Infectious complications in acute graft-versus-host disease after liver transplantation

Supavit Chesdachai1, Prowpanga Udompap2, Zachary A Yetmar1

  • 1Division of Public Health, Infectious Diseases and Occupational Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Insights

Infections after liver transplant graft-versus-host disease (GVHD) are common and deadly. Despite prophylaxis, severe infections led to mortality in 83% of patients, highlighting the need for optimized antimicrobial strategies.

Area of Science:

  • Transplantation Immunology
  • Infectious Diseases
  • Hepatology

Background:

  • Graft-versus-host disease (GVHD) post-liver transplantation (LT) is rare but associated with high mortality.
  • Infectious complications are the primary cause of death in GVHD patients following LT.
  • Current literature lacks detailed descriptions of infection patterns and antimicrobial management in this population.

Purpose of the Study:

  • To detail infectious complications in adult patients with acute GVHD after LT.
  • To analyze the characteristics and outcomes of infections in this specific patient group.
  • To inform antimicrobial management and prophylaxis strategies for GVHD post-LT.

Main Methods:

  • Retrospective review of adult LT recipients diagnosed with acute GVHD at Mayo Clinic Transplant Centers (January 1, 2010 – December 31, 2021).
  • Detailed description of infection characteristics for each case.
  • Analysis of antimicrobial prophylaxis regimens used based on neutropenia and CMV status.

Main Results:

  • Out of 4,585 LTs, 12 patients (0.3%) developed acute GVHD.
  • Median time to GVHD diagnosis was 49.0 days post-LT.
  • Ten of 12 patients (83.3%) experienced severe infections, leading to mortality.
  • Common infections included nosocomial bacteremia (vancomycin-resistant enterococci, gram-negative bacilli), invasive fungal infections, CMV reactivation, and Clostridioides difficile colitis.
  • Standard antimicrobial prophylaxis (levofloxacin, nebulized pentamidine, posaconazole, valganciclovir) was employed.

Conclusions:

  • Infectious complications are frequent and associated with exceptionally high mortality in GVHD post-LT, even with prophylaxis.
  • Individualized antimicrobial treatment, prophylaxis, and monitoring are crucial for managing GVHD.
  • Further research is necessary to optimize antimicrobial practices in this high-risk patient cohort.

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