1. Comparative analysis of galactomannan lateral flow assay, galactomannan enzyme immunoassay and <scp>BAL</scp> culture for diagnosis of <scp>COVID</scp> ‐19‐associated pulmonary aspergillosis
- Author
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Mona Ghazanfari, Jamshid Yazdani Charati, Lotfollah Davoodi, Amir Arastehfar, Maryam Moazeni, Mahdi Abastabar, Iman Haghani, Sabah Mayahi, Martin Hoenigl, Weihua Pan, and Mohammad T. Hedayati
- Subjects
Invasive Pulmonary Aspergillosis ,Antifungal Agents ,COVID-19 ,Galactose ,Dermatology ,General Medicine ,Sensitivity and Specificity ,Immunoenzyme Techniques ,Mannans ,COVID-19 Testing ,Infectious Diseases ,Humans ,Pulmonary Aspergillosis ,Bronchoalveolar Lavage Fluid - Abstract
Galactomannan Enzyme Immunoassay (GM-EIA) is proved to be a cornerstone in the diagnosis of COVID-19-associated pulmonary aspergillosis (CAPA), its use is limited in middle and low-income countries, where the application of simple and rapid test, including Galactomannan Lateral Flow Assay (GM-LFA), is highly appreciated. Despite such merits, limited studies directly compared GM-LFA with GM-EIA. Herein we compared the diagnostic features of GM-LFA, GM-EIA and bronchoalveolar lavage (BAL) culture for CAPA diagnosis in Iran, a developing country.Diagnostic performances of GM-LFA and GM-EIA in BAL (GM indexes ≥1) and serum (GM indexes0.5), i.e. sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) and areas under the curve (AUC), were evaluated using BAL (n = 105) and serum (n = 101) samples from mechanically ventilated COVID-19 patients in intensive care units. Patients were classified based on the presence of host factors, radiological findings and mycological evidences according to 2020 ECMM/ISHAM consensus criteria for CAPA diagnosis.The Aspergillus GM-LFA for serum and BAL samples showed a sensitivity of 56.3% and 60.6%, specificity of 94.2% and 88.9%, PPV of 81.8% and 71.4%, NPV of 82.3% and 83.1%, when compared with BAL culture, respectively. GM-EIA showed sensitivities of 46.9% and 54.5%, specificities of 100% and 91.7%, PPVs of 100% and 75%, NPVs of 80.2% and 81.5% for serum and BAL samples, respectively.Our study found GM-LFA as a reliable simple and rapid diagnostic tool, which could circumvent the shortcomings of culture and GM-EIA and be pivotal in timely initiation of antifungal treatment.
- Published
- 2022