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Objectives: Rising prevalence of multidrug-resistant organisms (MDRO) is a major health problem in patients with liver cirrhosis. The impact of MDRO colonization in liver transplantation (LT) candidates and recipients on mortality has not been determined in detail., Methods: Patients consecutively evaluated and listed for LT in a tertiary German liver transplant center from 2008 to 2018 underwent screening for MDRO colonization including methicillin-resistant Staphylococcus aureus (MRSA), multidrug-resistant gram-negative bacteria (MDRGN), and vancomycin-resistant enterococci (VRE). MDRO colonization and infection status were obtained at LT evaluation, planned and unplanned hospitalization, three months upon graft allocation, or at last follow-up on the waiting list., Results: In total, 351 patients were listed for LT, of whom 164 (47%) underwent LT after a median of 249 (range 0-1662) days. Incidence of MDRO colonization increased during waiting time for LT, and MRDO colonization was associated with increased mortality on the waiting list (HR = 2.57, p<0.0001. One patients was colonized with a carbapenem-resistant strain at listing, 9 patients acquired carbapenem-resistant gram-negative bacteria (CRGN) on the waiting list, and 4 more after LT. In total, 10 of these 14 patients died., Conclusions: Colonization with MDRO is associated with increased mortality on the waiting list, but not in short-term follow-up after LT. Moreover, colonization with CRGN seems associated with high mortality in liver transplant candidates and recipients., Competing Interests: Philip G. Ferstl, Consultancies: SNIPR Biome. Wolf O. Bechstein: Consultancies/speaker fees: Astellas, Chiesi, Gore Deutschland, Medupdate GmbH, MCI, MCN, Novartis. Michael Hogardt, Grants: Gilead, Kirmser Foundation, German CF Foundation; Speaker’s fees: Thieme Science, Chiesi GmbH. Haitham Mutlak, Speaker’s fees: Orion Pharma, Löwenstein Medical, Pfizer, Getinge. Christoph Stephan, Speaker’s fees: AbbVie, LÄK-Hessen, Gilead, Hexal, Janssen, MSD, Pfizer, Roche, TAD, ViiV; Consultancies: AbbVie, Gilead, Janssen, MSD, ViiV. Nina Weiler, Consultancy: Astellas and Novartis, Travel support: AbbVie, Astellas, Biotest, and Novartis. Jonel Trebicka, Speaker’s fees and/or consultancies: Gore, Bayer, Alexion, MSD, Gilead, Intercept, Norgine, Grifols, Versantis, and Martin Pharmaceutical. Stefan Zeuzem: Speaker’s fees: Abbvie, Gilead, Merck/MSD, Consultancy: Abbvie, Gilead, Intercept, Janssen. Oliver Waidmann, Consultancies: Amgen, Bayer, BMS, Celgene, Eisai, Incyte, Ipsen, Merck Serono, MSD, Novartis, Roche, Servier, Shire; Speaker’s fees: Bayer, BMS, Celgene, Eisai, Ipsen, Novartis, Roche, Shire; Travel support: Abbvie, Bayer, BMS, Gilead, Ipsen, Merck; Grants: Basilea, Incyte, Else Kröner-Fresenius-Stiftung, Medac, Merck Serono, MSD. Martin-Walter Welker, Consultancies / speaker’s fees: AbbVie, Amgen, Bayer, Chiesis, BMS, Gilead, Novartis, Roche; Travel Support: AbbVie, Astellas, Bayer, BMS, Novartis, Janssen, Roche. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Background & Aims: Infections with multidrug-resistant gram-negative bacteria are significantly impairing the prognosis of patients with liver disease. In particular, carbapenem resistance further narrows therapeutic options. This study investigates the impact of carbapenem-resistant gram-negative bacteria on the outcome of patients with liver disease and cirrhosis., Methods: Between January 2011 and July 2015, 132 patients treated at the tertiary liver transplant centre at University Hospital Frankfurt, Germany, were tested positive for carbapenem-resistant gram-negative bacteria and retrospectively analysed in this study. Risk factors for fatal outcome were evaluated using multivariate regression analysis. Competing-risk analysis was performed on patients tested positive for Enterobacteriaceae or non-fermenting species, for example, Pseudomonas aeruginosa, Acinetobacter baumannii, Stenotrophomonas maltophilia. Subgroup analysis of cirrhotic patients was performed on a matched cohort of cirrhotic patients, comparable model for end-stage liver disease and tested negative for carbapenem-resistant gram-negative bacteria., Results: 97 (73.5%) and 35 (26.5%) patients were infected or colonised with carbapenem-resistant gram-negative bacteria respectively. Within the observation period, 61/132 (46.2%) patients died, with sepsis being the leading cause (38/61, 62.3%). Decompensated liver disease, sepsis and admission to intensive care unit were independent risk factors for fatal outcome. Lethal sepsis in patients positive for non-fermenting bacteria was significantly more frequent than in those positive for Enterobacteriaceae, independently from liver function. Subgroup analysis of cirrhotic patients showed that sepsis (54.9% vs 13%) and lethal sepsis were significantly more frequent after detection of carbapenem-resistant gram-negative bacteria, independently from localisation of pathogen detection., Conclusions: Patients with advanced liver disease are prone to fatal infections caused by carbapenem-resistant gram-negative bacteria., (© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)