Combination of Mycological Criteria: a Better Surrogate to Identify COVID-19-Associated Pulmonary Aspergillosis Patients and Evaluate Prognosis?
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Diagnosis of coronavirus disease 2019 (COVID-19)-associated pulmonary aspergillosis (CAPA) remains unclear especially in nonimmunocompromised patients. The aim of this study was to evaluate seven mycological criteria and their combination in a large homogenous cohort of patients. All successive patients ( = 176) hospitalized for COVID-19 requiring mechanical ventilation and who clinically worsened despite appropriate standard of care were included over a 1-year period. Direct examination, culture, Aspergillus quantitative PCR (-qPCR), and galactomannan testing were performed on all respiratory samples ( = 350). Serum galactomannan, β-d-glucan, and plasma -qPCR were also assessed. The criteria were analyzed alone or in combination in relation to mortality rate. Mortality was significantly different in patients with 0, ≤2, and ≥3 positive criteria (log rank test, = 0.04) with death rate of 43.1, 58.1, and 76.4%, respectively. Direct examination, plasma qPCR, and serum galactomannan were associated with a 100% mortality rate. Bronchoalveolar lavage (BAL) galactomannan and positive respiratory sample culture were often found as isolated markers (28.1 and 34.1%) and poorly repeatable when a second sample was obtained. Aspergillus DNA was detected in 13.1% of samples (46 of 350) with significantly lower quantitative cycle (Cq) when associated with at least one other criterion (30.2 versus 35.8) ( < 0.001). A combination of markers and/or blood biomarkers and/or direct respiratory sample examination seems more likely to identify patients with CAPA. -qPCR may help identifying false-positive results of BAL galactomannan testing and culture on respiratory samples while quantifying fungal burden accurately.
Sun C, Cai X, Zhong H, Lu Y, Li Y, Cai Y Microbiol Spectr. 2025; 13(3):e0294524.
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Gibert C, Tirard-Collet P, Miossec C, Dupont D, Persat F, Wallon M J Clin Microbiol. 2024; 62(11):e0079124.
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Goncalves S, Pereira I, Feys S, Cunha C, Chamilos G, Hoenigl M mBio. 2024; 15(6):e0198223.
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van Grootveld R, van Paassen J, Claas E, Heerdink L, Kuijper E, de Boer M Med Mycol. 2024; 62(5).
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