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聚合酶链反应联合量子点荧光分析在疑似血流感染患者中鉴定细菌和酵母菌的临床评估。

Clinical evaluation of polymerase chain reaction coupled with quantum dot fluorescence analysis in the identification of bacteria and yeasts in patients with suspected bloodstream infections.

机构信息

College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China.

Department of Infectious Disease, Zhejiang Provincial People's Hospital, Hangzhou, China.

出版信息

Microb Biotechnol. 2023 Apr;16(4):827-837. doi: 10.1111/1751-7915.14226. Epub 2023 Feb 1.

Abstract

Bloodstream infections are serious and complex infectious diseases that often require a rapid diagnosis. Polymerase chain reaction coupled with quantum dot fluorescence analysis (PCR-QDFA) is a novel diagnostic technique. This study aimed to evaluate the diagnostic performance of PCR-QDFA for pathogen detection in patients with suspected bloodstream infections (BSIs). It evaluates 29 kinds of common pathogens (24 bacteria and 5 yeasts) from blood culture bottles. The results of PCR-QDFA identification and traditional microbial laboratory identification were compared, and the latter was used as the 'gold standard' to analyse the diagnostic performance of the PCR-QDFA. In total, 517 blood culture bottles were included in this study. The PCR-QDFA identified microorganisms in 368/422 (87.2%) samples with monomicrobial growth. For the pathogens on the PCR-QDFA list, the assay showed a higher sensitivity of 97.4% (368/378). When polymicrobial growth was analysed, the PCR-QDFA successfully detected 19/25 (76%) microorganisms on the PCR-QDFA list. In addition, 82/82 negative blood culture bottles also showed no pathogens by PCR-QDFA with a specificity of 100%. In conclusion, the PCR-QDFA assay could identify a majority of the common pathogens encountered in clinical practice, showing excellent diagnostic performance for pathogen detection in patients with suspected BSIs.

摘要

血流感染是严重且复杂的传染病,通常需要快速诊断。聚合酶链反应结合量子点荧光分析(PCR-QDFA)是一种新型诊断技术。本研究旨在评估 PCR-QDFA 检测疑似血流感染(BSI)患者病原体的诊断性能。它评估了来自血培养瓶的 29 种常见病原体(24 种细菌和 5 种酵母)。将 PCR-QDFA 鉴定结果与传统微生物实验室鉴定结果进行比较,后者作为“金标准”分析 PCR-QDFA 的诊断性能。本研究共纳入 517 个血培养瓶。PCR-QDFA 在 368/422(87.2%)个单培养生长样本中鉴定出微生物。对于 PCR-QDFA 列表上的病原体,该检测方法的灵敏度为 97.4%(368/378)。在分析多培养生长时,PCR-QDFA 成功检测到 PCR-QDFA 列表上的 19/25(76%)微生物。此外,82/82 个阴性血培养瓶也通过 PCR-QDFA 未检测到病原体,特异性为 100%。总之,PCR-QDFA 检测法可鉴定出临床实践中遇到的大多数常见病原体,对疑似 BSI 患者的病原体检测具有出色的诊断性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2e0/10034622/27208227da40/MBT2-16-827-g002.jpg

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