Multidrug-resistant bacterial infections in patients with decompensated cirrhosis and with acute-on-chronic liver failure in Europe.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
03 2019
Historique:
received: 27 03 2018
revised: 23 10 2018
accepted: 28 10 2018
pubmed: 6 11 2018
medline: 23 9 2020
entrez: 5 11 2018
Statut: ppublish

Résumé

Antibiotic resistance has been increasingly reported in patients with decompensated cirrhosis in single-center studies. Prospective investigations reporting broad epidemiological data are scarce. We aimed to analyze epidemiological changes in bacterial infections in patients with decompensated cirrhosis. This was a prospective evaluation of 2 series of patients hospitalized with decompensated cirrhosis. The Canonic series included 1,146 patients from Northern, Southern and Western Europe in 2011. Data on epidemiology, clinical characteristics of bacterial infections, microbiology and empirical antibiotic schedules were assessed. A second series of 883 patients from Eastern, Southern and Western Europe was investigated between 2017-2018. A total of 455 patients developed 520 infections (39.7%) in the first series, with spontaneous bacterial peritonitis, urinary tract infections and pneumonia the most frequent infections. Nosocomial episodes predominated in this series. Nearly half of the infections were culture-positive, of which 29.2% were caused by multidrug-resistant organisms (MDROs). MDR strains were more frequently isolated in Northern and Western Europe. Extended-spectrum beta-lactamase-producing Enterobacteriaceae were the most frequent MDROs isolated in this series, although prevalence and type differed markedly among countries and centers. Antibiotic resistance was associated with poor prognosis and failure of antibiotic strategies, based on third-generation cephalosporins or quinolones. Nosocomial infection (odds ratio [OR] 2.74; p < 0.001), intensive care unit admission (OR 2.09; p = 0.02), and recent hospitalization (OR 1.93; p = 0.04) were identified as independent predictors of MDR infection. The prevalence of MDROs in the second series (392 infections/284 patients) was 23%; 38% in culture-positive infections. A mild increase in the rate of carbapenem-resistant Enterobacteriaceae was observed in this series. MDR bacterial infections constitute a prevalent, growing and complex healthcare problem in patients with decompensated cirrhosis and acute-on-chronic liver failure across Europe, negatively impacting on prognosis. Strategies aimed at preventing the spread of antibiotic resistance in cirrhosis should be urgently evaluated. Infections caused by bacteria resistant to the main antibiotic families are prevalent in patients with cirrhosis. This study demonstrates that this healthcare problem is increasing and extends through all European regions. Infections caused by these difficult to treat bacteria resolve less frequently and often cause the death of the patient. The type of resistant bacteria varies markedly among different hospitals.

Sections du résumé

BACKGROUND & AIMS
Antibiotic resistance has been increasingly reported in patients with decompensated cirrhosis in single-center studies. Prospective investigations reporting broad epidemiological data are scarce. We aimed to analyze epidemiological changes in bacterial infections in patients with decompensated cirrhosis.
METHODS
This was a prospective evaluation of 2 series of patients hospitalized with decompensated cirrhosis. The Canonic series included 1,146 patients from Northern, Southern and Western Europe in 2011. Data on epidemiology, clinical characteristics of bacterial infections, microbiology and empirical antibiotic schedules were assessed. A second series of 883 patients from Eastern, Southern and Western Europe was investigated between 2017-2018.
RESULTS
A total of 455 patients developed 520 infections (39.7%) in the first series, with spontaneous bacterial peritonitis, urinary tract infections and pneumonia the most frequent infections. Nosocomial episodes predominated in this series. Nearly half of the infections were culture-positive, of which 29.2% were caused by multidrug-resistant organisms (MDROs). MDR strains were more frequently isolated in Northern and Western Europe. Extended-spectrum beta-lactamase-producing Enterobacteriaceae were the most frequent MDROs isolated in this series, although prevalence and type differed markedly among countries and centers. Antibiotic resistance was associated with poor prognosis and failure of antibiotic strategies, based on third-generation cephalosporins or quinolones. Nosocomial infection (odds ratio [OR] 2.74; p < 0.001), intensive care unit admission (OR 2.09; p = 0.02), and recent hospitalization (OR 1.93; p = 0.04) were identified as independent predictors of MDR infection. The prevalence of MDROs in the second series (392 infections/284 patients) was 23%; 38% in culture-positive infections. A mild increase in the rate of carbapenem-resistant Enterobacteriaceae was observed in this series.
CONCLUSIONS
MDR bacterial infections constitute a prevalent, growing and complex healthcare problem in patients with decompensated cirrhosis and acute-on-chronic liver failure across Europe, negatively impacting on prognosis. Strategies aimed at preventing the spread of antibiotic resistance in cirrhosis should be urgently evaluated.
LAY SUMMARY
Infections caused by bacteria resistant to the main antibiotic families are prevalent in patients with cirrhosis. This study demonstrates that this healthcare problem is increasing and extends through all European regions. Infections caused by these difficult to treat bacteria resolve less frequently and often cause the death of the patient. The type of resistant bacteria varies markedly among different hospitals.

Identifiants

pubmed: 30391380
pii: S0168-8278(18)32511-X
doi: 10.1016/j.jhep.2018.10.027
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

398-411

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2018 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Auteurs

Javier Fernández (J)

Liver ICU, Liver Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain; European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHED), ISCIII, Spain. Electronic address: Jfdez@clinic.ub.es.

Verónica Prado (V)

Liver ICU, Liver Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain.

Jonel Trebicka (J)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain; University of Bonn, Germany.

Alex Amoros (A)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

Thierry Gustot (T)

Liver Transplant Unit, Erasme Hospital, Brussels, Belgium.

Reiner Wiest (R)

Department of Medicine and Surgery, Inselspital, University of Bern, Bern, Switzerland.

Carme Deulofeu (C)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

Elisabet Garcia (E)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

Juan Acevedo (J)

South West Liver Unit, Derriford Hospital, UK.

Valentin Fuhrmann (V)

University Medical Center Hamburg-Eppendorf, Germany.

François Durand (F)

Hopital Beaujon, Paris, France.

Cristina Sánchez (C)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

Maria Papp (M)

Department of Internal Medicine, Division of Gastroenterology, Faculty of Medicine, University of Debrecen, Hungary.

Paolo Caraceni (P)

University of Bologna, Italy.

Victor Vargas (V)

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHED), ISCIII, Spain; Hospital Vall d'Hebron, Barcelona, Spain.

Rafael Bañares (R)

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHED), ISCIII, Spain; Hospital Gregorio Marañon, Madrid, Spain.

Salvatore Piano (S)

University of Padova, Padova, Italy.

Martin Janicko (M)

Pavol Jozef Safarik University in Kosice, Slovakia.

Agustin Albillos (A)

Hospital Universitario Ramon y Cajal, Madrid, Spain.

Carlo Alessandria (C)

San Giovanni Battista Hospital, Turin, Italy.

German Soriano (G)

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHED), ISCIII, Spain; Hospital of Santa Creu i Sant Pau, Barcelona, Spain.

Tania M Welzel (TM)

University Hospital of Frankfurt, Germany.

Wim Laleman (W)

University UZ Leuven, Belgium.

Alexander Gerbes (A)

Department of Medicine II, Liver Centre Munich, University Hospital, LMU Munich, Germany.

Andrea De Gottardi (A)

Department of Medicine and Surgery, Inselspital, University of Bern, Bern, Switzerland.

Manuela Merli (M)

Sapienza University of Rome, Italy.

Minneke Coenraad (M)

Leiden University Medical Centre, Netherlands.

Faouzi Saliba (F)

Centre Hepato-Biliare, Hòpital Paul Brousse, Paris, France.

Marco Pavesi (M)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

Rajiv Jalan (R)

ILDH, Division of Medicine, University College London Medical School, London, United Kingdom.

Pere Ginès (P)

Liver ICU, Liver Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHED), ISCIII, Spain.

Paolo Angeli (P)

University of Padova, Padova, Italy.

Vicente Arroyo (V)

European Foundation of Chronic Liver Failure (EF-Clif), Barcelona, Spain.

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