Lack of Association Between Rifaximin and Drug-resistant Infections: A global multicenter inpatient cirrhosis cohort

Background/Aims: Infections with drug-resistant organisms (DROs) are associated with poor outcomes in cirrhosis.Rifaximin, widely used for hepatic encephalopathy (HE) could promote cross-resistance, but data regarding clinical impact are conflicting.Aim: Determine predictors of DROs in a global cirrhosis inpatient cohort focusing on pre-admission rifaximin use.Methods: From the global CLEARED consortium, we focused on cirrhosis inpatients with infections on/during admission.Clinical/demographic/medications especially rifaximin details were recorded.The primary outcome was DRO development.Multivariable regression for DRO development including clinical, medications, and country income were performed.Results: 2,949 infected inpatients (55.3 years, 62.9% male) were included.12.2% of all and 24.4% of culture-positive infections developed DROs; these patients had higher HE (39 vs.31%,p=0.003),AKI/HRS (25 vs 19%,p=0.006),lactulose(55 vs.47%,p=0.008)and rifaximin use (34 vs 27%,p=0.006) on crude comparisons but country-income distributions were similar.29.7% were on pre-admission rifaximin, mostly HE-related; they had more advanced cirrhosis and from low/low-middle-income countries.Daptomycin was used in 1.5%, linked with DROs (5.0 vs 1.0%, p<0.0001) without difference in rifaximin use (1.4 vs.1.7%,p=0.61).On adjusted analysis, MELD-Na (1.03,95% CI:1.02-1.04,p<0.001)increased, whereas male sex (0.73,95%CI:0.58-0.92,p=0.008)and HBV (0.65,95%CI:0.45-0.92,p=0.020)decreased DRO.Rifaximin was not associated with DROs overall (OR:1.07,95%CI:0.80-1.43,p=0.65) or within income strata (High:1.07,95%CI:0.59-1.92,p=0.82,Upper-middle:1.18,95%CI:0.74-1.85,p=0.49,low/lowmiddle:1.04,95%CI:0.60-1.81,p=0.90)despite sensitivity analyses.Conclusion: In this large global cohort of hospitalized patients with cirrhosis and infections, 12% developed infections involving DROs.30% had pre-admission rifaximin use which was not linked with daptomycin use, or with with DRO development on adjusted analysis overall or across country income groups.

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Journal
Clinical and Molecular Hepatology
Published
2026-04-15
DOI
https://doi.org/10.3350/cmh.2026.0228
Primary Topic
Travel-related health issues
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article
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article

Lack of Association Between Rifaximin and Drug-resistant Infections: A global multicenter inpatient cirrhosis cohort

Jacob George, Ramazan Idılman, Scott Silvey, Brian J. Bush et al.
Clinical and Molecular Hepatology
Travel-related health issues
article

Lack of Association Between Rifaximin and Drug-resistant Infections: A global multicenter inpatient cirrhosis cohort

Jacob George, Ramazan Idılman, Scott Silvey, Brian J. Bush, Aldo Torre, PC Hayes, Mario Silva, Ashok Choudhury, Mark Topazian, Wai-Kay Seto, Jasmohan S Bajaj, Florence Wong, On behalf of the EXPLANTORREDO-TAVR Registry Investigators, Qing Xie, Patrick S Kamath
article en

Abstract

Background/Aims: Infections with drug-resistant organisms (DROs) are associated with poor outcomes in cirrhosis.Rifaximin, widely used for hepatic encephalopathy (HE) could promote cross-resistance, but data regarding clinical impact are conflicting.Aim: Determine predictors of DROs in a global cirrhosis inpatient cohort focusing on pre-admission rifaximin use.Methods: From the global CLEARED consortium, we focused on cirrhosis inpatients with infections on/during admission.Clinical/demographic/medications especially rifaximin details were recorded.The primary outcome was DRO development.Multivariable regression for DRO development including clinical, medications, and country income were performed.Results: 2,949 infected inpatients (55.3 years, 62.9% male) were included.12.2% of all and 24.4% of culture-positive infections developed DROs; these patients had higher HE (39 vs.31%,p=0.003),AKI/HRS (25 vs 19%,p=0.006),lactulose(55 vs.47%,p=0.008)and rifaximin use (34 vs 27%,p=0.006) on crude comparisons but country-income distributions were similar.29.7% were on pre-admission rifaximin, mostly HE-related; they had more advanced cirrhosis and from low/low-middle-income countries.Daptomycin was used in 1.5%, linked with DROs (5.0 vs 1.0%, p<0.0001) without difference in rifaximin use (1.4 vs.1.7%,p=0.61).On adjusted analysis, MELD-Na (1.03,95% CI:1.02-1.04,p<0.001)increased, whereas male sex (0.73,95%CI:0.58-0.92,p=0.008)and HBV (0.65,95%CI:0.45-0.92,p=0.020)decreased DRO.Rifaximin was not associated with DROs overall (OR:1.07,95%CI:0.80-1.43,p=0.65) or within income strata (High:1.07,95%CI:0.59-1.92,p=0.82,Upper-middle:1.18,95%CI:0.74-1.85,p=0.49,low/lowmiddle:1.04,95%CI:0.60-1.81,p=0.90)despite sensitivity analyses.Conclusion: In this large global cohort of hospitalized patients with cirrhosis and infections, 12% developed infections involving DROs.30% had pre-admission rifaximin use which was not linked with daptomycin use, or with with DRO development on adjusted analysis overall or across country income groups.

Clinical and Molecular Hepatology
Universidade Federal do Rio Grande do Sul (BR), Mayo Clinic (US), Ankara University (TR), Shanghai Jiao Tong University (CN), University of Toronto (CA), Millennium Institute (BR), Ruijin Hospital (CN), Hunter Holmes McGuire VA Medical Center (US), Hospital de Clínicas de Porto Alegre (BR), Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán (MX), Institute of Liver and Biliary Sciences (IN), Mayo Clinic in Arizona (US), Westmead Institute (AU), Mayo Clinic in Florida (US), St. Paul's Hospital Millennium Medical College (ET), Virginia Commonwealth University Medical Center (US), University of Hong Kong (HK), University of Edinburgh (GB)
No poverty
Openalex Percentile: Top 19%
Travel-related health issues
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