医学
锝Tc 99m倍他米比
心脏病学
内科学
灌注
动脉
组织病理学
放射性核素血管造影
闪烁照相术
狭窄
核医学
放射科
心力衰竭
病理
射血分数
作者
Habib A. Dakik,Jimmy F. Howell,Gerald M. Lawrie,Rafael Espada,Donald G. Weilbaecher,Zhixu He,John J. Mahmarian,Mario S. Verani
出处
期刊:Circulation
[Ovid Technologies (Wolters Kluwer)]
日期:1997-11-04
卷期号:96 (9): 2892-2898
被引量:133
标识
DOI:10.1161/01.cir.96.9.2892
摘要
Assessment of myocardial viability by 99mTc-sestamibi remains controversial. Accordingly, we investigated the use of sestamibi as a marker of myocardial viability, defined by histopathology, and for predicting improvement of myocardial function after coronary artery bypass graft surgery (CABG).99mTc-sestamibi perfusion tomography and radionuclide angiography were performed within 2 days before CABG in 21 patients with > or = 75% stenosis of the left anterior descending coronary artery and resting anterior wall dyssynergy. During CABG, transmural myocardial biopsies were obtained from the dyssynergic anterior wall and from normal myocardial segments to determine the extent of viable myocardium by histopathology. Improvement of regional left ventricular function was evaluated by radionuclide angiography at 6 to 8 weeks after CABG. There was a good correlation (r=.85, P<.001) between the quantified sestamibi activity and the extent of viable myocardium determined morphometrically. Among 21 biopsied dyssynergic myocardial segments, 11 improved their function after CABG and 10 failed to improve. Biopsied segments with improved postoperative function had significantly higher sestamibi activity (81+/-5% versus 49+/-16%, P<.0001) and significantly lower extent of interstitial fibrosis (7+/-4% versus 31+/-21%, P=.0002) than segments that failed to improve. A 55% threshold of 99mTc-sestamibi activity had positive and negative predictive values of 79% and 100%, respectively, for recovery of function after CABG in the biopsied segments.Myocardial 99mTc-sestamibi activity correlates well with the extent of viable myocardium and predicts improvement in regional function after CABG. This lends support to the use of sestamibi as a myocardial viability agent.
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