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静脉注射肌球蛋白特异性抗体后患者心肌坏死的闪烁显像定量分析。

Scintigraphic quantification of myocardial necrosis in patients after intravenous injection of myosin-specific antibody.

作者信息

Khaw B A, Gold H K, Yasuda T, Leinbach R C, Kanke M, Fallon J T, Barlai-Kovach M, Strauss H W, Sheehan F, Haber E

出版信息

Circulation. 1986 Sep;74(3):501-8. doi: 10.1161/01.cir.74.3.501.

Abstract

The Fab fragments of antimyosin antibodies, labeled with 99mTc, were used in the scintigraphic examination of 30 patients with myocardial infarction. The ability to detect necrosis and determine its extent from the antimyosin scan were compared with the results of quantitative regional wall motion analysis by contrast ventriculography at 10 to 14 days and 99mTc-pyrophosphate imaging. Antimyosin images recorded by planar and single photon-emission computed tomography (SPECT) delineated areas of myocardial necrosis in 27 of 30 patients (90%) compared with a 91% sensitivity of pyrophosphate in 21 of 23 patients. Infarct size was determined by both antimyosin and pyrophosphate SPECT images. Results by both techniques showed a significant correlation with computer-derived hypokinetic segment length (r = .79 for both, p = .002) and peak creatine kinase (r = .9 for both, p less than .01). Although sensitivity for and correlations with markers of necrosis were similar with both techniques, infarct size by pyrophosphate SPECT was 1.7 times larger than infarct size by antimyosin SPECT (p less than .01). Certain zones in the infarct area were differentially labeled; the nature and irreversibility of injury within these zones remains to be clarified.

摘要

用99mTc标记的抗肌球蛋白抗体的Fab片段对30例心肌梗死患者进行了闪烁扫描检查。将抗肌球蛋白扫描检测坏死及其范围的能力与10至14天时通过对比心室造影进行的定量局部室壁运动分析结果以及99mTc - 焦磷酸盐显像结果进行了比较。通过平面和单光子发射计算机断层扫描(SPECT)记录的抗肌球蛋白图像在30例患者中的27例(90%)中勾勒出心肌坏死区域,相比之下,23例患者中的21例焦磷酸盐的敏感性为91%。梗死大小通过抗肌球蛋白和焦磷酸盐SPECT图像确定。两种技术的结果均显示与计算机得出的运动减弱节段长度有显著相关性(两者r = 0.79,p = 0.002)以及与肌酸激酶峰值有显著相关性(两者r = 0.9,p < 0.01)。虽然两种技术对坏死标志物的敏感性和相关性相似,但焦磷酸盐SPECT测定的梗死大小比抗肌球蛋白SPECT测定的梗死大小大1.7倍(p < 0.01)。梗死区域内的某些区域有不同的标记;这些区域内损伤的性质和不可逆性仍有待阐明。

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