Abstract

BackgroundTo assess the performance of Candida albicans germ tube antibody (CAGTA), (1 → 3)-ß-D-glucan (BDG), mannan antigen (mannan-Ag), anti-mannan antibodies (mannan-Ab), and Candida DNA for diagnosing invasive candidiasis (IC) in ICU patients with severe abdominal conditions (SAC).MethodsA prospective study of 233 non-neutropenic patients with SAC on ICU admission and expected stay ≥ 7 days. CAGTA (cutoff positivity ≥ 1/160), BDG (≥80, 100 and 200 pg/mL), mannan-Ag (≥60 pg/mL), mannan-Ab (≥10 UA/mL) were measured twice a week, and Candida DNA only in patients treated with systemic antifungals. IC diagnosis required positivities of two biomarkers in a single sample or positivities of any biomarker in two consecutive samples. Patients were classified as neither colonized nor infected (n = 48), Candida spp. colonization (n = 154) (low-grade, n = 130; high-grade, n = 24), and IC (n = 31) (intra-abdominal candidiasis, n = 20; candidemia, n = 11).ResultsThe combination of CAGTA and BDG positivities in a single sample or at least one of the two biomarkers positive in two consecutive samples showed 90.3 % (95 % CI 74.2–98.0) sensitivity, 42.1 % (95 % CI 35.2–98.8) specificity, and 96.6 % (95 % CI 90.5–98.8) negative predictive value. BDG positivities in two consecutive samples had 76.7 % (95 % CI 57.7–90.1) sensitivity and 57.2 % (95 % CI 49.9–64.3) specificity. Mannan-Ag, mannan-Ab, and Candida DNA individually or combined showed a low discriminating capacity.ConclusionsPositive Candida albicans germ tube antibody and (1 → 3)-ß-D-glucan in a single blood sample or (1 → 3)-ß-D-glucan positivity in two consecutive blood samples allowed discriminating invasive candidiasis from Candida spp. colonization in critically ill patients with severe abdominal conditions. These findings may be helpful to tailor empirical antifungal therapy in this patient population.

Highlights

  • To assess the performance of Candida albicans germ tube antibody (CAGTA), (1 → 3)-ß-D-glucan (BDG), mannan antigen, anti-mannan antibodies, and Candida DNA for diagnosing invasive candidiasis (IC) in intensive care unit (ICU) patients with severe abdominal conditions (SAC)

  • We investigated the performance of these five tests, alone and in combination, for discriminating IC in critically ill patients with severe abdominal conditions (SAC)

  • Design and study population Between November 1, 2012 and February 28, 2014, all consecutive adult non-neutropenic patients with SAC on ICU admission and an expected stay of ≥ 7 days were included in a prospective, cohort, observational, and multicenter study

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Summary

Introduction

To assess the performance of Candida albicans germ tube antibody (CAGTA), (1 → 3)-ß-D-glucan (BDG), mannan antigen (mannan-Ag), anti-mannan antibodies (mannan-Ab), and Candida DNA for diagnosing invasive candidiasis (IC) in ICU patients with severe abdominal conditions (SAC). Accurate and timely diagnosis of invasive candidiasis (IC) from the patient’s perspective and to optimize antifungal therapy in the intensive care unit (ICU) setting remains a topic of great interest [1,2,3,4,5,6]. The use of single or combined biomarkers, such as (1 → 3)-ß-D-glucan (BDG), Candida albicans germ tube antibody (CAGTA), mannan antigen (mannan-Ag), anti-mannan antibodies (mannan-Ab), and polymerase chain reaction (PCR) detection of Candida DNA has received increasing attention [7,8,9,10], but the appropriate incorporation into clinical practice remains controversial. We investigated the performance of these five tests, alone and in combination, for discriminating IC in critically ill patients with severe abdominal conditions (SAC)

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