Perfusion fluid-related infections in liver transplant recipients: A 5-year, single-center, retrospective study

Andrea Lombardi1,2, Giulia Renisi1, Daniele Dondossola2,3

  • 1Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Infectious Diseases Unit, Milan, Italy.

Abstract

Insights

Perfusion fluid (PRF) in liver transplantation (LTx) can transmit infections to recipients (LTRs). While rare, PRF-related infections (PRF-RI) significantly increase LTR mortality and morbidity.

Area of Science:

  • Transplantation Medicine
  • Infectious Diseases
  • Organ Preservation

Background:

  • Perfusion fluid (PRF) is crucial for maintaining liver graft viability during liver transplantation (LTx).
  • PRF may serve as a potential route for transmitting infections to liver transplant recipients (LTRs).
  • Limited systematic research exists on PRF as an infection source in LTx.

Purpose of the Study:

  • To investigate the incidence of positive PRF cultures (PRF+) and PRF-related infections (PRF-RI) in LTRs.
  • To identify factors associated with PRF+ and PRF-RI.
  • To assess the impact of PRF-RI on LTR outcomes, including 1-year mortality.

Main Methods:

  • A 5-year single-center retrospective study (January 2017 - December 2021) included 234 LTRs.
  • Analysis of PRF culture results, PRF-RI incidence, and associated risk factors.
  • Evaluation of 1-year overall and infection-related mortality.

Main Results:

  • Positive PRF cultures (PRF+) occurred in 13.2% of LTx, with high-risk microorganisms identified in 67.6% of cases.
  • Perfusion fluid-related infections (PRF-RI) developed in 1.7% of LTRs.
  • Isolation of multiple microorganisms in PRF culture significantly increased PRF-RI risk (OR 37.5, p = .01). PRF-RI were linked to longer ICU stays and higher 1-year mortality (p = .001).

Conclusions:

  • Although PRF+ is uncommon, PRF-RI develops in a small proportion of LTRs.
  • PRF-RI is associated with increased morbidity and mortality following liver transplantation.
  • Vigilance for PRF contamination is warranted to mitigate potential adverse outcomes in LTRs.