Evaluation of the EUROIMMUN Aspergillus antigen immunoenzyme assay in serum and bronchoalveolar lavage fluid samples

被引:0
作者
Roiz-Mesones, Maria Pia [1 ,2 ]
de Malet Pintos-Fonseca, Ana [1 ,2 ]
Ahedo-Garcia, Noelia [1 ]
de Alegria-Puig, Carlos Ruiz [1 ,2 ]
机构
[1] Hosp Univ Marques Valdecilla, Serv Microbiol, Santander, Spain
[2] IDIVAL, Santander, Spain
来源
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA | 2023年 / 41卷 / 03期
关键词
Galactomannan; Aspergillus antigen; ELISA; Serum samples; Bronchoalveolar lavage fluid; CROSS-REACTIVITY;
D O I
10.1016/j.eimc.2021.08.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: The most widely used marker for the diagnosis of invasive aspergillosis (IA) is the detection of galactomannan by ELISA. This study describes the evaluation of the results obtained by Euroimmun Aspergillus antigen ELISA (EIA-GM-E) in serum samples and bronchoalveolar lavage fluid (BAL) from patients at risk of IA, and compares these results with those obtained by Bio-Rad Galactomannan EIA (EIA-GM-BR).Methods: Anonymous retrospective case-control comparative study in 64 serum samples and 28 BAL from 51 patients.Results: Overall agreement of the results of the two assays was observed in 72 of 92 samples (78.3%). The sensitivity of EIA-GM-BR and EIA-GM-E in serum samples was 88.9% and 43.2%, respectively, and 100% and 88.9% for BAL. The specificity of EIA-GM-BR and EIA-GM-E in serum samples was 91.9% for both assays, and 68.4% and 84.2% in BAL. There were no statistically significant differences in the results of both assays.Conclusions: Both methods show good results for the discrimination of patients with IA when BAL is tested, or serum in case of EIA-GM-BR.(c) 2021 Sociedad Espan tilde ola de Enfermedades Infecciosas y Microbiologi acute accent a Cli acute accent nica. Published by Elsevier Espan tilde a, S.L.U. All rights reserved.
引用
收藏
页码:176 / 180
页数:5
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