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Infection and Prophylaxis During Normothermic Liver Perfusion: Audit of Incidence and Pharmacokinetics of Antimicrobial Therapy.

Authors :
Qureshi S
Elliott H
Noel A
Swift L
Fear C
Webster R
Brown NM
Gaurav R
Butler AJ
Watson CJE
Source :
Transplantation [Transplantation] 2024 Jun 01; Vol. 108 (6), pp. 1376-1382. Date of Electronic Publication: 2024 Jan 10.
Publication Year :
2024

Abstract

Background: Ex situ normothermic liver perfusion (NMP) in a blood-based perfusate is associated with a risk of microbe growth, resulting in life-threatening posttransplant sepsis. Antibiotics are widely used, but the pharmacokinetics of these agents are unknown as is their efficacy. We wished to assess the perfusate concentrations of the meropenem and fluconazole that we use and to audit the incidence of infection with this antimicrobial therapy.<br />Methods: Fluconazole and meropenem (100 mg each) were added to the perfusate before NMP began, and serial samples were taken and assayed for drug concentrations. Perfusate cultures were available from 210 of the 242 perfusions performed between February 1, 2018, and April 6, 2023; these were reviewed.<br />Results: Following administration of 100 mg fluconazole, levels fell slightly from a median of 24.9 mg/L at 1 h to 22.6 mg/L at 10 h. In contrast, meropenem concentrations fell over time, from a median of 21.8 mg/L at 1 h to 9.4 mg/L at 10 h. There were 4 significant microorganisms grown in the perfusions, including 3 Candida species and an Enterococcus faecium . All the Candida -infected livers were transplanted with no adverse consequences, the recipients being treated with anidulafungin upon identification of the infecting organism; the Enterococcus -infected liver was not transplanted.<br />Conclusions: Serious infection is a risk with NMP but appears to be mitigated with a protocol combining fluconazole and meropenem. This combination may not be appropriate in areas where resistance is prevalent. Routine culture of NMP perfusate is essential to identify breakthrough organisms early and enable recipient treatment.<br />Competing Interests: C.W. received speaker fees from OrganOx Ltd and was an advisory board member for Jazz Pharmaceuticals and Nefro Health. A.B. holds a share of a patent in connection with the OrganOx metra. The other authors declare no conflicts of interest.<br /> (Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.)

Details

Language :
English
ISSN :
1534-6080
Volume :
108
Issue :
6
Database :
MEDLINE
Journal :
Transplantation
Publication Type :
Academic Journal
Accession number :
38196099
Full Text :
https://doi.org/10.1097/TP.0000000000004897