Objective : The purpose of this study was to clarify the diagnostic accuracy of 3 electrocardiographic (ECG) indexes including Q waves in V
1 [QV
1 (+)], Q waves in V
1 and V
2 [QV
1V
2 (+)], and absence of septal q waves in V
6 [qV
6 (-)] for prediction of myocardial infarction (MI) in the interventricular septal area (IVS) using 201-T1C1 myocardial scintigraphy. In addition, we also evaluated the relationship between these ECG indexes and the site of the culprit lesions in the left anterior descending artery (LAD).
Patients : This study consisted of 115 patients (100 males; mean age, 60 years) with anteroseptal MI who underwent 201-T1C1 myocardial scintigraphy in our hospital between January 1994 and December 1997. One hundred six of them also underwent coronary angiography (CAG). Methods : On extent maps obtained from SPECT images of 201-T1C1 scintigraphy, the area of MI occupying the IVS area, using the proportion of the defect area in the IVS, was expressed as % defect area (%DA). Three patterns of %DA were defined as follows. A : 50%≤%DA≤100%; B : 70%≤%DA≤100%; and C : 90%≤%DA≤100%. Results : On scintigraphic evaluations, %DA in patients with each of the 3 ECG indexes was significantly larger than %DA in patients without them (p=0.0002, p=0.0008, and p=0.0008, respectively). QV
1 (+) and qV
6 (-) showed good sensitivities only for pattern C (79% and 75%, respectively), but all ECG indexes showed low sensitivities for patterns A and B. Regarding specificity, QV
1V
2 (+) showed the best values (76% for pattern A, 68% for pattern B, and 68% for pattern C) among the 3 ECG indexes. For prediction of the culprit lesion located proximal to the origin of the first septal branch, qV6 (-) showed a relatively good sensitivity (67%) and specificity (67%) Conclusions : For prediction of MI in the IVS area, QV
1 (+) and qV
6 (-) showed good sensitivities when the MI was sufficiently large in size. QV
1V
2 (+) showed relatively good specificities irrespective of the MI size. qV
6 (-) was the best predictive index for the culprit lesions located in the proximal site of the LAD.
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