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The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease

BACKGROUND: A retrospective analysis was conducted to explore the sensitivity and specificity of metagenomic next-generation sequencing (mNGS) in blood, cerebrospinal fluid, and pleural effusion samples in children with invasive pneumococcal disease (IPD), and the impact of detection timing on progn...

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Autores principales: Guo, Fang, Kang, Lei, Xu, Meixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753463/
https://www.ncbi.nlm.nih.gov/pubmed/35070842
http://dx.doi.org/10.21037/tp-21-533
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author Guo, Fang
Kang, Lei
Xu, Meixian
author_facet Guo, Fang
Kang, Lei
Xu, Meixian
author_sort Guo, Fang
collection PubMed
description BACKGROUND: A retrospective analysis was conducted to explore the sensitivity and specificity of metagenomic next-generation sequencing (mNGS) in blood, cerebrospinal fluid, and pleural effusion samples in children with invasive pneumococcal disease (IPD), and the impact of detection timing on prognosis and cost. METHODS: Children with IPD admitted to Hebei Children’s Hospital from 1 January 2017 to 1 March 2021 were allocated to 1 of 3 groups according to the clinical symptoms and lesions (Group 1: bacteremia; Group 2: meningitis; Group 3: pleurisy). Taking Alere BinaxNow(®) Streptococcus pneumoniae (S. pneumoniae) antigen detection and blood culture as the gold standard, receiver operating characteristic (ROC) was used to establish the diagnostic value of mNGS. RESULTS: A total of 96 cases were enrolled in the study, comprising Group 1 (n=65), Group 2 (n=17), and Group 3 (n=14). The positive rate of mNGS test was 62.5% (n=60), and the total coincidence rate was 75.0%. Delayed mNGS was found to have no significant effect on the 30-day survival rate; however, the species-specific read number (SSRN) of S. pneumoniae detected by mNGS in the early stage of the disease was higher, and it could significantly reduce the hospitalization days and costs (P<0.05). CONCLUSIONS: The sensitivity and specificity of mNGS are high in the identification of S. pneumoniae in blood, cerebrospinal fluid, and pleural effusion samples, and the SSRN of S. pneumoniae is related to the interval from onset to sample collection. Early mNGS detection has no significant effect on the 30-day survival rate among children with IPD, but it can reduce hospitalization costs and duration.
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spelling pubmed-87534632022-01-21 The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease Guo, Fang Kang, Lei Xu, Meixian Transl Pediatr Original Article BACKGROUND: A retrospective analysis was conducted to explore the sensitivity and specificity of metagenomic next-generation sequencing (mNGS) in blood, cerebrospinal fluid, and pleural effusion samples in children with invasive pneumococcal disease (IPD), and the impact of detection timing on prognosis and cost. METHODS: Children with IPD admitted to Hebei Children’s Hospital from 1 January 2017 to 1 March 2021 were allocated to 1 of 3 groups according to the clinical symptoms and lesions (Group 1: bacteremia; Group 2: meningitis; Group 3: pleurisy). Taking Alere BinaxNow(®) Streptococcus pneumoniae (S. pneumoniae) antigen detection and blood culture as the gold standard, receiver operating characteristic (ROC) was used to establish the diagnostic value of mNGS. RESULTS: A total of 96 cases were enrolled in the study, comprising Group 1 (n=65), Group 2 (n=17), and Group 3 (n=14). The positive rate of mNGS test was 62.5% (n=60), and the total coincidence rate was 75.0%. Delayed mNGS was found to have no significant effect on the 30-day survival rate; however, the species-specific read number (SSRN) of S. pneumoniae detected by mNGS in the early stage of the disease was higher, and it could significantly reduce the hospitalization days and costs (P<0.05). CONCLUSIONS: The sensitivity and specificity of mNGS are high in the identification of S. pneumoniae in blood, cerebrospinal fluid, and pleural effusion samples, and the SSRN of S. pneumoniae is related to the interval from onset to sample collection. Early mNGS detection has no significant effect on the 30-day survival rate among children with IPD, but it can reduce hospitalization costs and duration. AME Publishing Company 2021-12 /pmc/articles/PMC8753463/ /pubmed/35070842 http://dx.doi.org/10.21037/tp-21-533 Text en 2021 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Guo, Fang
Kang, Lei
Xu, Meixian
The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title_full The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title_fullStr The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title_full_unstemmed The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title_short The application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
title_sort application value of metagenomic next-generation sequencing in children with invasive pneumococcal disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753463/
https://www.ncbi.nlm.nih.gov/pubmed/35070842
http://dx.doi.org/10.21037/tp-21-533
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