Materne R, Van Beers B E, Smith A M, Leconte I, Jamart J, Dehoux J P, Keyeux A, Horsmans Y
Department of Radiology, Université Catholique de Louvain, St-Luc University Hospital, B-1200 Brussels, Belgium.
Clin Sci (Lond). 2000 Dec;99(6):517-25.
Various liver diseases lead to significant alterations of the hepatic microcirculation. Therefore, quantification of hepatic perfusion has the potential to improve the assessment and management of liver diseases. Most methods used to quantify liver perfusion are invasive or controversial. This paper describes and validates a non-invasive method for the quantification of liver perfusion using computed tomography (CT). Dynamic single-section CT of the liver was performed after intravenous bolus administration of a low-molecular-mass iodinated contrast agent. Hepatic, aortic and portal-venous time-density curves were fitted with a dual-input one-compartmental model to calculate liver perfusion. Validation studies consisted of simultaneous measurements of hepatic perfusion with CT and with radiolabelled microspheres in rabbits at rest and after adenosine infusion. The feasibility and reproducibility of the CT method in humans was assessed by three observers in 10 patients without liver disease. In rabbits, significant correlations were observed between perfusion measurements obtained with CT and with microspheres (r=0.92 for total liver perfusion, r=0.81 for arterial perfusion and r=0.85 for portal perfusion). In patients, total liver plasma perfusion measured with CT was 112+/-28 ml.min(-1).100 ml(-1), arterial plasma perfusion was 18+/-12 ml.min(-1).100 ml(-1) and portal plasma perfusion was 93+/-31 ml.min(-1).100 ml(-1). The measurements obtained by the three observers were not significantly different from each other (P>0.1). Our results indicate that dynamic CT combined with a dual-input one-compartmental model provides a valid and reliable method for the non-invasive quantification of perfusion in the normal liver.
多种肝脏疾病会导致肝微循环的显著改变。因此,肝灌注的量化有潜力改善肝脏疾病的评估和管理。大多数用于量化肝灌注的方法具有侵入性或存在争议。本文描述并验证了一种使用计算机断层扫描(CT)量化肝灌注的非侵入性方法。在静脉推注低分子量碘化造影剂后,对肝脏进行动态单层面CT扫描。将肝、主动脉和门静脉的时间 - 密度曲线用双输入单室模型进行拟合,以计算肝灌注。验证研究包括在兔子静息状态和腺苷输注后,同时用CT和放射性标记微球测量肝灌注。10名无肝脏疾病的患者由三名观察者评估CT方法在人体中的可行性和可重复性。在兔子中,CT测量与微球测量的灌注结果之间存在显著相关性(全肝灌注r = 0.92,动脉灌注r = 0.81,门静脉灌注r = 0.85)。在患者中,CT测量的全肝血浆灌注为112±28 ml·min⁻¹·100 ml⁻¹,动脉血浆灌注为18±12 ml·min⁻¹·100 ml⁻¹,门静脉血浆灌注为93±31 ml·min⁻¹·100 ml⁻¹。三名观察者获得的测量结果彼此之间无显著差异(P>0.1)。我们的结果表明,动态CT结合双输入单室模型为正常肝脏灌注的非侵入性量化提供了一种有效且可靠的方法。