全心双嘧达莫应激心肌灌注MRI对冠状动脉病变的检测。

Bonpei Takase, Masayoshi Nagata, Teruyoshi Kihara, Akira Kameyawa, Kumiko Noya, Takemi Matsui, Fumitaka Ohsuzu, Masayuki Ishihara, Akira Kurita
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引用次数: 22

摘要

最近开发了一种全心脏覆盖的MRI序列,该序列采用了快速梯度回波和回波平面采集成像(FastCard EchoTrain)的混合技术。使用这一序列,首次心肌灌注MRI被证明是一种在临床环境中检测冠状动脉疾病(CAD)的良好无创方式。此外,延迟增强MRI的临床用途最近也有报道。本研究的目的是:(1)探讨双嘧达莫应激首次心肌灌注MRI诊断冠心病(> 50%狭窄)的准确性;(2)阐明额外的延迟增强MRI是否具有临床意义。我们对102例(66 +/- 9岁)怀疑患有CAD或新病变的连续患者(有充分证据的既往心肌梗死(MI))进行了首次心肌灌注MRI检查。采用1.5 T心脏磁共振成像仪(GE CV/i),在双嘧达莫输注(0.56 mg/kg)应激下注射钆(0.1 mmol/kg),获得左心室8张短轴磁共振图像。15分钟后,注射氨茶碱(250 mg),静息状态下重复第一次灌注MRI,以评估是否存在灌注缺损和延迟增强。灌注缺损和延迟增强的存在是根据视觉定性分析确定的,由两个独立的读者同意,他们对任何临床信息都是盲的。根据应力和休息的结果,没有记录任何患者的缺损、可逆缺损或固定缺损伴或不伴延迟增强。磁共振成像显示冠心病76例,其中24例心肌梗死伴新发病变,26例无冠心病。应激灌注缺损诊断CAD的敏感性为93%,特异性为85%。固定缺陷诊断既往心肌梗死的敏感性为86%,特异性为66%。固定缺陷伴延迟强化的患者梗死相关动脉狭窄比未伴任何强化的患者更为显著(11/26 vs 15/20, P < 0.05)。使用FastCard EchoTrain进行双嘧达莫应激第一次心肌灌注MRI是临床上诊断CAD的一种有用和准确的方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole-heart dipyridamole stress first-pass myocardial perfusion MRI for the detection of coronary artery disease.

A whole-heart coverage MRI sequence, which employes a hybrid of fast gradient echo and echo planar acquisition imaging (FastCard EchoTrain), has recently been developed. Using this sequence, a first-pass myocardial perfusion MRI was shown to be a good noninvasive modality for detecting coronary artery disease (CAD) in a clinical setting. In addition, the clinical usefulness of delayed enhanced MRI has recently been reported. The objectives of this study were (1) to investigate the accuracy of dipyridamole stress first-pass myocardial perfusion MRI for diagnosing CAD (> 50% stenosis) and (2) to clarify whether additional delayed enhancement MRI has any clinical significance. We performed first-pass myocardial perfusion MRI in 102 consecutive patients (66 +/- 9 years old) suspected to have CAD or new lesions in patients with well-documented prior myocardial infarction (MI). Using a 1.5 T cardiac MR imager (GE CV/i), eight short axis MR images of the left ventricle were acquired by injecting gadolinium (0.1 mmol/kg) under dipyridamole infusion stress (0.56 mg/kg). Fifteen minutes later, aminophylline (250 mg) was injected and first-pass perfusion MRI was repeated in the resting state in order to evaluate both the presence of perfusion defect and delayed enhancement. The presence of perfusion defect and delayed enhancement was determined based on a visual qualitative analysis by the agreement of two separate readers who were blinded to any clinical information. Based on the stress and rest findings, no defect, reversible defect, or fixed defect with or without delayed enhancement was recorded in any patient. The MR findings revealed 76 CAD patients, including 24 MI patients with new lesions and 26 patients without CAD on coronary angiography. The presence of stress perfusion defect had a 93% sensitivity and an 85% specificity for diagnosing CAD. A fixed defect showed an 86% sensitivity and a 66% specificity for diagnosing a prior MI. Patients with a fixed defect with delayed enhancement had more significant stenosis in the infarct related artery than in those without any enhancement (11/26 vs 15/20, P < 0.05). Dipyridamole stress first-pass myocardial perfusion MRI using the FastCard EchoTrain was found to be a clinically useful and accurate modality for diagnosing CAD.

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