Multidrug-Resistant Bacteria and Disease Progression in Patients with End-Stage Liver Disease and after Liver Transplantation.


Journal

Journal of gastrointestinal and liver diseases : JGLD
ISSN: 1842-1121
Titre abrégé: J Gastrointestin Liver Dis
Pays: Romania
ID NLM: 101272825

Informations de publication

Date de publication:
01 Sep 2019
Historique:
received: 21 06 2019
accepted: 13 07 2019
entrez: 14 9 2019
pubmed: 14 9 2019
medline: 16 4 2020
Statut: epublish

Résumé

Multidrug-resistant (MDR) pathogens represent an emerging challenge in end-stage liver disease and in liver transplant recipients. We evaluated the impact of MDR bacteria upon clinical outcomes in patients with end-stage liver disease (n = 777) at the time of enrollment on the liver transplant (LTx) waiting list, after first LTx (n = 645), and after second LTx (n = 128). Colonization/infection with MDR bacteria was present in 72/777 patients on the waiting list, in 98/645 patients at first LTx, and in 46/128 patients at second LTx. While on the LTx waiting list, the time until first hydropic decompensation (p = 0.021), hepatic encephalopathy (p < 0.001) and hepatorenal syndrome (p < 0.001) was reduced in the presence of MDR bacteria, which remained an independent risk factor of poor survival in multivariate analysis (p < 0.001). Following first and second liver transplant, MDR bacteria were associated with an increased risk of infection-related deaths (first LTx: p < 0.001; second LTx: p = 0.037) and reduced actuarial survival (first LTx: p < 0.001; second LTx: p = 0.046). We showed that MDR pathogens are associated with poor outcomes before, after first and after recurrent LTx.

Sections du résumé

BACKGROUND BACKGROUND
Multidrug-resistant (MDR) pathogens represent an emerging challenge in end-stage liver disease and in liver transplant recipients.
METHODS METHODS
We evaluated the impact of MDR bacteria upon clinical outcomes in patients with end-stage liver disease (n = 777) at the time of enrollment on the liver transplant (LTx) waiting list, after first LTx (n = 645), and after second LTx (n = 128).
RESULTS RESULTS
Colonization/infection with MDR bacteria was present in 72/777 patients on the waiting list, in 98/645 patients at first LTx, and in 46/128 patients at second LTx. While on the LTx waiting list, the time until first hydropic decompensation (p = 0.021), hepatic encephalopathy (p < 0.001) and hepatorenal syndrome (p < 0.001) was reduced in the presence of MDR bacteria, which remained an independent risk factor of poor survival in multivariate analysis (p < 0.001). Following first and second liver transplant, MDR bacteria were associated with an increased risk of infection-related deaths (first LTx: p < 0.001; second LTx: p = 0.037) and reduced actuarial survival (first LTx: p < 0.001; second LTx: p = 0.046).
CONCLUSIONS CONCLUSIONS
We showed that MDR pathogens are associated with poor outcomes before, after first and after recurrent LTx.

Identifiants

pubmed: 31517327
doi: 10.15403/jgld-212
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

303-310

Auteurs

Kilian Friedrich (K)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. . kilianfriedrich@gmx.de.

Jessica Krempl (J)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. Jessica.krempl@med.uni-heidelberg.de.

Shigehiko Schamoni (S)

Department of Computational Linguistics, University of Heidelberg, Heidelberg, Germany. schamoni@cl.uni-heidelberg.de.

Theresa Hippchen (T)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. theresa.hippchen@med.uni-heidelberg.de.

Jan Pfeiffenberger (J)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. jan.pfeiffenberger@med.uni-heidelberg.de.

Christian Rupp (C)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. christian.rupp@med.uni-heidelberg.de.

Daniel Nils Gotthardt (DN)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. daniel.gotthardt@med.uni-heidelberg.de.

Philip Houben (P)

Department of General, Visceral and Tansplant Surgery, University Hospital of Heidelberg, Heidelberg, Germany. philip.houben@med.uni-heidelberg.de.

Rebecca Von Haken (R)

Department of Anaesthesiology, University Hospital of Heidelberg, Heidelberg, Germany. Rebecca.vonhaken@med.uni-heidelberg.de.

Alexandra Heininger (A)

Department of Infectious Diseases, Medical Microbiology and Hygiene, Division Hospital and Environmental Hygiene, Heidelberg University Hospital, Heidelberg, Germany. alexandra.heininger@med.uni-heidelberg.de.

Thorsten Brenner (T)

Department of Anaesthesiology, University Hospital of Heidelberg, Heidelberg, Germany. thorsten.brenner@med.uni-heidelberg.de.

Arianeb Mehrabi (A)

Department of General, Visceral and Tansplant Surgery, University Hospital of Heidelberg, Heidelberg, Germany. arianeb.mehrabi@med.uni-heidelberg.de.

Karl-Heinz Weiss (KH)

Department of Internal Medicine IV, University Hospital of Heidelberg, Heidelberg, Germany. karl-heinz.weiss@med.uni-heidelberg.de.

Markus Mieth (M)

Department of General, Visceral and Tansplant Surgery, University Hospital of Heidelberg, Heidelberg, Germany. markus.mieth@med.uni-heidelberg.de.

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