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Impact of acquisition time-window on clinical whole-body PET parametric imaging

机译:采集时间窗口对临床全身PET参数成像的影响

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Whole-body PET parametric imaging can combine the benefit of extended axial field-of-view (FOV) in multi-bed scans with that of generating time activity curves (TACs) in dynamic scans. We have recently proposed such a framework capable of delivering whole-body FDG Patlak images in clinically feasible scan times. The design of the acquisition protocol was limited to a single time-window and the standard Patlak graphical analysis method. However, the relatively long FDG half-life and uptake, compared to clinically acceptable acquisition time-windows, render the choice of this window critical. The major FDG kinetic components can be estimated from the early and intermediate TAC segments. On the contrary, at later time-windows, tumor contrast may be overall higher. In addition, the standard Patlak method does not account for tracer uptake reversibility, a property that becomes more apparent at later acquisition time-windows for certain tumors, thus increasing the probability for larger bias at later times. Consequently, the choice of the optimal time-window can be critical and should constitute an important design aspect of multi-bed dynamic protocols. In the present work we assessed the impact of a sliding acquisition time-window on whole-body FDG PET parametric images. This included incremental shift of a 6-pass acquisition time-window (~35min) along an extended scan period of 0-90min post injection, using both real patient kinetic data as well as realistic 4D simulations of the state-of-the-art Siemens Biograph mCT scanner. We also propose the selective application of a generalized Patlak method accounting for uptake reversibility. Our simulated and clinical results demonstrate that both Patlak methods (standard and generalized) result in enhanced tumor-to-background contrast as well as contrast-to-noise ratios with minimal bias at an early acquisition time window (10-45min post injection) with the generalized method exhibiting systematically superior performance.
机译:全身PET参数成像可以将多床扫描中扩展轴向视场(FOV)的优势与动态扫描中生成时间活动曲线(TAC)的优势相结合。我们最近提出了一种这样的框架,该框架能够在临床可行的扫描时间内提供全身FDG Patlak图像。采集协议的设计仅限于单个时间窗口和标准的Patlak图形分析方法。但是,与临床上可接受的采集时间窗口相比,相对较长的FDG半衰期和吸收时间使该窗口的选择变得至关重要。 FDG的主要动力学成分可以从TAC的早期和中期进行估算。相反,在较晚的时间窗口内,肿瘤对比度总体上可能更高。另外,标准的Patlak方法没有考虑到示踪剂摄取的可逆性,该属性在某些肿瘤的较晚采集时间窗口变得更加明显,因此增加了在较晚时间出现较大偏差的可能性。因此,最佳时间窗口的选择可能至关重要,并且应该构成多床动态协议的重要设计方面。在当前的工作中,我们评估了滑动采集时间窗口对全身FDG PET参数图像的影响。这包括使用真实患者动力学数据以及最新技术的逼真的4D模拟,在注射后0-90​​min的扩展扫描期间内,经过6次采集的时间窗口(约35分钟)的增量偏移西门子Biograph mCT扫描仪。我们还建议考虑到吸收可逆性的广义Patlak方法的选择性应用。我们的模拟和临床结果表明,Patlak方法(标准方法和通用方法)均可在早期采集时间窗(注射后10-45分钟)内以最小的偏差提高肿瘤与背景的对比度以及对比度与噪声比。具有系统优越性能的通用方法。

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