Intensive Care Antifungal Stewardship Programme Based on T2Candida PCR and Candida Mannan Antigen: A Prospective

Jannik Helweg-Larsen1, Morten Steensen2, Finn Møller Pedersen3

  • 1Department of Infectious Diseases, Rigshospitalet, 2100 Copenhagen, Denmark.

Insights

Non-culture-based biomarkers like T2Candida and mannan antigen improve diagnosis and antifungal treatment for invasive candidiasis. Combining these tests reduced unnecessary antifungal use in sepsis patients, though overall consumption remained unchanged.

Area of Science:

  • Infectious Diseases
  • Clinical Microbiology
  • Critical Care Medicine

Background:

  • Invasive candidiasis (IC) diagnosis and antifungal treatment (AFT) can be improved by non-culture-based biomarkers.
  • Antifungal stewardship programs (AFSP) aim to optimize antifungal use, especially in high-risk patients.
  • T2Candida and Candida mannan antigen (MAg) are emerging biomarkers for IC detection.

Purpose of the Study:

  • To evaluate an antifungal stewardship program (AFSP) incorporating T2Candida and MAg screening in intensive care unit (ICU) patients.
  • To assess the diagnostic performance of T2Candida and MAg, individually and in combination, for invasive candidiasis.
  • To determine the impact of this AFSP on antifungal consumption and treatment decisions.

Main Methods:

  • Prospective study in two tertiary ICUs over one year, including 219 non-neutropenic sepsis patients at high risk for IC.
  • Collected 504 T2Candida and MAg samples for parallel testing.
  • Evaluated AFSP impact on AFT initiation, discontinuation, and antifungal consumption, comparing biomarker performance against proven/likely IC.

Main Results:

  • Invasive candidiasis was proven in 13.2% of patients. T2Candida/MAg combination showed improved sensitivity (70%) and specificity (90%) when tested within 3 days of AFT initiation.
  • The combined biomarkers contributed to early AFT initiation (13%), early discontinuation (25%), and avoiding AFT (24%).
  • While unnecessary treatment was reduced, overall antifungal use did not decrease compared to the previous year. T2Candida performance was lower than reported but improved with MAg.

Conclusions:

  • An AFSP utilizing T2Candida and MAg screening can reduce unnecessary antifungal exposure in high-risk ICU patients.
  • Combining T2Candida and MAg enhances diagnostic performance for invasive candidiasis.
  • Further optimization is needed to impact overall antifungal consumption despite improved stewardship.

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