Radiology Imaging Sciences, National Institutes of Health Clinical Center, Bethesda, MD, USA.
Computed Tomography Division, Siemens Healthcare GmbH, Forchheim, Germany.
Med Phys. 2017 Oct;44(10):5120-5127. doi: 10.1002/mp.12301. Epub 2017 Aug 20.
To demonstrate the feasibility of spectral imaging using photon-counting detector (PCD) x-ray computed tomography (CT) for simultaneous material decomposition of three contrast agents in vivo in a large animal model.
This Institutional Animal Care and Use Committee-approved study used a canine model. Bismuth subsalicylate was administered orally 24-72 h before imaging. PCD CT was performed during intravenous administration of 40-60 ml gadoterate meglumine; 3.5 min later, iopamidol 370 was injected intravenously. Renal PCD CT images were acquired every 2 s for 5-6 min to capture the wash-in and wash-out kinetics of the contrast agents. Least mean squares linear material decomposition was used to calculate the concentrations of contrast agents in the aorta, renal cortex, renal medulla and renal pelvis.
Using reference vials with known concentrations of materials, we computed molar concentrations of the various contrast agents during each phase of CT scanning. Material concentration maps allowed simultaneous quantification of both arterial and delayed renal enhancement in a single CT acquisition. The accuracy of the material decomposition algorithm in a test phantom was -0.4 ± 2.2 mM, 0.3 ± 2.2 mM for iodine and gadolinium solutions, respectively. Peak contrast concentration of gadolinium and iodine in the aorta, renal cortex, and renal medulla were observed 16, 24, and 60 s after the start each injection, respectively.
Photon-counting spectral CT allowed simultaneous material decomposition of multiple contrast agents in vivo. Besides defining contrast agent concentrations, tissue enhancement at multiple phases was observed in a single CT acquisition, potentially obviating the need for multiphase CT scans and thus reducing radiation dose.
展示基于光子计数探测器(PCD)X 射线计算机断层扫描(CT)的光谱成像技术在活体大动物模型中同时对三种对比剂进行物质分解的可行性。
本机构动物护理和使用委员会批准的研究使用犬模型。在成像前 24-72 小时口服水杨酸铋。在静脉注射 40-60ml 钆喷酸葡胺的同时进行 PCD CT;3.5 分钟后,静脉内注射碘帕醇 370。为了捕捉对比剂的洗脱动力学,使用 PCD CT 对肾脏进行连续 2 秒采集,共 5-6 分钟。最小均方线性物质分解用于计算主动脉、肾皮质、肾髓质和肾盂中的对比剂浓度。
使用已知浓度材料的参考小瓶,我们在 CT 扫描的每个阶段计算出各种对比剂的摩尔浓度。物质浓度图允许在单次 CT 采集同时定量动脉期和延迟期肾增强。在测试体模中,物质分解算法的准确性为-0.4±2.2mM,碘和钆溶液分别为 0.3±2.2mM。在每次注射开始后 16、24 和 60 秒,分别观察到主动脉、肾皮质和肾髓质中钆和碘的峰值对比浓度。
光子计数能谱 CT 允许在活体中同时对多种对比剂进行物质分解。除了定义对比剂浓度外,还在单次 CT 采集观察到多个相位的组织增强,可能无需进行多期 CT 扫描,从而降低辐射剂量。