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心脏计算机断层扫描血管造影术中使用舒张末期和舒张末期成像进行冠状动脉解读及射血分数相关性分析的最佳阶段:对前瞻性触发的影响

Optimal phase for coronary interpretations and correlation of ejection fraction using late-diastole and end-diastole imaging in cardiac computed tomography angiography: implications for prospective triggering.

作者信息

Isma'eel Hussain, Hamirani Yasmin S, Mehrinfar Ramona, Mao Songshuo, Ahmadi Naser, Larijani Vahid, Nair Subu, Budoff Matthew J

机构信息

Beirut Cardiac Institute, Founding Faculty Lebanese American University, Beirut, Lebanon.

出版信息

Int J Cardiovasc Imaging. 2009 Oct;25(7):739-49. doi: 10.1007/s10554-009-9481-y. Epub 2009 Jul 25.

DOI:10.1007/s10554-009-9481-y
PMID:19633922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2729417/
Abstract

A typical acquisition protocol for multi-row detector computed tomography (MDCT) angiography is to obtain all phases of the cardiac cycle, allowing calculation of ejection fraction (EF) simultaneously with plaque burden. New MDCT protocols scanner, designed to reduce radiation, use prospectively acquired ECG gated image acquisition to obtain images at certain specific phases of the cardiac cycle with least coronary artery motion. These protocols do not we allow acquisition of functional data which involves measurement of ejection fraction requiring end-systolic and end-diastolic phases. We aimed to quantitatively identify the cardiac cycle phase that produced the optimal images as well as aimed to evaluate, if obtaining only 35% (end-systole) and 75% (as a surrogate for end-diastole) would be similar to obtaining the full cardiac cycle and calculating end diastolic volumes (EDV) and EF from the 35th and 95th percentile images. 1,085 patients with no history of coronary artery disease were included; 10 images separated by 10% of R-R interval were retrospectively constructed. Images with motion in the mid portion of RCA were graded from 1 to 3; with '1' being no motion, '2' if 0 to <1 mm motion, and '3' if there is >1 mm motion and/or non-interpretable study. In a subgroup of 216 patients with EF > 50%, we measured left ventricular (LV) volumes in the 10 phases, and used those obtained during 25, 35, 75 and 95% phase to calculate the EF for each patient. The average heart rate (HR) for our patient group was 56.5 +/- 8.4 (range 33-140). The distribution of image quality at all heart rates was 958 (88.3%) in Grade 1, 113 (10.42%) in Grade 2 and 14 (1.29%) in Grade 3 images. The area under the curve for optimum image quality (Grade 1 or 2) in patients with HR > 60 bpm for phase 75% was 0.77 +/- 0.04 [95% CI: 0.61-0.87], while for similar heart rates the area under the curve for phases 75 + 65 + 55 + 45% combined was 0.92 +/- 0.02. LV volume at 75% phase was strongly correlated with EDV (LV volume at 95% phase) (r = 0.970, P < 0.001). There was also a strong correlation between LVEF (75_35) and LVEF (95_35) (r = 0.93, P < 0.001). Subsequently, we developed a formula to correct for the decrement in LVEF using 35-75% phase: LVEF (95_35) = 0.783 x LVEF (75_35) + 20.68; adjusted R(2) = 0.874, P < 0.001. Using 64 MDCT scanners, in order to acquire >90% interpretable studies, if HR < 60 bpm 75% phase of RR interval provides optimal images; while for HR > 60 analysis of images in 4 phases (75, 35, 45 and 55%) is needed. Our data demonstrates that LVEF can be predicted with reasonable accuracy by using data acquired in phases 35 and 75% of the R-R interval. Future prospective acquisition that obtains two phases (35 and 75%) will allow for motion free images of the coronary arteries and EF estimates in over 90% of patients.

摘要

多排探测器计算机断层扫描(MDCT)血管造影的典型采集方案是获取心动周期的所有阶段,以便在计算斑块负荷的同时计算射血分数(EF)。新的MDCT协议扫描仪旨在减少辐射,采用前瞻性心电门控图像采集,在心动周期的某些特定阶段获取冠状动脉运动最小的图像。这些协议不允许采集涉及测量射血分数(需要收缩末期和舒张末期阶段)的功能数据。我们旨在定量确定产生最佳图像的心动周期阶段,并评估仅获取35%(收缩末期)和75%(作为舒张末期的替代)是否与获取整个心动周期并从第35和95百分位数图像计算舒张末期容积(EDV)和EF相似。纳入1085例无冠状动脉疾病史的患者;回顾性构建了间隔为R-R间期10%的10幅图像。右冠状动脉中部有运动的图像从1到3分级;“1”表示无运动,“2”表示运动0至<1毫米,“3”表示运动>1毫米和/或研究无法解读。在216例EF>50%的患者亚组中,我们在10个阶段测量了左心室(LV)容积,并使用在第25、35、75和95%阶段获得的数据计算每位患者的EF。我们患者组的平均心率(HR)为56.5±8.4(范围33-140)。所有心率下图像质量的分布为1级958例(88.3%),2级1... 展开

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/2f9f518584c0/10554_2009_9481_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/2f9f518584c0/10554_2009_9481_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/368e8b42c93c/10554_2009_9481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/bdf0f09ab309/10554_2009_9481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/858341e04b72/10554_2009_9481_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/a66a1497cde6/10554_2009_9481_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/3191e5e1eaf5/10554_2009_9481_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29da/2729417/2f9f518584c0/10554_2009_9481_Fig6_HTML.jpg

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