Wackers F J, Gibbons R J, Verani M S, Kayden D S, Pellikka P A, Behrenbeck T, Mahmarian J J, Zaret B L
Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, Connecticut 06510.
J Am Coll Cardiol. 1989 Oct;14(4):861-73. doi: 10.1016/0735-1097(89)90456-7.
Technetium-99m isonitrile is a new myocardial perfusion imaging agent that accumulates according to the distribution of myocardial blood flow. However, unlike thallium-201, it does not redistribute over time. This imaging agent was used with serial quantitative planar imaging to assess the initial risk area of infarction, its change over time and the relation to infarct-related artery patency in 30 patients with a first acute myocardial infarction. Twenty-three of 30 patients were treated with recombinant tissue-type plasminogen activator (rt-PA) within 4 h after the onset of chest pain. Seven patients were treated in the conventional manner without thrombolytic therapy. Technetium-99m isonitrile was injected before or at the initiation of thrombolytic therapy, and imaging was performed several hours later. These initial images demonstrated the area at risk. Repeat imaging was performed 18 to 48 h later and at 6 to 14 days after the onset of myocardial infarction to visualize the ultimate extent of infarction. The initial area at risk varied greatly (range defect integral 2 to 61) both in patients treated with rt-PA and in those who received conventional treatment. For the total group, the initial imaging defect decreased in size in 20 patients and was unchanged or larger in 10 patients. Patients with a patent infarct-related artery had a significantly greater decrease in defect size than did patients with persistent coronary occlusion (-51 +/- 38% versus -1 +/- 26%, p = 0.0001). All patients with a decrease in defect size greater than 30% had a patent infarct-related artery. In 12 patients who also had predischarge quantitative exercise thallium-201 imaging, good agreement existed between the extent and severity of myocardial perfusion defect on the last technetium-99m isonitrile study before discharge and that noted on delayed thallium-201 imaging. It is concluded that serial planar technetium-99m isonitrile myocardial imaging in patients with acute myocardial infarction undergoing thrombolytic therapy offers a new quantitative noninvasive approach for assessment of the initial risk zone as well as the success of reperfusion.
锝-99m异腈是一种新型心肌灌注显像剂,它根据心肌血流分布进行聚集。然而,与铊-201不同,它不会随时间重新分布。本显像剂用于30例首次发生急性心肌梗死患者,采用系列定量平面显像来评估梗死的初始危险区、其随时间的变化以及与梗死相关动脉通畅情况的关系。30例患者中有23例在胸痛发作后4小时内接受了重组组织型纤溶酶原激活剂(rt-PA)治疗。7例患者采用传统方式治疗,未进行溶栓治疗。在溶栓治疗前或开始时注射锝-99m异腈,数小时后进行显像。这些初始图像显示了危险区。在心肌梗死发作后18至48小时以及6至14天进行重复显像,以观察梗死的最终范围。接受rt-PA治疗的患者和接受传统治疗的患者,初始危险区差异很大(范围缺损积分2至61)。对于整个组,20例患者初始显像缺损大小减小,10例患者不变或增大。梗死相关动脉通畅的患者缺损大小的减小明显大于持续性冠状动脉闭塞的患者(-51±38%对-1±26%,p = 0.0001)。所有缺损大小减小超过30%的患者梗死相关动脉均通畅。在12例出院前也进行了定量运动铊-201显像的患者中,出院前最后一次锝-99m异腈研究的心肌灌注缺损范围和严重程度与延迟铊-201显像时的情况有很好的一致性。结论是,对接受溶栓治疗的急性心肌梗死患者进行系列平面锝-99m异腈心肌显像,为评估初始危险区以及再灌注成功提供了一种新的定量无创方法。