Association between gut colonization of vancomycin-resistant enterococci and liver transplant outcomes.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Jun 2022
Historique:
revised: 11 02 2022
received: 22 10 2021
accepted: 20 02 2022
pubmed: 6 3 2022
medline: 23 6 2022
entrez: 5 3 2022
Statut: ppublish

Résumé

Vancomycin-resistant enterococci (VRE) colonization is common in liver transplant recipients and has been associated with worse posttransplant outcomes. We conducted a retrospective cohort study at the University of Alberta Hospital including patients who underwent a liver transplant between September 2014 and December 2017. Of 343 patients, 68 (19.8%) had pretransplant VRE colonization and 27 (27/275, 9.8%) acquired VRE posttransplant, 67% were males and the median age was 56.5 years. VRE colonized patients at baseline had higher MELD scores and required longer posttransplant hospitalization. VRE colonization was associated with increased risk of early acute kidney injury (AKI) (64% vs. 52%, p = .044), clinically significant bacterial/fungal infection (29% vs. 17%, p = .012) and invasive VRE infection (5% vs. 1%, p = .017). Mortality at 2 years was 13% in VRE-colonized versus 7% in noncolonized (p = .085). On multivariate analysis, VRE colonization increased the risk of posttransplant AKI (HR 1.504, 95% CI: 1.077-2.100, p = .017) and clinically significant bacterial or fungal infection at 6 months (HR 2.038, 95% CI: 1.222-3.399, p = .006), and was associated with nonsignificant trend toward increased risk of mortality at 2 years posttransplant (HR 1.974 95% CI 0.890-4.378; p = .094). VRE colonization in liver transplant patients is associated with increased risk of early AKI, clinically significant infections, and a trend toward increased mortality at 2 years.

Sections du résumé

BACKGROUND BACKGROUND
Vancomycin-resistant enterococci (VRE) colonization is common in liver transplant recipients and has been associated with worse posttransplant outcomes.
METHODS METHODS
We conducted a retrospective cohort study at the University of Alberta Hospital including patients who underwent a liver transplant between September 2014 and December 2017.
RESULTS RESULTS
Of 343 patients, 68 (19.8%) had pretransplant VRE colonization and 27 (27/275, 9.8%) acquired VRE posttransplant, 67% were males and the median age was 56.5 years. VRE colonized patients at baseline had higher MELD scores and required longer posttransplant hospitalization. VRE colonization was associated with increased risk of early acute kidney injury (AKI) (64% vs. 52%, p = .044), clinically significant bacterial/fungal infection (29% vs. 17%, p = .012) and invasive VRE infection (5% vs. 1%, p = .017). Mortality at 2 years was 13% in VRE-colonized versus 7% in noncolonized (p = .085). On multivariate analysis, VRE colonization increased the risk of posttransplant AKI (HR 1.504, 95% CI: 1.077-2.100, p = .017) and clinically significant bacterial or fungal infection at 6 months (HR 2.038, 95% CI: 1.222-3.399, p = .006), and was associated with nonsignificant trend toward increased risk of mortality at 2 years posttransplant (HR 1.974 95% CI 0.890-4.378; p = .094).
CONCLUSIONS CONCLUSIONS
VRE colonization in liver transplant patients is associated with increased risk of early AKI, clinically significant infections, and a trend toward increased mortality at 2 years.

Identifiants

pubmed: 35247208
doi: 10.1111/tid.13821
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13821

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Diana Chiang (D)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Tanis C Dingle (TC)

Department of Laboratory Medicine & Pathology, University of Alberta, Edmonton, Alberta, Canada.
Alberta Precision Laboratories, Edmonton, Alberta, Canada.

Sara Belga (S)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Dima Kabbani (D)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Rahima A Bhanji (RA)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Jens Walter (J)

Department of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Alberta, Canada.
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada.
Department of Medicine and APC Microbiome Ireland, University College Cork, Cork, Ireland.
School of Microbiology, University College Cork, Cork, Ireland.

Juan G Abraldes (JG)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Carlos Cervera (C)

Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

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