Cargando…

Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia

PURPOSE: Severe community-acquired pneumonia (SCAP) is the leading cause of death among patients with infectious diseases worldwide. This study aimed to evaluate the effectiveness of metagenomic next-generation sequencing (mNGS) through detecting pathogens in bronchoalveolar lavage fluid (BALF) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Dongmei, Abudouaini, Maidina, Kerimu, Munire, Leng, Qiuping, Wu, Hongtao, Aynazar, Amar, Zhong, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423567/
https://www.ncbi.nlm.nih.gov/pubmed/37581165
http://dx.doi.org/10.2147/IDR.S421721
_version_ 1785089481514156032
author Lu, Dongmei
Abudouaini, Maidina
Kerimu, Munire
Leng, Qiuping
Wu, Hongtao
Aynazar, Amar
Zhong, Zhiwei
author_facet Lu, Dongmei
Abudouaini, Maidina
Kerimu, Munire
Leng, Qiuping
Wu, Hongtao
Aynazar, Amar
Zhong, Zhiwei
author_sort Lu, Dongmei
collection PubMed
description PURPOSE: Severe community-acquired pneumonia (SCAP) is the leading cause of death among patients with infectious diseases worldwide. This study aimed to evaluate the effectiveness of metagenomic next-generation sequencing (mNGS) through detecting pathogens in bronchoalveolar lavage fluid (BALF) and identifying risk factors for recovery in SCAP patients. PATIENTS AND METHODS: This prospective study recruited 158 SCAP patients admitted to respiratory intensive care unit that were randomly divided into control and study groups, with receiving conventional tests and the same conventional tests plus mNGS, respectively. The diagnostic efficiency of mNGS was evaluated by comparing with conventional tests. Furthermore, univariate and multivariate logistic regression analyses were performed to determine the independent risk factors for recovery in SCAP patients, and a nomogram prediction model was established based on these factors. RESULTS: Within the study group, the pathogen detection rate was significantly higher with mNGS than that with conventional tests (84.81% vs 45.57%, P < 0.001), with a positive coincidence rate of 94.44%. Acinetobacter baumannii (21.52%, 17/79), Candida albicans (17.72%, 14/79), and Klebsiella pneumonia (15.19%, 12/79) were the top three common pathogens detected by mNGS. Of note, the improvement rate of patients in the study group was significantly higher than that in the control group. The further analysis revealed that the increased levels of interleukin-6, blood urea nitrogen, procalcitonin, the longer length of hospital stay, and bacterial infection were independent risk factors for recovery of SCAP patients, while mNGS detection status was a protective factor. The predictive model showed a good performance for the modeling and validation sets. CONCLUSION: Early mNGS exhibited a superior diagnostic efficiency to conventional tests in SCAP patients, which can reduce the risk of death in SCAP patients. Moreover, the clinical factors could also be used for the management and prognosis prediction of SCAP patients.
format Online
Article
Text
id pubmed-10423567
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-104235672023-08-14 Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia Lu, Dongmei Abudouaini, Maidina Kerimu, Munire Leng, Qiuping Wu, Hongtao Aynazar, Amar Zhong, Zhiwei Infect Drug Resist Original Research PURPOSE: Severe community-acquired pneumonia (SCAP) is the leading cause of death among patients with infectious diseases worldwide. This study aimed to evaluate the effectiveness of metagenomic next-generation sequencing (mNGS) through detecting pathogens in bronchoalveolar lavage fluid (BALF) and identifying risk factors for recovery in SCAP patients. PATIENTS AND METHODS: This prospective study recruited 158 SCAP patients admitted to respiratory intensive care unit that were randomly divided into control and study groups, with receiving conventional tests and the same conventional tests plus mNGS, respectively. The diagnostic efficiency of mNGS was evaluated by comparing with conventional tests. Furthermore, univariate and multivariate logistic regression analyses were performed to determine the independent risk factors for recovery in SCAP patients, and a nomogram prediction model was established based on these factors. RESULTS: Within the study group, the pathogen detection rate was significantly higher with mNGS than that with conventional tests (84.81% vs 45.57%, P < 0.001), with a positive coincidence rate of 94.44%. Acinetobacter baumannii (21.52%, 17/79), Candida albicans (17.72%, 14/79), and Klebsiella pneumonia (15.19%, 12/79) were the top three common pathogens detected by mNGS. Of note, the improvement rate of patients in the study group was significantly higher than that in the control group. The further analysis revealed that the increased levels of interleukin-6, blood urea nitrogen, procalcitonin, the longer length of hospital stay, and bacterial infection were independent risk factors for recovery of SCAP patients, while mNGS detection status was a protective factor. The predictive model showed a good performance for the modeling and validation sets. CONCLUSION: Early mNGS exhibited a superior diagnostic efficiency to conventional tests in SCAP patients, which can reduce the risk of death in SCAP patients. Moreover, the clinical factors could also be used for the management and prognosis prediction of SCAP patients. Dove 2023-08-09 /pmc/articles/PMC10423567/ /pubmed/37581165 http://dx.doi.org/10.2147/IDR.S421721 Text en © 2023 Lu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Lu, Dongmei
Abudouaini, Maidina
Kerimu, Munire
Leng, Qiuping
Wu, Hongtao
Aynazar, Amar
Zhong, Zhiwei
Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title_full Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title_fullStr Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title_full_unstemmed Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title_short Clinical Evaluation of Metagenomic Next-Generation Sequencing and Identification of Risk Factors in Patients with Severe Community-Acquired Pneumonia
title_sort clinical evaluation of metagenomic next-generation sequencing and identification of risk factors in patients with severe community-acquired pneumonia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423567/
https://www.ncbi.nlm.nih.gov/pubmed/37581165
http://dx.doi.org/10.2147/IDR.S421721
work_keys_str_mv AT ludongmei clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT abudouainimaidina clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT kerimumunire clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT lengqiuping clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT wuhongtao clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT aynazaramar clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia
AT zhongzhiwei clinicalevaluationofmetagenomicnextgenerationsequencingandidentificationofriskfactorsinpatientswithseverecommunityacquiredpneumonia