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Background <p>Intra-abdominal candidiasis (IAC) is a severe form of invasive candidiasis that affects critically ill patients and is associated with a high mortality rate and persistent diagnostic delays. Conventional fungal culture from peritoneal fluid remains slow and has insufficient sensitivity. Molecular assays promote early diagnosis, but data from critically ill populations remain scarce.</p> Objectives <p>We evaluated the diagnostic performance of the OLM CandID Real-Time PCR assay directly applied to peritoneal fluid samples obtained from a previously established multicenter cohort of critically ill patients with suspected or confirmed IAC.</p> Methods <p>OLM CandID Real-Time PCR is a quantitative PCR assay for detecting <i>C. albicans</i>,<i> C. glabrata</i>,<i> C. parapsilosis</i>,<i> C. tropicalis</i>,<i> C. krusei</i>, and <i>C. dubliniensis</i>. Binary PCR results were compared with those of fungal culture as the reference standard. Secondary analyses analyzed quantitative PCR values to better understand culture-negative/PCR-positive discordances using ROC-derived cycle threshold (Ct) cutoffs.</p> Results <p>Fifty-seven patients, mainly with postoperative peritonitis, were included. Among the culture-positive samples, <i>C. albicans</i> was predominant. Using binary interpretation, the PCR achieved 100% sensitivity (95% CI 100–100) and 60% specificity (95% CI 38–81); the positive and negative predictive values were 82% (95% CI 71–93) and 100% (95% CI 100–100), respectively. In the secondary Ct-based analysis, ROC-derived threshold determination was feasible for <i>C. albicans</i> (<i>n</i> = 35) and <i>C. tropicalis</i> (<i>n</i> = 12). For <i>C. albicans</i> and <i>C. tropicalis</i>, the ROC AUC values were 0.92 (95% CI 0.75-1) and 0.90 (95% CI 0.66-1), respectively, and applying the optimal Ct cutoffs (30.75 and 34.63 respectively) yielded 100% specificity and 100% positive predictive value for both species.</p> Conclusions <p>OLM CandID Real-Time PCR applied directly to peritoneal fluid demonstrated strong analytical performance for the detection of <i>Candida</i> in critically ill patients with suspected IAC. The assay showed high concordance with culture results, supporting its feasibility for rapid microbiological assessment. Discordant PCR-positive/culture-negative results were mainly associated with high Ct values, likely reflecting low fungal burden, detection of non-viable DNA, or analytical over-detection. These findings are exploratory and highlight the need for prospective studies to determine the clinical relevance of quantitative PCR results and their role in guiding antifungal management.</p> Trial registration <p>The study was registered with ClinicalTrials.gov (ID number 07005258, first registered on March 6, 2025).</p>

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Analytical performance of species-targeted quantitative PCR for intra-abdominal candidiasis in critically ill patients: a proof-of-concept post hoc analysis from the pBDG2 multicenter study

  • 期刊论文

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  • 发表日期：

    2026年2月10日

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  • Emmanuel Novy,
  • Arnaud Schaeffer,
  • Maxime Nguyen,
  • Frédéric Dalle,
  • Julien Pottecher,
  • Valérie Letscher-Bru,
  • Guillaume Louis,
  • Charlotte Stephan,
  • Amandine Luc,
  • Marie Machouart,
  • Anne Debourgogne

摘要

Background

Intra-abdominal candidiasis (IAC) is a severe form of invasive candidiasis that affects critically ill patients and is associated with a high mortality rate and persistent diagnostic delays. Conventional fungal culture from peritoneal fluid remains slow and has insufficient sensitivity. Molecular assays promote early diagnosis, but data from critically ill populations remain scarce.

Objectives

We evaluated the diagnostic performance of the OLM CandID Real-Time PCR assay directly applied to peritoneal fluid samples obtained from a previously established multicenter cohort of critically ill patients with suspected or confirmed IAC.

Methods

OLM CandID Real-Time PCR is a quantitative PCR assay for detecting C. albicans, C. glabrata, C. parapsilosis, C. tropicalis, C. krusei, and C. dubliniensis. Binary PCR results were compared with those of fungal culture as the reference standard. Secondary analyses analyzed quantitative PCR values to better understand culture-negative/PCR-positive discordances using ROC-derived cycle threshold (Ct) cutoffs.

Results

Fifty-seven patients, mainly with postoperative peritonitis, were included. Among the culture-positive samples, C. albicans was predominant. Using binary interpretation, the PCR achieved 100% sensitivity (95% CI 100–100) and 60% specificity (95% CI 38–81); the positive and negative predictive values were 82% (95% CI 71–93) and 100% (95% CI 100–100), respectively. In the secondary Ct-based analysis, ROC-derived threshold determination was feasible for C. albicans (n = 35) and C. tropicalis (n = 12). For C. albicans and C. tropicalis, the ROC AUC values were 0.92 (95% CI 0.75-1) and 0.90 (95% CI 0.66-1), respectively, and applying the optimal Ct cutoffs (30.75 and 34.63 respectively) yielded 100% specificity and 100% positive predictive value for both species.

Conclusions

OLM CandID Real-Time PCR applied directly to peritoneal fluid demonstrated strong analytical performance for the detection of Candida in critically ill patients with suspected IAC. The assay showed high concordance with culture results, supporting its feasibility for rapid microbiological assessment. Discordant PCR-positive/culture-negative results were mainly associated with high Ct values, likely reflecting low fungal burden, detection of non-viable DNA, or analytical over-detection. These findings are exploratory and highlight the need for prospective studies to determine the clinical relevance of quantitative PCR results and their role in guiding antifungal management.

Trial registration

The study was registered with ClinicalTrials.gov (ID number 07005258, first registered on March 6, 2025).