TY - JOUR
T1 - The Use of Rifaximin in Patients With Cirrhosis
AU - for the Liverhope Consortium
AU - Caraceni, Paolo
AU - Vargas, Victor
AU - Solà, Elsa
AU - Alessandria, Carlo
AU - de Wit, Koos
AU - Trebicka, Jonel
AU - Angeli, Paolo
AU - Mookerjee, Rajeshwar P.
AU - Durand, François
AU - Pose, Elisa
AU - Krag, Aleksander
AU - Bajaj, Jasmohan S.
AU - Beuers, Ulrich
AU - Ginès, Pere
AU - Juanola, Adrià
AU - Napoleone, Laura
AU - Carol, Marta
AU - Avitabile, Emma
AU - Thu, Ann Ma
AU - Cervera, Marta
AU - Pérez, Martina
AU - Belén Rubio-Garcia, Ana
AU - Ardiaca, Alicia
AU - Vives, Adriana
AU - Pich, Judit
AU - Fabrellas, Núria
AU - Zaccherini, Giacomo
AU - Chiappa, Maria Teresa
AU - Jiménez, César
AU - Palacio, Ester
AU - Campion, Daniela
AU - Lanzillotti, Tommaso
AU - Piano, Salvatore
AU - Nicolao, Gea
AU - Uschner, Frank
AU - Graf_Dirmeier, Sabine
AU - Francoz, Claire
AU - Roux, Olivier
AU - Esnault, Vanessa
AU - Helder, Jeltje
AU - Aban, Marites
AU - Kazankov, Konstantin
AU - Korenjak, Marko
AU - Kamath, Patrick
AU - Abraldes, Juan G.
AU - Watson, Hugh
N1 - Funding Information:
The Liverhope Consortium investigators: Hospital Clinic de Barcelona and IDIBAPS: Adrià Juanola, Laura Napoleone, Marta Carol, Emma Avitabile, Ann Ma Thu, Marta Cervera, Martina Pérez, Ana Belén Rubio-Garcia, Alicia Ardiaca, Adriana Vives, Judit Pich University of Barcelona, School of Medicine and Health Sciences: Núria Fabrellas University of Bologna: Giacomo Zaccherini; Maria Teresa Chiappa Hospital Vall d’Hebron: César Jiménez, Ester Palacio University of Torino: Daniela Campion, Tommaso Lanzillotti University of Padova: Salvatore Piano, Gea Nicolao Goethe-University Frankfurt: Frank Uschner, Sabine Graf_Dirmeier Hospital Beaujon: Claire Francoz, Olivier Roux, Vanessa Esnault Amsterdam University Medical Centers, location AMC : Jeltje Helder Royal Free Hospital: Marites Aban, Konstantin Kazankov ELPA: Marko Korenjak Mayo Clinic Rochester: Patrick Kamath University Hospital of Alberta: Juan G. Abraldes Evotec: Hugh Watson. We thank Roser Poblet and Nicki van Berckel for their work in the preparation of the manuscript.
Publisher Copyright:
© 2021 The Authors. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.
PY - 2021/9
Y1 - 2021/9
N2 - Rifaximin is an oral nonsystemic antibiotic with minimal gastrointestinal absorption and broad-spectrum antibacterial activity covering both gram-positive and gram-negative organisms. Rifaximin is currently used worldwide in patients with cirrhosis for preventing recurrent HE because its efficacy and safety have been proven by large randomized clinical trials. In the last decade, experimental and clinical evidence suggest that rifaximin could have other beneficial effects on the course of cirrhosis by modulating the gut microbiome and affecting the gut-liver axis, which in turn can interfere with major events of the pathophysiological cascade underlying decompensated cirrhosis, such as systemic inflammatory syndrome, portal hypertension, and bacterial infections. However, the use of rifaximin for prevention or treatment of other complications, including spontaneous bacterial peritonitis or other bacterial infections, is not accepted because evidence by clinical trials is still very weak. The present review deals in the first part with the potential impact of rifaximin on pathogenic mechanisms in liver diseases, whereas in the second part, its clinical effects are critically discussed. It clearly emerges that, because of its potential activity on multiple pathogenic events, the efficacy of rifaximin in the prevention or management of complications other than HE deserves to be investigated extensively. The results of double-blinded, adequately powered randomized clinical trials assessing the effect of rifaximin, alone or in combination with other drugs, on hard clinical endpoints, such as decompensation of cirrhosis, acute-on-chronic liver failure, and mortality, are therefore eagerly awaited.
AB - Rifaximin is an oral nonsystemic antibiotic with minimal gastrointestinal absorption and broad-spectrum antibacterial activity covering both gram-positive and gram-negative organisms. Rifaximin is currently used worldwide in patients with cirrhosis for preventing recurrent HE because its efficacy and safety have been proven by large randomized clinical trials. In the last decade, experimental and clinical evidence suggest that rifaximin could have other beneficial effects on the course of cirrhosis by modulating the gut microbiome and affecting the gut-liver axis, which in turn can interfere with major events of the pathophysiological cascade underlying decompensated cirrhosis, such as systemic inflammatory syndrome, portal hypertension, and bacterial infections. However, the use of rifaximin for prevention or treatment of other complications, including spontaneous bacterial peritonitis or other bacterial infections, is not accepted because evidence by clinical trials is still very weak. The present review deals in the first part with the potential impact of rifaximin on pathogenic mechanisms in liver diseases, whereas in the second part, its clinical effects are critically discussed. It clearly emerges that, because of its potential activity on multiple pathogenic events, the efficacy of rifaximin in the prevention or management of complications other than HE deserves to be investigated extensively. The results of double-blinded, adequately powered randomized clinical trials assessing the effect of rifaximin, alone or in combination with other drugs, on hard clinical endpoints, such as decompensation of cirrhosis, acute-on-chronic liver failure, and mortality, are therefore eagerly awaited.
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U2 - 10.1002/hep.31708
DO - 10.1002/hep.31708
M3 - Review article
C2 - 33421158
AN - SCOPUS:85102703299
SN - 0270-9139
VL - 74
SP - 1660
EP - 1673
JO - Hepatology
JF - Hepatology
IS - 3
ER -