Evidence map›Paper›PMID 40301532›Full record

ArticlePediatric research2025

Evaluation of a fully automatic nucleic acid amplification system for detecting four respiratory pathogens.

Ying-Ying Chen, Wen-Qing Xiang, Ya-Jun Guo, Zheng Shen, Wei Li

Abstract readEvaluation Study
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In one paragraph

Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ying-Ying ChenDepartment of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.
Wen-Qing XiangDepartment of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.
Ya-Jun GuoDepartment of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.
Zheng ShenDepartment of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.
Wei LiDepartment of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China. chweige@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV), adenovirus (ADV), human parainfluenza virus (hPIV), and Mycoplasma pneumoniae (MP) are prevalent pathogens causing acute respiratory infections (ARIs) in children. Prompt and precise detection of these pathogens is essential for early differentiation. This study sought to assess the diagnostic efficacy of a fully automatic real-time fluorescence PCR assay utilizing microfluidic technology (PCR-MT) for the rapid detection of RSV, hPIV, ADV, and MP in children in a hospital setting in Zhejiang, China.

methodsThe study was conducted on 420 children with ARIs from March to December 2022 at our hospital. Throat swab samples were collected and detected for RSV, hPIV, ADV, and MP using both PCR-capillary electrophoresis fragment analysis (PCR-CEFA) and PCR-MT. The results obtained from the PCR-MT method were compared with those from PCR-CEFA.

resultsWith PCR-CEFA as the gold standard, the sensitivity and specificity of the PCR-MT method were as follows: 94.4% and 100.0% for RSV, 96.0% and 99.1% for hPIV, 100.0% and 98.6% for ADV, and 93.5% and 98.8% for MP, respectively.

conclusionThe PCR-MT method demonstrates substantial potential for clinical application in the early diagnosis of RSV, hPIV, ADV, and MP in an outpatient setting, offering robust sensitivity and specificity. IMPACT: Rapid, accurate, and convenient multiple pathogen detection technologies represent a significant area of research in the medical field. The method evaluated in this study enables simultaneous detection of four pathogens on a single chip, covering various subtypes, with results available within half an hour. Although some multi-pathogen detection chips are already commercially available, they may still have limitations such as sensitivity, specificity, and cost. Ongoing technological advancements could make pathogen detection more efficient, accurate, and economical. Continued attention to the development, validation, and optimization of these technologies in clinical practice will better serve patients.

Indexed as

Mycoplasma pneumoniaeNucleic Acid Amplification TechniquesReal-Time Polymerase Chain ReactionRespiratory Tract InfectionsAdenoviridaeAutomationChildChild, PreschoolChinaFemaleHumansInfantMaleRespiratory Syncytial VirusesRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus Infections

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.