Reversible (ischemic) and mild-moderate irreversible (nonischemic) thallium defects represent regions with viable myocardium. Since the mere presence of viable myocardium does not necessarily indicate ischemic myocardium, we investigated whether stress-induced reversible thallium defects are more accurate in predicting recovery of function after revascularization compared to nonischemic but viable myocardium (mild-moderate irreversible thallium defects). We studied 11 patients with chronic coronary artery disease who underwent pre- and post-revascularization quantitative stress-redistribution-reinjection thallium, gated magnetic resonance imaging (MRI) and radionuclide angiography. Mean LV ejection fraction at rest increased from 31 plus/minus 8% pre-revascularization to 38 plus/minus 11% post-revascularization (p<0.05). Two to four MRI and thallium transaxial slices were matched and analyzed per patient. For each slice, pre- and post-revascularization systolic wall thickening was visually assessed in 5 regions by MRI. From a total of 137 revascularized regions, 62 regions had abnormal wall motion pre-revascularization, of which 42 improved post-revascularization and 20 did not improve. Among the 42 abnormal regions which improved post-revascularization, 21 (50%) exhibited reversible thallium defects and only 2 had mild-moderate irreversible defects. In contrast, of the 20 abnormal regions that did not improve post-revascularization, 14 (70%) demonstrated mild-moderate irreversible defects and only 3 had reversible thallium defects (p<0.0001). These data suggest that when performing stress studies, most mild-moderate irreversible thallium regions represent an admixture of viable (nonischemic) and scarred myocardium that may not improve post-revascularization. On the other hand, the identification of reversible thallium defect on stress in an asynergic region more accurately predicts recovery of function after revascularization.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Intramural Research (Z01)
Project #
1Z01HL004926-04
Application #
2576840
Study Section
Cell Biology Integrated Review Group (CB)
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1996
Total Cost
Indirect Cost
Name
National Heart, Lung, and Blood Institute
Department
Type
DUNS #
City
State
Country
United States
Zip Code