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mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study

Whether metagenomic next-generation sequencing (mNGS) could benefit patients with suspected severe central nervous system (CNS) infection in terms of diagnosis and antibiotic treatment remains unknown. We retrospectively analyzed 79 patients with suspected CNS infection and undertook mNGS. The value...

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Autores principales: Feng, Li, Chen, Jiaxin, Luo, Qiuyan, Su, Miao, Chen, Peisong, Lai, Rong, Shen, Cunzhou, Zhou, Hongyan, Wang, Haiyan, Sun, Xunsha, Chen, Ling, Xia, Han, Feng, Huiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985444/
https://www.ncbi.nlm.nih.gov/pubmed/36879645
http://dx.doi.org/10.1515/biol-2022-0578
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author Feng, Li
Chen, Jiaxin
Luo, Qiuyan
Su, Miao
Chen, Peisong
Lai, Rong
Shen, Cunzhou
Zhou, Hongyan
Wang, Haiyan
Sun, Xunsha
Chen, Ling
Xia, Han
Feng, Huiyu
author_facet Feng, Li
Chen, Jiaxin
Luo, Qiuyan
Su, Miao
Chen, Peisong
Lai, Rong
Shen, Cunzhou
Zhou, Hongyan
Wang, Haiyan
Sun, Xunsha
Chen, Ling
Xia, Han
Feng, Huiyu
author_sort Feng, Li
collection PubMed
description Whether metagenomic next-generation sequencing (mNGS) could benefit patients with suspected severe central nervous system (CNS) infection in terms of diagnosis and antibiotic treatment remains unknown. We retrospectively analyzed 79 patients with suspected CNS infection and undertook mNGS. The value of mNGS was investigated in terms of identification of pathogen and guidance for the adjustment of antibiotic treatment. The relationship between the time of initiating mNGS since onset and the Glasgow Outcome Scale (GOS) score after 90-day follow-up were analyzed. Fifty out of 79 cases with suspicious severe CNS infection were finally diagnosed. Despite previous routine laboratory tests, mNGS further promoted the accurate identification of pathogens in 23 cases (47.9%). The sensitivity, specificity, and accuracy of mNGS test in this study were 84.0, 79.3, and 82.3%, respectively. Furthermore, mNGS facilitated the adjustment of empirical antibiotic treatments in 38 cases (48.1%). The time of taking mNGS since onset had an insignificant weak positive correlation with GOS after 90-day follow-up (r = −0.73, P = 0.08). mNGS facilitated the accurate identification of pathogens in suspicious severe CNS infections and promoted the accurate antibiotic therapy even empirical antibiotics were administrated. It should be taken as early as possible to improve the clinical outcome of patients with suspicious severe CNS infection.
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spelling pubmed-99854442023-03-05 mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study Feng, Li Chen, Jiaxin Luo, Qiuyan Su, Miao Chen, Peisong Lai, Rong Shen, Cunzhou Zhou, Hongyan Wang, Haiyan Sun, Xunsha Chen, Ling Xia, Han Feng, Huiyu Open Life Sci Research Article Whether metagenomic next-generation sequencing (mNGS) could benefit patients with suspected severe central nervous system (CNS) infection in terms of diagnosis and antibiotic treatment remains unknown. We retrospectively analyzed 79 patients with suspected CNS infection and undertook mNGS. The value of mNGS was investigated in terms of identification of pathogen and guidance for the adjustment of antibiotic treatment. The relationship between the time of initiating mNGS since onset and the Glasgow Outcome Scale (GOS) score after 90-day follow-up were analyzed. Fifty out of 79 cases with suspicious severe CNS infection were finally diagnosed. Despite previous routine laboratory tests, mNGS further promoted the accurate identification of pathogens in 23 cases (47.9%). The sensitivity, specificity, and accuracy of mNGS test in this study were 84.0, 79.3, and 82.3%, respectively. Furthermore, mNGS facilitated the adjustment of empirical antibiotic treatments in 38 cases (48.1%). The time of taking mNGS since onset had an insignificant weak positive correlation with GOS after 90-day follow-up (r = −0.73, P = 0.08). mNGS facilitated the accurate identification of pathogens in suspicious severe CNS infections and promoted the accurate antibiotic therapy even empirical antibiotics were administrated. It should be taken as early as possible to improve the clinical outcome of patients with suspicious severe CNS infection. De Gruyter 2023-03-03 /pmc/articles/PMC9985444/ /pubmed/36879645 http://dx.doi.org/10.1515/biol-2022-0578 Text en © 2023 the author(s), published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Feng, Li
Chen, Jiaxin
Luo, Qiuyan
Su, Miao
Chen, Peisong
Lai, Rong
Shen, Cunzhou
Zhou, Hongyan
Wang, Haiyan
Sun, Xunsha
Chen, Ling
Xia, Han
Feng, Huiyu
mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title_full mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title_fullStr mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title_full_unstemmed mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title_short mNGS facilitates the accurate diagnosis and antibiotic treatment of suspicious critical CNS infection in real practice: A retrospective study
title_sort mngs facilitates the accurate diagnosis and antibiotic treatment of suspicious critical cns infection in real practice: a retrospective study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985444/
https://www.ncbi.nlm.nih.gov/pubmed/36879645
http://dx.doi.org/10.1515/biol-2022-0578
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