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. 2019 Nov 1;57(8):987-996.
doi: 10.1093/mmy/myz002.

Use of Aspergillus fumigatus real-time PCR in bronchoalveolar lavage samples (BAL) for diagnosis of invasive aspergillosis, including azole-resistant cases, in high risk haematology patients: the need for a combined use with galactomannan

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Use of Aspergillus fumigatus real-time PCR in bronchoalveolar lavage samples (BAL) for diagnosis of invasive aspergillosis, including azole-resistant cases, in high risk haematology patients: the need for a combined use with galactomannan

Malgorzata Mikulska et al. Med Mycol. .

Abstract

Diagnosis of invasive aspergillosis (IA) is challenging, particularly in high-risk patients with lung lesions other than typical according to 2008-EORTC/MSG criteria. Even if microbiology is positive, they still remain unclassified according to 2008-EORTC/MSG. Quantitative polymerase chain reaction (qPCR) provides new mycological documentation of IA. This retrospective study assessed Aspergillus fumigatus real time qPCR (MycoGENIE®) in BAL to diagnose IA and identify azole-resistant strains. Clinical, radiological, and microbiological data from 114 hematology patients (69% HSCT recipients; 29% on mould active agents) from years 2012-2017 were collected; and 123 BAL samples were tested with qPCR (cutoff: Ct < 40) and galactomannan (GM, Platelia®, cutoff: 0.5 ODI). Patients were classified as proven/probable, possible, and no-IA. "Atypical-IA" referred to patients with lesions other than typical according to 2008-EORTC/MSG and positive mycology. Proven IA was diagnosed in two cases (1.6%), probable in 28 (22.8%), possible in 27 (22%), atypical in 14 (11.4%). qPCR was positive in 39 samples (31.7%). Sensitivity and specificity of qPCR for proven/probable IA (vs no-IA; atypical-IA excluded) were 40% (95% confidence interval [CI]: 23-59) and 69% (95%CI: 55-81), respectively. Sensitivity of qPCR was higher when combined with GM (83%, 95%CI: 65-94) and in those receiving mould-active agents at BAL (61%, 95%CI: 32-86). One sample had TR34/L98H mutation. In conclusion, in high-risk hematology patients with various lung lesions, A. fumigatus qPCR in BAL contributes to diagnosing IA, particularly if combined with GM and in patients receiving mould-active agents might allow detecting azole-resistant mutations in culture negative samples.

Keywords: Aspergillus fumigatus PCR; BAL; HSCT; galactomannan; invasive aspergillosis.

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Figures

Figure 1.
Figure 1.
Number of patients with results positive for invasive aspergillosis according to radiological criteria, BAL galactomannan (GM) and BAL Aspergillus fumigatus qPCR.

References

    1. Kosmidis C, Denning DW. The clinical spectrum of pulmonary aspergillosis. Thorax. 2015; 70: 270–277. - PubMed
    1. Patterson TF, Thompson GR, 3rd, Denning DW et al. .. Practice guidelines for the diagnosis and management of aspergillosis: 2016 Update by the Infectious Diseases Society of America. Clin Infect Dis. 2016; 63: e1–e60. - PMC - PubMed
    1. Ullmann AJ, Aguado JM, Arikan-Akdagli S et al. .. Diagnosis and management of Aspergillus diseases: executive summary of the 2017 ESCMID-ECMM-ERS guideline. Clin Microbiol Infect. 2018; 24: e1–e38. - PubMed
    1. Bongomin F., Gago S. Global and multinational prevalence of fungal diseases-estimate precision. J Fungi. 2017; 3: E57. - PMC - PubMed
    1. Meis JF, Chowdhary A. Clinical implications of globally emerging azole resistance in Aspergillus fumigatus. Philos Trans R Soc London B Biol Sci. 2016; 371. doi:10.1098/rstb.2015.0460. - DOI - PMC - PubMed

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