肝CT灌注成像作为评估慢性丙型肝炎纤维化和肝硬化患者肝实质血流动力学的无创方法

G. Stashuk, Y. Moysyuk, D. Smirnova, O. Sumtsova
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引用次数: 1

摘要

目的:探讨肝脏计算机断层扫描(CT)灌注成像是否可以评估慢性丙型肝炎(CVHC)纤维化和肝硬化患者的血流动力学。研究对象和方法。这项前瞻性研究在莫斯科地区研究和临床研究所放射诊断部进行,纳入了61名因CVHC导致肝纤维化和肝硬化的患者,其中26名患者接受了抗病毒治疗(AVT),并在治疗结束后24周实现了持续病毒学应答(SVR)。所有患者均在256层Philips ICT计算机断层扫描仪(荷兰)上进行肝脏CT灌注成像。通过计算曲线的斜率,测量每位患者III、VII、VIII肝段的动脉、门静脉、总灌注及肝脏灌注指数参数。结果。将AVT后达到SVR且未接受特异性治疗的患者灌注参数值与纤维化、代偿、亚代偿和失代偿肝硬化组进行比较。在肝纤维化组中,AVT后SVR达到SVR的患者门脉和总灌注值高于未接受特异性治疗的患者(p = 0.001和p = 0.002;分别)。在同一组中,未行AVT的患者肝脏灌注指数高于治疗组(p = 0.028)。AVT后SVR达到代偿性肝硬化患者的总灌注值明显高于未治疗的患者(p = 0.008)。失代偿肝硬化组特异性治疗后门静脉灌注高于非avt组(p = 0.012)。亚代偿性肝硬化组在比较不同治疗条件下肝脏灌注参数值时,差异无统计学意义。结论。肝CT灌注成像不能显示AVT后CVHC患者肝组织在纤维化和肝硬化情况下的血流动力学变化。
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Liver CT Perfusion Imaging as a Non-Invasive Method for Assessing Hemodynamics of the Hepatic Parenchyma in Patients with Fibrosis and Cirrhosis as a Result of Chronic Viral Hepatitis C
Objective: to determine whether liver computed tomography (CT) perfusion imaging can assess hemodynamics in patients with fibrosis and cirrhosis as a result of chronic viral hepatitis C (CVHC). Subjects and methods. The prospective study conducted at the Department of Radiation Diagnosis, M.F. Vladimirsky Moscow Regional Research and Clinical Institute, enrolled 61 patients with liver fibrosis and cirrhosis as a result of CVHC, of whom 26 patients had received antiviral therapy (AVT) and achieved a sustained virological response (SVR) at 24 weeks after the end of treatment. All the patients underwent liver CT perfusion imaging on a 256-slice Philips ICT computed tomography scanner (Netherlands). The parameters of arterial, portal, general perfusion and hepatic perfusion index were measured in each patient in his/her liver segments III, VII, and VIII, by calculating the slope of a curve. Results. The values of perfusion parameters in patients who had undergone AVT and attained SVR and who had received no specific treatment were compared with those in the fibrosis, compensated, subcompensated, and decompensated liver cirrhosis groups. In the liver fibrosis group, the patients who had achieved SVR after AVT had higher portal and total perfusion values than those who had received no specific treatment (p = 0.001 and p = 0.002; respectively). In the same group, the liver perfusion index was higher in the patients who had not undergone AVT than in the treated patients (p = 0.028). The values of total perfusion were statistically significantly higher in patients with compensated liver cirrhosis who had attained SVR after AVT than in the untreated patients (p = 0.008). In the decompensated liver cirrhosis group, portal perfusion after specific treatment was higher than in the non-AVT group (p = 0.012). The subcompensated liver cirrhosis group showed no statistically significant differences when comparing the values of liver perfusion parameters depending on the availability of treatment. Conclusion. Liver CT perfusion imaging cannot give an idea of how the hemodynamics of liver tissue changes in the presence of fibrosis and cirrhosis in patients with CVHC after AVT.
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