Widding A, Hesse B, Gadsboll N
Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet, University of Copenhagen, Denmark.
Eur J Nucl Med. 1997 Jan;24(1):42-5. doi: 10.1007/BF01728307.
The aim of this study was to compare technetium-99m labelled tetrofosmin and sestamibi myocardial perfusion single-photon emission tomography (SPET) with one common sestamibi reference file for bull's eye imaging, with quantitation of the extent and severity of perfusion defects. Twenty patients suspected or known to have coronary artery disease participated in the study. Patients first underwent routine sestamibi myocardial SPET over 2 days, receiving doses of 400-600 MBq at stress and 600-800 MBq at rest. Then within the same week a 1-day tetrofosmin myocardial SPET study was performed, with a dose of 300 MBq at stress, followed 2.5 h later by a dose of 750 MBq at rest. Bull's eye images were generated for visual evaluation. Black-out defects according to the Cequal software analysis were only recorded if they comprised more than 10 pixels in men and 20 in women. According to the Cequal program, extent score and severity scores were expressed as number of pixels and deviations below reference limits. Five patients had normal myocardial SPET imaging with both radiotracers, while 15 had reversible, irreversible or partially reversible defects. The concordance of the results was high. The only two significant differences were that one patient had a reversible defect which appeared to be located in different myocardial regions (LAD vs RCA), and another patient had a defect that was partially reversible with sestamibi but irreversible with tetrofosmin. The results showed very high correlation coefficients for the extent and severity scores (linear correlation coefficient values of 0.99 and 0.94, respectively). In conclusion, it appears that changing between sestamibi and tetrofosmin has little influence on the interpretation of bull's eye images from the data file of a common reference population using one of the tracers.
本研究的目的是比较锝-99m标记的替曲膦和甲氧基异丁基异腈心肌灌注单光子发射断层扫描(SPET),使用一个常见的甲氧基异丁基异腈参考文件进行靶心图成像,并对灌注缺损的范围和严重程度进行定量分析。20例疑似或已知患有冠状动脉疾病的患者参与了本研究。患者首先在2天内接受常规甲氧基异丁基异腈心肌SPET检查,负荷量为400 - 600 MBq,静息量为600 - 800 MBq。然后在同一周内进行为期1天的替曲膦心肌SPET检查,负荷量为300 MBq,2.5小时后静息量为750 MBq。生成靶心图用于视觉评估。仅当男性患者的缺损超过10像素、女性患者超过20像素时,才根据Cequal软件分析记录为黑屏缺损。根据Cequal程序,范围评分和严重程度评分分别表示为像素数量和低于参考限值的偏差。5例患者使用两种放射性示踪剂时心肌SPET成像均正常,而15例患者有可逆、不可逆或部分可逆的缺损。结果的一致性很高。仅有的两个显著差异是,一名患者有一个可逆缺损,其在不同心肌区域(左前降支与右冠状动脉)出现,另一名患者有一个缺损,用甲氧基异丁基异腈时部分可逆,用替曲膦时不可逆。结果显示范围评分和严重程度评分的相关系数非常高(线性相关系数值分别为0.99和0.94)。总之,使用其中一种示踪剂从共同参考人群的数据文件对靶心图进行解读时,在甲氧基异丁基异腈和替曲膦之间切换似乎对其影响很小。