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From the Department of Nuclear Medicine and Division of Cardiology, Hôpital Hôtel-Dieu de Montréal, Université de Montréal, Montréal, Canada
Correspondence: For reprints contact: Dr. Raymond Taillefer, Département de Médecine Nucléaire, Hôtel-Dieu de Montréal, 3840 St-Urbain St., Montreal, Quebec, H2W 1T8, Canada.
ABSTRACT
Technetium-99m-sestamibi (MIBI) and 99mTc-teboroxime (TEBO) are two new myocardial perfusion imaging agents. The purpose of this prospective study was to compare MIBI and TEBO to 201Tl planar imaging. Eighteen patients with significant coronary artery disease on coronary angiogram were submitted to three treadmill stress tests performed within 3 mo and were imaged with the three radiopharmaceuticals as follows.
Patients achieved similar levels of exercise. A blinded reading was performed by three observers. The left ventricle was divided into three segments/view and ischemic/normal wall ratios were also determined. Segmental comparison showed an agreement in 85% (138/162) of the segments between Tl and TEBO, in 92% (149/162) between Tl and MIBI and in 84% (136/162) between MIBI and TEBO. Abnormal Tl, MIBI and TEBO studies were seen in 16 (89%), 16 (89%) and 15 (83%) patients, respectively, detecting 77, 75 and 65 abnormal segments. Ischemic-to-normal wall ratios were 0.75 ± 0.06, 0.73 ± 0.08 and 0.78 ± 0.08 for Tl, MIBI and TEBO, respectively. In conclusion, although the biologic characteristics of these agents are different, this study showed a good correlation between them in detection of significant coronary artery disease (high pretest likelihood population).
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