PVT In Patients With Chronic Liver Disease Dominique-Charles Valla Hôpital Beaujon, APHP, Université Paris-7, Inserm CR3B Cooperation Bilharz-Beaujon Cairo - March 16-18, 2008
PVT in Patients with Cirrhosis Epidemiology Manifestations Causal factors Therapy
Prevalence of Overt PVT in Cirrhosis Screening for HCC 0.6 % In-Hospital 7.0 % Necropsy 8.0 % Before LTx or PSS 15.0 % Okuda et al. Gastroenterology 1985;89: Chang et al. J Pathol Bacteriol 1965;89:
Incidence of PVT in Patients with Cirrhosis Amitrano, Endoscopy Francoz et al. Gut % pt/yr Listed for liver transplantation Sclerotherapy 12% pt/yr
Prevalence of Occult PVT in Cirrhosis Liver explants Wanless et al. Hepatology 1995;21: Small mural thrombus 64 % Large veins (intimal fibrosis) 25 % Small veins (intimal fibrosis) 36 % % Veins involved
Prevalence of Overt PVT in Schistosomiasis Preoperative 5 % Splenectomy/Devascularization 19 % Distal splenorenal shunt50 % Widman. Hepatogastroenterology 2003
PVT in Patients with Cirrhosis Epidemiology Manifestations Causal factors Therapy
PVT and Cirrhosis: Associations Portal hypertensive bleeding Failure to control bleeding Ascites Hepatic encephalopathy Hyperdynamic circulation Intestinal ischemia or infarction Nonami Hepatology Orloff J Gastrointest Surg D’Amico Hepatology Amitrano J Hepatol 2004.
PVT and Cirrhosis: Associations Nonami et al. Hepatology 1992;16: At LTxNLiver weight PVT 6317 g/Kg No PVT40121 g/Kg P <.02
Thrombosis Advanced Liver Disease Decreased Portal Blood Inflow Blood stasis Wall changes (PHT) Thrombosis Advanced Liver Disease
PVT in Patients with Cirrhosis Epidemiology Manifestations Causal factors Therapy
THROMBOSIS External Factors Environmental Local factors Internal Factors Prothrombotic Disorders Causes For Venous Thrombosis Acquired Inherited
Inherited Prothrombotic Disorders Loss of function Inhibitors (PC, PS, AT) Uncommon (< 0.1%) High risk Dg: Plasma level Gain of function Factors (FV, FII) Common (> 2.0%) Moderate risk Dg: DNA analysis
Acquired Prothrombotic Disorders Common Moderate risk Inflammatory states Malignancy Hyperhomocysteinemia … Uncommon High risk Myeloproliferative dis. APL syndrome PNH Behcet’s disease …
Inherited Prothrombotic Disorders Loss of function Inhibitors (PC, PS, AT) Uncommon (< 0.1%) High risk Dg: Plasma level Gain of function Factors (FV, FII) Common (> 2.0%) Moderate risk Dg: DNA analysis
Coagulation Inhibitors in Cirrhosis Romero-Gomez. J Clin Gastroenterol % Protein C Protein S Antithrombin A B C 50% 0% 75% Child-Pugh BC A BC A BC A
Acquired Prothrombotic Disorders Common Moderate risk Inflammatory states Malignancy Hyperhomocysteinemia … Uncommon High risk Myeloproliferative dis. APL syndrome PNH Behcet’s disease …
PVT and Cirrhosis: Antiphospholipid Ab Mangia, Am J Gastroenterol Dalekos, Eur J Gastro Hepato Munoz-Rodriguez, J Hepatol Prieto, Hepatology Quintarelli, J Hepatol Violi, Hepatology Romero-Gomez J Clin gastro 2000 ACL common in chronic liver diseases (20%) Usually non specific (low fluctuating titer, no LA)
Risk Factors for Portal Vein Thrombosis. Cirrhosis without HCC Univariate:Age, Child-Pugh class, Surgery for portal hypertension Endoscopic sclerotherapy Prothrombotic features Mangia, Am J Gastroenterol Nonami, Hepatology Davidson, Transplantation *Amitrano, J Hepatol 2004.
PVT and Cirrhosis: Prothrombotic Disorders With PVTNo PVT p Amitrano et al. Hepatology 2000;31: F. V Leiden F. II gene mutation C677T MTHFR At least one Two or more 13 % 35 % 43 % 70 % 22 % NS <.05 <.01 7 % 2 % 5 % 14 % 0
Risk Factors for Portal Vein Thrombosis. Cirrhosis without HCC Univariate:Age, Child-Pugh class, Surgery for portal hypertension Endoscopic sclerotherapy Prothrombotic features Mangia, Am J Gastroenterol Nonami, Hepatology Davidson, Transplantation *Amitrano, J Hepatol Multivariate:G20210A FII (OR 5.94*)
PVT in Patients with Cirrhosis Epidemiology Manifestations Causal factors Therapy
PVT and Cirrhosis: Why to treat? To prevent aggravation ? To facilitate transplantation
Portal Vein Thrombosis Clinical results of anticoagulant therapy In patients without cirrhosis In patients with cirrhosis
Acute PVT: Complete Recanalization Pts at risk: Time to recanalization (months) Recanalization (%)
Chronic Portal Vein Thrombosis Condat et al. Gastroenterology 2001; 120:490 Thrombosis 6.0 yes no yes no Anticoagulation 1.2 Bleeding 7 17 per 100 patients per year p = p = 0.212
Orr et al. Hepatology 2005; 42: 212A (AASLD San Francisco 2005) Chronic portomesenteric venous thrombosis HR for Death yes no Warfarine p=0.038
Patients on the Waiting List for LTx PVT before transplantation (n = 29) Anticoagulation (n = 19) Recanalization (n = 8) Francoz, Gut 2005 No anticoagulation (n = 10) Recanalization (n = 0)
TIPS for PVT in Cirrhosis Limited data Feasible and safe Risk of obstruction unclear Risk of encephalopathy unclear Benefit unclear Senzolo Alim Pharmacol Therap Van Ha Cardiovasc Intervent Radiol Bauer Liver Transplant 2006
PVT and Cirrhosis: Summary Common in end-stage cirrhosis Uncommon in well-compensated cirrhosis Causal factors: surgery, stasis, thrombophilias A marker for severity: certainly A cause for aggravation: uncertain A limitation for liver transplantation: certainly
PVT and Cirrhosis: What we do in Beaujon Objectives:Recanalization (recent thrombus) Prevention of thrombus extension Indications:→ Child A with thrombophilia → Patients listed for LTx Monitoring:Anti-Xa 0.5 U/ml Factor II 25% to 35%
Hemostasis in Cirrhosis Normal thrombin generation in platelet-poor plasma. Decreased thrombin generation in severely thrombocytopenic blood. Elevated levels of vWF support platelet adhesion despite reduced functional capacities. Caldwell. Hepatology 2006
INR in Patients with Cirrhosis Not related to prothrombin levels along the same regression line as for Vitamin K antagonists. Due to uncarboxylated metabolites of coagulation factors Interlaboratory variability. → Adjustment based on Factor II level 25-35%?
Patients on the Waiting List for LTx PVT before transplantation 24 Complete 3 Recanalization 0 Francoz, ILTS 2008 Partial 21 Recanalization* 15 * No post-OLT PVT
Recanalisation 83 % Anticoagulation (alone, n = 27) Condat. Hepatology 2000 Thrombolysis (in situ, n = 20) 75 % Acute Portal Vein Thrombosis Holliingshead. J Vasc Interv Radiol 2005
Acute Portal Vein Thrombosis Major Bleeding 60% Thrombolysis (in situ, n = 20) 5% Anticoagulation (alone, n = 27) Condat. Hepatology 2000 Holliingshead. J Vasc Interv Radiol 2005 %