Future liver remnant growth after various portal vein embolization regimens: a quantitative comparison

被引:6
|
作者
Biggemann, Lorenz [1 ]
Uhlig, Johannes [1 ]
Streit, Ulrike [1 ]
Sack, Henrik [1 ]
Guo, Xiao Chao [2 ]
Jung, Carlo [3 ]
Ahmed, Saheeb [1 ]
Lotz, Joachim [1 ]
Mueller-Wille, Rene [1 ]
Hosseini, Ali Seif Amir [1 ]
机构
[1] Univ Med Ctr Goettingen, Dept Diagnost & Intervent Radiol, Robert Koch Str 40, D-37075 Gottingen, Germany
[2] Univ Beijing, Peking Univ Hosp 1, Dept Radiol, Beijing, Peoples R China
[3] Univ Med Ctr Gottingen, Dept Gastroenterol & Gastrointestinal Oncol, Gottingen, Germany
关键词
Portal vein embolization; future liver remnant; ethylene vinyl alcohol; HEPATOCELLULAR-CARCINOMA; MAJOR HEPATECTOMY; 2-STAGE HEPATECTOMY; HEPATIC RESECTION; HYPERTROPHY; LIGATION; METASTASES; SAFETY; FEASIBILITY; INDUCTION;
D O I
10.1080/13645706.2019.1582067
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: To compare the efficacy of right portal vein embolization using ethylene vinyl alcohol (EVOH-PVE) compared to other embolic agents and surgical right portal vein ligation (PVL). Material and methods: Patients with right sided liver malignancies scheduled for extensive surgery and receiving induction of liver hypertrophy via right portal vein embolization/ligature between 2010-2016 were retrospectively evaluated. Treatments included were ethylene vinyl alcohol copolymer (Onyx (R), EVOH-PVE), ethiodized oil (Lipiodol(R), Lipiodol/PVA-PVE), polyvinyl alcohol (PVA-PVE) or surgical ligature (PVL). Liver segments S2/3 were used to assess hypertrophy. Primary outcome was future liver remnant growth in ml/day. Results: Forty-one patients were included (EVOH-PVE n = 11; Lipiodol/PVA-PVE n = 10; PVA-PVE n = 8; PVL n = 12), the majority presenting with cholangiocarcinoma and colorectal metastases (n = 11; n = 27). Pre-interventional liver volumes were comparable (p = .095). Liver hypertrophy was successfully induced in all but one patient receiving Lipiodol/PVA-PVE. Liver segment S2/3 growth was largest for EVOH-PVE (5.38 ml/d) followed by PVA-PVE (2.5 ml/d), with significantly higher growth rates than PVL (1.24 ml/d; p < .001; p = .007). No significant difference was evident for Lipiodol/PVA-PVE (1.43 ml/d, p = .809). Conclusions: Portal vein embolization using EVOH demonstrates fastest S2/3 growth rates compared to other embolic agents and PVL, potentially due to its permanent portal vein embolization and induction of hepatic inflammation.
引用
收藏
页码:98 / 106
页数:9
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