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Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes

This study aimed to evaluate the impact of precise treatment administered according to the results of metagenomic next-generation sequencing (mNGS) on the clinical outcomes of patients with spinal infections. In this multicenter retrospective study, the clinical data of 158 patients with spinal infe...

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Autores principales: Zhang, Guang, Zhang, Hongqi, Hu, XiaoJiang, Xu, Dongcheng, Tang, Bo, Tang, Mingxing, Liu, Shaohua, Li, Yanbing, Xu, Wen, Guo, Chaofeng, Gao, Qile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945583/
https://www.ncbi.nlm.nih.gov/pubmed/36844401
http://dx.doi.org/10.3389/fcimb.2023.1076525
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author Zhang, Guang
Zhang, Hongqi
Hu, XiaoJiang
Xu, Dongcheng
Tang, Bo
Tang, Mingxing
Liu, Shaohua
Li, Yanbing
Xu, Wen
Guo, Chaofeng
Gao, Qile
author_facet Zhang, Guang
Zhang, Hongqi
Hu, XiaoJiang
Xu, Dongcheng
Tang, Bo
Tang, Mingxing
Liu, Shaohua
Li, Yanbing
Xu, Wen
Guo, Chaofeng
Gao, Qile
author_sort Zhang, Guang
collection PubMed
description This study aimed to evaluate the impact of precise treatment administered according to the results of metagenomic next-generation sequencing (mNGS) on the clinical outcomes of patients with spinal infections. In this multicenter retrospective study, the clinical data of 158 patients with spinal infections who were admitted to Xiangya Hospital Central South University, Xiangya Boai Rehabilitation Hospital, The First Hospital of Changsha, and Hunan Chest Hospital from 2017 to 2022 were reviewed. Among these 158 patients, 80 patients were treated with targeted antibiotics according to the mNGS results and were assigned to the targeted medicine (TM) group. The remaining 78 patients with negative mNGS results and those without mNGS and negative microbial culture results were treated with empirical antibiotics and assigned to the empirical drug (EM) group. The impact of targeted antibiotics based on the mNGS results on the clinical outcomes of patients with spinal infections in the two groups was analyzed. The positive rate of mNGS for diagnosing spinal infections was significantly higher than that of microbiological culture (X (2)=83.92, P<0.001), procalcitonin (X (2)=44.34, P<0.001), white blood cells (X (2)=89.21, P < 0.001), and IGRAs (Interferon-gamma Release Tests) (X (2) = 41.50, P < 0.001). After surgery, C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) showed a decreasing trend in the patients with spinal infections in both the TM and EM groups. The decrease in CRP was more obvious in the TM group than in the EM group at 7, 14 days, 3, and 6 months after surgery (P<0.05). The decrease in ESR was also significantly obvious in the TM group compared with the EM group at 1 and 6 months after surgery (P<0.05). The time taken for CRP and ESR to return to normal in the TM group was significantly shorter than that in the EM group (P<0.05). There was no significant difference in the incidence of poor postoperative outcomes between the two groups. The positive rate of mNGS for the diagnosis of spinal infection is significantly higher than that of traditional detection methods. The use of targeted antibiotics based on mNGS results could enable patients with spinal infections to achieve a faster clinical cure.
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spelling pubmed-99455832023-02-23 Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes Zhang, Guang Zhang, Hongqi Hu, XiaoJiang Xu, Dongcheng Tang, Bo Tang, Mingxing Liu, Shaohua Li, Yanbing Xu, Wen Guo, Chaofeng Gao, Qile Front Cell Infect Microbiol Cellular and Infection Microbiology This study aimed to evaluate the impact of precise treatment administered according to the results of metagenomic next-generation sequencing (mNGS) on the clinical outcomes of patients with spinal infections. In this multicenter retrospective study, the clinical data of 158 patients with spinal infections who were admitted to Xiangya Hospital Central South University, Xiangya Boai Rehabilitation Hospital, The First Hospital of Changsha, and Hunan Chest Hospital from 2017 to 2022 were reviewed. Among these 158 patients, 80 patients were treated with targeted antibiotics according to the mNGS results and were assigned to the targeted medicine (TM) group. The remaining 78 patients with negative mNGS results and those without mNGS and negative microbial culture results were treated with empirical antibiotics and assigned to the empirical drug (EM) group. The impact of targeted antibiotics based on the mNGS results on the clinical outcomes of patients with spinal infections in the two groups was analyzed. The positive rate of mNGS for diagnosing spinal infections was significantly higher than that of microbiological culture (X (2)=83.92, P<0.001), procalcitonin (X (2)=44.34, P<0.001), white blood cells (X (2)=89.21, P < 0.001), and IGRAs (Interferon-gamma Release Tests) (X (2) = 41.50, P < 0.001). After surgery, C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) showed a decreasing trend in the patients with spinal infections in both the TM and EM groups. The decrease in CRP was more obvious in the TM group than in the EM group at 7, 14 days, 3, and 6 months after surgery (P<0.05). The decrease in ESR was also significantly obvious in the TM group compared with the EM group at 1 and 6 months after surgery (P<0.05). The time taken for CRP and ESR to return to normal in the TM group was significantly shorter than that in the EM group (P<0.05). There was no significant difference in the incidence of poor postoperative outcomes between the two groups. The positive rate of mNGS for the diagnosis of spinal infection is significantly higher than that of traditional detection methods. The use of targeted antibiotics based on mNGS results could enable patients with spinal infections to achieve a faster clinical cure. Frontiers Media S.A. 2023-02-08 /pmc/articles/PMC9945583/ /pubmed/36844401 http://dx.doi.org/10.3389/fcimb.2023.1076525 Text en Copyright © 2023 Zhang, Zhang, Hu, Xu, Tang, Tang, Liu, Li, Xu, Guo and Gao 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
Zhang, Guang
Zhang, Hongqi
Hu, XiaoJiang
Xu, Dongcheng
Tang, Bo
Tang, Mingxing
Liu, Shaohua
Li, Yanbing
Xu, Wen
Guo, Chaofeng
Gao, Qile
Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title_full Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title_fullStr Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title_full_unstemmed Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title_short Clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
title_sort clinical application value of metagenomic next-generation sequencing in the diagnosis of spinal infections and its impact on clinical outcomes
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945583/
https://www.ncbi.nlm.nih.gov/pubmed/36844401
http://dx.doi.org/10.3389/fcimb.2023.1076525
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