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评价一种 PCR-电喷雾电离质谱平台,用于直接从前瞻性采集的支气管肺泡灌洗液标本中检测和鉴定真菌病原体。

Evaluation of a PCR-electrospray ionization mass spectrometry platform for detection and identification of fungal pathogens directly from prospectively collected bronchoalveolar lavage specimens.

机构信息

Division of Medical Microbiology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Chongqing Key Laboratory of Infectious Diseases and Parasitic Diseases, Department of Infectious Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Ibis Biosciences, Abbott, Carlsbad, CA, USA.

出版信息

Diagn Microbiol Infect Dis. 2020 May;97(1):114988. doi: 10.1016/j.diagmicrobio.2020.114988. Epub 2020 Jan 15.

Abstract

The incidence of invasive fungal infections is on the rise worldwide due to the growth of the immunocompromised population. We report here the use of a diagnostic assay that utilizes a universal extraction method, broad spectrum PCR amplification and analysis via electrospray ionization mass spectrometry (PCR/ESI-MS) to detect and identify more than 200 pathogenic fungi directly from bronchoalveolar lavage (BAL) specimens in less than 8 hours. In this study, we describe both analytical and clinical performance of the assay, when run with prospectively collected clinical BAL specimens. In 146 patients with probable and possible fungal infections defined by EORTC/MSG (European Organization for Research and Treatment of Cancer/Mycoses Study Group) criteria, the PCR/ESI-MS assay demonstrated a sensitivity of 90.9% (95% CI: 76.4-96.9%) and a specificity of 82.3% (95% CI: 74.2-88.2%). This data demonstrates the utility of a non-culture based broad fungal targets molecular diagnostic tool for rapid and accurate diagnosis of invasive fungal infections in patients at risk of developing fungal diseases.

摘要

由于免疫功能低下人群的增加,全球侵袭性真菌感染的发病率呈上升趋势。我们在此报告一种诊断检测方法的应用,该方法使用通用提取方法、广谱 PCR 扩增和电喷雾电离质谱分析(PCR/ESI-MS),可直接从支气管肺泡灌洗液(BAL)标本中检测和鉴定 200 多种致病性真菌,整个过程不到 8 小时。在这项研究中,我们描述了该检测方法的分析和临床性能,当与前瞻性采集的临床 BAL 标本一起运行时。在 146 例符合 EORTC/MSG(欧洲癌症研究与治疗组织/真菌病研究组)标准的疑似和可能真菌感染患者中,PCR/ESI-MS 检测方法的敏感性为 90.9%(95%CI:76.4-96.9%),特异性为 82.3%(95%CI:74.2-88.2%)。这些数据表明,一种非培养的广谱真菌靶标分子诊断工具可用于快速准确地诊断有发生真菌病风险的患者的侵袭性真菌感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d379/7127232/c5f1332e4d9f/gr1_lrg.jpg

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