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Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection

OBJECTIVE: To evaluate the diagnostic value of metagenomic next-generation sequencing (mNGS) in sepsis and bloodstream infection (BSI). METHODS: A retrospective analysis of patients diagnosed with sepsis and BSI at the First Affiliated Hospital of Zhengzhou University from January 2020 to February 2...

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Autores principales: Qin, Cuihong, Zhang, Shuguang, Zhao, Yingying, Ding, Xianfei, Yang, Fei, Zhao, Yangchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950395/
https://www.ncbi.nlm.nih.gov/pubmed/36844396
http://dx.doi.org/10.3389/fcimb.2023.1117987
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author Qin, Cuihong
Zhang, Shuguang
Zhao, Yingying
Ding, Xianfei
Yang, Fei
Zhao, Yangchao
author_facet Qin, Cuihong
Zhang, Shuguang
Zhao, Yingying
Ding, Xianfei
Yang, Fei
Zhao, Yangchao
author_sort Qin, Cuihong
collection PubMed
description OBJECTIVE: To evaluate the diagnostic value of metagenomic next-generation sequencing (mNGS) in sepsis and bloodstream infection (BSI). METHODS: A retrospective analysis of patients diagnosed with sepsis and BSI at the First Affiliated Hospital of Zhengzhou University from January 2020 to February 2022 was conducted. All the patients underwent blood culture and were divided into mNGS group and non-mNGS group according to whether mNGS was performed or not. The mNGS group was further divided into early group (< 1 day), intermediate group (1–3 days), and late group (> 3 days) according to the time of mNGS inspection. RESULTS: In 194 patients with sepsis and BSI, the positive rate of mNGS for identifying pathogens was significantly higher than that of blood culture (77.7% vs. 47.9%), and the detection period was shorter (1.41 ± 1.01 days vs. 4.82 ± 0.73 days); the difference was statistically significant (p < 0.05). The 28-day mortality rate of the mNGS group (n = 112) was significantly lower than that of the non-mNGS group (n = 82) (47.32% vs. 62.20%, p = 0.043). The total hospitalization time for the mNGS group was longer than that for the non-mNGS group (18 (9, 33) days vs. 13 (6, 23) days, p = 0.005). There was no significant difference in the ICU hospitalization time, mechanical ventilation time, vasoactive drug use time, and 90-day mortality between the two groups (p > 0.05). Sub-group analysis of patients in the mNGS group showed that the total hospitalization time and the ICU hospitalization time in the late group were longer than those in the early group (30 (18, 43) days vs. 10 (6, 26) days, 17 (6, 31) days vs. 6 (2, 10) days), and the ICU hospitalization time in the intermediate group was longer than that in the early group (6 (3, 15) days vs. 6 (2, 10) days); the differences were statistically significant (p < 0.05). The 28-day mortality rate of the early group was higher than that of the late group (70.21% vs. 30.00%), and the difference was statistically significant (p = 0.001). CONCLUSIONS: mNGS has the advantages of a short detection period and a high positive rate in the diagnosis of pathogens causing BSI and, eventually, sepsis. Routine blood culture combined with mNGS can significantly reduce the mortality of septic patients with BSI. Early detection using mNGS can shorten the total hospitalization time and the ICU hospitalization time of patients with sepsis and BSI.
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spelling pubmed-99503952023-02-25 Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection Qin, Cuihong Zhang, Shuguang Zhao, Yingying Ding, Xianfei Yang, Fei Zhao, Yangchao Front Cell Infect Microbiol Cellular and Infection Microbiology OBJECTIVE: To evaluate the diagnostic value of metagenomic next-generation sequencing (mNGS) in sepsis and bloodstream infection (BSI). METHODS: A retrospective analysis of patients diagnosed with sepsis and BSI at the First Affiliated Hospital of Zhengzhou University from January 2020 to February 2022 was conducted. All the patients underwent blood culture and were divided into mNGS group and non-mNGS group according to whether mNGS was performed or not. The mNGS group was further divided into early group (< 1 day), intermediate group (1–3 days), and late group (> 3 days) according to the time of mNGS inspection. RESULTS: In 194 patients with sepsis and BSI, the positive rate of mNGS for identifying pathogens was significantly higher than that of blood culture (77.7% vs. 47.9%), and the detection period was shorter (1.41 ± 1.01 days vs. 4.82 ± 0.73 days); the difference was statistically significant (p < 0.05). The 28-day mortality rate of the mNGS group (n = 112) was significantly lower than that of the non-mNGS group (n = 82) (47.32% vs. 62.20%, p = 0.043). The total hospitalization time for the mNGS group was longer than that for the non-mNGS group (18 (9, 33) days vs. 13 (6, 23) days, p = 0.005). There was no significant difference in the ICU hospitalization time, mechanical ventilation time, vasoactive drug use time, and 90-day mortality between the two groups (p > 0.05). Sub-group analysis of patients in the mNGS group showed that the total hospitalization time and the ICU hospitalization time in the late group were longer than those in the early group (30 (18, 43) days vs. 10 (6, 26) days, 17 (6, 31) days vs. 6 (2, 10) days), and the ICU hospitalization time in the intermediate group was longer than that in the early group (6 (3, 15) days vs. 6 (2, 10) days); the differences were statistically significant (p < 0.05). The 28-day mortality rate of the early group was higher than that of the late group (70.21% vs. 30.00%), and the difference was statistically significant (p = 0.001). CONCLUSIONS: mNGS has the advantages of a short detection period and a high positive rate in the diagnosis of pathogens causing BSI and, eventually, sepsis. Routine blood culture combined with mNGS can significantly reduce the mortality of septic patients with BSI. Early detection using mNGS can shorten the total hospitalization time and the ICU hospitalization time of patients with sepsis and BSI. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950395/ /pubmed/36844396 http://dx.doi.org/10.3389/fcimb.2023.1117987 Text en Copyright © 2023 Qin, Zhang, Zhao, Ding, Yang and Zhao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Qin, Cuihong
Zhang, Shuguang
Zhao, Yingying
Ding, Xianfei
Yang, Fei
Zhao, Yangchao
Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title_full Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title_fullStr Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title_full_unstemmed Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title_short Diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
title_sort diagnostic value of metagenomic next-generation sequencing in sepsis and bloodstream infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950395/
https://www.ncbi.nlm.nih.gov/pubmed/36844396
http://dx.doi.org/10.3389/fcimb.2023.1117987
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