TY - JOUR
T1 - Hepatic encephalopathy is not a contraindication to pre-emptive TIPS in high-risk patients with cirrhosis with variceal bleeding
AU - Rudler, Marika
AU - Hernández-Gea, Virginia
AU - Procopet, Bogdan Dumitru
AU - Giráldez, Alvaro
AU - Amitrano, Lucio
AU - Villanueva, Càndid
AU - Ibañez, Luis
AU - Silva-Junior, Gilberto
AU - Genesca, Joan
AU - Bureau, Christophe
AU - Trebicka, Jonel
AU - Bañares, Rafael
AU - Krag, Aleksander
AU - Llop, Elba
AU - Laleman, Wim
AU - Palazon, Jose Maria
AU - Castellote, Jose
AU - Rodrigues, Susana
AU - Gluud, Lise Lotte
AU - Noronha Ferreira, Carlos
AU - Canete, Nouria
AU - Rodríguez, Manuel
AU - Ferlitsch, Arnulf
AU - Mundi, Jose Luis
AU - Gronbaek, Henning
AU - Hernandez-Guerra, Manuel
AU - Sassatelli, Romano
AU - Dell'Era, Alessandra
AU - Senzolo, Marco
AU - Abraldes, Juan G.
AU - Romero-Gómez, Manuel
AU - Zipprich, Alexander
AU - Casas, Meritxell
AU - Masnou, Helena
AU - Larrue, Hélène
AU - Primignani, Massimo
AU - Nevens, Frederik
AU - Calleja, Jose Luis
AU - Schwarzer, Remy
AU - Jansen, Christian
AU - Robic, Marie Angèle
AU - Conejo, Irene
AU - Martínez Gonzalez, Javier
AU - Catalina, Maria Vega
AU - Albillos, Agustín
AU - Alvarado, Edilmar
AU - Guardascione, Maria Anna
AU - Mallet, Maxime
AU - Tripon, Simona
AU - Casanovas, Georgina
AU - Bosch, Jaume
AU - Garcia-Pagan, Juan Carlos
AU - Thabut, Dominique
N1 - Funding Information:
CB has received speaker fees from GORE and is a board member in Alfa Wassemran/Norgine. VH-G, AG, JB, AA, DT and FN have received speaker fees from GORE. J-CG-P has consultant fees from GORE, and Shionogi and Cook grants from GORE and Novartis. JT has speaking and/or consulting fees from GORE, Bayer, Alexion, MSD, Gilead, Intercept, Norgine, Grifols, Versantis and Martin Pharmaceuticals. RB has received speaker fees from GORE and Grifols, unrelated to the submitted work.
Publisher Copyright:
© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2023/4
Y1 - 2023/4
N2 - Background: A pre-emptive transjugular intrahepatic portosystemic shunt (pTIPS) reduces mortality in high-risk patients with cirrhosis (Child-Pugh C/B+active bleeding) with acute variceal bleeding (AVB). Real-life studies point out that <15% of patients eligible for pTIPS ultimately undergo transjugular intrahepatic portosystemic shunt (TIPS) due to concerns about hepatic encephalopathy (HE). The outcome of patients undergoing pTIPS with HE is unknown. We aimed to (1) assess the prevalence of HE in patients with AVB; (2) evaluate the outcome of patients presenting HE at admission after pTIPS; and (3) determine if HE at admission is a risk factor for death and post-TIPS HE. Patients and methods: This is an observational study including 2138 patients from 34 centres between October 2011 and May 2015. Placement of pTIPS was based on individual centre policy. Patients were followed up to 1 year, death or liver transplantation. Results: 671 of 2138 patients were considered at high risk, 66 received pTIPS and 605 endoscopic+drug treatment. At admission, HE was significantly more frequent in high-risk than in low-risk patients (39.2% vs 10.6%, p<0.001). In high-risk patients with HE at admission, pTIPS was associated with a lower 1-year mortality than endoscopic+drug (HR 0.374, 95% CI 0.166 to 0.845, p=0.0181). The incidence of HE was not different between patients treated with pTIPS and endoscopic+drug (38.2% vs 38.7%, p=0.9721), even in patients with HE at admission (56.4% vs 58.7%, p=0.4594). Age >56, shock, Model for End-Stage Liver Disease score >15, endoscopic+drug treatment and HE at admission were independent factors of death in high-risk patients. Conclusion: pTIPS is associated with better survival than endoscopic treatment in high-risk patients with cirrhosis with variceal bleeding displaying HE at admission.
AB - Background: A pre-emptive transjugular intrahepatic portosystemic shunt (pTIPS) reduces mortality in high-risk patients with cirrhosis (Child-Pugh C/B+active bleeding) with acute variceal bleeding (AVB). Real-life studies point out that <15% of patients eligible for pTIPS ultimately undergo transjugular intrahepatic portosystemic shunt (TIPS) due to concerns about hepatic encephalopathy (HE). The outcome of patients undergoing pTIPS with HE is unknown. We aimed to (1) assess the prevalence of HE in patients with AVB; (2) evaluate the outcome of patients presenting HE at admission after pTIPS; and (3) determine if HE at admission is a risk factor for death and post-TIPS HE. Patients and methods: This is an observational study including 2138 patients from 34 centres between October 2011 and May 2015. Placement of pTIPS was based on individual centre policy. Patients were followed up to 1 year, death or liver transplantation. Results: 671 of 2138 patients were considered at high risk, 66 received pTIPS and 605 endoscopic+drug treatment. At admission, HE was significantly more frequent in high-risk than in low-risk patients (39.2% vs 10.6%, p<0.001). In high-risk patients with HE at admission, pTIPS was associated with a lower 1-year mortality than endoscopic+drug (HR 0.374, 95% CI 0.166 to 0.845, p=0.0181). The incidence of HE was not different between patients treated with pTIPS and endoscopic+drug (38.2% vs 38.7%, p=0.9721), even in patients with HE at admission (56.4% vs 58.7%, p=0.4594). Age >56, shock, Model for End-Stage Liver Disease score >15, endoscopic+drug treatment and HE at admission were independent factors of death in high-risk patients. Conclusion: pTIPS is associated with better survival than endoscopic treatment in high-risk patients with cirrhosis with variceal bleeding displaying HE at admission.
KW - cirrhosis
KW - hepatic encephalopathy
KW - oesophageal varices
KW - Liver Cirrhosis/complications
KW - Severity of Illness Index
KW - End Stage Liver Disease
KW - Humans
KW - Hepatic Encephalopathy/etiology
KW - Esophageal and Gastric Varices/complications
KW - Gastrointestinal Hemorrhage/etiology
KW - Contraindications
U2 - 10.1136/gutjnl-2022-326975
DO - 10.1136/gutjnl-2022-326975
M3 - Journal article
C2 - 36328772
AN - SCOPUS:85139230191
SN - 0017-5749
VL - 72
SP - 749
EP - 758
JO - GUT
JF - GUT
IS - 4
ER -