Risk Factors Associated With Invasive Fungal Infections in Kidney Transplant Patients

Sara Leitheiser1, Andrew Harner2, Jennifer L Waller3

  • 1Department of Medicine, Medical College of Georgia at Augusta University, Augusta, GA.

Abstract

Insights

Kidney transplant patients face a higher risk of invasive fungal infections (IFI). Key risk factors include older age, diabetes, bacterial pneumonia, and urinary tract infections, informing diagnosis and treatment.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Immunology

Background:

  • Kidney transplant recipients (KTRs) are a vulnerable population with an elevated risk of invasive fungal infections (IFI).
  • Understanding specific risk factors is crucial for preventing and managing IFI in KTRs.

Purpose of the Study:

  • To identify demographic, clinical, and medication-associated risk factors for IFI in kidney transplant recipients.
  • To analyze the incidence and types of IFI in KTRs using a large national database.

Main Methods:

  • Retrospective analysis of the United States Renal Data System (USRDS) database.
  • Inclusion of kidney transplant patients who underwent transplantation between 2005 and 2008.
  • Identification of IFI cases using ICD-9 codes and categorization into specific fungal groups (Candida, Histoplasmosis, Aspergillosis, Cryptococcosis, Other mycoses).
  • Statistical modeling to determine relative risks (RR) and adjusted relative risks (aRR) for various factors.

Main Results:

  • A total of 57,188 KTRs were analyzed, with 1,218 experiencing 1,343 IFI diagnoses (median time to infection: 495 days).
  • The most common IFI types were "Other" mycoses (37%) and Aspergillosis (22%).
  • Increased risk for any IFI was associated with age ≥65 years. Top clinical risk factors included diabetes (aRR=1.71), bacterial pneumonia (aRR=1.62), and urinary tract infection (UTI) (aRR=1.34).
  • Mycophenolate mofetil use was linked to a reduced risk of candidemia.

Conclusions:

  • IFI risk in KTRs is multifactorial, influenced by demographics, comorbidities, and specific fungal pathogens.
  • Identifying these risk factors provides a clinical profile to guide the diagnosis and presumptive treatment of IFI in this high-risk population.

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