Davis Jessica P E, Lim Joseph K, Francis Fadi F, Ahn Joseph
Division of Gastroenterology and Hepatology, Department of Medicine, Washington DC Veterans Affairs Medical Center, Washington, District of Columbia.
Section of Digestive Diseases and Yale Liver Center, Yale School of Medicine, New Haven, Connecticut.
Gastroenterology. 2025 Feb;168(2):396-404.e1. doi: 10.1053/j.gastro.2024.10.038. Epub 2024 Dec 20.
Portal vein thromboses (PVTs) are common in patients with cirrhosis and are associated with advanced portal hypertension and mortality. The treatment of PVTs remains a clinical challenge due to limited evidence and competing risks of PVT-associated complications vs bleeding risk of anticoagulation. Significant heterogeneity in PVT phenotype based on anatomic, host, and disease characteristics, and an emerging spectrum of therapeutic options further complicate PVT management. This Clinical Practice Update (CPU) aims to provide best practice advice for the evaluation and management of PVT in cirrhosis, including the role of direct oral anticoagulants and endovascular interventions.
This expert review was commissioned and approved by the American Gastroenterological Association (AGA) Institute CPU Committee and the AGA Governing Board to provide timely guidance on a topic of high clinical importance to the AGA membership, and underwent internal peer review by the CPU Committee and external peer review through standard procedures of Gastroenterology. These Best Practice Advice statements were drawn from a review of the published literature and from expert opinion. Because systematic reviews were not performed, these Best Practice Advice statements do not carry formal ratings regarding the quality of evidence or strength of the presented considerations. Best Practice Advice Statements BEST PRACTICE ADVICE 1: Asymptomatic patients with compensated cirrhosis do not require routine screening for PVT. BEST PRACTICE ADVICE 2: Patients with cirrhosis with PVTs identified on Doppler ultrasound should undergo cross-sectional imaging with computed tomography or magnetic resonance imaging to confirm the diagnosis, evaluate for malignancy, and document the degree of lumen occlusion, clot extent, and chronicity. BEST PRACTICE ADVICE 3: Patients with cirrhosis and PVT do not require a hypercoagulable workup in the absence of additional thromboemboli or laboratory abnormalities or family history suggestive of thrombophilia. BEST PRACTICE ADVICE 4: Patients with cirrhosis and PVT with evidence of intestinal ischemia require urgent anticoagulation to minimize ischemic injury. If available, these patients should be managed by a multidisciplinary team, including gastroenterology and hepatology, interventional radiology, hematology, and surgery. BEST PRACTICE ADVICE 5: Consider observation, with repeat imaging every 3 months until clot regression, in patients with cirrhosis without intestinal ischemia and recent (<6 months) thrombosis involving the intrahepatic portal vein branches or when there is <50% occlusion of the main portal vein, splenic vein, or mesenteric veins. BEST PRACTICE ADVICE 6: Anticoagulation should be considered in patients with cirrhosis without intestinal ischemia who develop recent (<6 months) PVT that is >50% occlusive or involves the main portal vein or mesenteric vessels. Patients who have increased benefit of recanalization include those with involvement of more than 1 vascular bed, those with thrombus progression, potential liver transplantation candidates, and those with inherited thrombophilia. BEST PRACTICE ADVICE 7: Anticoagulation is not advised for patients with cirrhosis with chronic (>6 months) PVT with complete occlusion with collateralization (cavernous transformation). BEST PRACTICE ADVICE 8: Patients with cirrhosis and PVT warrant endoscopic variceal screening if they are not already on nonselective beta-blocker therapy for bleeding prophylaxis. Avoid delays in the initiation of anticoagulation for PVT, as this decreases the odds of portal vein recanalization. BEST PRACTICE ADVICE 9: Vitamin K antagonists, low-molecular-weight heparin, and direct oral anticoagulants are all reasonable anticoagulant options for patients with cirrhosis and PVT. Decision making should be individualized and informed by patient preference and Child-Turcotte-Pugh class. Direct oral anticoagulants may be considered in patients with compensated Child-Turcotte-Pugh class A and Child-Turcotte-Pugh class B cirrhosis and offer convenience as their dosages are independent of international normalized ratio monitoring. BEST PRACTICE ADVICE 10: Patients with cirrhosis on anticoagulation for PVT should have cross-sectional imaging every 3 months to assess response to treatment. If clot regresses, anticoagulation should be continued until transplantation or at least clot resolution in nontransplantation patients. BEST PRACTICE ADVICE 11: Portal vein revascularization with transjugular intrahepatic portosystemic shunting may be considered for selected patients with cirrhosis and PVT who have additional indications for transjugular intrahepatic portosystemic shunting, such as those with refractory ascites or variceal bleeding. Portal vein revascularization with transjugular intrahepatic portosystemic shunting may also be considered for transplantation candidates if recanalization can facilitate the technical feasibility of transplantation.
门静脉血栓形成(PVT)在肝硬化患者中很常见,与晚期门静脉高压和死亡率相关。由于证据有限以及PVT相关并发症的风险与抗凝出血风险相互竞争,PVT的治疗仍然是一项临床挑战。基于解剖、宿主和疾病特征的PVT表型存在显著异质性,以及新兴的一系列治疗选择,进一步使PVT的管理复杂化。本临床实践更新(CPU)旨在为肝硬化患者PVT的评估和管理提供最佳实践建议,包括直接口服抗凝剂和血管内介入治疗的作用。
本专家综述由美国胃肠病学会(AGA)研究所CPU委员会和AGA理事会委托并批准,旨在为对AGA成员具有高度临床重要性的主题提供及时指导,并通过胃肠病学标准程序接受CPU委员会的内部同行评审和外部同行评审。这些最佳实践建议声明来自对已发表文献的综述和专家意见。由于未进行系统评价,这些最佳实践建议声明未对所提供考虑因素的证据质量或强度进行正式评级。最佳实践建议 1:代偿期肝硬化的无症状患者无需常规筛查PVT。最佳实践建议 2:经多普勒超声检查发现有PVT的肝硬化患者应接受计算机断层扫描或磁共振成像的横断面成像,以确诊、评估是否存在恶性肿瘤,并记录管腔阻塞程度、血栓范围和慢性程度。最佳实践建议 3:在没有额外血栓栓塞、实验室异常或提示血栓形成倾向的家族史的情况下,肝硬化合并PVT的患者无需进行高凝检查。最佳实践建议 4:有肠缺血证据的肝硬化合并PVT患者需要紧急抗凝,以尽量减少缺血性损伤。如果可行,这些患者应由多学科团队管理,包括胃肠病学和肝病学、介入放射学、血液学和外科。最佳实践建议 5:对于无肠缺血且近期(<6个月)血栓形成累及肝内门静脉分支或主门静脉、脾静脉或肠系膜静脉阻塞<50%的肝硬化患者,可考虑观察,每3个月重复成像直至血栓消退。最佳实践建议 6:对于无肠缺血且近期(<6个月)发生PVT且阻塞>50%或累及主门静脉或肠系膜血管的肝硬化患者,应考虑抗凝。再通获益增加的患者包括累及多个血管床的患者、血栓进展的患者、潜在肝移植候选者以及患有遗传性血栓形成倾向的患者。最佳实践建议 7:对于慢性(>6个月)PVT且完全阻塞并伴有侧支循环形成(海绵样变性)的肝硬化患者,不建议抗凝。最佳实践建议 8:肝硬化合并PVT的患者如果尚未接受非选择性β受体阻滞剂治疗以预防出血,则需要进行内镜下静脉曲张筛查。避免因PVT而延迟开始抗凝,因为这会降低门静脉再通的几率。最佳实践建议 9:维生素K拮抗剂、低分子肝素和直接口服抗凝剂对肝硬化合并PVT的患者都是合理的抗凝选择。决策应个体化,并根据患者偏好和Child-Turcotte-Pugh分级来决定。对于代偿期Child-Turcotte-Pugh A级和Child-Turcotte-Pugh B级肝硬化患者,可考虑使用直接口服抗凝剂,因其剂量与国际标准化比值监测无关,使用方便。最佳实践建议 10:接受PVT抗凝治疗的肝硬化患者应每3个月进行横断面成像,以评估治疗反应。如果血栓消退,抗凝应持续至移植或至少在非移植患者中血栓溶解。最佳实践建议 11:对于有经颈静脉肝内门体分流术(TIPS)其他适应证(如难治性腹水或静脉曲张出血)的特定肝硬化合并PVT患者,可考虑进行TIPS门静脉再血管化。如果再通可促进移植的技术可行性,对于移植候选者也可考虑TIPS门静脉再血管化。