Literature DB >> 8249853

Technetium-99m teboroxime regional myocardial washout in subjects with and without coronary artery disease.

T Chua1, H Kiat, G Germano, W Palmas, K Takemoto, J Friedman, D S Berman.   

Abstract

The aim of this study was to test the hypothesis that regional myocardial washout of technetium-99m teboroxime is slowed in the presence of coronary stenosis. Washout was assessed in 33 catheterized patients and in 13 with a low likelihood of coronary artery disease, using a triple detector camera and dynamic single-photon emission computed tomography, with serial 1-minute acquisitions after injection of 20 to 25 mCi of teboroxime at the third minute of adenosine-induced hyperemia. Washout was measured as the percent change in counts between the first, second and third minutes after injection, as measured in 6 short-axis myocardial regions of interest. Myocardial regions were classified as ischemic (> or = 50% diameter stenosis and no prior myocardial infarct), infarcted, normal (no significant coronary stenosis) or "low likelihood" (from the 13 patients with a low likelihood of coronary artery disease). Teboroxime washout was significantly (p < 0.001) slowed in the ischemic myocardium (12.7 +/- 8.3%) compared with the normal (18.5 +/- 5.7%), low-likelihood (17.8 +/- 6.1%) and infarcted (17.8 +/- 4.4%) zones. There was regional variability in washout rates (% washout/min), with the anterior wall having the lowest (13.8 +/- 3.4%/min) and the inferior wall the highest (20.7 +/- 7.9%/min) values. In regard to individual coronary territories, 21 of 41 ischemic, noninfarcted territories (51%) had abnormal washout compared with 3 of 43 normal territories (7%) (p = 0.001). In conclusion, regional washout of teboroxime is detectably slowed in ischemic, noninfarcted myocardium. The clinical value of washout analysis in teboroxime single-photon emission computed tomography warrants further investigation.

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Year:  1993        PMID: 8249853     DOI: 10.1016/0002-9149(93)90893-h

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  6 in total

1.  Technetium 99m-labeled teboroxime: death in utero, infanticide, or failure to thrive?

Authors:  R J Burns
Journal:  J Nucl Cardiol       Date:  1995 Jan-Feb       Impact factor: 5.952

2.  The birth of a new radiopharmaceutical. Clinical investigative perspective.

Authors:  F J Wackers
Journal:  J Nucl Cardiol       Date:  1995 Jan-Feb       Impact factor: 5.952

3.  Compartmental modeling of technetium-99m-labeled teboroxime with dynamic single-photon emission computed tomography: comparison with static thallium-201 in a canine model.

Authors:  E V Di Bella; S G Ross; D J Kadrmas; H S Khare; P E Christian; S McJames; A G Gullberg
Journal:  Invest Radiol       Date:  2001-03       Impact factor: 6.016

4.  Myocardial technetium 99m-labeled teboroxime clearance derived from canine scans differentiates severity of stenosis after dipyridamole.

Authors:  G Johnson; D K Glover; C B Hebert; R D Okada
Journal:  J Nucl Cardiol       Date:  1994 Jul-Aug       Impact factor: 5.952

5.  Static Versus Dynamic Teboroxime Myocardial Perfusion SPECT in Canines.

Authors:  D J Kadrmas; E V R Di Bella; H S Khare; P E Christian; G T Gullberg
Journal:  IEEE Trans Nucl Sci       Date:  2000-06-01       Impact factor: 1.679

6.  Myocardial clearance of technetium-99m-teboroxime in reperfused injured canine myocardium.

Authors:  David R Okada; Gerald Johnson; Robert D Okada
Journal:  EJNMMI Res       Date:  2014-08-01       Impact factor: 3.138

  6 in total

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