Hom J, Dankbaar J W, Schneider T, Cheng S-C, Bredno J, Wintermark M
Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, Calif 94143-0628, USA.
AJNR Am J Neuroradiol. 2009 Aug;30(7):1366-70. doi: 10.3174/ajnr.A1592. Epub 2009 Apr 15.
A previous study demonstrated the need to use delayed acquisition rather than first-pass data for accurate blood-brain barrier permeability surface product (BBBP) calculation from perfusion CT (PCT) according to the Patlak model, but the optimal duration of the delayed acquisition has not been established. Our goal was to determine the optimal duration of the delayed PCT acquisition to obtain accurate BBBP measurements while minimizing potential motion artifacts and radiation dose.
We retrospectively identified 23 consecutive patients with acute ischemic anterior circulation stroke who underwent a PCT study with delayed acquisition. The Patlak model was applied for the full delayed acquisition (90-240 seconds) and also for truncated analysis windows (90-210, 90-180, 90-150, 90-120 seconds). Linear regression of Patlak plots was performed separately for the full and truncated analysis windows, and the slope of these regression lines was used to indicate BBBP. The full and truncated analysis windows were compared in terms of the resulting BBBP values and the quality of the Patlak fitting.
BBBP values in the infarct and penumbra were similar for the full 90- to 240-second acquisition (95% confidence intervals for the infarct and penumbra: 1.62-2.47 and 1.75-2.41 mL x100 g(-1) x min(-1), respectively) and the 90- to 210-second analysis window (1.82-2.76 and 2.01-2.74 mL x 100 g(-1) x min(-1), respectively). BBBP values increased significantly with shorter acquisitions. The quality of the Patlak fit was excellent for the full 90- to 240-second and 90- to 210-second acquisitions, but it degraded with shorter acquisitions.
The duration for the delayed PCT acquisition should be at least 210 seconds, because acquisitions shorter than 210 seconds lead to significantly overestimated BBBP values.
先前的一项研究表明,根据Patlak模型,从灌注CT(PCT)准确计算血脑屏障通透表面积乘积(BBBP)需要使用延迟采集数据而非首过数据,但延迟采集的最佳时长尚未确定。我们的目标是确定延迟PCT采集的最佳时长,以获得准确的BBBP测量值,同时将潜在的运动伪影和辐射剂量降至最低。
我们回顾性纳入了23例连续的急性缺血性前循环卒中患者,这些患者均接受了延迟采集的PCT检查。将Patlak模型应用于整个延迟采集期(90 - 240秒)以及截断分析窗(90 - 210、90 - 180、90 - 150、90 - 120秒)。分别对整个和截断分析窗进行Patlak图的线性回归,并将这些回归线的斜率用于表示BBBP。比较整个和截断分析窗所得的BBBP值以及Patlak拟合的质量。
在整个90至240秒采集期(梗死灶和半暗带的95%置信区间分别为:1.62 - 2.47和1.75 - 2.41 mL×100 g⁻¹×min⁻¹)和90至210秒分析窗(分别为1.82 - 2.76和2.01 - 2.74 mL×100 g⁻¹×min⁻¹)中,梗死灶和半暗带的BBBP值相似。采集时间越短,BBBP值显著升高。对于整个90至240秒和90至210秒采集期,Patlak拟合质量极佳,但采集时间越短,拟合质量下降。
延迟PCT采集的时长应至少为210秒,因为短于210秒的采集会导致BBBP值被显著高估。