DEB-TACE和lipodol - tace后门静脉损伤:基于动脉门静脉造影时计算机断层成像的评价。

Masashi Tamura, Seishi Nakatsuka, Hideyuki Torikai, Manabu Misu, Jitsuro Tsukada, Kentaro Tamura, Nobutake Ito, Masanori Inoue, Hideki Yashiro, Masahiro Jinzaki
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摘要

目的:通过动脉门静脉造影时计算机断层成像的评价,揭示药物洗脱珠经动脉化疗栓塞和Lipiodol经动脉化疗栓塞对门静脉灌注的影响,探讨经动脉化疗栓塞后门静脉损伤的易感因素。材料和方法:本回顾性队列分析纳入了2013年10月至2015年4月期间在动脉门静脉造影期间接受经动脉化疗栓塞和术前/随访计算机断层扫描的49例肝细胞癌患者。对比术前和随访的门静脉造影ct,发现门静脉造影随访ct提示门静脉损伤的新变化:小灌注缺损、大灌注缺损、门静脉狭窄/消失或梗阻。计算药物洗脱珠经动脉化疗栓塞和Lipiodol经动脉化疗栓塞后门静脉损伤的频率,并分析门静脉损伤与临床变量的关系。最后,进行了多因素logistic回归分析,并对潜在的混杂因素进行了调整,以确定导致门静脉损伤的因素。结果:本研究纳入24例药物洗脱珠经动脉化疗栓塞患者和25例脂醇经动脉化疗栓塞患者。药物洗脱珠经动脉化疗栓塞后出现小灌注缺损、门静脉狭窄/消失或阻塞的频率明显高于脂醇经动脉化疗栓塞后(70.8% [17/24]vs. 20% [5/25]);P < 0.001;41.7% [10/24] vs. 12% [3/25];P = 0.019)。结论:药物洗脱珠经动脉化疗栓塞后门静脉损伤发生率明显高于脂醇经动脉化疗栓塞,药物洗脱珠经动脉化疗栓塞是经动脉化疗栓塞后门静脉损伤的独立预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Portal Vein Damage after DEB-TACE and Lipiodol-TACE: Based on Evaluation by Computed Tomography during Arterial Portography.

Purpose: To reveal the effect of drug-eluting beads transarterial chemoembolization and Lipiodol transarterial chemoembolization on portal perfusion, and to identify factors predisposing portal vein damage after transarterial chemoembolization, based on evaluation by computed tomography during arterial portography.

Material and methods: This retrospective cohort analysis included 49 patients with hepatocellular carcinoma who underwent transarterial chemoembolization and preprocedural/follow-up computed tomography during arterial portography between October 2013 and April 2015. The preprocedural and follow-up computed tomography during arterial portography were compared to identify the following new changes suggestive of portal vein damage in the follow-up computed tomography during arterial portography: small perfusion defects, large perfusion defects, and narrowing/disappearance or portal vein obstruction. The frequency of portal vein damage after drug-eluting beads transarterial chemoembolization and Lipiodol transarterial chemoembolization was calculated, and relationships between portal vein damage and clinical variables were analyzed. Finally, a multivariate logistic regression analysis with adjustments for potentially confounding factors was performed to identify factors predisposing portal vein damage.

Results: The analysis included 24 patients who underwent drug-eluting beads transarterial chemoembolization and 25 who underwent Lipiodol transarterial chemoembolization. Emergence of small perfusion defects and narrowing/disappearance or obstruction of portal vein were observed at a significantly higher frequency following drug-eluting beads transarterial chemoembolization than following Lipiodol transarterial chemoembolization (70.8% [17/24] vs. 20% [5/25]; p < 0.001; 41.7% [10/24] vs. 12% [3/25]; p = 0.019). Drug-eluting beads transarterial chemoembolization and selectivity of transarterial chemoembolization (selective [

Conclusions: Portal vein damage occurred at a significantly higher frequency following drug-eluting beads transarterial chemoembolization than following Lipiodol transarterial chemoembolization, and drug-eluting beads transarterial chemoembolization was an independent predictor of portal vein damage after transarterial chemoembolization.

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