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The assessment of myocardial viability
remains clinically important,
yet diagnostically challenging. Tamaki et
al
1 probe various
approaches with positron emission
tomography (PET). Since myocardial
viability refers to a state of
reversible impairment of contractile
function, the authors correctly
measure the accuracy of each
approach against the postrevascularization
outcome in systolic
segmental wall motion as a yardstick of myocardial
viability.
The investigators conclude that (1) severe flow reductions
accurately
define myocardium as nonviable. In contrast, mild to modest
reductions
discriminate only poorly between viable and nonviable
tissue.
(2) The addition of stress-induced defects incrementally
improves
the identification of viable myocardium, even though the
reasons
for such improvement remain uncertain. (3) The combined
evaluation
of rest blood flow and
18F-deoxyglucose uptake
as a tracer of
exogenous glucose utilization distinguishes most
reliably between
viable and nonviable myocardium. As the authors acknowledge,
the
latter observation on the high
predictive accuracy of blood
flow metabolism patterns
represents an extension of their earlier
work.
2 3
Together with other previous
investigations,
4 5 6 7 the
present data further strengthen the case of flow metabolism
patterns
as accurate indexes of the myocardial state. Yet, the study
does
not answer clinically or therapeutically critical questions.
It
would have been important to know the effects of revascularization
on
global left ventricular function, clinical symptoms, or both
and how
such changes might relate to mismatches and their
extent.
4 8 Thus, we must rely on changes in segmental
function as surrogates
of changes in global function.
Although the negative predictive accuracy of the flow metabolism
matches, 92%, . . . [Full Text of this Article]
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