首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Value of Serial Quantification of Fungal DNA by a Real-Time PCR-Based Technique for Early Diagnosis of Invasive Aspergillosis in Patients with Febrile Neutropenia
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Value of Serial Quantification of Fungal DNA by a Real-Time PCR-Based Technique for Early Diagnosis of Invasive Aspergillosis in Patients with Febrile Neutropenia

机译:基于实时PCR的真菌DNA序列定量技术对发热性中性粒细胞减少症患者侵袭性曲霉病的早期诊断价值

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摘要

A study was designed to assess the reliability of the serial detection of Aspergillus sp. DNA to diagnose invasive aspergillosis (IA) in patients with febrile neutropenia. Two blood and two serum samples were taken weekly from 83 patients. A total of 2,244 samples were analyzed by real-time quantitative PCR. Twelve (14.4%) patients were diagnosed with IA. Taking two consecutive positive results as the diagnostic criterion, PCR detected 11 cases, with 4 false positives, giving sensitivity, specificity, positive, and negative predictive values of 91.6%, 94.4%, 73.3%, and 98.5%, respectively. On analyzing in conjunction with high-resolution chest tomography (HRCT) and galactomannan (GM) testing, the combination of serial PCR and GM detected 100% of aspergillosis cases, with a positive predictive value of 75.1%. This diagnostic strategy presented, according to CART analysis, a receiver-operator curve with an area under the curve of 0.97 (95% confidence interval, 0.895 to 1.032; P < 0.01), with a relative risk of IA 6.92 times higher than the control population and with predictive success of 95.2%. As regards early diagnosis, the serial detection of Aspergillus DNA took on average 21 days less than HRCT and 68 days less than GM. The serial detection of Aspergillus DNA using real-time quantitative PCR has great diagnostic applicability, which increases when combined with GM quantification.
机译:设计了一项研究,以评估连续检测曲霉菌的可靠性。用于诊断发热性中性粒细胞减少症的侵袭性曲霉病(IA)的DNA。每周从83名患者中采集两份血液和两份血清样本。通过实时定量PCR分析了总共2,244个样品。十二名(14.4%)患者被诊断出患有IA。以连续两次阳性结果为诊断标准,PCR检测到11例,其中假阳性4例,敏感性,特异性,阳性和阴性预测值分别为91.6%,94.4%,73.3%和98.5%。在结合高分辨率胸部断层扫描(HRCT)和半乳甘露聚糖(GM)检测进行分析时,连续PCR和GM的结合检测出100%的曲霉病病例,阳性预测值为75.1%。根据CART分析,此诊断策略呈现出接收者-操作者曲线,曲线下面积为0.97(95%置信区间,0.895至1.032; P <0.01),IA的相对危险度比对照组高6.92倍人口,预测成功率为95.2%。关于早期诊断,连续检测曲霉DNA比HRCT平均少21天,比GM平均少68天。使用实时定量PCR进行的曲霉DNA的连续检测具有很好的诊断适用性,与GM定量结合使用时,这种检测会增加。

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