带有轴向和横向间隙的全身 PET 系统设计:病变定量和可探测性研究

Min Gao, Margaret E. Daube-Witherspoon, Joel S. Karp, Suleman Surti
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引用次数: 0

摘要

高灵敏度全身PET可实现更快的扫描、更低的剂量和动态的多器官成像。然而,长轴向视场扫描仪较高的系统成本阻碍了其广泛应用。本文研究了成本效益高的全身PET稀疏设计对病灶量化和可检测性的影响。方法:以PennPET Explorer (PPEx)为模型,考虑3种具有相同142 cm AFOV的稀疏配置,包括仅轴向间隙(AGs)、仅横向间隙(tgg)和AGs与tgg混合(MG)的设计,保留的检测器分数(DFs)范围为71% ~ 40%。来自PPEx的人类数据被用来模拟稀疏设计,通过丢弃响应线作为缺失检测器的代理。我们将病变事件嵌入到重建前肺和肝脏不同摄取的结果列表数据中。一种广义的扫描统计方法被用来测量病变的可检测性和量化,作为病变摄取和扫描时间的函数。结果:相对于完全填充的系统,71%的AG设计表现良好,但当DF降低到58%时,容易受到图像伪影的影响。TG设计在DF为58%时表现良好,但需要两倍的扫描时间才能达到类似的病变可检测性,并且随着DF进一步降低,在60厘米以下容易出现横向视场截断。DF为58%的MG设计需要3倍的扫描时间才能达到类似的病变可检测性,并且即使DF降低到40%也没有伪影的证据。结论:具有无伪影图像的稀疏设计在补偿了随扫描时间增加而降低的灵敏度后,可以提供与完全填充的PPEx相当的病变量化和可检测性。由于AG设计更容易受到较低DF的图像伪影的影响,因此仅使用AG的系统并不是大幅降低成本的最佳选择。对于给定的DF, TG设计提供了比AG或MG设计更高的相对灵敏度,导致更短的扫描时间,以达到相当的病变可检测性。然而,随着DF的减小,横向视场截断量的增加限制了这种设计选择。如果增加扫描持续时间以补偿更高的灵敏度损失,则MG设计可以最大限度地降低成本(最低DF)。具有长AFOV的PET稀疏设计为将此类系统以较低的成本引入常规临床应用提供了技术解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total-Body PET System Designs with Axial and Transverse Gaps: A Study of Lesion Quantification and Detectability

High-sensitivity total-body PET enables faster scans, lower doses, and dynamic multiorgan imaging. However, the higher system cost of a scanner with a long axial field of view (AFOV) hinders its wider application. This paper investigates the impact on the lesion quantification and detectability of cost-effective total-body PET sparse designs. Methods: Using the PennPET Explorer (PPEx) as a model, 3 sparse configurations with the same 142-cm AFOV were considered, including designs with only axial gaps (AGs), only transverse gaps (TGs), and a mixture of AGs and TGs (MG), with retained detector fractions (DFs) ranging from 71% to 40%. Human data from the PPEx were used to emulate sparse designs by discarding lines of response as a proxy for missing detectors. We embedded lesion events in the resultant list data with varying uptakes in the lung and liver before reconstruction. A generalized scan statistics methodology was used to measure lesion detectability and quantification as a function of lesion uptake and scan duration. Results: Relative to a fully populated system, an AG design with 71% performs well but is susceptible to image artifacts as the DF decreases to 58%. A TG design performs well with a DF of 58% but requires twice the scan time to achieve similar lesion detectability and is susceptible to transverse field-of-view truncation below 60 cm as the DF is further decreased. An MG design with a DF of 58% requires 3 times the scan time to achieve similar lesion detectability, and with no evidence of artifacts even as the DF is decreased to 40%. Conclusion: Sparse designs with artifact-free images can provide comparable lesion quantification and detectability to the fully populated PPEx after compensating for the reduced sensitivity with increased scan time. Because an AG design is more susceptible to image artifacts with a lower DF, a system with only AGs is not an optimal choice for dramatic cost reduction. A TG design provides a higher relative sensitivity than AG or MG designs for a given DF, leading to a shorter scan time to achieve comparable lesion detectability. However, the increased truncation of the transverse field of view with decreasing DF limits this design choice. An MG design allows for the greatest cost reduction (lowest DF) if the scan duration is increased to compensate for the higher loss in sensitivity. Sparse designs of PET with a long AFOV provide a technologic solution for introducing such systems at reduced cost into routine clinical use.

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