Epidemiology of systemic mycoses among renal-transplant recipients in India

George Tharayil John1, Viswanathan Shankar, Girish Talaulikar

  • 1Department of Nephrology, Christian Medical College Hospital, Vellore, Tamil Nadu, India. george@cmcvellore.ac.in

Transplantation
|June 7, 2003
PubMed
Abstract

Insights

Systemic mycoses significantly impact tropical renal transplant recipients, with Cytomegalovirus disease and chronic liver disease being key risk factors. Survival rates are poor with mycoses, highlighting the need for improved prevention and treatment strategies.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Transplantation Immunology

Background:

  • Systemic mycoses pose a significant threat to renal transplant recipients in tropical regions.
  • Understanding the epidemiology and risk factors is crucial for improving patient outcomes.

Purpose of the Study:

  • To analyze the incidence, risk factors, outcomes, and postmortem findings of systemic mycoses in renal transplant recipients.
  • To identify specific factors associated with increased risk of mycoses and mortality.

Main Methods:

  • Prospective data collection from 1,476 primary renal transplant recipients between 1986 and 2000.
  • Analysis included cumulative incidence, timing, risk factors, outcomes, and postmortem data for 30 patients with systemic mycoses.

Main Results:

  • 110 episodes of systemic mycoses occurred in 98 patients; Aspergillus, Cryptococcus, and Candida were the most common pathogens.
  • Cytomegalovirus (CMV) disease and chronic liver disease significantly increased the risk of mycoses. Tuberculosis (TB) was a common coinfection.
  • Cyclosporine (CsA) use was linked to a higher risk of mycoses early post-transplant. Survival probability was significantly lower for patients with systemic mycoses (25.6% at 10 years) compared to those without (75.5%).

Conclusions:

  • CMV disease, chronic liver disease, and hyperglycemia are significant risk factors for systemic mycoses in renal transplant recipients.
  • Tuberculosis is an important coinfection, and CsA use increases early post-transplant mycoses risk.
  • Systemic mycoses drastically increase mortality risk, although recent survival rates show improvement.

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