Comparison of 2 real-time PCR assays for diagnosis of Pneumocystis jirovecii pneumonia in human immunodeficiency virus (HIV) and non-HIV immunocompromised patients

被引:25
作者
Montesinos, Isabel [1 ]
Brancart, Francoise [1 ]
Schepers, Kinda [2 ]
Jacobs, Frederique [2 ]
Denis, Olivier [1 ]
Delforge, Marie-Luce [1 ]
机构
[1] Univ Libre Bruxelles, Hop Erasme, Dept Microbiol, B-1070 Brussels, Belgium
[2] Univ Libre Bruxelles, Hop Erasme, Infect Dis, B-1070 Brussels, Belgium
关键词
Pneumocystis jirovecii pneumonia; Quantitative real-time PCR; BRONCHOALVEOLAR LAVAGE SPECIMENS; CLINICAL-SIGNIFICANCE; CARINII-PNEUMONIA; INFECTED PATIENTS; COLONIZATION; DNA; DIFFERENTIATION; EPIDEMIOLOGY; FLUID; ERA;
D O I
10.1016/j.diagmicrobio.2015.03.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A total of 120 bronchoalveolar lavage specimens from HIV and non-HIV immunocompromised patients, positive for Pneumocystis jirovecii by an "in house" real-time polymerase chain reaction (PCR), were evaluated by the Bio-Evolution Pneumocystis real-time PCR, a commercial quantitative assay. Patients were classified in 2 categories based on clinical and radiological findings: definite and unlikely Pneumocystis pneumonia (PCP). For the "in house" PCR, cycle threshold 34 was established as cut-off value to discriminate definite PCP from unlikely PCP with 65% and 85% of sensitivity and specificity, respectively. For the Bio-Evolution quantitative PCR, a cut-off value of 2.8 x 10(5) copies/mL was defined with 72% and 82% of sensitivity and specificity, respectively. Overlapped zones of results for definite and unlikely PCP were observed. Quantitative PCR is probably a useful tool for PCP diagnosis. However, for optimal management of PCP in non-HIV immunocompromised patients, operational thresholds should be assessed according to underlying diseases and other clinical and radiological parameters. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 147
页数:5
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