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Terlipressin therapy is associated with increased risk of colonisation with multidrug-resistant bacteria in patients with decompensated cirrhosis.
Mücke, Marcus M; Hernández-Tejero, María; Gu, Wenyi; Kuhn, Michael; Janz, Malte; Keller, Marisa I; Fullam, Anthony; Altepeter, Laura; Mücke, Victoria T; Finkelmeier, Fabian; Schwarzkopf, Katharina M; Cremonese, Carla; Hunyady, Peter-Merton; Heilani, Myriam W; Uschner, Frank Erhard; Schierwagen, Robert; Brol, Maximilian J; Fischer, Julia; Klein, Sabine; Peiffer, Kai-Henrik; Hogardt, Michael; Shoaie, Saeed; Coenraad, Minneke J; Bojunga, Jörg; Arroyo, Vicente; Zeuzem, Stefan; Kempf, Volkhard A J; Welsch, Christoph; Laleman, Wim; Bork, Peer; Fernandez, Javier; Trebicka, Jonel.
Afiliação
  • Mücke MM; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Hernández-Tejero M; Liver ICU, Liver Unit, Hospital Clinic, University of Barcelona, IDIBAPS and CIBERehd, Barcelona, Spain.
  • Gu W; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Kuhn M; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Janz M; Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Keller MI; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Fullam A; Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Altepeter L; Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Mücke VT; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Finkelmeier F; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Schwarzkopf KM; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Cremonese C; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Hunyady PM; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Heilani MW; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Uschner FE; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Schierwagen R; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Brol MJ; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Fischer J; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Klein S; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Peiffer KH; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Hogardt M; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Shoaie S; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Coenraad MJ; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Bojunga J; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Arroyo V; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
  • Zeuzem S; Department of Internal Medicine B, Muenster University Clinic, University of Münster, Münster, Germany.
  • Kempf VAJ; Institute of Medical Microbiology and Infection Control, Goethe University Frankfurt, Germany University Center for Infectious Diseases, University Hospital Frankfurt, Frankfurt, Germany.
  • Welsch C; University Center of Competence for Infection Control, State of Hesse, Germany.
  • Laleman W; Centre for Host-Microbiome Interactions, Dental Institute, King's College London, London, UK.
  • Bork P; Science for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Fernandez J; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Trebicka J; Medical Clinic 1, University Hospital, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Aliment Pharmacol Ther ; 59(7): 877-888, 2024 04.
Article em En | MEDLINE | ID: mdl-38414095
ABSTRACT

BACKGROUND:

Patients with cirrhosis are susceptible to develop bacterial infections that trigger acute decompensation (AD) and acute-on-chronic liver failure (ACLF). Infections with multidrug-resistant organisms (MDRO) are associated with deleterious outcome. MDRO colonisation frequently proceeds MDRO infections and antibiotic therapy has been associated with MDRO colonisation.

AIM:

The aim of the study was to assess the influence of non-antibiotic medication contributing to MDRO colonisation.

METHODS:

Three hundred twenty-four patients with AD and ACLF admitted to the ICU of Frankfurt University Hospital with MDRO screening were included. Regression models were performed to identify drugs associated with MDRO colonisation. Another cohort (n = 129) from Barcelona was included to validate. A third multi-centre cohort (n = 203) with metagenomic sequencing data of stool was included to detect antibiotic resistance genes.

RESULTS:

A total of 97 patients (30%) were identified to have MDRO colonisation and 35 of them (11%) developed MDRO infection. Patients with MDRO colonisation had significantly higher risk of MDRO infection than those without (p = 0.0098). Apart from antibiotic therapy (odds ratio (OR) 2.91, 95%-confidence interval (CI) 1.82-4.93, p < 0.0001), terlipressin therapy in the previous 14 days was the only independent covariate associated with MDRO colonisation in both cohorts, the overall (OR 9.47, 95%-CI 2.96-30.23, p < 0.0001) and after propensity score matching (OR 5.30, 95%-CI 1.22-23.03, p = 0.011). In the second cohort, prior terlipressin therapy was a risk factor for MDRO colonisation (OR 2.49, 95% CI 0.911-6.823, p = 0.075) and associated with risk of MDRO infection during follow-up (p = 0.017). The validation cohort demonstrated that antibiotic inactivation genes were significantly associated with terlipressin administration (p = 0.001).

CONCLUSIONS:

Our study reports an increased risk of MDRO colonisation in patients with AD or ACLF, who recently received terlipressin therapy, while other commonly prescribed non-antibiotic co-medications had negligible influence. Future prospective trials are needed to confirm these results.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacorresistência Bacteriana Múltipla / Antibacterianos Limite: Humans Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacorresistência Bacteriana Múltipla / Antibacterianos Limite: Humans Idioma: En Revista: Aliment Pharmacol Ther Assunto da revista: FARMACOLOGIA / GASTROENTEROLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha