Chen Hui, Liu Lei, Qi Xingshun, He Chuangye, Wu Feifei, Fan Daiming, Han Guohong
aDepartment of Liver Disease and Digestive Interventional Radiology bState Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Diseases, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Eur J Gastroenterol Hepatol. 2016 Jan;28(1):82-9. doi: 10.1097/MEG.0000000000000482.
Portal vein thrombosis (PVT) is a frequent event in patients with cirrhosis. The effects of anticoagulation on these patients were still unclear, especially for more advanced PVT. The aim of this study was to retrospectively assess the resolution of PVT and liver disease progression in a large cohort of cirrhotic patients with PVT with or without anticoagulation therapy.
We analyzed data from 66 cirrhotic patients with PVT from January 2002 to June 2014. Thirty patients were anticoagulated with warfarin and 36 patients were untreated. PVT and hepatic decompensation were evaluated.
For anticoagulated patients, the thrombosis had improved in 15 (68.2%) patients, was stable in four patients (18.2%), and progressed in three patients (13.6%). For untreated patients, the thrombosis had improved in four patients (25%), was stable in six patients (37.5%), and progressed in six patients (37.5%). The anticoagulation group had significantly better recanalization rates than the untreated group (P=0.011). Degree of superior mesenteric vein (P=0.032, hazard ratio: 15.4; 95% confidence interval: 1.3-200) was a significant predictor. In addition, anticoagulation can effectively improve PVT with a degree less than 75% in the main portal vein compared with untreated patients (6/6 vs. 2/6, P=0.030). The probability of hepatic decompensation at 1 year was 15.6 and 17.9% between the anticoagulation and the untreated groups (P=0.847). Albumin (P=0.06, hazard ratio: 0.860; 95% confidence interval: 0.772-0.959) was a significant predictor.
Anticoagulation with warfarin might result in the resolution of more advanced PVT effectively and safely in patients with liver cirrhosis. In addition, we did not demonstrate the benefit of anticoagulation for the decompensation or death.
门静脉血栓形成(PVT)在肝硬化患者中较为常见。抗凝治疗对这些患者的影响仍不明确,尤其是对于病情更严重的PVT患者。本研究的目的是回顾性评估大量伴有或不伴有抗凝治疗的肝硬化合并PVT患者的PVT消退情况及肝病进展情况。
我们分析了2002年1月至2014年6月期间66例肝硬化合并PVT患者的数据。30例患者接受华法林抗凝治疗,36例患者未接受治疗。对PVT和肝失代偿情况进行了评估。
接受抗凝治疗的患者中,15例(68.2%)血栓情况改善,4例(18.2%)稳定,3例(13.6%)进展。未接受治疗的患者中,4例(25%)血栓情况改善,6例(37.5%)稳定,6例(37.5%)进展。抗凝组的再通率显著高于未治疗组(P = 0.011)。肠系膜上静脉程度(P = 0.032,风险比:15.4;95%置信区间:1.3 - 200)是一个显著的预测因素。此外,与未治疗患者相比,抗凝治疗可有效改善主门静脉中程度小于75%的PVT(6/6 vs. 2/6,P = 0.030)。抗凝组和未治疗组1年时肝失代偿的概率分别为15.6%和17.9%(P = 0.847)。白蛋白(P = 0.06,风险比:0.860;95%置信区间:0.772 - 0.959)是一个显著的预测因素。
华法林抗凝治疗可能有效且安全地使肝硬化患者更严重的PVT消退。此外,我们未证明抗凝治疗对肝失代偿或死亡有益处。