Diagnostic potential of nested PCR, galactomannan EIA, and Beta-D-glucan for invasive aspergillosis in pediatric patients

被引:60
作者
Badiee, Parisa [1 ]
Alborzi, Abdolvahab [1 ]
Karimi, Mahammad [1 ]
Pourabbas, Bahman [1 ]
Haddadi, Pedram [2 ]
Mardaneh, Jalal [3 ,4 ]
Moieni, Mahsa [1 ]
机构
[1] Shiraz Univ Med Sci, Prof Alborzi Clin Microbiol Res Ctr, Shiraz, Iran
[2] Shiraz Univ Med Sci, Student Res Comm, Shiraz, Iran
[3] Univ Tehran Med Sci, Sch Publ Hlth, Dept Pathobiol, Tehran, Iran
[4] Univ Tehran Med Sci, Publ Hlth Res Inst, Tehran, Iran
来源
JOURNAL OF INFECTION IN DEVELOPING COUNTRIES | 2012年 / 6卷 / 04期
关键词
galactomannan; D-glucan; nested-PCR; hematologic disorder; aspergillosis; REAL-TIME PCR; FUNGAL-INFECTIONS; PULMONARY ASPERGILLOSIS; ENZYME-IMMUNOASSAY; ASSAY; ANTIGENEMIA; SERUM; DNA; FREQUENCY; ADULT;
D O I
10.3855/jidc.2110
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Limited specific data and investigations are available for invasive aspergillosis (IA) in pediatric patients. We evaluated the diagnostic potential of three noninvasive tests including the Platelia Aspergillus EIA kit for using galactomannan antigen, (1,3)-beta-D-glucan Detection Reagent Kit, and nested-PCR for Aspergillus DNA in sera. We evaluated the diagnostic potential of three noninvasive tests including EIA for galactomannan antigen (Platelia Aspergillus), nested PCR assay for Aspergillus DNA and test for (1 -> 3)-beta-D-glucan (Glucatell assay Kit). Methodology: All pediatric patients treated at the hematology/oncology unit who were at increased risk of developing invasive aspergillosis were enrolled. Clinical samples were examined for Aspergillus infections by mycological methods. Serial blood samples were collected twice weekly and evaluated by noninvasive tests. Results: We analyzed 230 consecutive blood samples from 62 pediatric patients. The incidence rate of invasive aspergillosis in the patients was found to be 27.4%, and the etiologic agents were Aspergillus flavus, Aspergillus fumigatus, and Aspergillus spp. The sensitivity, specificity, positive and negative predictive values, and likelihood ratios for positive and negative results of galactomannan in patients with proven and probable IA were 90%, 92%, 81.8%, 96%, 11.25, and 0.1; for beta-D-glucan they were 50%, 46%, 26%, 70.6%, 0.9, 0.9; and for nested-PCR they were 80%, 96.2%, 88.9%, 92.6%, 21, and 0.2, respectively. Conclusions: The conventional methods are not able to detect IA, due to the lack of valid and proper sampling. Galactomannan and nested-PCR tests in serum, with enough accuracy and reliability, can serve as noninvasive methods for the detection of IA in pediatric patients. However, the beta-D-glucan test cannot serve as an efficient diagnostic tool in those with hematologic disorders.
引用
收藏
页码:352 / 357
页数:6
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