Reevaluating the Value of (1,3)-β-D-Glucan for the Diagnosis of Intra-Abdominal Candidiasis in Critically Ill

Emmanuel Novy1,2, Mathieu Esposito1, Anne Debourgogne2,3

  • 1Department of Anesthesiology, Critical Care and Perioperative Medicine, Surgical Intensive Care Unit, CHRU-Nancy, F-54000 Nancy, France.

PubMed

Insights

Peritoneal fluid (1,3)-β-D-glucan (BDG) shows promise for diagnosing intra-abdominal candidiasis (IAC) in critically ill patients. Serum BDG is less specific for IAC, but peritoneal BDG may help differentiate fungal from bacterial infections.

Area of Science:

  • Critical Care Medicine
  • Mycology
  • Clinical Diagnostics

Background:

  • Intra-abdominal candidiasis (IAC) presents diagnostic and treatment challenges in critically ill patients.
  • Conventional fungal cultures are slow, delaying essential antifungal therapy.
  • (1,3)-β-D-glucan (BDG) is a fungal cell wall biomarker with potential for IAC diagnosis, but its utility is limited by false positives in intensive care unit (ICU) settings.

Purpose of the Study:

  • To review the diagnostic value of BDG in serum and peritoneal fluid for intra-abdominal candidiasis (IAC).
  • To assess the potential of peritoneal BDG as a diagnostic tool for IAC in critically ill patients.

Main Methods:

  • Systematic review of studies evaluating BDG in serum and peritoneal fluid for IAC diagnosis.
  • Analysis of BDG performance in differentiating IAC from other conditions, including bacterial peritonitis and candidemia.
  • Discussion of practical aspects, advantages, and limitations of BDG testing in ICU patients.

Main Results:

  • Serum BDG effectively excludes candidemia but shows low specificity for diagnosing IAC in critically ill patients.
  • Peritoneal fluid BDG demonstrates higher specificity in distinguishing IAC from bacterial peritonitis.
  • Current data suggest peritoneal BDG may serve as a valuable complementary diagnostic marker for IAC.

Conclusions:

  • Peritoneal fluid BDG offers improved diagnostic accuracy for IAC compared to serum BDG in critically ill patients.
  • Further research is required to establish optimal diagnostic thresholds and clinical utility of peritoneal BDG.
  • Peritoneal BDG holds potential to enhance timely and targeted antifungal treatment for intra-abdominal candidiasis.