Suppr超能文献

宏基因组下一代测序在重症监护下儿科患者血流感染中的应用价值

Application Value of Metagenomic Next-Generation Sequencing for Bloodstream Infections in Pediatric Patients Under Intensive Care.

作者信息

Nan Xiangzhen, Zhang Yean, Su Nana, Yang Lei, Pan Guoquan

机构信息

Department of Pediatric Intensive Care Unit, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, People's Republic of China.

出版信息

Infect Drug Resist. 2022 Apr 18;15:1911-1920. doi: 10.2147/IDR.S357162. eCollection 2022.

Abstract

PURPOSE

This study aimed to analyze the application value of metagenomic next-generation sequencing (mNGS) as a basis for the proper adjustment of the clinical treatment of bloodstream infections (BSIs) in pediatric patients under intensive care.

METHODS

We retrospectively enrolled 46 pediatric patients with clinically diagnosed BSIs who were hospitalized in the pediatric intensive care unit of the Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University from June 2018 to July 2021. Blood samples were collected for cultivation and for mNGS detection of pathogens.

RESULTS

Among the 46 children, the average turnaround time for blood culture tests was 3.2 days, and the results revealed pathogens in three children (6.5%). The average turnaround time for mNGS was 2.2 days, and pathogens were found in 30 children (65.2%). The difference in positivity rates between blood culture and mNGS was significant (<0.05). Blood culture tests found three pathogens, while mNGS identified 28 pathogens, indicating that mNGS detected significantly more types of pathogens than the traditional diagnostic method for pathogenic microorganisms. In some children, more than one pathogen was detected.

CONCLUSION

mNGS can help identify pathogenic microorganisms associated with BSI in some pediatric patients under intensive care.

摘要

目的

本研究旨在分析宏基因组下一代测序(mNGS)作为重症监护下小儿患者血流感染(BSIs)临床治疗合理调整依据的应用价值。

方法

我们回顾性纳入了2018年6月至2021年7月在温州医科大学附属第二医院育英儿童医院儿科重症监护病房住院的46例临床诊断为BSIs的小儿患者。采集血样进行病原菌培养及mNGS检测。

结果

46例患儿中,血培养检测的平均周转时间为3.2天,结果显示3例患儿(6.5%)检出病原菌。mNGS的平均周转时间为2.2天,30例患儿(65.2%)检出病原菌。血培养与mNGS的阳性率差异有统计学意义(<0.05)。血培养检测出3种病原菌,而mNGS鉴定出28种病原菌,表明mNGS检测出的病原菌种类明显多于传统病原微生物诊断方法。部分患儿检测出不止一种病原菌。

结论

mNGS有助于识别部分重症监护下小儿患者中与BSI相关的病原微生物。

相似文献

1
Application Value of Metagenomic Next-Generation Sequencing for Bloodstream Infections in Pediatric Patients Under Intensive Care.
Infect Drug Resist. 2022 Apr 18;15:1911-1920. doi: 10.2147/IDR.S357162. eCollection 2022.
3
Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection.
Front Cell Infect Microbiol. 2023 Feb 10;13:1117987. doi: 10.3389/fcimb.2023.1117987. eCollection 2023.
5
Diagnostic Value of Metagenomic Next-Generation Sequencing for Pulmonary Infection in Intensive Care Unit and Non-Intensive Care Unit Patients.
Front Cell Infect Microbiol. 2022 Aug 15;12:929856. doi: 10.3389/fcimb.2022.929856. eCollection 2022.
6
Metagenomic next-generation sequencing technology for detection of pathogens in blood of critically ill patients.
Int J Infect Dis. 2021 Feb;103:81-87. doi: 10.1016/j.ijid.2020.11.166. Epub 2020 Nov 20.
8
The diagnostic value of metagenomic next⁃generation sequencing in infectious diseases.
BMC Infect Dis. 2021 Jan 13;21(1):62. doi: 10.1186/s12879-020-05746-5.

引用本文的文献

1
The impact of neutrophil count on the results of metagenomic next-generation sequencing in immunocompromised febrile children.
Heliyon. 2024 Jun 11;10(12):e32816. doi: 10.1016/j.heliyon.2024.e32816. eCollection 2024 Jun 30.
2
A case report of diagnosis of cat-scratch disease using metagenomic next-generation sequencing.
Front Cell Infect Microbiol. 2024 Jan 15;13:1322651. doi: 10.3389/fcimb.2023.1322651. eCollection 2023.
3
Performance of next-generation sequencing for diagnosis of blood infections by .
Front Cell Infect Microbiol. 2023 Dec 1;13:1278482. doi: 10.3389/fcimb.2023.1278482. eCollection 2023.
4
Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection.
Front Cell Infect Microbiol. 2023 Feb 10;13:1117987. doi: 10.3389/fcimb.2023.1117987. eCollection 2023.
5
The diagnostic value of blood metagenomic next-generation sequencing in patients with acute hematogenous osteomyelitis.
Front Cell Infect Microbiol. 2023 Jan 27;13:1106097. doi: 10.3389/fcimb.2023.1106097. eCollection 2023.
7
Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease.
Front Cell Infect Microbiol. 2022 Sep 16;12:946849. doi: 10.3389/fcimb.2022.946849. eCollection 2022.

本文引用的文献

1
The Microbiology of Bloodstream Infection: 20-Year Trends from the SENTRY Antimicrobial Surveillance Program.
Antimicrob Agents Chemother. 2019 Jun 24;63(7). doi: 10.1128/AAC.00355-19. Print 2019 Jul.
2
Laboratory validation of a clinical metagenomic sequencing assay for pathogen detection in cerebrospinal fluid.
Genome Res. 2019 May;29(5):831-842. doi: 10.1101/gr.238170.118. Epub 2019 Apr 16.
6
Rapid Detection of Powassan Virus in a Patient With Encephalitis by Metagenomic Sequencing.
Clin Infect Dis. 2018 Feb 10;66(5):789-792. doi: 10.1093/cid/cix792.
7
Diagnosis of Sepsis with Cell-free DNA by Next-Generation Sequencing Technology in ICU Patients.
Arch Med Res. 2016 Jul;47(5):365-371. doi: 10.1016/j.arcmed.2016.08.004.
8
Attributable mortality of central line associated bloodstream infection: systematic review and meta-analysis.
Infection. 2015 Feb;43(1):29-36. doi: 10.1007/s15010-014-0689-y. Epub 2014 Oct 21.
9
The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform.
PLoS One. 2014 Oct 20;9(10):e110240. doi: 10.1371/journal.pone.0110240. eCollection 2014.
10
Actionable diagnosis of neuroleptospirosis by next-generation sequencing.
N Engl J Med. 2014 Jun 19;370(25):2408-17. doi: 10.1056/NEJMoa1401268. Epub 2014 Jun 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验