Beta-(1,3)-D-glucan (BG) detection is an emerging tool to diagnose invasive fungal infections (IFIs). Invasive aspergillosis (IA) is the second most common IFI in immunocompromised intensive care unit (ICU) patients.We retrospectively analyzed the serum BG concentration (Fungitell; Associates of Cape Cod) in immunocompromised ICU patients with proven IA and in immunocompromised ICU patients in whom autopsy failed to show IFI. The study was performed in a 17-bed medical ICU in a 1,900-bed referral hospital. Patients at risk for IA were eligible for inclusion when at least two additional clinical signs were present. Patients with other IFIs were excluded. Fourteen patients with IA and 33 patients who had no IFI were eligible for inclusion. Serum BG levels were significantly higher in patients with IA than patients without an IFI (P < 0.01). Using a cutoff of 140 pg/ml, the sensitivity and specificity were 85.7 and 69.7%, respectively; the positive and negative predictive values were 54.5 and 92.0%, respectively. The positive and negative likelihood ratios were 2.83 and 0.21, respectively. Although serum BG concentrations were higher in immunocompromised ICU patients with IA than in patients with the same risk factors who did not have IFI on autopsy, the moderate performance characteristics of this test limit its use as a diagnostic test for IA in this population.The incidence of invasive fungal infections (IFIs) has markedly increased in recent decades. Despite development of new antifungal drugs, the mortality rate from IFIs remains high, particularly in intensive care unit (ICU) patients. Invasive aspergillosis (IA) is the second most common IFI in immunocompromised ICU patients. The prognosis of IA is poor; mortality rates up to 100% have been reported in mechanically ventilated chronic obstructive pulmonary disease patients with IA (2), and in nonneutropenic critically ill patients with IA, rates up to 89% were published (5). A retrospective study in our medical ICU showed an observed mortality rate of 80% in patients suffering from IA, compared to a predicted mortality rate of 48% (14).An important determinant of the prognosis is the time lag between the onset of infection and the administration of antifungal drugs (3,25). This phase can be long due to diagnostic difficulties. Classical methods such as culture and biopsy are invasive and time-consuming tools (9). Detection of fungal cell wall components is a rapid and attractive tool to diagnose IFIs. Beta-(1,3)-D-glucan (BG) is one of those components and is present in a wide variety of pathogenic fungi such as Candida spp., Fusarium spp., Aspergillus spp., and Pneumocystis spp. The cell wall of Zygomycetes does not contain BG; Cryptococcus spp. have a capsule that captures BG before it is released into the bloodstream (12). BG is also present in the fungal wall of Penicillium spp. and Paecilomyces spp., which can cause contamination of the sample.Aspergillus spp. have galactomannan (GM) as another important cell wall component. GM is released into the blood...